Cargando…
Mitochondrial bioenergetic dysfunction in the D2.mdx model of Duchenne muscular dystrophy is associated with microtubule disorganization in skeletal muscle
In Duchenne muscular dystrophy, a lack of dystrophin leads to extensive muscle weakness and atrophy that is linked to cellular metabolic dysfunction and oxidative stress. This dystrophinopathy results in a loss of tethering between microtubules and the sarcolemma. Microtubules are also believed to r...
Autores principales: | Ramos, Sofhia V., Hughes, Meghan C., Delfinis, Luca J., Bellissimo, Catherine A., Perry, Christopher G. R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529311/ https://www.ncbi.nlm.nih.gov/pubmed/33002037 http://dx.doi.org/10.1371/journal.pone.0237138 |
Ejemplares similares
-
Social stress is lethal in the mdx model of Duchenne muscular dystrophy
por: Razzoli, Maria, et al.
Publicado: (2020) -
The Effect of Vitamin D Supplementation on Skeletal Muscle in the mdx Mouse Model of Duchenne Muscular Dystrophy
por: Debruin, Danielle A., et al.
Publicado: (2019) -
Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H(2)O(2) emission during impaired oxidative phosphorylation
por: Hughes, Meghan C., et al.
Publicado: (2019) -
Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy
por: Rybalkin, Sergei D, et al.
Publicado: (2013) -
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy
por: Hammers, David W., et al.
Publicado: (2020)