Altered nuclear dynamics in MDX myofibers

Duchenne muscular dystrophy (DMD) is a genetic disorder in which the absence of dystrophin leads to progressive muscle degeneration and weakness. Although the genetic basis is known, the pathophysiology of dystrophic skeletal muscle remains unclear. We examined nuclear movement in wild-type (WT) and...

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Detalhes bibliográficos
Publicado no:J Appl Physiol (1985)
Main Authors: Iyer, Shama R., Shah, Sameer B., Valencia, Ana P., Schneider, Martin F., Hernández-Ochoa, Erick O., Stains, Joseph P., Blemker, Silvia S., Lovering, Richard M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5401960/
https://ncbi.nlm.nih.gov/pubmed/27979987
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/japplphysiol.00857.2016
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