Showing results (171-180 of 187) with videos related to

Sort By:
Pageof 19
BMC Medical Genetics|September 17, 2016
Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case reportMarie-Cécile Gaillard, Francesca Puppo, Stéphane Roche, et al.
Human Molecular Genetics|August 23, 2013
DUX4 and DUX4 downstream target genes are expressed in fetal FSHD musclesMaxime Ferreboeuf, Virginie Mariot, Bettina Bessières, et al.
Molecular Carcinogenesis|March 10, 2017
Activation of mutated TRPA1 ion channel by resveratrol in human prostate cancer associated fibroblasts (CAF)Eric Vancauwenberghe, Lucile Noyer, Sandra Derouiche, et al.
Journal of Medical Genetics|October 26, 2010
Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type IbStéphanie Maupetit-Méhouas, Virginie Mariot, Christelle Reynès, et al.
Oncotarget|April 14, 2016
Targeting of short TRPM8 isoforms induces 4TM-TRPM8-dependent apoptosis in prostate cancer cellsGabriel Bidaux, Anne-Sophie Borowiec, Charlotte Dubois, et al.
The American Journal of Pathology|August 9, 2012
Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHDYvonne D Krom, Julie Dumonceaux, Kamel Mamchaoui, et al.
Annals of Neurology|May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophyVirginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Antibodies (Basel, Switzerland)|August 23, 2022
Anticalin N- or C-Terminal on a Monoclonal Antibody Affects Both Production and In Vitro FunctionalityNicolas Aubrey, Valérie Gouilleux-Gruart, Christine Dhommée, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|March 14, 2012
Ferromagnetic Mn-doped Si0.3Ge0.7 nanodots self-assembled on Si(100)P De Padova, B Olivieri, J-M Mariot, et al.
Pageof 19