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J-GLOBAL ID:201702231721289121   Reference number:17A1607373

NUP98-HOXC13 fusion gene in acute myeloid leukemia: Pediatric case

急性骨髄性白血病におけるNUP98-HOXC13融合遺伝子:小児症例
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Material:
Volume: 59  Issue: 10  Page: 1105-1106  Publication year: 2017 
JST Material Number: U0706A  ISSN: 1442-200X  Document type: Article
Article type: 短報  Country of issue: United States (USA)  Language: ENGLISH (EN)
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Clinical oncology in general  ,  Blood cell tumors(=neoplasms)  ,  Research methods in genetics 
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Reference (5):
  • Taga T, Tomizawa D, Takahashi H, Adachi S. Acute myeloid leukemia in children: Current status and future directions. Pediatr. Int. 2016; 58: 71-80.
  • Tosic N, Stojiljkovic M, Colovic N, Colovic M, Pavlovic S. Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: Case report and literature review. Cancer Genet. Cytogenet. 2009; 193: 98-103.
  • Taketani T, Taki T, Nakamura T et al. High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes. Leukemia 2010; 24: 1975-7.
  • Chou WC, Chen CY, Hou HA et al. Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients. Leukemia 2009; 23: 1303-10.
  • Xu H, Valerio DG, Eisold ME et al. NUP98 fusion proteins interact with the NSL and MLL1 complexes to drive leukemogenesis. Cancer Cell 2016; 30: 863-78.
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