(Q41160185)

27 September 2017

1 reference

title

Dystrophin-associated proteins and the muscular dystrophies: a glossary (English)

1 reference

27 September 2017

Brown RH Jr

1

1 reference

27 September 2017

1 January 1996

1 reference

27 September 2017

1 reference

27 September 2017

6

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27 September 2017

19-24

1 reference

27 September 2017

1

1 reference

Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution.

27 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

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/10.1111%2FJ.1750-3639.1996.TB00779.X

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Association of dystrophin and an integral membrane glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

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/10.1111%2FJ.1750-3639.1996.TB00779.X

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Nitric oxide in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Dystrophin at the plasma membrane of human muscle fibers shows a costameric localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Cloned human brain nitric oxide synthase is highly expressed in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Dystrophin colocalizes with beta-spectrin in distinct subsarcolemmal domains in mammalian skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Primary structure of dystrophin-related protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1996.TB00779.X

10.1111/J.1750-3639.1996.TB00779.X

21 January 2018

Identifiers

DOI

1 reference

27 September 2017

1 reference

PubMed ID

8866744