Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy (Q28144192)

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12 December 2019

title

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy (English)

1 reference

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12 December 2019

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Dystroglycan 1

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Sarcospan

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Sarcoglycan, beta (dystrophin-associated glycoprotein)

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Sarcoglycan, gamma (dystrophin-associated glycoprotein)

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Creatine kinase, brain

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Sarcoglycan, delta (dystrophin-associated glycoprotein)

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Sarcoglycan, alpha (dystrophin-associated glycoprotein)

1 reference

1 reference

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3

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12 December 2019

Kevin P Campbell

12

1 reference

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12 December 2019

Ramón Coral

1 reference

ORCID Public Data File 2021

author name string

R Coral-Vazquez

1

1 reference

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12 December 2019

R D Cohn

2

1 reference

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12 December 2019

J A Hill

4

1 reference

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12 December 2019

R M Weiss

5

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12 December 2019

R L Davisson

6

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12 December 2019

V Straub

7

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12 December 2019

R Barresi

8

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12 December 2019

D Bansal

9

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12 December 2019

R F Hrstka

10

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12 December 2019

R Williamson

11

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12 December 2019

language of work or name

English

0 references

publication date

1 August 1999

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12 December 2019

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12 December 2019

volume

98

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12 December 2019

issue

4

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12 December 2019

page(s)

465-474

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy.

1 reference

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7 January 2021

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

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

1 reference

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7 January 2021

Microvascular spasm in the cardiomyopathic Syrian hamster: a preventable cause of focal myocardial necrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

1 reference

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7 January 2021

Management of vasospastic angina--role of nicorandil.

1 reference

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7 January 2021

The sarcoglycan complex in limb-girdle muscular dystrophy

1 reference

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7 January 2021

Heart involvement in muscular dystrophies due to sarcoglycan gene mutations

1 reference

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7 January 2021

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

1 reference

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7 January 2021

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Delineation of genomic deletion in cardiomyopathic hamster.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

The role of cytoskeletal proteins in cardiomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981975-3

7 January 2021

10.1016/S0092-8674(00)81975-3

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

2887183

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10481911%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

2887183

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2887183