DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder linked to contractions of the D4Z4 repeat array in the subtelomeric region of chromosome 4q. By comparing genome-wide gene expression data from muscle biopsies of patients with FSHD to those of 11 other neuromuscular dis...

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Detaylı Bibliyografya
Asıl Yazarlar: Dixit, Manjusha, Ansseau, Eugénie, Tassin, Alexandra, Winokur, Sara, Shi, Rongye, Qian, Hong, Sauvage, Sébastien, Mattéotti, Christel, van Acker, Anne M., Leo, Oberdan, Figlewicz, Denise, Barro, Marietta, Laoudj-Chenivesse, Dalila, Belayew, Alexandra, Coppée, Frédérique, Chen, Yi-Wen
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2007
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2084313/
https://ncbi.nlm.nih.gov/pubmed/17984056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0708659104
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