Resolution of skeletal muscle inflammation in mdx dystrophic mouse is accompanied by increased immunoglobulin and interferon-γ production

Mdx mouse, the animal model of Duchenne muscular dystrophy, develops an X-linked recessive inflammatory myopathy with an apparent sustained capacity for muscle regeneration. We analysed whether changes in the skeletal muscle during myonecrosis and regeneration would correlate with functional alterat...

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Hlavní autoři: Lagrota-Candido, Jussara, Vasconcellos, Rita, Cavalcanti, Marta, Bozza, Marcelo, Savino, Wilson, Quirico-Santos, Thereza
Médium: Artigo
Jazyk:Inglês
Vydáno: Blackwell Science Inc 2002
Témata:
Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2517677/
https://ncbi.nlm.nih.gov/pubmed/12383191
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1365-2613.2002.00221.x
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