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Genetic induction of hypometabolism by ablation of MC4R does not suppress ALS-like phenotypes in the G93A mutant SOD1 mouse model

Dysfunction and death of motor neurons leads to progressive paralysis in amyotrophic lateral sclerosis (ALS). Recent studies have reported organism-level metabolic dysfunction as a prominent but poorly understood feature of the disease. ALS patients are hypermetabolic with increased resting energy e...

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Detalles Bibliográficos
Autores principales: Doshi, Shachee, Gupta, Preetika, Kalb, Robert G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640619/
https://www.ncbi.nlm.nih.gov/pubmed/29030576
http://dx.doi.org/10.1038/s41598-017-13304-4

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