Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Moreover, individuals with both the Asp/Asp genotype of the Glu(298)-->Asp polymorphism and at least one C allele of the T(786)-->C variant in the promoter region of the eNOS gene had an increased risk of CAD (odds ratio = 4.0; P <0.001) and a significantly higher mean Duke score (26.2 +/- 2.9 vs 45.2 +/- 3.7; P = 0.002) compared with individuals with the TT genotype and the Glu allele.
|
12600950 |
2003 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Multiple logistic regression analysis revealed a significant and independent association of eNOS T-786C polymorphism and other putative risk factors with CAD/TVD in T2DM individuals.
|
23182401 |
2013 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Odds ratio (OR) and 95% confidence interval (CI) were used to evaluate the association between NOS3 10G/T and G24943A polymorphisms as well as CAD risk.
|
27443477 |
2017 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Odds ratios with 95% confidence intervals were used to evaluate associations between endothelial nitric oxide synthase polymorphisms and coronary artery disease.
|
30789045 |
2019 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Only the -786 T/C polymorphism in the 5' flanking region of the NOS3 gene was significantly associated with early CAD in our population.
|
11485372 |
2001 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our findings indicate that high numbers of CA repeats in intron 13 of the eNOS gene are associated with an excess risk of coronary artery disease.
|
10762001 |
2000 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our findings show that the 27-bp VNTR polymorphic locus, but not the c.894G>T polymorphic locus, is associated with CAD and that it may regulate NOS3 pre-mRNA splicing in a length-dependent manner.
|
30447355 |
2019 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our findings, for the first time, indicate that NOS3 T allele strongly interacts with CETP B1 allele to augment the risk of CAD and T2DM in the population of Western Iran.
|
23157875 |
2012 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Our study does not support the conclusion that the eNOS Asp298 allele contributes to the development of premature CAD.
|
11579346 |
2001 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Patients with coronary artery disease had significantly higher ratios of eNOS T/C and C/C genotypes, which include the C allele, than the T/T genotype.
|
19761682 |
2009 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in the endothelial nitric oxide synthase ( eNOS ) gene (- 786T > C and 894G > T ) enhance endothelial dysfunction and have been studied in relation to coronary artery disease (CAD).
|
20846926 |
2010 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recent genetic studies have shown an association between the -786TC polymorphism in the endothelial nitric oxide synthase gene (NOS3) and coronary artery diseases, but any possible association with hypertension has been controversial.
|
21194529 |
2011 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recently, a common polymorphism in exon 7 of the eNOS gene (894G-->T) has been reported to be a strong risk factor for coronary artery disease.
|
9731617 |
1998 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Recently, an endothelial nitric oxide synthase (ecNOS) gene polymorphism, the 27-bp repeat in intron 4 (ecNOS4), was reported to be related to the pathogenesis of coronary heart disease and terminal renal failure.
|
9535806 |
1998 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Relationship between hemorheology and Glu(298)Asp polymorphism of endothelial nitric oxide synthase gene in patients with coronary artery disease.
|
19434512 |
2010 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
CTD_human |
Role of nitric oxide-producing and -degrading pathways in coronary endothelial dysfunction in chronic kidney disease.
|
17267746 |
2007 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
RPA1 thus apparently functions as a repressor protein in the -786T-->C mutation-related reduction of eNOS gene transcription associated with the development of coronary artery disease.
|
11063722 |
2000 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Several studies have evaluated the association between the G894T polymorphism located in an exon of endothelial nitric oxide synthase (eNOS) and the risk of premature CAD.
|
29100441 |
2017 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Several studies have shown that the T-786C polymorphism in 5'-flanking region of the endothelial nitric oxide synthase (eNOS) gene is associated with coronary artery disease in non-diabetic population.
|
16401309 |
2005 |
Coronary Artery Disease
|
0.500 |
Biomarker
|
disease |
BEFREE |
Several studies have suggested that ALDH2 polymorphism plays an important role in the progress of CAD through multiple mechanisms, including the regulation of alcohol consumption, inflammation, endothelial progenitor cells, oxidative stress, asymmetric dimethylarginine, endothelial nitric oxide synthase, and other CAD-promoting factors.
|
25263942 |
2014 |
Coronary Artery Disease
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
Shear stress insensitivity of endothelial nitric oxide synthase expression as a genetic risk factor for coronary heart disease.
|
15375006 |
2004 |
Coronary Artery Disease
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
Short-term transdermal estradiol enhances nitric oxide synthase III and estrogen receptor mRNA expression in arteries of women with coronary artery disease.
|
16207548 |
2005 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The ecNOS gene a/b polymorphism and the NADH/NADPH oxidase p22 phox gene C242T polymorphism were found to be significantly associated with the development of CAD in Korean male patients less than 51 years old.
|
11530961 |
2001 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The eNOS gene harbours a common polymorphism in intron 4 (4a/b), and some clinical studies have suggested an association of the rare a-allele with coronary artery disease (CAD) and myocardial infarction (MI).
|
12226742 |
2002 |
Coronary Artery Disease
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The endothelial nitric oxide synthase (eNOS) (4a/b) gene polymorphism contributes to coronary heart disease and hypertension risk.
|
12923396 |
2003 |