(Q47858156)

6 February 2018

title

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer (English)

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6 February 2018

author name string

Holt KH

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6 February 2018

Lim LE

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6 February 2018

Straub V

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6 February 2018

Venzke DP

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6 February 2018

Duclos F

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6 February 2018

Anderson RD

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6 February 2018

Davidson BL

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6 February 2018

Campbell KP

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6 February 2018

publication date

1 May 1998

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6 February 2018

published in

Molecular Cell

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6 February 2018

volume

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6 February 2018

issue

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6 February 2018

page(s)

841-848

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6 February 2018

Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs

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Dystrophin expression improves myofiber survival in mdx muscle following intramuscular plasmid DNA injection.

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Membrane organization of the dystrophin-glycoprotein complex

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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

Expression of Deletion-Containing Dystrophins in mdx Muscle: Implications for Gene Therapy and Dystrophin Function

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Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

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

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

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7 January 2021

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

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β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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7 January 2021

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7 January 2021

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

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7 January 2021

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

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7 January 2021

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

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7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

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7 January 2021

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

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7 January 2021

A genetic linkage map of the Syrian hamster and localization of cardiomyopathy locus on chromosome 9qa2.1-b1 using RLGS spot-mapping

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7 January 2021

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

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7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

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7 January 2021

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

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7 January 2021

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Identifiers

DOI

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6 February 2018

1 reference

6 February 2018