Endothelial nitric oxide synthase gene promoter polymorphism (T-786C) may be associated with advanced retinopathy of prematurity

被引:7
作者
Shastry, Barkur S. [1 ]
机构
[1] Oakland Univ, Dept Biol Sci, Rochester, MI 48063 USA
关键词
eNOS Gene; G894T Polymorphism; Gene Promoter Polymorphism; Retinal Vascular Disease; eNOS Polymorphism;
D O I
10.1007/s00417-012-2231-1
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
引用
收藏
页码:2251 / 2253
页数:3
相关论文
共 9 条
[1]   Genetic susceptibility to retinopathy of prematurity [J].
Bizzarro, Matthew J. ;
Hussain, Naveed ;
Jonsson, Baldvin ;
Feng, Rui ;
Ment, Laura R. ;
Gruen, Jeffrey R. ;
Zhang, Heping ;
Bhandari, Vineet .
PEDIATRICS, 2006, 118 (05) :1858-1863
[2]  
Brooks SE, 2001, INVEST OPHTH VIS SCI, V42, P222
[3]   The G894T polymorphism on endothelial nitric oxide synthase gene is associated with premature coronary artery disease in a Turkish population [J].
Cam, SF ;
Sekuri, C ;
Tengiz, I ;
Ercan, E ;
Sagcan, A ;
Akin, M ;
Berdeli, A .
THROMBOSIS RESEARCH, 2005, 116 (04) :287-292
[4]  
Kimura H, 2003, ACTA BIOCHIM POL, V50, P49
[5]   T-786→C mutation in the 5′-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm [J].
Nakayama, M ;
Yasue, H ;
Yoshimura, M ;
Shimasaki, Y ;
Kugiyama, K ;
Ogawa, H ;
Motoyama, T ;
Saito, Y ;
Ogawa, Y ;
Miyamoto, Y ;
Nakao, K .
CIRCULATION, 1999, 99 (22) :2864-2870
[6]  
Rusai K, 2008, MOL VIS, V14, P286
[7]   Genetic susceptibility to advanced retinopathy of prematurity (ROP) [J].
Shastry, Barkur S. .
JOURNAL OF BIOMEDICAL SCIENCE, 2010, 17
[8]   eNOS4 polymorphism of the endothelial nitric oxide synthase predicts risk for severe diabetic retinopathy [J].
Taverna, MJ ;
Sola, A ;
Guyot-Argenton, C ;
Pacher, N ;
Bruzzo, F ;
Chevalier, A ;
Slama, G ;
Reach, G ;
Selam, JL .
DIABETIC MEDICINE, 2002, 19 (03) :240-245
[9]   Endothelial Nitric Oxide Synthase genotypes in the etiology of retinopathy of prematurity in premature infants [J].
Yanamandra, Krishna ;
Napper, Dawn ;
Pramanik, Arun ;
Bocchini, Joseph A., Jr. ;
Dhanireddy, Ramasubbareddy .
OPHTHALMIC GENETICS, 2010, 31 (04) :173-177