The Ubr2 Gene is Expressed in Skeletal Muscle Atrophying as a Result of Hind Limb Suspension, but not Merg1a Expression Alone

Skeletal muscle (SKM) atrophy is a potentially debilitating condition induced by muscle disuse, denervation, many disease states, and aging. The ubiquitin proteasome pathway (UPP) contributes greatly to the protein loss suffered in muscle atrophy. The MERG1a K(+) channel is known to induce UPP activ...

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Detalles Bibliográficos
Autores principales: Hockerman, Gregory H., Dethrow, Nicole M., Hameed, Sohaib, Doran, Maureen, Jaeger, Christine, Wang, Wen-Horng, Pond, Amber L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2014
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163950/
https://www.ncbi.nlm.nih.gov/pubmed/26913136
http://dx.doi.org/10.4081/ejtm.2014.3319

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