(Q28298383)

2

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B Apostol

3

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V Straub

4

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J C Lee

5

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V Allamand

6

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D P Venzke

7

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Y Sunada

8

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C R Moomaw

9

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C J Leveille

10

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C A Slaughter

11

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T O Crawford

12

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J D McPherson

13

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K P Campbell

Journal of Biological Chemistry

14

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language of work or name

English

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publication date

13 December 1996

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published in

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volume

271

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issue

50

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page(s)

32321-9

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cites work

Association of dystrophin and an integral membrane glycoprotein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Glycoprotein complex anchoring dystrophin to sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Analysis of the actin-binding domain of alpha-actinin by mutagenesis and demonstration that dystrophin contains a functionally homologous domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Syntrophin binds to an alternatively spliced exon of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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.271.50.32321

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.271.50.32321

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

β–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.271.50.32321

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.271.50.32321

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.271.50.32321

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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/10.1074%2FJBC.271.50.32321

On the classification, natural history and treatment of the myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Development of a microsatellite genetic map spanning 5q31–q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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/10.1074%2FJBC.271.50.32321

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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.271.50.32321

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.271.50.32321

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Construction and characterization of a normalized cDNA library

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.50.32321

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.271.50.32321

21 January 2018

Identifiers

DOI

10.1074/JBC.271.50.32321

1 reference

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Fatcat ID

release_2hfleb7v65gojlepp2kzniruoa

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PubMed publication ID

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https://api.fatcat.wiki/v0/release/2hfleb7v65gojlepp2kzniruoa