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On the Protective Effects of Gene SNPs Against Human Cancer.

作者信息

Tan Hua

机构信息

School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

出版信息

EBioMedicine. 2018 Jul;33:4-5. doi: 10.1016/j.ebiom.2018.06.027. Epub 2018 Jun 27.

DOI:10.1016/j.ebiom.2018.06.027
PMID:29954716
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6085566/
Abstract
摘要

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本文引用的文献

1
Base Excision Repair Gene Polymorphisms and Wilms Tumor Susceptibility.碱基切除修复基因多态性与肾母细胞瘤易感性。
EBioMedicine. 2018 Jul;33:88-93. doi: 10.1016/j.ebiom.2018.06.018. Epub 2018 Jun 21.
2
Identification of candidate protective variants for common diseases and evaluation of their protective potential.常见疾病候选保护性变异体的鉴定及其保护潜力评估。
BMC Genomics. 2017 Aug 3;18(1):575. doi: 10.1186/s12864-017-3964-3.
3
Adding Protective Genetic Variants to Clinical Reporting of Genomic Screening Results: Restoring Balance.在基因组筛查结果的临床报告中加入保护性基因变异：恢复平衡
JAMA. 2017 Apr 18;317(15):1527-1528. doi: 10.1001/jama.2017.1533.
4
The association between gene SNPs and cancer predisposition: Correlation or causality?基因单核苷酸多态性与癌症易感性之间的关联：相关性还是因果关系？
EBioMedicine. 2017 Feb;16:8-9. doi: 10.1016/j.ebiom.2017.01.047. Epub 2017 Feb 1.
5
Protective alleles and modifier variants in human health and disease.人类健康与疾病中的保护等位基因和修饰变体。
Nat Rev Genet. 2015 Dec;16(12):689-701. doi: 10.1038/nrg4017. Epub 2015 Oct 27.
6
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.
7
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.拉丁裔女性乳腺癌全基因组关联研究确定了6q25上的新型保护性变异。
Nat Commun. 2014 Oct 20;5:5260. doi: 10.1038/ncomms6260.
8
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.
9
Protective association exhibited by the single nucleotide polymorphism (SNP) rs1052133 in the gene human 8-oxoguanine DNA glycosylase (hOGG1) with the risk of squamous cell carcinomas of the head & neck (SCCHN) among north Indians.单核苷酸多态性（SNP）rs1052133 在基因人 8-氧鸟嘌呤 DNA 糖基化酶（hOGG1）中与北印度人头颈部鳞状细胞癌（SCCHN）风险的保护关联。
Indian J Med Res. 2011 Jun;133(6):605-12.
10
SNPs in cancer research and treatment.癌症研究与治疗中的单核苷酸多态性
Br J Cancer. 2004 Feb 23;90(4):747-51. doi: 10.1038/sj.bjc.6601574.