Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 33 Records) |
| Query Trace: Syndrome and NPM1[original query] |
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| The impact on outcome of the addition of all-trans retinoic acid to intensive chemotherapy in younger patients with nonacute promyelocytic acute myeloid leukemia: overall results and results in genotypic subgroups defined by mutations in NPM1, FLT3, and CEBPA. Blood 2010 Feb 115 (5): 948-56. Burnett Alan K, Hills Robert K, Green Claire, Jenkinson Sarah, Koo Kenneth, Patel Yashma, Guy Carol, Gilkes Amanda, Milligan Donald W, Goldstone Anthony H, Prentice Archibald G, Wheatley Keith, Linch David C, Gale Rosemary |
| Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission. Blood 2010 Aug 116 (7): 1132-5. Nibourel Olivier, Kosmider Olivier, Cheok Meyling, Boissel Nicolas, Renneville Aline, Philippe Nathalie, Dombret Hervé, Dreyfus François, Quesnel Bruno, Geffroy Sandrine, Quentin Samuel, Roche-Lestienne Catherine, Cayuela Jean-Michel, Roumier Christophe, Fenaux Pierre, Vainchenker William, Bernard Olivier A, Soulier Jean, Fontenay Michaëla, Preudhomme Clau |
| FLT3 and NPM1 mutations in myelodysplastic syndromes: Frequency and potential value for predicting progression to acute myeloid leukemia. American journal of clinical pathology 2011 Jan 135 (1): 62-9. Bains Ashish, Luthra Rajyalakshmi, Medeiros L Jeffrey, Zuo Zhua |
| SF3B1 mutation is a rare event in Chinese patients with acute and chronic myeloid leukemia. Clinical biochemistry 2013 Feb . Yang J, Qian J, Yao DM, Qian SX, Qian W, Lin J, Xiao GF, Wang CZ, Deng ZQ, Ma JC, Chen XX |
| DNMT3A R882 mutations in patients with cytogenetically normal acute myeloid leukemia and myelodysplastic syndrome. Blood cells, molecules & diseases 0 53 (1-2): 61-6. El Ghannam Doaa, Taalab Mona M, Ghazy Hayam F, Eneen Asmaa |
| Persistence of DNMT3A mutations at long-term remission in adult patients with AML. British journal of haematology 2014 Nov 167 (4): 478-86. Pløen Gro G, Nederby Line, Guldberg Per, Hansen Maria, Ebbesen Lene H, Jensen Uffe Birk, Hokland Peter, Aggerholm An |
| IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association. Oncotarget 2015 Oct . Debarri Houria, Lebon Delphine, Roumier Christophe, Cheok Meyling, Marceau-Renaut Alice, Nibourel Olivier, Geffroy Sandrine, Helevaut Nathalie, Rousselot Philippe, Gruson Bérengère, Gardin Claude, Chretien Marie-Lorraine, Sebda Shéhérazade, Figeac Martin, Berthon Céline, Quesnel Bruno, Boissel Nicolas, Castaigne Sylvie, Dombret Hervé, Renneville Aline, Preudhomme Clau |
| The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes. British journal of haematology 2016 Mar . Olsson Linda, Zettermark Sofia, Biloglav Andrea, Castor Anders, Behrendtz Mikael, Forestier Erik, Paulsson Kajsa, Johansson Bert |
| FLT3-ITD, NPM1, and DNMT3A Gene Mutations and Risk Factors in Normal Karyotype Acute Myeloid Leukemia and Myelodysplastic Syndrome Patients in Upper Northern Thailand. Asian Pacific journal of cancer prevention : APJCP 2017 11 18 (11): 3031-3039. Mevatee Piyanan, Tantiworawit Adisak, Traisathit Patrinee, Puaninta Chaniporn, Mevatee Umnat, Angsuchawan Sirinda, Bumroongkit Kanokk |
| Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group. Haematologica 2018 2 103 (5): 822-829. Ferret Yann, Boissel Nicolas, Helevaut Nathalie, Madic Jordan, Nibourel Olivier, Marceau-Renaut Alice, Bucci Maxime, Geffroy Sandrine, Celli-Lebras Karine, Castaigne Sylvie, Thomas Xavier, Terré Christine, Dombret Hervé, Preudhomme Claude, Renneville Ali |
| Pattern associated leukemia immunophenotypes and measurable disease detection in acute myeloid leukemia or myelodysplastic syndrome with mutated NPM1. Cytometry. Part B, Clinical cytometry 2018 11 96 (1): 67-72. Zhou Yi, Moon Andres, Hoyle Eric, Fromm Jonathan R, Chen Xueyan, Soma Lori, Salipante Stephen J, Wood Brent L, Wu Dav |
| Clinicopathologic and genetic characterization of nonacute NPM1-mutated myeloid neoplasms. Blood advances 2019 5 3 (9): 1540-1545. Patel Sanjay S, Ho Caleb, Ptashkin Ryan N, Sadigh Sam, Bagg Adam, Geyer Julia T, Xu Mina L, Prebet Thomas, Mason Emily F, Seegmiller Adam C, Morgan Elizabeth A, Steensma David P, Winer Eric S, Wong Waihay J, Hasserjian Robert P, Weinberg Olga |
| The Clinical impact of PTPN11 mutations in adults with acute myeloid leukemia. Leukemia 2020 6 35 (3): 691-700. Alfayez Mansour, Issa Ghayas C, Patel Keyur P, Wang Feng, Wang Xuemei, Short Nicholas J, Cortes Jorge E, Kadia Tapan, Ravandi Farhad, Pierce Sherry, Assi Rita, Garcia-Manero Guillermo, DiNardo Courtney D, Daver Naval, Pemmaraju Naveen, Kantarjian Hagop, Borthakur Gaut |
| [Clinical analysis of gene mutation characteristics and mutation burden in myelodysplastic syndrome]. Zhonghua yi xue za zhi 2020 4 100 (12): 933-937. Lü X D, Li Y W, Guo Z, Xin Y P, Hu J Y, Fan R H, Song Y |
| [Analysis of ASXL1 gene variant in patients with myelodysplastic syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Feb 37 (2): 110-115. Chen Meiyu, Liu Jie, Chao Hongying, Qin Wei, Jiang Naike, Lu Xuzhang, Cen Ling, Jiang Yu, Cai Xiaohui, Zhang Ri, Wang Qi |
| [Analysis of RUNX1 Gene Mutation in Patients with Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2020 Feb 28 (1): 202-208. Cai Xiao-Hui, Chen Mei-Yu, Chao Hong-Ying, Jiang Nai-Ke, Lu Xu-Zhang, Han Wen-Min, Qin Wei, Jia Zhu-X |
| Differential U2AF1 mutation sites, burden and co-mutation genes can predict prognosis in patients with myelodysplastic syndrome. Scientific reports 2020 10 10 (1): 18622. Wang Haiqiong, Guo Yongbo, Dong Zhenkun, Li Tao, Xie Xinsheng, Wan Dingming, Jiang Zhongxing, Yu Jifeng, Guo Ro |
| Clinicopathologic Characterization of Hypocellular Acute Myeloid Leukemia (AML) Showed Fewer Genetic Abnormalities Involving Cell Proliferation and NPM1 When Compared With Nonhypocellular AML. American journal of clinical pathology 2020 Oct . Carlsen Eric, Bailey Nathanael G, Aggarwal Nidhi, Illar Gwendolyn M, Wild Matthew, Yatsenko Svetlana A, Rea Bryan, Liu Yen-Ch |
| The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms. Blood 2022 6 140 (7): 716-755. Li Peng, Brown Sara, Williams Margaret, White Thomas, Xie Wei, Cui Wei, Peker Deniz, Lei Li, Kunder Christian A, Wang Huan-You, Murray Sarah S, Vagher Jennie, Kovacsovics Tibor, Patel Jay |
| [Analysis of Gene Mutation Characteristics and Prognosis of Elderly Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Jun 30 (3): 755-759. Zhou Nai-Cen, Li Guo-Hui, Qin Wei-Wei, Wang Wen-Qing, Guo Huai-Peng, Liu Cong, Liu |
