Dalila Laoudj‐Chenivesse
Centre National de la Recherche Scientifique(FR)Inserm(FR)Université de Montpellier(FR)Physiologie et Médecine Expérimentale du Coeur et des Muscles(FR)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Neurogenetic and Muscular Disorders Research, RNA Research and Splicing, Cardiomyopathy and Myosin Studies, Genetic Neurodegenerative Diseases
Most-Cited Works
- → DUX4 , a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1(2007)371 cited
- → The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein(2007)317 cited
- → Mutations in GJB6 cause hidrotic ectodermal dysplasia(2000)287 cited
- → The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression(2011)206 cited
- → DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?(2012)153 cited
- → Myoblasts from affected and non‐affected FSHD muscles exhibit morphological differentiation defects(2008)143 cited