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No association of the cytotoxic T-lymphocyte associated gene CTLA4 +49A/G polymorphisms with Crohn’s disease and ulcerative colitis in Hungarian population samples

机译:匈牙利人群样本中细胞毒性T淋巴细胞相关基因CTLA4 + 49A / G多态性与克罗恩病和溃疡性结肠炎无关联

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摘要

AIM: ududThe goal of the current work was to analyse the prevalence of the +49A/G variant of the cytotoxic T-lymphocyte antigen 4 gene (CTLA4) in Hungarian patients with Crohnos disease (CD) and ulcerative colitis (UC).ududMETHODS: ududA total of 130 unrelated subjects with CD and 150 with UC, and 170 matched controls were genotyped for the single nucleotide polymorphism (SNP). The genotypes were determined by using PCR/RFLP test.ududRESULTS: ududThe G allele frequency and the prevalence of the GG genotype were 38.1% and 12.3% in the CD group, 40.6% and 18.6% in the UC patients, and 37.4% and 15.9% in the control group, respectively.ududCONCLUSION: ududThe results of the current study show that carriage of the +49G SNP in heterozygous or in homozygous form does not confer risk either for CD or for UC in the Hungarian population.ud
机译:目的: ud ud当前工作的目标是分析匈牙利克罗诺斯病(CD)和溃疡性结肠炎(UC)患者的细胞毒性T淋巴细胞抗原4基因(CTLA4)+ 49A / G变异的患病率方法: ud ud方法:共有130位CD无关受试者和150位UC受试者,以及170位匹配的对照进行了单核苷酸多态性(SNP)基因分型。通过PCR / RFLP测试确定基因型。 ud ud结果: ud udCD组的G等位基因频率和GG基因型患病率分别为38.1%和12.3%,UC患者为40.6%和18.6%。结论: ud ud本研究结果表明,+ 49G SNP以杂合或纯合形式携带不会给CD或CD带来风险。匈牙利人口中的UC。 ud

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