Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Sylvie Taviaux"'
Autor:
Francois P. Duhoux, Geneviève Ameye, Virginie Lambot, Christian Herens, Frédéric Lambert, Sophie Raynaud, Iwona Wlodarska, Lucienne Michaux, Catherine Roche-Lestienne, Elise Labis, Sylvie Taviaux, Elise Chapiro, Florence Nguyen-Khac, Stéphanie Struski, Sophie Dobbelstein, Nicole Dastugue, Eric Lippert, Frank Speleman, Nadine Van Roy, An De Weer, Katrina Rack, Pascaline Talmant, Steven Richebourg, Francine Mugneret, Isabelle Tigaud, Marie-Joëlle Mozziconacci, Sophy Laibe, Nathalie Nadal, Christine Terré, Jeanne-Marie Libouton, Anabelle Decottignies, Miikka Vikkula, Hélène A. Poirel
Publikováno v:
PLoS ONE, Vol 6, Iss 12 (2011)
Externí odkaz:
https://doaj.org/article/b949280337144bf482ac838d8fd89850
Autor:
Francois P Duhoux, Geneviève Ameye, Virginie Lambot, Christian Herens, Frédéric Lambert, Sophie Raynaud, Iwona Wlodarska, Lucienne Michaux, Catherine Roche-Lestienne, Elise Labis, Sylvie Taviaux, Elise Chapiro, Florence Nguyen-Khac, Stéphanie Struski, Sophie Dobbelstein, Nicole Dastugue, Eric Lippert, Frank Speleman, Nadine Van Roy, An De Weer, Katrina Rack, Pascaline Talmant, Steven Richebourg, Francine Mugneret, Isabelle Tigaud, Marie-Joëlle Mozziconacci, Sophy Laibe, Nathalie Nadal, Christine Terré, Jeanne-Marie Libouton, Anabelle Decottignies, Miikka Vikkula, Hélène A Poirel, Groupe Francophone de Cytogénétique Hématologique (GFCH), Belgian Cytogenetic Group for Hematology and Oncology (BCG-HO)
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26311 (2011)
Fluorescence in situ hybridization was performed to characterize 81 cases of myeloid and lymphoid malignancies with cytogenetic 1p36 alterations not affecting the PRDM16 locus. In total, three subgroups were identified: balanced translocations (N = 2
Externí odkaz:
https://doaj.org/article/83442896cbc6471683b7214a16f968ec
Autor:
Fanny Pineau, Isabelle Rivals, Maurane Reveil, Isabelle Vachier, Raphaël Chiron, Laura Brosseau, Margot Drevait, Davide Caimmi, Mireille Claustres, Sylvie Taviaux, Albertina De Sario
Publikováno v:
Genes
Genes, MDPI, 2021, 12 (3), pp.441. ⟨10.3390/genes12030441⟩
Genes, Vol 12, Iss 441, p 441 (2021)
Volume 12
Issue 3
Genes, MDPI, 2021, 12 (3), pp.441. ⟨10.3390/genes12030441⟩
Genes, Vol 12, Iss 441, p 441 (2021)
Volume 12
Issue 3
Cystic fibrosis (CF) is a chronic genetic disease that mainly affects the respiratory and gastrointestinal systems. No curative treatments are available, but the follow-up in specialized centers has greatly improved the patient life expectancy. Robus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50193198cba3170c2035e30beea33619
https://hal.archives-ouvertes.fr/hal-03189670/document
https://hal.archives-ouvertes.fr/hal-03189670/document
Autor:
Fanny, Pineau, Davide, Caimmi, Sylvie, Taviaux, Maurane, Reveil, Laura, Brosseau, Isabelle, Rivals, Margot, Drevait, Isabelle, Vachier, Mireille, Claustres, Raphaël, Chiron, Albertina, De Sario
Publikováno v:
Genes
Cystic fibrosis (CF) is a chronic genetic disease that mainly affects the respiratory and gastrointestinal systems. No curative treatments are available, but the follow-up in specialized centers has greatly improved the patient life expectancy. Robus
Autor:
David Grand, Peter Coopman, Sylvie Taviaux, Isabelle Rouquette, Beno ⁱt Béganton, Jean-Louis Pujol, Jérôme Solassol, Sylvain Godreuil, Estelle Clermont, Julien Mazieres, Pierre Brousset, Patricia Audran, Isabelle Serre, Julie A. Vendrell, Valérie Costes, Vanessa Szablewski
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2017, 7 (1), pp.12510. ⟨10.1038/s41598-017-12679-8⟩
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Scientific Reports, 2017, 7 (1), pp.12510. ⟨10.1038/s41598-017-12679-8⟩
Scientific Reports, Nature Publishing Group, 2017, 7 (1), pp.12510. ⟨10.1038/s41598-017-12679-8⟩
