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Plos One|December 29, 2012
FSHD myotubes with different phenotypes exhibit distinct proteomesAlexandra Tassin, Baptiste Leroy, Dalila Laoudj-Chenivesse, et al.
Journal of Cellular and Molecular Medicine|December 5, 2012
DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?Alexandra Tassin, Dalila Laoudj-Chenivesse, Céline Vanderplanck, et al.
Scientific Reports|July 11, 2020
Induction of a local muscular dystrophy using electroporation in vivo: an easy tool for screening therapeuticsAline Derenne, Alexandra Tassin, Thuy Hang Nguyen, et al.
Skeletal Muscle|December 16, 2023
Hypoxia enhances human myoblast differentiation: involvement of HIF1α and impact of DUX4, the FSHD causal geneThuy-Hang Nguyen, Lise Paprzycki, Alexandre Legrand, et al.
International Journal of Molecular Sciences|March 28, 2024
The DUX4-HIF1α Axis in Murine and Human Muscle Cells: A Link More Complex Than ExpectedThuy-Hang Nguyen, Maelle Limpens, Sihame Bouhmidi, et al.
The EMBO Journal|October 4, 2008
An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologiesDarko Bosnakovski, Zhaohui Xu, Eun Ji Gang, et al.
Plos One|October 16, 2009
DUX4c is up-regulated in FSHD. It induces the MYF5 protein and human myoblast proliferationEugénie Ansseau, Dalila Laoudj-Chenivesse, Aline Marcowycz, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2007
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1Manjusha Dixit, Eugénie Ansseau, Alexandra Tassin, et al.
Skeletal Muscle|March 7, 2023
The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteinsClothilde Claus, Moriya Slavin, Eugénie Ansseau, et al.
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