Pubmed abstracts for Protein-Protein Interaction search result :

Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
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Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.61871913
Based on the pattern of distribution of the SG proteins in patients with LGMD2C and 2D , and on the observed decreased abundance of dystrophin through WB in some sarcoglycans ( SG ) patients , we have recently suggested that alpha , beta and delta subunits of sarcoglycan complex might be more closely associated and that gamma SG might interact more directly with dystrophin . 0.61871913^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.58967143
The correlation between phenotype and type of deletion agreed with the reading frame theory , except for two BMD and two DMD cases . . 0.58967143^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.98413973
We have investigated the possible association between BMD and two polymorphisms in 135 beta thalassaemic patients : ( 1 ) a substitution G > Tau in a regulatory region of the COLIA 1 gene encoding for the major protein of bone ( type 1 collagen ) , and ( 2 ) a one base deletion in intron 4 ( 713 8del C ) of transforming growth factor beta 1 ( TGF beta 1 ) gene . 0.98413973^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The absence of dystrophin leads to a dramatic reduction of the dystrophin associated proteins ( 156DAG , 59DAP , 50DAG , 43DAG and 35DAG ) in the sarcolemma of patients with Duchenne muscular dystrophy and mdx mice . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystrophin associated glycoprotein complex is classified into two subcomplexes : the dystroglycan complex ( 156DAG and 43DAG ) and the sarcoglycan complex ( 50DAG , A3b , and 35DAG ) . ^^^ We examined muscles from five SCARMD patients and found that dystrophin and 43DAG were present in almost normal levels while 35DAG and the newly identified protein A3b in addition to 50DAG were absent or greatly reduced . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Selective defect in dystrophin associated glycoproteins 50DAG ( A 2 ) and 35DAG ( A 4 ) in the dystrophic hamster : an animal model for severe childhood autosomal recessive muscular dystrophy ( SCARMD ) . ^^^ Antibodies against dystrophin , utrophin and DAGs including 50DAG ( A 2 ) , 43DAG ( A3a ) and 35DAG ( A 4 ) were employed for the examination . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A monoclonal antibody MA 4 2 against a dystrophin associated protein 35DAG ( A 4 ) was established and applied to examine the distribution of 35DAG in monkey tissue and its expression in DMD patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Here we demonstrate the co localization of Dp 116 ( a 116 kDa protein product of the DMD gene ) , full size utrophin , alpha and beta dystroglycan , 59DAP and 35DAG in a thin rim surrounding the outermost layer of myelin sheath of peripheral nerve fibers . ^^^ Dystrophin associated proteins are comprised of an extracellular glycoprotein of 156 kDa ( 156DAG ) , transmembrane glycoproteins of 50 kDa ( 50DAG ) , 43 kDa ( 43DAG ) and 35 kDa ( 35DAG ) , and a cytoskeletal protein of 59 kDa ( 59DAP ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The dystrophin associated proteins are classified into three groups : ( 1 ) alpha and beta dystroglycan , ( 2 ) adhalin , 35DAG and A3b , and ( 3 ) members of the syntrophin family . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the 4 cases adhalin was completely absent in muscle sections , whereas dystrophin and the other members of the dystrophin associated protein complex were normal , except for the 35 kDa dystrophin associated glycoprotein which was decreased as usually observed in SCARMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We investigated the expression of the DAPs beta dystroglycan , alpha sarcoglycan , gamma sarcoglycan and syntrophin as well as utrophin in the muscles of 13 Duchenne muscular dystrophy ( DMD ) carriers ( with variable percentages of dystrophin deficient fibers and with a range of clinical symptoms ) , 2 Becker muscular dystrophy ( BMD ) carriers ( expressing a highly truncated protein in some fibers ) , 2 girls with a DMD like phenotype , and 11 BMD carriers with almost normal dystrophin expression ( reduced or patchy distribution in a few fibers only and rare dystrophin deficient fibers ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
One form of this disorder , limb girdle muscular dystrophy type 2C ( LGMD 2C ) , is prevalent in northern Africa and has been shown to be associated with a single mutation in the gene encoding the dystrophin associated protein gamma sarcoglycan . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A previous study identified a single base pair deletion in the gene encoding the dystrophin associated protein gamma sarcoglycan in a number of Tunisian muscular dystrophy patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : We studied muscle biopsy specimens from 18 patients with LGMD using immunofluorescence with antibodies against dystrophin C terminus , beta dystroglycan , alpha sarcoglycan , gamma sarcoglycan , and the laminin subunits merosin , beta 1 , and gamma 1 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These regions showed weak staining for dystrophin , beta dystroglycan as well as alpha and gamma sarcoglycan . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We combined magnetic resonance ( MR ) imaging and phosphorus magnetic resonance spectroscopy ( 31P MRS ) to study skeletal muscle in seven patients with limb girdle muscular dystrophy ( LGMD ) with a variable deficiency of the alpha , beta , and gamma sarcoglycan but normal dystrophin expression on muscle biopsy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To reduce ascertainment bias , biopsies with dystrophic ( n=131 ) and non dystrophic myopathic ( n=71 ) changes were studied with antibodies to dystrophin , alpha , beta , and gamma sarcoglycan , beta dystroglycan , and laminin alpha 2 , and results were correlated with clinical phenotype . ^^^ Two patients with mutations identified in gamma sarcoglycan had abnormal dystrophin ( by immunocytochemistry and immunoblot ) , showing that abnormalities of dystrophin may be a secondary phenomenon . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
INTRODUCTION : Limb Girdle Muscular Dystrophy type 2C ( LGMD2C ) is an autosomal recessive dystrophy due to the deficit of gamma sarcoglycan , one of the proteins of the dystrophin associated proteins complex ( DAP ) . ^^^ RESULTS : The patients presented a severe muscular dystrophy with a dystrophic pattern in the muscle biopsy , normal immunolabeling for dystrophin , very weak for alpha , beta and delta sarcoglycan and absent for gamma sarcoglycan . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Gamma sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin . gamma Sarcoglycan is a transmembrane , dystrophin associated protein expressed in skeletal and cardiac muscle . ^^^ Vital staining with Evans blue dye revealed that muscle lacking gamma sarcoglycan developed membrane disruptions like those seen in dystrophin deficient muscle . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In this study we have examined a large population of Italian myopathic patients to determine the frequency of ( alpha , beta and gamma sarcoglycan deficiency and to correlate molecular defects with clinical phenotypes ; to exclude the presence of primary dystrophinopathies both genetic and immunological analysis of dystrophin was performed . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Using catalytic histochemistry and immunohistochemistry on rat skeletal muscle NOS 1 was colocalized in the costameres together with dystrophin , beta dystroglycan , alpha , beta and gamma sarcoglycan , beta 1 integrin , vinculin , paxillin and caveolin 3 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Ultrastructural localization of alpha , beta and gamma sarcoglycan and their mutual relation , and their relation to dystrophin , beta dystroglycan and beta spectrin in normal skeletal myofiber . ^^^ Ultrastructural localization of alpha , beta and gamma sarcoglycan and their mutual relation , and their relation to dystrophin , beta dystroglycan and beta spectrin were investigated in normal skeletal myofibers . ^^^ Double immunogold labeling disclosed the close association of alpha , beta and gamma sarcoglycan each other and alpha , beta , gamma sarcoglycan with dystrophin or beta dystroglycan , and this was confirmed by statistical analysis . ^^^ This study demonstrated that alpha , beta and gamma sarcoglycan are closely located to one another and to dystrophin and beta dystroglycan at the muscle plasma membrane . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Immunocytochemistry demonstrated normal spectrin and dystrophin , reduced alpha sarcoglycan and absent gamma sarcoglycan indicating a gamma sarcoglycanopathy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The DGC relative levels for the slow muscle soleus and the fast muscle EDL differed significantly : dystrophin , beta dystroglycan , and gamma sarcoglycan levels were 130 % , 110 % and 120 % higher in the soleus , respectively . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To determine if delta sarcoglycan deficiency occurred in other world populations , to identify the range of mutations and clinical phenotypes , and to test for the biochemical consequences of delta sarcoglycan gene mutations , we studied Duchenne like and limb girdle muscular dystrophy patients who we had previously shown not to exhibit gene mutations of dystrophin , alpha , beta , or gamma sarcoglycan for delta sarcoglycan mutations ( n = 54 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Desmin immunoreactivity ( IR ) was detected by 3 days in vitro ( DIV 3 ) , IR for developmental heavy chain myosin , vimentin , utrophin , and beta dystroglycan , as well as alpha , beta , and gamma sarcoglycan , a day later . delta Sarcoglycan was found by DIV 7 ; dystrophin could be detected only by DIV 11 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Within the better preserved parts of the muscles , i . e . , those without signs of necrotic processes , dystrophin , spectrin , and some of the dystrophin associated proteins ( beta dystroglycan , alpha sarcoglycan , and gamma sarcoglycan ) disappeared from sarcolemma of many fibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Immunohistochemical staining demonstrated the synthesis and correct subsarcolemmal localization of dystrophin and gamma sarcoglycan in the mdx mouse after intramuscular delivery of antisense oligoribonucleotide : liposome complexes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystrophin , beta , delta sarcoglycan and beta dystroglycan are first expressed in the myotome at the 4th week of human embryogenesis , followed by gamma sarcoglycan and merosin at the 6th week of development ; alpha sarcoglycan appears only at the level of the muscular fibre at the end of the embryonic period . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This ischemic loss of dystrophin was a specific event in that no ischemic loss of sarcolemmal alpha sarcoglycan , gamma sarcoglycan , alphaDG , or betaDG was observed . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Therefore , we investigated all three intracellular / extracellular linkage systems of the sarcolemma using antibodies against dystrophin , beta dystroglycan , gamma sarcoglycan , vinculin , beta 1 integrin , laminin , and spectrin . ^^^ Immunoconfocal microscopy and Western blotting revealed that the rank order of sensitivity was the following : dystrophin , beta dystroglycan , gamma sarcoglycan , vinculin , spectrin , integrin and laminin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
RESULTS : We validate the temporal Hotelling T 2 test on muscular gene expression data from four mouse strains which were profiled at different ages : dystrophin , beta sarcoglycan and gamma sarcoglycan deficient mice , and wild type mice . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Animals lacking dystrophin or gamma SG were used to identify DGC components critical for sensing dynamic mechanical load . ^^^ Extensor digitorum longus muscles from 7 wk old normal ( C 57 ) , dystrophin null ( mdx ) , and gamma SG null ( gsg ( / ) ) mice were subjected to a series of eccentric contractions , after which ERK1 / 2 phosphorylation levels were determined . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A complete deficiency was found in 9 patients : 2 / 12 with classical merosin positive congenital MD ( CMD ) , 1 / 12 with Severe Childhood Autosomal Recessive MD ( DLMD ) , but with a positive IF pattern for the proteins of the sarcoglycan complex : 3 / 14 with mild limb girdie MD ( 1LGMD2A and 2 yet unclassified ) , 1 / 10 with sarcoglycanopathies ( LGMD2C ) , and 2 / 6 with Xp 21 Duchenne MD ( DMD ) . ^^^ Patients within the same family , and with the same disease ( DMD , LGMD2A , LGMD2C ) , were discordant for ACTN 3 deficiency . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Kinetic and electrophoretic studies indicate that the PK isozyme found in the serum from affected patients and from heterozygotes for the DMD gene is mainly the M 1 type PK , which is the only PK isozyme found in skeletal muscle and brain and the major component from myocardium . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum CPK was measured in 135 families with Duchenne muscular dystrophy ( DMD ) and 19 with the Becker type ( BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The results show that type IIC fibers were remarkably increased and type IIB fibers was deficiency in DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Sample size , type of fabric , and fabric pore size affected pH , DMD , and CD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Becker type muscular dystrophy ( BMD ) is reported in two brothers . ^^^ Mild neuronal losses in the spinal cord may explain the mixed type of neurogenic myogenic features in the skeletal muscles of adult BMD patients . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The central portion of the dystrophin gene locus is a preferential site for deletions causing progressive muscular dystrophy of the Duchenne type ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A third type of calcium current could be recorded on a non negligible number of human skeletal muscle cells ( normal and Duchenne dystrophic ( DMD ) ) in primary culture . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The muscle type but not the brain type dystrophin mRNA is found in cloned skeletal muscle cells and its presence is correlated with the appearance of multinucleated fibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This mRNA differs in coding content and tissue distribution from the known muscle type and brain type 14 kb DMD mRNAs which code for dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A 10 year follow up study by orthogonal Frank lead electrocardiography was performed on 25 patients with progressive muscular dystrophy of the Duchenne type ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Muscle biopsy demonstrated Becker type muscular dystrophy with dystrophin of low molecular weight . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Polymerase chain reaction ( PCR ) was used to study the presence of gene deletion ( the most prominent type of mutations ) in some families afflicted by Duchenne muscular dystrophy / Becker muscular dystrophy ( DMD / BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Absence of dystrophin in two patients with Becker type Xp 21 muscular dystrophy . ^^^ Two patients with Xp 21 muscular dystrophy Becker type showed absence of dystrophin in muscle biopsy tested with 4 antibodies ( polyclonal anti 60 kDa , monoclonal against the rod domain , the C terminus and the N terminus ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Clustered dystrophin deficient fibers were constituted to regenerating basophilic fibers ( mainly type 2C fiber ) based on histochemical stainings . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
One possible mechanism for the high frequency of DMD in Indians is the presence of repetitive elements in the wild type gene which predispose to mutations . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) was significantly decreased in Type 1 diabetic men and women as well in Type 2 men , when compared with a non diabetic matched population . ^^^ In Type 1 women , BMD was reduced from 0 . 97 + / 0 . 10 to 0 . 90 + / 0 . 10 g . cm 2 ( p = 0 . 023 ) in the femoral neck . ^^^ In Type 2 men , BMD in Ward ' s triangle was also significantly lower than in controls : 0 . 69 + / 0 . 14 vs 0 . 76 + / 0 . 19 g . cm 2 , respectively ( p = 0 . 001 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The second type has the features of the typical Duchenne muscular dystrophy ( DMD ) and has abnormal dystrophin . ^^^ The first type is characterized by normal dystrophin assays and affects girls and boys in an autosomal recessive pattern of inheritance . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystrophin transcripts were shown to be alternatively spliced in a pattern characteristic of both tissue type and developmental stage . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The relative tissue content of dystrophin has been evaluated in the slow twitch soleus ( primarily type 1 fibers ) and fast twitch vastus lateralis ( primarily type IIb fibers ) muscles of the rat and mouse , as well as in human biopsy samples from the vastus lateralis and gluteus maximus muscles , using a sensitive immunochemical assay . ^^^ This difference is not entirely explained by the higher total sarcolemmal surface of the smaller soleus muscle type 1 fibers , and is therefore attributed to a higher content of dystrophin in the type 1 fibers compared to type IIb fibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Treatment of this type of muscular dystrophy may soon mean the routine use of steroids and later include direct injection of an artificial gene for dystrophin . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
When these two were subclassified into five subgroups , different results were seen in terms of BMD value in the proximal femur and fracture types ; intracapsular fracture type 1 showed BMD values equivalent to those of controls ; on the other hand , type 2 showed significantly lower BMD value than controls , and the BMD distribution in the proximal femur among the extracapsular fracture subgroups 1 3 differed , although all of them showed significantly lower BMD values than controls . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The total number of boiled egg fibers was 235 with 192 in DMD and 43 in other disorders . 197 of 235 ( 83 . 8 % ) had the same type for both inner and outer parts and remaining 38 ( 16 . 2 % ) had different types for their inner parts . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the predicted secondary structure of the mRNA precursor , exon 19 of dystrophin Kobe is paired with intron sequences , whereas a large part of exon sequence from wild type is paired with itself and folded into a large hairpin structure . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Immunohistochemical studies of muscle biopsies from patients with Duchenne muscular dystrophy ( DMD ) showed that the number of alpha actinin positive type IIb fibers was essentially normal in preclinical patients . ^^^ ATPase histochemistry showed that a few type IIb fibers were present in muscle from symptomatic DMD patients but lacked the fast isoform of alpha actinin . ^^^ The data suggest that type IIb fibers are affected early in DMD . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The increasing rate of the changes in the P complex together with those in TU U was ascertained in patients suffering from DM without CSHD , DMD , CHD in the presence of both type 1 and type 2 DM . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Gait has been continued on 1 year and 7 months to 3 years and 8 months according to the evolving type of Duchenne Muscular Dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Degenerating and regenerating muscle fibers , in serotonin induced myopathy ( SM ) of rats , were investigated histochemically , immunohistochemically and electron microscopically with polyclonal antibodies against dystrophin , type 4 collagen and laminin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A unique Japanese family with both Fukuyama type congenital muscular dystrophy ( FCMD ) and Duchenne muscular dystrophy ( DMD ) is described . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The most frequent causes for the 10 linked muscular dystrophy of the allelic Duchenne ( DMD ) or Becker ( BMD ) type are partial deletions of the dystrophin gene . ^^^ The splicing of exon 46 to exon 51 resulted in a reading frameshift , indicating that this mutation is likely to be responsible for a DMD type of dystrophy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CT findings of muscular dystrophy : limb girdle type ( LG ) , myotonic type ( MYD ) and Duchenne type ( DMD ) ] . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In this study , we have taken advantage of this phenomenon , called illegitimate transcription , to analyze the muscle type dystrophin mRNA in easily accessible cells such as lymphoid cells , fibroblasts , and peripheral blood cells from Duchenne and Becker muscular dystrophies with known internal gene deletion . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The complete 14 kb cDNA for the gene causing the 10 linked recessive muscular dystrophy ( MD ) type Duchenne ( DMD ) and Becker ( BMD ) has recently been cloned and made available for deletion / duplication screening in patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The subjects were 7 cases of muscular dystrophy ; 1 Duchenne type ( DMD ) , 3 limb girdle type , 2 facioscapulohumeral type ( FSH ) , 1 Fukuyama type ( FCMD ) ; and 1 myotonic dystrophy ( MyD ) ; 5 mitochondrial myopathies ; 11 inflammatory myopathies including 6 polymyositis and 3 myopathy associated with collagen disease ; 5 endocrinological myopathies including 2 periodic paralysis ; and , 11 cases of neurogenic amyotrophies [ 4 amyotrophic lateral sclerosis ( ALS ) , 4 spinal progressive muscular atrophy ( SPMA ) and 3 other types ] . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Many patients with aluminum induced osteopathy had type 2 patterns , with decreased BMD in cortical bone . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Because the daily activity of patients with rapidly progressive type of muscular dystrophy such as DMD is at a very low level , they do not require pacing therapy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Study of 55 cases of progressive muscular dystrophies ( 34 Duchenne , 12 Duchenne with residual dystrophin and 9 Becker patients ) comparing age , age at the initial symptoms , duration of symptoms , levels of serum enzymes , degree of disability measured by the Vignos and Archibald scale , and the type and amount of dystrophin found in the muscle biopsies by immunofluorescence . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We examined the expression of dystrophin by immunohistochemical and immunoblot analyses in the skeletal and cardiac muscles of Xmdx / X+ heterozygous mice , which were obtained by mating male mdx mice ( Xmdx / Y ) with female wild type mice ( X+ / X+ ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
