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首页> 外文期刊>International journal of immunogenetics >Lack of association between GTF2H4 genetic variants and AERD development and FEV(1) decline by aspirin provocation.
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Lack of association between GTF2H4 genetic variants and AERD development and FEV(1) decline by aspirin provocation.

机译:GTF2H4遗传变异与AERD发育和FEV(1)之间的缺乏联系因阿司匹林的刺激而下降。

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摘要

Aspirin-exacerbated respiratory disease (AERD) is prevalent in about 10% of asthma patients and is characterized by a severe decline in forced expiratory volume in 1-s (FEV(1) ), an important phenotype for total lung capacity, upon ingestion of aspirin. The general transcription factor IIH subunit 4 (GTF2H4) is positioned at 6p21.33, a part of the major histocompatibility complex (MHC) class II region that contains a number of genes that play an important role in the immune system. In addition, genetic variants in another general transcription factor IIH gene have revealed significant association with lung disease. To investigate whether GTF2H4 genetic variants could be a causative factor for AERD development and FEV(1) decline by aspirin provocation, five common single-nucleotide polymorphisms (SNPs) were genotyped in 93 patients with AERD and 96 aspirin-tolerant asthma (ATA) controls.
机译:阿司匹林加剧的呼吸系统疾病(AERD)在大约10%的哮喘患者中普遍存在,其特征是被强迫摄入的呼气量在1 s内急剧下降(FEV(1)),这是摄入总肺容量后的重要表型。阿司匹林。通用转录因子IIH亚基4(GTF2H4)位于6p21.33,它是主要组织相容性复合体(MHC)II类区域的一部分,该区域包含许多在免疫系统中起重要作用的基因。此外,另一种通用转录因子IIH基因的遗传变异已显示出与肺部疾病显着相关。为了研究GTF2H4遗传变异是否可能是AERD发生和FEV(1)因阿司匹林激增而下降的原因,对93名AERD患者和96名阿司匹林耐受性哮喘(ATA)对照患者的5种常见单核苷酸多态性(SNP)进行了基因分型。

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