Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Disease Progression and RUNX1[original query] |
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ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia. Advances in hematology 2010 1 2009 924301. Gmidène Abir, Elghezal Hatem, Sennana Hlima, Ben Youssef Yosra, Meddeb Balkiss, Elloumi Moez, Khlif Abderrahim, Saad A |
Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms. Blood 2010 1 115 (14): 2882-90. Thoennissen Nils H, Krug Utz O, Lee Dhong Hyun Tony, Kawamata Norihiko, Iwanski Gabriela B, Lasho Terra, Weiss Tamara, Nowak Daniel, Koren-Michowitz Maya, Kato Motohiro, Sanada Masashi, Shih Lee-Yung, Nagler Arnon, Raynaud Sophie D, Müller-Tidow Carsten, Mesa Ruben, Haferlach Torsten, Gilliland D Gary, Tefferi Ayalew, Ogawa Seishi, Koeffler H Phill |
Genetic modifiers of cardiorespiratory fitness response to lifestyle intervention. Medicine and science in sports and exercise 2014 Feb 46 (2): 302-11. Peter Inga, Papandonatos George D, Belalcazar L Maria, Yang Yao, Erar Bahar, Jakicic John M, Unick Jessica L, Balasubramanyam Ashok, Lipkin Edward W, Delahanty Linda M, Wagenknecht Lynne E, Wing Rena R, McCaffery Jeanne M, Huggins Gordon S, |
SF3B1 mutations in patients with myelodysplastic syndromes: the mutation is stable during disease evolution. American journal of hematology 2014 Aug 89 (8): E109-15. Lin Chien-Chin, Hou Hsin-An, Chou Wen-Chien, Kuo Yuan-Yeh, Wu Shang-Ju, Liu Chieh-Yu, Chen Chien-Yuan, Tseng Mei-Hsuan, Huang Chi-Fei, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Huang Shang-Yi, Hsu Szu-Chun, Ko Bor-Sheng, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
Dynamics of ASXL1 mutation and other associated genetic alterations during disease progression in patients with primary myelodysplastic syndrome. Blood cancer journal 2014 4 e177. Chen T-C, Hou H-A, Chou W-C, Tang J-L, Kuo Y-Y, Chen C-Y, Tseng M-H, Huang C-F, Lai Y-J, Chiang Y-C, Lee F-Y, Liu M-C, Liu C-W, Liu C-Y, Yao M, Huang S-Y, Ko B-S, Hsu S-C, Wu S-J, Tsay W, Chen Y-C, Tien H |
Splicing factor mutations predict poor prognosis in patients with de novo acute myeloid leukemia. Oncotarget 2016 Jan . Hou Hsin-An, Liu Chieh-Yu, Kuo Yuan-Yeh, Chou Wen-Chien, Tsai Cheng-Hong, Lin Chien-Chin, Lin Liang-In, Tseng Mei-Hsuan, Chiang Ying-Chieh, Liu Ming-Chih, Liu Chia-Wen, Tang Jih-Luh, Yao Ming, Li Chi-Cheng, Huang Shang-Yi, Ko Bor-Sheng, Hsu Szu-Chun, Chen Chien-Yuan, Lin Chien-Ting, Wu Shang-Ju, Tsay Woei, Tien Hwei-Fa |
Pancreatic Insufficiency in Cystic Fibrosis: Influence of Inflammatory Response Genes. Pancreas 2018 Jan 47 (1): 99-109. Marson Fernando Augusto Lima, Bertuzzo Carmen Sílvia, de Araujo Tânia Kawasaki, Hortencio Taís Daiene Russo, Ribeiro Antônio Fernando, Ribeiro José Dirc |
ETV6/RUNX1-positive childhood acute lymphoblastic leukemia in China: excellent prognosis with improved BFM protocol. Italian journal of pediatrics 2018 8 44 (1): 94. Wang Yu, Zeng Hui-Min, Zhang Le-Pi |
Sorafenib and omacetaxine mepesuccinate as a safe and effective treatment for acute myeloid leukemia carrying internal tandem duplication of Fms-like tyrosine kinase 3. Cancer 2019 10 126 (2): 344-353. Zhang Chunxiao, Lam Stephen S Y, Leung Garret M K, Tsui Sze-Pui, Yang Ning, Ng Nelson K L, Ip Ho-Wan, Au Chun-Hang, Chan Tsun-Leung, Ma Edmond S K, Yip Sze-Fai, Lee Harold K K, Lau June S M, Luk Tsan-Hei, Li Wa, Kwong Yok-Lam, Leung Anskar Y |
