Výsledky vyhledávání - Samuel Quentin

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  1. 1
    FLT3-ITD impedes retinoic acid, but not arsenic, responses in murine acute promyelocytic leukemias

    FLT3-ITD impedes retinoic acid, but not arsenic, responses in murine acute promyelocytic leukemias Autor Cécile Esnault, Ramy Rahmé, Kim L. Rice, Caroline Berthier, Coline Gaillard, Samuel Quentin, Anne-Lise Maubert, Scott C. Kogan, Hugues de Thé

    Vydáno 2019
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  2. 2
    Meningioma progression in mice triggered by Nf2 and Cdkn2ab inactivation

    Meningioma progression in mice triggered by Nf2 and Cdkn2ab inactivation Autor Matthieu Peyre, Anat Stemmer‐Rachamimov, Estelle Clermont‐Taranchon, Samuel Quentin, N El-Taraya, Christine Walczak, Andreas Volk, Michiko Niwa‐Kawakita, Narjesse Karboul, Marco Giovannini, Michel Kalamarides

    Vydáno 2012
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  3. 3
    First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

    First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis Autor Éric Pasmant, P. Goussard, Laetitia Baranes, Ingrid Laurendeau, Samuel Quentin, P Ponsot, Yann Consigny, Olivier Farges, Bertrand Condat, Dominique Vidaud, Michel Vidaud, Jian‐Min Chen, Béatrice Parfait

    Vydáno 2011
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  4. 4
    Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission

    Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission Autor Olivier Nibourel, Olivier Kosmider, Meyling Cheok, Nicolas Boissel, Aline Renneville, N Philippe, Hervé Dombret, François Dreyfus, Bruno Quesnel, Sandrine Geffroy, Samuel Quentin, Catherine Roche‐Lestienne, Jean‐Michel Cayuela, Christophe Roumier, Pierre Fenaux, William Vainchenker, Olivier Bernard, Jean Soulier, Michaëla Fontenay, Claude Preudhomme

    Vydáno 2010
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  5. 5
    PAX5 P80R mutation identifies a novel subtype of B-cell precursor acute lymphoblastic leukemia with favorable outcome

    PAX5 P80R mutation identifies a novel subtype of B-cell precursor acute lymphoblastic leukemia with favorable outcome Autor Marie Passet, Nicolas Boissel, François Sigaux, Colombe Saillard, Mario Bargetzi, Ibrahima Ba, Xavier Thomas, Carlos Graux, Yves Chalandon, Thibaut Leguay, Étienne Lengliné, Johanna Konopacki, Samuel Quentin, Éric Delabesse, Mårina Lafage‐Pochitaloff, Cédric Pastoret, Nathalie Grardel, Vahid Asnafi, Véronique Lhéritier, Jean Soulier, Hervé Dombret, Emmanuelle Clappier

    Vydáno 2018
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  6. 6
    Structural Basis of PML-RARA Oncoprotein Targeting by Arsenic Unravels a Cysteine Rheostat Controlling PML Body Assembly and Function

    Structural Basis of PML-RARA Oncoprotein Targeting by Arsenic Unravels a Cysteine Rheostat Controlling PML Body Assembly and Function Autor Pierre Bercier, Qian Qian Wang, Ning Zang, Jie Zhang, Chang Yang, Yasen Maimaitiyiming, Majdouline Abou-Ghali, Caroline Berthier, Chengchen Wu, Michiko Niwa‐Kawakita, Thassadite Dirami, Marie‐Claude Geoffroy, Omar Ferhi, Samuel Quentin, Shirine Benhenda, Yasumitsu Ogra, Zoher Gueroui, Chun Zhou, Hua Naranmandura, Hugues de Thé, Valérie Lallemand-Breitenbach

    Vydáno 2023
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  7. 7
    Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

    Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions Autor Samuel Quentin, Wendy Cuccuini, Raphaël Ceccaldi, Olivier Nibourel, Corinne Pondarré, Marie‐Pierre Pagès, Nadia Vasquez, Catherine Dubois d’Enghien, Jérôme Larghero, Régis Peffault de Latour, Vanderson Rocha, Jean‐Hugues Dalle, Pascale Schneider, Mauricette Michallet, Gérard Michel, André Baruchel, François Sigaux, Éliane Gluckman, Thierry Leblanc, Dominique Stoppa‐Lyonnet, Claude Preudhomme, Gèrard Socié, Jean Soulier

    Vydáno 2011
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  8. 8
    Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

    Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum Autor Alain Sarasin, Samuel Quentin, Nathalie Droin, Mourad Sahbatou, Véronique Saada, Nathalie Auger, Yannick Boursin, Philippe Dessen, Anna Raimbault, Vahid Asnafi, J.‐L. Schmutz, Alain Taı̈eb, Carlos Frederico Martins Menck, Filippo Rosselli, Laurianne Drieu La Rochelle, Caroline Robert, Flore Sicre de Fontbrune, Marie Sébert, Thierry Leblanc, Patricia Kannouche, Stéphane de Botton, Éric Solary, Jean Soulier

    Vydáno 2019
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  9. 9
    Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly

    Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly Autor Sandrine Vuillaumier‐Barrot, C. Bouchet-Séraphin, M. Chelbi, Louise Devisme, Samuel Quentin, Steven Gazal, Annie Laquerrière, Catherine Fallet‐Bianco, Philippe Loget, Sylvie Odent, Dominique Carles, Anne Bazin, Jacqueline Aziza, Alix Clémenson, Fabien Guimiot, Maryse Bonnière, Sophie Monnot, Christine Bôle‐Feysot, Jean‐Pierre Bernard, Laurence Lœuillet, Marie Gonzalès, Koryna Socha, Bernard Grandchamp, Tania Attié‐Bitach, Férechté Encha‐Razavi, Nathalie Seta

