FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes

Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle disorder linked to a contraction of the D4Z4 repeat array in the 4q35 subtelomeric region. This deletion induces epigenetic modifications that affect the expression of several genes located in the vicinity. In each D4Z4 element, w...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Tassin, Alexandra, Leroy, Baptiste, Laoudj-Chenivesse, Dalila, Wauters, Armelle, Vanderplanck, Céline, Le Bihan, Marie-Catherine, Coppée, Frédérique, Wattiez, Ruddy, Belayew, Alexandra
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2012
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3525578/
https://ncbi.nlm.nih.gov/pubmed/23272181
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0051865
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