Virginie Courtois

Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

Fabrice Cailloux, Fernande Gauthier‐Barichard, Corinne Mimault et al. · European Journal of Human Genetics · 2000 · 185 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Brain Development +10

Proteolipoprotein Gene Analysis in 82 Patients with Sporadic Pelizaeus-Merzbacher Disease: Duplications, the Major Cause of the Disease, Originate More Frequently in Male Germ Cells, but Point Mutations Do Not

Corinne Mimault, G Giraud, Virginie Courtois et al. · The American Journal of Human Genetics · 1999 · 131 citations · Full text

Mendelian Disorder, Sporadic Pelizaeus-merzbacher Disease, Proteolipoprotein Gene Analysis +9

Antibiotic-free selection in E. coli: new considerations for optimal design and improved production

Isabelle Peubez, Nicolas Chaudet, Charlotte Mignon et al. · Microbial Cell Factories · 2010 · 64 citations · Full text

Surface plasmon resonance imaging (SPRI) system and real-time monitoring of DNA biochip for human genetic mutation diagnosis of DNA amplified samples

Ilaria Mannelli, Virginie Courtois, Pierre Lecaruyer et al. · Sensors and Actuators B Chemical · 2006 · 54 citations

Real-time Monitoring, Genetic Testing, Engineering +13

New <i>Otx2</i> mRNA isoforms expressed in the mouse brain

Virginie Courtois, Gilles Chatelain, Zhi‐Yan Han et al. · Journal of Neurochemistry · 2003 · 36 citations