Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Albert, Najman"'
Autor:
Graciela Rabadan Moraes, Florence Pasquier, Christophe Marzac, Eric Deconinck, Carlotta Caterina Damanti, Gwendoline Leroy, Mira El‐Khoury, Wassim El Nemer, Jean‐Jacques Kiladjian, Hana Raslova, Albert Najman, William Vainchenker, Caroline Marty, Christine Bellanné‐Chantelot, Isabelle Plo
Publikováno v:
British Journal of Haematology. 198:131-136
Autor:
Graciela, Rabadan Moraes, Florence, Pasquier, Christophe, Marzac, Eric, Deconinck, Carlotta Caterina, Damanti, Gwendoline, Leroy, Mira, El-Khoury, Wassim, El Nemer, Jean-Jacques, Kiladjian, Hana, Raslova, Albert, Najman, William, Vainchenker, Caroline, Marty, Christine, Bellanné-Chantelot, Isabelle, Plo
Publikováno v:
British journal of haematologyREFERENCES. 198(1)
Myeloproliferative neoplasms (MPN) are mainly sporadic but inherited variants have been associated with higher risk development. Here, we identified an EPOR variant (EPOR
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:
Sabina I. Swierczek, Donghoon Yoon, Christine Bellanné-Chantelot, Soo Jin Kim, Cécile Saint-Martin, Francois Delhommeau, Albert Najman, Josef T. Prchal
Publikováno v:
Haematologica, Vol 96, Iss 5 (2011)
TET2 mutations are found in polycythemia vera and it was initially reported that there is a greater TET2 mutational burden than JAK2V617F in polycythemia vera stem cells and that TET2 mutations precede JAK2V617F. We quantified the proportion of TET2,
Externí odkaz:
https://doaj.org/article/06f8e7eab89a4e7ba1a4876da408e923
Autor:
Albert Najman, Guigon M
Publikováno v:
Malignant Cell Secretion ISBN: 9780429276064
Malignant Cell Secretion
Malignant Cell Secretion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bf5125143749ccfa71ccbd4af14fffd
https://doi.org/10.1201/9780429276064-8
https://doi.org/10.1201/9780429276064-8
Publikováno v:
Hématologie. 17:331-341
Les formes familiales de syndromes myeloproliferatifs (SMP) peuvent etre divisees en deux grands groupes. Le premier groupe correspond aux formes familiales de SMP bcr-abl-negatif, compatibles avec une transmission autosomique dominante a penetrance
Autor:
Yves Plumelle, Albert Najman, Dominique Bordessoule, Isabelle Plo, Sabrina Dupont, William Vainchenker, Olivier Bernard, François Delhommeau, Alain Devidas, Christine Bellanné-Chantelot, Christine Chomienne, Françoise Isnard, Gwendoline Leroy, Chloé James, Cécile Saint-Martin, Martine Gardembas-Pain, André Delannoy, Gérard Panelatti
Publikováno v:
Blood
Blood, American Society of Hematology, 2009, 114 (8), pp.1628-32. ⟨10.1182/blood-2009-01-197525⟩
Blood, American Society of Hematology, 2009, 114 (8), pp.1628-32. ⟨10.1182/blood-2009-01-197525⟩
The JAK2V617F mutation does not elucidate the phenotypic variability observed in myeloproliferative neoplasm (MPN) families. A putative tumor suppressor gene, TET2, was recently implicated in MPN and myelodysplastic syndromes through the identificati
Autor:
Raphaël David, Stachowiak J, B. Rio, G. A. Voisin, Norbert-Claude Gorin, J. Jansen, G. Le Blanc, P. Poncelet, Luc Douay, J. P. Laporte, M. Lopez, Albert Najman, Salmon C, Duhamel G, R. Zittoun, M. C. Liance, Deloux J, P. Cazellas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1c7828255fc2345ba9b495f5b3636a9
https://doi.org/10.1159/000411719
https://doi.org/10.1159/000411719
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
Autor:
Christine Bellanné-Chantelot, Myriam Labopin, Florence Bellanger, Claudia de Toma, Véronique Barbu, Gilles Thomas, William Vainchenker, Albert Najman, Isabelle Chaumarel, François Delhommeau, Nicole Casadevall
Publikováno v:
Blood. 108:346-352
To study the prevalence of the Val617Phe JAK2 mutation in familial cases of myeloproliferative disorder (MPD) and its possible implication as a predisposing genetic factor, we analyzed 72 families including 174 patients (81 polycythemia vera [PV], 68