She had two sons with Duchenne type muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The activity of serum creatine phosphokinase ( CPK ) was determined in 80 female members of 23 families with affected members of Duchenne type muscular dystrophy ( DMD ) and compared with the values of a control group of 100 unaffected women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystonia musculorum deformans ( DMD ) is an idiopathic movement disorder which usually involves pediatric age group and progresses to the generalized type . ^^^ These findings suggest that some patients diagnosed as idiopathic spasmodic torticollis are in an early stage of DMD and that this particular type progresses more likely to the generalized form than other types of adult onset DMD . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study included 15 patients with Duchenne muscular dystrophy ( DMD ) , 8 patients with Fukuyama type congenital muscular dystrophy ( FCMD ) and 2 sisters with non Fukuyama type congenital muscular dystrophy ( nFCMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Cardiac involvement is common in patients with Duchenne type muscular dystrophy ( DMD ) . ^^^ We named it ' cardiac type ' DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The result of AO staining showed that the number of regenerating IIc type fibers in DMD increased by 5 20 % . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The BMD appears to be similar in different caucasian populations when the same type of equipment is used , but the values can not be compared with the results obtained with other equipment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Of these three major groups only the slow twitch ( type 1 ; 14 / 24 ; 58 % ) and the fast twitch intermediate ( type IIA ; 3 / 24 ; 13 % ) fibres were found in the DMD muscle , indicating that fast twitch fibres of type IIB were in very low proportion in DMD muscle . 4 . ^^^ The results demonstrate that DMD leads to marked diminution in the ability of most individual skeletal muscle fibres to develop tension , and causes changes in the overall fibre type distribution in afflicted muscles . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This sort of deletion ( designated as DMD Kobe ) might be classified as a new type of DMD gene abnormality . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral content ( BMC ) and bone mineral density ( BMD ) of lumbar spine have been measured in 695 healthy postmenopausal and 64 type 1 osteoporotic Belgian , Caucasian females . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Our results demonstrate that the brain type promoter of the dystrophin gene is highly specific to neurons , in which there is a significant increase in the amount of brain specific messenger RNA during the course of in vitro maturation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The similarity in clinical features of 10 linked Becker muscular dystrophy ( BMD ) and the autosomal recessive limb girdle ( LGD ) type of adult muscular dystrophy makes differential diagnosis of the isolated male case difficult . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In orders to search for possible events in the pathogenesis of Duchenne muscular dystrophy ( DMD ) , the activity of erythrocyte superoxide dismutase has been determined in thirty seven patients and fifteen carriers of DMD , comparison to fourty five age matched normal controls , seventeen cases of infantile , Kugelberg Welander type spinal muscle atrophy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
There was a very strong correlation of clinical diagnoses with the type of dystrophin abnormality ; all Duchenne muscular dystrophy patient muscle contained no detectable dystrophin , Becker muscular dystrophy patient muscle had clearly abnormal dystrophin , and unrelated diseases showed normal dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) was assessed in 28 women with type 2 diabetes mellitus and compared to 207 age matched nondiabetic women . ^^^ Thus , women with type 2 diabetes are not at increased risk for diminished BMD and may be protected against bone loss . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Sequential changes of the cardiomyopathy in Duchenne muscular dystrophy by 201Tl myocardial SPECT ] . 201Tl myocardial SPECT was performed to evaluate cardiomyopathy in Duchenne type of progressive muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Following the strategy outlined in an accompanying paper , we studied 32 10 linked muscular dystrophy families ( 29 Duchenne [ DMD ] and three Becker [ BMD ] type ) for abnormalities of HindIII and BglII fragments detected by the entire dystrophin cDNA . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Of the approximately 170 families with 10 linked muscular dystrophy of the Duchenne ( DMD ) and Becker ( BMD ) type in Finland , we have studied 90 unrelated patients for intragenic deletions by using the cDNA probes described by Koenig et al . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Fibre type differentiation was carried out on 20 biopsies from Duchenne Muscular Dystrophy ( DMD ) sufferers using the acid preincubated reaction for myofibrillar ATPase . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Cell and fiber type distribution of dystrophin . ^^^ The dystrophin content of brain and spinal cord , however , is found not to correlate with any type of muscle cell , and it is suggested that neurons express dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In Duchenne ' s muscular dystrophy ( DMD ) as well as in congenital muscular dystrophies ( CMD ) the extensive proliferation of connective tissue consisted mainly of fibronectin and type 1 and 3 collagens . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We investigated the relationship of CT determined vertebral bone mineral density ( BMD ) , type of renal osteodystrophy , N terminal PTH levels and fracture history in 31 dialysis patients . ^^^ A low BMD was not predictive of fracture history but the type of renal osteodystrophy was . ^^^ In conclusion we found that patients with osteitis fibrosa had increased BMD compared to normal while those with low turnover osteodystrophy had decreased BMD , but that the N terminal PTH level was a better predictor of the type of bone disease present than was BMD . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 2B deficiency was again common in DMD as well as occurring in some BMD cases . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The chromosomes of a male patient who suffers from Duchenne muscular dystrophy ( DMD ) with a molecular deletion were examined with an improved high resolution R type replication banding technique . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Right heart catheterization was performed in 8 patients with progressive muscular dystrophy of the Duchenne type ( DMD ) at the advanced stage . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Haplotypes for 7 flanking and 16 `` intragenic ' ' 10 linked DNA polymorphisms were determined in 204 members of 31 families with Duchenne ( DMD ) and 27 members of 4 families with Becker type muscular dystrophy ( BMD ) and combined with CK and pedigree data to estimate carrier and fetal risks . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The same types of collagen , i . e . , type 1 and type 3 were synthesized by myogenic cells from DMD patients and controls . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The role of collagen type 3 and 4 ( Coll 3 , 4 ) in Duchenne muscular dystrophy ( DMD ) was investigated by the indirect immunofluorescence technique ( IIF ) both in muscle biopsies and derived cell cultures . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Using these criteria the families from Erfurt and Warsaw could be clearly separated into classical Duchenne ( DMD ) and classical Becker ( BMD ) type patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Wild type , dematiaceous Wangiella dermatitidis ( DMD 368 ) and melanin deficient mutant ( Mel 3 ) strains derived therefrom were compared for pathogenic and virulent effects in Swiss albino mice following intravenous infection . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The identification of a mouse 10 linked mutant showing muscular dystrophy , mdx , has provided a candidate mouse genetic homologue to the DMD locus ; the relatively mild pathological features of mdx suggest it may have more in common with mutations of the Becker muscular dystrophy type at the same human locus , however . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Degenerating and regenerating fibers were not as frequent in FCMD as in DMD , whereas the number of type 2C fibers in the former was about twice that in the latter . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In women aged over 40 years , compared with adequate controls of the same body type , real time ultrasound imaging may provide additional evidence and thus help in the detection of BMD carriers . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The overall findings differed from those of the Fukuyama type congenital muscular dystrophy ( FCMD ) and Duchenne muscular dystrophy ( DMD ) in which more active fiber necrosis and regeneration are seen . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It appears , therefore , that at least one type of membrane repair system functions normally in DMD fibroblasts . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Undifferentiated type 2C fibers , which are dark on ATPase staining with both alkaline and acid preincubation , comprised on average 16 . 1 % of the muscle fibers in 12 patients with Duchenne muscular dystrophy ( DMD ) . ^^^ Since most of the opaque ( hyaline , dark ) fibers , which previously have been thought to be precursors of necrotic fibers , behaved as differentiated type 1 or type 2 fibers , the presence of type 2C fibers in DMD may not reflect `` dedifferentiation ' ' of fiber type , but rather indicate an active regenerating process . ^^^ It remains unknown whether the type 2C fiber segments in DMD develop into fully differentiated functional fibers or remain as incompletely regenerated fibers . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It is useful to distinguish three types in DMD : major involvement or type 1 , severe involvement or type 2 , moderate or mild involvement or type III . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A balanced de novo ( 10 ; 9 ) translocation was observed in a patient with progressive muscular dystrophy of Duchenne ' s type ( DMD ) , Turner ' s syndrome , epilepsy and mental retardation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Recently , Pickard et al reported decreased `` capping ' ' in lymphocytes from patients with Duchenne type muscular dystrophy ( DMD ) as well as female carriers of the DMD trait . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Although there was no qualitative difference in the muscle histochemistry between FCMD and Duchenne muscular dystrophy ( DMD ) , there was a greater proportion of type 2C fibers and fibrosis was present at the early infantile stage of FCMD . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Although early onset type MMD and DMD fibroblasts have lower maximal cell densities than fibroblasts from age matched control individuals do in medium containing 10 % fetal bovine serum , we could not reveal any abnormalities in exogeneous cholesterol requirements for proliferation of MMD fibroblasts . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The behavior of the tubular system in muscles from six patients with Fukuyama type congenital muscular dystrophy ( FCMD ) was examined by electron microscopy using a lanthanum nitrate stain for a comparison with that in Duchenne muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The increased hydroxylation of proline residues of collagen ( composed of type 1 and type 3 ) could be the cause for the enhanced degradation of collagen in DMD fibroblasts . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 1 fibers of DMD were more diverse in the composition of MLC than those of controls ; 55 % of type 1 fibers of DMD contained distinct fast type MLC 3 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Carriers of muscular dystrophy occasionally revealed a slight increase in anti type 3 collagen fluorescence , but no abnormalities in collagen disposition were observed in foetuses `` at risk ' ' for DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In normal fibroblasts , approximately 48 % of the total CK activity was of the MM type , 40 % was of the BB type , and 12 % was of the MB type with no significant differences apparent between normal and DMD groups . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the DMD group 30 % presented a severe restrictive respiratory syndrome associated with a life span of less than 20 years ( Type 1 ) , 40 % had a serious restrictive syndrome and variable mortality ( Type 2 ) , and the remaining 30 % had a moderate restrictive respiratory syndrome ( Type 3 ) . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In many fibers of the biopsy specimens from patients with DMD , activation by strontium revealed a pattern intermediate between those shown by the usual type 1 and type 2 fibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Total activity of creatine kinase ( CK ) , lactate dehydrogenase ( LD ) , aldolase ( Ald ) , glutamico oxaloacetic transaminase ( GOT ) , and LD isoenzyme distribution was studied in serum and muscle biopsies from normal persons and 117 patients with different types of muscular dystrophy : 82 Duchenne type ( DMD ) , 12 BEcker type , 7 facioscapulohumeral ( FSHMD ) , and 16 limb girdle ( LGMD ) . ^^^ The mean muscle M / H ratio was 6 . 4 in controls , 1 . 8 in early DMD , 0 . 1 in late DMD , 3 . 0 in Becker type , 3 . 8 in FSHMD and 3 . 9 in LGMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The features of regional wall motion abnormalities of the left ventricle were analysed in 11 patients of congestive cardiomyopathy ( CCM ) in comparison with 22 patients of progressive muscular dystrophy ( DMD ) of Duchenne type who showed an abnormal motion of the left ventricle by echocardiography . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It was based on 514 males with Duchenne type muscular dystrophy ( DMD ) from five of nineteen hospitals for muscular disease in Japan . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The vacuolar membrane stained positively with antibodies raised to dystrophin , dystrophin associated glycoproteins , laminin and type 4 collagen , and it was identical to the sarcolemma and its basal lamina . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The basis for a type of familial dilated cardiomyopathy without substantial skeletal muscle involvement , caused by a mutation in the dystrophin gene , has been explored . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the Type 2 diabetic postmenopausal women , fat mass and lean body mass correlated positively with total body bone mineral density ( BMD ) ( r = 0 . 53 and 0 . 68 ) , and with total body bone mineral content ( BMC ) ( r = 0 . 58 and 0 . 77 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
For this type of transplantation , no significant difference in the percentage of normal dystrophin mRNA was observed between immunosuppressed mice and those not immunosuppressed . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) was measured by dual energy 10 ray absorptiometry and bone turnover was assessed by serum markers of bone metabolism ( osteocalcin , procollagen 1 peptide , cross linked telopeptide of type 1 collagen and alkaline phosphatase activity ) , In women with adult onset GHD ( N = 19 ) and in men with childhood onset GHD ( N = 15 ) , total body , spine and hip BMD was significantly reduced at baseline compared to Swedish age and sex matched control material . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
DESIGN : A nonrandomized , prospective , descriptive study of 11 patients with spinal muscular atrophy type 2 ( SMA 2 ) and 14 patients with Duchenne muscular dystrophy ( DMD ) . ^^^ Although 7 of the 11 patients with SMA type 2 had FVC below 1 . 2 L and some of them had an EK sum score higher ( indicating more disability ) than some patients with DMD who needed mechanical ventilation , none of them required mechanical ventilation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We studied changes in blood gas data from 32 patients with Duchenne type muscular dystrophy ( DMD ) , who were followed for more than 5 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Characterization of the recombinant C terminal domain of dystrophin : phosphorylation by calmodulin dependent protein kinase 2 and dephosphorylation by type 2B protein phosphatase . ^^^ Type 2C phosphatase ( SMP 2 ) and type 1 protein phosphatases [ SMP 3 , SMP 4 , and myosin associated phosphatase ( PP1M ) of smooth muscle and skeletal muscle protein phosphatase 1c ] were ineffective in dephosphorylating the C terminal region of dystrophin . ( ABSTRACT TRUNCATED AT 250 WORDS ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) of the spine and the different regions of interest ( ROI ) of the hip were measured by dual energy 10 ray absorptiometry in 278 healthy Belgian postmenopausal women and 93 postmenopausal type 1 osteoporotic females in order to : a ) determine the normal range for lumbar and hip BMD values ; b ) define an `` hypothetical ' ' fracture threshold in this population ; c ) determine the preferential region to be considered for clinical use in type 1 osteoporosis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Localisation of striated muscle type dystrophin . ^^^ We investigated dystrophin localization , using three antisera raised against different domains of skeletal muscle type of dystrophin , in the smooth muscle structures of the skin , using immunohistochemical methods with monoclonal antibodies against dystrophin , in 24 patients with various neuromuscular diseases , and in a normal control . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) was studied in 21 children and adolescents with type 1 diabetes and in age and sex matched healthy controls . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Knowledge of risk was associated with the type of disease in the family ( p < 0 . 001 ) ( inheritance of DMD was poorly understood by relevant subjects ) and was positively associated with the participant ' s level of education ( p < 0 . 05 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The type and the level of injury of the cervical spine were not related to the changes of BMD , age or gender of the patient , whereas the local osteoporosis was mostly reversible in the follow up evaluation of 5 6 months . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Distinction of Becker ' s muscular dystrophy from limb girdle type by dystrophin analysis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Multiplex PCR of the DMD gene showed in frame type deletion from exon 45 to 48 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum osteocalcin and C terminal propeptide of type 1 procollagen did not correlate with the observed differences in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It is concluded that lumbar BMD is normal in type 1 diabetic patients , although the degree of metabolic control , age and duration of the disease may affect it . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Immunoblotting studies demonstrated dystrophin of low molecular mass and quantity in BMD patients with deletion mutations , while a low quantity of dystrophin with an apparent wild type molecular mass was observed in nearly half the BMD patients without detectable deletions . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystrophin analysis together with a genetic DMD locus study led us to diagnose Becker type muscular dystrophy , with truncated dystrophin and a gene deletion extending from exon 45 to 48 . ^^^ Prevalent cardiac involvement in dystrophin Becker type mutation . ^^^ Dystrophin analysis together with a genetic DMD locus study led us to diagnose Becker type muscular dystrophy , with truncated dystrophin and a gene deletion extending from exon 45 to 48 . ^^^ Prevalent cardiac involvement in a Becker type mutation of the dystrophin gene further confirms clinical variability of dystrophinopathies . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The results indicate that in this animal model of type 1 diabetes , spine and femoral BMD do not increase comparable to control despite weight and blood glucose control . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The expression of embryonic , fetal , and fast / slow myosin isoforms in type IIC fibers in TDLMD and DMD suggest different fiber type transformations in these two diseases . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To address the physiologic responses associated with these effects on bone mineral density ( BMD ) , we assessed mRNA transcripts reflecting activities of osteoblasts ( type 1 collagen , osteocalcin , osteopontin , and alkaline phosphatase ) , osteoclasts [ tartrate resistant acid phosphatase ( TRAP ) ] , and cell proliferation ( histone H 4 ) in the spine and femur of these rats . ^^^ CT increased spine BMD while increasing type 1 collagen and decreasing TRAP and histone mRNAs . ^^^ In the femur , where CT had no effect on BMD , it decreased type 1 collagen and histone H 4 mRNA but did not affect TRAP . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Unusual expression and very mild course of Xp 21 muscular dystrophy ( Becker type ) in a 60 year old man with 26 percent deletion of the dystrophin gene . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Methods of molecular genetics ( Southern ' s hybridization and DNA amplification by the PCR method ) were used to search the DNA of patients suffering from the Duchenne ( DMD ) and the Becker ( BMD ) type of progressive muscular dystrophy for deletions in the dystrophin gene . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Muscle biopsies on the injected and control muscles obtained 1 yr after the injections showed only a small increase in the number of dystrophin positive fibers and the presence of numerous small type 2 fibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These included 249 cases of Duchenne muscular dystrophy ( DMD ) , 3 Becker muscular dystrophies ( BMD ) , 14 limb girdle muscular dystrophies ( LGMD ) , 3 fascioscapulohumeral muscular dystrophies ( FSH ) , 18 Fukuyama type congenital muscular dystrophies ( FCMD ) and 17 myotonic dystrophies ( MyD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 1 vacuoles , found in all diseases , were lined by laminin , dystrophin , and beta spectrin and arose from infoldings of the basal lamina and sarcolemma into splitting or branching fibers . ^^^ Type 2 vacuoles were lined by dystrophin and beta spectrin and were most common in adult acid maltase deficiency , chloroquine myopathy , and periodic paralysis . ^^^ Type 3 vacuoles were lined by small patches of dystrophin and beta spectrin and occurred in any vacuolar myopathy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
