Literature DB >> 8580726

How does dystrophin deficiency lead to muscle degeneration?--evidence from the mdx mouse.

A McArdle1, R H Edwards, M J Jackson.   

Abstract

The mdx mouse has a defect in the same gene as boys with Duchenne muscular dystrophy, which results in the absence of the protein product, dystrophin. A large number of recent studies have used the mdx mouse model to examine the potential role of dystrophy in normal muscle and the mechanisms by which dystrophin-deficiency leads to myopathy. This review discusses critically the results of these studies and their relevance to understanding the mechanisms by which dystrophin-deficiency leads to muscle necrosis.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8580726     DOI: 10.1016/0960-8966(95)00001-4

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  21 in total

1.  Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice.

Authors:  Stephen Hollingworth; Ulrike Zeiger; Stephen M Baylor
Journal:  J Physiol       Date:  2008-09-04       Impact factor: 5.182

Review 2.  The role of mechanobiology in progression of rotator cuff muscle atrophy and degeneration.

Authors:  Michael C Gibbons; Anshuman Singh; Adam J Engler; Samuel R Ward
Journal:  J Orthop Res       Date:  2017-08-11       Impact factor: 3.494

3.  Changes in mechanosensitive channel gating following mechanical stimulation in skeletal muscle myotubes from the mdx mouse.

Authors:  Alfredo Franco-Obregón; Jeffry B Lansman
Journal:  J Physiol       Date:  2002-03-01       Impact factor: 5.182

4.  Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides.

Authors:  T A Rando; M H Disatnik; L Z Zhou
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

Review 5.  Mechanisms of resistance to pathogenesis in muscular dystrophies.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1999-05       Impact factor: 3.396

6.  Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice.

Authors:  Sonia Messina; Domenica Altavilla; M'hammed Aguennouz; Paolo Seminara; Letteria Minutoli; Maria C Monici; Alessandra Bitto; Anna Mazzeo; Herbert Marini; Francesco Squadrito; Giuseppe Vita
Journal:  Am J Pathol       Date:  2006-03       Impact factor: 4.307

7.  Alteration of excitation-contraction coupling mechanism in extensor digitorum longus muscle fibres of dystrophic mdx mouse and potential efficacy of taurine.

Authors:  A De Luca; S Pierno; A Liantonio; M Cetrone; C Camerino; S Simonetti; F Papadia; D C Camerino
Journal:  Br J Pharmacol       Date:  2001-03       Impact factor: 8.739

8.  Gadolinium reduces short-term stretch-induced muscle damage in isolated mdx mouse muscle fibres.

Authors:  Ella W Yeung; Stewart I Head; David G Allen
Journal:  J Physiol       Date:  2003-10-15       Impact factor: 5.182

9.  The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres.

Authors:  Christopher E Woods; David Novo; Marino DiFranco; Julio L Vergara
Journal:  J Physiol       Date:  2004-03-05       Impact factor: 5.182

10.  Sustained dystrophin expression induced by peptide-conjugated morpholino oligomers in the muscles of mdx mice.

Authors:  Natee Jearawiriyapaisarn; Hong M Moulton; Brian Buckley; Jennifer Roberts; Peter Sazani; Suthat Fucharoen; Patrick L Iversen; Ryszard Kole
Journal:  Mol Ther       Date:  2008-06-10       Impact factor: 11.454

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.