Defective Regulation of MicroRNA Target Genes in Myoblasts from Facioscapulohumeral Dystrophy Patients

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant hereditary neuromuscular disorder linked to the deletion of an integral number of 3.3-kb-long macrosatellite repeats (D4Z4) within the subtelomeric region of chromosome 4q. Most genes identified in this region are overexpressed i...

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Detalhes bibliográficos
Main Authors: Dmitriev, Petr, Stankevicins, Luiza, Ansseau, Eugenie, Petrov, Andrei, Barat, Ana, Dessen, Philippe, Robert, Thomas, Turki, Ahmed, Lazar, Vladimir, Labourer, Emmanuel, Belayew, Alexandra, Carnac, Gilles, Laoudj-Chenivesse, Dalila, Lipinski, Marc, Vassetzky, Yegor S.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2013
Assuntos:
Molecular Bases of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3853252/
https://ncbi.nlm.nih.gov/pubmed/24145033
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M113.504522
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