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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2007
Aiheet:
Biological Sciences
Linkit: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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