Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation

BACKGROUND: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder associated with the partial deletion of integral numbers of 3.3 kb D4Z4 DNA repeats within the subtelomere of chromosome 4q. A number of candidate FSHD genes, adenine nucleotide translocator 1 g...

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Detalles Bibliográficos
Autores principales: Bodega, Beatrice, Ramirez, Gabriella Di Capua, Grasser, Florian, Cheli, Stefania, Brunelli, Silvia, Mora, Marina, Meneveri, Raffaella, Marozzi, Anna, Mueller, Stefan, Battaglioli, Elena, Ginelli, Enrico
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719609/
https://www.ncbi.nlm.nih.gov/pubmed/19607661
http://dx.doi.org/10.1186/1741-7007-7-41

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