As bisphosphonates are able to decrease bone resorption , especially in high bone turnover states , we investigated the potential effects of etidronate disodium ( EHDP ) on L T 4 induced bone loss in the rat model by assessing BMD and gene expression of osteoblast ( osteocalcin , osteopontin , type 1 collagen , and alkaline phosphatase ) , osteoclast ( tartrate resistant acid phosphatase ) , and cell growth ( histone ) markers in the skeleton . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To address potential involvement of muscle basal lamina and membrane cytoskeleton proteins in the etiology of non dystrophinopathy muscular dystrophies , we examined the immunostaining intensity and distribution of laminin subunits ( A , B 1 , B 2 and M ) , type 4 collagen , dystrophin and spectrin in skeletal muscle biopsies from 64 myopathic patients ( 17 Fukuyama congenital muscular dystrophy : FCMD , 13 congenital muscular dystrophy unrelated to FCMD : other CMD , 16 Duchenne muscular dystrophy : DMD , and 18 other neuromuscular diseases . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
PCR analysis demonstrated the presence of the muscle type dystrophin mRNA in all AF cell cultures . ^^^ The brain type dystrophin mRNA was also detected in some of these cultures . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In both the DMD and BMD carriers , a significant reduction in type 2B fibres , as well as an increase in type 2C and fetal myosin containing fibres was found as has also been reported in DMD patients . ^^^ Altered dystrophin expression was observed more frequently in type 2 than type 1 fibres . ^^^ Dystrophin deficiency was found in a high percentage of type 2C fibres as well as in all fibres expressing fetal myosin ; this suggests that dystrophin deficient fibres are more susceptible to degeneration , leading to regeneration . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The programme included among other things age , bone age , bone maturity difference ( BMD : difference age minus bone age ) height , type and severity of asthma ( measured by means of scope of therapy ) . ^^^ The degree of BMD showed a significant dependence on age and type of asthma but not on the duration of the disease , severity or glucocorticoid therapy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It is located more than 2000 kb 3 ' to the muscle and brain type dystrophin promoters and only 150 kb from the 3 ' end of the gene , suggesting that in most DMD patients the expression of Dp 71 is unaffected . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Identification of the gene coding for the protein ( dystrophin ) which is lacking or abnormal in Duchenne or Becker type human muscular dystrophies was a decisive turning point in neuro muscular pathology . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In 1990 we examined 25 patients with Duchenne Muscular Dystrophy ( DMD ) or Spinal Muscular Atrophy type 2 ( SMA 2 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Three cases out of 15 with Duchenne muscular dystrophy ( DMD ) , and one case out of 3 with limb girdle type muscular dystrophy which had previously been diagnosed on the basis of clinical data , were found to have non dystrophin related muscular dystrophy , and Becker muscular dystrophy ( BMD ) , respectively . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Two other patients with a deletion of exon 47 showed progressive muscular atrophy and weakness ; they were considered to be typical BMD in both clinical features and the type of gene deletion . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The type of testosterone treatment was also not associated with significant differences in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Identification of the defective gene and the absent gene product dystrophin can substantiate the clinical evidence for manifesting 10 linked Duchenne type muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The 5 ' sequences , corresponding to the first exon , of DT in the retina was mainly the brain type , whereas in the 3 ' region of DT that corresponds to the C terminal domain of dystrophin , some additional RT PCR products were detected . ^^^ It was thus concluded that dystrophin really expresses in the mouse retina and most of the retinal dystrophin proteins belong to the brain type isoform . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The severe Duchenne muscular dystrophy ( DMD ) and the more benign Becker type ( BMD ) are allelic conditions , controlled by a defective gene at Xp 21 , caused by the absence ( DMD ) or a defect in quantity or quality ( BMD ) of the protein dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
One type of hereditary cardiomyopathy is caused by defects in the dystrophin gene in Duchenne and Becker muscular dystrophy patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the two Becker dystrophy type biopsies the expression of dystrophin varied . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These results suggest that the dystrophin expression is abnormal in this group of children and that this type of abnormalities can not be differentiated from early Becker muscular dystrophy nor childhood autosomal recessive muscular dystrophy through immunohystochemistry alone . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD of patients with continuous and mixed types of OPLL was higher than that of those with the segmental type . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystroglycan expression in the wild type and mdx mouse neural retina : synaptic colocalization with dystrophin , dystrophin related protein but not laminin . ^^^ Using immunohistochemistry , we find that alpha and beta DG are expressed in the outer plexiform layer of both wild type and mdx retina , where both dystrophin and dystrophin related protein ( DRP ) , but not laminin are present . ^^^ Western blot analysis revealed the expression of several dystrophin isoforms in wild type and mdx retina , possibly explaining the unaltered expression of alpha and beta dystroglycan in the mdx central nervous system ( CNS ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
After the first 3 months of trial , BMD was unaffected , and the urinary output of collagen pyridinoline , deoxypyridinoline cross links , and hydroxyproline ( all markers of bone resorption ) were increased , but serum markers , the carboxy terminal telopeptide of type 1 collagen ( marker of bone resorption ) and that of bone specific alkaline phosphatase ( marker of bone formation ) did not change . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The most significant correlation with BMD was the type of physical activity . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We explored the relation between BMD and parity , age , body mass index ( BMI ) , type of menopause , and level of exercise . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The effects of fasting for 48 h were investigated in C57BL / 10 ( wild type ) and age matched C57BL / 10 dystrophin deficient ( mdx ) mice . 2 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Representative values of H ( E ) were determined for patients undergoing each type of BMD procedure . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The authors carried out a study of children with progressive muscular dystrophy of Duchenne type ( DMD ) , giving special attention to physiatrical follow up , having in mind that the practice of exercises has been debated very much in the specialized literature . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp 21 muscular dystrophy patients ( Duchenne and Becker type ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The correlation between phenotype and type of deletion agreed with the reading frame theory except for one DMD case . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Slopes for total bone mineral density ( BMD ) for each scan type ranged between 0 . 994 and 1 . 029 , the best value being found for forearm ( 1 . 000 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In dystrophinopathy [ DMD and BMD ] , positivity was seen mainly in type 2 fibers with no correlation to the opaque fibers and histochemical Ca2+ loading fibers in DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The spectacular progress concerning dystrophin and its pathology , the dystrophinopathies , has led to a somewhat arbitrarily separated heterogeneous group of nondystrophinopathic muscular dystrophies that currently comprise the Emery Dreifuss type , the nosologically heterogeneous autosomal recessive limb girdle muscular dystrophy , the severe childhood autosomal recessive muscular dystrophy , the merosin positive and negative congenital muscular dystrophies , the autosomal recessive distal muscular dystrophy of Miyoshi , the facio scapulo humeral muscular dystrophy , and myotonic dystrophy , both the adult and neonatal variants . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To assess the mechanisms of osteopenia in inflammatory bowel disease ( IBD ) , the serum markers of bone formation ( osteocalcin and carboxyterminal propeptide of type 1 procollagen ( PICP ) ) and bone degradation ( carboxyterminal telopeptide of type 1 collagen ( ICTP ) ) , the bone mineral density ( BMD ) of the lumbar spine and the proximal femur and calcium intake of 150 unselected IBD patients and 73 healthy controls were investigated . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We have examined healthy women ( 51 premenopausal women and 30 postmenopausal women ; age 28 59 ) for lumbar bone mineral density ( BMD ) by dual energy 10 ray absorptiometry ( DXA ) and assessed metabolic bone markers , such as type 1 procollagen carboxy terminal propeptide ( P1CP ) , pyridinoline ( PYR ) , deoxypyridinoline ( DPYR ) , osteocalcin ( BGP ) and alkaline phosphatase ( ALP ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The result of analysis of quantification method of the first type showed that age and menopause had a marked effect on BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In conclusion , the higher BMD demonstrated in the ice hockey players seems to be site specific and may well be associated with the type and magnitude of loading from predominantly ice hockey . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The age normalized BMD findings ( Z scores ) were correlated with multiple variables , including measures of growth and nutrition , type of malignancy , and various treatments , including use of steroids , methotrexate , or cranial irradiation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Lack of dystrophin , a protein localized to the inner surface of the sarcolemma of the muscle fiber , is the cause of Duchenne type muscular dystrophy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The serum markers of bone formation ( carboxy terminal propeptide of type 1 collagen , PICP ) and resorption ( pyridinoline cross links containing telopeptide of type 1 collagen , ICTP ) , as well as urinary resorption markers , pyridinoline ( Pyr ) and deoxypyridinoline ( Dpyr ) , were studied in 78 year old women with high ( n = 18 ) and low ( n = 17 ) bone mineral density ( BMD ) measured from the calcaneus and tibia . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We concluded that ( 1 ) physical activity during adolescence may contribute significantly towards increasing BMD of athletes and ( 2 ) the training type may provide a specific stimulus for increasing BMD at specific localized sites experienced in training . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The bone mineral density ( BMD ) of the vertebrae ( L 2 4 ) , proximal femur , and total body bone mineral content ( tb BMC ) ( women only ) , as well as urinary N terminal crosslinked fragment of type 1 collagen ( NTX ) , serum osteocalcin , bone isozyme of alkaline phosphatase , and caboxyterminal propeptide of type 1 procollagen levels were measured . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density of the vertebral body in the osteoporotic fracture group was compared with that in the osteoporotic group to investigate the correlation among BMD , age distribution , and fracture type , and to estimate fracture threshold in the osteoporotic fracture group . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Soccer playing and training appears to have a beneficial effect on bone mass in young females , and it seems that there is a site specific skeletal response to the type of loading subjected to each BMD site . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured bone mineral density ( BMD ) at lumbar ( L 2 L4 ) vertebrae and proximal femurs of 385 healthy Chinese women aged 40 70 years and 156 healthy Chinese men aged 20 85 , and four markers bone alkaline phosphatase isozyme ( BAP ) , procollagen 1 C terminal propeptide ( PICP ) , osteocalcin ( BGP ) in serum , and a bone resorption marker , urinary cross linked N telopeptide of type 1 collagen ( NTX ) , of these subjects . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : To investigate calcium intake and its association with bone mineral density ( BMD ) and the type and extent of the disease in patients with inflammatory bowel disease ( IBD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At baseline , lumbar spine , femoral neck , trochanter , and Ward ' s triangle BMD values were decreased , and serum bone Gla protein , bone alkaline phosphatase , and urinary pyridinoline , deoxypyridinoline , and N terminal telopeptide of type 1 collagen were increased compared with control values ( by paired t test , P = 0 . 02 , 0 . 03 , 0 . 01 , 0 . 05 , 0 . 002 , 0 . 02 , 0 . 02 , 0 . 007 , and 0 . 006 , respectively ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Translational reading frame of the dystrophin gene was derived from ' Border type ' analysis of exons flanking the intragenic deletions . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the present study , the relationship between the BsmI , ApaI , and TaqI polymorphisms in the VDR gene , and the bone mineral density ( BMD ) at the lumbar spine , the femoral neck ( FN ) , and the proximal radius was investigated in a large group of elderly women ( 75 . 5 + / 5 . 0 years ) of Caucasian origin and in 84 Type 1 osteoporotic women ( 66 . 6 + / 8 . 4 years ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The demonstrated high bone mass seems to be related to the type of loading subjected to each BMD site . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We studied the immunolocalization of Dp 116 ( a 116 kDa protein product of the dystrophin gene ) , vinculin , talin , vimentin , desmin , spectrin and titin in the sural nerve biopsies of 25 patients with peripheral neuropathies of different origin . 4 patients presented with HMSN type 1 , 4 with HMSN type 2 , 2 with HNPP , 4 with CIDP , 5 with chronic axonal neuropathy of unknown origin , 3 with vasculitic neuropathy , 3 with diabetic neuropathy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Neurophysiological abnormalities did not correlate with type , site and size of alteration in the dystrophin gene . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
However , the function of brain type dystrophin remains insufficiently clear . ^^^ With this background , in order to study the cell specific regulation of brain type dystrophin expression in mice , we generated transgenic mice carrying the 2 . 1 kb 5 ' fragment of the mouse brain type dystrophin gene , fused to the coding region of the bacterial lacZ gene . ^^^ These results suggest that the 2 . 1 kb 5 ' fragment of the mouse brain type dystrophin gene contains the regulatory element required for its expression in the cerebral cortex , but not in the hippocampus . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD was assessed with dual energy 10 ray absorptiometry , and serum concentrations of osteocalcin , carboxy terminal propeptide of type 1 procollagen ( PICP ) , and carboxy terminal cross linked telopeptide of type 1 collagen ( ICTP ) were measured . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Ultrasound has also been shown to correlate better with the type of hip fracture ( intertrochanteric or cervical ) than BMD and to provide comparable diagnostic sensitivity to spine BMD in vertebral fractures . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
No significant differences were found in lumbar spine BMD between normals and alcoholics regardless of the type of alcohol consumption and duration of alcoholism . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Neuronal type nitric oxide synthase mu is enriched in fast twitch fibers and binds to syntrophin , a component of the sarcolemmal dystrophin glycoprotein complex . ^^^ Interestingly , the highest levels of neuronal type nitric oxide synthase mu in muscle are found complexed with dystrophin at the sarcolemma of intrafusal fibers in muscle spindles . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The myocardial cells observed were classified into four types , according to staining pattern : normal for both actin and dystrophin ( Type 1 ) : normal for actin , but abnormal for dystrophin ( Type 2 ) ; abnormal for actin , but normal for dystrophin ( Type 3 ) ; and abnormal for both actin and dsytrophin ( Type 4 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The main goal of this study was to determine and characterise the types of mutations in two monogenic human disorders : cystic fibrosis ( CF ) and Duchenne / Becker muscular dystrophy ( DMD , BMD ) and the susceptibility allele frequency in a polygenic disease : type 1 insulin dependent diabetes mellitus ( IDDM ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Patients with DMD or SMA type 3 should be stabilized after loss of walking ability and definitive confinement to wheel chair , if the curve is more than 20 degrees 30 degrees Cobb and progressive and forced vital capacity ( FVC ) is > 35 % . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In order to study the regulatory mechanism of developmental and tissue specific expression of the muscle type dystrophin gene in mice , transgenic mice were generated carrying the 900 bp genomic fragment derived from the muscle type dystrophin promoter region fused to the bacterial lacZ gene . ^^^ Based on these findings , the relationship between defects in muscle type promoter and the diseases caused by abnormal dystrophin expression is discussed . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Long term testosterone treatment maintained BMD in the age dependent reference range in all 72 hypogonadal men , independent of the type of hypogonadism . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Moreover , the absence of labelled adherens junctions indicates the presence of full length dystrophin at this type of junction in the normal mouse superior cervical ganglion . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Duchenne ( DMD ) and Becker ( BMD ) type muscular dystrophies are allelic 10 linked recessive disorders caused by mutations in the gene encoding dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Skeletal involvement was studied by measuring : ( a ) the main biomarkers of bone turnover : serum alkaline phosphatase total activity ( AP ) , bone GLA protein ( BGP ) , serum carboxy terminal propeptide of type 1 collagen ( PICP ) , serum type 1 cross linked N telopeptide ( ICTP ) , and urinary pyridinoline and deoxypyridinoline corrected for creatinine ( Pyr / Cr , D Pyr / Cr ) and urinary calcium / creatinine ratio ( Ca / Cr ) ; ( b ) bone mineral density ( BMD ) , as measured by quantitative computed tomography both at lumbar spine and distal radius , and by dual 10 ray absorptiometry both at lumbar spine and at three femoral sites ( Ward ' s triangle , femoral neck , and great trochanter ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The Bombelli hypertrophic type showed significantly better improvement than the atrophic type , but there was no correlation between the value of the BMD , and the postoperative result . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Biochemical bone markers ( pyridinoline [ PYR ] , deoxypyridinoline [ DPYR ] , procollagen type 1 carboxy terminal peptide [ PICP ] ) and bone mineral density ( BMD ) were measured at baseline and at 6 , 12 , and 24 months . ^^^ Initial ESR influenced the percent change in BMD at 1 year ( r = 0 . 35 , P = 0 . 05 ) , while cumulative steroid dose , mean ESR , and type of steroid used did not . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Previous studies on adult rat and mouse skeletal muscles have shown the spatial association of nitric oxide synthase ( NOS ) 1 to the dystrophin complex ( DC ) in the sarcolemma of type 2 fibers and , in combination with the NMDA receptor 1 ( NMDAR 1 ) , an accumulation of the enzyme at the neuromuscular junctions ( NMJ ) of this fiber type . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In addition , we tested the hypothesis that allelic variation at the Vitamin D receptor ( VDR ) , and the type 1 collagen gene ( COL1A1 and COL1A2 ) loci influence BMD . ^^^ While several studies suggest that VDR genotype is an important determinant of BMD , we did not find this association in our population , nor did we identify an association between allelic variation at the type 1 collagen gene loci and BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In conclusion , treatment with high doses of T 4 caused BMD to decrease substantially , particularly at the femur , whereas near physiological doses of T 4 prevented bone loss associated with OVX , and regardless of bone type ( trabecular or cortical ) , the skeleton site seems to be a more important determinant of the effects of thyroid hormone on bone mass . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Reduced bone mineral density ( BMD ) , termed diabetic osteopenia , has been reported in patients with insulin dependent ( Type 1 ) diabetes mellitus ( IDDM ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Although the age and sex matched BMD was different among the kinds of HRA ( 98 . 6 % for cimetidine , 101 . 3 % for ranitidine , and 85 . 5 % for famotidine ) , the relationship between the BMD and type of drug was not significant by multivariate analysis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD , serum PRL , testosterone , dihydrotestosterone , and osteocalcin ( OC ) , and urinary cross linked N telopeptides of type 1 collagen ( Ntx ) levels were measured before and every 6 months during treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured bone mineral density ( BMD ) using dual energy 10 ray absorptiometry ( DXA ) , bone resorption using urinary cross linked N terminal telopepides of type 1 collagen ( NTx ) , and bone formation using osteocalcin ( BGP ) and bone alkaline phosphatase ( BAP ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Histochemical analysis revealed that the dystrophin deficiency was associated with a decrease in the percentage of type 1 myofibers in all three cats . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We examined the association of BMD levels and their change over a 3 year period , and polymorphisms of the estrogen receptor ( ER ) , vitamin D receptor ( VDR ) , type 1 collagen , osteonectin , osteopontin , and osteocalcin genes in pre and perimenopausal women who were part of the Michigan Bone Health Study , a population based longitudinal study of BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In particular the colocalization of vinculin and talin and the presence of the integrins confers to this system the description of the adherens junctions type cell ECM , while the presence of dystrophin in correspondence to both A and 1 bands with Z line negative is important for the stabilization of the membrane of the skeletal muscle fiber . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured bone mineral density ( BMD ) of the lumbar spine ( L 2 L4 ) , and serum ICTP , carboxyterminal propeptide of type 1 procollagen ( PICP ) and other conventional serum biochemical markers , e . g . bone gla protein ( BGP ) , alkaline phosphatase , calcium and phosphate at the entry and 6 months later . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BACKGROUND : Most patients with progressive muscular dystrophy of the Duchenne type ( DMD ) die of respiratory failure at approximately 20 years of age . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Low incidence of osteoporosis in a two year follow up of early community based patients with rheumatoid arthritis . 52 patients with early rheumatoid arthritis ( RA ) were followed with regular measurements of bone mineral density ( BMD ) and serum markers of type 1 collagen metabolism in order to determine whether they develop osteoporosis during the first two years of the disease course and if the changes in type 1 collagen metabolites reflect the alterations in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Muscle type promoter and its first intron abnormalities in dystrophin gene in patients with Duchenne muscular dystrophy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
