Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 33 Records) |
| Query Trace: Leukemia and RUNX1T1[original query] |
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| Exome sequencing identifies recurring FLT3 N676K mutations in core-binding factor leukemia. Blood 2013 Sep 122 (10): 1761-9. Opatz Sabrina, Polzer Harald, Herold Tobias, Konstandin Nikola P, Ksienzyk Bianka, Zellmeier Evelyn, Vosberg Sebastian, Graf Alexander, Krebs Stefan, Blum Helmut, Hopfner Karl-Peter, Kakadia Purvi M, Schneider Stephanie, Dufour Annika, Braess Jan, Sauerland Maria Cristina, Berdel Wolfgang E, Büchner Thomas, Woermann Bernhard J, Hiddemann Wolfgang, Spiekermann Karsten, Bohlander Stefan K, Greif Philipp |
| NPM1 Gene Type A Mutation in Bulgarian Adults with Acute Myeloid Leukemia: A Single-Institution Study. Turkish journal of haematology : official journal of Turkish Society of Haematology 2014 Mar 31 (1): 40-8. Balatzenko Gueorgui, Spassov Branimir, Stoyanov Nikolay, Ganeva Penka, Dikov Tihomit, Konstantinov Spiro, Hrischev Vasil, Romanova Malina, Toshkov Stavri, Guenova Margari |
| FLT3 expression and IL10 promoter polymorphism in acute myeloid leukemia with RUNX1-RUNX1T1. Molecular biology reports 2015 Feb 42 (2): 451-6. Kim Myungshin, Kim Jiyeon, Kim Jung Rok, Han Eunhee, Park Joonhong, Lim Jihyang, Kim Yonggoo, Han Kyungja, Kim Hee-Je, Min Woo-Sung, Cho B |
| High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome. Leukemia 2014 Jul 28 (7): 1449-58. Krauth M-T, Eder C, Alpermann T, Bacher U, Nadarajah N, Kern W, Haferlach C, Haferlach T, Schnittger |
| Low WT1 transcript levels at diagnosis predicted poor outcomes of acute myeloid leukemia patients with t(8;21) who received chemotherapy or allogeneic hematopoietic stem cell transplantation. Chinese journal of cancer 2016 35 (1): 46. Qin Ya-Zhen, Wang Yu, Zhu Hong-Hu, Gale Robert Peter, Zhang Mei-Jie, Jiang Qian, Jiang Hao, Xu Lan-Ping, Chen Huan, Zhang Xiao-Hui, Liu Yan-Rong, Lai Yue-Yun, Jiang Bin, Liu Kai-Yan, Huang Xiao-J |
| [Genetic abnormalities in core binding factor acute myeloid leukemia]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2017 9 58 (8): 991-998. Ishikawa Yuic |
| Molecular Characterization of Pediatric Acute Myeloid Leukemia: Results of a Multicentric Study in Brazil. Archives of medical research 2016 11 47 (8): 656-667. Andrade Francianne Gomes, Noronha Elda Pereira, Brisson Gisele Dallapicola, Dos Santos Vicente Bueno Filipe, Cezar Ingrid Sardou, Terra-Granado Eugênia, Thuler Luiz Claudio Santos, Pombo-de-Oliveira Maria S, |
| ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis. Genes, chromosomes & cancer 2017 Jan . Yamato Genki, Shiba Norio, Yoshida Kenichi, Shiraishi Yuichi, Hara Yusuke, Ohki Kentaro, Okubo Jun, Okuno Haruna, Chiba Kenichi, Tanaka Hiroko, Kinoshita Akitoshi, Moritake Hiroshi, Kiyokawa Nobutaka, Tomizawa Daisuke, Park Myoung-Ja, Sotomatsu Manabu, Taga Takashi, Adachi Souichi, Tawa Akio, Horibe Keizo, Arakawa Hirokazu, Miyano Satoru, Ogawa Seishi, Hayashi Yasuhi |
| Mediation analysis reveals common mechanisms of RUNX1 point mutations and RUNX1/RUNX1T1 fusions influencing survival of patients with acute myeloid leukemia. Scientific reports 2018 Jul 8 (1): 11293. Hornung Roman, Jurinovic Vindi, Batcha Aarif M N, Bamopoulos Stefanos A, Rothenberg-Thurley Maja, Amler Susanne, Sauerland Maria Cristina, Berdel Wolfgang E, Wörmann Bernhard J, Bohlander Stefan K, Braess Jan, Hiddemann Wolfgang, Lehmann Sören, Mareschal Sylvain, Spiekermann Karsten, Metzeler Klaus H, Herold Tobias, Boulesteix Anne-Lau |
| CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia. Cancer 2018 Jun . Zhang Yang, Wang Fang, Chen Xue, Zhang Yu, Wang Mingyu, Liu Hong, Cao Panxiang, Ma Xiaoli, Wang Tong, Zhang Jianping, Zhang Xian, Lu Peihua, Liu Hongxi |
