Cargando…

Association of the CYP1A1 rs4646903 polymorphism with susceptibility and severity of coronary artery disease

Given the significant physical, mental, and economic problems of coronary artery disease (CAD), it is important for communities to help reduce these costs. The Cytochrome P450 Family 1 Subfamily A Member 1) CYP1A1 (enzyme is known to cause coronary artery disease through various mechanisms. Therefor...

Descripción completa

Detalles Bibliográficos
Autores principales:	Eskandari, Mahsa, Awsat Mellati, Ali, Mahmoodi, Khalil, Kamali, Koorosh, Soltanpour, Mohammad Soleiman
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Shiraz University 2021
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310655/ https://www.ncbi.nlm.nih.gov/pubmed/34316491 http://dx.doi.org/10.22099/mbrc.2021.39141.1574

Ejemplares similares

Assessment of the role of plasma nitric oxide levels, T-786C genetic polymorphism, and gene expression levels of endothelial nitric oxide synthase in the development of coronary artery disease
por: Mahmoodi, Khalil, et al.
Publicado: (2017)

Plasma concentration, genetic variation, and gene expression levels of matrix metalloproteinase 9 in Iranian patients with coronary artery disease
por: Mahmoodi, Khalil, et al.
Publicado: (2017)

CYP1A1 rs1048943 and rs4646903 polymorphisms associated with laryngeal cancer susceptibility among Asian populations: a meta‐analysis
por: Zeng, Wei, et al.
Publicado: (2015)

Liver X Receptor as a Possible Drug Target for Blood-Brain Barrier Integrity
por: Eskandari, Mahsa, et al.
Publicado: (2022)

A preliminary study of the association between the ABCA1 gene promoter DNA methylation and coronary artery disease risk
por: Ghaznavi, Habib, et al.
Publicado: (2018)

Association between CYP1A1 rs4646903 T > C genetic variations and male infertility risk: A meta-analysis
por: Cao, DeHong, et al.
Publicado: (2019)

Association of Nitric Oxide Levels and Endothelial Nitric Oxide Synthase G894T Polymorphism with Coronary Artery Disease in the Iranian Population
por: Mahmoodi, Khalil, et al.
Publicado: (2016)

The association between NFKB1 -94ATTG ins/del and NFKB1A 826C/T genetic variations and coronary artery disease risk
por: Seidi, Abbas, et al.
Publicado: (2018)

Association between CYP1A1 rs4646903 T > C genetic variations and male infertility risk: A meta-analysis: Erratum
Publicado: (2019)

Genotype of Null Polymorphisms in Genes GSTM1, GSTT1, CYP1A1, and CYP1A1*2A (rs4646903 T>C)/CYP1A1*2C (rs1048943 A>G) in Patients with Larynx Cancer in Southeast Spain
por: Sánchez-Siles, Mariano, et al.
Publicado: (2020)

Associations between CYP1A1 rs1048943 A > G and rs4646903 T > C genetic variations and colorectal cancer risk: Proof from 26 case-control studies
por: Zhu, Xueru, et al.
Publicado: (2016)

Association Study of the ATP - Binding Cassette Transporter A1 (ABCA1) Rs2230806 Genetic Variation with Lipid Profile and Coronary Artery Disease Risk in an Iranian Population
por: Ghaznavi, Habib, et al.
Publicado: (2018)

Promoter Hypermethylation of Wnt/β-catenin Signaling Pathway Inhibitor WIF-1 Gene and its Association with MTHFR C677T Polymorphism in Patients with Colorectal Cancer
por: Jalilvand, Ahmad, et al.
Publicado: (2020)

Association study between DNA methylation and genetic variation of APOE gene with the risk of coronary artery disease
por: Ghaznavi, Habib, et al.
Publicado: (2018)

Polymorphisms CYP2R1 rs10766197 and CYP27B1 rs10877012 in Multiple Sclerosis: A Case-Control Study
por: Martinez-Hernandez, A., et al.
Publicado: (2021)

NFKB1 gene rs28362491 polymorphism is associated with the susceptibility of acute coronary syndrome
por: Jin, Si-Yu, et al.
Publicado: (2019)

Vitamin D Receptor rs2228570 and rs731236 Polymorphisms are Susceptible Factors for Systemic Lupus Erythematosus
por: Salimi, Saeedeh, et al.
Publicado: (2019)

