Cargando…

Chromosome 9p21.3 is Associated with Early-Onset Coronary Heart Disease in the Irish Population

Coronary heart disease (CHD) remains a leading cause of death across the world. A region on chromosome 9p21.3 has been recently reported to be associated with CHD. We evaluated 3 SNPs and 3 common haplotypes in the 9p21.3 region in 1494 individuals from 580 Irish families, where at least 1 member ha...

Descripción completa

Detalles Bibliográficos
Autores principales:	Meng, Weihua, Hughes, Anne E., Patterson, Chris C., Belton, Christine, Kee, Frank, McKeown, Pascal P.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	IOS Press 2008
Materias:	Other
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827790/ https://www.ncbi.nlm.nih.gov/pubmed/18957718 http://dx.doi.org/10.1155/2008/375617

Ejemplares similares

Genetic variants of Complement factor H gene are not associated with premature coronary heart disease: a family-based study in the Irish population
por: Meng, Weihua, et al.
Publicado: (2007)

Lack of MEF2A Δ7aa mutation in Irish families with early onset ischaemic heart disease, a family based study
por: Horan, Paul G, et al.
Publicado: (2006)

Polymorphism on Chromosome 9p21.3 Is Associated with Severity and Early-Onset CAD in Type 2 Diabetic Tunisian Population
por: Abid, Kaouthar, et al.
Publicado: (2015)

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)

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)

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)

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)

Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia
por: Ma, Yuanlin, et al.
Publicado: (2015)

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

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)

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

The Matrix Metalloproteinase-3 (MMP-3) 5A/6A Promoter Polymorphism Is Not Associated with Ischaemic Heart Disease: Analysis Employing a Family Based Approach
por: McGlinchey, Paul G., et al.
Publicado: (2004)

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)

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)

Clinical characterization of chromosome 5q21.1–21.3 microduplication: A case report
por: Chen, Shuang, et al.
Publicado: (2020)

Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese population
por: Yan, Jianjun, et al.
Publicado: (2016)

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)

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)

Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering
por: Abe, Satoshi, et al.
Publicado: (2010)

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)

Interaction between a variant of chromosome 9p21.3 locus and diet antioxidant capacity on metabolic syndrome in Tehrani adults
por: Mirzababaei, Atieh, et al.
Publicado: (2018)

Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study
por: Semaev, Sergey, et al.
Publicado: (2023)

Human chromosome 3p21.3 carries TERT transcriptional regulators in pancreatic cancer
por: Yagyu, Takuki, et al.
Publicado: (2021)

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry
por: Scheffold, Thomas, et al.
Publicado: (2011)

An extra chromosome 9 derived from either a normal chromosome 9 or a derivative chromosome 9 in a patient with acute myeloid leukemia positive for t(9;11)(p21.3;q23.3): A case report
por: Gao, Man, et al.
Publicado: (2019)

Antibody prevalence to avian influenza virus subtypes H5, H7 and H9 in falcons, captive and wild birds, United Arab Emirates, 2003–2006
por: Jöstl, Nicola, et al.
Publicado: (2023)

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)

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)

Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort
por: Ernst, Florian D, et al.
Publicado: (2010)

Deletions at the chromosome 3 common eliminated region 1 on 3p21.3 in human breast tumors
por: Petursdottir, ThE, et al.
Publicado: (2005)

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)

Detection and control of an ongoing international outbreak of hepatitis A among the Irish Traveller community beginning September 2020
por: Kelly, David, et al.
Publicado: (2022)

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)

Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A
por: Spena, Silvia, et al.
Publicado: (2022)

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)

Mediating Effect of Diabetes Mellitus on the Association Between Chromosome 9p21.3 Locus and Myocardial Infarction Risk: A Case-Control Study in Shanghai, China
por: Wu, Zhijun, et al.
Publicado: (2018)

4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects
por: Iourov, Ivan Y., et al.
Publicado: (2018)

A replicative association study of Chromosome 6p21.3 with susceptibility to leprosy in an Indian population - 'a string hypothesis'
por: Ali, Shafat, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_p13ltbkbkfg38k50vo4rfame8c