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急性髓系白血病FLT3基因突变的研究 被引量:7

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摘要 FLT3(FMS-like tyrosine kinase-3)即FMS样酪氨酸激酶3,是Ⅲ型RTK家族成员之一,其蛋白结构包括5个免疫球蛋白(Ig)样结构域组成的胞外区,1个跨膜区,1个近膜区(JM),以及胞内由激酶插入区分隔而成的两个酪氨酸激酶(TK)区。目前研究发现,FLT3基因突变主要包括两种形式:串联重复突变(FLT3-ITD)和Asp835点突变,在急性白血病尤其是急性髓系白血病(AML)发生中起重要作用。我们较为全面地分析273例AML患者FLT3基因突变和单核苷酸多态性(SNP),希望最终能为靶向治疗AML提供线索。
出处 《中华血液学杂志》 CAS CSCD 北大核心 2007年第2期124-126,共3页 Chinese Journal of Hematology
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参考文献7

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二级参考文献16

  • 1王莉红,周春林,张新伟,陈森,王敏,王建祥.FLT3基因内部串联重复突变与急性白血病的关系及临床意义[J].中华血液学杂志,2004,25(7):393-396. 被引量:35
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共引文献35

同被引文献68

  • 1王莉红,周春林,张新伟,陈森,王敏,王建祥.FLT3基因内部串联重复突变与急性白血病的关系及临床意义[J].中华血液学杂志,2004,25(7):393-396. 被引量:35
  • 2颜灵芝,陈苏宁,梁建英,冯宇峰,岑建农,何军,常伟荣,朱子玲,潘金兰,吴亚芳,薛永权,吴德沛.急性髓系白血病患者NPM1基因突变分析[J].中华血液学杂志,2007,28(5):289-293. 被引量:17
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  • 7Frohling S, Schlenk RF, Breitruck J, et al. Prognostic significance of activating FLT3 mutations in younger adults ( 16 to 60 years ) with acute myeloid leukemia and normal cytogenetics: a study of the AML Study Group Ulm. Blood, 2002 ; 100 : 4372 - 4380.
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