首页> 美国卫生研究院文献>other >Disease-Associated SNPs From non-Coding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells
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Disease-Associated SNPs From non-Coding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells

机译:来自幼年特发性关节炎非编码区的与疾病相关的SNP位于人类嗜中性粒细胞和CD4 + T细胞的功能基因组元件之内或附近

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摘要

BackgroundJuvenile idiopathic arthritis (JIA) is considered a complex trait in which the environment interacts with inherited genes to produce a phenotype that shows broad inter-individual variance. A recently completed genome-wide association study (GWAS) identified 24 regions of genetic risk for JIA, for example. However, as is typical for GWAS, most of the regions of genetic risk for JIA (22 of 24) were in non-coding regions of the genome. The studies reported here were undertaken to identify functional elements (other than genes) that might be located within the regions of genetic risk.
机译:背景幼年特发性关节炎(JIA)被认为是一种复杂的特征,在该特征中,环境与遗传基因相互作用产生一种表型,该表型表现出广泛的个体差异。例如,最近完成的全基因组关联研究(GWAS)确定了JIA的24个遗传风险区域。但是,就像GWAS一样,大多数JIA的遗传风险区域(24个中的22个)都位于基因组的非编码区域。此处进行的研究旨在确定可能位于遗传风险区域内的功能元件(基因除外)。

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