| Apoptosis: A biomarker of high-risk phenotype in pediatric acute myeloid leukemia? International journal of laboratory hematology 2018 11 41 (1): 141-147. Tyagi Anudishi, Pramanik Raja, Bakhshi Radhika, Vishnubhatla Sreenivas, Bakhshi Same |
| Accurate and Sensitive Analysis of Minimal Residual Disease in Acute Myeloid Leukemia Using Deep Sequencing of Single Nucleotide Variations. The Journal of molecular diagnostics : JMD 2018 10 21 (1): 149-162. Delsing Malmberg Erik, Rehammar Anna, Pereira Mariana B, Abrahamsson Jonas, Samuelsson Tore, Ståhlman Sara, Asp Julia, Tierens Anne, Palmqvist Lars, Kristiansson Erik, Fogelstrand Lin |
| Distinct gene alterations with a high percentage of myeloperoxidase-positive leukemic blasts in de novo acute myeloid leukemia. Leukemia research 2018 Jan 65 34-41. Kamijo Rena, Itonaga Hidehiro, Kihara Rika, Nagata Yasunobu, Hata Tomoko, Asou Norio, Ohtake Shigeki, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Miyano Satoru, Ogawa Seishi, Naoe Tomoki, Kiyoi Hitoshi, Miyazaki Yasus |
| Prognostic Role of Postinduction Minimal Residual Disease and Myeloid Sarcoma Type Extramedullary Involvement in Pediatric RUNX1-RUNX1T1 (+) Acute Myeloid Leukemia. Journal of pediatric hematology/oncology 2019 11 42 (3): e132-e139. Lee Jae Wook, Kim Seongkoo, Jang Pil-Sang, Chung Nack-Gyun, Cho Bin, Im Soo Ah, Kim Myungsh |
| Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations. HemaSphere 2019 11 3 (1): e178. Höllein Alexander, Nadarajah Niroshan, Meggendorfer Manja, Jeromin Sabine, Kern Wolfgang, Haferlach Claudia, Haferlach Torst |
| Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients. Blood 2019 1 133 (10): 1140-1151. Christen Friederike, Hoyer Kaja, Yoshida Kenichi, Hou Hsin-An, Waldhueter Nils, Heuser Michael, Hills Robert K, Chan Willy, Hablesreiter Raphael, Blau Olga, Ochi Yotaro, Klement Piroska, Chou Wen-Chien, Blau Igor-Wolfgang, Tang Jih-Luh, Zemojtel Tomasz, Shiraishi Yuichi, Shiozawa Yusuke, Thol Felicitas, Ganser Arnold, Löwenberg Bob, Linch David C, Bullinger Lars, Valk Peter J M, Tien Hwei-Fang, Gale Rosemary E, Ogawa Seishi, Damm Freder |
| Next-generation sequencing-based genetic landscape and its clinical implications for Chinese acute myeloid leukemia patients. Cancer cell international 2019 1 18 215. Cao Xin-Xin, Cai Hao, Mao Yue-Ying, Wu Qi, Zhang Lu, Zhou Dao-Bin, Li Ji |
| Machine learning derived genomics driven prognostication for acute myeloid leukemia with RUNX1-RUNX1T1. Leukemia & lymphoma 2020 8 61 (13): 3154-3160. Shaikh Anam Fatima, Kakirde Chinmayee, Dhamne Chetan, Bhanshe Prasanna, Joshi Swapnali, Chaudhary Shruti, Chatterjee Gaurav, Tembhare Prashant, Prasad Maya, Roy Moulik Nirmalya, Gokarn Anant, Bonda Avinash, Nayak Lingaraj, Punatkar Sachin, Jain Hasmukh, Bagal Bhausaheb, Shetty Dhanalaxmi, Sengar Manju, Narula Gaurav, Khattry Navin, Banavali Shripad, Gujral Sumeet, P G Subramanian, Patkar Nikh |
| Allogeneic hematopoietic stem cell transplantation can improve the prognosis of high-risk pediatric t(8;21) acute myeloid leukemia in first remission based on MRD-guided treatment. BMC cancer 2020 Jun 20 (1): 553. Hu Guan-Hua, Cheng Yi-Fei, Lu Ai-Dong, Wang Yu, Zuo Ying-Xi, Yan Chen-Hua, Wu Jun, Sun Yu-Qian, Suo Pan, Chen Yu-Hong, Chen Huan, Jia Yue-Ping, Liu Kai-Yan, Han Wei, Xu Lan-Ping, Zhang Le-Ping, Huang Xiao-J |
| [The prognostic value of cloned genetic mutations detected by second-generation sequencing in RUNX1-RUNX1T1 positive acute myeloid leukemia patients receiving intensive consolidation therapy]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2020 4 41 (3): 210-215. Yu J Q, Xue S L, Li Z, Wang J, Wang C, Chu X L, Han R, Tao T, Qiu Q C, Wu D |
