The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference42 articles.
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2. Identification of novel mutations in theMTM1 gene causing severe and mild forms of X-linked myotubular myopathy
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1. Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy;Journal of Clinical Investigation;2023-09-15
2. Inactivating the lipid kinase activity of PI3KC2β is sufficient to rescue myotubular myopathy in mice;JCI Insight;2023-05-08
3. Roles of protein tyrosine phosphatases in hepatocellular carcinoma progression (Review);Oncology Reports;2023-01-19
4. Structural rationale to understand the effect of disease-associated mutations on Myotubularin;Current Research in Structural Biology;2023
5. Disrupted T‐tubular network accounts for asynchronous calcium release in MTM1‐deficient skeletal muscle;The Journal of Physiology;2022-12-08
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