Non-toxic ubiquitous over-expression of utrophin in the mdx mouse (Q43762845)

26 November 2017

title

Non-toxic ubiquitous over-expression of utrophin in the mdx mouse (English)

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26 November 2017

Fisher R

1

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26 November 2017

Tinsley JM

2

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26 November 2017

Phelps SR

3

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26 November 2017

Squire SE

4

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26 November 2017

Townsend ER

5

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26 November 2017

Martin JE

6

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26 November 2017

Davies KE

7

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26 November 2017

language of work or name

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1 November 2001

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26 November 2017

published in

Neuromuscular Disorders

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26 November 2017

volume

11

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26 November 2017

issue

8

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26 November 2017

page(s)

713-721

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The structural and functional diversity of dystrophin

26 November 2017

cites work

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

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Glycoprotein complex anchoring dystrophin to sarcolemma

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

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Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin

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Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein

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Differential Association of Syntrophin Pairs with the Dystrophin Complex

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An autosomal transcript in skeletal muscle with homology to dystrophin

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Primary structure of dystrophin-related protein

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Utrophin: a structural and functional comparison to dystrophin

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Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.

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Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in prol

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Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells

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7 January 2021

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

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

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

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X chromosome-linked muscular dystrophy (mdx) in the mouse

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Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

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Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice

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Expression of full-length utrophin prevents muscular dystrophy in mdx mice

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Utrophin: a potential replacement for dystrophin?

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7 January 2021

Dystrophin associated proteins fail in filling dystrophin's shoes

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7 January 2021

The human ubiquitin C promoter directs high ubiquitous expression of transgenes in mice

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7 January 2021

beta-dystrobrevin, a member of the dystrophin-related protein family

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7 January 2021

Further aspects of muscular dystrophy in mdx mice

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7 January 2021

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

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7 January 2021

Molecular and functional analysis of the utrophin promoter

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7 January 2021

A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy

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7 January 2021

10.1016/S0960-8966(01)00220-6

Identifiers

DOI

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26 November 2017

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