(Q47858156)

6 February 2018

title

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

1 reference

6 February 2018

author name string

Holt KH

1

1 reference

6 February 2018

Lim LE

2

1 reference

6 February 2018

Straub V

3

1 reference

6 February 2018

Venzke DP

4

1 reference

6 February 2018

Duclos F

5

1 reference

6 February 2018

Anderson RD

6

1 reference

6 February 2018

Davidson BL

7

1 reference

6 February 2018

Campbell KP

8

1 reference

6 February 2018

publication date

1 May 1998

1 reference

6 February 2018

published in

Molecular Cell

1 reference

6 February 2018

volume

1

1 reference

6 February 2018

issue

6

1 reference

6 February 2018

page(s)

841-848

1 reference

6 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Expression of Escherichia coli beta-galactosidase and rat HPRT in the CNS of Macaca mulatta following adenoviral mediated gene transfer

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Expression of deletion-containing dystrophins in mdx muscle: implications for gene therapy and dystrophin function

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Defective association of dystrophin with sarcolemmal glycoproteins in the cardiomyopathic hamster heart

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Loss, restoration, and maintenance of plasma membrane integrity

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

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%2FS1097-2765%2800%2980083-0

7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

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%2FS1097-2765%2800%2980083-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Dystrophin-associated proteins in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980083-0

7 January 2021

10.1016/S1097-2765(00)80083-0

Identifiers

DOI

1 reference

6 February 2018

PubMed ID

9660967

1 reference

6 February 2018