rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Polymorphism in rs10865710, rs1805192 and rs4646903 and interaction between rs1805192 and rs4646903 were related with increased CAD susceptibility.
|
28415751 |
2017 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
We investigated the relationship of the Pro 12 Ala PPARγ2 polymorphism with the presence and severity of coronary artery disease (CAD) assessed by Gensini score (Gs).
|
23652363 |
2013 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
The results of the present study demonstrated that possessing the A allele of RAGE -374T/A polymorphism by diabetic CAD patients and possessing the-374T/Ala12 haplotype of RAGE -374T/A and PPAR-γ Pro12 Ala polymorphisms by the patients group were the most important risk factors for CAD.
|
21861709 |
2012 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
The meta-analysis of the association of PPARG P12A, C161T polymorphism and coronary heart disease.
|
22987045 |
2012 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Our results demonstrated that the PPARγ2 Pro12Ala polymorphism might be risk-conferring locus for the progression of CAD among Caucasians, but not among Asians.
|
23300871 |
2012 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Association of the PPARG Pro12Ala polymorphism with type 2 diabetes and incident coronary heart disease in a Hong Kong Chinese population.
|
22515931 |
2012 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Our aim was to evaluate the role of the Pro12Ala PPARγ2 polymorphism on the risk of coronary artery disease (CAD) in an Italian population with a case-controlled genetic association study in which 478 CAD patients and 218 controls were genotyped for the Pro12Ala polymorphism.CAD was diagnosed by angiography.
|
21206011 |
2010 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
We hypothesized that polymorphisms of PPARgamma Pro12Ala, LPL HindIII and LPL Ser447X influence severity of coronary artery disease (CAD) in an Indian population.
|
20430250 |
2010 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
The aim was to investigate if the polymorphism PPARgamma2 Pro12Ala, which encodes a less efficient transcription factor, was associated with risk of acute coronary disease and if there were interactions between this polymorphism and factors that modify PPARgamma activity, such as alcohol intake, smoking, and use of non-steroidal anti-inflammatory medicine.
|
19500413 |
2009 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
We investigated the effects of carriership of the Pro12Ala variant on angiographic and cardiovascular event outcomes in male patients with symptomatic coronary artery disease (CAD).
|
19228871 |
2009 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Further studies on the correlation between Pro12Ala</span> polymorphism and CAD should be carried out in a larger Korean population in the future.
|
17322631 |
2007 |
rs1805192
|
|
Coronary Artery Disease
|
|
0.100 |
GeneticVariation
|
BEFREE |
Peroxisome proliferator-activated receptor-gamma2 P12A polymorphism and risk of coronary heart disease in US men and women.
|
15920035 |
2005 |