Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Lymphoma and FBXW7[original query] |
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FBXW7 and NOTCH1 mutations in childhood T cell acute lymphoblastic leukaemia and T cell non-Hodgkin lymphoma. British journal of haematology 2009 Apr 145 (2): 198-206. Park Myoung-Ja, Taki Tomohiko, Oda Megumi, Watanabe Tomoyuki, Yumura-Yagi Keiko, Kobayashi Ryoji, Suzuki Nobuhiro, Hara Junichi, Horibe Keizo, Hayashi Yasuhi |
Clinical impact of NOTCH1 and/or FBXW7 mutations, FLASH deletion, and TCR status in pediatric T-cell lymphoblastic lymphoma. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Jun 30 (16): 1966-73. Callens Celine, Baleydier Frederic, Lengline Etienne, Ben Abdelali Raouf, Petit Arnaud, Villarese Patrick, Cieslak Agata, Minard-Colin Veronique, Rullier Anne, Moreau Anne, Baruchel André, Schmitt Claudine, Asnafi Vahid, Bertrand Yves, Macintyre Elizabe |
Incidence and prognostic relevance of genetic variations in T-cell lymphoblastic lymphoma in childhood and adolescence. Blood 2013 Apr 121 (16): 3153-60. Bonn Bettina R, Rohde Marius, Zimmermann Martin, Krieger David, Oschlies Ilske, Niggli Felix, Wrobel Grazyna, Attarbaschi Andishe, Escherich Gabriele, Klapper Wolfram, Reiter Alfred, Burkhardt Birg |
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%. Genes, chromosomes & cancer 2014 Jun 53 (6): 524-36. Mühlbacher Verena, Zenger Melanie, Schnittger Susanne, Weissmann Sandra, Kunze Franziska, Kohlmann Alexander, Bellos Frauke, Kern Wolfgang, Haferlach Torsten, Haferlach Claud |
TP53 mutations are common in mantle cell lymphoma, including the indolent leukemic non-nodal variant. Annals of diagnostic pathology 2019 5 41 38-42. Sakhdari Ali, Ok Chi Young, Patel Keyur P, Kanagal-Shamanna Rashmi, Yin C Cameron, Zuo Zhuang, Hu Shimin, Routbort Mark J, Luthra Rajyalakshmi, Medeiros L Jeffrey, Khoury Joseph D, Loghavi San |
Prognostic Role of Minimal Disseminated Disease and NOTCH1/FBXW7 Mutational Status in Children with Lymphoblastic Lymphoma: The AIEOP Experience. Diagnostics (Basel, Switzerland) 2021 9 11 (9): . Lovisa Federica, Gallingani Ilaria, Varotto Elena, Pasin Cristiano, Carraro Elisa, Michielotto Barbara, Garbin Anna, Damanti Carlotta Caterina, Pizzi Marco, d'Amore Emanuele S G, Piglione Matilde, Muggeo Paola, Buffardi Salvatore, Vinti Luciana, Folsi Veronica Maria, Onofrillo Daniela, Biffi Alessandra, Buldini Barbara, Pillon Marta, Mussolin La |
Toward Pediatric T Lymphoblastic Lymphoma Stratification Based on Minimal Disseminated Disease and NOTCH1/FBXW7 Status. HemaSphere 2021 9 5 (10): e641. Trinquand Amélie, Plesa Adriana, Abdo Chrystelle, Subtil Fabien, Aladjidi Nathalie, Rigaud Charlotte, Touzart Aurore, Lhermitte Ludovic, Petit Arnaud, Michaux Katell, Jung Charlotte, Chassagne-Clement Catherine, Asnafi Vahid, Bertrand Yves, Garnier Nathalie, Macintyre Elizabe |
CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis. Signal transduction and targeted therapy 2021 Jan 6 (1): 10. Huang Yao-Hui, Cai Kun, Xu Peng-Peng, Wang Li, Huang Chuan-Xin, Fang Ying, Cheng Shu, Sun Xiao-Jian, Liu Feng, Huang Jin-Yan, Ji Meng-Meng, Zhao Wei- |
Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma. Pediatric blood & cancer 2022 Aug e29926. Salmerón-Villalobos Julia, Ramis-Zaldivar Joan Enric, Balagué Olga, Verdú-Amorós Jaime, Celis Verónica, Sábado Constantino, Garrido Marta, Mato Sara, Uriz Javier, Ortega M José, Gutierrez-Camino Angela, Sinnett Daniel, Illarregi Unai, Carron Máxime, Regueiro Alexandra, Galera Ana, Gonzalez-Farré Blanca, Campo Elias, Garcia Noelia, Colomer Dolors, Astigarraga Itziar, Andrés Mara, Llavador Margarita, Martin-Guerrero Idoia, Salaverria Itzi |
Prognostic Significance of Comprehensive Gene Mutations and Clinical Characteristics in Adult T-Cell Acute Lymphoblastic Leukemia Based on Next-Generation Sequencing. Frontiers in oncology 2022 3 12 811151. Yin Hua, Hong Mei, Deng Jun, Yao Lan, Qian Chenjing, Teng Yao, Li Tingting, Wu Qiuli |
Genomic signatures and prognosis of advanced stage Chinese pediatric T cell lymphoblastic lymphoma by whole exome sequencing. Frontiers in pediatrics 2023 9 11 1224966. Qinglin Liu, Xiang Yu, Jinquan Wen, Nange Yin, Xin Liao, Pinli Zou, Yuxia Guo, Lin Song, Jianwen Xi |
Clinical significance of genetic profiling based on different anatomic sites in patients with mucosal melanoma who received or did not receive immune checkpoint inhibitors. Cancer cell international 2023 8 23 (1): 187. Hai-Yun Wang, Ye Liu, Ling Deng, Kuntai Jiang, Xin-Hua Yang, Xiao-Yan Wu, Kai-Hua Guo, Fang Wa |
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- Page last updated:Apr 22, 2024
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