(Q45888822)

17 December 2017

title

Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy (English)

1 reference

17 December 2017

author name string

Gardner KL

1

1 reference

17 December 2017

Kearney JA

2

1 reference

17 December 2017

Edwards JD

3

1 reference

17 December 2017

Rafael-Fortney JA

4

1 reference

17 December 2017

publication date

1 May 2006

1 reference

17 December 2017

published in

Gene Therapy

1 reference

17 December 2017

volume

13

1 reference

17 December 2017

issue

9

1 reference

17 December 2017

page(s)

744-751

1 reference

17 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.gt.3302686

exact match

0 references

cites work

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Membrane organization of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Forced expression of dystrophin deletion constructs reveals structure-function correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Dystroglycan, a scaffold for the ERK-MAP kinase cascade

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin-associated protein complex and inhibits myofibre degeneration in nude/mdx mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Systemic delivery of genes to striated muscles using adeno-associated viral vectors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Overcoming adeno-associated virus vector size limitation through viral DNA heterodimerization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Trans-splicing vectors expand the utility of adeno-associated virus for gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Recombinant AAV-mediated gene delivery using dual vector heterodimerization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

Cardiomyopathic features associated with muscular dystrophy are independent of dystrophin absence in cardiovasculature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

7 January 2021

The mutant mdx: inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

7 January 2021

Contraction times and fiber types in patients with progressive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

7 January 2021

Concatamerization of adeno-associated virus circular genomes occurs through intermolecular recombination.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302686

7 January 2021

Identifiers

DOI

10.1038/SJ.GT.3302686

1 reference

17 December 2017

Dimensions Publication ID

1027459839

0 references

1 reference

17 December 2017