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The intracellular Ca²⁺ channel MCOLN1 is required for sarcolemma repair to prevent muscular dystrophy.

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第一作者： Xiping,Cheng

第一单位： Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA.

作者： Xiping,Cheng ^[1] ; Xiaoli,Zhang ^[1] ; Qiong,Gao ^[1] ; Mohammad,Ali Samie ^[1] ; Marlene,Azar ^[1] ; Wai Lok,Tsang ^[1] ; Libing,Dong ^[1] ; Nirakar,Sahoo ^[1] ; Xinran,Li ^[1] ; Yue,Zhuo ^[1] ; Abigail G,Garrity ^[2] ; Xiang,Wang ^[1] ; Marc,Ferrer ^[3] ; James,Dowling ^[4] ; Li,Xu ^[5] ; Renzhi,Han ^[5] ; Haoxing,Xu ^[2]

作者单位： Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA. ^[1] 1] Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA. [2] Neuroscience Graduate Program, University of Michigan, Ann Arbor, Michigan, USA. ^[2] National Center for Advancing Translational Science, National Institutes of Health, Maryland, USA. ^[3] 1] Department of Pediatrics, University of Michigan Medical Center, Ann Arbor, Michigan, USA. [2] Division of Neurology, Hospital for Sick Children, Toronto, Ontario, Canada [3] Program of Genetic and Genome Biology, Hospital for Sick Children, Toronto, Ontario, Canada [4] Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada [5] Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada. ^[4] Department of Cell and Molecular Physiology, Loyola University Chicago Health Sciences Division, Chicago, Illinois, USA. ^[5]