首页> 外文期刊>Biotechnology & Biotechnological Equipment >The Tumor Necrosis Factor-A (TNF-A) Gene -308 G/A Polymorphism and the Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (Trail) Gene Polymorphisms in Behcet'S Disease
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The Tumor Necrosis Factor-A (TNF-A) Gene -308 G/A Polymorphism and the Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (Trail) Gene Polymorphisms in Behcet'S Disease

机译:白塞氏病的肿瘤坏死因子-A(TNF-A)基因-308 G / A多态性和肿瘤坏死因子相关的凋亡诱导配体(Trail)基因多态性。

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Behcet's disease (BD) is a chronic, multisystemic inflammatory disease. The specific etiology of BD remains elusive, but the interaction between infectious-agent exposure and genetic factors may have a role. In this report, we aim to investigate the possible association between pathogenesis of the BD and TNF-???± gene 308A/G (rs1800629) polymorphism and the TRAIL gene (Arg141His, G422A (rs6557634), Thr209Arg, C626G (rs20575) and Glu228Ala, A683C (rs20576)) polymorphisms in people from southeast of Turkey. The study population consisted of 55 BD patients and 80 healthy subjects. All samples were collected and studied between July 2009 and January 2010. Polymorphisms were detected by polymerase chain reaction restriction fragment length-polymorphism (PCR-RFLP) analysis . The patients and healthy control groups were similar with respect to their ages and sex characteristic. Statistically, there was not significant difference between the BD patients and healthy control groups in terms of TRAIL Arg141His, G422A ( rs6557634) polymorphism , TRAIL Thr209Arg, C626G ( rs20575), TRAIL Glu228Ala, A683C ( rs20576) and TNF-???±-308 G/A (rs1800629) polymorphisms . We could not detect statistically significant difference between the BD patients and healthy control groups according to TNF-???±-308 G/A (rs1800629) , TRAIL Arg141His, G422A ( rs6557634), TRAIL Thr209Arg, C626G ( rs20575) and TRAIL Glu228Ala, A683C ( rs20576) gene polymorphism.
机译:白塞氏病(BD)是一种慢性多系统性炎症性疾病。 BD的具体病因仍然难以捉摸,但传染源暴露与遗传因素之间的相互作用可能起作用。在本报告中,我们旨在研究BD和TNF-α±基因308A / G(rs1800629)多态性与TRAIL基因(Arg141His,G422A(rs6557634),Thr209Arg,C626G(rs20575)和Glu228Ala,A683C(rs20576))多态性,来自土耳其东南部。研究人群包括55名BD患者和80名健康受试者。在2009年7月至2010年1月之间收集并研究了所有样品。通过聚合酶链反应限制片段长度多态性(PCR-RFLP)分析检测了多态性。患者和健康对照组的年龄和性别特征相似。从统计学上讲,在BD患者和健康对照组之间,TRAIL Arg141His,G422A(rs6557634)多态性,TRAIL Thr209Arg,C626G(rs20575),TRAIL Glu228Ala,A683C(rs20576)和TNF-α±- 308 G / A(rs1800629)多态性。根据TNF-α--- 308 G / A(rs1800629),TRAIL Arg141His,G422A(rs6557634),TRAIL Thr209Arg,C626G(rs20575)和TRAIL Glu228Ala,我们无法检测到BD患者与健康对照组之间的统计学差异。 ,A683C(rs20576)基因多态性。

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