Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Abnormalities and FBXW7[original query] |
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| NOTCH1/FBXW7 mutation identifies a large subgroup with favorable outcome in adult T-cell acute lymphoblastic leukemia (T-ALL): a Group for Research on Adult Acute Lymphoblastic Leukemia (GRAALL) study. Blood 2009 Apr 113 (17): 3918-24. Asnafi Vahid, Buzyn Agnès, Le Noir Sandrine, Baleydier Frédéric, Simon Arnauld, Beldjord Kheira, Reman Oumedaly, Witz Francis, Fagot Thierry, Tavernier Emmanuelle, Turlure Pascal, Leguay Thibaut, Huguet Françoise, Vernant Jean-Paul, Daniel Francis, Béné Marie-Christine, Ifrah Norbert, Thomas Xavier, Dombret Hervé, Macintyre Elizabe |
| Impact of complex NOTCH1 mutations on survival in paediatric T-cell leukaemia. BMC cancer 2012 12 (1): 9. Mansur Marcela Braga, Hassan Rocio, Barbosa Thayana C, Splendore Alessandra, Jotta Patricia Y, Yunes José Andrés, Wiemels Joseph L, Pombo-de-Oliveira Maria |
| B-cell receptor configuration and mutational analysis of patients with chronic lymphocytic leukaemia and trisomy 12 reveal recurrent molecular abnormalities. Hematological oncology 2014 Mar 32 (1): 22-30. Falisi Erika, Novella Elisabetta, Visco Carlo, Guercini Nicola, Maura Francesco, Giaretta Ilaria, Pomponi Fabrizio, Nichele Ilaria, Finotto Silvia, Montaldi Annamaria, Neri Antonino, Rodeghiero Frances |
| Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2013 Dec 31 (34): 4333-42. Trinquand Amélie, Tanguy-Schmidt Aline, Ben Abdelali Raouf, Lambert Jérôme, Beldjord Kheira, Lengliné Etienne, De Gunzburg Noémie, Payet-Bornet Dominique, Lhermitte Ludovic, Mossafa Hossein, Lhéritier Véronique, Bond Jonathan, Huguet Françoise, Buzyn Agnès, Leguay Thibaud, Cahn Jean-Yves, Thomas Xavier, Chalandon Yves, Delannoy André, Bonmati Caroline, Maury Sebastien, Nadel Bertrand, Macintyre Elizabeth, Ifrah Norbert, Dombret Hervé, Asnafi Vah |
| The molecular profile of adult T-cell acute lymphoblastic leukemia: mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL. Genes, chromosomes & cancer 2013 Jan . Grossmann V, Haferlach C, Weissmann S, Roller A, Schindela S, Poetzinger F, Stadler K, Bellos F, Kern W, Haferlach T, Schnittger S, Kohlmann A |
| Oncogenetics and minimal residual disease are independent outcome predictors in adult patients with acute lymphoblastic leukemia. Blood 2014 Jun 123 (24): 3739-49. Beldjord Kheira, Chevret Sylvie, Asnafi Vahid, Huguet Françoise, Boulland Marie-Laure, Leguay Thibaut, Thomas Xavier, Cayuela Jean-Michel, Grardel Nathalie, Chalandon Yves, Boissel Nicolas, Schaefer Beat, Delabesse Eric, Cavé Hélène, Chevallier Patrice, Buzyn Agnès, Fest Thierry, Reman Oumedaly, Vernant Jean-Paul, Lhéritier Véronique, Béné Marie C, Lafage Marina, Macintyre Elizabeth, Ifrah Norbert, Dombret Hervé, |
| Impact of PTEN abnormalities on outcome in pediatric patients with T-cell acute lymphoblastic leukemia treated on the MRC UKALL2003 trial. Leukemia 2015 Jul . Jenkinson S, Kirkwood A A, Goulden N, Vora A, Linch D C, Gale R |
| Collecting duct carcinoma of the kidney is associated with CDKN2A deletion and SLC family gene up-regulation. Oncotarget 2016 Apr . Wang Jianmin, Papanicolau-Sengos Antonios, Chintala Sreenivasulu, Wei Lei, Liu Biao, Hu Qiang, Miles Kiersten Marie, Conroy Jeffrey M, Glenn Sean T, Costantini Manuela, Magi-Galluzzi Cristina, Signoretti Sabina, Choueiri Toni, Gallucci Michele, Sentinelli Steno, Fazio Vito M, Poeta Maria Luana, Liu Song, Morrison Carl, Pili Rober |
| Frequent HRAS Mutations in Malignant Ectomesenchymoma: Overlapping Genetic Abnormalities With Embryonal Rhabdomyosarcoma. The American journal of surgical pathology 2016 Feb . Huang Shih-Chiang, Alaggio Rita, Sung Yun-Shao, Chen Chun-Liang, Zhang Lei, Kao Yu-Chien, Agaram Narasimhan P, Wexler Leonard H, Antonescu Cristina |
| Next-generation sequencing and FISH studies reveal the appearance of gene mutations and chromosomal abnormalities in hematopoietic progenitors in chronic lymphocytic leukemia. Journal of hematology & oncology 2017 Apr 10 (1): 83. Quijada-Álamo Miguel, Hernández-Sánchez María, Robledo Cristina, Hernández-Sánchez Jesús-María, Benito Rocío, Montaño Adrián, Rodríguez-Vicente Ana E, Quwaider Dalia, Martín Ana-África, García-Álvarez María, Vidal-Manceñido María Jesús, Ferrer-Garrido Gonzalo, Delgado-Beltrán María-Pilar, Galende Josefina, Rodríguez Juan-Nicolás, Martín-Núñez Guillermo, Alonso José-María, García de Coca Alfonso, Queizán José A, Sierra Magdalena, Aguilar Carlos, Kohlmann Alexander, Hernández José-Ángel, González Marcos, Hernández-Rivas Jesús-Mar |
| Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases. The American journal of surgical pathology 2017 Nov . El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi |
| Prognostic and predictive role of gene mutations in chronic lymphocytic leukemia: results from the pivotal phase III study COMPLEMENT1. Haematologica 2020 Jan 105 (10): 2440-2447. Tausch Eugen, Beck Philipp, Schlenk Richard F, Jebaraj Billy J, Dolnik Anna, Yosifov Deyan Y, Hillmen Peter, Offner Fritz, Janssens Ann, Babu Govind K, Grosicki Sebastian, Mayer Jiri, Panagiotidis Panagiotis, McKeown Astrid, Gupta Ira V, Skorupa Alexandra, Pallaud Celine, Bullinger Lars, Mertens Daniel, Döhner Hartmut, Stilgenbauer Steph |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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