Repression of phosphatidylinositol transfer protein α ameliorates the pathology of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a progressive muscle wasting disease caused by X-linked inherited mutations in the DYSTROPHIN (DMD) gene. Absence of dystrophin protein from the sarcolemma causes severe muscle degeneration, fibrosis, and inflammation, ultimately leading to cardiorespiratory fail...

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Dettagli Bibliografici
Pubblicato in:Proc Natl Acad Sci U S A
Autori principali: Vieira, Natassia M., Spinazzola, Janelle M., Alexander, Matthew S., Moreira, Yuri B., Kawahara, Genri, Gibbs, Devin E., Mead, Lillian C., Verjovski-Almeida, Sergio, Zatz, Mayana, Kunkel, Louis M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: National Academy of Sciences 2017
Soggetti:
Biological Sciences
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5468635/
https://ncbi.nlm.nih.gov/pubmed/28533404
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1703556114
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