Cargando…
Biochemical and Functional Comparisons of mdx and Sgcg (−/−) Muscular Dystrophy Mouse Models
Mouse models have provided an essential platform to investigate facets of human diseases, from etiology, diagnosis, and prognosis, to potential treatments. Muscular dystrophy (MD) is the most common human genetic disease occurring in approximately 1 in 2500 births. The mdx mouse, which is dystrophin...
Autores principales: | Roberts, Nathan W., Holley-Cuthrell, Jenan, Gonzalez-Vega, Magdalis, Mull, Aaron J., Heydemann, Ahlke |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433636/ https://www.ncbi.nlm.nih.gov/pubmed/26064876 http://dx.doi.org/10.1155/2015/131436 |
Ejemplares similares
-
The superhealing MRL background improves muscular dystrophy
por: Heydemann, Ahlke, et al.
Publicado: (2012) -
Increased AMP‐activated protein kinase in skeletal muscles of Murphy Roth Large mice and its potential role in altered metabolism
por: Berhanu, Tirsit K., et al.
Publicado: (2014) -
Successful metabolic adaptations leading to the prevention of high fat diet-induced murine cardiac remodeling
por: Roberts, Nathan W., et al.
Publicado: (2015) -
Intraosseous transplant of dystrophin expressing chimeric (DEC) cells improves skeletal muscle function in mdx mouse model of Duchenne muscular dystrophy
por: Malik, Mohammad, et al.
Publicado: (2021) -
Skeletal Muscle Metabolism in Duchenne and Becker Muscular Dystrophy—Implications for Therapies
por: Heydemann, Ahlke
Publicado: (2018)