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Linking genetic variants to kidney disease via the epigenome
Nature Genetics ( IF 31.7 ) Pub Date : 2022-06-23 , DOI: 10.1038/s41588-022-01098-9


The largest GWAS for kidney function so far provided the starting point for integrated multi-stage annotation of genetic loci. Whole kidney and single-cell epigenomic information is crucial for translating GWAS information to the identification of causal genes and pathogenetic (and potentially targetable) cellular and molecular mechanisms of kidney disease.

中文翻译:

通过表观基因组将遗传变异与肾脏疾病联系起来

迄今为止最大的肾功能 GWAS 为基因位点的集成多阶段注释提供了起点。全肾和单细胞表观基因组信息对于将 GWAS 信息转化为识别肾脏疾病的致病基因和致病(和潜在可靶向的)细胞和分子机制至关重要。
更新日期:2022-06-23
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