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 |
PHF6 Mutations in Hematologic Malignancies. Frontiers in oncology 2021 8 11 704471. Kurzer Jason H, Weinberg Olga |
Impact of Integrated Genetic Information on Diagnosis and Prognostication for Myeloproliferative Neoplasms in the Next-Generation Sequencing Era. Journal of clinical medicine 2021 Mar 10 (5): . Lee Jong-Mi, Lee Howon, Eom Ki-Seong, Lee Sung-Eun, Kim Myungshin, Kim Yongg |
Integration Analysis of JAK2 or RUNX1 Mutation With Bone Marrow Blast Can Improve Risk Stratification in the Patients With Lower Risk Myelodysplastic Syndrome. Frontiers in oncology 2020 10 610525. Fang Ying, Guo Juan, Wu Dong, Wu Ling-Yun, Song Lu-Xi, Zhang Zheng, Zhao You-Shan, Chang Chun-Ka |
Cytogenetic and molecular aberrations and worse outcome for male patients in systemic mastocytosis. Theranostics 2021 1 11 (1): 292-303. Kluin-Nelemans Hanneke C, Jawhar Mohamad, Reiter Andreas, van Anrooij Bjorn, Gotlib Jason, Hartmann Karin, Illerhaus Anja, Oude Elberink Hanneke N G, Gorska Aleksandra, Niedoszytko Marek, Lange Magdalena, Scaffidi Luigi, Zanotti Roberta, Bonadonna Patrizia, Perkins Cecelia, Elena Chiara, Malcovati Luca, Shoumariyeh Khalid, von Bubnoff Nikolas, Müller Sabine, Triggiani Massimo, Parente Roberta, Schwaab Juliana, Kundi Michael, Fortina Anna Belloni, Caroppo Francesca, Brockow Knut, Zink Alexander, Fuchs David, Angelova-Fischer Irena, Yavuz Akif Selim, Doubek Michael, Mattsson Mattias, Hagglund Hans, Panse Jens, Simonowski Anne, Sabato Vito, Schug Tanja, Jentzsch Madlen, Breynaert Christine, Várkonyi Judit, Kennedy Vanessa, Hermine Olivier, Rossignol Julien, Arock Michel, Valent Peter, Sperr Wolfgang |
Comprehensive Analysis of Acquired Genetic Variants and Their Prognostic Impact in Systemic Mastocytosis. Cancers 2022 5 14 (10): . González-López Oscar, Muñoz-González Javier I, Orfao Alberto, Álvarez-Twose Iván, García-Montero Andrés |
Co-Occurring CSF3R W791* Germline and Somatic T618I Driver Mutations Induce Early CNL and Clonal Progression to Mixed Phenotype Acute Leukemia. Current oncology (Toronto, Ont.) 2022 2 29 (2): 805-815. Adam Franziska C, Szybinski Jakub, Halter Jörg P, Cantoni Nathan, Wenzel Friedel, Leonards Katharina, Brkic Sime, Passweg Jakob R, Touw Ivo, Maxson Julia E, Meyer Sara |
BCR-ABL1 is a secondary event after JAK2V617F in a patient with essential thrombocythemia who develop chronic myeloid leukemia. Blood science (Baltimore, Md.) 2022 12 4 (4): 199-204. Zhang Yanqing, Bi Hailiang, Wang Ying, Chen Long, Pan Jiaqi, Xu Ping, Wang Wei, Yang Shaob |
The clinical phenotype of germline RUNX1 mutations in relation to the accompanying somatic variants and RUNX1 isoform expression. Genes, chromosomes & cancer 2023 6 . David Cabrerizo Granados, Indira Barbosa, Panagiotis Baliakas, Eva Hellström-Lindberg, Vanessa Lund |
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- Page last updated:May 06, 2024
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