    Vydáno 2012
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  10. 10
    Concurrent <i>CDX2 cis</i>-deregulation and <i>UBTF::ATXN7L3</i> fusion define a novel high-risk subtype of B-cell ALL

    Concurrent <i>CDX2 cis</i>-deregulation and <i>UBTF::ATXN7L3</i> fusion define a novel high-risk subtype of B-cell ALL Autor Marie Passet, Rathana Kim, Stéphanie Gachet, François Sigaux, Julie Chaumeil, Ava Galland, Tom Sexton, Samuel Quentin, Lucie Hernandez, Lise Larcher, Hugo Bergugnat, Tao Ye, Nezih Karasu, Aurélie Caye, Beate Heizmann, Isabelle Duluc, Patrice Chevallier, Philippe Rousselot, Françoise Huguet, Thibaut Leguay, Mathilde Hunault, Françoise Pflumio, Jean‐Noël Freund, Camille Lobry, Véronique Lhéritier, Hervé Dombret, Claire Domon‐Dell, Jean Soulier, Nicolas Boissel, Emmanuelle Clappier

    Vydáno 2022
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  11. 11
    Actinomycin D Targets NPM1c-Primed Mitochondria to Restore PML-Driven Senescence in AML Therapy

    Actinomycin D Targets NPM1c-Primed Mitochondria to Restore PML-Driven Senescence in AML Therapy Autor Hsin-Chieh Wu, Domitille Rérolle, Caroline Berthier, Rita Hleihel, Takashi Sakamoto, Samuel Quentin, Shirine Benhenda, Claudia Morganti, Chengchen Wu, Lidio Conte, Sylvie Rimsky, Marie Sébert, Emmanuelle Clappier, Sylvie Souquère, Stéphanie Gachet, Jean Soulier, Sylvère Durand, Jennifer J. Trowbridge, Paule Bénit, Pierre Rustin, Hiba El Hajj, Emmanuel Raffoux, Lionel Adès, Raphaël Itzykson, Hervé Dombret, Pierre Fenaux, Olivier Espéli, Guido Kroemer, Lorenzo Brunetti, Tak W. Mak, Valérie Lallemand-Breitenbach, Ali Bazarbachi, Brunangelo Falini, Keisuke Ito, Maria Paola Martelli, Hugues de Thé

    Vydáno 2021
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  12. 12
    A landscape of germ line mutations in a cohort of inherited bone marrow failure patients

    A landscape of germ line mutations in a cohort of inherited bone marrow failure patients Autor Olivier Bluteau, Marie Sébert, Thierry Leblanc, Régis Peffault de Latour, Samuel Quentin, Élodie Lainey, Lucie Hernandez, Jean‐Hugues Dalle, Flore Sicre de Fontbrune, Étienne Lengliné, Raphaël Itzykson, Emmanuelle Clappier, Nicolas Boissel, Nadia Vasquez, Mélanie Da Costa, Julien Masliah-Planchon, Wendy Cuccuini, Anna Raimbault, Louis De Jaegere, Lionel Adès, Pierre Fenaux, Sébastien Maury, Claudine Schmitt, Marc Müller, Carine Domenech, Nicolas Blin, Bénédicte Bruno, Isabelle Pellier, Mathilde Hunault, Stéphane Blanche, Arnaud Petit, Guy Leverger, Gérard Michel, Yves Bertrand, André Baruchel, Gerard Socié, Jean Soulier

    Vydáno 2017
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  13. 13
    Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia

    Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia Autor Marie Sébert, Stéphanie Gachet, Thierry Leblanc, Alix Rousseau, Olivier Bluteau, Rathana Kim, Raouf Ben Abdelali, Flore Sicre de Fontbrune, Loïc Maillard, Carèle Fedronie, Valentine Murigneux, Léa Bellenger, Naïra Naouar, Samuel Quentin, Lucie Hernandez, Nadia Vasquez, Mélanie Da Costa, Pedro Henrique Prata, Lise Larcher, Marie de Tersant, Matthieu Duchmann, Anna Raimbault, Franck Trimoreau, Odile Fenneteau, Wendy Cuccuini, Nathalie Gachard, Nathalie Auger, Giulia Tueur, Maud Blanluet, Claude Gazin, Michèle Souyri, Francina Langa‐Vives, Aarón Méndez-Bermúdez, Hélène Lapillonne, Étienne Lengliné, Emmanuel Raffoux, Pierre Fenaux, Lionel Adès, Édouard Forcade, Charlotte Jubert, Carine Domenech, Marion Strullu, Bénédicte Bruno, Nimrod Buchbinder, Caroline Thomas, Arnaud Petit, Guy Leverger, Gérard Michel, Marina Cavazzana, Éliane Gluckman, Yves Bertrand, Nicolas Boissel, André Baruchel, Jean‐Hugues Dalle, Emmanuelle Clappier, Éric Gilson, Ludovic Deriano, Sylvie Chevret, François Sigaux, Gèrard Socié, Dominique Stoppa‐Lyonnet, Hugues de Thé, Christophe Antoniewski, Dominique Bluteau, Régis Peffault de Latour, Jean Soulier

    Vydáno 2023
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