HuGE Literature Finder
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Integrated clinical genotype-phenotype characteristics of early T-cell precursor acute lymphoblastic leukemia. Cancer 2022 Oct . Ye Matthew T, Wang Yi, Zuo Zhuang, Calin Steliana, He Hua, Tang Zhenya, Jabbour Elias J, Borthakur Gautam, Zhang Yizhuo, Yang Yaling, You M Jam |
Metastatic grade 1 meningioma lacking genetic abnormalities commonly associated with bad prognosis. Pathology, research and practice 2022 Aug 238 154089. Barresi Valeria, Lawlor Rita T, Mafficini Andrea, Gilioli Eliana, Scarpa Al |
Prognostic and predictive impact of genetic markers in patients with CLL treated with obinutuzumab and venetoclax. Blood 2020 Mar . Tausch Eugen, Schneider Christof, Robrecht Sandra, Zhang Can, Dolnik Anna, Bloehdorn Johannes, Bahlo Jasmin, Al-Sawaf Othman, Ritgen Matthias, Fink Anna Maria, Eichhorst Barbara, Kreuzer Karl-Anton, Tandon Maneesh, Humphrey Kathryn, Jiang Yanwen, Schary William, Bullinger Lars, Mertens Daniel, Porro Lurà Michele, Kneba Michael, Döhner Hartmut, Fischer Kirsten, Hallek Michael, Stilgenbauer Steph |
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. Eugen Tausch , Philipp Beck , Richard F Schlenk , Billy J Jebaraj , Anna Dolnik , Deyan Y Yosifov , Peter Hillmen , Fritz Offner , Ann Janssens , K Govind Babu , Sebastian Grosicki , Jiri Mayer , Panagiotis Panagiotidis , Astrid McKeown , Ira V Gupta , Alexandra Skorupa , Celine Pallaud , Lars Bullinger , Daniel Mertens , Hartmut Döhner , Stephan Stilgenbaue |
THE SPECTRUM OF TP53, SF3B1, AND NOTCH1 MUTATIONS IN CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS EXPOSED TO IONIZING RADIATION DUE TO THE CHORNOBYL NPP ACCIDENT. Problemy radiatsiinoi medytsyny ta radiobiolohii 2018 Dec 23 283-301. Bilous N I, Abramenko I V, Chumak A A, Dyagil I S, Martina Z V, Saenko V, Bazyka D |
Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working group. Genes, chromosomes & cancer 2018 Sep . Roos-Weil Damien, Nguyen-Khac Florence, Chevret Sylvie, Touzeau Cyrille, Roux Clémence, Lejeune Julie, Cosson Adrien, Mathis Stéphanie, Feugier Pierre, Leprêtre Stéphane, Béné Marie-Christine, Baron Marine, Raynaud Sophie, Struski Stéphanie, Eclache Virginie, Sutton Laurent, Lesty Claude, Merle-Béral Hélène, Cymbalista Florence, Ysebaert Loïc, Davi Frédéric, Leblond Véronique, |
Targetable Alterations in Adult Patients With Soft-Tissue Sarcomas: Insights for Personalized Therapy. JAMA oncology 2018 May . Lucchesi Carlo, Khalifa Emmanuel, Laizet Yec'han, Soubeyran Isabelle, Mathoulin-Pelissier Simone, Chomienne Christine, Italiano Antoi |
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 |
Co-existence of PHF6 and NOTCH1 mutations in adult T-cell acute lymphoblastic leukemia. Oncology letters 2016 Jul 12 (1): 16-22. Li Min, Xiao Lichan, Xu Jingyan, Zhang Run, Guo Jingjing, Olson Justin, Wu Yujie, Li Jianyong, Song Chunhua, Ge Zhe |
A SNaPshot of potentially personalized care: Molecular diagnostics in gynecologic cancer. Gynecologic oncology 2016 Apr 141 (1): 108-12. Penson R T, Sales E, Sullivan L, Borger D R, Krasner C N, Goodman A K, Del Carmen M G, Growdon W B, Schorge J O, Boruta D M, Castro C M, Dizon D S, Birrer M |
CD49d prevails over the novel recurrent mutations as independent prognosticator of overall survival in chronic lymphocytic leukemia. Leukemia 2016 Apr . Dal Bo M, Bulian P, Bomben R, Zucchetto A, Maria Rossi F, Pozzo F, Tissino E, Benedetti D, Bittolo T, Nanni P, Cattarossi I, Zaina E, Chivilò H, Degan M, Zaja F, Pozzato G, Chiarenza A, Di Raimondo F, Del Principe M I, Del Poeta G, Rossi D, Gaidano G, Gattei |
