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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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Bibliografske podrobnosti
izdano v:Dis Model Mech
Main Authors: de Luna, Noemí, Brull, Astrid, Guiu, Josep Maria, Lucia, Alejandro, Martin, Miguel Angel, Arenas, Joaquin, Martí, Ramon, Andreu, Antoni L., Pinós, Tomàs
Format: Artigo
Jezik:Inglês
Izdano: The Company of Biologists 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4415898/
https://ncbi.nlm.nih.gov/pubmed/25762569
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.020230
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