Cargando…

Potential Impact of COMT-rs4680 G > A Gene Polymorphism in Coronary Artery Disease

Purpose: Catechol-O-methyltransferase (COMT) plays a central role in DNA repair and estrogen-induced carcinogenesis. The nonsynonymous single nucleotide polymorphism (SNP) in exon 4 G > A or Val108 > 158Met or rs4680 G > A influences COMT enzyme activity. The three phenotypes of the COMT en...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mir, Rashid, Bhat, Musadiq, Javid, Jamsheed, Jha, Chandan, Saxena, Alpana, Banu, Shaheen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2018
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162781/ https://www.ncbi.nlm.nih.gov/pubmed/30011860 http://dx.doi.org/10.3390/jcdd5030038

Ejemplares similares

Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study
por: Jha, Chandan K, et al.
Publicado: (2019)

Reply to Comment: Evaluation of the Association of Omentin 1 rs2274907 A > T and rs2274908 G > A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case–Control Study
por: Jha, Chandan K., et al.
Publicado: (2020)

Evaluation of the Association of COMT Rs4680 Polymorphism with Swimmers’ Competitive Performance
por: Zmijewski, Piotr, et al.
Publicado: (2021)

Association Between the rs4680 Polymorphism of the COMT Gene and Personality Traits among Combat Sports Athletes
por: Humińska-Lisowska, Kinga, et al.
Publicado: (2023)

The Influence of 5-HTTLPR, BDNF Rs6265 and COMT Rs4680 Polymorphisms on Impulsivity in Bipolar Disorder: The Role of Gender
por: Boscutti, Andrea, et al.
Publicado: (2022)

Frequency Distribution of COMT Polymorphisms in Greek Patients with Schizophrenia and Controls: A Study of SNPs rs737865, rs4680, and rs165599
por: Maria, Kotrotsou, et al.
Publicado: (2012)

Effects of COMT rs4680 and BDNF rs6265 polymorphisms on brain degree centrality in Han Chinese adults who lost their only child
por: Qi, Rongfeng, 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)

Associations between the COMT rs4680 Gene Polymorphism and Personality Dimensions and Anxiety in Patients with a Diagnosis of Other Stimulants Dependence
por: Chmielowiec, Krzysztof, et al.
Publicado: (2022)

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)

Influence of COMT (rs4680) and DRD2 (rs1076560, rs1800497) Gene Polymorphisms on Safety and Efficacy of Methylphenidate Treatment in Children with Fetal Alcohol Spectrum Disorders
por: Śmiarowska, Małgorzata, et al.
Publicado: (2022)

Evidence for the contribution of COMT gene Val158/108Met polymorphism (rs4680) to working memory training‐related prefrontal plasticity
por: Zhao, Wan, et al.
Publicado: (2020)

Association of rs4680 COMT, rs6280 DRD3, and rs7322347 5HT2A With Clinical Features of Youth-Onset Schizophrenia
por: Morozova, Anna, et al.
Publicado: (2019)

Parent-Adolescent Conflict, Depressive Symptoms, and Non-Suicidal Self-Injury among Chinese Adolescents: The Moderating Effect of the COMT Gene rs4680 Polymorphism
por: Deng, Yuting, et al.
Publicado: (2022)

Association between Catechol-O-methyltransferase rs4680 (G > A) polymorphism and lung cancer risk
por: Tan, Xiang, et al.
Publicado: (2014)

Haplotypic and Genotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Polymorphisms and Treatment Resistance in Schizophrenia
por: Sagud, Marina, et al.
Publicado: (2018)

LDLR rs688 TT Genotype and T Allele Are Associated with Increased Susceptibility to Coronary Artery Disease—A Case-Control Study
por: Jha, Chandan K., et al.
Publicado: (2018)

Genotypic and Haplotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Gene Polymorphisms with Particular Clinical Symptoms in Schizophrenia
por: Sagud, Marina, et al.
Publicado: (2023)

Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study
por: De Marchis, Maria Laura, et al.
Publicado: (2015)

Polymorphism T81C in H-RAS Oncogene Is Associated With Disease Progression in Imatinib (TKI) Treated Chronic Myeloid Leukemia Patients
por: Mir, Rashid, et al.
Publicado: (2015)

