Céline Vanderplanck

University of Mons — Belgium

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index550citations14works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(12), Neurogenetic and Muscular Disorders Research(8), RNA Research and Splicing(5), Cardiomyopathy and Myosin Studies(3), Adipose Tissue and Metabolism(2)

Publications14 total

Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei
Skeletal Muscle·2018· 19 citedOpen Access
Additional file 2: Figure S2. of Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei
Figshare·2018Open Access
Antisense Oligonucleotides Used to Target the DUX4 mRNA as Therapeutic Approaches in FaciosScapuloHumeral Muscular Dystrophy (FSHD)
Genes·2017· 67 citedOpen Access
Transcription factors DUX4 and DUX4c associate with mRNP granules in the cytoplasm of fusing myoblasts: a new function in translation regulation?
2016
Antisense strategies targeting DUX4 and DUX4c for the treatment of Facioscapulohumeral muscular dystrophy.
2016
Antisense strategies targeting DUX4 and DUX4c as therapeutic approaches for facioscapulohumeral muscular dystrophy (FSHD)
Neuromuscular Disorders·2015
The Role of D4Z4-Encoded Proteins in the Osteogenic Differentiation of Mesenchymal Stromal Cells Isolated from Bone Marrow
Stem Cells and Development·2015· 14 cited
FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes
PLoS ONE·2012· 33 citedOpen Access
<scp>DUX</scp>4 expression in <scp>FSHD</scp> muscle cells: how could such a rare protein cause a myopathy?
Journal of Cellular and Molecular Medicine·2012· 151 citedOpen Access
The FSHD Atrophic Myotube Phenotype Is Caused by DUX4 Expression
PLoS ONE·2011· 204 citedOpen Access
SUPPRESSION OF DUX4 OR DUX4C EXPRESSION BY ANTISENSE STRATEGIES IN A THERAPEUTIC APPROACH FOR FSHD
2011
DUX4c Is Up-Regulated in FSHD. It Induces the MYF5 Protein and Human Myoblast Proliferation
PLoS ONE·2009· 62 citedOpen Access
Investigations on the molecular mechanism of a muscular dystrophy (FSHD) by proteomic and metabonomic analyses of primary myoblast cultures
2009
D.P.1.09 Study of DUX4 and DUX4c in facioscapulohumeral muscular dystrophy
Neuromuscular Disorders·2008

Frequent Co-authors

Alexandra Belayew(14), Frédérique Coppée(13), Eugénie Ansseau(12), Alexandra Tassin(11), Dalila Laoudj‐Chenivesse(11), Sébastien Charron(6), Armelle Wauters(5), Céline Lancelot(5), Marietta Barro(4), Baptiste Leroy(4), Ruddy Wattiez(4), Steve D. Wilton(3), Sébastien Sauvage(2), Kelly Vancutsem(2), Steve Wilton D.(2), Aline Derenne(2), Stéphanie Conotte(2), Virginie Dudome(2), Alexandre Legrand(2), Nadia Stricwant(1)