A Report of High Triglyceride Level in Cord Blood of Iranian Newborns
por: Kazemi, Seyed Ali Naghi, et al.
Publicado: (2013)

Polymorphisms in Phase I (CYP450) Genes CYP1A1 (rs4646421), CYP1B1 (rs1056836), CYP19A1 (rs749292) and CYP2C8 (rs1058930) and Their Relation to Risk of Breast Cancer: A Case-Control Study in Mazandaran Province in North of Iran
por: Golmohammadzadeh, Golpar, et al.
Publicado: (2019)

Prognostic Value of CYP1A2 (rs2069514 and rs762551) Polymorphisms in COVID-19 Patients
por: Bozkurt, I, et al.
Publicado: (2023)

Comparative Proteomics Study of Streptozotocin-induced Diabetic Nephropathy in Rats Kidneys Transfected with Adenovirus-mediated Fibromodulin Gene
por: Maleki, Akram, et al.
Publicado: (2014)

CYP17A1 rs743572 polymorphism might contribute to endometriosis susceptibility: evidences from a case–control study
por: Cong, Lili, et al.
Publicado: (2018)

LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population
por: K. Jha, Chandan, et al.
Publicado: (2019)

Association of RB1 rs9568036 and CDKN1A rs1801270 Polymorphisms with Retinoblastoma Susceptibility
por: Azimi, Fatemeh, et al.
Publicado: (2022)

Association of CYP1A1 rs1048943 Polymorphism with Prostate Cancer in Iraqi Men Patients
por: Hoidy, Wisam H, et al.
Publicado: (2019)

Impact of rs2414096 polymorphism of CYP19 gene on susceptibility of polycystic ovary syndrome and hyperandrogenism in Kashmiri women
por: Ashraf, Sairish, et al.
Publicado: (2021)

Polymorphisms of CYP1A1 and GSTM1 Genes and Susceptibility to Oral Cancer
por: Cha, In-Ho, et al.
Publicado: (2007)

Association of Methylenetetrahydrofolate Reductase C677T Polymorphism with Hyperhomocysteinemia and Deep Vein Thrombosis in the Iranian Population
por: Ghaznavi, Habib, et al.
Publicado: (2015)

Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis
por: Ghaznavi, Habib, et al.
Publicado: (2016)

CYP1A2 rs762551 polymorphism contributes to cancer susceptibility: a meta-analysis from 19 case-control studies
por: Wang, Hongge, et al.
Publicado: (2012)

Association between myeloperoxidase rs2333227 polymorphism and susceptibility to coronary heart disease
por: Zhang, Yi-Qing, et al.
Publicado: (2020)

Polymorphism in CYP1A1 and CYP2D6 genes: possible association with susceptibility to lung cancer.
por: Hirvonen, A, et al.
Publicado: (1993)

Rs420137, rs386360 and rs7763726 polymorphisms in fibronectin type III domain containing 1 are associated with susceptibility to coronary heart disease: Analysis in the Han population
por: He, Xiaodan, et al.
Publicado: (2022)

CYP27B1 Gene Polymorphism rs10877012 in Patients Diagnosed with Colorectal Cancer
por: Latacz, Maria, et al.
Publicado: (2020)

ADORA2A rs5760423 and CYP1A2 rs762551 Polymorphisms as Risk Factors for Parkinson’s Disease
por: Siokas, Vasileios, et al.
Publicado: (2021)

Association among VKORC1 rs9923231, CYP4F2 rs2108622, GGCX rs11676382 polymorphisms and acute ischemic stroke
por: Iluţ, Silvina, et al.
Publicado: (2023)

Co-Administration of Vitamin E and Atorvastatin Improves Insulin Sensitivity and Peroxisome Proliferator-Activated Receptor-γ Expression in Type 2 Diabetic Patients: A Randomized Double-Blind Clinical Trial
por: Tabaei, Banafsheh Sadat, et al.
Publicado: (2022)

Single-Nucleotide Polymorphism rs7251246 in ITPKC Is Associated with Susceptibility and Coronary Artery Lesions in Kawasaki Disease
por: Kuo, Ho-Chang, et al.
Publicado: (2014)

CYP1B1 Polymorphisms and Susceptibility to Prostate Cancer: A Meta-Analysis
por: Zhang, Hongtuan, et al.
Publicado: (2013)

The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population
por: Qrafli, Mounia, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_p9t7s3stmbbkl7bfd8plul4jtm