miR-196a2 (rs11614913) polymorphism is associated with coronary artery disease, but not with in-stent coronary restenosis.
José Manuel FragosoJulian Ramírez-BelloMarco Antonio Martínez-RíosMarco Antonio Peña-DuqueRosalinda Posadas-SánchezHilda Delgadillo-RodríguezMayra Jiménez-MoralesCarlos Posadas-RomeroGilberto Vargas-AlarconPublished in: Inflammation research : official journal of the European Histamine Research Society ... [et al.] (2018)
Our data suggests that the T allele of the miRNA-196a2 C/T (rs11614913) polymorphism is associated with the risk of developing CAD, but no association with restenosis was observed.
Keyphrases
- coronary artery disease
- percutaneous coronary intervention
- cell proliferation
- cardiovascular events
- coronary artery bypass grafting
- long non coding rna
- electronic health record
- long noncoding rna
- big data
- aortic stenosis
- coronary artery
- type diabetes
- cardiovascular disease
- heart failure
- data analysis
- artificial intelligence
- atrial fibrillation
- deep learning
- transcatheter aortic valve replacement
- aortic valve
- ejection fraction