单核苷酸多态性分析技术及其在肿瘤研究中的应用
被引量：3
Techniques of SNP analysis in cancer research
摘要
单核苷酸多态性 (SNP)是第 3代遗传标记 ,由于其在基因组中分布的高密度性 ,被认为在多基因疾病的诊断及治疗方面有着广阔的应用前景。
出处
《国外医学（肿瘤学分册）》
2003年第3期189-193,共5页
Foreign Medical Sciences (Cancer Section)
基金
国家杰出青年科学基金项目 ( 3 0 12 5 0 2 6)
国家重点基础研究发展规划 ( 973 )项目基金项目 (G19980 5 12 0 5 )
国家高技术研究发展计划 ( 863 )基金项目 ( 2 0 0 1AA2 2 115 1)
参考文献24
-
1Wang DG, Fan JB, Siao CJ, et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphimas in the human genome[J]. Science, 1998, 280(5366): 107-1082.
-
2Kwok PY, Deng Q, Zakeri H, et al. Increasing the information content of STS-based genome maps: identifying polymorphisaaas in mapped STSs[J]. Genommics, 1996, 31(1):123-126.
-
3Cargill M, Altshuler D, Ireland J, et al. Characterization of singlenucleotide polymorphimas in coding regions of human genes[J]. Nat Genet, 1999, 22(3) :231-238.
-
4Halushka MK, Fan JB, Bentley K, et al. Patterns of single-nucleotide polyrnorphisms in candidate genes for blood-pressure homeostasis[J]. Nat Genet, 1999, 22(3):239-247.
-
5Shi MM, Myrand SP, Bleavins MR, et al. High throughput genotyping for the detection of a single nucleotide polymorphism in NAD(P)H quinone oxidoreductase (DT diaphorase) using TaqMan probes[J]. Mol Pathol, 1999,52(5) :295-299.
-
6Ahmadian A, Gharizadeh B, Gustafsson AC, et al. Single-nucleotide polymorphism analysis by pyrosequencing [ J ]. Anal Biochem,2000, 280( 1 ) : 103-110.
-
7O'Donovan MC, Oefner PJ, Roberts SC, et al. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection[J]. Genomics, 1998, 52(1):44-49.
-
8Jones AC, Austin J, Hansen N, et al. Optimal temperature selection for mutation detection by denaturing FIPLC and comparison to singlestranded conformation polymorphism and heteroduplex analysis [ J ].Clin Chem, 1999, 45(8 Pt 1) : 1133-1140.
-
9Giordano M,Oefner PJ, Underhill PA, et al. Identification by denaturing high-performance liquid chromatography of numaerous polymorphisms in a candidate region for multiple sclerosis susceptibility[J].Genomics, 1999,56 (3) : 247-253.
-
10Myakishev MV, Khripin Y, Hu S, et al. High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers[J]. Genome Res, 2001, 11(1):163-169.
同被引文献36
-
1欧雪玲,伍新尧.基质辅助激光解析-电离-飞行时间质谱法检测单核苷酸多态性的研究进展[J].中华检验医学杂志,2004,27(8):539-541. 被引量：2
-
2Kai-FengPan,You-YongLu,Wan-GuoLiu,LianZhang,Wei-ChengYou.Detection of frameshift mutations of RIZ in gastric cancers with microsatellite instability[J].World Journal of Gastroenterology,2004,10(18):2719-2722. 被引量：4
-
3许玲,孙大志,余志红.肿瘤基因单核苷酸多态性研究及个体化医疗的思考[J].世界华人消化杂志,2005,13(5):592-595. 被引量：12
-
4Wei Zh,Jirong Long,Yu-Tang Gao et al.Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1(J).Nat Genet,2009,41(3):324.
-
5Jie Liang,Peizhan Chen,Zhibin Hu et al.Genetic variants in fibroblast growth factor receptor 2(FGRF2)contribute to sus-ceptibility of breast cancer in Chinese women(J).Carcino-genesis,2008,29(12):2341.
-
6Collins F S;P artinos A;Jordan E.New goals for the US Human Genome Project,1998.
