期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
蒙汉民族ASAP1、NRAMP1、SP110基因表达水平与结核病易感性关联分析
1
作者 宁鹏媛 董丽 +6 位作者 郝金奇 崔晓钢 杨彩婷 王爱欣 郝明媛 余艳琴 吴长新 《中国动物传染病学报》 CAS 北大核心 2022年第3期40-47,共8页
结核病(TB)发病具有种族易感性的分布特点,揭示结核病种族易感性的发病机制对明确结核病的高危人群、制定相应的防控策略具有重要作用。本研究从宿主易感相关基因转录水平出发,探讨ASAP1、NRAMP1和SP110表达水平与蒙古族和汉族结核病发... 结核病(TB)发病具有种族易感性的分布特点,揭示结核病种族易感性的发病机制对明确结核病的高危人群、制定相应的防控策略具有重要作用。本研究从宿主易感相关基因转录水平出发,探讨ASAP1、NRAMP1和SP110表达水平与蒙古族和汉族结核病发病的关联程度。基于病例-对照研究设计,收集蒙古族和汉族96例结核病患者和126例健康人群静脉血,采用实时荧光定量PCR的方法检测易感性关联基因ASAP1、NRAMP1和SP110的mRNA表达水平,并分析不同民族间、结核患者与健康对照组间基因表达水平的差异。蒙古族结核患者结核易感基因ASAP1、NRAMP1 mRNA表达水平明显高于对照组(P<0.05),汉族结核病患者NRAMP1表达水平高于对照组(P<0.05)。蒙古族女性结核病患者,SP110的表达显著性差异(P<0.05)。汉族ASAP1、SP110 mRNA表达在结核病患者与对照之间没有显著差异。蒙汉民族结核病发病易感性与宿主基因ASAP1、NRAMP1和SP110表达有关,尤其是女性人群。提示结核病防治过程中可参考这些易感基因的表达评估结核病高危人群。 展开更多
关键词 蒙古族 汉族 结核病 易感性关联基因 MRNA表达
下载PDF
No association between IRF3 polymorphism and susceptibility to hepatitis B virus infection in Chinese patients 被引量:3
2
作者 Fang Yan,Feng Lv,Xu Li,Hua-Fa Yin,Department of Infectious Diseases,The First Affiliated Hospital of Anhui Medical University,Hefei 230032,Anhui Province,China Yu-Feng Gao,Department of Hepatopathy,The Second Affiliated Hospital of Anhui Medical University,Hefei 230601,Anhui Province,China Tian-Chen Zhang,Department of Epidemiology and Biostatistics,School of Public Health,Anhui Medical University,Hefei 230032,Anhui Province,China 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第4期388-392,共5页
AIM:To investigate the association between three tag single nucleotide polymorphisms (tagSNPs) in inter-feron regulatory factors (IRF3) and the genetic suscep-tibility to chronic hepatitis B virus (HBV) infection.METH... AIM:To investigate the association between three tag single nucleotide polymorphisms (tagSNPs) in inter-feron regulatory factors (IRF3) and the genetic suscep-tibility to chronic hepatitis B virus (HBV) infection.METHODS:We performed a case-control study of 985 Chinese cases of chronic HBV infection and 294 self-limiting HBV-infected individuals as controls.Three tagSNPs in IRF3 (rs10415576,rs2304204,rs2304206) were genotyped with the Multiplex SNaPshot technique.The genotype and allele frequencies were calculatedand analyzed.RESULTS:The three SNPs showed no significant geno-type/allele associations with chronic HBV infection.Overall allele P values were:rs10415576,P=0.0908,odds ratio (OR) [95% confidence interval (CI)]=1.1798 (0.9740-1.4291);rs2304204,P=0.5959,OR (95% CI)=1.0597 (0.8552-1.3133);rs2304206,P=0.8372,OR (95% CI)=1.0250 (0.8097-1.2976).Overall genotype P values were:rs10415576,P=0.2106;rs2304204,P=0.8458;rs2304206,P=0.8315.There were no statisti-cally significant differences between patients with chron-ic HBV infection and controls.Haplotypes generated by these three SNPs were also not significantly different between the two groups.CONCLUSION:The three tagSNPs of IRF3 are not asso-ciated with HBV infection in the Han Chinese population. 展开更多
关键词 Chronic hepatitis B virus infection Interferon regulatory factors tag single nucleotide polymorphisms Genetic susceptibility HAPLOTYPE
下载PDF
Association between Two Polymorphisms of Follicle Stimulating Hormone Receptor Gene and Susceptibility to Polycystic Ovary Syndrome: a Meta-analysis 被引量:3
3
作者 Lei Qiu Jing Liu Qi-ming Hei 《Chinese Medical Sciences Journal》 CAS CSCD 2015年第1期44-50,共7页
Objective To investigate the association between two polymorphisms of follicle stimulating hormone receptor (FSHR) gene and polycystic ovary syndrome (PCOS) susceptibility. Methods Case-control studies on relatio... Objective To investigate the association between two polymorphisms of follicle stimulating hormone receptor (FSHR) gene and polycystic ovary syndrome (PCOS) susceptibility. Methods Case-control studies on relationship of Thr307Ala and Asn680Ser polymorphisms in FSHR gene and PCOS susceptibility were searched from PubMed, ISI web of knowledge, EBSCO, and China National Knowledge Infrastructure (CNKI) databases up to March 21, 2013. The pooled odds ratio (OR) and 95% confidence interval (CO were calculated using fixed- or random-effect model based on heterogeneity test in 5 genotype models analyses. Results A total of 11 studies were included in the Meta-analysis. The random-effect analysis showed Asn680Ser was significantly associated with the reduced susceptibility to PCOS with dominant model (Asn/Asn+Asn/Ser vs. Ser/Ser, OR=0.83, 95% CI: 0.69-1.00), recessive model (Asn/Asn vs. Asn/Ser+ Ser/Ser, OR=0.84, 95% CI: 0.72-0.98), homozygote comparison (Ash/Ash vs. Ser/Ser, 0R=0.79, 95% CI: 0.63-0.98), and the allele contrast (Asn vs. Ser, OR=0.87, 95% CI: 0.79-0.97) respectively(P=0.02, I2=56.0%), being protective factors for PCOS. However, no significant associations were found between Thr307Ala and PCOS. Conclusion There might be a significant association between Asn680Ser polymorphism and PCOS. 展开更多
关键词 follicle stimulating hormone receptor polycystic ovary syndrome META-ANALYSIS single-nucleotide polymorphism
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部