首页> 美国卫生研究院文献>The Open Neurology Journal >Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine
【2h】

Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine

机译:C19p13上作为偏头痛候选者的NOTCH3和TNFSF7基因的研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

To investigate the migraine locus around the C19p13 region through analysis of the NOTCH3 gene (C19p13.2-p13.1), previously shown to be a gene involved in CADASIL and the TNFSF7 gene (C19p13), homologous to the ligands of TNF-alpha and TNF-beta, genes that have previously been associated with migraine. The NOTCH3 gene was analysed by sequencing all exons with known CADASIL mutations in a typical (non-familial hemiplegic) migraine family (MF1) that has previously been shown to be linked to C19p13. The TNFSF7 gene was investigated through SNP association analysis using a matched case-control migraine population. NOTCH3 gene sequencing results for affected members of MF1 proved to be negative for all known sequence variants giving rise to mutations for CADASIL. TNFSF7 gene chi-square results showed non-significant P values across all populations tested against controls, except for the MO subgroup which displayed a possible association with the TNFSF7 SNP (genotype, allele analysis P = 0.036, P = 0.017 respectively). Our results suggest that common migraine is not caused by any known CADASIL mutations in the NOTCH3 gene of interest. However, the TNFSF7 gene displayed signs of involvement in a MO affected population and indicates that further independent studies of this marker are warranted.
机译:通过分析NOTCH3基因(C19p13.2-p13.1)来研究C19p13区域附近的偏头痛位点,该基因先前已证明是与CADASIL和TNFSF7基因(C19p13)有关的基因,与TNF-alpha的配体同源和TNF-beta,以前与偏头痛相关的基因。通过对典型(非家族性偏瘫)偏头痛家族(MF1)中具有已知CADASIL突变的所有外显子进行测序,对NOTCH3基因进行了分析,该家族先前已显示与C19p13相关。使用匹配的病例对照偏头痛人群,通过SNP关联分析研究了TNFSF7基因。事实证明,对于所有已知的序列变异,MF1受影响成员的NOTCH3基因测序结果均为阴性,从而导致CADASIL突变。 TNFSF7基因卡方结果显示,与对照组相比,所有对照组的P值均无显着性差异,除了MO亚组与TNFSF7 SNP可能存在关联(基因型,等位基因分析分别为P = 0.036,P = 0.017)。我们的结果表明,普通的偏头痛不是由目标NOTCH3基因中任何已知的CADASIL突变引起的。然而,TNFSF7基因表现出参与MO感染人群的迹象,并表明有必要对该标志物进行进一步的独立研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号