Cargando…
Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility
Large-scale genome-wide association studies (GWAS) have revealed that rs10757278 polymorphism (or its proxy rs1333049) on chromosome 9p21 is associated with myocardial infarction (MI) susceptibility in individuals of Caucasian ancestry. Following studies in other populations investigated this associ...
Autores principales: | Chen, Guangyuan, Fu, Xiuhua, Wang, Guangyu, Liu, Guiyou, Bai, Xiuping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463723/ https://www.ncbi.nlm.nih.gov/pubmed/26006241 http://dx.doi.org/10.3390/ijms160511678 |
Ejemplares similares
-
Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population
por: Bogari, Neda, et al.
Publicado: (2021) -
Case–Control Study on the Interaction Effects of rs10757278 Polymorphisms at 9p21 Locus and Traditional Risk Factors on Coronary Heart Disease in Xinjiang, China
por: Lu, Wu-Hong, et al.
Publicado: (2020) -
Association of Single-Nucleotide Polymorphisms of rs2383206, rs2383207, and rs10757278 With Stroke Risk in the Chinese Population: A Meta-analysis
por: Hu, Xuemei, et al.
Publicado: (2022) -
Corrigendum: Association of single-nucleotide polymorphisms of rs2383206, rs2383207, and rs10757278 with stroke risk in the Chinese population: A meta-analysis
por: Hu, Xuemei, et al.
Publicado: (2022) -
CDH1 rs9929218 variant at 16q22.1 contributes to colorectal cancer susceptibility
por: Han, Peng, et al.
Publicado: (2016)