STUDY DESIGN : Lumbar spine ( L 1 L4 ) and femoral neck BMD , serum osteocalcin ( OC ) , urinary cross linked N telopeptides of type 1 collagen ( Ntx ) levels were evaluated at study entry , in patients and controls , and were repeated after 6 and 12 months in the 39 patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Polymorphisms at the vitamin D receptor ( VDR ) , estrogen receptor , ( ER ) , collagen type 1 , and interleukin 6 ( IL 6 ) gene loci have been correlated to BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
No association was observed between BMD and time elapsed since BMT , type of conditioning regimen , gonadal function , steroid intake or graft versus host disease . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aim of this study was to determine the correlation between changes in collagen metabolites ( ICTP , mature cross linked carboxy terminal telopeptide of type 1 collagen ; PINP , the amino terminal propeptide of type 1 procollagen ) and bone mineral density ( BMD ) in 206 pre and post menopausal breast cancer patients with non metastatic disease . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study aimed to explore multiple determinants of BMD ( bone mineral density ) in 99 women with long standing type 1 diabetes , recruited from a population based register of insulin users . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Calcium intake and type of sport practised did not exert a significant influence on BMC of the distal radius and BMD of the L 2 to L 4 vertebrae in boys . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Reduced BMD was unrelated to gender , disease type , lifetime corticosteroid dose , but inversely correlated with disease duration ( r = 0 . 36 , p < 0 . 05 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Polymorphisms at the binding site of the Sp 1 transcription factor of the collagen type 1 alpha 1 gene have recently been suggested to be an important marker for low bone mineral density ( BMD ) and vertebral fracture in a population of predominantly postmenopausal British women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 1 patients showed a lower BMD of hip ( 83+ / 2 % , Z score ) and lumbar spine ( 93+ / 2 % ) than Type 2 diabetics ( 93+ / 5 % , 101+ / 5 % respectively ) , reaching significance in the female subgroups ( P < 0 . 05 ) . ^^^ In Type 1 patients , BMD of hip correlated negatively with IGFBP 1 ( r= 0 . 34 , P < 0 . 05 ) and IGFBP 4 ( r= 0 . 3 , P < 0 . 05 ) but positively with IGFBP 5 ( r=0 . 37 , P < 0 . 05 ) , which was independent of age , diabetes duration , height , weight and body mass index , as assessed by partial correlation analysis . ^^^ In 20 Type 2 patients in whom immunoreactive proinsulin could be detected , significant positive correlations were found between proinsulin and BMD of hip ( r=0 . 63 , P < 0 . 005 ) , IGF 1 ( r=0 . 59 , P < 0 . 01 ) as well as IGFBP 3 ( r=0 . 49 , P < 0 . 05 ) . ^^^ Type 1 and Type 2 patients with macroalbuminuria showed a lower BMD of hip , lower IGFBP 5 but higher IGFBP 4 levels , suggesting that diabetic nephropathy may contribute to bone loss by a disturbed IGF system . ^^^ In conclusion , the findings of this study support the hypothesis that the imbalance between individual IGF system components and the lack of endogenous proinsulin may contribute to the lower BMD in Type 1 diabetics . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To evaluate whether DNA polymorphisms of the VDR ( vitamin D receptor ) , COL1A1 ( alpha 1 type 1 collagen ) , and COL2A1 ( alpha 1 type 2 collagen ) genes , which have previously been linked to bone mineral density ( BMD ) and / or osteoarthritis ( OA ) , are also associated with OA of the hip ( OAH ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Mean BMD was significantly lower at the hip of patients with previous bowel resection ( diff in means = 0 . 53 , 95 % CI 0 . 97 , 0 . 08 , P = 0 . 02 ) , but type of surgery was not significant . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study demonstrated the decrease of bone mineral density ( BMD ) in the type 2 collagen ( CII ) induced arthritis ( CIA ) model in rats and the relationship between BMD and paw edema and the effect of dexamethasone 21 phosphate ( DEX ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Nonsteroidal anti inflammatory drugs ( NSAIDs ) are known to inhibit synthesis of prostaglandins and may help prevent bone loss , but no study has shown the differential association of type or dose of NSAID compound with bone mineral density ( BMD ) . ^^^ The purpose of this study was to determine the relation of NSAIDs by type and dose to BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Immunohistochemical analyses revealed that expression of GDNF in regeneration muscle fibers was up regulated in polymyositis ( PM ) and Duchenne type muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Recent data show that a G T transition polymorphism of the Sp 1 binding site at the collagen type 1 alpha 1 gene ( Sp 1 polymorphism ) is associated significantly with bone mineral density ( BMD ) and osteoporotic fracture in British women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Thus , the type of hip fracture was found to be independent of the value of BMD , BMI , and the length of the patient ' s hip axis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Adjustment for age , physical activity , calcium intake , BMI , breastfeeding , testing site , and menopausal type indicated a significant ( P for trend = 0 . 0013 ) positive association of grip strength with BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Histologic type of thyroid neoplasia , doses of thyroid hormones , thyroid hormone levels and duration of follow up , were not associated with changes in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Every patient was submitted to auxological evaluations , dual 10 ray absorptiometry to measure bone mineral density ( BMD ) , and to the determination of bone metabolic markers of osteoclastic activity ( total urinary hydroxylysylpyridinoline crosslinks , carboxyterminal pyridinoline crosslinked telopeptide of type 1 collagen [ ICTP ] ) and of osteoblastic activity ( bone Gla protein [ BGP ] and carboxyterminal propeptide of type 1 procollagen [ PIPC ] ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We compared BMD according to the type of epileptic drug being taken and theorized that phenytoin , barbiturates , and acetazolamide reduced BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A especial type of CMD caused by absence of alpha 2 chain ( or merosin ) of laminin 2 , a tissue specific protein from muscle basement membrane which anchors extracellular matrix to dystrophin , is the paradigm of a muscular dystrophy produced by extracellular abnormalities . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Histochemically , the masses were present in both type 1 and 2 fibers , and exhibited almost similar stained patterns to the tubular aggregates , but were dystrophin , GRP 78 and clathrin positive . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) , serum osteocalcin and type 1 collagen C telopeptide ( ICTP ) were assessed in a cohort of 31 ( 16 males ) adults who had received cranial irradiation in childhood as part of their treatment for acute lymphoblastic leukaemia ( ALL ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : Polymorphism of the vitamin D receptor ( VDR ) , collagen alpha 1 type 1 ( Col 1 alpha 1 ) , and oestrogen receptor ( ER ) genes have been shown to account for some of the heritability of bone mineral density ( BMD ) in adults . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At baseline , prior fracture , femoral neck BMD by dual energy 10 ray absorptiometry ( DXA ) , heel BUA and urinary type 1 collagen C telopeptide breakdown products ( CTX ) were assessed . ^^^ However , this increased sensitivity was also obtained simply by increasing the BMD and BUA cutoffs , suggesting that a combination of CTX with BMD / BUA is not useful for that type of treatment strategy . ^^^ If DXA or ultrasound is not available , the combination of a bone resorption marker with a history of any type of fracture after the age of 50 years gave a predictive value similar to that obtained with femoral neck BMD or heel BUA alone , for both types of treatment strategy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To investigate whether peripheral neuropathy ( PN ) , as part of the microangiopathic complex , affects bone mineral density ( BMD ) of the peripheral or the axial skeleton in patients with type 1 diabetes . ^^^ CONCLUSIONS : The present results suggest that in patients with type 1 diabetes , PN may be an independent risk factor for reduced BMD in the affected limbs as well as in the skeleton in general . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In retinae from wild type and mdx3Cv mice , dystrophin and beta dystroglycan were concentrated in small extensions of rod and cone photoreceptor terminals protruding into the outer plexiform layer . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The differences in BMD between the groups seem to be site specific and may be associated with the type and magnitude of loading during off season training and preferentially during ice hockey . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Femoral neck BMD , serum osteocalcin ( OC ) , bone specific alkaline phosphatase ( BAP ) and type 1 procollagen carboxy terminal propeptide ( PICP ) , as well as urine free deoxypyridoline ( Dpd ) cross links , N telopeptide ( NTx ) and C telopeptide ( CTx ) cross links of type 1 of collagen were measured in 45 CINA patients and 36 normal subjects . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
However , there was no significant difference in the deficit in BMD in any of the genotypes , either before or after adjusting for age , sex , body mass index , disease type , age at onset of disease , disease duration , cumulative steroid dosage , smoking status and dietary calcium intake . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To investigate whether the severity of GHD was correlated with the degree of bone mass and turnover impairment , we evaluated BMD at the lumbar spine and femoral neck ; circulating insulin like growth factor 1 ( IGF 1 ) , IGF binding protein 3 ( IGFBP 3 ) , and osteocalcin levels , and urinary cross linked N telopeptides of type 1 collagen ( Ntx ) levels in 101 adult hypopituitary patients and 35 sex and age matched healthy subjects . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
DESIGN AND METHODS : BMD with dual energy 10 ray absorptiometry , serum type 1 procollagen carboxy terminal propeptide ( PICP ) , serum type 1 collagen carboxy terminal telopeptide ( ICTP ) and serum IGF 1 were assessed in 71 adults with GH deficiency . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The main results of this study show that the mean diameter of type 2 fibers is usually markedly larger than that of type 1 fibers in DMD although the number of type 2 fibers is severely reduced . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Best ' s macular dystrophy ( BMD ) , also known as vitelliform macular degeneration type 2 ( VMD 2 ; OMIM 153700 ) , is an autosomal dominant form of macular degeneration with mainly juvenile onset . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
There was also no correlation between the estimated blood loss and the type of gene mutation found causing DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The failure of the observed increase in BMD to translate into a reduced fracture risk may be due , in part , to the number and type of falls sustained by subjects with OA . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At study entry , all subjects underwent BMD assessment at the lumbar spine and measurement of serum osteocalcin ( OC ) and cross linked N telopeptides of type 1 collagen ( Ntx ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In women treated with ALN ( 5 mg ) , change from baseline at month 6 in urine N telopeptide cross links of type 1 collagen ( NTX ) and osteocalcin ( OC ) correlated with change from baseline at month 24 in spine , hip , and total body bone mineral density ( BMD ) [ r = 0 . 28 to 0 . 31 ( NTX ) and r = 0 . 16 to 0 . 25 ( OC ) , P < 0 . 001 ] . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The only criterion for inclusion was the absolute proof of this type of disease through clinical assessments , an immunohistochemical muscle study ( dystrophin positive ) and linkage study . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) was measured , and blood and urine samples of all participants were examined to obtain values for eight biochemical markers : alkaline phosphatase ( ALP ) , bone Gla protein ( BGP ) , type 1 procollagen ( carboxyterminal peptide of type 1 procollagen ; PICP ) , cross linked carboxyterminal telopeptide region of type 1 collagen ( ICTP ) , and urinary excretion of calcium ( Ca ) , phosphate ( P ) , pyridinoline ( Pyr ) , and deoxypyridinoline ( D Pyr ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Baseline bone markers ( serum alkaline phosphatase [ AP ] , serum bone AP , serum pyridinoline crosslinked telopeptide of type 1 collagen , urinary hydroxyproline , urinary osteocalcin ) , as well as baseline histomorphometric indices of bone turnover ( eroded and labeled surface , bone formation rate , activation frequency , and cortical porosity ) were positively correlated with changes in spinal BMD over 6 months ( p < 0 . 05 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Significant brain atrophy was observed in 21 out of 63 cases of Duchenne muscular dystrophy ( DMD ) , 7 out of 15 Becker muscular dystrophy ( BMD ) , no case of 2 female dystrophinopathy ( F dyst ) , 11 out of 21 limb girdle muscular dystrophy ( LG ) , all cases of 10 Fukuyama type congenital muscular dystrophy ( FCMD ) , 2 out of 5 fascioscapulohumeral muscular dystrophy ( FSH ) , and 32 out of 44 myotonic dystrophy ( MyD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The purpose of this prospective study was to characterize the changes in serum levels of two proteins produced during the synthesis and degradation of type 1 collagen , i . e . , the carboxyterminal propeptide of type 1 procollagen ( PICP ) and the pyridinoline cross linked carboxyterminal telopeptide of type 1 collagen ( ICTP ) , respectively , after oophorectomy , and to assess the degree of correlation between changes in the serum values of these proteins and changes in bone mineral density ( BMD ) of the lumbar spine . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We examined whether the polymorphism for BsmI restriction enzyme in the vitamin D receptor ( VDR ) gene influenced radial ( distal third ) and lumbar ( L 2 L4 ) bone mineral density ( BMD ) , phospho calcium metabolism ( calcium , phosphate , intact parathyroid hormone , 25 hydroxyvitamin D , and 1 , 25 dihydroxyvitamin D ) , biochemical markers of bone formation ( osteocalcin and carboxy terminal propeptide of type 1 procollagen ) and bone resorption ( carboxy terminal telopeptide of type 1 collagen and urinary cross linked N telopeptides of type 1 collagen ) , insulin like growth factor 1 and insulin like growth factor binding protein 3 , and growth in 209 healthy prepubertal children ( 112 males and 97 females ) aged 7 . 1 10 . 0 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the whole population , higher baseline levels of bone formation ( serum osteocalcin and serum type 1 collagen N terminal propeptide ) and bone resorption markers ( urinary N telopeptides ; urinary and serum C telopeptides ) were significantly associated with faster BMD loss ( r = 0 . 19 to 0 . 30 , p < 0 . 001 ) , independently of age . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study therefore examined the frequency and severity of the skeletal changes in predialysis chronic renal failure by measurements of bone mineral density ( BMD ) , biochemical markers of bone turnover ( osteocalcin , bone specific alkaline phosphatase , carboxy terminal propeptide of type 1 collagen , and carboxy terminal telopeptide of type 1 collagen ) , parathyroid hormone ( PTH ) , ionized calcium ( Ca++ ) , phosphate ( P ) , and vitamin D metabolites . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Duration of treatment and type of AED were not independent factors for reduction in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The cross linked carboxyterminal telopeptide of type 1 collagen ( ICTP ) correlated negatively with BMD ( r = 0 . 45 , P = 0 . 045 ) as did bone specific alkaline phosphatase ( BAP ; r = 0 . 64 , P = 0 . 002 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Biochemical markers of bone turnover ( osteocalcin , procollagen type 1 C terminal propeptide ( PICP ) , immunoreactive free deoxypyridinoline ( iFDpd ) , N terminal crosslinked telopeptides of type 1 collagen ( NTx ) ) , BMD at the spine and femoral neck , and serum cortisol concentrations were measured at baseline and 12 months later . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Baseline serum osteocalcin , serum pyridinoline crosslinked telopeptide of Type 1 collagen and several histomorphometric indices of trabecular bone turnover ( eroded and labeled surfaces , bone formation rate , and activation frequency ) also correlated positively with the subsequent increase in whole body BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study attempts to investigate the influence of menopause type on bone mineral density ( BMD ) changes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSIONS : We conclude that bone turnover was increased in type 1 diabetic patients with incipient stage of diabetic nephropathy but there was no difference in BMD as compared with type 1 diabetic patients without nephropathy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured total body BMD and biochemical markers of bone resorption ( urinary pyridinium crosslinks and telopeptides of type 1 collagen ) and bone formation ( serum bone alkaline phosphatase , propeptides of type 1 procollagen [ PINP ] and osteocalcin ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Univariate and multivariate analyses revealed that BMD was significantly associated with the age and sex of patients , but was not influenced by the type of gastrectomy ( partial versus total ) and years after operation ( < 20 versus 20 < ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These findings clearly demonstrate a considerably high BMC and BMD in professional volleyball players which seems to be related to the loading type of exercise they perform . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Highly purified normal myoblasts derived from the m . soleus and m . gastrocnemius white of normal mice were transplanted into the m . soleus ( containing 70 % of type 1 fibers ) and gastrocnemius white ( 100 % of type 2 fibers ) of dystrophin deficient mdx mice . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
