Suppr超能文献

利用二核苷酸重复多态性检测人类TP53基因座杂合性缺失

Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism.

作者信息

Jones M H, Nakamura Y

机构信息

Department of Biochemistry, Cancer Institute, Tokyo, Japan.

出版信息

Genes Chromosomes Cancer. 1992 Jul;5(1):89-90. doi: 10.1002/gcc.2870050113.

Abstract

Loss of heterozygosity at the TP53 locus occurs frequently in many types of cancer and requires polymorphic markers for detection. Several polymorphisms at the TP53 locus have been described previously, and polymerase chain reaction (PCR)-based assays have been developed to detect these polymorphisms. However, these polymorphisms have relatively low levels of heterozygosity and are often uninformative. We report here the detection of loss of heterozygosity at the TP53 locus in various human cancers by using a highly informative dinucleotide repeat polymorphism.

摘要

TP53基因座杂合性缺失在多种癌症中频繁发生,检测需要多态性标记。此前已描述了TP53基因座的几种多态性,并已开发基于聚合酶链反应(PCR)的检测方法来检测这些多态性。然而,这些多态性的杂合性水平相对较低,且常常提供不了有用信息。我们在此报告,通过使用一种信息丰富的二核苷酸重复多态性来检测各种人类癌症中TP53基因座的杂合性缺失。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验