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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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: American Physiological Society 2017
Assuntos:
Research Article
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares