Cargando…

Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese population

BACKGROUND: Genome-wide association studies have reported that the 9p21.3 locus confers risk for coronary artery disease (CAD). However, it is not known whether rs10811656 is linked with CAD in a Chinese population. Thus, the purpose of this study was to investigate the potential association between...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yan, Jianjun, Zeng, Jinmei, Xie, Zhiyong, Liu, Dongchen, Wang, Liansheng, Chen, Zhong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979187/ https://www.ncbi.nlm.nih.gov/pubmed/27507036 http://dx.doi.org/10.1186/s12944-016-0296-2

Ejemplares similares

Influence of Chromosome 9p21.3 rs1333049 Variant on Telomere Length and Their Interactive Impact on the Prognosis of Coronary Artery Disease
por: Borghini, Andrea, et al.
Publicado: (2023)

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)

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)

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)

A study of the association of rs12040273 with susceptibility and severity of coronary artery disease in a Chinese Han population
por: Yang, Bo, et al.
Publicado: (2018)

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)

The 9p21.3 risk locus for coronary artery disease: A 10-year search for its mechanism
por: Almontashiri, Naif A.M.
Publicado: (2017)

Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population
por: Kalpana, Bellary, et al.
Publicado: (2019)

Chromosome 9p21.3 is Associated with Early-Onset Coronary Heart Disease in the Irish Population
por: Meng, Weihua, et al.
Publicado: (2008)

Association in a Chinese population of a genetic variation in the early B-cell factor 1 gene with coronary artery disease
por: Li, Yafei, et al.
Publicado: (2017)

The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3
por: Kim, Daniel S, et al.
Publicado: (2014)

Analysis of the 9p21.3 sequence associated with coronary artery disease reveals a tendency for duplication in a CAD patient
por: Kouprina, Natalay, et al.
Publicado: (2018)

Association of rs10757274 and rs2383206 Polymorphisms on 9p21 locus with Coronary Artery Disease in Turkish Population
por: Yayla, Çağrı, et al.
Publicado: (2016)

Analysis of Polymorphism rs1333049 (Located at 9P21.3) in the White Population of Western Siberia and Associations with Clinical and Biochemical Markers
por: Shakhtshneider, Elena, et al.
Publicado: (2019)

Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran
por: Golabgir Khademi, Khadijeh, et al.
Publicado: (2016)

Analysis on the polymorphisms of site RS4977574, and RS1333045 in region 9p21 and the susceptibility of coronary heart disease in Chinese population
por: Hua, Lei, et al.
Publicado: (2020)

Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population
por: Lin, Xiaoming, et al.
Publicado: (2017)

Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population
por: Bogari, Neda, et al.
Publicado: (2021)

Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran
por: Foroughmand, Ali Mohammad, et al.
Publicado: (2015)

Chromosome 9p21.3 polymorphism in a Chinese Han population is associated with angiographic coronary plaque progression in non-diabetic but not in type 2 diabetic patients
por: Wang, Wei, et al.
Publicado: (2010)

Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease
por: Silander, Kaisa, et al.
Publicado: (2009)

Comments on: Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran
por: Michael H., Preuß, et al.
Publicado: (2016)

The Chromosome 9p21.3 Coronary Heart Disease Risk Allele Is Associated with Altered Gene Expression in Normal Heart and Vascular Tissues
por: Pilbrow, Anna P., et al.
Publicado: (2012)

A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia
por: Othman, Moneeb A. K., et al.
Publicado: (2014)

Hypertension and the roles of the 9p21.3 risk locus: Classic findings and new association data
por: Gallo, Juan E., et al.
Publicado: (2020)

High shear stress enhances endothelial permeability in the presence of the risk haplotype at 9p21.3
por: Teng, Evan L., et al.
Publicado: (2021)

MACHETE identifies interferon-encompassing chromosome 9p21.3 deletions as mediators of immune evasion and metastasis
por: Barriga, Francisco M., et al.
Publicado: (2022)

Single-nucleotide polymorphism rs731384 is associated with plasma lipid levels and the risk of coronary artery disease in Chinese populations
por: Zhao, Chenhui, et al.
Publicado: (2018)

On the Wegener granulomatosis associated region on chromosome 6p21.3
por: Szyld, Paweł, et al.
Publicado: (2006)

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)

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis
por: Chen, Suet Nee, et al.
Publicado: (2009)

A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma
por: Frigerio, Simona, et al.
Publicado: (2014)

Polymorphism of 9p21.3 Locus Is Associated with 5-Year Survival in High-Risk Patients with Myocardial Infarction
por: Szpakowicz, Anna, et al.
Publicado: (2014)

Polymorphism of 9p21.3 Locus Is Associated with 5-Year Survival in High-Risk Patients with Myocardial Infarction
por: Szpakowicz, Anna, et al.
Publicado: (2013)

Effect of 9p21.3 (lncRNA and CDKN2A/2B) variant on lipid profile
por: Wei, Baozhu, et al.
Publicado: (2022)

Deletion of the murine ortholog of human 9p21.3 locus promotes atherosclerosis by increasing macrophage proinflammatory activity
por: Kettunen, Sanna, et al.
Publicado: (2023)

Targeted sequencing of the 9p21.3 region reveals association with reduced disease risks in Ashkenazi Jewish centenarians
por: Zhu, Yizhou, et al.
Publicado: (2023)

Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland
por: Clark, Jeremy S. C., et al.
Publicado: (2022)

HDAC9 Variant Rs2107595 Modifies Susceptibility to Coronary Artery Disease and the Severity of Coronary Atherosclerosis in a Chinese Han Population
por: Wang, Xue-bin, et al.
Publicado: (2016)

Association of the single nucleotide polymorphism in chromosome 9p21 and chromosome 9q33 with coronary artery disease in Chinese population
por: Li, Qi, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_bp8b2ir9flvvcatf9sj635q7ei