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TEL-AML1阳性儿童急性淋巴细胞白血病IgH及TCRγ基因重排的研究 被引量:3

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摘要 t(12;21)是儿童急性淋巴细胞白血病(ALL)中最常见的染色体易位,占B-ALL的16%-36%^[1];该易位导致12p13上的TEL基因与21q22上的AML1基因融合,形成TEL-AML1融合基因。已有研究证实单独TEL-AML1融合基因并不能导致白血病发生,提示还存在其他协同因素^[2]。
出处 《中华血液学杂志》 CAS CSCD 北大核心 2008年第6期408-409,共2页 Chinese Journal of Hematology
基金 基金资助:新世纪优秀人才支持计划(NCET-05-0173)
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参考文献8

  • 1Romana SP, Poirel H, Leconiat M, et al. High frequency of t( 12; 21 ) in childhood B-lineage acute lymphoblastic leukemia. Blood, 1995, 86: 4263-4269.
  • 2Rothman R, Trakhtenbrot L, Bielorai B, et al. Co-existence of multiple subclones in TEL-AML1 at diagnosis of acute lymphoblas- tic leukaemia in association with submicroscopic deletion of AML1. Br J Haematol, 2005, 129:491-498.
  • 3van Dongen JJ, Langerak AW, Broggemann M, et al. Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receplor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936. Leukemia ,2003,17:2257-2317.
  • 4林冬,刘世和,竺晓凡,薄丽津,李承文,陈玉梅,刘旭平,秦爽,代芸,王建祥.t(12;21)儿童急性淋巴细胞白血病的研究[J].中华血液学杂志,2004,25(1):17-21. 被引量:9
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二级参考文献10

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共引文献8

同被引文献24

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