Associated Papers
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
Association of Paraoxonase-1 (p.L55M) and Paraoxonase-2 (p.S311C) polymorphisms with coronary artery disease in North Indian Punjabi population.
Bhat MA et al.
Frontiers in Endocrinology, 2025
A Case-Control Study Supports Genetic Contribution of the PON Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver Disease.
Van Dijck E et al.
Antioxidants (basel, Switzerland), 2024
Paraoxonase 2 Deficiency Causes Mitochondrial Dysfunction in Retinal Pigment Epithelial Cells and Retinal Degeneration in Mice.
Sreekumar PG et al.
Antioxidants (basel, Switzerland), 2023
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease.
Menezes JF et al.
Scientific Reports, 2023
Proteomic Exploration of Paraoxonase 1 Function in Health and Disease.
Jakubowski H
International Journal of Molecular Sciences, 2023
Germline genetic variants are associated with development of insulin-dependent diabetes in cancer patients treated with immune checkpoint inhibitors.
Caulfield JI et al.
Journal for Immunotherapy of Cancer, 2023
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.
Boukhalfa W et al.
Frontiers in Aging Neuroscience, 2023
Paraoxonase 2 (PON2) Deficiency Reproduces Lipid Alterations of Diabetic and Inflammatory Glomerular Disease and Affects TRPC6 Signaling.
Hagmann H et al.
Cells, 2022
Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.
Shi M et al.
Journal of the American Heart Association, 2022
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Young WJ et al.
Nature Communications, 2022
Coronary Heart Disease in Type 2 Diabetes Mellitus: Genetic Factors and Their Mechanisms, Gene-Gene, and Gene-Environment Interactions in the Asian Populations.
Zarkasi KA et al.
International Journal of Environmental Research and Public Health, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations.
Pei J et al.
Clinical Epigenetics, 2021
The Relevance of Noncoding DNA Variations of Paraoxonase Gene Cluster in Atherosclerosis-Related Diseases.
Wysocka A et al.
International Journal of Molecular Sciences, 2021
Association between human paraoxonase 2 protein and efficacy of acetylcholinesterase inhibiting drugs used against Alzheimer's disease.
Parween F et al.
Plos One, 2021
Paraoxonase single nucleotide variants show associations with polycystic ovary syndrome: a meta-analysis.
Kunjantarachot A et al.
Reproductive Biology and Endocrinology : Rb&e, 2020
WTAP and BIRC3 are involved in the posttranscriptional mechanisms that impact on the expression and activity of the human lactonase PON2.
Carusone TM et al.
Cell Death & Disease, 2020
Importance of paraoxonase 1 (PON1) as an antioxidant and antiatherogenic enzyme in the cardiovascular complications of type 2 diabetes: Genotypic and phenotypic evaluation.
Shokri Y et al.
Diabetes Research and Clinical Practice, 2020
Susceptibility of PON1/PON2 Genetic Variations to Ischemic Stroke Risk in a Chinese Han Population.
Pan Y et al.
Pharmacogenomics and Personalized Medicine, 2020
Association of SOD2 A16V and PON2 S311C polymorphisms with polycystic ovary syndrome in Chinese women.
Liu Q et al.
Journal of Endocrinological Investigation, 2019
Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patients.
Bhuvaneshwar K et al.
Bmc Cancer, 2019
Paraoxonase 1 Gene L55M Polymorphism and Paraoxonase 1 Activity in Obstructive Sleep Apnea Patients.
Płóciniczak A et al.
Advances in Experimental Medicine and Biology, 2019
Paraoxonase 1 (PON1)-L55M among common variants in the coding region of the paraoxonase gene family may contribute to the glycemic control in type 2 diabetes.
Mahrooz A et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2018
Genetic polymorphisms in amyotrophic lateral sclerosis: Evidence for implication in detoxification pathways of environmental toxicants.
Dardiotis E et al.
Environment International, 2018
PON2 and PPARG polymorphisms as biomarkers of risk for coronary heart disease.
González-Castro TB et al.
Biomarkers in Medicine, 2018
Paraoxonase (PON)-1: a brief overview on genetics, structure, polymorphisms and clinical relevance.
Shunmoogam N et al.
Vascular Health and Risk Management, 2018
Association of PON2 Gene Polymorphisms (Ser311Cys and Ala148Gly) With the Risk of Developing Type 2 Diabetes Mellitus in the Chinese Population.
Ren H et al.
Frontiers in Endocrinology, 2018
Paraoxonase-2 variants potentially influence insulin resistance, beta-cell function, and their interrelationships with alanine aminotransferase in type 2 diabetes.
Qujeq D et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences, 2018
A Meta-Analysis on the Relationship of the PON Genes and Alzheimer Disease.
Nie Y et al.
Journal of Geriatric Psychiatry and Neurology, 2017
Regulation of the epithelial Na+ channel by paraoxonase-2.
Shi S et al.
The Journal of Biological Chemistry, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK.
Morgan S et al.
Brain : a Journal of Neurology, 2017
Paraoxonase 1 and 2 gene variants and the ischemic stroke risk in Gran Canaria population: an association study and meta-analysis.
Rodríguez-Esparragón F et al.
The International Journal of Neuroscience, 2017
Association Between Paraoxonase 2 Ser311Cys Polymorphism and Coronary Heart Disease Risk: A Meta-Analysis.
Chen ML et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2016
Antioxidant-related gene polymorphisms associated with the cardio-ankle vascular index in young Russians.
Sorokin AV et al.
Cardiology in the Young, 2016
Association Between Paraoxonase Gene Polymorphisms and Intracerebral Hemorrhage in a Korean Population.
Park HJ et al.
Journal of Molecular Neuroscience : Mn, 2015
Identification of HPV integration and gene mutation in HeLa cell line by integrated analysis of RNA-Seq and MS/MS data.
Sun H et al.
Journal of Proteome Research, 2015
Association between Genetic Variants and Diabetes Mellitus in Iranian Populations: A Systematic Review of Observational Studies.
Khodaeian M et al.
Journal of Diabetes Research, 2015
Targeted exon capture and sequencing in sporadic amyotrophic lateral sclerosis.
Couthouis J et al.
Plos Genetics, 2014
Renin-angiotensin system genetic polymorphisms and brain white matter lesions in older Australians.
Assareh AA et al.
American Journal of Hypertension, 2014
Genes involved in the regulation of vascular homeostasis determine renal survival rate in patients with chronic glomerulonephritis.
Litovkina O et al.
Gene, 2014
Gene-environment interaction among GSTT1, PON2 polymorphisms and organic solvents on gestational age in a Chinese women cohort.
Li S et al.
Journal of Assisted Reproduction and Genetics, 2014
Genetic score based on high-risk genetic polymorphisms and early onset of ischemic heart disease in an Italian cohort of ischemic patients.
Vecoli C et al.
Thrombosis Research, 2014
Antioxidant defense enzyme genes and asthma susceptibility: gender-specific effects and heterogeneity in gene-gene interactions between pathogenetic variants of the disease.
Polonikov AV et al.
Biomed Research International, 2014
Association of paraoxonase gene polymorphisms with diabetic nephropathy and retinopathy.
Wang J et al.
Molecular Medicine Reports, 2013
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing.
Kenna KP et al.
Journal of Medical Genetics, 2013
Association of paraoxonase polymorphisms with carotid artery atherosclerosis in essential hypertension patients.
Han L et al.
Genetics and Molecular Research : Gmr, 2013
Association of polymorphism of ser311cys paraoxonase-2 gene with type 2 diabetes mellitus in iran.
Andalib S et al.
International Journal of Preventive Medicine, 2013