Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice (Q73851362)

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7 November 2019

title

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

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7 November 2019

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22 November 2024

N. Deconinck

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22 November 2024

J. Tinsley

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22 November 2024

F. De Backer

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22 November 2024

R. Fisher

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22 November 2024

D. Kahn

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22 November 2024

S. Phelps

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22 November 2024

K. Davies

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22 November 2024

J. M. Gillis

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22 November 2024

language of work or name

English

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National Center for Biotechnology Information

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22 November 2024

publication date

1 November 1997

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7 November 2019

November 1997

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9359695

full work available at URL

22 November 2024

http://www.nature.com/articles/nm1197-1216

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https://api.crossref.org/works/10.1038/NM1197-1216

http://www.nature.com/articles/nm1197-1216.pdf

22 November 2024

file format

Portable Document Format

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https://api.crossref.org/works/10.1038/NM1197-1216

22 November 2024

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7 November 2019

volume

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7 November 2019

issue

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7 November 2019

page(s)

1216-1221

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Utrophin: a structural and functional comparison to dystrophin

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Primary structure of dystrophin-related protein

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal andmdxmice Immunological evidence

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Localization and quantitation of the chromosome 6-encoded dystrophin-related protein in normal and pathological human muscle

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Utrophin: a potential replacement for dystrophin?

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Utrophin muscles in on the action

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

The mdx mouse skeletal muscle myopathy: II. Contractile properties

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

A noninvasive procedure to detect muscle weakness in the mdx mouse

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Intracellular Ca2+ concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Increased calcium influx in dystrophic muscle

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Calcium/calmodulin-dependent regulation of the NH2-terminal F-actin binding domain of utrophin

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Developmental regulation of mechanosensitive calcium channels in skeletal muscle from normal and mdx mice.

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Time course of changes in plasma membrane permeability in the dystrophin-deficient mdx mouse

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNM1197-1216

7 January 2021

Identifiers

DOI

10.1038/NM1197-1216

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359695%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

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