Sophie Aubert

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

Alice Bourdon, Limor Minai, Valérie Serre et al. · Nature Genetics · 2007 · 517 citations

Genome Instability, Mitochondrial Function, P53-controlled Ribonucleotide Reductase +10

Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells

Maxime Feyeux, Fany Bourgois-Rocha, Amanda Redfern et al. · Human Molecular Genetics · 2012 · 71 citations · Full text

Genetics, Genomic Mechanism, Gene Characterization +20

Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells

Christine Varela, Jérôme Alexandre Denis, Jérôme Polentes et al. · Journal of Clinical Investigation · 2012 · 57 citations · Full text

Genetics, Hesc Derivatives, Stem Cell Biology +19

Allele-Specific Silencing of Mutant Huntingtin in Rodent Brain and Human Stem Cells

Valérie Drouet, Marta Ruiz, Diana Zala et al. · PLoS ONE · 2014 · 54 citations · Full text

Hd Rat, Genetics, Mutant Huntingtin +20

A new pathway encompassing calpain 3 and its newly identified substrate cardiac ankyrin repeat protein is involved in the regulation of the nuclear factor‐κB pathway in skeletal muscle

Lydie Laure, Nathalie Danièle, Laurence Suel et al. · FEBS Journal · 2010 · 45 citations · Full text

Cardiac Muscle, Molecular Regulation, Cytoskeleton +21