Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouse (Q74702690)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12206802%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Multivariate evaluation of the functional recovery obtained by the overexpression of utrophin in skeletal muscles of the mdx mouse (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12206802%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

main subject

multivariate statistics

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1 reference

Jean-Marie Gillis

1

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12 November 2019

publication date

1 October 2002

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12 November 2019

published in

Neuromuscular Disorders

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12 November 2019

volume

12 Suppl 1

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12 November 2019

page(s)

S90-4

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Primary structure of dystrophin-related protein

12 November 2019

cites work

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

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

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

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7 January 2021

Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse

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A noninvasive procedure to detect muscle weakness in the mdx mouse

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

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

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

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

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

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7 January 2021

Increased calcium influx in dystrophic muscle

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Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice

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

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7 January 2021

Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice

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7 January 2021

Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers

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7 January 2021

Hypoosmotic shocks induce elevation of resting calcium level in Duchenne muscular dystrophy myotubes contracting in vitro

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy

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

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7 January 2021

10.1016/S0960-8966(02)00088-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12206802%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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