Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitro

McArdle disease, also termed ‘glycogen storage disease type V’, is a disorder of skeletal muscle carbohydrate metabolism caused by inherited deficiency of the muscle-specific isoform of glycogen phosphorylase (GP-MM). It is an autosomic recessive disorder that is caused by mutations in the PYGM gene...

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Detalles Bibliográficos
Autores principales: de Luna, Noemí, Brull, Astrid, Guiu, Josep Maria, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L., Pinós, Tomàs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415898/
https://www.ncbi.nlm.nih.gov/pubmed/25762569
http://dx.doi.org/10.1242/dmm.020230

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415898/
https://www.ncbi.nlm.nih.gov/pubmed/25762569
http://dx.doi.org/10.1242/dmm.020230

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