|
CDKN2B-AS1
|
0.180 |
GeneticVariation
|
disease |
BEFREE |
There was no association between clinical severity and recurrence with variants rs2383207 (CDKN2B-AS1) for atherothrombotic IS and variants rs879324 (ZFHX3), rs966221 (PDE4D), and rs152312 (PDE4D) for cardioembolic IS.
|
31757599 |
2020 |
|
CDKN2B-AS1
|
0.180 |
GeneticVariation
|
disease |
BEFREE |
Mutations in gene locations of CDKN2B-AS1 (Rs2383206), HDAC9 (Rs11984041), NINJ2 (Rs12425791), NAA25 (Rs17696736) are not risk factors for ischemic stroke in childhood.
|
30656483 |
2019 |
|
CDKN2B-AS1
|
0.180 |
Biomarker
|
disease |
BEFREE |
In this study, we used oxygen-glucose deprivation (OGD) to stimulate rat adrenal medulla-derived pheochromocytoma cell line PC-12 to construct an <i>in vitro</i> IS cell model and investigated the role of ANRIL and the underlying mechanism.
|
31174432 |
2019 |
|
CDKN2B-AS1
|
0.180 |
Biomarker
|
disease |
BEFREE |
We found an association between rs2383207*A allele, nearby CDKN2B-AS1, and LAAS-IS [OR 2.35 (95% CI = 1.79-3.08); p = 4.66 × 10<sup>-10</sup>].
|
30738964 |
2019 |
|
CDKN2B-AS1
|
0.180 |
GeneticVariation
|
disease |
BEFREE |
This study aims to determine whether variants in the antisense noncoding RNA in the INK4 locus (ANRIL) gene are associated with IS in Han Chinese, as well as whether there is evidence of a gene-environment interactions.
|
29773352 |
2018 |
|
CDKN2B-AS1
|
0.180 |
GeneticVariation
|
disease |
BEFREE |
The ANRIL variants rs2383207 and rs1333049 were significantly associated with the risk of IS among males but not females in the Chinese Han population.
|
29881905 |
2018 |
|
CDKN2B-AS1
|
0.180 |
GeneticVariation
|
disease |
GWASCAT |
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
|
29531354 |
2018 |
|
CDKN2B-AS1
|
0.180 |
Biomarker
|
disease |
BEFREE |
ANRIL may increase the risk of ischemic stroke through regulation of the CARD8 pathway.
|
24385277 |
2014 |
|
CDKN2B-AS1
|
0.180 |
Biomarker
|
disease |
BEFREE |
ANRIL (antisense Non-coding RNA in the INK4 Locus (harboring the CDKN2A/B genes)) variants were related to a variety of vascular diseases (myocardial infarction, aortic and intracranial aneurysm), including ischaemic stroke.
|
22776031 |
2012 |