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RBM15-MKL1 (OTT-MAL) fusion transcript in an adult acute myeloid leukemia patient

  • Hui Hua Hsiao
  • , Ming Yu Yang
  • , Yi Chang Liu
  • , Hui Pin Hsiao
  • , Shih Bin Tseng
  • , Mei Chyn Chao
  • , Ta Chih Liu
  • , Sheng Fung Lin*
  • *此作品的通信作者
  • Kaohsiung Medical University

研究成果: 期刊稿件文獻綜述同行評審

22 引文 斯高帕斯(Scopus)

摘要

The t(1;22)(p13;q13) is a nonrandom chromosomal abnormality in acute leukemia with the fusion oncogene, RBM15-MKL1 (OTT-MAL), identified recently. However, this abnormality has been described only in infants and young children with acute megakaryoblastic leukemia (AMKL). We report a 59-year-old male patient with the diagnosis of acute myeloid leukemia, subtype M1, who harbors an abnormal chromosome +der(1)t(1;22)(p13;q13). The RBM15-MKL1 (OTT-MAL) fusion transcript was also confirmed by the reverse transcriptase-polymerase chain reaction. This unusual abnormality is rare in adult cases of leukemia, and in children it is restricted to AMKL. This report is accompanied by a review of the literature on the t(1;22)(p13;q13).

原文英語
頁(從 - 到)43-45
頁數3
期刊American Journal of Hematology
79
發行號1
DOIs
出版狀態已出版 - 05 2005
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UN SDG

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  1. SDG3 健康與福祉
    SDG3 健康與福祉

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