Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pascal Fuseau"'
Autor:
Marie‐Daniéla Dubois, Ivan Peyron, Olivier‐Nicolas Pierre‐Louis, Serge Pierre‐Louis, Johalène Rabout, Pierre Boisseau, Annika deJong, Sophie Susen, Jenny Goudemand, Rémi Neviere, Pascal Fuseau, Olivier D. Christophe, Peter J. Lenting, Cécile V. Denis, Caterina Casari
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 6, Iss 4, Pp n/a-n/a (2022)
Abstract Background Von Willebrand disease was diagnosed in two Afro‐Caribbean patients and sequencing of the VWF gene (VWF) revealed the presence of multiple variants located throughout the gene, including variants located in the D4 domain of VWF:
Externí odkaz:
https://doaj.org/article/b5a5473594134f32afc891cac997479f
Autor:
Christophe Ferrand, Philippe Saas, Etienne Daguindau, Anne Roggy, Sandrine Geffroy, Sabrina Bouyer, Pierre-Julien Viailly, Olivier Adotevi, Mary Callanan, Sabeha Biichle, Elizabeth Macintyre, Francine Garnache-Ottou, Tony Petrella, Jacques Colinge, Christophe Roumier, Florian Renosi, Véronique Harrivel, Véronique Salaun, Pascale Saussoy, Eric Deconinck, Ambre Giguelay, Fanny Angelot-Delettre, Jean Feuillard, Vahid Asnafi, Claude Preudhomme, Fabrice Jardin, Meyling Cheok, Pascal Fuseau, Lou Soret
Publikováno v:
Blood advances, Vol. 5, no.5, p. 1540-1551 (2021)
Blood Adv
Blood Adv
Oncogenesis and ontogeny of blastic plasmacytoid dendritic cell neoplasm (BPDCN) remain uncertain, between canonical plasmacytoid dendritic cells (pDCs) and AXL+ SIGLEC6+ DCs (AS-DCs). We compared 12 BPDCN to 164 acute leukemia by Affymetrix HG-U133
Autor:
Jean-Edouard Martin, Christine Bellanné-Chantelot, Olivier Caron, Pascal Fuseau, Nathalie Auger, Barbara Schmaltz-Panneau, Sophie Cotteret, Stéphane de Botton, Christophe Willekens, Florence Pasquier, Christophe Marzac, Jean-Baptiste Micol, Jean Pegliasco, Maureen Lopez, William Vainchenker, Adel Ben-Ali, Véronique Saada, Carole Bourdin, Flore Salviat, Odile Bera, Sabine Khalife-Hachem, Isabelle Plo, Cristina Castilla-Llorent, Philippe Helias, Jean-Côme Meniane, Samy Chraibi, Raouf Ben-Abdelali
Publikováno v:
Leukemia & Lymphoma. 62:1770-1773
Genetic predisposition to acute myeloid leukemia (AML) concerns a minority of adult patients. Development of high-throughput sequencing technologies over the last ten years allowed identification o...
Autor:
Pierre Hirsch, Barbara Schmaltz-Panneau, Jean-Henri Bourhis, Caroline Deswarte, Christophe Marzac, Christine Bellanné-Chantelot, Jean-Baptiste Micol, Christine Delaunay-Darivon, Flore Sicre de Fontbrune, Hélène Guermouche, Albert Najman, William Vainchenker, Céline Lemaitre, Jean-Côme Meniane, Eolia Brissot, Florence Pasquier, Philippe Pellet, Gwendoline Leroy, François Delhommeau, Patrick R. Benusiglio, Samy Chraibi, Isabelle Plo, Olivier Caron, Pascal Fuseau, Simona Lapusan, Pascale Cony-Makhoul, Odile Bera, Chrystelle Colas, Jean Pegliasco, Graciela Rabadan Moraes, Françoise Isnard
Publikováno v:
Leukemia. 36(1)
The germline predisposition associated with the autosomal dominant inheritance of the 14q32 duplication implicating ATG2B/GSKIP genes is characterized by a wide clinical spectrum of myeloid neoplasms. We analyzed 12 asymptomatic carriers and 52 patie
Autor:
Roseline Tang, Sophie Cotteret, Jean Pegliasco, Christine Bellanné-Chantelot, Véronique Saada, Clemence Legoupil, Olivier Caron, Pascal Fuseau, Adel Ben-Ali, Pascale Cornillet-Lefebvre, Raouf Benabelali, Stéphane de Botton, Jean-Henri Bourhis, Christophe Marzac, Jean-Edouard Martin, Jean-Baptiste Micol, Nathalie Auger, William Vainchenker, Isabelle Plo, Florence Pasquier, Jean-Côme Meniane, Jacques Delaunay, Christophe Willekens, Maureen Lopez, Samy Chraibi, Odile Bera, Philippe Helias, Barbara Panneau-Schmaltz, Christian Recher
Publikováno v:
Blood. 132:1482-1482
In 2015, a germline copy number variation of chromosome 14 (CNVdup14) including ATG2B and GSKIP genes was described as a predisposition genetic factor responsible of familial myeloproliferative neoplasms from French West Indies (Saliba et al, Nat Gen
Autor:
Hana Raslova, Eric Solary, Sabine Charrier, Jane Merlevede, Gaëlle Lenglet, Antonio Di Stefano, M'Boyba Diop, Véronique Della Valle, Gwendoline Leroy, Boris Keren, Cécile Saint-Martin, Christine Bellanné-Chantelot, Sarah Grosjean, Lise Secardin, Philippe Dessen, Caroline Marty, Nicole Casadevall, Emna Mahfoudhi, Najet Debili, Florence Pasquier, Isabelle Plo, Françoise Isnard, Joseph Saliba, Pascal Fuseau, Albert Najman, Jean-Côme Meniane, Olivier Bernard, Christine Delaunay-Darivon, Alberta Palazzo, William Vainchenker, Nathalie Droin
Publikováno v:
Nature Genetics
Nature Genetics, 2015, 47 (10), pp.1131-1140. ⟨10.1038/ng.3380⟩
Nature Genetics, Nature Publishing Group, 2015, 47 (10), pp.1131-1140. ⟨10.1038/ng.3380⟩
Nature Genetics, 2015, 47 (10), pp.1131-1140. ⟨10.1038/ng.3380⟩
Nature Genetics, Nature Publishing Group, 2015, 47 (10), pp.1131-1140. ⟨10.1038/ng.3380⟩
International audience; No major predisposition gene for familial myeloproliferative neoplasms (MPN) has been identified. Here we demonstrate that the autosomal dominant transmission of a 700-kb duplication in four genetically related families predis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aef0f5d0f376850b705b56dca3d58157
https://hal.science/hal-02881018/document
https://hal.science/hal-02881018/document