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Suppression of mTORC1 activation in acid-α-glucosidase-deficient cells and mice is ameliorated by leucine supplementation

Pompe disease is due to a deficiency in acid-α-glucosidase (GAA) and results in debilitating skeletal muscle wasting, characterized by the accumulation of glycogen and autophagic vesicles. Given the role of lysosomes as a platform for mTORC1 activation, we examined mTORC1 activity in models of Pompe...

詳細記述

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書誌詳細
出版年:Am J Physiol Regul Integr Comp Physiol
主要な著者: Shemesh, Adi, Wang, Yichen, Yang, Yingjuan, Yang, Gong-She, Johnson, Danielle E., Backer, Jonathan M., Pessin, Jeffrey E., Zong, Haihong
フォーマット: Artigo
言語:Inglês
出版事項: American Physiological Society 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4233288/
https://ncbi.nlm.nih.gov/pubmed/25231351
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpregu.00212.2014
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