Effect of catechol-O-methyltransferase (rs4680) single-nucleotide polymorphism on opioid-induced hyperalgesia in adults with chronic pain
por: Hooten, W Michael, et al.
Publicado: (2019)

Impact of Catechol-O-Methyltransferase Val 158Met (rs4680) Polymorphism on Breast Cancer Susceptibility in Asian Population
por: Rai, Vandana, et al.
Publicado: (2017)

Catechol-O-methyltransferase rs4680 and rs4818 haplotype association with treatment response to olanzapine in patients with schizophrenia
por: Nikolac Perkovic, Matea, et al.
Publicado: (2020)

Lack of Association between rs4680 Polymorphism in Catechol-O-Methyltransferase Gene and Alcohol Use Disorder: A Meta-Analysis
por: Jin, Xin-Rong, et al.
Publicado: (2020)

Clinical Utility of Amplification Refractory Mutation System-Based PCR and Mutation-Specific PCR for Precise and Rapid Genotyping of Angiotensin-Converting Enzyme 1 (ACE1-rs4646996 D>I) and Angiotensin-Converting Enzyme 2 (ACE2-rs4240157T>C) Gene Variations in Coronary Artery Disease and Their Strong Association with Its Disease Susceptibility and Progression
por: Yousif, Aadil, et al.
Publicado: (2022)

Clinical implications of cytosine deletion of exon 5 of P53 gene in non small cell lung cancer patients
por: Mir, Rashid, et al.
Publicado: (2016)

The Role of Catechol-O-Methyl Transferase Val(108/158)Met Polymorphism (rs4680) in the Effect of Green Tea on Resting Energy Expenditure and Fat Oxidation: A Pilot Study
por: Hursel, Rick, et al.
Publicado: (2014)

3255 Association between dopaminergic genetic variants, COMTrs4680 and DRD2rs1076560, and alcohol consumption and reward behaviors in non-dependent drinkers
por: Ortega, Nancy Elizabeth, et al.
Publicado: (2019)

Association study of single nucleotide polymorphism rs165599 of COMT gene, with schizophrenia and bipolar mood disorder in the south-west of Iran
por: Behbahani, Parisima, et al.
Publicado: (2015)

Comte
por: Marvin, Francis Sydney, 1863-1943
Publicado: (1941)

Count on dopamine: influences of COMT polymorphisms on numerical cognition
por: Júlio-Costa, Annelise, et al.
Publicado: (2013)

Pain in Parkinson's Disease Associated with COMT Gene Polymorphisms
por: Li, Wanjun, et al.
Publicado: (2014)

Analysis of the relationship between COMT polymorphisms and endometriosis susceptibility
por: Zhai, Jiajia, et al.
Publicado: (2019)

Interleukin-6 (IL-6)-597 A/G (rs1800797) & -174 G/C (rs1800795) gene polymorphisms in type 2 diabetes
por: Saxena, Madhukar, et al.
Publicado: (2014)

Differential Expression of Serum Proinflammatory Cytokine TNF-α and Genetic Determinants of TNF-α, CYP2C19*17, miR-423 Genes and Their Effect on Coronary Artery Disease Predisposition and Progression
por: Almassabi, Rehab F., et al.
Publicado: (2023)

Clinical Significance of Circulatory miRNA-21 as an Efficient Non-Invasive Biomarker for the Screening of Lung Cancer Patients
por: Abu-Duhier, F M, et al.
Publicado: (2018)

The IL-6 rs1800795 and rs1800796 polymorphisms are associated with coronary artery disease risk
por: Lu, Shuai, et al.
Publicado: (2020)

The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease
por: Nowak, Tomasz, et al.
Publicado: (2016)

COMT val158met Polymorphism and Neural Pain Processing
por: Schmahl, Christian, et al.
Publicado: (2012)

A Meta-Analysis on the Association Between TNFSF4 Polymorphisms (rs3861950 T > C and rs1234313 A > G) and Susceptibility to Coronary Artery Disease
por: Liu, Shuyan, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_i0hnat1q8n9okju0lm8hqrtd2f