Suppr超能文献

多因素遗传的罕见变异假说:以结直肠腺瘤易感性为模型

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.

作者信息

Fearnhead Nicola S, Winney Bruce, Bodmer Walter F

机构信息

Cancer Research U.K. Cancer and Immunogenetics Laboratory, Weatherall Institute of Molecular Medicine, Oxford, UK.

出版信息

Cell Cycle. 2005 Apr;4(4):521-5. doi: 10.4161/cc.4.4.1591. Epub 2005 Apr 7.

Abstract

The rare variant hypothesis postulates that genetic susceptibility to colorectal neoplasia within the general population is due to a number of low frequency variants in a variety of different genes. Each variant confers a moderate, but detectable, increase in relative risk of developing the disease. Recent evidence suggests that a quarter of patients with multiple adenomatous polyps are due to rare but functionally important variants in just five genes.

摘要

罕见变异假说假定,普通人群中结直肠肿瘤的遗传易感性归因于多种不同基因中的一些低频变异。每个变异都会使患该疾病的相对风险适度但可检测地增加。最近的证据表明,四分之一的多发性腺瘤性息肉患者是由仅五个基因中的罕见但功能重要的变异所致。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验