FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes-Reference-Cited by-同舟云学术

FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes

Published:2012-12-18 Issue:12 Volume:7 Page:e51865
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Tassin Alexandra,Leroy Baptiste,Laoudj-Chenivesse Dalila,Wauters Armelle,Vanderplanck Céline,Le Bihan Marie-Catherine,Coppée Frédérique,Wattiez Ruddy,Belayew Alexandra

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference58 articles.

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3. Richards M, Coppée F, Thomas N, Belayew A, Upadhyaya M (2011) Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Hum Genet. Available:http://www.ncbi.nlm.nih.gov/pubmed/21984394. Accessed 19 December 2011.

4. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy;PGM van Overveld;Nat Genet,2003

5. Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts;A Petrov;Proc Natl Acad Sci USA,2006

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