Associations of polymorphisms in LOXL1 and copper chaperone genes with pseudoexfoliation-syndrome-related cataract in a Chinese Uygur population

2020 ◽  
Vol 40 (7) ◽  
pp. 1841-1848
Author(s):  
Qinghe Jing ◽  
Dan Li ◽  
Wei Gao ◽  
Fan Zhang ◽  
Yi Lu ◽  
...  
2017 ◽  
Vol 2 (3) ◽  
pp. 82-87
Author(s):  
N. Lutsenko ◽  
◽  
O. Isakova ◽  
O. Rudycheva ◽  
T. Mihalchik

2015 ◽  
Vol 22 (6) ◽  
pp. 532-538 ◽  
Author(s):  
Dana Kahra ◽  
Tanumoy Mondol ◽  
Moritz Niemiec ◽  
Pernilla Wittung-Stafshede
Keyword(s):  

Hereditas ◽  
2021 ◽  
Vol 158 (1) ◽  
Author(s):  
Dilare Adi ◽  
Jialin Abuzhalihan ◽  
Jing Tao ◽  
Yun Wu ◽  
Ying-Hong Wang ◽  
...  

Abstract Background Coronary artery disease (CAD) is the leading cause of death worldwide. In this study, we aimed to explore whether some genetic variants of the human IDOL gene were associated with CAD among Chinese population in Xinjiang. Methods We designed two independent case–control studies. The first one included in the Han population (448 CAD patients and 343 controls), and the second one is the Uygur population (304 CAD patients and 318 controls). We genotyped three SNPs (rs2072783, rs2205796, and rs909562) of the IDOL gene. Results Our results revealed that, in the Han female subjects, for rs2205796, the distribution of alleles, dominant model (TT vs. GG + GT) and the additive model (GG + TT vs. GT) showed significant differences between CAD patients and the control subjects (P = 0.048, P = 0.014, and P = 0.032, respectively). Conclusions The rs2205796 polymorphism of the IDOL gene is associated with CAD in the Chinese Han female population in Xinjiang, China.


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