(Q43883312)

27 November 2017

Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice (English)

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27 November 2017

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Allamand V

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27 November 2017

Donahue KM

2

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27 November 2017

Straub V

3

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27 November 2017

Davisson RL

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27 November 2017

Davidson BL

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27 November 2017

Campbell KP

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27 November 2017

1 August 2000

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27 November 2017

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27 November 2017

7

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27 November 2017

1385-1391

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27 November 2017

16

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https://scigraph.springernature.com/pub.10.1038/sj.gt.3301247

27 November 2017

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cites work

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Association of dystrophin and an integral membrane glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Glycoprotein complex anchoring dystrophin to sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Assembly of the sarcoglycan complex. Insights for muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

The limb-girdle muscular dystrophies-multiple genes, multiple mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

The sarcoglycan complex in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

rAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Expression of the primary coxsackie and adenovirus receptor is downregulated during skeletal muscle maturation and limits the efficacy of adenovirus-mediated gene delivery to muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Immunology of gene therapy with adenoviral vectors in mouse skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Adenovirus-mediated gene transfer: influence of transgene, mouse strain and type of immune response on persistence of transgene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Expression of coxsackie adenovirus receptor and alphav-integrin does not correlate with adenovector targeting in vivo indicating anatomical vector barriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Next-generation adenoviral vectors: new and improved

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

Persistence in muscle of an adenoviral vector that lacks all viral genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Cytotoxic T-lymphocyte target proteins and their major histocompatibility complex class I restriction in response to adenovirus vectors delivered to mouse liver.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Myosin isoform transitions and physiological properties of regenerated and re-innervated soleus muscles of the rat

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3301247

7 January 2021

Identifiers

DOI

10.1038/SJ.GT.3301247

1 reference

Dimensions Publication ID

27 November 2017

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1 reference