Dysferlin, Annexin A1 and Mitsugumin-53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System with Stretch

Mutations in dysferlin cause an inherited muscular dystrophy due to defective membrane repair. Three interacting partners of dysferlin are also implicated in membrane resealing: caveolin-3 (in limb girdle muscular dystrophy type 1C), annexin A1, and the newly identified protein mitsugumin-53 (MG53)....

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Библиографические подробности
Опубликовано в: :J Neuropathol Exp Neurol
Главные авторы: Waddell, Leigh B., Lemcket, Frances A., Zheng, Xi F., Tran, Jenny, Evesson, Frances J., Hawkes, Joanne M., Lek, Angela, Street, Neil E., Lin, Peihui, Clarke, Nigel F., Landstrom, Andrew P., Ackerman, Michael J., Weisleder, Noah, Ma, Jianjie, North, Kathryn N., Cooper, Sandra T.
Формат: Artigo
Язык:Inglês
Опубликовано: 2011
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6309232/
https://ncbi.nlm.nih.gov/pubmed/21412170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0b013e31821350b0
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