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Genetics of Chronic Kidney Disease

机译:慢性肾脏病的遗传学

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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 pathogenesisofCKD. Renal failure susceptibility genes identified by these methods, such as MYH9, 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.
机译:当前的评论整理了关于慢性肾脏病(CKD)遗传学的已知知识,并着眼于全基因组评估对该病易感性遗传成分的新趋势。早期使用连锁和候选基因策略鉴定肾脏疾病易感性基因座的努力令人失望。最近,全基因组关联研究产生了非常有希望的结果,表明了许多潜在的候选基因和基因组区域可能有助于CKD的发病。通过这些方法鉴定的肾衰竭易感基因,例如MYH9,已对CKD的发病机理产生了新的见解。 CKD的全基因组关联研究开始定义肾脏疾病的基因组结构,并将影响我们对遗传变异如何影响此病易感性的理解。

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