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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 2, 2023. (Total: 221654Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Trisomy and TET2[original query]
A Modified Integrated Genetic Model for Risk Prediction in Younger Patients with Acute Myeloid Leukemia.
PloS one 2016 11 (4): e0153016.
Sloan Caroline E, Luskin Marlise R, Boccuti Anne M, Sehgal Alison R, Zhao Jianhua, Daber Robert D, Morrissette Jennifer J D, Luger Selina M, Bagg Adam, Gimotty Phyllis A, Carroll Mart
The high frequency of the U2AF1 S34Y mutation and its association with isolated trisomy 8 in myelodysplastic syndrome in Asians, but not in Caucasians.
Leukemia research 2017 9 61 96-103.
Kim Seon Young, Kim Kwantae, Hwang Byungjin, Im Kyongok, Park Si Nae, Kim Jung-Ah, Hwang Sang Mee, Bang Duhee, Lee Dong So
[Analysis of Clinical Characteristics in 31 Acute Myeloid Leukemia Patients with Chromosome 21 Aberrations].
Zhongguo shi yan xue ye xue za zhi 2017 8 25 (4): 992-997.
Yu Hai-Zhi, Cheng Zhao, Xie Si-Si, Yi Yi-Fang, Peng Hong-Li
Comparison of therapy-related and de novo core binding factor acute myeloid leukemia: A bone marrow pathology group study.
American journal of hematology 2020 4 95 (7): 799-808.
Rogers Heesun J, Wang Xiaoqiong, Xie Yan, Davis Adam R, Thakral Beenu, Wang Sa A, Borthakur Gautam, Cantu Miguel D, Margolskee Elizabeth M, Philip John K S, Sukhanova Madina, Bagg Adam, Bueso-Ramos Carlos E, Orazi Attilio, Arber Daniel A, Hsi Eric D, Hasserjian Robert
A rare case of acute promyelocytic leukemia with ider(17)(q10)t(15;17)(q22;q21) and favorable outcome.
Molecular cytogenetics 2020 4 13 13.
Liu Yongming, Xu Junqing, Chu Lina, Yu Limei, Zhang Yanhong, Ma Li, Wang Weihua, Zhang Yangyang, Xu Yimin, Liu Rimi
Cytogenetic and molecular landscape and its potential clinical significance in Hispanic CMML patients from Puerto Rico.
Oncotarget 2020 12 11 (47): 4411-4420.
Jiang Zeju, Sun Xinlai, Wu Zhao, Alhatem Albert, Zheng Ruifang, Liu Dongfang, Wang Yaqun, Kumar Dibyendu, Xia Changqing, You Bei, Wang He, Liu Chen, Jiang Jie-G
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome.
Blood advances 2021 9 6 (3): 793-807.
West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis
Prognostic impact of the adverse molecular-genetic profile on long-term outcomes following allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia.
Bone marrow transplantation 2021 Mar .
Daher-Reyes Georgina, Kim TaeHyung, Novitzky-Basso Igor, Kim Kyuoung Ha, Smith Adam, Stockley Tracy, Capochichi Jose-Mario, Al-Shaibani Zeyad, Pasic Ivan, Law Arjun, Lam Wilson, Michelis Fotios V, Gerbitz Armin, Viswabandya Auro, Lipton Jeffrey, Kumar Rajat, Mattsson Jonas, Schimmer Aaron, McNamara Caroline, Murphy Tracy, Maze Dawn, Gupta Vikas, Sibai Hassan, Chan Steven, Yee Karen, Minden Mark, Zhang Zhaolei, Schuh Andre, Kim Dennis D
[Clinical Characteristics of Acute Myeloid Leukemia Patients with RUNX1 Gene Mutation].
Zhongguo shi yan xue ye xue za zhi 2021 Oct 29 (5): 1411-1416.
Ni Zeng-Feng, Ma Li-Jie, Shi Li-Li, Shen Pan-Li, Zhao Jian-Qia
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