HMG CoA reductase inhibitors increase BMD in type 2 diabetes mellitus patients . ^^^ We studied the effect of HMG CoA reductase inhibitors on BMD of type 2 diabetes mellitus by a retrospective review of medical records . ^^^ These results suggest that HMG CoA reductase inhibitors may increase BMD of the femur in male patients with type 2 diabetes mellitus . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The collagen type Ialpha 1 Sp1 ( ColIA 1 ) polymorphism has been associated with reduced bone mineral density ( BMD ) and increased prevalence of osteoporosis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum levels of aminoterminal extension propeptides ( PINP ) , the carboxyterminal telopeptide ( ICTP ) , and the cross linked N telopeptides ( NTx ) of type 1 collagen were determined in 78 healthy , elderly men aged 76 + / 5 years in 1993 and 1996 and compared with bone mineral density ( BMD ) measurements of their lumbar spine , femoral neck , and total body regions made using dual 10 ray absorptiometry . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We projected an inquiry about the incidence rate and type of severe anaesthetic complications in an utmost large number of patients and families with Duchenne ( DMD ) and Becker type ( BMD ) muscular dystrophy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystrophin and utrophin influence fiber type composition and post synaptic membrane structure . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Nitric oxide is formed in skeletal muscle by the neuronal type nitric oxide synthase and the signalling function of dystrophin and related compounds are in part mediated by nitric oxide . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To determine the utility of bone markers in the management of postmenopausal women receiving HRT , we analyzed the relationship between changes in four markers ( serum osteocalcin and bone alkaline phosphatase [ BAP ] , serum and urinary C telopeptide of type 1 collagen [ CTX ] ) and changes in spine BMD in 569 women treated for 2 years with different doses of a matrix transdermal 17beta estradiol patch in two placebo controlled trials . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To assess the effect of type 1 and type 2 diabetes and insulin treatment on bone mineral density ( BMD ) in middle aged and elderly men and women . ^^^ RESEARCH DESIGN AND METHODS : We measured BMD and evaluated known determinants of osteoporosis in 56 type 1 and 68 type 2 diabetic patients and 498 nondiabetic community control subjects . ^^^ RESULTS : Among both sexes , BMD values were significantly lower in type 1 diabetic patients than in type 2 diabetic patients or the control subjects . ^^^ After further adjustments for confounding factors , the average BMD values were still lower in type 1 diabetic subjects than in type 2 diabetic subjects although with lesser significance . ^^^ CONCLUSIONS : The lower BMD in type 1 versus type 2 diabetic patients and control subjects probably results from more rapid bone loss after the onset of type 1 diabetes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In all patients , we performed a bone mineral density ( BMD ) analysis and simultaneously evaluated different biochemical parameters , intact parathyroid hormone ( iPTH ) , sexual hormone determinations that included total estradiol , follicle stimulating ( FSH ) , and luteinizing hormone and markers of bone resorption such as the procollagen type 1 cross linked carboxy terminal telopeptide ( ICTP ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
When comparing the association of the type of physical activity among the pubertal athletics by multiple regression analysis , height , physical activity , gymnastics , and Tanner stage emerged as significant variables and accounted for 54 . 7 % and 63 . 4 % of the total variation in BMD of the femoral neck and lumbar spine , respectively . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the present study we evaluated bone and collagen turnover ( bone Gla protein , BGP ; carboxyterminal telopeptide of type 1 collagen , ICTP ; aminoterminal propeptide of type 3 procollagen , PIIINP , respectively ) and bone mineral density ( BMD ) in 5 pre pubertal GH deficient thalassaemic children before and during rec GH treatment ( 0 . 6 IU / kg / week ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Twenty three subjects with Type 3 EDS and 23 matched controls underwent BMD measurement by dual Energy 10 ray absorptiometry ( DXA ) of the lumbar spine and femoral neck . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To determine the effect of metabolic control on bone mineral density ( BMD ) in type 1 diabetes mellitus ( type 1 DM ) , we studied BMD ( by dual energy 10 ray energy absorptiometry ) and bone remodeling parameters in 62 patients with type 1 DM both before and 7 years after commencement of intensive insulin therapy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To evaluate the role of pro alpha 2 ( 1 ) collagen in type 1 collagen structure / function in mineralized tissues , we examined age matched oim / oim , heterozygous ( oim / + ) , and wild type ( + / + ) mouse femurs and incisors for mineral composition ( calcium , phosphorus , magnesium , fluoride , sodium , potassium , and chloride ) by neutron activation analyses ( NAA ) , and bone mineral content ( BMC ) and bone mineral density ( BMD ) by dual energy 10 ray absorptiometry ( DEXA ) in a longitudinal study ( 7 weeks to 16 months of age ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured bone mineral density ( BMD ) , four markers of bone formation [ bone alkaline phosphatase ( bAP ) , osteocalcin ( Oc ) , N and C terminal propeptide of type 1 procollagen ( PINP and PICP respectively ) ] and five markers of bone resorption [ serum C terminal telopeptide of type 1 collagen ( CTx ) , urinary CTx , N terminal cross linked telopeptide ( NTx ) , free and total deoxypyridinoline ( fDpd and tDpd respectively ) ] in 28 healthy premenopausal women ( 45 . 7 + / 3 . 0 years ) , 15 early ( < 7 years ) healthy menopausal women ( 53 . 8 + / 3 . 1 years ) and 20 osteoporotic women ( 65 . 3 + / 8 . 2 years ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In a multivariate analysis among all subjects ( n = 50 ) , all BMD sites , except the femur diaphysis , distal femur , and proximal tibia , were significantly related to type of physical activity ( beta = 0 . 25 0 . 43 , P < 0 . 05 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Using multiple linear regression , the type of activity ( soccer player , nonactive ) independently predicted BMD of all dominant hip sites ( beta = 0 . 32 0 . 48 , P < 0 . 01 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To determine bone mineral density ( BMD ) at axial and appendicular sites in patients with type 1 diabetes mellitus and evaluate its relationship with metabolic control and disease duration . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Body weight , femur length , serum levels of osteocalcin ( OC ) , insulin like growth factor 1 ( IGF 1 ) , testosterone , and luteinizing hormone ( LH ) ; femur distal metaphyseal and middiaphyseal bone mineral density ( BMD ) and tibial metaphyseal gene expression for alpha 1 type 1 collagen ( Col 1 ) , OC , and bone alkaline phosphatase ( AP ) ; and femur strength by four point bending to failure were measured after 28 days of feeding and alendronate injections . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Outcome measures were hip and spine BMD and biochemical markers of bone resorption , including serum N telopeptide and C telopeptide cross linked collagen type 1 ( NTx and CTx , respectively ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
There was a marked reduction in bone remodeling markers , serum osteocalcin , and the ratio of urinary cross linked N : telopeptides of type 1 collagen to creatinine with alcohol consumption , suggesting that increased BMD with alcohol consumption could be due to reduced bone remodeling . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In 18 patients with hypothalamo pituitary diseases aged over 60 years and in 18 sex , age and BMI matched healthy subjects , the results of plasma IGF 1 and IGF BP 3 levels and the GH response to GHRH + arginine test ( GHRH + ATT ) were correlated to the results of body composition , serum osteocalcin ( OC ) and urinary cross linked N telopeptides of type 1 collagen ( Ntx ) and the bone mineral density ( BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At baseline , we recorded body mass index ( BMI ) , Hoehn and Yahr stage , and postmenopausal interval , and also measured bone mineral density ( BMD ) and serum concentrations of ionized calcium , intact parathyroid hormone ( PTH ) , pyridinoline cross linked carboxyterminal telopeptide of type 1 collagen ( ICTP ; a bone resorption marker ) , and 25 hydroxyvitamin ( 25 OHD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Patients with grade 2 and grade 3 of any fracture type had significantly lower BMD ( P < . 01 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A study was performed to investigate the possible relationship between Apa 1 , Bsm 1 , Taq 1 , and Fok 1 polymorphisms of the VDR gene and serum 1 , 25 dihydroxyvitamin D ( 1 , 25 [ OH ] 2D ) , osteocalcin , and propeptide of type 1 collagen ( PICP ) markers of bone turnover , total body calcium , and BMD of the total body , radius , lumbar spine , trochanter , and femoral neck in 39 young adult black men of 20 to 40 years of age and 44 age , height , and weight matched white men . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Recently , a G to T polymorphism in an Sp 1 site in the collagen type Ialpha 1 ( COLIA 1 ) gene was found to be associated with reduced BMD and with increased fracture risk . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In a cohort of 596 men , aged 51 85 yr , we measured bone mineral density ( BMD ) of the lumbar spine , hip , total body , and forearm ; serum levels of sex steroid hormones [ total and free testosterone , total estradiol ( 17betaE ( 2 ) ) , bioavailable estradiol ( bio 17betaE ( 2 ) ) , androstenedione , and sex hormone binding globulin ] ; and markers of bone turnover [ serum osteocalcin , bone alkaline phosphatase , N terminal extension propeptide of type 1 collagen , and beta isomerized C terminal telopeptide of collagen type 1 ( betaCTX ) ] , as well as urinary excretion of betaCTX and deoxypyridinoline ( DPyr ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD is a hereditary form of macular degeneration that may develop subretinal neovascularisation similar to the wet type of age related macular degeneration ( AMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum leptin levels also correlated well with the age adjusted z score for BMD ( P < 0 . 02 ) and were inversely correlated with levels of the carboxy terminal propeptide of type 1 procollagen ( P < 0 . 05 ) in females patients , but not in male patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : Medical records of all inpatients for the period March to October 1999 who were documented in pharmacy records as either having received continuous oral steroids for at least 3 months or who had at least 4 courses of oral steroids per year were examined for the following data : age , sex , medical condition for which steroids were required , dose and duration of steroid therapy , whether they were offered bone mineral density ( BMD ) scans , and whether they were offered drug prophylaxis for steroid induced osteoporosis and the type of drug prophylaxis offered . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In this study , to further characterize the regulation of muscle type of promoter , we analyzed promoter activity and tissue specificity using a total 14 kb fragment around the human dystrophin muscular specific exon 1 in vitro and in vivo . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The following variables were measured in both groups : QUS parameters at the heel ( BUA ; SOS ; Stiffness Index , SI ) ; bone mineral density ( BMD ) at both the lumbar spine ( LS ) and femoral neck ( FN ) by dual energy 10 ray absorptiometry ; and serum markers of bone turnover ( osteocalcin , procollagen type 1 N and C terminal propeptides ( PINP and PICP ) , bone alkaline phosphatase ( BAP ) , procollagen type 1 C terminal telopeptide ( ICTP ) and urinary type 1 collagen C telopepetide breakdown products ( CTX ) ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The type of endocrine therapy ( tamoxifen and toremifene ) had no significant influence on BMD changes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Mitochondrial distribution and function in skinned cardiac and skeletal muscle fibers from dystrophin deficient ( MDX ) and wild type mice were compared . ^^^ Irrespective of muscle type , the absence of dystrophin had no effect on the maximal capacity of oxidative phosphorylation , nor on coupling between oxidation and phosphorylation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To investigate whether there are any basic abnormalities of coagulation and fibrinolysis in muscular dystrophy , we measured serum levels of the MM isozyme of creatine kinase ( CK MM ) , fibrin and fibrinogen degradation products ( FDP ) , plasma levels of fibrinogen , antithrombin ( AT ) , and D dimer in 36 patients with Duchenne muscular dystrophy ( DMD ) , 11 with Becker muscular dystrophy ( BMD ) , 5 with Fukuyama congenital muscular dystrophy ( FCMD ) , 5 with myotonic dystrophy ( MyD ) , and 5 with spinal muscular atrophy ( SMA ) type 2 . ^^^ FDP levels were elevated in the patients with DMD , BMD , and FCMD ( 1 . 0 to 84 . 9 microg / ml ) , but not in the patients with MyD and SMA type 2 . ^^^ In DMD , BMD , and FCMD , FDP levels significantly correlated with CK MM , but not with age , fibrinogen , AT , D dimer , and type of dystrophy ( multiple regression analysis ; r ( 2 ) = 0 . 814 , P < 0 . 0001 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
DESIGN : Polymorphisms at the VDR FokI and ER PvuII and XbaI gene sites , serum bone specific alkaline phosphatase , urinary N telopeptide of type 1 collagen , and BMD at the lumbar spine and proximal femur were analyzed in 229 postmenopausal Korean women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At baseline and at 1 and 3 months after intervention , we measured serum intact osteocalcin , serum N terminal midfragment osteocalcin , serum C terminal telopeptide of type 1 collagen ( CTx ) , urinary deoxypyridinoline cross links , and urinary CTX : The BMD of the lumbar spine and the femoral neck was measured at baseline and after 1 and 2 years of intervention . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We recently demonstrated that children with type 1 diabetes mellitus ( DM ) have decreased lumbar spine bone mineral density ( BMD ) as early as four years after clinical diagnosis of the disease . ^^^ Lumbar spine and femoral neck BMD were measured by dual 10 ray absorptiometry , while bone turnover was assessed by the determination of the serum concentration of the carboxy terminal propeptide of type 1 collagen ( PICP ) and the carboxy terminal cross linked telopeptide of type 1 collagen ( N telopeptide ) . ^^^ In summary , early on after the diagnosis of type 1 DM , children present with decreased lumbar spine BMD and decreased bone formation markers . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The cumulative dose and number of days of glucocorticoid therapy and the number of days of cyclosporine or tacrolimus therapy showed significant associations with loss of BMD ; age , total body irradiation , diagnosis , and donor type did not . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the group receiving alfacalcidol plus menatetrenone , serum carboxylated osteocalcin ( OC ) ( p =0 . 0022 ) and lumbar BMD ( p=0 . 0029 ) increased and serum undercarboxylated OC ( p=0 . 0004 ) decreased significantly in comparison to the group receiving alfacalcidol ; further , the change of lumbar BMD showed an inverse correlation to the change of serum undercarboxylated OC ( r= 0 . 744 , p=0 . 0134 ) and positive correlations to the baseline values of bone turnover markers such as serum levels of intact OC , bone specific alkaline phosphatase and type 1 procollagen carboxyl extension peptide and urinary levels of deoxypyridinoline and N telopeptide of type 1 collagen . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These experiments revealed clear complex or non complex formation between members of the dystrophin system , depending on the muscle type analyzed . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Despite promoter tissue specificity , up regulation of the brain and Purkinje cell type dystrophin isoforms was described in skeletal muscle of 10 linked dilated cardiomyopathy ( XLDCM ) and BMD affected individuals . ^^^ We consider that muscle ectopic expression of the brain and Purkinje cell type isoforms has no favorable prognostic significance in DMD and BMD patients . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Metacarpal cortical BMD in bilateral hands was measured by computed 10 ray densitometry , and the levels of urinary cross linked N telopeptides of type 1 collagen ( NTx ) , as a bone resorption marker , were measured by an enzyme linked immunosorbent assay ( ELISA ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Clinical symptoms , levels of urinary cross linked N telopeptides of type 1 collagen ( NTx ) , and metacarpal cortical bone mineral density ( BMD ) were assessed before and just after the 6 months of treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aged female ER beta / mice further exhibited a significantly higher trabecular bone mineral density ( BMD ) as well as increased bone volume / total volume ( BV / TV ) compared with wild type ( wt ) mice . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We aimed at studying fracture risk in patients with Duchenne ' s muscular dystrophy ( DMD ) , Becker ' s muscular dystrophy ( BEMD ) , and spinal muscular atrophy type 2 and 3 ( SMA 2 and 3 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
There was a significant decrease in the number of type 2A myofibers in dystrophin deficient cats at both ages . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The first reported female patient with the Fukuyama type of congenital muscular dystrophy associated with a lack of C terminal domain of dystrophin is presented . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) , broadband ultrasonic attenuation ( BUA ) , and biochemical markers of bone formation ( serum osteocalcin , C terminal propeptide of type 1 collagen and bone alkaline phosphatase ) and resorption ( urinary deoxypyridinoline ) were assessed at baseline and 12 months . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bronchiolar clearance was studied in 7 boys in the age range of 8 to 17 years , 6 with Duchenne muscular dystrophy ( DMD ) and 1 with spinal muscular atrophy type 2 ( SMA 2 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Observed changes in BMD among DMPA users differed from women who used either type of pill ( P < . 002 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 2 diabetes mellitus was associated with increased BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To study bone mineral density ( BMD ) and bone remodeling factors at the time of diagnosis of adult onset type 1 diabetes mellitus ( DM ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We previously identified a polymorphism of a Sp 1 binding site in the Collagen Type 1 Alpha 1 gene ( COLIA 1 ) that has been associated with reduced BMD and an increased risk of osteoporotic fractures in several populations . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone resorption in post menopausal women with normal and low BMD assessed with biochemical markers specific for telopeptide derived degradation products of collagen type 1 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Previous studies have demonstrated that an Sp 1 binding site polymorphism in the collagen type 1 gene ( COLIA 1 ) is related to reduced bone mineral density ( BMD ) and osteoporotic fractures in certain populations , particularly in the elderly . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The BMD of COPD patients correlated positively with arterial pH ( r = 0 . 582 ; p < 0 . 001 ) , negatively with PCO 2 ( r = 0 . 442 ; p < 0 . 001 ) , and negatively with serum cross linked telopeptide of type 1 collagen ( ICTP ) , a bone resorption marker ( r = 0 . 444 ; p < 0 . 001 ) but not with serum osteocalcin , a bone formation marker . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Nonrecovered AN patients with binge eating / purging type showed a significantly reduced BMD compared with patients with the restricting type ( 0 . 87 + / 0 . 13 vs . 1 . 02 + / 0 . 08 g / cm2 ; P = 0 . 02 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A polymorphic binding site of the Sp 1 transcription factor in the gene encoding the alpha 1 chain of type 1 collagen is associated with bone mineral density ( BMD ) and , independently , with fracture risk in postmenopausal women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Another method used to obtain a carcinogenic potency value based on a 25 % increase in incidence above the background rate is the estimation of a T 25 derived from a benchmark dose ( BMD ) response model fit to the chronic bioassay data for the specified tumor type . ^^^ In each of the 2 year bioassays , a tumor type was selected based on statistical and biological significance , and both EU T 25 and BMD T 25 estimates were determined for that end point . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To explore the relationship between vitamin D receptor ( VDR ) gene polymorphisms and bone mineral density ( BMD ) in patients with type 2 diabetes mellitus ( DM ) and to better understand the pathogenesis of osteoporosis . ^^^ CONCLUSION : These findings suggest a small influence of VDR gene polymorphism on the BMD of patients with type 2 DM . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
T and L type calcium currents and contractile responses induced by membrane depolarisations as well as intracellular calcium transients induced by three kinds of stimulus ( superfusions of acetylcholine , high K+ or caffeine containing media ) were recorded by means of whole cell patch clamp and ratiometric cytofluorimetry in co cultured FSHD myotubes which presented a sarcolemmal localisation of dystrophin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Herpes simplex virus type 1 ( HSV 1 ) amplicon vectors were evaluated for feasibility in gene therapy of Duchenne ' s muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The metacarpal BMD of the nondominant hand was measured by computed 10 ray densitometry , and the levels of urinary cross linked N telopeptides of type 1 collagen ( NTx ) , as a marker of bone resorption , were measured with an enzyme linked immunosorbent assay . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MEASUREMENTS : Bone mineral density ( BMD ) at lumbar spine , serum osteocalcin ( OC ) , and urinary N telopeptides of type 1 collagen ( Ntx ) levels . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In conclusion , BMD and body composition in children with rheumatic disease treated with CS are influenced by physical activity , as well as corticosteroid treatment and type of rheumatic disease . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
