Cargando…
Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy
The loss of dystrophin produces a mechanically fragile sarcolemma, causing muscle membrane disruption and muscle loss. The degree to which exercise alters muscular dystrophy has been evaluated in humans with Duchenne Muscular Dystrophy (DMD) and in mouse models including the mdx mouse but with incon...
Autores principales: | Zelikovich, Aaron S., Quattrocelli, Mattia, Salamone, Isabella M., Kuntz, Nancy L., McNally, Elizabeth M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453911/ https://www.ncbi.nlm.nih.gov/pubmed/30962487 http://dx.doi.org/10.1038/s41598-019-42203-z |
Ejemplares similares
-
Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy
por: Quattrocelli, Mattia, et al.
Publicado: (2021) -
An Open Label Exploratory Clinical Trial Evaluating Safety and Tolerability of Once-Weekly Prednisone in Becker and Limb-Girdle Muscular Dystrophy
por: Zelikovich, Aaron S., et al.
Publicado: (2022) -
Biochemical and Functional Comparisons of mdx and Sgcg
(−/−) Muscular Dystrophy Mouse Models
por: Roberts, Nathan W., et al.
Publicado: (2015) -
A gene-edited mouse model of limb-girdle muscular dystrophy 2C for testing exon skipping
por: Demonbreun, Alexis R., et al.
Publicado: (2019) -
Intermittent prednisone treatment in mice promotes exercise tolerance in obesity through adiponectin
por: Quattrocelli, Mattia, et al.
Publicado: (2022)