(Q72640306)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894483%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

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

1 reference

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28 October 2019

3

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28 October 2019

author name string

Greenberg DS

1

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28 October 2019

Sunada Y

2

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28 October 2019

Yaffe D

4

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28 October 2019

Nudel U

5

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28 October 2019

publication date

1 December 1994

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28 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894483%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

volume

8

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28 October 2019

page(s)

340-344

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28 October 2019

issue

4

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https://scigraph.springernature.com/pub.10.1038/ng1294-340

28 October 2019

exact match

0 references

cites work

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Glycoprotein complex anchoring dystrophin to sarcolemma

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Characterization and cell type distribution of a novel, major transcript of the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Dp71, the nonmuscle product of the Duchenne muscular dystrophy gene is associated with the cell membrane.

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Specificity of dystrophin analysis improved with monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal andmdxmice Immunological evidence

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Dystrophin expression in Duchenne patients with "in-frame" gene deletions.

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1294-340

7 January 2021

Identifiers

DOI

10.1038/NG1294-340

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7894483%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference