about
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscle.Loss of catalytically inactive lipid phosphatase myotubularin-related protein 12 impairs myotubularin stability and promotes centronuclear myopathy in zebrafishLack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathwaysReceptor activator of NF-kappaB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unitIncreased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weakness.Phosphatase-dead myotubularin ameliorates X-linked centronuclear myopathy phenotypes in miceMyotubularin phosphoinositide phosphatases in human diseases.Myotubularin and PtdIns3P remodel the sarcoplasmic reticulum in muscle in vivo.Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophyPrimary T-tubule and autophagy defects in the phosphoinositide phosphatase Jumpy/MTMR14 knockout mice muscle
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description
hulumtuese
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researcher
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ricercatrice
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wetenschapper
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հետազոտող
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name
Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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type
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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Leonela Amoasii
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0000-0001-7960-2749