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The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality

최리화 장미애 유건희 이승태 김희진 김선희 2014년

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' The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality' 의 주제별 논문영향력
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' The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality' 의 참고문헌

  • The inv(11)(p15q22) chromosome translocation of therapy-related myelodysplasia with NUP98-DDX10 and DDX10-NUP98 fusion transcripts
    Ikeda T Int J Hematol 69 160-164 [1999]
  • The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10
    Arai Y Blood 89 3936-3944 [1997]
  • Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization
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  • Nucleoporins and nucleocytoplasmic transport in hematologic malignancies
    Takeda A Semin Cancer Biol 27 3-10 [2014]
  • NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern
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