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Down-regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophy

✍ Scribed by L Gannoun-Zaki; S Fournier-Bidoz; G Le Cam; C Chambon; Ph Millasseau; J.J Léger; C.A Dechesne


Book ID
115931557
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
887 KB
Volume
375
Category
Article
ISSN
0014-5793

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The mdx mouse has a genetically homologous disease to Duchenne muscular dystrophy in humans. The disease progression, however, is not accompanied by the same level of fatty infiltration and muscle degeneration as occurs in humans. Thus, the presence of histological/ pathological changes in living md