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首页> 外文期刊>Osteoarthritis and cartilage >Discovery and analysis of methylation quantitative trait loci (mQTLs) mapping to novel osteoarthritis genetic risk signals
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Discovery and analysis of methylation quantitative trait loci (mQTLs) mapping to novel osteoarthritis genetic risk signals

机译:甲基化定量特性基因座(MQTLS)映射到新型骨关节炎遗传风险信号的发现与分析

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摘要

Objective: Osteoarthritis (OA) is polygenic with over 90 independent genome-wide association loci so far reported. A key next step is the identification of target genes and the molecular mechanisms through which this genetic risk operates. The majority of OA risk-conferring alleles are predicted to act by modulating gene expression. DNA methylation at CpG dinucleotides may be a functional conduit through which this occurs and is detectable by mapping methylation quantitative trait loci, or mQTLs. This approach can therefore provide functional insight into OA risk and will prioritize genes for subsequent investigation. That was our goal, with a focus on the largest set of OA loci yet to be reported.
机译:目的:骨关节炎(OA)是迄今为止有超过90个独立基因组关联基因座的多种子项。 下一步是靶基因的鉴定和这种遗传风险运作的分子机制。 大多数OA风险赋予等位基因预测通过调节基因表达来作用。 CpG二核苷酸的DNA甲基化可以是官能导管,通过该功能导管,这通过映射甲基化定量性状基因座或MQTLs来检测。 因此,这种方法可以提供对OA风险的功能洞察,并优先考虑基因进行后续调查。 这是我们的目标,重点是尚未报道的最大的OA座位。

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