Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Vincent Fregona"'
Autor:
Laëtitia Largeaud, Vincent Fregona, Laura Jamrog, Camille Hamelle, Stephanie Dufrechou, Naïs Prade, Esmaa Sellam, Pauline Enfedaque, Manon Bayet, Sylvie Hebrard, Christine Didier, Eric Delabesse, Bastien Gerby, Marlène Pasquet, Cyril Broccardo
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100052- (2023)
Externí odkaz:
https://doaj.org/article/72d4ea3cd74f437583e68904497e20da
Autor:
Laetitia Largeaud, Matthew Collin, Nils Monselet, Francois Vergez, Vincent Fregona, Lise Larcher, Pierre Hirsch, Nicolas Duployez, Audrey Bidet, Isabelle Luquet, Jacinta Bustamante, Stephanie Dufrechou, Nais Prade, Marie Nolla, Camille Hamelle, Suzanne Tavitian, Christophe Habib, Mateo Meynier, Christine Bellanne-Chantelot, Jean Donadieu, Flore Sicre de Fontbrune, Claire Fieschi, Alina Ferster, Francois Delhommeau, Eric Delabesse, Marlene Pasquet
Publikováno v:
Haematologica, Vol 108, Iss 6 (2023)
Germline GATA2 mutations predispose to myeloid malignancies resulting from the progressive acquisition of additional somatic mutations. Here we describe clinical and biological features of 78 GATA2-deficient patients. Hematopoietic stem and progenito
Externí odkaz:
https://doaj.org/article/66d570b4c75a4f039dacadeac2564635
Publikováno v:
Cancers, Vol 13, Iss 21, p 5511 (2021)
Our understanding of the hierarchical structure of acute leukemia has yet to be fully translated into therapeutic approaches. Indeed, chemotherapy still has to take into account the possibility that leukemia-initiating cells may have a distinct chemo
Externí odkaz:
https://doaj.org/article/fba48e79826043c6a263d7d90bb21e71
Autor:
Vincent Fregona
We are happy to share the First UNICORN ★ Protocol on behalf of the UNICORN Hemato. How to perform affordable immunofluorescence staining on bones or other tissues without cryostat This method is an adaptation from - Multicolor quantitative confoca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65867d8830aa5325be4028c5289506e0
https://doi.org/10.17504/protocols.io.14egn2zpzg5d/v1
https://doi.org/10.17504/protocols.io.14egn2zpzg5d/v1
Autor:
Virginie Eclache, John Boudjarane, Naïs Prade, Stéphanie Struski, Laetitia Largeaud, Cyril Broccardo, Joop H. Jansen, Christine Terré, Marie-Agnès Collonge-Rame, Pierre-Yves Juvin, Dominique Penther, Stéphanie Lagarde, Antoine Ittel, Véronique Mansat-De Mas, G Ameye, Isabelle Luquet, Marina Lafage-Pochitaloff, Carole Barin, David Rombaut, Bastien Gerby, Carine Gervais, Steven Richebourg, Oliver M. Dovey, Pierre Bories, Christine Lefebvre, Isabelle Radford-Weiss, Audrey Bidet, Isabelle Tigaud, George S. Vassiliou, Benedicte Ribourtout, Tobias Tekath, Michaela Fontenay, Lucienne Michaux, Sylvie Hébrard, Hélène Antoine-Poirel, Laura Jamrog, Vincent Fregona, Nathalie Nadal, Eric Delabesse, Véronique Baccini, Kosuke Yusa
Publikováno v:
Blood Advances, 6, 2, pp. 386-398
Blood Advances
Blood Advances, 6, 386-398
Blood Advances, The American Society of Hematology, 2021, ⟨10.1182/bloodadvances.2021005311⟩
Blood Advances
Blood Advances, 6, 386-398
Blood Advances, The American Society of Hematology, 2021, ⟨10.1182/bloodadvances.2021005311⟩