| Prospective evaluation of prognostic impact of KIT mutations on acute myeloid leukemia with RUNX1-RUNX1T1 and CBFB-MYH11. Blood advances 2020 Jan 4 (1): 66-75. Ishikawa Yuichi, Kawashima Naomi, Atsuta Yoshiko, Sugiura Isamu, Sawa Masashi, Dobashi Nobuaki, Yokoyama Hisayuki, Doki Noriko, Tomita Akihiro, Kiguchi Toru, Koh Shiro, Kanamori Heiwa, Iriyama Noriyoshi, Kohno Akio, Moriuchi Yukiyoshi, Asada Noboru, Hirano Daiki, Togitani Kazuto, Sakura Toru, Hagihara Maki, Tomikawa Tatsuki, Yokoyama Yasuhisa, Asou Norio, Ohtake Shigeki, Matsumura Itaru, Miyazaki Yasushi, Naoe Tomoki, Kiyoi Hitos |
| Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1-RUNX1T1 transcripts. British journal of haematology 2021 Jun . Sasaki Koji, Tsujimoto Shinichi, Miyake Mayuko, Uchiyama Yuri, Ikeda Junji, Yoshitomi Masahiro, Shimosato Yuko, Tokumasu Mayu, Matsuo Hidemasa, Yoshida Kenichi, Ohki Kentaro, Kaburagi Taeko, Yamato Genki, Hara Yusuke, Takeuchi Masanobu, Kinoshita Akitoshi, Tomizawa Daisuke, Taga Takashi, Adachi Souichi, Tawa Akio, Horibe Keizo, Hayashi Yasuhide, Matsumoto Naomichi, Ito Shuichi, Shiba Nor |
| The clinical characteristics and prognosis of Chinese acute myeloid leukemia patients with CSF3R mutations. International journal of laboratory hematology 2021 Nov . Chen Xiuhua, Xu Jing, Fang Fang, Xu Zhifang, Tan Yanhong, Chang JianMei, Muyey Daniel Muteb, Wang Hongw |
| Impact of KMT2A Rearrangement and CSPG4 Expression in Pediatric Acute Myeloid Leukemia. Cancers 2021 10 13 (19): . Hoffmeister Lina Marie, Orhan Eser, Walter Christiane, Niktoreh Naghmeh, Hanenberg Helmut, von Neuhoff Nils, Reinhardt Dirk, Schneider Mark |
| Both the subtypes of KIT mutation and minimal residual disease are associated with prognosis in core binding factor acute myeloid leukemia: a retrospective clinical cohort study in single center. Annals of hematology 2021 Jan . Duan Wenbing, Liu Xiaohong, Zhao Xiaosu, Jia Jinsong, Wang Jing, Gong Lizhong, Jiang Qian, Zhao Ting, Wang Yu, Zhang Xiaohui, Xu Lanping, Shi Hongxia, Chang Yingjun, Liu Kaiyan, Huang Xiaojun, Qin Yazhen, Jiang H |
| [Short-term efficacy of venetoclax combined with azacitidine in acute myeloid leukemia: a single-institution experience]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2022 4 43 (2): 134-140. Yu W J, Jia J S, Wang J, Tang F F, Gong L Z, Liu X H, Zhu X L, Zhao X S, Huang X J, Jiang |
| Comprehensive Mutation Profile in Acute Myeloid Leukemia Patients with RUNX1-RUNX1T1 or CBFB-MYH11 Fusions. Turkish journal of haematology : official journal of Turkish Society of Haematology 2022 4 39 (2): 84-93. Qin Wei, Chen Xiayu, Shen Hong Jie, Wang Zheng, Cai Xiaohui, Jiang Naike, Hua Haiyi |
| [Molecular Genetic Characteristics of Acute Myeloid Leukemia Patients with CBF?-MYH11 Positive]. Zhongguo shi yan xue ye xue za zhi 2022 12 30 (6): 1661-1667. Jiang Yu, Chao Hong-Ying, Lu Xu-Zhang, Wu Pin, Sun Xiao-Ch |
| TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia. Genes, chromosomes & cancer 2023 4 . Yusuke Hara, Norio Shiba, Kenichi Yoshida, Genki Yamato, Taeko Kaburagi, Yuichi Shiraishi, Kentaro Ohki, Yusuke Shiozawa, Machiko Kawamura, Hirohide Kawasaki, Manabu Sotomatsu, Takumi Takizawa, Hidemasa Matsuo, Akira Shimada, Nobutaka Kiyokawa, Daisuke Tomizawa, Takashi Taga, Etsuro Ito, Keizo Horibe, Satoru Miyano, Souichi Adachi, Tomohiko Taki, Seishi Ogawa, Yasuhide Hayas |
| A comprehensive analysis of cytogenetics, molecular profile, and survival among pediatric acute myeloid leukemia: a prospective study from a tertiary referral center. American journal of blood research 2023 2 12 (6): 177-189. Meena Jagdish Prasad, Makkar Harshita, Gupta Aditya Kumar, Bakhshi Sameer, Gupta Ritu, Thakral Deepshi, Chopra Anita, Tanwar Pranay, Upadhyay Ashish Datt, Pathak Nivedita, Seth Rach |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 25, 2023
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