Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis.

Alireza Azani,Asghar Hosseinzadeh,Roya Azadkhah,Ali Akbar Poursadegh Zonouzi,Ahmad Poursadegh Zonouzi,Younes Aftabi, Hourieh Khani,Leida Heidary,Shahla Danaii,Nasrin Bargahi,Nasser Pouladi,Sayed Mostafa Hosseini

European Journal of Obstetrics & Gynecology and Reproductive Biology（2017）

引用 16|浏览5

暂无评分

摘要

Our findings provide evidence to support the hypothesis that eNOS -786 T>C polymorphism and the -786C-4a-894G haplotype are associated with the high risk of RPL.

查看译文

关键词

Nitric oxide,Endothelial nitric oxide synthase,Polymorphism,Haplotype,Recurrent pregnancy loss,In silico

AI 理解论文

溯源树

样例

生成溯源树，研究论文发展脉络

Chat Paper

正在生成论文摘要