André Dautigny

Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation

Diana Rodriguez, Fernande Gauthier, Enrico Bertini et al. · The American Journal of Human Genetics · 2001 · 150 citations · Full text

Developmental Anomaly, Mendelian Disorder, Infantile Alexander Disease +11

Myelin/oligodendrocyte glycoprotein–deficient (MOG-deficient) mice reveal lack of immune tolerance to MOG in wild-type mice

Cécile Delarasse, Philippe Daubas, Lennart T. Mars et al. · Journal of Clinical Investigation · 2003 · 143 citations · Full text

cDNA and amino acid sequences of rainbow trout (Oncorhynchus mykiss) lysozymes and their implications for the evolution of lysozyme and lactalbumin

André Dautigny, Ellen M. Prager, Danièle Pham-Dinh et al. · Journal of Molecular Evolution · 1991 · 108 citations

Biology, Rainbow Trout, Phylogenetics +10

Connexin32 Mutations Associated with X-Linked Charcot–Marie–Tooth Disease Show Two Distinct Behaviors: Loss of Function and Altered Gating Properties

Catherine Ressot, Danielle Gomès, André Dautigny et al. · Journal of Neuroscience · 1998 · 104 citations · Full text

Genetics, Pathology, Cmtx Mutations +18

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene

Eva Nelis, Vincent Timmerman, Peter De Jonghe et al. · Human Genetics · 1994 · 98 citations

Mendelian Disorder, Genetic Disorder, Medicine +11