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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Bibliographic Details
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.
Format: Artigo
Language:Inglês
Published: American Society for Biochemistry and Molecular Biology 2013
Subjects:
Molecular Bases of Disease
Online Access: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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