Human Genome Epidemiology Literature Finder
|
Records 1 - 4 (of 4 Records) |
| Query Trace: Monosomy and SETBP1[original query] |
|---|
| Somatic SETBP1 mutations in myeloid malignancies. Nature genetics 2013 Aug 45 (8): 942-6. Makishima Hideki, Yoshida Kenichi, Nguyen Nhu, Przychodzen Bartlomiej, Sanada Masashi, Okuno Yusuke, Ng Kwok Peng, Gudmundsson Kristbjorn O, Vishwakarma Bandana A, Jerez Andres, Gomez-Segui Ines, Takahashi Mariko, Shiraishi Yuichi, Nagata Yasunobu, Guinta Kathryn, Mori Hiraku, Sekeres Mikkael A, Chiba Kenichi, Tanaka Hiroko, Muramatsu Hideki, Sakaguchi Hirotoshi, Paquette Ronald L, McDevitt Michael A, Kojima Seiji, Saunthararajah Yogen, Miyano Satoru, Shih Lee-Yung, Du Yang, Ogawa Seishi, Maciejewski Jaroslaw |
| SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations. Leukemia 2013 Sep 27 (9): 1852-60. Meggendorfer M, Bacher U, Alpermann T, Haferlach C, Kern W, Gambacorti-Passerini C, Haferlach T, Schnittger |
| Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression. American journal of hematology 2014 Feb 89 (2): 181-6. Hou Hsin-An, Kuo Yuan-Yeh, Tang Jih-Luh, Chou Wen-Chien, Yao Ming, Lai Yan-Jun, Lin Chien-Chin, Chen Chien-Yuan, Liu Chieh-Yu, Tseng Mei-Hsuan, Huang Chi-Fei, Chiang Ying-Chieh, Lee Fen-Yu, Liu Ming-Chih, Liu Chia-Wen, Huang Shang-Yi, Ko Bor-Sheng, Wu Shang-Ju, Tsay Woei, Chen Yao-Chang, Tien Hwei-Fa |
| [Clinical features and prognostic factors of advanced myelodysplastic syndromes in children]. Zhonghua yi xue za zhi 2024 7 104 (27): 2529-2534. C M Liu, Y L Chen, X C Wang, X L Li, W B An, Y Wan, Y Y Ren, X Chen, F Liu, Y Guo, X J Chen, L Zhang, Y Zou, Y M Chen, J Li, X J Guo, X F Zhu, W Y Ya |
- Page last reviewed:Feb 1, 2024
- Content source: