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...

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Detalles Bibliográficos
Autores principales: Tassin, Alexandra, Leroy, Baptiste, Laoudj-Chenivesse, Dalila, Wauters, Armelle, Vanderplanck, Céline, Le Bihan, Marie-Catherine, Coppée, Frédérique, Wattiez, Ruddy, Belayew, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525578/
https://www.ncbi.nlm.nih.gov/pubmed/23272181
http://dx.doi.org/10.1371/journal.pone.0051865

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525578/
https://www.ncbi.nlm.nih.gov/pubmed/23272181
http://dx.doi.org/10.1371/journal.pone.0051865

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