S. Lefebvre

Conformational transitions of the serotonin 5-HT3 receptor

Lucie Polovinkin, Ghérici Hassaı̈ne, Jonathan Perot et al. · Nature · 2018 · 172 citations · Full text

Life Sciences, Biochemistry, Pharmacology +14

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 · 149 citations

Medicine, Developmental Biology, Molecular Biology +15

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

Medicine, Genetics, Molecular Genetics +7

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

Life Sciences, Genetics, Molecular Genetics +11

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

Life Sciences, Genetics, Molecular Biology +16