Cargando…
The 9p21.3 risk locus for coronary artery disease: A 10-year search for its mechanism
The 9p21.3 risk locus is the first locus to be associated with an increased risk of coronary artery disease (CAD)-related events and many other phenotypes. This locus contains 59 single nucleotide polymorphisms (SNPs) in a region with multiple long range enhancers and long non-coding RNAs (lncRNAs)...
Autor principal: | Almontashiri, Naif A.M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taibah University
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694924/ https://www.ncbi.nlm.nih.gov/pubmed/31435240 http://dx.doi.org/10.1016/j.jtumed.2017.03.001 |
Ejemplares similares
-
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes
por: Rivera, Natalia V, et al.
Publicado: (2013) -
9p21.3 coronary artery disease risk locus and interferon alpha 21: Association study in an Asian Indian population
por: Kalpana, Bellary, et al.
Publicado: (2019) -
The Same Chromosome 9p21.3 Locus Is Associated With Type 2 Diabetes and Coronary Artery Disease in a Chinese Han Population
por: Cheng, Xiang, et al.
Publicado: (2011) -
The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population
por: Manjula, Gorre, et al.
Publicado: (2020) -
Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3
por: Benberin, Valeriy, et al.
Publicado: (2023)