(Q28138974)

1

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S A Moore

2

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C A Stolle

3

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J R Mendell

4

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K P Campbell

Journal of Biological Chemistry

5

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language of work or name

English

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publication date

8 December 2000

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published in

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volume

275

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page(s)

38554-60

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issue

49

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cites work

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Muscular dystrophies and the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

The sarcoglycan complex in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Neuronal nitric oxide synthase and dystrophin-deficient muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Dystroglycan inside and out.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Sarcoglycan isoforms in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Identification of the Syrian hamster cardiomyopathy gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Expression of dystrophin-associated protein 35DAG (A4) and 50DAG (A2) is confined to striated muscles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Sarcospan-deficient mice maintain normal muscle function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Delineation of genomic deletion in cardiomyopathic hamster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007799200