|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
We identified an exonic polymorphism in NOS3 (rs1799983, p.Glu298Asp; p = 2.2E-8, odds ratio [OR] = 1.05, 95% confidence interval [CI] = 1.04-1.07) and variants in an intron of COL4A1 (rs9521634; p = 3.8E-8, OR = 1.04, 95% CI = 1.03-1.06) and near DYRK1A (rs720470; p = 6.1E-9, OR = 1.05, 95% CI = 1.03-1.07) at genome-wide significance for stroke.
|
30383316 |
2018 |
|
rs1799983
|
|
T |
0.780 |
GeneticVariation |
GWASCAT |
We identified an exonic polymorphism in NOS3 (rs1799983, p.Glu298Asp; p = 2.2E-8, odds ratio [OR] = 1.05, 95% confidence interval [CI] = 1.04-1.07) and variants in an intron of COL4A1 (rs9521634; p = 3.8E-8, OR = 1.04, 95% CI = 1.03-1.06) and near DYRK1A (rs720470; p = 6.1E-9, OR = 1.05, 95% CI = 1.03-1.07) at genome-wide significance for stroke.
|
30383316 |
2018 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
In conclusion, genotypic polymorphisms of the eNOS Glu298Asp and Cav-1 14713A/29107A polymorphisms are associated with the elevated risk of LAA stroke among Han Chinese in Taiwan.
|
28346478 |
2017 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
AF patients with rs1799983 variants were more likely to have coronary artery disease or stroke than those without genetic variant at this gene (31.0% vs. 17.3%, p=0.004).
|
26256966 |
2015 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
However, the copresence of G894T and intron 4 VNTR risk-elevating genotypes in the same individual increased the risk of stroke seven times (odds ratio=7.083, 95% confidence interval=0.866-57.963, p=0.029).
|
25321404 |
2014 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
Thus, we examined the possible association of eNOS G894T variation with stroke severity and functional outcome.
|
22004707 |
2011 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
We tested a single nucleotide polymorphism (SNP) in endothelial nitric oxide synthase (NOS3) gene at codon 298 (single-nucleotide polymorphism rs1799983; p.Asp298Glu) in a cohort of 355 older (>75 years) stroke survivors, who had detailed cognitive assessments from 3 months poststroke, i.e., baseline when the patients were free of dementia and subsequently at annual intervals.
|
20691505 |
2011 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
In order to investigate the influence of genetic factors in childhood stroke, we compared the distributions of mutations/ polymorphisms affecting hemostasis and/or endothelial function (factor V [FV] Leiden, factor II [FII] G20210A, methylenetetrahydrofolate reductase [MTHFR] C677T, angiotensin-converting enzyme [ACE] insertion/deletion [ID], and endothelial nitric oxide synthase [eNOS] G894T) among children with stroke and controls.
|
19372095 |
2009 |
|
rs1799983
|
|
|
0.780 |
GeneticVariation |
BEFREE |
In pooled analysis of all patients, intron 4c, but not intron 4a, intron 4b or G894T alleles are associated with stroke (p < 0.01).
|
18070351 |
2007 |
|
rs375752214
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We examined the association between different polymorphisms frequently found in young patients with cryptogenic stroke [methylenetetrahydrofolate reductase (MTHFR) C677T, factor II (prothrombin) G20210A, factor V G1691A (Leiden), nitric oxide synthase 3 (NOS3) intron 4 VNTR, and apolipoprotein E (APOE) epsilon4 gene] in patients with a cerebral infarct caused by spontaneous cervical artery dissection.
|
20446941 |
2010 |
|
rs3918166
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Only 1 of the tested SNP (NOS3 rs3918166) was associated with both migraine and stroke.
|
19661472 |
2009 |