Cargando…

Association of rs10757274 and rs2383206 Polymorphisms on 9p21 locus with Coronary Artery Disease in Turkish Population

BACKGROUND AND OBJECTIVES: Genetic predisposition is an important risk factor for coronary artery disease (CAD). In this study, we aimed to evaluate the impact of rs10757274 and rs2383206 polymorphisms in chromosome 9p21 on presence and severity of CAD in a Turkish population. SUBJECTS AND METHODS:...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yayla, Çağrı, Okyay, Kaan, Yılmaz, Akın, Şahinarslan, Asife, Yar Sağlam, Atiye Seda, Eyiol, Azmi, Bolayır, Hasan Ata, Sezenöz, Burak, Menevşe, Sevda, Çengel, Atiye
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society of Cardiology 2016
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054172/ https://www.ncbi.nlm.nih.gov/pubmed/27721851 http://dx.doi.org/10.4070/kcj.2016.46.5.615

Ejemplares similares

Association between rs10757274 and rs2383206 SNPs as Genetic Risk Factors in Iranian Patients with Coronary Artery Disease
por: Aleyasin, Seyed Ahmad, et al.
Publicado: (2017)

Effect of API-1 and FR180204 on cell proliferation and apoptosis in human DLD-1 and LoVo colorectal cancer cells
por: Saglam, Atiye Seda Yar, et al.
Publicado: (2016)

Higher ultrafiltration rate is associated with right ventricular mechanical dispersion
por: Ünlü, Serkan, et al.
Publicado: (2019)

Prostaglandin F receptor expression in intrauterine tissues of pregnant rats
por: Anadol, Elvan, et al.
Publicado: (2014)

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)

Phenoxodiol sensitizes metastatic colorectal cancer cells to 5-fluorouracil- and oxaliplatin-induced apoptosis through intrinsic pathway
por: Yaylaci, Esra, et al.
Publicado: (2020)

The role of oxidative DNA damage and GSTM1, GSTT1, and hOGG1 gene polymorphisms in coronary artery disease risk
por: Kadıoğlu, Ela, et al.
Publicado: (2016)

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)

Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population
por: Nawaz, Syed Kashif, et al.
Publicado: (2015)

Metabolic Dysregulation of the Lysophospholipid/Autotaxin Axis in the Chromosome 9p21 Gene SNP rs10757274
por: Meckelmann, Sven W., et al.
Publicado: (2020)

Rs10757274 gene polymorphisms in coronary artery disease: A systematic review and a meta-analysis
por: Xu, Lang-Biao, et al.
Publicado: (2020)

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)

Turkish Society of Cardiology consensus report on the rational use of cardiac troponins in daily practice
por: Okyay, Kaan, et al.
Publicado: (2019)

Association between parathyroid hormone levels and the extensiveness of coronary artery disease
por: Alsancak, Yakup, et al.
Publicado: (2016)

Consensus paper on the evaluation and treatment of resistant hypertension by the Turkish Society of Cardiology
por: Şahinarslan, Asife, et al.
Publicado: (2020)

HDAC inhibitors, MS-275 and salermide, potentiates the anticancer effect of EF24 in human pancreatic cancer cells
por: Yar Saglam, Atiye Seda, et al.
Publicado: (2016)

Neutrophil-to-lymphocyte ratio is increased in patients with rheumatic mitral valve stenosis?
por: Akboğa, Mehmet Kadri, et al.
Publicado: (2015)

Heart rate variability in Eisenmenger syndrome and its correlation with echocardiographic parameters and plasma BNP, high sensitivity troponin-I level
por: Sezenöz, Burak, et al.
Publicado: (2017)

Interaction of type 2 diabetes mellitus with Chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case–control study in Chinese population
por: Zhang, Liu-wei, et al.
Publicado: (2014)

Investigation of chicken housekeeping genes using next-generation sequencing data
por: Hasanpur, Karim, et al.
Publicado: (2022)

Relationship Between MMP-1, MMP-9, TIMP-1, IL-6 and Risk Factors, Clinical Presentation, Extent and Severity of Atherosclerotic Coronary Artery Disease
por: Tanindi, Asli, et al.
Publicado: (2011)

The Evaluation of Diastolic Dysfunction with Tissue Doppler Echocardiography in Women with Subclinical Hypothyroidism and the Effect of L-Thyroxine Treatment on Diastolic Dysfunction: A Pilot Study
por: Erkan, Gulbanu, et al.
Publicado: (2011)

The effect of periodontal therapy on neopterin and vascular cell adhesion molecule-1 levels in chronic periodontitis patients with and without acute myocardial infarction: a case-control study
por: Turgut Çankaya, Zeynep, et al.
Publicado: (2018)

Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian Population
por: Razavian, Takavar, et al.
Publicado: (2020)

Association of FTO common variant (rs9939609) with body fat in Turkish individuals
por: AĞAGÜNDÜZ, Duygu, et al.
Publicado: (2019)

Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia
por: Bănescu, Claudia, et al.
Publicado: (2019)

Determinação do Tecido Cicatricial do Miocárdio no Fenômeno de Fluxo Coronário Lento e a Relação entre a Quantidade de Tecido Cicatricial e o Nt-ProBNP
por: Candemir, Mustafa, et al.
Publicado: (2020)

Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children
por: Buda, Piotr, et al.
Publicado: (2021)

Case-control study on PCSK9 R496W (rs374603772) and D374Y (rs137852912) mutations in Turkish patients with primary dyslipidemia
por: Eroğlu, Zuhal, et al.
Publicado: (2018)

Association of ESR1 (rs2234693 and rs9340799), CETP (rs708272), MTHFR (rs1801133 and rs2274976) and MS (rs185087) polymorphisms with Coronary Artery Disease (CAD)
por: Raina, Jyotdeep Kour, et al.
Publicado: (2020)

TIRAP Rs8177376, Rs611953, Rs3802814, and Rs8177374 Polymorphisms and Their Association with Cervical Cancer Phenotype and Prognosis
por: Bekampytė, Justina, et al.
Publicado: (2022)

PSMA6 (rs2277460, rs1048990), PSMC6 (rs2295826, rs2295827) and PSMA3 (rs2348071) genetic diversity in Latvians, Lithuanians and Taiwanese
por: Sjakste, Tatjana, et al.
Publicado: (2014)

Association between interleukin 6 polymorphisms (rs1800796, rs1800795, rs2069837, rs17147230, and rs1800797) and hepatocellular carcinoma susceptibility: a meta-analysis
por: Aleagha, Omid Emami, et al.
Publicado: (2020)

Genetic Variations of DAOA (rs947267 and rs3918342) and COMT Genes (rs165599 and rs4680) in Schizophrenia and Bipolar I Disorder
por: Ahmadi, Leila, et al.
Publicado: (2018)

Functional Analysis of the rs774872314, rs116171003, rs200231898 and rs201107751 Polymorphisms in the Human RORγT Gene Promoter Region
por: Ratajewski, Marcin, et al.
Publicado: (2017)

Increased serum YKL-40 level is associated with the presence and severity of metabolic syndrome
por: Akboğa, Mehmet Kadri, et al.
Publicado: (2016)

Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson’s disease risks
por: Bai, Ye, et al.
Publicado: (2017)

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis
por: Liu, Jia, et al.
Publicado: (2021)

The Correlation of Mouse Double Minute 4 (MDM4) Polymorphisms (rs4245739, rs1563828, rs11801299, rs10900598, and rs1380576) with Cancer Susceptibility: A Meta-Analysis
por: Chen, Jian, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_nk2auka5n0t5e38j1nf0v9sfiu