Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy

Monika M. Pichler; Claudia Bodner; Carina Fischer; Alexander J. Deutsch; Karin Hiden; Christine Beham-Schmid; Werner Linkesch; Christian Guelly; Heinz Sill; Albert W?lfler

首页> 外文期刊>British Journal of Haematology >Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy

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Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy

机译：对与治疗有关的和继发性急性髓细胞性白血病中异柠檬酸脱氢酶基因突变的评估，确定了由于单亲二体性而克隆发展为IDH2 R172K纯合性的患者

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《British Journal of Haematology》 |2011年第5期|669-672|共4页
作者
Monika M. Pichler; Claudia Bodner; Carina Fischer; Alexander J. Deutsch; Karin Hiden; Christine Beham-Schmid; Werner Linkesch; Christian Guelly; Heinz Sill; Albert W?lfler;
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Division of Haematology;

Centre for Medical Research;

Institute of Pathology Medical University of Graz Graz Austria. E-mail: albert.woelfler@medunigraz.at;

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1. Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy. [J] . Pichler MM, Bodner C, Fischer C, British Journal of Haematology . 2011,第5期

机译：对治疗相关性和继发性急性髓细胞性白血病中异柠檬酸脱氢酶基因突变的评估，确定了由于单亲二体性而克隆发展为IDH2 R172K纯合性的患者。
2. Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients [J] . Sadudee Chotirat, Wanna Thongnoppakhun, Orathai Promsuwicha, Journal of Hematology and Oncology . 2012,第5期

机译：新诊断的急性髓细胞性白血病患者中异柠檬酸脱氢酶1和2（IDH1和IDH2）代谢基因的分子改变以及其他基因突变
3. Mutation Analysis of IDH1/2 Genes in Unselected De novo Acute Myeloid Leukaemia Patients in India - Identification of A Novel IDH2 Mutation [J] . Sureshkumar Raveendran, Santhi Sarojam, Sangeetha Vijay, Asian Pacific Journal of Cancer Prevention . 2015,第9期

机译：印度未选定的de Novo急性髓白血病患者IDH1 / 2基因的突变分析 - 一种新型IDH2突变的鉴定
4. Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients [O] . Sadudee Chotirat, Wanna Thongnoppakhun, Orathai Promsuwicha, 2012

机译：新诊断的急性髓细胞性白血病患者中异柠檬酸脱氢酶1和2（IDH1和IDH2）代谢基因的分子改变以及其他基因突变
5. Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patients [O] . Chotirat, Sadudee, Thongnoppakhun, Wanna, Promsuwicha, Orathai, 2012

机译：新诊断的急性髓细胞性白血病患者中异柠檬酸脱氢酶1和2（IDH1和IDH2）代谢基因的分子改变以及其他基因突变

Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy

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