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Scientific Reports, 2017, 7 (1), pp.12510. ⟨10.1038/s41598-017-12679-8⟩
Rearrangements of the anaplastic lymphoma kinase (ALK) gene in non-small cell lung cancer (NSCLC) represent a novel molecular target in a small subset of tumors. Although ALK rearrangements are usually assessed by immunohistochemistry (IHC) and fluor
Autor:
Nicole Dastugue, Carole Barin, Christian Bastard, Olivier A. Bernard, Lisa J. Russell, Stéphanie Struski, Dominique Penther, Nathalie Nadal, Peter Vandenberghe, Isabelle Tigaud, Christine Lefebvre, Elise Chapiro, Florence Nguyen-Khac, Francine Mugneret, Marie-Joelle Mozziconacci, Christine J. Harrison, Eric Lippert, Pascaline Talmant, Sylvie Taviaux, Isabelle Radford-Weiss, Serge Romana, Hong-Anh Cung
Publikováno v:
Cancer Genetics. 206:162-173
Chromosomal translocations involving the immunoglobulin heavy chain locus (IGH@) are recurrent but rare in B-cell precursor acute lymphoblastic leukemia (BCP-ALL), and various partner genes have been described. Here, we report a new series of 29 case
Autor:
Cécile Borel, Jean Philippe Rault, Sylvie Taviaux, Sorin Visanica, Aranud Pigneux, Eric Lippert, Eric Delabesse, Pascaline Talmant, Nicole Dastugue, Faezeh Legrand, Nathalie Gachard, Marie-Joelle Mozziconacci, Valérie Cances-Lauwers, Christian Bastard, Christian Recher, Marie Agnes Collonges Rames, Norbert Vey, Francine Mugneret, Thomas Prebet
Publikováno v:
Leukemia Research. 36:1365-1369
The PICALM-MLLT10 fusion gene, generated by the t(10;11)(p12-13;q14-21) translocation, is a rare but recurrent event in acute leukemias. In this study, we assessed the characteristics and outcome of 18 PICALM-MLLT10 AML patients. As compared with non
Autor:
Lauren Veronese, Marc De Braekeleer, Christine Terré, Isabelle Radford-Weiss, Sylvie Taviaux, Nathalie Leporrier, Hélène Merle-Béral, Dominique Leroux, Hossein Mossafa, Florence Nguyen-Khac, Elise Chapiro, Sandra Fert-Ferrer, Evelyne Callet-Bauchu, Frederic Davi, Olivier Bernard, Laurent Sutton, Françoise Brizard, Claude Lesty, Stéphanie Struski, Christian Bastard, Isabelle Tigaud, Sophie Raynaud
Publikováno v:
Leukemia Research. 34:63-68
Using array-based CGH, we identified 2p gain in 22/78 (28%) untreated Binet stages B/C CLL, which was the second most frequent copy number change after 13q deletion. It never occurred as a sole abnormality and was associated with other changes (6q de
Autor:
M.J. Gregoire, Francine Mugneret, Marie-Pierre Pages, C Herens, F Nguyen Khac, Bruce Poppe, Catherine Helias, Joris Andrieux, Lucienne Michaux, Hélène Cavé, Roland Berger, Paola Ballerini, M J Mozziconacci, Franki Speleman, Pascaline Talmant, Maryvonne Busson, Sylvie Taviaux, Nicole Dastugue, Christian Bastard, Vahid Asnafi, Isabelle Radford, C Leonard, Olivier Bernard, Chrystele Bilhou-Nabera, Marina Lafage-Pochitaloff, C. Charrin, Laurent Mauvieux, J van den Akker, Pascale Cornillet-Lefebvre, Anne Hagemeijer, B. Quilichini, Christine Perot
Publikováno v:
Leukemia. 17:1851-1857
To accurately estimate the incidence of HOX11L2 expression, and determine the associated cytogenetic features, in T-cell acute lymphoblastic leukemia (T-ALL), the Groupe Francais de Cytogenetique Hematologique (GFCH) carried out a retrospective study
Autor:
Maximilian Muenke, Pierre Cau, Marguerite Gastaldi, Erich Roessler, Jean-Louis Bergé-Lefranc, Philippe Berta, Annick Massacrier, Sylvie Taviaux, Philippe Jay, Deeann Wallis
Publikováno v:
European Journal of Biochemistry. 267:2921-2928
A cDNA encoding a new human actin-related protein (ARP) was cloned. The corresponding protein is highly conserved with the previously described ARP3 protein, suggesting that it represents a second isoform of the human ARP3 subfamily. This new actin-r