Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

B J Wouters; M A Sanders; S Lugthart; W M C Geertsma-Kleinekoort; E van Drunen; H B Beverloo; B L?wenberg; P J M Valk; R Delwel

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Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

机译：节段性单亲二体性作为急性髓性白血病纯合CEBPA突变的复发机制

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《Leukemia》 |2007年第11期|共3页
作者
B J Wouters; M A Sanders; S Lugthart; W M C Geertsma-Kleinekoort; E van Drunen; H B Beverloo; B L?wenberg; P J M Valk; R Delwel;
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中图分类肿瘤学;
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1. Molecular Evaluation of CEBPA Gene Mutation in Normal Karyotype Acute Myeloid Leukemia: A Comparison of Two Methods and Report of Novel CEBPA Mutations from Indian Acute Myeloid Leukemia Patients [J] . Firoz Ahmad, Saket Rajput, Swarna Mandava, Genetic testing and molecular biomarkers . 2012,第7期

机译：正常核型急性髓性白血病中CEBPA基因突变的分子评估：两种方法的比较和印度急性髓性白血病患者新型CEBPA突变的报道
2. Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. [J] . Raghavan M, Smith LL, Lillington DM, Blood: The Journal of the American Society of Hematology . 2008,第3期

机译：节段性单亲二体性是复发性急性髓细胞性白血病中常见的遗传事件。
3. 250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies. [J] . Dunbar AJ, Gondek LP, OKeefe CL, Cancer research: The official organ of the American Association for Cancer Research, Inc . 2008,第24期

机译：250K单核苷酸多态性阵列核型分析可识别骨髓恶性肿瘤中获得性单亲二体性和纯合突变，包括c-Cbl的新型错义取代。
4. Ras gene mutation in acute myeloid leukemia and Myelodysplastic syndromes: a meta-analysis of its occurrence and prognostic relevance [C] . Cheng Jingru, Wang Peng, Zhang Tai, International Conference on Advanced Materials and Computer Science . 2016

机译：RAS基因突变在急性髓性白血病和髓细胞增强综合征中：荟萃分析其发生和预后相关性
5. Pharmacology Profiles of ALK and FLT3 Kinase Inhibitors against Non-Small-Cell Lung Cancer Cells and Acute Myeloid Leukemia Cells with Cancer Driver Mutations [D] . 森政道 2019

机译：ALK和FLT3激酶抑制剂对非小细胞肺癌细胞和急性髓系白血病细胞的癌症驱动突变的药理作用
6. 250K SNP array karyotyping identifies acquired uniparental disomy and homozygous mutations including novel missense substitutions of c-Cbl in myeloid malignancies [O] . Andrew J. Dunbar, Lukasz P. Gondek, Christine L. O’Keefe, -1

机译：250K SNP阵列核型分析可识别骨髓恶性肿瘤中获得的单亲二体性和纯合突变包括新的c-Cbl错义替换
7. Association between Acquired Uniparental Disomy and Homozygous Gene Mutation in Acute Myeloid Leukemias [O] . Jude Fitzgibbon, Lan-Lan Smith, Manoj Raghavan, 2005

机译：在急性髓性白血病中获得的发单人生物和纯合基因突变之间的关联

Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia

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