التفاصيل البيبلوغرافية
العنوان:
Genome-Wide Association and Functional Studies Identify
المؤلفون:
Yang, Li , Dao Wen, Wang , Yundai, Chen , Can, Chen , Jian, Guo , Shu, Zhang , Zhijun, Sun , Hu, Ding , Yan, Yao , Lei, Zhou , Ke, Xu , Chun, Song , Fan, Yang , Bin, Zhao , Han, Yan , Wen-Jing, Wang , Chong, Wu , Xiangfeng, Lu , Xueli, Yang , Jie, Dong , Guyan, Zheng , Shuhan, Tian , Yanjun, Cui , Lijuan, Jin , Gangqiong, Liu , Hanbin, Cui , Shenghuang, Wang , Feng, Jiang , Changhua, Wang , Jeanette, Erdmann , Linyao, Zeng , Shian, Huang , Jianfeng, Zhong , Yuehua, Ma , Wenjiang, Chen , Jianli, Sun , Wei, Lei , Shenghan, Chen , Shaoqi, Rao , Dongfeng, Gu , Heribert, Schunkert , Xiao-Li, Tian
المصدر:
Arteriosclerosis, thrombosis, and vascular biology . 38(4)
سنة النشر:
2017
مصطلحات موضوعية:
Adult , Male , China , Polycomb-Group Proteins , Coronary Artery Disease , Vascular Remodeling , Polymorphism, Single Nucleotide , Rats, Sprague-Dawley , Asian People , Gene Frequency , Risk Factors , Human Umbilical Vein Endothelial Cells , Animals , Humans , Carotid Stenosis , Genetic Predisposition to Disease , Cells, Cultured , Aged , Middle Aged , Coronary Vessels , Disease Models, Animal , Carotid Arteries , Phenotype , Female , Thrombospondins , Genome-Wide Association Study
الوصف:
The genetic contribution to coronary artery disease (CAD) remains largely unclear. We combined genetic screening with functional characterizations to identify novel loci and candidate genes for CAD.We performed genome-wide screening followed by multicenter validation in 8 cohorts consisting of 21 828 participants of Han ethnicity and identified 3 novel intragenic SNPs (single nucleotide polymorphisms), rs9486729 (We identify 3 novel loci associated with CAD and show that 2 genes
تدمد:
1524-4636
URL الوصول:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf6daf798ba1611b509aeeb473afbf32 https://pubmed.ncbi.nlm.nih.gov/29472232
رقم الانضمام:
edsair.pmid..........cf6daf798ba1611b509aeeb473afbf32
قاعدة البيانات:
OpenAIRE