|
CDKN2B-AS1
|
0.100 |
Biomarker
|
disease |
BEFREE |
The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.
|
30587704 |
2019 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Effects of ANRIL polymorphisms on the likelihood of coronary artery disease: A meta-analysis.
|
30387168 |
2019 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Effects of CDKN2B-AS1 polymorphisms on the susceptibility to coronary heart disease.
|
31496134 |
2019 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of CDKN2BAS gene polymorphism with periodontitis and Coronary Artery Disease from South Indian population.
|
31173806 |
2019 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
ANRIL polymorphism rs4977574 is associated with increased risk of coronary artery disease in Asian populations: A meta-analysis of 12,005 subjects.
|
30278588 |
2018 |
|
CDKN2B-AS1
|
0.100 |
Biomarker
|
disease |
BEFREE |
The interplay of LncRNA ANRIL and miR-181b on the inflammation-relevant coronary artery disease through mediating NF-κB signalling pathway.
|
30079603 |
2018 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of ANRIL Expression with Coronary Artery Disease in Type 2 Diabetic Patients.
|
29308617 |
2018 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Genome-wide association analysis of all-cause HF identified several suggestive loci ( P<1×10<sup>-6</sup>), the majority linked to upstream HF risk factors, ie, coronary artery disease ( CDKN2B-AS1 and MAP3K7CL) and atrial fibrillation ( PITX2).
|
30586722 |
2018 |
|
CDKN2B-AS1
|
0.100 |
Biomarker
|
disease |
BEFREE |
CDKN2B-AS may indirectly regulate coronary artery disease-associated genes via targeting miR-92a.
|
28760552 |
2017 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The lncRNA ANRIL is located at a genetic susceptibility locus for coronary artery diseases and type 2 diabetes.
|
28122089 |
2017 |
|
CDKN2B-AS1
|
0.100 |
Biomarker
|
disease |
BEFREE |
Effect of Circular ANRIL on the Inflammatory Response of Vascular Endothelial Cells in a Rat Model of Coronary Atherosclerosis.
|
28683453 |
2017 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The prominent lncRNA antisense noncoding RNA in the INK4 locus (ANRIL), which has been unequivocally associated with coronary artery disease through genome-wide association studies (GWAS), serves as an example to demonstrate the features of each individual database.
|
27049585 |
2016 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.
|
26999117 |
2016 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
CDKN2BAS polymorphisms are associated with coronary heart disease risk a Han Chinese population.
|
27741513 |
2016 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: a case-control study and a meta-analysis.
|
25268619 |
2014 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
ANRIL has long been considered as the strongest candidate gene at the 9p21 locus, robustly associated with stroke and coronary artery disease.
|
24385277 |
2014 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Our thorough genomic characterization of 9p21.3 suggests common variants likely account for observed disease associations and provides further support for the hypothesis that complex regulatory variation affecting ANRIL and CDKN2B gene expression may contribute to increased risk for clinically apparent and subclinical coronary artery disease and aortic disease.
|
23315372 |
2013 |
|
CDKN2B-AS1
|
0.100 |
Biomarker
|
disease |
BEFREE |
Although ANRIL has been proven to be associated with coronary heart disease, its roles in stroke are inconsistent, and sparse data are available regarding hemorrhagic stroke.
|
22034006 |
2012 |
|
CDKN2B-AS1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Significantly reduced expression of all INK4/ARF transcripts (p15(INK4b), p16(INK4a), ARF and ANRIL) was found in PBTL of individuals harboring a common SNP (rs10757278) associated with increased risk of coronary artery disease, stroke and aortic aneurysm.
|
19343170 |
2009 |