|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our aim of this study was to investigate the association of the rs12425791, rs11833579 and rs12904 in the binding site of miR-200c with the risk of IS.
|
31077198 |
2019 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
NINJ2 gene rs12425791 confers a susceptible factor for IS, while there is no association between NINJ2 gene rs11833579 and IS.
|
31258083 |
2019 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
New evidence from this case-control study and meta-analysis indicates that 12</span>p13 rs12425791</span>/rs118</span>33579 polymorphisms are associated with ischemic stroke</span> susceptibility in Asian populations.
|
31679297 |
2019 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our meta-analysis shows that SNP rs11833579 is not related to ischemic stroke in the Asian population.
|
25096477 |
2014 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The present study suggests A allele of rs11833579 may play a role in mediating susceptibility to IS and</span> it may increase the risk of IS together with smoking.
|
24664524 |
2014 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
These findings indicated that rs12425791 and rs11833579 on chromosome 12p13 may be useful biomarkers for predicting the prognosis of patients with the LAA subtype of ischaemic stroke.
|
24995625 |
2014 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Two single-nucleotide polymorphisms rs11833579 and rs12425791 located on chromosome 12p13 were reported to be associated with ischemic stroke in Caucasians.
|
23270316 |
2013 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This meta-analysis suggest that rs12425791 is relative to ischemic stroke risk under dominant model in Asian population, but not for rs11833579.
|
22795341 |
2012 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Association between 12p13 SNPs rs11833579/rs12425791 near NINJ2 gene and ischemic stroke in East Asian population: evidence from a meta-analysis.
|
22297388 |
2012 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This is a precedent study that found genetic variants of rs12425791 and rs11833579 on chromosome 12p13 are independent predictors of stroke-related mortality or stroke recurrence in patients with incident ischemic stroke in Taiwan.
|
22212150 |
2012 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Recently, a genome-wide association study reported an association between two single nucleotide polymorphisms (SNPs) rs11833579 and rs12425791 near NINJ2 gene and ischemic stroke in Caucasians.
|
21722921 |
2011 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The A allele of SNP rs11833579 on chromosome 12p13 may play a role in mediating susceptibility to IS in the Han Chinese population in a recessive model.
|
21832970 |
2011 |
|
rs11833579
|
|
|
0.100 |
GeneticVariation |
BEFREE |
No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population.
|
21376321 |
2011 |