期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
ADRA2B gene insertion/deletion polymorphism and artery compliance
1
作者 ZHANG Hai-feng LI Xin-li +7 位作者 XIE Si-feng ZHU Jian WANG Zhen-zhen LIANG Li-rong CAO Ke-jiang DE Wei YUAN Li HUANG Jun 《Chinese Medical Journal》 SCIE CAS CSCD 2005年第21期1797-1802,共6页
Background The ADRA2B gene insertion/deletion (I/D) polymorphism is associated with various cardiovascular and metabolic phenotypes. Large (C1) and small (C2) artery compliance, assessed by pulse wave analysis, ... Background The ADRA2B gene insertion/deletion (I/D) polymorphism is associated with various cardiovascular and metabolic phenotypes. Large (C1) and small (C2) artery compliance, assessed by pulse wave analysis, is considered as sensitive markers or risk factors for cardiovascular disease. Therefore whether the ADRA2B I/D polymorphism is associated with CI and C2 need to be investigated. Methods A total of 227 men and 243 women were enrolled in a Chinese family-based study. C1 and C2 were measured by pulse wave analysis. ADRA2B genotypes were determined by polymerase chain reaction. Statistical methods included generalized estimation equations and quantitative transmission disequilibrium test. Results The II (31.9%), ID (46.8%) and DD (21.3%) genotype frequencies were in Hardy-Weinberg equilibrium (P = 0. 73 ). The covariates selected by stepwise regression for C1 and C2 were age, systolic pressure and gender. The population based association analysis showed that C1 and C2 were not associated with ADRA2B genotype both before (C1 : P =0. 28; C2: P =0. 27) and after (C1 : P =0. 58; C2: P =0. 18) the adjustment. The family-based analyses of 128 informative offspring showed that transmission of the D-allele was not associated with C1 orC2, both before (CI: P=0.42; C2: P=0.85) and after (CI: P=0.31; C2: P= 0. 82) the adjustment. Conclusion The study do not support that the ADRA2B gene I/D polymorphism has a major gene effect on C1 or C2 in the Chinese population of current sample size. 展开更多
关键词 large artery compliance small artery compliance adra2b gene
原文传递
人类情绪记忆的行为与神经遗传学研究进展述评 被引量:2
2
作者 邹吉林 周仁来 《心理科学》 CSSCI CSCD 北大核心 2013年第4期1004-1008,共5页
情绪记忆及其增强效应存在广泛的个体差异,这种个体差异可能有其神经与遗传基础。近来的行为遗传学与神经遗传学证实人类ADRA2B基因缺失突变以及BDNF Val66Met基因的多态性与情绪记忆增强及其神经机制的个体差异相联系。本文重点介绍与... 情绪记忆及其增强效应存在广泛的个体差异,这种个体差异可能有其神经与遗传基础。近来的行为遗传学与神经遗传学证实人类ADRA2B基因缺失突变以及BDNF Val66Met基因的多态性与情绪记忆增强及其神经机制的个体差异相联系。本文重点介绍与人类情绪记忆相关的这两种基因,梳理了行为与神经遗传学研究的最新进展,指出未来应关注更多候选基因,并重视多个脑区之间的交互作用;还应使用情绪面孔刺激探索BDNF Val66Met基因多态性对情绪记忆编码和提取的影响等。 展开更多
关键词 情绪记忆 adra2b BDNF 基因多态性 突变 杏仁核
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部