M Ménasche

Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis

Emeline F. Nandrot, Éric Dufour, Alexandra Provost et al. · Neurobiology of Disease · 2000 · 134 citations · Full text

Knockout Mouse, Homozygous Deletion, Signal Transduction +13

Sirt1 Involvement in rd10 Mouse Retinal Degeneration

Carolina O. Jaliffa, Ilhame Ameqrane, Anouk Dansault et al. · Investigative Ophthalmology & Visual Science · 2009 · 94 citations · Full text

A subset of patients with epithelial basement membrane corneal dystrophy have mutations inTGFBI/BIGH3

Sandrine Boutboul, Graeme C. Black, John E. Moore et al. · Human Mutation · 2006 · 83 citations

VEGF and KDR Gene Expression during Human Embryonic and Fetal Eye Development

Kari ̈n Gogat, Laurence Le Gat, Loi ̈c Van Den Berghe et al. · Investigative Ophthalmology & Visual Science · 2003 · 79 citations

Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.

Anouk Dansault, Gabriel David, C. Schwartz et al. · PubMed · 2007 · 74 citations