DMD is the more severe type with an onset at 2 3 years of age . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Previous studies have shown that a polymorphic Sp 1 binding site in the collagen type 1 alpha 1 gene ( COLIA 1 ) is associated with bone mineral density ( BMD ) and osteoporotic vertebral fracture . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Best ' s macular dystrophy ( BMD ) , also known as vitelliform macular degeneration type 2 , is an autosomal dominant disease that causes loss of vision . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MAIN OUTCOME MEASURES : Changes from baseline in spine and total hip BMD , total body BMC , and biochemical markers of bone turnover ( serum osteocalcin and urinary cross linked N telopeptides of type 1 collagen ) , assessed at 6 month intervals and compared among treatment groups with a modified intention to treat approach . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aim of this study was to compare the biochemical markers of bone formation ( serum collagen type 1 C terminal propeptide ) and resorption ( serum deoxypyridinoline DPD and pyridinoline PYR ) with the bone mineral density ( BMD ) at lumbar spine , femoral neck , and forearm in patients with end stage renal disease on haemodialysis ( HD ) versus continuous ambulatory peritoneal dialysis ( CAPD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Our aim was to investigate the association between femur BMD and hip fracture type at different ages . ^^^ Logistic multiple regression showed that the association between hip fracture type and BMD was independent of age , weight , height , time between fracture occurrence and DXA assessment , number of concomitant diseases and number of drugs administered when BMD was evaluated at total proximal femur ( p < 0 . 001 ) , trochanter ( p < 0 . 001 ) , and intertrochanteric area ( p < 0 . 01 ) . ^^^ Moreover , we show that the role played by BMD as a determinant of the hip fracture type varies with age . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At the Children ' s Hospital of the Johannes Gutenberg University in Mainz , Germany , 7 children with type 1 Gaucher disease presented with reduced BMD in the distal ulna , and after 18 24 months of ERT , these patients demonstrated increases in BMD at this site . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Despite a similar increase in parameters of bone turnover ( osteocalcin [ OC ] , procollagen type 1 carboxy terminal propeptide [ PICP ] , and pyridinolines ( [ PYD ] ) in male and female GH treated patients compared with controls , the effects on BMC and BMD as evaluated by dual energy 10 ray absorptiometry were gender specific . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We devised non radioactive PCR assays for the DMD ( mdx3Cv ) and DMD ( mdx4Cv ) mouse dystrophin point mutations , in which mutant and wild type reactions electrophoresed separately diagnose whether the DNA carries the mutant , wild type , or both alleles . ^^^ This simple and reliable assay facilitates the use of these mutant mouse models , which have an extended inflammatory phase ( DMD ( mdx3Cv ) ) , less reversion to wild type ( DMD ( mdx4Cv ) ) , and reduced expression of dystrophin mRNAs arising from internal promoter usage than the DMD ( mdx ) mouse . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD was measured at baseline and then after 6 and 12 months of supplementation as were the biochemical markers bone specific alkaline phosphatase , amino terminal propeptide extension of type 1 collagen , deoxypyridinoline , calcitonin , intact parathyroid hormone , calcidiol , and urinary Ca . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In an effort to identify factors responsible for susceptibility to low BMD in the Irish population , we investigated its possible association with polymorphisms in the Osteoprotegerin ( OPG ) gene , Type 1 collagen alpha 1 ( COLIA 1 ) Sp 1 binding site and vitamin D receptor ( VDR ) start codon . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To determine whether soluble adhesion molecules are affected in muscular dystrophy , we measured serum levels of creatine kinase ( CK ) , soluble vascular cell adhesion molecule 1 ( sVCAM 1 ) , soluble intercellular adhesion molecule 1 ( sICAM 1 ) , soluble ( s ) E selectin , and fibrin and fibrinogen degradation products ( FDP ) in 25 patients with Duchenne muscular dystrophy ( DMD ) , 7 with Becker muscular dystrophy , 7 with Fukuyama type congenital muscular dystrophy , 6 with myotonic dystrophy ( MyD ) , and 5 with spinal muscular atrophy ( SMA ) type 2 , and also serum sVCAM 1 , sICAM 1 , and sE selectin in 9 healthy controls . ^^^ The levels of sVCAM 1 in the patients with DMD were 367 . 0 852 . 0 ng / ml ( 552 . 8 + / 23 . 1 ) and significantly elevated than those in the patients with MyD , SMA type 2 , and controls . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD was measured by DXA , while bone turnover was evaluated by serum osteocalcin ( OC ) , bone alkaline phosphatase ( B ALP ) , and serum and urinary type 1 collagen C telopeptide ( CTXs and CTXu ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To investigate into the changes of bone mineral density ( BMD ) in Type 2 diabetes mellitus with nephropathy ( DN ) and without nephropathy ( DM ) . ^^^ METHODS : BMD of lumbar vertebrae 1 4 and femur in 93 cases of Type 2 diabetes mellitus ( 41 cases of DN and 52 cases of DM ) were measured with dual energy 10 ray absorptiometry ( DEXA ) and were compared with age , sex , and BMI matched normal control group . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD of the lumbar supine ( dual emission 10 rays absorptiometry ) and bone resorption ( deoxypyridinoline , aminoterminal telopeptide of type 1 collagen , and carboxyterminal telopeptide of type 1 collagen ) and formation ( propeptide of type 1 procollagen , osteocalcin , and bone specific alkaline phosphatase ) markers were examined at baseline ( before the surgery ) , 6 and 12 months after the start of tamoxifen treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : The urinary levels of pyridinoline ( Pyr ) and deoxypyridinoline ( D pyr ) , the serum levels of type 1 carboxy terminal pyridinoline cross linked telopeptide ( ICTP ) , and lumbar bone mineral density ( BMD ) , were compared in 80 Japanese women after menopause or oophorectomy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSION : These data support the findings that the COL1A1 gene polymorphism is associated with low BMD and fracture risk , and suggest a possible physiologic effect on total body turnover of type 1 collagen . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These increases in BMD as well as the BMD increases at the femoral neck , trochanter , and total body and the reductions of biochemical markers of bone resorption ( urinary cross linked N telopeptides of type 1 collagen [ NTx ] ) and bone formation ( serum bone specific alkaline phosphatase [ BSAP ] ) were similar for the three dosing regimens . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In conclusion , some lifetime factors and low S Ca , low S 25 ( OH ) D , high S CT , and low BMD of the upper femur seem to be related to the risk of hip fracture , and low BMD and low S CT seem to be related to the trochanteric fracture type in postmenopausal women . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
AIM : To analyze whether bone mineral density ( BMD ) and bone resorption status are influenced by long term metabolic control and duration of disease in adolescents with long standing type 1 diabetes mellitus . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone ages and BMD were measured every 12 months by dual energy 10 ray absorptiometry , as were serum concentrations of the carboxy terminal propeptide of type 1 collagen ( PICP ) and the carboxy terminal cross linked telopeptide of type 1 collagen ( ICPT ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
A decreased amount of full length dystrophin and a 360 kDa polypeptide lacking the COOH terminus were detectable in the patient ' s muscle biopsy ; accordingly , transcript analysis revealed the expression of a wild type messenger RNA together with a shorter frameshifted one . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Seven genes , including interleukin 1 receptor antagonist ( IL 1ra ) , IL 1receptor type 2 ( IL 1RII ) , insulin like growth factor binding protein 4 ( IGFBP 4 ) , transforming growth factor beta ( TGF beta ) , granulocyte colony stimulating factor receptor ( G CSFR ) , leukemia inhibitory factor receptor ( LIFR ) , and soluble IL 4 receptor ( sIL 4R ) were selected as probable candidate genes for the trabecular bone sparing effect of estrogen , as the mRNA levels of these genes were highly correlated ( r 2 > 0 . 65 ) to the trabecular BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Linear multiple regression showed that the association between BMD and Barthel Index score was independent of 10 confounding variables : age , body mass index , fracture type , pressure ulcers , cognitive impairment , neurologic diseases , total lymphocyte count as a nutritional index , time between fracture occurrence and DXA assessment , comorbidity , and surgical procedure . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The different subcellular distributions of dystrophin immunoreactivity might reflect diverse roles played by full length isoforms in each cell type . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We investigated polymorphisms of the following five commonly used markers of four prominent BMD candidate genes with the purpose of identifying useful genetic markers for osteoporosis genetic research in Chinese : the Sp 1 and RsaI polymorphisms of the collagen type 1 alpha l ( Col1a1 ) gene , the 174G / C promoter polymorphism of the interleukin 6 ( IL 6 ) gene , the Asn363Ser polymorphism of the glucocorticoid receptor ( GR ) gene , and the T > C polymorphism in intron 5 of the transforming growth factor beta ( 1 ) ( TGF beta ( 1 ) ) gene . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The molecular background of an intermediate type of dystrophinopathy [ Duchenne and Becker muscular dystrophy ( DMD / BMD ) ] remains to be clarified , and out of frame and in frame mutations of the dystrophin gene are shown to be causes of DMD and BMD , respectively . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Lumbar spine ( L 1 L4 ) and femoral neck ( FN ) BMD were measured by dual energy 10 ray absorptiometry ( DEXA ) at time 0 ( T 0 ) , after 6 ( T 6 ) and 12 ( T 12 ) months ; at the same time , serum bone specific alkaline phosphatase ( BALP ) and urinary N terminal telopeptide of type 1 collagen normalized by creatinine ( NTx / cr ) were determined at T 0 , T 6 and T 12 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSION : Evidence of a linear relationship between BMD change and total and exercise specific weight lifted in a 1 yr strength training program reinforces the positive association between this type of exercise and BMD in postmenopausal women . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Longitudinal study of a BMD patient indicated that such abnormalities were dynamic and changed in type and degree with time . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSION : JGG can efficiently prevent type 1 primary osteoporosis or delay its occurrence by enhancing the function of endocrine system , coordinating the action of calcium related hormone , reducing bone turnover rate and increasing BMD . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
PATIENTS AND METHODS : Bone mineral density ( BMD ) at lumbar spine , serum osteocalcin ( OC ) and urinary cross linked N telopeptides of type 1 collagen ( Ntx ) levels were measured at diagnosis and 2 years after cure of Cushing ' s disease ( CD ) in six patients with childhood onset and nine with adulthood onset disease . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : We measured BMD and elevated known determinants of BMD ( bone markers ) in 35 patients with DISH related type 2 diabetes mellitus , 47 type 2 female diabetics , and 52 female controls with no systemic disease and no drug administration . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
RT PCR for dystrophin tissue specific exon 1 revealed that only muscle type promoter , but not non muscle type promoter ( brain and Purkinje cell type ) , was activated immediately after banding . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Lumbar spine and proximal femur ( trochanter , femoral neck , total hip ) BMD were measured by dual energy 10 ray absorptiometry ; serum osteocalcin and creatinine corrected urinary C telopeptide of type 1 collagen ( u CTX / Cr ) excretion were measured by ELISA . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To analyse the interest of baseline levels and short term ( 3 months ) changes in serum osteocalcin ( BGP ) , serum bone specific alkaline phosphatase ( BALP ) and urinary C telopeptide of type 1 collagen / creatinine ratio ( U CTX ) to predict 3 years changes in bone mineral density ( BMD ) and spinal deformity index ( SDI ) in postmenopausal osteoporotic women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : The investigation of the effect of time and type of menopause on bone mineral density ( BMD ) at different ages . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Adynamic bone disease ( ABD ) has attracted attention as the most frequent type of renal osteodystrophy , but there are few reports about the bone mineral density ( BMD ) in ABD patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Sex , diagnosis , use of total body irradiation , stem cell source and type of graft ( auto versus allo ) did not significantly predict BMD change over the first 12 months . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Effects of 1 year treatment with troglitazone , a member of the TZDs , on bone mineral density ( BMD ) and bone metabolism were examined in 25 Japanese type 2 diabetic patients . ^^^ The percent change of BMD was negatively correlated with that of serum leptin , whereas it was not associated with changes of bone metabolic markers , type 1 collagen N telopeptide ( NTx ) , bone alkaline phosphatase ( ALP ) , body mass index , or HbA1c . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Most of the studies conducted in recent years reveal that bone mineral density ( BMD ) values of type 2 DM patients are not decreased and even increased when compared with healthy control groups . ^^^ In this study we evaluated bone turnover in 57 postmenopausal type 2 DM patients utilizing biochemical markers for bone formation and resorption , and BMD measurements . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MAIN OUTCOME MEASURE ( S ) : Serum levels of leptin , osteocalcin ( OC ) , bone alkaline phosphatase ( B ALP ) , urinary deoxypyridinoline ( DPyr ) , and N telopeptide of type 1 collagen ( NTX ) as well as LS BMD using dual energy 10 ray absorptiometry ( DEXA ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
For the PvuII and XbaI polymorphisms in these IL 6 D / D and D / E genotypes , the FN BMD was higher in pp in comparison with Pp ( P = 0 . 036 ) , and lumbar spine BMD was higher in 20 type , comparing with 20 and 20 genotype ( P = 0 . 005 and 0 . 031 , respectively ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Their MFA score was compared with treatment method , fracture type , and bone mineral density ( BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : Bone mineral density ( BMD ) of lumbar vertebrae 2 4 , femoral neck , Ward ' s triangle and trochanter in 27 COPD male patients , 25 male control subjects and 25 healthy persons were determined using dual energy 10 ray absorptiometry , patient ' s Syndrome type , their blood levels of total protein , albumin , alkaline phosphatase , bone glaprotein , hydroxyproline , calcium , phosphate , urine levels of calcium / creatine and phosphorous / creatine as well as arterial blood gas were also determined . ^^^ RESULTS : The BMD in COPD patients accompanied with respiratory failure or with course > 10 years was higher than that in COPD patients without respiratory failure or with course < or = 10 years , BMD in COPD patients of Fei Pi Shen type was lower than that in those of Fei Pi , but the urine hydroxyprdine in the former was higher than that in the latter ( all P < 0 . 05 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
RESULTS : The femoral neck ( FN ) BMD ( Z score ) was higher in pp compared to Pp ( 0 . 01 + / 0 . 12 vs . 0 . 35 + / 0 . 09 , P < 0 . 05 ) while lumbar spine BMD ( Z score ) was higher in 20 type compared to 20 and 20 genotypes ( 0 . 01 + / 0 . 45 vs 1 . 53 + / 0 . 17 , 1 . 29 + / 0 . 10 , < 0 . 001 and 0 . 001 , respectively ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Dystroglycan associated intracellular proteins such as dystrophin , dystrobrevin , sarcoglycans , plectin and caveolin 3 are responsible for causing severe ( Duchenne type ) and moderate forms ( Becker , LGMDs ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
AIMS : To evaluate the relationship between serum bioactive IL 6 levels and BMD at the femoral neck of post menopausal women with Type 1 diabetes . ^^^ METHODS : We studied BMD , urine excretion of deoxypirydynoline crosslinks , serum bioactive IL 6 and soluble IL 6 receptor ( sIL 6R ) levels in 20 post menopausal women with Type 1 diabetes mellitus , and compared these results with 20 matched healthy post menopausal controls . ^^^ RESULTS : Post menopausal women with Type 1 diabetes had significantly lower BMD at the femoral neck and increased serum bioactive IL 6 levels compared with the control group , but no relationship was observed between these variables in a multiple regression analysis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Reduced BMD and increased joint destruction were associated with : at the forearm and femoral neck , high Larsen score , low weight , and old age ( R ( 2 ) =0 . 381 , p < 0 . 001 ; R ( 2 ) =0 . 372 , p < 0 . 001 , respectively ) ; at the total hip , low weight , high Larsen score , and dose of injected glucocorticosteroids ( R ( 2 ) =0 . 435 , p < 0 . 001 ) ; at the lumbar spine , low weight , reduced cartilage oligomeric matrix protein , and increased carboxyterminal propeptide of type 1 procollagen ( R ( 2 ) =0 . 248 , p < 0 . 001 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Taking this into consideration the aim of the present study was to assess new markers of bone metabolism : serum CrossLaps degradation products of C terminal telopeptides of type 1 collagen tartrate resistant acid phosphatase ( TRAP ) and bone specific alkaline phosphatase ( bALP ) , as well as their correlations with bone mineral disease ( BMD ) in kidney transplant recipients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MAIN OUTCOME MEASURES : Efficacy parameters were the relative changes from baseline in spine ( L 1 4 ) and hip BMD , and biochemical markers of bone turnover ( serum and urinary C telopeptide of collagen type 1 ( CTx ) , osteocalcin , and alkaline phosphatase ) measured by dual energy 10 ray absorptiometry and enzyme immunoassays , respectively . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We report the results of bone mineral density ( BMD ) measurements in type 2 diabetic patients , in comparison to healthy controls . ^^^ In this prospective study , a total of 277 subjects ( aged 30 60 years ) with type 2 diabetes mellitus , outpatients at the Cukurova Medical School Hospital , were evaluated for BMD at L ( 1 ) L ( 4 ) lumbar vertebrae and at the femur ( neck , trochanter , Ward ' s triangle and total ) by DEXA ( dual energy 10 ray absorptiometry ) . ^^^ Type 2 diabetic patients may have lower , similar or higher BMD measurements at different ages and anatomic regions , so each patient should be evaluated individually . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD of the lumbar spine ( L 1 L4 ) measured by DXA , urinary cross linked N terminal telopeptides of type 1 collagen ( NTX ) level measured by enzyme linked immunosorbent assay , and back pain evaluated by face scale score were assessed at baseline and every 6 months . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : In 109 post menopausal women beginning either tibolone 2 . 5 mg ( n=29 ) , tibolone 1 . 25 mg ( n=42 ) or estradiol 2 mg plus norethisterone acetate 1 mg ( E 2 + NETA ) ( n=38 ) , we assessed body composition , total and regional BMD by dual energy 10 ray absorptiometry , and the serum bone alkaline phosphatase ( BAP ) , osteocalcin and the urinary excretion to type 1 collagen C telopeptide ( CTX ) at baseline and after 2 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : Type 1 diabetes has been associated with decreased bone mineral density ( BMD ) . ^^^ The aims of this study were to assess BMD in a cohort of young women with type 1 diabetes compared with nondiabetic control subjects and to evaluate the possible association of BMD with diabetes duration , HbA ( 1c ) , and biomarkers of bone metabolism . ^^^ RESEARCH DESIGN AND METHODS : BMD was measured by dual energy 10 ray absortiometry scan in 39 teenage ( age 13 19 years ) and 33 post teenage females ( age 20 37 years ) with type 1 diabetes and 91 female age matched control subjects . ^^^ RESULTS : After adjustment for age and BMI , BMD values were significantly lower at the femoral neck and lateral spine in women with type 1 diabetes older than age 20 years compared with control subjects but not in the case subjects younger than age 20 years , nor at the anterio posterior spine , wrist , or whole body . ^^^ CONCLUSIONS : This study indicates that women with type 1 diabetes exhibit BMD differences early in life with significant differences already present in the post teenage years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The BMD of the lumbar spine ( L 1 L4 ) measured by dual energy 10 ray absorptiometry , urinary crosslinked N terminal telopeptides of type 1 collagen ( NTX ) measured by an enzyme linked immunosorbent assay , and back pain evaluated by the face scale score were assessed at baseline , 6 months , and 12 months . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Our findings demonstrate that the sensitivity to GH in target tissues is growth period and tissue type dependent and that continuous GH treatment is necessary to maintain body fat loss but not BMD gain during a 3 7 wk follow up . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The interaction between Sillence type and BMD in osteogenesis imperfecta . ^^^ BMD served as a marker , representing the amount of bone tissue available for vertebral load bearing , and the Sillence classification , either type 1 or III / IV , as a marker representing the quality of the organic bone matrix . ^^^ Independent associations were observed between the prevalence of vertebral deformities and ( 1 ) Sillence type ( OR : 5 . 7 , 95 % Cl : 1 . 2 26 . 8 ) , ( 2 ) BMD ( OR : 0 . 003 , 95 % Cl : 0 0 . 25 ) and ( 3 ) body weight ( OR : 1 . 15 , 95 % Cl : 1 . 05 1 . 25 ) . ^^^ Prevalent vertebral deformities were associated with low BMD / body weight ratios ( OR : 0 . 04 , 95 % Cl : 0 . 008 0 . 2 ) in OI type 1 , but no association was found in type III / IV . ^^^ It was concluded that BMD and Sillence type have independent relationships with vertebral deformities . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSION : The noninvasive assessment of BMD using a DQCT scan employing a low dose protocol may be used to estimate expected primary stability depending on BMD , implant type and preparation procedure . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The major aim of the present study was to investigate whether the genetic effects of these genotypes on cancellous and cortical hand BMD , in the same elderly women ( N = 122 ) , are possibly mediated through circulating levels of parathyroid hormone ( PTH ) and / or 25 hydroxyvitamin D [ 25 ( OH ) D ] , and may be related to biochemical markers of bone turnover ( propeptide of type 1 procollagen [ PICP ] and osteocalcin ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 1 diabetes is associated with modest reductions in bone mineral density ( BMD ) but type 2 diabetes is often characterized by elevated BMD . ^^^ This paradox of higher BMD but increased fracture risk in type 2 diabetes may be explained by a combination of more frequent falls and poorer bone quality . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In the present study , we simultaneously test linkage and / or association of the collagen type 1 alpha 2 ( COL1A2 ) gene with bone mineral density ( BMD ) and bone area . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Chromosomal loci including 1p36 , 2p22 25 , 11q12 13 , parathyroid hormone receptor type 1 ( PTHR 1 ) , interleukin 6 ( IL 6 ) , interleukin 1 alpha ( IL 1alpha ) and type 2 collagen A1 / vitamin D receptor ( COL11A1 / VDR ) have been linked or shown suggestive linkage with BMD in other populations . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BACKGROUND : Our purpose was to determine whether type 2 diabetes is associated with altered bone mineral density ( BMD ) and whether fasting serum insulin levels are correlated with BMD . ^^^ CONCLUSIONS : These results suggest that Mexican American women with type 2 diabetes have higher BMD compared to their nondiabetic counterparts , with the association independent of obesity at hip , although not at spine or forearm . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To examine the relationships between serum leptin and bone metabolism , we measured bone mineral density ( BMD ) at the spine and the hip , fasting serum leptin , and osteocalcin and urinary excretion of C terminal crosslinking telopeptide of type 1 collagen ( CTX ) , as markers of bone formation and resorption , respectively , in 121 postmenopausal women aged 54 + / 5 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
