期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
Nicotinic Acetylcholine Receptor α4 Subunit Gene Variation Associated with Attention Deficit Hyperactivity Disorder
1
作者 黄雪竹 徐勇 +6 位作者 李茜茜 刘破资 杨元 张付全 郭田友 杨闯 郭兰婷 《Tsinghua Science and Technology》 SCIE EI CAS 2009年第4期534-540,共7页
Previous pharmacological, human genetics, and animal models have implicated the nicotinic ace- tylcholine receptor α4 subunit (CHRNA4) gene in the pathogenesis of attention deficit/hyperactivity disorder (ADHD). ... Previous pharmacological, human genetics, and animal models have implicated the nicotinic ace- tylcholine receptor α4 subunit (CHRNA4) gene in the pathogenesis of attention deficit/hyperactivity disorder (ADHD). The objective of this study is to examine the genetic association between single nucleotide poly- morphisms in the CHRNA4 gene (rs2273502, rs1044396, rs1044397, and rs3827020 loci) and ADHD. Both case-control and family-based designs are used. Children aged 6 to 16 years were interviewed and assessed with the children behavior checklist and the revised conner' parent rating scale to identify probands. No significant differences in the frequency distribution of genotypes or alleles were found between the case and control groups. However, further haplotype analyses showed the CCGG haplotype on risk for ADHD in 164 case-control samples and the standard transmission disequilibrium test analyses suggest that the allele C of rs2273502 was over-trensferred in 98 ADHD parent-offspring trios. These findings suggest that the CHRNA4 gene may play a role in the pathogenesis of ADHD. 展开更多
关键词 nicotinic acetylcholine receptora4 subunit (chrna4) attention deficit hyperactivity disorder (ADHD) POLYMORPHISM ASSOCIATION GENETICS
原文传递
Association of nicotinic acetylcholine receptor subunit alpha-4 polymorphisms with smoking behaviors in Chinese male smokers 被引量:3
2
作者 CHU Cheng-jing YANG Yan-chun +1 位作者 WEI Jin-xue ZHANG Lan 《Chinese Medical Journal》 SCIE CAS CSCD 2011年第11期1634-1638,共5页
Background it has been reported that the nicotinic acetylcholine receptor subunit a4 gene (CHRNA4) might be associated with smoking behaviors in the previous studies. Up to now, there are few reports on the relation... Background it has been reported that the nicotinic acetylcholine receptor subunit a4 gene (CHRNA4) might be associated with smoking behaviors in the previous studies. Up to now, there are few reports on the relationship between CHRNA4 and smoking initiation, in this study, we tried to explore the role of two polymorphisms in CHRNA4 (rs1044396 and rs1044397) in smoking initiation and nicotine dependence in Chinese male smokers. Methods Nine hundred and sixty-six Chinese male lifetime nonsmokers and smokers were assessed by the Fagerstr6m test for nicotine dependence (FTND), smoking quantity (SQ) and the heaviness of smoking index (HSI). 展开更多
关键词 smoking initiation nicotine dependence nicotinic acetylcholine receptor subunit a4 gene association study
原文传递
汉族儿童热性惊厥与CHRNA4和SYN2基因多态性的关联研究 被引量:1
3
作者 任晓暾 孙素真 +1 位作者 刘芳 王晓明 《中华实用儿科临床杂志》 CAS CSCD 北大核心 2013年第24期1864-1867,共4页
目的探讨神经元烟碱乙酰胆碱受体α-4亚单位基因(CHRNA4基因)和突触蛋白Ⅱ基因(SYN2基因)的单核苷酸多态性(SNP)是否可作为北方汉族儿童单纯性热性惊厥(FS)发病的基因标志物。方法用SNaPshotSNP分型技术对北方汉族141例单纯性F... 目的探讨神经元烟碱乙酰胆碱受体α-4亚单位基因(CHRNA4基因)和突触蛋白Ⅱ基因(SYN2基因)的单核苷酸多态性(SNP)是否可作为北方汉族儿童单纯性热性惊厥(FS)发病的基因标志物。方法用SNaPshotSNP分型技术对北方汉族141例单纯性FS患儿(病例组)和130例健康儿童(健康对照组)进行CHRNA4基因rs1044396、SYN2基因rs3773364位点分型,比较SNP基因型和等位基因频率的差异。结果病例组与健康对照组在rs1044396和rs3773364的基因型和等位基因频率的差异均无统计学意义(P均〉0.05);对CHRNA4基因rsl0443963种基因型A/A、A/G、G/G的Fs患儿的临床资料比较,显示首次惊厥的年龄差异具有统计学意义(x2=17.206,P〈0.001),而SYN2基因rs3773364的3种基因型C/C、C/T、T/T的FS患儿在性别、首次惊厥年龄和首次惊厥时体温的差异均有统计学意义(x2=21.458、8.717、10.424,P均〈0.05)。结论无论CHRNA4基因rs1044396还是SYN2基因rs3773364的多态性可能均与北方汉族儿童FS的发病无关联,但对患儿首次惊厥的年龄和体温有一定影响。 展开更多
关键词 热性惊厥 单核苷酸多态性 神经元烟碱乙酰胆碱受体α-4亚单位 突触蛋白Ⅱ
原文传递
吸烟和CHRNA4基因簇上rs3787140位点多态性与肺癌的关联
4
作者 张亚雷 何萍 +1 位作者 何绮华 江梅 《国际呼吸杂志》 2018年第11期807-811,共5页
目的探讨在中国男性人群中吸烟、烟碱型乙酰胆碱受体亚单位α4(CHRNA4)上rs3787140位点多态性与肺癌的关联。方法采用病例-对照研究设计,共收集204例男性原发性肺癌病例和821名正常健康男性对照者。采用结构式问卷调查人口学特征、吸... 目的探讨在中国男性人群中吸烟、烟碱型乙酰胆碱受体亚单位α4(CHRNA4)上rs3787140位点多态性与肺癌的关联。方法采用病例-对照研究设计,共收集204例男性原发性肺癌病例和821名正常健康男性对照者。采用结构式问卷调查人口学特征、吸烟行为及健康相关行为等信息,并采集静脉血检测CHRNA4基因簇上单核苷酸多态性位点rs3787140的多态性。应用Kruskal-Walis检验方法和多因素logistic回归模型分析吸烟、CHRNA4基因簇上的基因多态性与肺癌的关联。结果采用多因素logistic回归校正混杂因素后,rs3787140基因多态性与患者的病理类型及解剖位置无关;rs3787140基因型分布在吸烟与不吸烟的人群中的差异无统计学意义;rs3787140的基因多态性并不增加发生肺癌的风险,未发现rs3787140的多态性和吸烟对肺癌存在交互作用。结论吸烟和CHRNA4rs3787140多态性及其交互作用并非肺癌发生的危险因素。 展开更多
关键词 吸烟 烟碱型乙酰胆碱受体亚单位α4 肺癌 基因多态性
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部