Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Jamrog"'
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:
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
Autor:
Bastien Gerby, Stéphane J. C. Mancini, Marine Dubois, Laurent Delpy, Michel Cogné, Cyril Broccardo, Laura Jamrog, Naïs Prade, Nelly Rouquié, Charlotte Cresson, Sylvie Hébrard, Stéphanie Lagarde, Eric Delabesse, Sophie Péron
Publikováno v:
Oncotarget
Oncotarget, Impact journals, 2018, 9 (67), ⟨10.18632/oncotarget.26003⟩
Oncotarget, Impact journals, 2018, 9 (67), pp.32841-32854. ⟨10.18632/oncotarget.26003⟩
Oncotarget, 2018, 9 (67), pp.32841-32854. ⟨10.18632/oncotarget.26003⟩
Oncotarget, Impact journals, 2018, 9 (67), ⟨10.18632/oncotarget.26003⟩
Oncotarget, Impact journals, 2018, 9 (67), pp.32841-32854. ⟨10.18632/oncotarget.26003⟩
Oncotarget, 2018, 9 (67), pp.32841-32854. ⟨10.18632/oncotarget.26003⟩
International audience; Pax5 is the guardian of the B cell identity since it primes or enhances the expression of B cell specific genes and concomitantly represses the expression of B cell inappropriate genes. The tight regulation of Pax5 is therefor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a12041f56f799448e0fb364179adc33b
https://hal.archives-ouvertes.fr/hal-02343994
https://hal.archives-ouvertes.fr/hal-02343994