RESULTS : Excessive decrease in BMD was evidenced , which seemed to relate to the duration as well as type of treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At 18 mo , preoperative serum bone alkaline phosphatase was associated univariately with BMD loss in zones 1 ( r = 0 . 407 , p = 0 . 048 ) and 7 ( r = 0 . 543 , p = 0 . 006 ) and urinary N telopeptide cross linked collagen type 1 ( NTX ) was associated univariately with that in zone 7 ( r = 0 . 520 , p = 0 . 009 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured BMD by dual energy 10 ray absorptiometry ( DXA ) and quantitative bone ultrasound ( QUS ) , as well as the serum levels of osteocalcin ( OC ) , bone specific alkaline phosphatase ( BAP ) , osteoprotegerin ( OPG ) and its ligand RANKL , and the urinary concentration of the C terminal telopeptides of type 1 collagen ( CrossLaps ) , in 36 patient ( 20 male and 16 female ) with serious atherosclerotic involvement of the carotid and / or femoral artery to investigate the underlying mechanism of vascular and osseous disorders . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The defect in the lattice organization was also noted to be a characteristic of type 4 collagen , nidogen , perlecan , beta 1 ( D ) integrin , dystrophin and vinculin . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
L 1 L4 BMD z score was not related to weight , pre existing renal disease , gender , donor source , type of renal replacement therapy prior to transplantation , or rejection events . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
PURPOSE : This study was designed to elucidate the different decrease patterns of bone mineral density ( BMD ) in the distal tenth and third of the radius and ulna that influence the incidence of fractures , the fracture type , and redisplacement after closed reduction and casting . ^^^ The relationship between BMD , type of fracture , and radiographic parameters ( radial length , radial inclination , and palmar tilt ) determined after closed reduction and at bone union were examined . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We studied whether the combination of bone geometry and BMD could further improve the determination of hip fracture risk and fracture type . ^^^ The results confirm that the combination of BMD and radiological measures of upper femur geometry improve the assessment of the risk of hip fracture and fracture type compared to BMD alone , and that bone geometry plays an important role in the evaluation of bone strength . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : To study body composition and bone mineral density ( BMD ) in adult patients with long standing type 1 diabetes mellitus . ^^^ RESEARCH DESIGN AND METHODS : In a population based study , body composition and BMD were evaluated by dual energy 10 ray absorptiometry in 38 patients with type 1 diabetes since childhood , compared with 38 age and sex matched controls . ^^^ CONCLUSION : Patients with long standing type 1 diabetes with onset in childhood and adolescence seem to show only minor differences in body composition and no difference in BMD compared with closely matched healthy controls . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Decreases in serum BSAP ( bone specific alkaline phosphatase ) and serum or urine NTX ( N terminal telopeptide crosslink of type 1 collagen ) on high dose therapy were not predictive of an improvement in BMD , but a decrease in serum CrossLaps did predict an improvement in BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Type 1 herpes simplex virus ( HSV 1 ) based vectors , which are naturally capable of carrying large DNA fragments like the 14 kb dystrophin cDNA , have been studied for their ability to transduce muscle cells . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Aim : To evaluate bone turnover and bone mineral density ( BMD ) in MPS type 3 patients . ^^^ METHODS : We evaluated serum markers of bone formation or resorption , and measured BMD using dual energy 10 ray absorptiometry ( DEXA ) , in three patients with MPS type 3 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MATERIAL AND METHODS : For this purpose , we calculated BMI , and measured spinal ( BMD ( SP ) ) and femoral bone mineral density ( BMD ( FN ) ) and biochemical markers of bone formation ( serum osteocalcin ( S OC ) , serum procollagen type 1 C propeptide ( S PICP ) , serum bone specific alkaline phosphatase ( S B ALP ) ) and resorption ( urine N and C terminal cross linking telopeptide of type 1 collagen ( U NTX 1 and U CTX 1 ) , pyridinoline ( U PYD ) and deoxypyridinoline ( U DPD ) ) in 130 healthy postmenopausal women , aged 46 85 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The purpose of our study was to investigate associations of serum adiponectin with BMD ( DXA and QCT ) , FM ( DXA and QCT ) , and serum leptin and soluble leptin receptor levels in 38 women and 42 men ( age 39 81 , BMI 17 55 , 86 % with type 2 diabetes ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Important unanswered questions remain about the optimal relationship between intensity , amount and type of PA , and BMD and later risk of osteoporosis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In conclusion , the gymnasts had significantly higher ( p < 0 . 05 ) BMD than the runners , suggesting BMD is influenced by the type of mechanical loading . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : This study evaluated the effects of a 12 month rhGH therapy on bone metabolism parameters ; alkaline phosphatase ( AP ) , osteocalcin ( OC ) , procollagen 1 carboxyterminal propeptide ( PICP ) , telopeptide ICTP , serum crosslaps , n terminal propeptide of type 3 procollagen ( PIIINP ) and intact parathyroid hormone ( iPTH ) , as well as on BMD of the lumbar spine and the femoral neck in 19 malnourished HD patients ( 10 females , 9 males ) with a mean age of 59 . 3 + / 13 . 4 yrs . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum levels of three bone formation markers bone alkaline phosphatase ( BAP ) , osteocalcin ( OC ) , and N terminal propeptide of type 1 collagen ( PINP ) and three bone resorption markers type 1 collagen cross linked N telopeptide ( NTx ) , deoxypyridinoline ( DPD ) , and pyridinoline ( PYD ) were measured simultaneously in 85 predialysis CRF patients ( serum creatinine 3 . 5 + / 1 . 9 mg / dl , 61 . 0 + / 10 . 9 years old , 54 males and 31 females , 36 diabetics and 49 nondiabetics ) to examine the relationships between these markers and bone mineral density ( BMD ) of the distal radius , as measured by peripheral quantitative computed tomography ( pQCT ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Insulin like growth factor 1 ( IGF 1 ) gene microsatellite repeat polymorphism was found to be associated with osteoporosis in some studies and collagen type 1 alpha 1 ( COLIA 1 ) SP 1 `` s ' ' allele was associated with lower bone mineral density ( BMD ) in PBC . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At linear multiple regression [ dependent variable = femur BMD ; independent variables = age , weight , height , body mass index , fracture type , term fracture DXA , Barthel index score , FBM , lean body mass , serum PTH , serum 25 ( OH ) vitamin D and leptin ] , FBM was positively associated with BMD measured at all the five sites . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Total and regional bone mineral density ( BMD ) was determined by dual energy 10 ray absorptiometry , while bone turnover was evaluated by specific biochemical markers : bone specific alkaline phosphatase ( B ALP ) , osteocalcin , and urinary type 1 collagen C telopeptide . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : Alendronate sodium ( ALN ) increases bone mineral density ( BMD ) in heterogeneous populations of postmenopausal women , but its effect is unknown in women with type 2 diabetes . ^^^ CONCLUSIONS : ALN increased BMD relative to placebo in older women with type 2 diabetes and was generally well tolerated as a treatment for osteoporosis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MATERIALS AND METHODS : We measured biochemical markers of bone turnover ( bone specific alkaline phosphatase [ bone ALP ] , intact N terminal propeptide of type 1 collagen , and C terminal crosslinked telopeptide of type 1 collagen ) and BMD of the spine and hip at baseline and after 1 year of alendronate or placebo . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Logistic multiple regression showed no meaningful associations between PHPT and sex , age , weight , height , fracture type ( cervical or trochanteric ) , and femoral BMD in the hip fracture patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
No dose response association between ICS and BMD , or difference in BMD by type of ICS was found . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We investigated the effect of HMG CoA reductase inhibitors on BMD in patients with Type 2 diabetes mellitus . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The association between type 2 diabetes , BMD , and bone volume was examined to determine the effect of lean and fat mass and fasting insulin in the Health , Aging , and Body Composition Study , which included white and black well functioning men and women 70 79 years of age ( N = 2979 ) . ^^^ INTRODUCTION : The purpose of this study was to determine if the association between type 2 diabetes and higher BMD observed in older white women is seen in elderly white men and blacks and to evaluate if higher BMD in diabetic individuals is accounted for by lean mass , fat mass , or fasting insulin differences . ^^^ Type 2 diabetes was associated with a 4 5 % higher total hip BMD in all race gender groups of elderly adults , independent of body composition and fasting insulin levels . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Mutations in the human vitelliform macular dystrophy type 2 ( VMD 2 ) gene are known to cause autosomal dominant Best macular dystrophy ( BMD ) , a degenerative disorder of the central retina . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
At baseline , we recorded body mass index ( BMI ) , a score of Mini Mental State Examination ( MMSE ) and bone mineral density ( BMD ) , and measured serum concentrations of ionized calcium , intact parathyroid hormone ( PTH ) , pyridinoline cross linked carboxyterminal telopeptide of type 1 collagen ( ICTP ) , intact bone Gla protein ( BGP ) , 25 hydroxyvitamin ( 25 OHD ) and 1 , 25 dihydroxyvitamin D ( 1 , 25 [ OH ] 2D ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Older age , previous self reported fracture after age 50 , maternal history of hip fracture after age 50 , greater height at age 25 , impaired cognition , slower walking speed , nulliparity , type 2 diabetes mellitus , Parkinson ' s disease , and depth perception each independently predicted a 1 . 17 to 1 . 83 fold increase in hip fracture risk , whereas each SD ( 0 . 13 g / cm2 ) decrease in hip BMD was independently associated with a 1 . 84 fold increase in risk . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : To examine early changes in biochemical markers of bone turnover and bone mineral density ( BMD ) in a clinical trial of anti resorptive agent alendronate versus alfacalcidol in postmenopausal women with type 2 diabetes mellitus . ^^^ Urinary N telopeptide cross linked collagen type 1 ( NTx ) , one of biochemical markers , and radial bone mineral density ( BMD ) were measured as a marker of bone turnover . ^^^ CONCLUSION : Alendronate that produces reduction in urinary NTx and inhibition of decrease in BMD may have a clinical significance to reduce the risk of bone fracture in postmenopausal type 2 diabetic women . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Partial gene deletion is the major type of mutation leading to Duchenne muscular dystrophy ( DMD ) and its mild allelic form , Becker muscular dystrophy ( BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The purpose of this study was to investigate the heritability of BMD as determined by QCT and DXA in 124 women and 120 men ( age 39 83 years , BMI 17 75 , 84 % type 2 diabetics ) from 101 families ( 232 sibling pairs ) in the Diabetes Heart Study . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
BMD and Z score at the distal radius were significantly lower in type 2 diabetic patients than those in control subjects , and in type 2 diabetic patients , the Z score at the distal radius was lower than that at their own lumbar spine and femoral neck . ^^^ In type 2 diabetic patients , negative correlation between BMD and the mean HbA1c during the previous 2 years was found significantly at the distal radius in both genders and at the femoral neck in women . ^^^ These results indicate the selective cortical bone loss in type 2 diabetes and suggest the importance of also determining BMD at the radius and keeping good metabolic control to prevent bone loss in type 2 diabetic patients . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Primary endpoint of the study was the change in bone metabolism evaluated by N telopeptide of type 1 collagen and bone specific alkaline phosphatase ; the secondary endpoint was BMD variation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Moreover , both plasmin activity and alpha enolase plasminogen receptor expression were significantly augmented in injury induced regenerating muscle of wild type mice and in the dystrophic muscle of mdx mice , an animal model of Duchenne muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Since Albright first proposed the concept of `` diabetic osteopenia ' ' , many studies have investigated the levels of bone mineral density ( BMD ) and the risk of osteoporosis in type 1 and type 2 diabetes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Collagen type 1 alpha 2 ( COL1A2 ) and parathyroid hormone ( PTH ) / PTH related peptide receptor ( PTHR 1 ) are two prominent candidate genes for bone mineral density ( BMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Among the SNPs analyzed , the B+ type of the VDR gene tended to be associated with a lower BMD , and pp type of the ER gene digested by the PvuII enzyme in females indicated a significantly lower BMD than that in males . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This report provides evidence indicating that treatment with oral alendronate may have the potential to decrease bone turnover , improve the lumbar BMD , reduce back pain , and prevent new fragile fractures in premenopausal women with OI type I . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Differences in the levels of urinary metabolites and BMD among the different variants were analyzed by analysis of covariance , whereas differences in free estradiol index , urinary N telopeptide of type 1 collagen ( NTx ) , and bone size were compared by one way ANOVA . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In order to utilize other antibiotics with less side effects than gentamicin , we have shown that negamycin , a dipeptide antibiotic with read through activity in prokaryotes , restored dystrophin in skeletal and cardiac muscles of mdx mouse , an animal model for Duchenne type muscular dystrophy caused by nonsense mutation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : To determine the association between serum concentrations of osteocalcin , the carboxyterminal propeptide of type 1 collagen ( PICP ) and the carboxyterminal cross linked telopeptide of type 1 collagen ( ICTP ) measured early in the training season and the risk of DMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
To search for a correlation between alterations in chaotic brain states and mood disorders , we compared the fractal dimension of the electroencephalographic ( EEG ) signal in patients going through a manic episode of bipolar mood disorder ( BMD ) type 1 to a control group of healthy adults and showed that the EEG fractal dimension is significantly augmented in our patients . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
RESEARCH DESIGN AND METHODS : Total body BMC and BMD of 184 overweight Latino children ( 106 boys , 78 girls , 11 . 9 + / 1 . 7 years ) with a family history of type 2 diabetes were measured using dual energy 10 ray absorptiometry . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Preliminary in vitro studies indicate that the extent of post translational modifications of collagen which can be reflected in vivo by the measurement of the urinary ratio between native and isomerised type 1 collagen play a role in determining the mechanical competence of cortical bone , independently of BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
An increase in forearm BMD and a decrease in the level of urinary crosslinked N telopeptides of type 1 collagen ( NTx ) were observed in January 2003 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To study the relationships of serum bone alkaline phosphatase ( sBAP ) , serum osteocalcin ( sOC ) and the ratio of urine cross linked N telopeptide of collagen type 1 ( uNTX ) / creatine ( Cr ) with age and bone mineral density ( BMD ) in healthy women aged 20 80 years . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
While type 1 diabetes is generally associated with a mild reduction in bone mineral density ( BMD ) , type 2 diabetes , more prevalent in old subjects , is frequently linked to a normal or high BMD . ^^^ Studies on experimental models of diabetes have suggested an altered bone structure that may help to explain the elevated risk of fractures observed in these animals and may as well help to explain the paradox of an incremented risk of fractures in type 2 diabetic elderly in the presence of normal or elevated BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : Premature menopause is a known risk factor for osteoporosis , whilst the influence of type 2 diabetes on bone mineral density ( BMD ) is still controversial . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The mdx mice are a model for the human disease , Duchenne muscular dystrophy ( DMD ) , and the Lama 2 null mice are a model for human congenital muscular dystrophy type 1A ( MDC1A ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In all subjects the following parameters were assessed : bone mineral density ( BMD ) of the total body , L 2 L4 vertebrae and femoral neck ( DEXA ) , serum total PTH ( 1 PTH ) and PTH 1 84 level , as well as the difference between total PTH and PTH 1 84 ( reported as PTH 7 84 ) , activity of alkaline phosphatase ( AP ) , serum concentration of collagen type 1 cross linked C telopeptide , osteocalcin ( OC ) , creatinine ( creat ) , 25 OH D , total calcium ( Ca ( total ) ) and phosphorus ( P ) concentration . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Although type 2 diabetes is not associated with lower BMD , older diabetic adults have a higher prevalence of other risk factors for fracture , including more frequent falls , functional limitations , and diabetic complications . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In type 1 OI , some patients appear normal without investigating bone mineral density ( BMD ) by DXA . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
