S
Sylvie Taviaux
Researcher at University of Montpellier
Publications - 44
Citations - 2107
Sylvie Taviaux is an academic researcher from University of Montpellier. The author has contributed to research in topics: Gene & Complementary DNA. The author has an hindex of 23, co-authored 44 publications receiving 1989 citations. Previous affiliations of Sylvie Taviaux include Centre national de la recherche scientifique & French Institute of Health and Medical Research.
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Journal ArticleDOI
The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
Philippe Jay,Claire Rougeulle,Annick Massacrier,Anne Moncla,Marie Geneviève Mattei,Perrine Malzac,Nathalie Roeckel,Sylvie Taviaux,J.-L. B. Lefranc,Pierre Cau,Philippe Berta,Marc Lalande,Françoise Muscatelli +12 more
TL;DR: A complete lack of NDN expression in P WS brain and f ibroblasts indicates that the gene is expressed exclusively from the paternal allele in these tissues and suggests a possible role of this new gene in PWS.
Journal ArticleDOI
Distribution of olfactory receptor genes in the human genome
Sylvie Rouquier,Sylvie Taviaux,Barbara J. Trask,Véronique Brand-Arpon,G van den Engh,Jacques Demaille,Dominique Giorgi +6 more
TL;DR: It is demonstrated that members of the olfactory receptor (OR) gene family are distributed on all but a few human chromosomes and through FISH analysis, it is shown that OR sequences reside at more than 25 locations in the human genome.
Journal ArticleDOI
Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH).
Nicole Dastugue,Marina Lafage-Pochitaloff,Marie-Pierre Pages,Isabelle Radford,Christian Bastard,Pascaline Talmant,M J Mozziconacci,Claude Léonard,Christelle Bilhou-Nabera,Christine Cabrol,Anne-Marie Capodano,Pascale Cornillet-Lefebvre,Michel Lessard,Francine Mugneret,Christine Perot,Sylvie Taviaux,Odile Fenneteaux,Eliane Duchayne,Roland Berger +18 more
TL;DR: The morphologic and cytogenetic findings indicated that M7 might be a secondary leukemia more often than suggested by preceding history, particularly among adults.
Journal ArticleDOI
Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases.
Nicole Véronique Smadja,Dominique Leroux,Jean Soulier,Sylvie Dumont,Catherine Arnould,Sylvie Taviaux,Jean Louis Taillemite,Christian Bastard +7 more
TL;DR: It is confirmed that 14q32t are much more frequent in hypodiploid than in hyperdiploid MM (P < 0.0001) and that cryptic t(4;14)(p16;q32) is strongly associated with hypodi ploid karyotypes (P< 0.01).
Journal ArticleDOI
Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogénétique Hématologique study
Etienne Coyaud,Etienne Coyaud,Stéphanie Struski,Naïs Prade,Julien Familiades,Julien Familiades,Ruth Eichner,Ruth Eichner,Cathy Quelen,Cathy Quelen,Marina Bousquet,Marina Bousquet,Francine Mugneret,Pascaline Talmant,Marie-Pierre Pages,Christine Lefebvre,Dominique Penther,Eric Lippert,Nathalie Nadal,Sylvie Taviaux,Bruce Poppe,Isabelle Luquet,Laurence Baranger,Virginie Eclache,Isabelle Radford,Carole Barin,Marie-Joelle Mozziconacci,Marina Lafage-Pochitaloff,Hélène Antoine-Poirel,C. Charrin,Christine Perot,Christine Terré,Pierre Brousset,Nicole Dastugue,Cyril Broccardo +34 more
TL;DR: It is probable that gene fusions occur early, whereas deletions should be regarded as a late/secondary event, and strongly suggest that PAX5 fusion genes are early players in leukemogenesis.