NPM1 gene deletions in myelodysplastic syndromes with 5q- and complex karyotype.
作者信息
Ammatuna Emanuele, Panetta Paola, Agirre Xabier, Ottone Tiziana, Lavorgna Serena, Calasanz Maria José, Lo-Coco Francesco
出版信息
Haematologica. 2011 May;96(5):784-5. doi: 10.3324/haematol.2010.038620. Epub 2011 Mar 10.
Abstract
摘要
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Mutations and promoter methylation status of NPM1 in myeloproliferative disorders.骨髓增殖性疾病中NPM1的突变与启动子甲基化状态
Haematologica. 2006 Aug;91(8):1147-8. Epub 2006 Jul 25.
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Prognostic factors and life expectancy in myelodysplastic syndromes classified according to WHO criteria: a basis for clinical decision making.根据世界卫生组织标准分类的骨髓增生异常综合征的预后因素和预期寿命：临床决策的基础
J Clin Oncol. 2005 Oct 20;23(30):7594-603. doi: 10.1200/JCO.2005.01.7038. Epub 2005 Sep 26.
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Role of nucleophosmin in embryonic development and tumorigenesis.核磷蛋白在胚胎发育和肿瘤发生中的作用。
Nature. 2005 Sep 1;437(7055):147-53. doi: 10.1038/nature03915. Epub 2005 Jul 6.
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Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia.通过毛细管电泳同时检测急性髓系白血病中的NPM1和FLT3-ITD突变
Leukemia. 2005 Aug;19(8):1479-82. doi: 10.1038/sj.leu.2403846.
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Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31.伴有包括q31带在内的5号染色体长臂缺失的骨髓增生异常综合征患者的临床、形态学、细胞遗传学及预后特征
Leukemia. 2004 Jan;18(1):113-9. doi: 10.1038/sj.leu.2403189.
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Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia.骨髓增生异常综合征中5号染色体缺失的细胞遗传学和分子诊断
Br J Haematol. 2000 Sep;110(4):847-55. doi: 10.1046/j.1365-2141.2000.02285.x.
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5q-, twenty-five years later: a synopsis.
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Leukemia. 1996 Dec;10(12):1883-90.
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Distinct haematological disorder with deletion of long arm of no. 5 chromosome.伴有5号染色体长臂缺失的独特血液系统疾病。
Nature. 1974 Oct 4;251(5474):437-8. doi: 10.1038/251437a0.
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