肾脏疾病
候选基因
全基因组关联研究
遗传学
遗传关联
遗传建筑学
疾病
发病机制
医学
基因组
遗传倾向
基因
生物
生物信息学
单核苷酸多态性
基因型
数量性状位点
病理
内科学
作者
Conall M. O’Seaghdha,Caroline S. Fox
出处
期刊:Nephron
[S. Karger AG]
日期:2010-11-11
卷期号:118 (1): c55-c63
被引量:24
摘要
The current review collates what is already known of the genetics of chronic kidney disease (CKD), and focuses on new trends in genome-wide assessment of the inherited component of susceptibility to this condition. Early efforts to identify kidney disease susceptibility genetic loci using linkage and candidate gene strategies proved disappointing. More recently, genome-wide association studies have yielded highly promising results suggesting a number of potential candidate genes and genomic regions that may contribute to the pathogenesis of CKD. Renal failure susceptibility genes identified by these methods, such as <i>MYH9</i>, have yielded novel insights into the pathogenesis of CKD. Genome-wide association studies of CKD are beginning to define the genomic architecture of kidney disease and will impact our understanding of how genetic variation influences susceptibility to this condition.
科研通智能强力驱动
Strongly Powered by AbleSci AI