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本文引用的文献

1
BARD1 Gene Polymorphisms Confer Nephroblastoma Susceptibility.BARD1 基因多态性与肾母细胞瘤易感性相关。
EBioMedicine. 2017 Feb;16:101-105. doi: 10.1016/j.ebiom.2017.01.038. Epub 2017 Jan 31.
2
Genome-wide mutational spectra analysis reveals significant cancer-specific heterogeneity.全基因组突变谱分析揭示了显著的癌症特异性异质性。
Sci Rep. 2015 Jul 27;5:12566. doi: 10.1038/srep12566.
3
Identification of a functional SNP in the 3'UTR of CXCR2 that is associated with reduced risk of lung cancer.鉴定CXCR2基因3'非翻译区中一个与降低肺癌风险相关的功能性单核苷酸多态性（SNP）。
Cancer Res. 2015 Feb 1;75(3):566-75. doi: 10.1158/0008-5472.CAN-14-2101. Epub 2014 Dec 5.
4
Cancer genome landscapes.肿瘤基因组图谱。
Science. 2013 Mar 29;339(6127):1546-58. doi: 10.1126/science.1235122.
5
A novel missense-mutation-related feature extraction scheme for 'driver' mutation identification.一种新型的错义突变相关特征提取方案，用于“驱动”突变识别。
Bioinformatics. 2012 Nov 15;28(22):2948-55. doi: 10.1093/bioinformatics/bts558. Epub 2012 Oct 7.
6
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.常见的 BARD1 变异影响高危神经母细胞瘤的易感性。
Nat Genet. 2009 Jun;41(6):718-23. doi: 10.1038/ng.374. Epub 2009 May 3.
7
A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk.KRAS基因3'非翻译区中一个与let-7微小RNA互补位点的单核苷酸多态性增加了非小细胞肺癌的发病风险。
Cancer Res. 2008 Oct 15;68(20):8535-40. doi: 10.1158/0008-5472.CAN-08-2129.
8
MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells.微小RNA海绵：哺乳动物细胞中小RNA的竞争性抑制剂
Nat Methods. 2007 Sep;4(9):721-6. doi: 10.1038/nmeth1079. Epub 2007 Aug 12.
9
Natural selection on human microRNA binding sites inferred from SNP data.从单核苷酸多态性（SNP）数据推断人类微小RNA结合位点上的自然选择。
Nat Genet. 2006 Dec;38(12):1452-6. doi: 10.1038/ng1910. Epub 2006 Oct 29.
10
Genetics of global gene expression.全球基因表达的遗传学
Nat Rev Genet. 2006 Nov;7(11):862-72. doi: 10.1038/nrg1964.

The association between gene SNPs and cancer predisposition: Correlation or causality?

作者信息

Tan Hua

机构信息

Center for Bioinformatics & Systems Biology, Department of Radiology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

EBioMedicine. 2017 Feb;16:8-9. doi: 10.1016/j.ebiom.2017.01.047. Epub 2017 Feb 1.

DOI:10.1016/j.ebiom.2017.01.047
PMID:28163041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5474513/
Abstract
摘要