No significant relationship was found between BMD losses and the cast type . ^^^ CONCLUSION : Our results show that BMD losses and deterioration in reduction following treatment of CF occur irrespective of which type of casting is used . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The present study was designed to examine whether the prevalence of vertebral fracture in female HD patients with type 2 DM , age 65 years and older , might be increased , and the relation of this fracture to bone mineral density ( BMD ) determined by dual 10 ray absorptiometry ( DXA ) , since few data are available on the effect of DM on bone strength at lumbar spine . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Measurements included the following : femur bone area ( BA ) , mineral content ( BMC ) , density ( BMD ) , morphometry and ex vivo release of prostaglandin E ( 2 ) ( PGE ( 2 ) ) ; plasma osteocalcin and C terminal telopeptides of type 1 collagen . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Measurements included : bone area ( BA ) , mineral content ( BMC ) , and density ( BMD ) of whole body , lumbar spine , and excised femurs ; biomarkers of bone modeling were plasma osteocalcin and urinary cross linked N telopeptides of type 1 collagen ( NTx ) , tibial ex vivo release of prostaglandin E ( 2 ) ( PGE ( 2 ) ) , plasma insulin like growth factor 1 ( IGF 1 ) , and tissue fatty acids . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The effect of age , sex , and type of thalassaemia and hormonal factors on BMD was assessed . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The purpose of this study was to determine whether early changes in the urinary levels of cross linked N terminal telopeptides of type 1 collagen ( NTX ) during alendronate treatment would be correlated with the 1 year response of lumbar bone mineral density ( BMD ) in postmenopausal Japanese women with osteoporosis . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The correlation between BMD phenotype and type of deletion suggests that , in the distal rod domain region , the deletion size may not be as crucial as the particular combination of missing exons . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Secondary endpoints included change in lumbar spine BMD and change in markers of bone turnover ( bone specific alkaline phosphatase and urinary type 1 collagen cross linked N telopeptide ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aim of the study was to analyse bone mineral density ( BMD ) in patients with familial amyloid polyneuropathy ( FAP ) type 1 ( Val 30 Met ) and to compare them with a population of patients with other neuromuscular disorders . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
This study investigated and compared the gait of two patients with spinal muscular atrophy , type 2 ( SMA 2 ) and two patients with Duchenne muscular dystrophy ( DMD ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
HPV types 16 and 33 were more prevalent in women , amongst those containing a single hrHPV type , with moderate dyskaryosis or worse ( > BMD ) than in women with normal cytology , but only in case of underlying > or =CIN2 ( OR 4 . 10 , 95 % CI 2 . 98 5 . 64 and OR 2 . 68 , 95 % CI 1 . 39 5 . 15 , respectively ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Physical activity increased cortical BMD in wild type runners but not in the HZK runners at the age of 9 months . ^^^ There were only minor changes in BMD and mechanical and structural properties between sedentary HZK mice and their wild type controls . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Without information on BMD , the age adjusted risk for any type of fracture increased significantly with lower BMI . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aim was to investigate whether the addition of supervised high intensity progressive resistance training to a moderate weight loss program ( RT+WLoss ) could maintain bone mineral density ( BMD ) and lean mass compared to moderate weight loss ( WLoss ) alone in older overweight adults with type 2 diabetes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Three patients ( 1 with BS type 2 and 2 with BS type 3 ) presented reduced lumbar spine BMD or overt osteopenia ( BMD Z scores : 2 . 3 , 1 . 3 , and 1 . 1 ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Only body mass index ( BMI ) was correlated with BMD in the type 1 diabetic group , and only BMI and age were correlated with BMD in type 2 diabetics . ^^^ We did not find any significant difference in peripheral BMD between patients with type 1 diabetes , type 2 diabetes and controls . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In view of the reported associations between the BMD and polymorphisms in the collagen type 1 alpha 1 gene ( COL1A1 ) , vitamin D receptor ( VDR ) , estrogen receptor ( ER ) alpha and calcitonin receptor ( CTR ) genes , an association study was performed between VDR , COL1A1 , CTR and ER genotypes and lumbar spine , femoral neck and Ward ' s triangle BMD in postmenopausal Spanish women . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
After the mice had been killed , paws were collected for histology , one femur for bone mineral density ( BMD ) and sera for analyses of markers of bone resorption ( RatLaps ; type 1 collagen cross links , bone formation ( osteocalcin ) and cartilage destruction ( cartilage oligomeric matrix protein ) , and for the evaluation of antigen specific and innate immune responsiveness . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The losses of the lumbar BMD in patients with liver cirrhosis and the metacarpal BMD in hemiplegic patients after stroke are prevented , and the lumbar BMD is possibly increased , preventing fragile fractures in adult patients with osteogenesis imperfecta type 1 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured BMD and body composition ( dual energy 10 ray absorptiometry ) and carboxy terminal peptide of type 1 procollagen and N telopeptide levels . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
AIM : To investigate the influence of interleukin 6 ( IL 6 ) , collagen type 1alpha1 ( COL1A1 ) , and vitamin D receptor gene ( VDR ) single nucleotide polymorphisms ( SNP ) on BMD in patients with Crohn ' s disease . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Average absolute intrapair BMD difference between hip subregions was 0 . 038+ / 0 . 001 g / cm2 and was unaffected by the presence or type of positioning flaw . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The transforming growth factor ( TGF ) beta pathway was strongly induced in symptomatic patients , with expression of TGFbeta type 2 receptor and apoptosis signal regulating kinase 1 proteins on subsets of mature DMD myofibers . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
It is feasible to select different QUS methods , one type being optimized to assess microarchitectural properties of bone structure and another to assess BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The aim of this study was to assess the efficacy of ERT on bone involvement in a group of 12 type 1 Gaucher disease ( GD 1 ) patients by monitoring biochemical indices of bone resorption / formation and BMD measured by dual energy 10 ray absorptiometry ( DEXA ) . ^^^ Serum ( calcium , phosphorus , bone alkaline phosphatase isoenzyme , carboxyterminal propeptide of type 1 procollagen ( PICP ) , carboxyterminal telopeptide of type 1 collagen ( ICTP ) , osteocalcin , intact parathyroid hormone ) and urinary ( calcium , phosphorus , hydroxyproline and free deoxypyridinoline ) markers of bone metabolism and lumbar BMD were measured at baseline , after 6 and 12 months , and then every year for a mean ERT follow up period of 4 . 5 years ( range 4 . 4 6 years ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
METHODS : BMD , levels of parathyroid hormone ( PTH ) , osteocalcin , C terminal cross linking telopeptide of type 1 collagen ( CTX ) , calcium , alkaline phosphates ( ALP ) , cytokines as TNF alpha , interleukin ( IL ) 1beta , IL 2r , IL 6 , and IL 8 were studied in 54 children with chronic hepatitis B ( 4 15 years old ) treated with interferon alone ( n = 19 ) or in combination with lamivudine ( n = 35 ) for six months and as controls in 50 age matched healthy children . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Effects of angiotensin 1 converting enzyme inhibitor and angiotensin 2 type 1 receptor blocker on the right ventricular sarcoglycans and dystrophin after left coronary artery ligation . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Mice with a targeted deletion of either the cannabinoid receptor type 1 ( Cnr 1 ) or type 2 ( Cnr 2 ) gene show an alteration of bone mass , and pharmacological modification of both receptors can regulate osteoclast activity and BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The NOS guidelines recommend a triage approach in which patients ' bone mineral density ( BMD ) measurements are interpreted using upper and lower thresholds specific to each type of pDXA device . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These results suggest that a number of candidate genes located in the excluded regions , such as interleukin 6 receptor ( IL6R ) gene , type 1 collagen alpha 1 ( COL1A1 ) gene and bone morphogenetic protein 3 ( BMP 3 ) gene are unlikely to have a substantial effect on BMD variation in this Caucasian population . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The effect of exercise on bone mineral density ( BMD ) depends on the type of activity engaged in . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The influence of muscle type and dystrophin deficiency on murine expression profiles . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Myotonic dystrophy ( DM ) type 1 is associated with an expansion of ( > 50 ) CTG repeats within the 3 ' untranslated region ( UTR ) of the dystrophin myotonin protein kinase gene ( dmpk ) . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
However , the residual expression of middle genes at late stages continues at a higher rate in cells infected with a dmd mutant than with the wild type . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
CONCLUSIONS : The stability of the morpholino structural type , and the fact that it can be delivered to muscle in the absence of a delivery reagent , render this compound eminently suitable for consideration for therapeutic exon skipping to address dystrophin mutations . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The interaction between the adaptor / scaffolding protein dystrobrevin and the motor protein kinesin may play a role in the transport and targeting of components of the dystrophin associated protein complex to specific sites in the cell , with the differences in the binding properties of dystrobrevin isoforms reflecting their functional diversity within the same cell type . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
In addition , bone mineral density ( BMD ) is a convenient predictor for fracture and the type 1 diabetes is associated with modest reductions in BMD . ^^^ However , type 2 diabetes can be related to the elevated BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We examine the attitudes of pediatricians and pediatric subspecialists toward screening for cystic fibrosis ( CF ) , Duchenne muscular dystrophy ( DMD ) , fragile 10 , and type 1 diabetes . ^^^ Those who would personally choose testing of their own infants were highly likely to support newborn screening for CF ( 98 % ) , DMD ( 94 % ) , and fragile 10 ( 98 % ) , but only 78 % of those who would personally opt for newborn screening of type 1 diabetes would also endorse population based screening . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Expression of the skeletal muscle dystrophin dystroglycan complex and syntrophin nitric oxide synthase complex is severely affected in the type 2 diabetic Goto Kakizaki rat . ^^^ Immunohistochemical studies revealed that the reduction in the dystrophin dystroglycan complex does not induce obvious signs of muscle pathology , and is neither universal in all fibres , nor fibre type specific . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MAIN OUTCOME MEASURES : BMD ( lumbar spine , total femur , femoral neck , distal forearm , and total body ) and biochemical markers ( serum intact amino terminal propeptide of type 1 procollagen , type 1 collagen cross linked C telopeptide , and osteocalcin ) were measured at baseline and follow up visits . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
There were greater responses in BMD and growth in children with milder OI ( type 1 ) than those with more severe disease ( types 3 and 4 ) , but there were no significant effects of age or pubertal stage . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum osteocalcin , C telopeptide of type 1 collagen , and BMD at lumbar spine and proximal femur were measured . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The BMD of the lumbar spine ( L 1 L4 ) measured by DXA , the urinary cross linked N terminal telopeptides of type 1 collagen ( NTX ) level measured by the enzyme linked immunosorbent assay , and back pain evaluated by the face scale score were assessed at baseline , 6 months , and 12 months . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Urinary type 1 collagen N telopeptide ( NTx ) and serum osteocalcin ( OC ) at baseline , 3 , and 6 months after treatment as well as spine and femoral neck BMD at baseline and 12 months were measured . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
We measured bone mineral density ( BMD ) and urinary type 1 collagen N telopeptide ( uNTX ) in 35 postoperative patients including 25 with pituitary tumor ( PT ) , 6 with craniopharyngioma ( CP ) , and 4 others who had not been on sex hormone replacement , raloxifene , or bisphosphonate therapy . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : To determine whether middle aged premenopausal women with type 1 diabetes had more self reported fractures and lower bone mineral density ( BMD ) compared with nondiabetic women . ^^^ Type 1 diabetes was associated with lower total hip BMD ( 0 . 890 vs . 0 . 961 g / cm2 ; P < 0 . 001 ) , femoral neck BMD ( 0 . 797 vs . 0 . 847 g / cm2 ; P = 0 . 001 ) , whole body BMD ( 1 . 132 vs . 1 . 165 g / cm2 ; P < 0 . 01 ) , and lower calcaneal BUA ( 71 . 6 vs . 84 . 9 dB / MHz ; P < 0 . 001 ) after multivariate adjustment . ^^^ BMD was 3 8 % lower in type 1 diabetic compared with control women and calcaneal BUA was 15 % lower . ^^^ In the type 1 diabetic women , reduced monofilament detection and blindness were both associated with lower BMD . ^^^ CONCLUSIONS : Lower BMD in premenopausal women with type 1 diabetes may substantially increase their risk of developing osteoporosis after menopause . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
TYPE OF STUDY : A 2 year prospective cohort study with assessment of patient evaluation of knee performance , clinical scoring of surgical results , and measurement of BMD in the tibia and calcaneus . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
MATERIALS AND METHODS : We analysed bone mineral density ( BMD ) measured at the hip , spine and forearm using dual energy 10 ray absorptiometry in 34 patients with type 1 and 194 patients with type 2 diabetes . ^^^ RESULTS : After adjusting for age and BMI , there was a lower BMD at total hip ( p < 0 . 001 ) and femoral neck ( p=0 . 012 ) in type 1 men vs control subjects , but type 1 women and matched controls had similar BMD at each site . ^^^ There was a higher BMD at total hip ( p=0 . 006 ) , femoral neck ( p=0 . 026 ) and forearm ( p < 0 . 001 ) in type 2 women vs control subjects , but diabetes status was not associated with BMD in type 2 men after adjustment for age and BMI . ^^^ Serum oestradiol , BMI , C terminal telopeptide of collagen type 1 and male sex were consistently and independently associated with BMD at forearm , hip and femoral neck and explained 61 , 55 and 50 % of the total variance in BMD , respectively , at these sites . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Weight , type 2 diabetes and thiatzide use were associated with higher radius BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Auxological parameters , total bone mineral content ( TBMC ) and density ( TBMD ) , leg BMC and BMD , lumbar BMD , fat mass ( FM ) and lean tissue mass ( LTM ) , blood 25 hydroxyvitamin D ( 25 OHD ) , parathyroid hormone ( PTH ) , osteocalcin ( OC ) and urinary N terminal telopeptide of type 1 collagen ( NTx ) were determined at the start of therapy and after 1 and 2 years of treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Structural cooperativity in spectrin type repeats motifs of dystrophin . ^^^ Dystrophin is a member of the spectrin family of proteins , which are characterized as being predominantly composed the spectrin type repeat , a triple alpha helical bundle motif present in multiple tandem copies , producing a rod like shape . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Greater 1 and 3 month increases in turnover , particularly the formation marker N propeptide of type 1 collagen , were associated with greater increases in areal BMD . ^^^ Each sd increase in the 3 month change of N propeptide of type 1 collagen was associated with an a 21 % greater increase in QCT spine trabecular BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) at L 2 L4 according to dual energy 10 ray absorptiometry ( DXA ) , the administration of corticosteroids or methotrexate , and urinary excretion of N telopeptide of type 1 collagen ( NTx ) were also recorded . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Moment correlation coefficients were calculated to determine the effect of BMD on peak torque and pullout force for each type of screw . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Changes in hip BMD and in the level of serum C telopeptide of type 1 collagen ( CTX ) were also measured , as were safety and tolerability . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Thirty six wheelchair bound subjects and 19 age matched controls were evaluated using measurements of bone mineral density ( BMD ) at the calcaneus and forearm ( PIXI , Madison , WI ) , amplitude dependent speed of sound at the hand phalanges ( quantitative ultrasound DBM Sonic 1200 , IGEA , Modena , Italy ) , carboxyterminal telopeptide of type 1 collagen and bone alkaline phosphatase . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Historical low weight , duration of nucleoside reverse transcriptase inhibitor use , and FSH were significantly associated with lumbar BMD , whereas duration of HIV , BMI , historical low weight , smoking pack years , N telopeptide of type 1 collagen , viral load , 25 hydroxyvitamin D , and osteocalcin were associated with hip BMD at baseline . ^^^ In the HIV group , longitudinal changes in BMD were not associated with current protease inhibitor , nucleoside reverse transcriptase inhibitor , or non nucleoside reverse transcriptase inhibitor use but were associated with CD 4 count , weight , FSH , N telopeptide of type 1 collagen , and baseline BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Serum osteocalcin , bone alkaline phosphatase , C telopeptide of type 1 collagen , and BMD at the lumbar spine and femoral neck were measured . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Total DPD is good predictor of change bone mineral density ( BMD ) in bone antiresorptive drugs , however , free DPD is inferior to type 1 collagen N telopeptide ( NTX ) . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The linkage and / or association of 13 polymorphic loci of seven candidate genes ( estrogen receptor alpha [ ERalpha ] and beta [ ERbeta ] , calcium sensing receptor , vitamin D receptor , collagen type 1alpha1 , low density lipoprotein [ LDL ] receptor related protein 5 [ LRPS ] , and transforming growth factor beta 1 ) were evaluated in 177 southern Chinese pedigrees of 674 subjects , with each pedigree identified through a proband having a BMD Z score of 1 . 28 or less at the hip or spine . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
When analyzed by pubertal stage , BMI , lean body mass ( LBM ) , FM , and total bone mineral density ( BMD ) were significantly higher in pubertal girls with type 1 diabetes compared to prepubertal ones . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The vitamin D receptor gene ( VDR ) , the collagen type 1 alpha 1 gene ( COLIA 1 ) and estrogen receptor gene ( ER ) alpha have been most widely investigated and found to play a role in regulating BMD , but the effects are modest and together probably account for less than 5 % of the heritable contribution to BMD . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
These data suggest that areal BMD measured by DXA and trabecular volumetric BMD measured by QCT are not associated with type 2 diabetes independently from BMI . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Hybrid spectrin type repeats produced by exon skipping in dystrophin . ^^^ The structure of the dystrophin protein is highly modular , with the most common module being a motif termed the spectrin type repeat , or STR , of which there are 24 . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The purposes of this study were to describe the response to enalapril and its relation to dystrophin mutation type , ventricular size , or age at the onset of left ventricular ( LV ) systolic dysfunction . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVE : The objective of the study was to determine whether TZD use is associated with changes in bone mineral density ( BMD ) in older adults with type 2 diabetes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Although type 2 diabetes is often characterized by normal or high bone mineral density ( BMD ) , diabetes is associated with increased risk of fracture . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Bone mineral density ( BMD ) is the best predictor for fractures of primary osteoporosis , and increased risk for fractures of the type 1 diabetes is associated with the decrease of BMD , but not on the type 2 diabetes . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
Negative correlation between BMD and HbA1C in patients with type 2 diabetes ] . ^^^ BMD and Z score at the distal radius were significantly lower in type 2 diabetic patients than those in control subjects . ^^^ In type 2 diabetic patients , negative correlation between BMD and the mean HbA ( 1C ) during the last 2 years was found significantly at the distal radius in both sexes . ^^^ These results indicate the selective cortical bone loss in type 2 diabetes , and suggest the importance of evaluating BMD at the radius as well and keeping good metabolic control to prevent bone loss in type 2 diabetic patients . . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
OBJECTIVES : To analysis bone mineral density ( BMD ) and bone turnover markers in children and adolescents with type 1 diabetes mellitus ( DM 1 ) and to establish possible correlations with duration of the disease and degree of metabolic control . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
The BMD of the lumbar spine ( L 2 L4 ) was measured by dual energy 10 ray absorptiometry , and urinary cross linked N telopeptides of type 1 collagen ( NTX ) were assessed at baseline , 6 months , and 12 months after treatment . ^^^
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA
Interacting proteins: Q13326 and P11532	Pubmed	SVM Score :0.0
NA