| Therapy-related myeloid neoplasms with normal karyotype show distinct genomic and clinical characteristics compared to their counterparts with abnormal karyotype. British journal of haematology 2022 3 197 (6): 736-744. Tariq Hamza, Barnea Slonim Liron, Coty Fattal Zachary, Alikhan Mir B, Segal Jeremy, Gurbuxani Sandeep, Helenowski Irene B, Zhang Hui, Sukhanova Madina, Lu Xinyan, Altman Jessica K, Chen Qing C, Behdad Am |
| Higher RUNX1 expression levels are associated with worse overall and leukaemia-free survival in myelodysplastic syndrome patients. EJHaem 2022 12 3 (4): 1209-1219. Wang Yu-Hung, Yao Chi-Yuan, Lin Chien-Chin, Chen Chi-Ling, Hsu Chia-Lang, Tsai Cheng-Hong, Hou Hsin-An, Chou Wen-Chien, Tien Hwei-Fa |
| UBTF tandem duplications are rare but recurrent alterations in adult AML and associated with younger age, myelodysplasia, and inferior outcome. Blood cancer journal 2023 5 13 (1): 88. Julia-Annabell Georgi, Sebastian Stasik, Jan-Niklas Eckardt, Sven Zukunft, Marita Hartwig, Christoph Röllig, Jan Moritz Middeke, Uta Oelschlägel, Utz Krug, Tim Sauer, Sebastian Scholl, Andreas Hochhaus, Tim H Brümmendorf, Ralph Naumann, Björn Steffen, Hermann Einsele, Markus Schaich, Andreas Burchert, Andreas Neubauer, Kerstin Schäfer-Eckart, Christoph Schliemann, Stefan W Krause, Mathias Hänel, Richard Noppeney, Ulrich Kaiser, Claudia D Baldus, Martin Kaufmann, Carsten Müller-Tidow, Uwe Platzbecker, Wolfgang E Berdel, Hubert Serve, Gerhard Ehninger, Martin Bornhäuser, Johannes Schetelig, Frank Kroschinsky, Christian Thiede, |
| Wilms' tumor 1 expression combined with genetic mutations for prognostic assessment in MDS. Leukemia & lymphoma 2023 3 1-9. Pan Danqi, Zhao Wenshu, Jiang Qianli, Yin Changxin, He Han, Liao Libin, Ye Jieyu, Dai M |
| Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China. Cancer medicine 2023 2 . Li Junnan, Pei Li, Liang Simin, Xu Shuangnian, Wang Yi, Wang Xiao, Liao Yi, Zhan Qian, Cheng Wei, Yang Zesong, Tang Xiaoqiong, Zhang Hongbin, Xiao Qing, Chen Jianbin, Liu Lin, Wang |
| The Impact of Mutation of Myelodysplasia-Related Genes in De Novo Acute Myeloid Leukemia Carrying NPM1 Mutation. Cancers 2023 1 15 (1): . Wang Yi, Quesada Andres E, Zuo Zhuang, Medeiros L Jeffrey, Yin C Cameron, Li Shaoying, Xu Jie, Borthakur Gautam, Li Yisheng, Yang Chao, Abaza Yasmin, Gao Juehua, Lu Xinyan, You M James, Zhang Yizhuo, Lin P |
| Prognostic mutations identified by whole-exome sequencing and validation of the Molecular International Prognostic Scoring System in myelodysplastic syndromes after allogeneic haematopoietic stem cell transplantation. British journal of haematology 2024 8 . Hong Wang, Xueqian Li, Jiaqian Qi, Hong Liu, Tiantian Chu, Xiaoyan Xu, Huiying Qiu, Chengcheng Fu, Xiaowen Tang, Changgeng Ruan, Depei Wu, Yue H |
| Influence of genetic co-mutation on chemotherapeutic outcome in NPM1-mutated and FLT3-ITD wild-type AML patients. Cancer medicine 2024 8 13 (15): e70102. Quan Wu, Yujiao Zhang, Baoyi Yuan, Yun Huang, Ling Jiang, Fang Liu, Ping Yan, Jiaying Cheng, Zhiquan Long, Xuejie Jia |
| Chromothripsis in myeloid malignancies. Annals of hematology 2024 5 . Chien-Yuan Ch |
| [Analysis of Gene Mutation and Clinical Characteristics Related to Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2025 1 32 (6): 1798-1806. Yu-Feng Wang, Yan-Li Yang, Ying-Hua Ge |
- Page last reviewed:Feb 1, 2024
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