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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Trisomy and RUNX1[original query]
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
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
Prognostic impact of RUNX1 and ETV6 gene copy number on pediatric B-cell precursor acute lymphoblastic leukemia with or without hyperdiploidy.
International journal of hematology 2016 Jul .
Kutlay Nuket Yurur, Pekpak Esra, Alt?ner Sule, Ileri Talia, Vicdan Arzu Nedime, Dinçaslan Handan, Ince Elif Unal, Tukun Fatma Ajl
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
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
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
A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia.
Cancer genetics 2022 7 266-267 69-73.
Yang Fei, Akkari Yassmine, Fan Guang, Olson Susan, Moore Steph
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