Catherine Massart

Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

Giuseppe Novelli, Antoine Muchir, Federica Sangiuolo et al. · The American Journal of Human Genetics · 2002 · 532 citations · Full text

Lmna-encoding Lamin A/c, Mendelian Disorder, Genetic Disorder +3

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Takuro Arimura, A. Leclerc, Catherine Massart et al. · Human Molecular Genetics · 2004 · 318 citations · Full text

Inter-method variability in PTH measurement: Implication for the care of CKD patients

J.C. Souberbielle, Anne Boutten, M.-C. Carlier et al. · Kidney International · 2006 · 284 citations

Hemodialysis, Urology, Renal Function +8

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations

Antoine Muchir, Jacques Médioni, M. Laluc et al. · Muscle & Nerve · 2004 · 168 citations

Nuclear Structure, Genetics, Pathology +18

Isolation of 10 differentially expressed cDNAs in p53-induced apoptosis: activation of the vertebrate homologue of the drosophila seven in absentia gene.

Robert Amson, Mona Nemani, Jean-Pierre Roperch et al. · Proceedings of the National Academy of Sciences · 1996 · 161 citations · Full text

Tumor Biology, Systems Biology, Cell Regulation +14