Mutually exclusive mutations in NOTCH1 and PIK3CA associated with clinical prognosis and chemotherapy responses of esophageal squamous cell carcinoma in China. Oncotarget 2015 Oct . Song Bin, Cui Heyang, Li Yaoping, Cheng Caixia, Yang Bin, Wang Fang, Kong Pengzhou, Li Hongyi, Zhang Ling, Jia Zhiwu, Bi Yanghui, Wang Jiaqian, Zhou Yong, Liu Jing, Wang Juan, Zhao Zhenxiang, Zhang Yanyan, Hu Xiaoling, Shi Ruyi, Yang Jie, Liu Haiyan, Yan Ting, Li Yike, Xu Enwei, Qian Yu, Xi Yanfeng, Guo Shiping, Chen Yunqing, Wang Jinfen, Li Guodong, Liang Jianfang, Jia Junmei, Chen Xing, Guo Jiansheng, Wang Tong, Zhang Yanbo, Li Qingshan, Wang Chuangui, Cheng Xiaolong, Zhan Qimin, Cui Yongpi |
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 |
14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma. Genes, chromosomes & cancer 2014 Aug 53 (8): 657-66. Cosson Adrien, Chapiro Elise, Belhouachi Nabila, Cung Hong-Anh, Keren Boris, Damm Frederik, Algrin Caroline, Lefebvre Christine, Fert-Ferrer Sandra, Luquet Isabelle, Gachard Nathalie, Mugneret Francine, Terre Christine, Collonge-Rame Marie-Agnes, Michaux Lucienne, Rafdord-Weiss Isabelle, Talmant Pascaline, Veronese Lauren, Nadal Nathalie, Struski Stephanie, Barin Carole, Helias Catherine, Lafage Marina, Lippert Eric, Auger Nathalie, Eclache Virginie, Roos-Weil Damien, Leblond Veronique, Settegrana Catherine, Maloum Karim, Davi Frederic, Merle-Beral Helene, Lesty Claude, Nguyen-Khac Florence, |
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, |
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 |
Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance. Genes, chromosomes & cancer 2013 Oct 52 (10): 920-7. López Cristina, Delgado Julio, Costa Dolors, Villamor Neus, Navarro Alba, Cazorla Maite, Gómez Cándida, Arias Amparo, Muñoz Concha, Cabezas Sandra, Baumann Tycho, Rozman María, Aymerich Marta, Colomer Dolors, Pereira Arturo, Cobo Francesc, López-Guillermo Armando, Campo Elías, Carrió A |
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 |
Mutations of NOTCH1 are an independent predictor of survival in chronic lymphocytic leukemia. Blood 2012 Jan 119 (2): 521-9. Rossi Davide, Rasi Silvia, Fabbri Giulia, Spina Valeria, Fangazio Marco, Forconi Francesco, Marasca Roberto, Laurenti Luca, Bruscaggin Alessio, Cerri Michaela, Monti Sara, Cresta Stefania, Famà Rosella, De Paoli Lorenzo, Bulian Pietro, Gattei Valter, Guarini Anna, Deaglio Silvia, Capello Daniela, Rabadan Raul, Pasqualucci Laura, Dalla-Favera Riccardo, Foà Robin, Gaidano Gianlu |
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 |
Late recurrence of childhood T-cell acute lymphoblastic leukemia frequently represents a second leukemia rather than a relapse: first evidence for genetic predisposition. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2011 Apr 29 (12): 1643-9. Szczepanski Tomasz, van der Velden Vincent H J, Waanders Esmé, Kuiper Roland P, Van Vlierberghe Pieter, Gruhn Bernd, Eckert Cornelia, Panzer-Grümayer Renate, Basso Giuseppe, Cavé Hélène, Stadt Udo Zur, Campana Dario, Schrauder André, Sutton Rosemary, van Wering Elisabeth, Meijerink Jules P P, van Dongen Jacques J |
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 |
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- Page last updated:Jan 26, 2023
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