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The First Korean Case of NUP98-NSD1 and a Novel SNRK-ETV6 Fusion in a Pediatric Therapy-related Acute Myeloid Leukemia Patient Detected by Targeted RNA Sequencing

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참고문헌 (10)

  1. Zhong Yiming, "Application of Next Generation Sequencing in Laboratory Medicine", Annals of Laboratory Medicine, 41(1), pp.25~43 (2021), 대한진단검사의학회[DOI]
  2. Hollink IH, "NUP98", NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern, 2011, pp.118, 3645~3656
  3. Niktoreh N, "Mutated WT1, FLT3-ITD, and NUP98-NSD1 fusion in various combinations define a poor prognostic group in pediatric acute myeloid leukemia", J Oncol, 2019, pp.1609128~ (2019)
  4. Franks TM, "Nup98 recruits the Wdr82-Set1A", COMPASS complex to promoters to regulate H3K4 trimethylation in hematopoietic progenitor cells, 2017, pp.31, 2222~2234
  5. Li MM, "Standards and guidelines for the interpretation and reporting of sequence variants in cancer: a joint consensus recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists", J Mol Diagn, 19, pp.4~23 (2017)
  6. Kivioja JL, "Dasatinib and navitoclax act synergistically to target NUP98-NSD1(+)", FLT3-ITD(+) acute myeloid leukemia, 2019, pp.33, 1360~1372
  7. Mitani Y, "Successful treatment of acute myeloid leukemia co-expressing NUP98", NSD1 and FLT3, Int J Hematol, pp.2019, 110[DOI]
  8. Braekeleer E, "ETV6 fusion genes in hematological malignancies: a review", Leuk Res, 36, pp.945~961 (2012)
  9. Kertesz N, "Cloning and characterization of human and mouse SNRK sucrose non-fermenting protein (SNF-1)-related kinases", Gene, 294, pp.13~24 (2002)
  10. Block AW, "Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: report from an international workshop", Genes Chromosomes Cancer, 33, pp.401~412 (2002)

관련 논문AI추천

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