S. Lefebvre

Conformational transitions of the serotonin 5-HT3 receptor

Lucie Polovinkin, Ghérici Hassaı̈ne, Jonathan Perot et al. · Nature · 2018 · 163 citations · Full text

Neurotransmitter, Receptor (Biochemistry), Molecular Biology +6

The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy

P Burlet, Céline Huber, Solange Bertrandy et al. · Human Molecular Genetics · 1998 · 147 citations

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.

Lydie Bürglen, Thierry Seroz, Pierre Miniou et al. · PubMed · 1997 · 99 citations

Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

Lydie Bürglen, Jeanne Amiel, Louis Viollet et al. · Journal of Clinical Investigation · 1996 · 92 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +18

The RNA-Binding Properties of SMN: Deletion Analysis of the Zebrafish Orthologue Defines Domains Conserved in Evolution

Solange Bertrandy, P Burlet, Olivier Clermont et al. · Human Molecular Genetics · 1999 · 88 citations