Ngā hua rapu - Quentin, Samuel

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

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Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma mā Guenat, David, Quentin, Samuel, Rizzari, Carmelo, Lundin, Catarina, Coliva, Tiziana, Edery, Patrick, Fryssira, Helen, Bermont, Laurent, Ferrand, Christophe, Soulier, Jean, Borg, Christophe, Rohrlich, Pierre-Simon

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

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Reversal of microRNA-150 silencing disadvantages crizotinib-resistant NPM-ALK(+) cell growth mā Hoareau-Aveilla, Coralie, Valentin, Thibaud, Daugrois, Camille, Quelen, Cathy, Mitou, Géraldine, Quentin, Samuel, Jia, Jinsong, Spicuglia, Salvatore, Ferrier, Pierre, Ceccon, Monica, Giuriato, Sylvie, Gambacorti-Passerini, Carlo, Brousset, Pierre, Lamant, Laurence, Meggetto, Fabienne

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Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease mā Masliah-Planchon, Julien, Dupont, Céline, Vartzelis, George, Trimouille, Aurélien, Eymard-Pierre, Eléonore, Gay-Bellile, Mathilde, Renaldo, Florence, Dorboz, Imen, Pagan, Cécile, Quentin, Samuel, Elmaleh, Monique, Kotsogianni, Christina, Konstantelou, Elissavet, Drunat, Séverine, Tabet, Anne-Claude, Boespflug-Tanguy, Odile

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Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies mā Delahaye, Andrée, Bitoun, Pierre, Drunat, Séverine, Gérard-Blanluet, Marion, Chassaing, Nicolas, Toutain, Annick, Verloes, Alain, Gatelais, Frédérique, Legendre, Marie, Faivre, Laurence, Passemard, Sandrine, Aboura, Azzedine, Kaltenbach, Sophie, Quentin, Samuel, Dupont, Céline, Tabet, Anne-Claude, Amselem, Serge, Elion, Jacques, Gressens, Pierre, Pipiras, Eva, Benzacken, Brigitte

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

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

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

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

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