The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy

Facioscapulohumeral muscular dystrophy (FSHD), a dominant hereditary disease with a prevalence of 7 per 100,000 individuals, is associated with a partial deletion in the subtelomeric D4Z4 repeat array on chromosome 4q. The D4Z4 repeat contains a strong transcriptional enhancer that activates promote...

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Détails bibliographiques
Auteurs principaux: Dmitriev, Petr, Petrov, Andrei, Ansseau, Eugenie, Stankevicins, Luiza, Charron, Sébastien, Kim, Elena, Bos, Tomas Jan, Robert, Thomas, Turki, Ahmed, Coppée, Frédérique, Belayew, Alexandra, Lazar, Vladimir, Carnac, Gilles, Laoudj, Dalila, Lipinski, Marc, Vassetzky, Yegor S.
Format: Artigo
Langue:Inglês
Publié: American Society for Biochemistry and Molecular Biology 2011
Sujets:
Molecular Bases of Disease
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3247939/
https://ncbi.nlm.nih.gov/pubmed/21937448
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.254052
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