首页> 美国卫生研究院文献>Arthritis Research >Characterization of the HLA-DRβ1 third hypervariable region amino acid sequence according to charge and parental inheritance in systemic sclerosis
【2h】

Characterization of the HLA-DRβ1 third hypervariable region amino acid sequence according to charge and parental inheritance in systemic sclerosis

机译:HLA-DRβ1第三高变区氨基酸序列的表征根据系统性硬化中的电荷和亲本遗传

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

BackgroundSpecific HLA class II alleles are associated with systemic sclerosis (SSc) risk, clinical characteristics, and autoantibodies. HLA nomenclature initially developed with antibodies as typing reagents defining DRB1 allele groups. However, alleles from different DRB1 allele groups encode the same third hypervariable region (3rd HVR) sequence, the primary T-cell recognition site, and 3rd HVR charge differences can affect interactions with T cells. We considered 3rd HVR sequences (amino acids 67–74) irrespective of the allele group and analyzed parental inheritance considered according to the 3rd HVR charge, comparing SSc patients with controls.
机译:背景特定的HLA II类等位基因与全身性硬化症(SSc)风险,临床特征和自身抗体相关。 HLA命名法最初是用抗体作为定义DRB1等位基因组的分型试剂而开发的。但是,来自不同DRB1等位基因组的等位基因编码相同的第三高变区(3rd HVR)序列,主要T细胞识别位点,并且第三HVR电荷差异会影响与T细胞的相互作用。我们考虑了第三个HVR序列(氨基酸67-74),与等位基因组无关,并分析了根据第三个HVR收费考虑的父母遗传,将SSc患者与对照组进行了比较。

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