-
7Clifford R;Edmonson M;Hu Y.Expression based genetic/physical maps of single nucleotide polymorphisms identified by the cancer genome anatomy project,2000(08).
-
8ChakravartiA.To a future of genetic medicine[J],2001(6822).
-
9Cann R L.Genetic clues to dispersal in human populations:retracing the past from the present[J],2001(5509).
-
10Buren M von.A spelt specific gamma gliadin gene:discovery and detection,2000(02).
引证文献3
-
1王羚郦,何华.变性高效液相色谱法及其在基因变异检测中的研究进展[J].药物分析杂志,2006,26(5):706-711. 被引量：3
-
2董文甫,李艳红,张春香,任有蛇,岳文斌.单核苷酸多态(SNP)相关技术研究及其应用[J].现代畜牧兽医,2006(8):48-51. 被引量：1
-
3杨学习,李欣.乳腺癌易感基因单核苷酸多态性与个体化预防[J].中国妇幼保健,2012,27(24):3834-3835. 被引量：1
二级引证文献5
-
1黄禾根,张贵英.彩色多普勒超声在乳腺癌筛查中的应用价值[J].医学信息（医学与计算机应用）,2014,0(20):142-142. 被引量：2
-
2黄耀江,李雪,董明盛,刘越.人类基因组中单核苷酸多态性的检测技术[J].生物学通报,2007,42(6):1-3.
-
3柴逸峰,朱臻宇,李翔.药物分析(Ⅰ)[J].分析试验室,2008,27(8):83-122. 被引量：1
-
4段辉丽,刘文恩.变性高效液相色谱对ESBLs基因分型的研究进展[J].国际检验医学杂志,2009,30(11):1082-1083. 被引量：1
-
5陈孝梅,李永胜,蔺哲广,吉挺.SNP分子标记在蜜蜂中的应用[J].中国蜂业,2020,71(5):60-62.
-
1张晓玲,王慧琴,刘新梅,赵宗峰,张艳君,吴卫东.p16基因启动子区甲基化与新疆维吾尔族银屑病相关性研究[J].中华实用诊断与治疗杂志,2015,29(11):1082-1083. 被引量：2
-
2李莉,鲁英,杨晓燕,欧江华,齐新.新疆乳腺癌患者外周血中p16基因甲基化的检测意义[J].东南大学学报（医学版）,2014,33(6):691-696. 被引量：2
-
3王珺楠,刘斌,宋春莉.TLR4基因多态性SNP896A>G、SNP1196C>T与冠心病的相关性研究[J].中国实用医药,2009,4(11):5-6. 被引量：7
-
4黄红艳,朱月永.MicroRNA在肝癌中的研究进展[J].中华全科医学,2010,8(8):1038-1039. 被引量：1
-
5赵瑾,田俏梅,吴白平.非小细胞肺癌胸腔积液与小活检标本中EGFR基因突变检测的比较[J].黑龙江医药科学,2014,37(3):109-110. 被引量：2
-
6念馨,张旭祥,刘华,苏艳丹.等位特异PCR检测FOXC2检测基因多态性实验方法研究[J].医学信息,2011,24(17):5727-5728.
-
7王璇,王建东,罗春英,马恒辉,时姗姗,周晓军.结直肠癌中K-ras基因突变的检测及其临床病理学意义[J].医学研究生学报,2013,26(1):19-22. 被引量：21
-
8喻巍,梁剑平,杨德松,王文祥,周勇,李旭,张百华,唐金明,吴劼,吴智宁.连续100例肺癌术后EGFR基因突变检测结果分析[J].肿瘤药学,2016,6(2):150-153. 被引量：4
-
9李莉,鲁英,欧江华,齐新,杨晓燕.新疆乳腺癌患者RASSF1A基因甲基化的分析[J].现代预防医学,2014,41(18):3340-3343.
-
10牛晓敏,艾星浩,陆舜.肺癌的全基因组关联研究进展[J].中国肺癌杂志,2009,12(7):792-798. 被引量：1
