(Q28141128)

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Subcellular fractionation of dystrophin to the triads of skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Glycoprotein complex anchoring dystrophin to sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Muscular dystrophies and the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

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.274.53.38171

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.274.53.38171

Dystrophin-associated proteins in muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

Muscle degeneration without mechanical injury in sarcoglycan deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

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.274.53.38171

Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Molecular organization of sarcoglycan complex in mouse myotubes in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

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.274.53.38171

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

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.274.53.38171

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.274.53.38171

Identification of the Syrian hamster cardiomyopathy gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Bidirectional signaling between sarcoglycans and the integrin adhesion system in cultured L6 myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Developmental progression of myosin gene expression in cultured muscle cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

Homologous recombination at c-fyn locus of mouse embryonic stem cells with use of diphtheria toxin A-fragment gene in negative selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Comparison of two methods of preparing enzyme-antibody conjugates: Application of these conjugates for enzyme immunoassay

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

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.274.53.38171

alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Laminin polymerization induces a receptor-cytoskeleton network

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171

The one-to-four rule and paralogues of sex-determining genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.53.38171