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[High throughput sequencing combined with DNA-PCR for detection of 51 kinds of hematologic malignancy related gene mutations in patients with myelodysplastic syndromes].

作者信息

Wang K, Chao H Y, Wu P, He C, Zhang R, Shen H J, Chen S N

机构信息

Jiangsu Institute of Hematology, the First Affiliated Hospital of Soochow University, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health, Suzhou 215006, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2018 May 14;39(5):431-434. doi: 10.3760/cma.j.issn.0253-2727.2018.05.018.

DOI:10.3760/cma.j.issn.0253-2727.2018.05.018
PMID:29779357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7342906/
Abstract
摘要

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本文引用的文献

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[Gene mutations from 511 myelodysplastic syndromes patients performed by targeted gene sequencing].[通过靶向基因测序对511例骨髓增生异常综合征患者进行的基因突变分析]
Zhonghua Xue Ye Xue Za Zhi. 2017 Dec 14;38(12):1012-1016. doi: 10.3760/cma.j.issn.0253-2727.2017.12.002.
2
New Insight Into the Biology, Risk Stratification, and Targeted Treatment of Myelodysplastic Syndromes.骨髓增生异常综合征生物学、风险分层及靶向治疗的新见解
Am Soc Clin Oncol Educ Book. 2017;37:480-494. doi: 10.1200/EDBK_175397.
3
Clinical implications of mutations in a Southeast Asian cohort of acute myeloid leukaemia patients.
东南亚急性髓系白血病患者队列中突变的临床意义
J Clin Pathol. 2017 Aug;70(8):669-676. doi: 10.1136/jclinpath-2016-204195. Epub 2017 Jan 18.
4
TP53 and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes.TP53与地西他滨在急性髓系白血病和骨髓增生异常综合征中的应用
N Engl J Med. 2016 Nov 24;375(21):2023-2036. doi: 10.1056/NEJMoa1605949.
5
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Curr Hematol Malig Rep. 2016 Dec;11(6):441-448. doi: 10.1007/s11899-016-0356-8.
6
RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features.RUNX1 突变与急性髓系白血病的独特临床病理及遗传学特征相关。
Leukemia. 2016 Nov;30(11):2160-2168. doi: 10.1038/leu.2016.126. Epub 2016 May 3.
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Molecular and Cellular Mechanisms of Myelodysplastic Syndrome: Implications on Targeted Therapy.骨髓增生异常综合征的分子与细胞机制：对靶向治疗的启示
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