Key Points We detail at clinical, cytological, cytogenetic, and molecular levels 113 cases of MDS and MDS/MPN with del(11q), a rare recurrent event.CADM1, a tumor suppressor gene identified initially in solid tumors, ATM, CBL, and KMT2A are deleted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a801474f49c15e8392848015e288927
https://repository.ubn.ru.nl/handle/2066/244555
https://repository.ubn.ru.nl/handle/2066/244555
Autor:
Vincent Fregona, Manon Bayet, Mathieu bouttier, Laetitia Largeaud, Camille Hamelle, Laura Jamrog, Naïs Prade, Stéphanie Lagarde, Sylvie Hebard, Marlène Pasquet, Christine Didier, Ahmed Khamlichi, Cyril Broccardo, Eric Delabesse, Stéphane Mancini, bastien Gerby
Publikováno v:
Experimental Hematology. 111:S86-S87
Autor:
Eric Delabesse, Vincent Fregona, Céline Villenet, Catherine Roche-Lestienne, Céline Berthon, Stephanie Dufrechou, José Fernandes, Nathalie Helevaut, Brigitte Nelken, Sylvie Hébrard, Naïs Prade, Bastien Gerby, Stéphanie Poulain, Laura Jamrog, Claude Preudhomme, Nicolas Duployez, Cyril Broccardo, Aurélie Caillault, Laetitia Largeaud, Martin Figeac, Sophie Lejeune, Alice Marceau-Renaut, Sandrine Geffroy, Camille Hamelle, Laurène Fenwarth
Publikováno v:
Blood
Blood, American Society of Hematology, 2021, 137 (10), pp.1424-1428. ⟨10.1182/blood.2020005756⟩
Blood, 2021, 137 (10), pp.1424-1428. ⟨10.1182/blood.2020005756⟩
Blood, American Society of Hematology, 2021, 137 (10), pp.1424-1428. ⟨10.1182/blood.2020005756⟩
Blood, 2021, 137 (10), pp.1424-1428. ⟨10.1182/blood.2020005756⟩
International audience; No abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f85c8f5d950364f93af95d090c7c02
https://hal.archives-ouvertes.fr/hal-03426713/document
https://hal.archives-ouvertes.fr/hal-03426713/document
Autor:
Esmaa Sellam, Vincent Fregona, Cyril Broccardo, Naïs Prade, Laetitia Largeaud, Camille Hamelle, Stephanie Dufrechou, Manon Bayet, Christine Didier, Eric Delabesse, Sylvie Hébrard, Marlène Pasquet, Laura Jamrog, Bastien Gerby
Publikováno v:
Blood. 138:27-27
Germline GATA2 mutations are identified in a complex disorder termed GATA2 deficiency syndrome. Clinical heterogeneous manifestations are associated with a wide diversity of molecular alterations (missense, frameshift, nonsense, intronic or splicing
Autor:
Guillaume Chemin, Sylvie Hébrard, Chloé Oudinet, Ngoc Sa Nguyen Huu, Pierre Brousset, Stéphanie Lagarde, Laura Jamrog, Vincent Fregona, Cyril Broccardo, Bastien Gerby, Cathy Quelen, Eric Delabesse, Marina Bousquet, Stéphane J. C. Mancini, Naïs Prade, Nelly Rouquié, Charlotte Cresson, Marlène Pasquet, Lucie Coster, Ahmed Amine Khamlichi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2018, 115 (41), pp.10357-10362. ⟨10.1073/pnas.1721678115⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2018, 115 (41), pp.10357-10362. ⟨10.1073/pnas.1721678115⟩
International audience; PAX5 is a well-known haploinsufficient tumor suppressor gene in human B-cell precursor acute lymphoblastic leukemia (B-ALL) and is involved in various chromosomal translocations that fuse a part of PAX5 with other partners. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0897d5cf8c5dd337cf3b8d30ccb25c7b
https://hal.archives-ouvertes.fr/hal-02351122
https://hal.archives-ouvertes.fr/hal-02351122