Identification and characterization of the dystrophin anchoring site on beta-dystroglycan (Q24316047)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7592992%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

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

1 reference

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21 October 2019

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GOA release 2020-03-11

author

Kevin P Campbell

5

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21 October 2019

author name string

D Jung

1

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21 October 2019

B Yang

2

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21 October 2019

J Meyer

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7592992%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

J S Chamberlain

4

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21 October 2019

language of work or name

English

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publication date

1 November 1995

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Journal of Biological Chemistry

21 October 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7592992%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

270

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21 October 2019

page(s)

27305-27310

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21 October 2019

issue

45

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Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain

21 October 2019

cites work

1 reference

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7 January 2021

Deletion analysis of the dystrophin-actin binding domain.

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7 January 2021

Dystrophin isoforms and/or cross-reactive proteins on neurons and glial cells in control and mdx central nervous systems.

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7 January 2021

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

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7 January 2021

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

1 reference

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7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

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7 January 2021

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

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7 January 2021

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

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7 January 2021

Ca2+ channel regulation by a conserved beta subunit domain

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7 January 2021

Characterization and subcellular localization of the dystrophin-protein 71 (Dp71) from brain

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7 January 2021

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy.

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7 January 2021

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice

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7 January 2021

Characterization and localization of a 77 kDa protein related to the dystrophin gene family

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7 January 2021

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

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7 January 2021

SH3 domain-mediated interaction of dystroglycan and Grb2

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7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1074%2FJBC.270.45.27305

7 January 2021

Syntrophin binds to an alternatively spliced exon of dystrophin

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7 January 2021

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

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7 January 2021

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

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7 January 2021

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

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7 January 2021

A novel dystrophin isoform is required for normal retinal electrophysiology.

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7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

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7 January 2021

Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

1 reference

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7 January 2021

Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

1 reference

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7 January 2021

An intact cysteine-rich domain is required for dystrophin function

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7 January 2021

Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma

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7 January 2021