Associated Papers
LOX-1 variants modulate the severity of cardiovascular disease: state of the art and future directions.
Lubrano V et al.
Molecular and Cellular Biochemistry, 2024
Are IVS4 SNPs of OLR1 gene associated with coronary artery disease: Is there a linkage between IVS4 SNPs?
Kurnaz-Gomleksiz O et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University, 2018
Association of the LOX-1 rs1050283 Polymorphism with Risk for Atherosclerotic Cerebral Infarction and its Effect on sLOX-1 and LOX-1 Expression in a Chinese Population.
Guo X et al.
Journal of Atherosclerosis and Thrombosis, 2017
LOX-1 gene variants and maternal levels of plasma oxidized LDL and malondialdehyde in patients with gestational diabetes mellitus.
Aydemir B et al.
Archives of Gynecology and Obstetrics, 2016
Association of LOXIN, a new functional splicing isoform of the OLR1 gene, with severity and prognostic localization of critical coronary artery stenoses.
Cappelletti A et al.
Journal of Cardiovascular Medicine (hagerstown, Md.), 2014
Genetic influence in liver steatosis prevalence and proatherothrombotic/inflammatory profile in familial combined hyperlipoproteinemia.
Santilli F et al.
International Journal of Cardiology, 2013
Oxidized LDL receptor 1 gene polymorphism in patients with metabolic syndrome.
Palmieri VO et al.
European Journal of Clinical Investigation, 2013
Effect of lectin-like oxidized LDL receptor-1 polymorphism on liver disease, glucose homeostasis, and postprandial lipoprotein metabolism in nonalcoholic steatohepatitis.
Musso G et al.
The American Journal of Clinical Nutrition, 2011
Loxin polymorphism is associated with increased resistin levels and with oxidative status.
Gambino R et al.
Clinical Biochemistry, 2011
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events.
Predazzi IM et al.
Annals of Human Biology, 2010
IVS4-14 A/G and IVS4-73 C/T polymorphisms in OLR1 gene in patients with ischemic cerebrovascular diseases.
Vietri MT et al.
Genetic Testing and Molecular Biomarkers, 2010
[Association of APOA5 gene polymorphism with levels of lipids and atherosclerotic cerebral infarction in Chinese].
Li J et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2007
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants.
Chen JM et al.
Human Genetics, 2006
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease.
Trabetti E et al.
European Journal of Human Genetics : Ejhg, 2006
Association of OLR1 gene polymorphisms with the risk of coronary artery disease: A systematic review and meta-analysis.
Salehipour P et al.
Heart & Lung : the Journal of Critical Care, 0