11号染色体长臂存在缺失的骨髓增生异常综合征与SF3B1突变的高频率相关。 - Suppr

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超能文献

MDS with deletions in the long arm of chromosome 11 are associated with a high frequency of SF3B1 mutations.

作者信息

Stengel A, Kern W, Meggendorfer M, Haferlach T, Haferlach C

机构信息

MLL Munich Leukemia Laboratory, Munich, Germany.

出版信息

Leukemia. 2017 Sep;31(9):1995-1997. doi: 10.1038/leu.2017.180. Epub 2017 Jun 8.

DOI:10.1038/leu.2017.180

PMID:28592886

Abstract

摘要

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本文引用的文献

The impact of TP53 mutations and TP53 deletions on survival varies between AML, ALL, MDS and CLL: an analysis of 3307 cases.TP53 突变和缺失对 AML、ALL、MDS 和 CLL 患者生存的影响不同：对 3307 例病例的分析。

Leukemia. 2017 Mar;31(3):705-711. doi: 10.1038/leu.2016.263. Epub 2016 Sep 29.

The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.2016 年版世界卫生组织髓系肿瘤和急性白血病分类。

Blood. 2016 May 19;127(20):2391-405. doi: 10.1182/blood-2016-03-643544. Epub 2016 Apr 11.

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes.944例骨髓增生异常综合征患者的基因损伤图谱

Leukemia. 2014 Feb;28(2):241-7. doi: 10.1038/leu.2013.336. Epub 2013 Nov 13.

Clinical and biological implications of driver mutations in myelodysplastic syndromes.骨髓增生异常综合征中驱动突变的临床和生物学意义。

Blood. 2013 Nov 21;122(22):3616-27; quiz 3699. doi: 10.1182/blood-2013-08-518886. Epub 2013 Sep 12.

Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes.验证低危骨髓增生异常综合征患者的预后模型和突变的影响。

J Clin Oncol. 2012 Sep 20;30(27):3376-82. doi: 10.1200/JCO.2011.40.7379. Epub 2012 Aug 6.

Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes.骨髓增生异常综合征患者中 SRSF2、U2AF1 和 ZRSR2 突变的频率及其预后影响。

Blood. 2012 Apr 12;119(15):3578-84. doi: 10.1182/blood-2011-12-399337. Epub 2012 Mar 2.

New comprehensive cytogenetic scoring system for primary myelodysplastic syndromes (MDS) and oligoblastic acute myeloid leukemia after MDS derived from an international database merge.新的原发性骨髓增生异常综合征（MDS）和 MDS 衍生的少突细胞急性髓系白血病的综合细胞遗传学评分系统，源自国际数据库合并。

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