About: The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study

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About: The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1996 (uk) article scientifique publié en 1996 (fr) im Oktober 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 1996 (ast) scientific article published on 01 October 1996 (en)
publication date	wds:Q59660648-E33F5674-D2AB-4F15-A9A0-8264B7E53FED
publication date	1996-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q59660648-0FACD5E1-5997-4E0F-A564-9B1AB4C4D66C wds:Q59660648-15F9E4E3-6DC0-4D5E-AABB-AB3BF155898C wds:Q59660648-3AA911FF-1437-474D-B53C-85474DBBA0B1 wds:Q59660648-7E1B9F05-7E60-4044-8025-D52C9BFEE8CB wds:Q59660648-CF305318-DA9E-4E20-8D96-23D49EF7A342 wds:Q59660648-E65719CA-5A18-4023-842A-257AFAD8AB01 wds:Q59660648-EEE92A7D-30F3-4C32-BA09-E5234ECAA63C wds:Q59660648-FA149DEA-E323-48B8-A5B3-466AB44EC4C5
author name string	A Evans D Arveiler F Cambien G Luc J M Bard S M Herrmann H Blanc O Poirier
rdfs:label	The Gln/Arg polymorphism of human paraoxonase (nl) The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study (en)
skos:prefLabel	The Gln/Arg polymorphism of human paraoxonase (nl) The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study (en)
name	The Gln/Arg polymorphism of human paraoxonase (nl) The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study (en)
author	wds:Q59660648-0F4FD8A6-AAD7-448D-B082-8DB921D78F57
author	Pedro Marques-Vidal
title	wds:Q59660648-AF530D9C-619E-432A-80B4-CA276289A6FF
title	The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study (en)
page(s)	wds:Q59660648-41C2D51D-CDBE-4111-8732-48D4ADED3792
page(s)	299-303
instance of	wds:Q59660648-8377795F-C1D4-417E-8619-25FD93C60731
instance of	scholarly article
main subject	wds:Q59660648-4B78A6A2-F08F-4E66-B58B-3217492834EE
main subject	myocardial infarction
PubMed ID	wds:Q59660648-2FB8ED81-6D0B-42AE-A431-302B9A62A6B7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8902155
PubMed ID	8902155
published in	wds:Q59660648-4187C57E-9EDE-4B72-BA44-D2E6D5BDD1A7
published in	Atherosclerosis
issue	wds:Q59660648-BC002EB8-845A-4C92-8691-5599CDE614CA
volume	wds:Q59660648-61419E6E-AB59-41FB-9122-0E47C640E464
issue	2
volume	126
DOI	wds:Q59660648-C1C08DCA-E95F-4426-AFDF-385A399BA083
DOI	http://dx.doi.org/10.1016/0021-9150(96)05917-5
DOI	10.1016/0021-9150(96)05917-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59660648
is cites work of	DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease Evidence for association between paraoxonase gene polymorphisms and atherosclerotic diseases Does paraoxonase play a role in susceptibility to cardiovascular disease? Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites. Atheroprotective mechanisms of HDL. Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies. Effect of the human serum paraoxonase 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification The paraoxonase Leu-Met54 and Gln-Arg191 gene polymorphisms are not associated with the risk of coronary heart disease Distribution of paraoxonase-1 gene polymorphisms and enzyme activity in a Peruvian population Serum paraoxonase activity and phenotype distribution in Turkish subjects with coronary heart disease and its relationship to serum lipids and lipoproteins Human serum paraoxonase Serum paraoxonase (PON1) 55 and 192 polymorphism and paraoxonase activity and concentration in non-insulin dependent diabetes mellitus Genetic variations of the paraoxonase gene in patients with coronary artery disease A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin PON2 gene variants are associated with clinical manifestations of cardiovascular disease in familial hypercholesterolemia patients Exploring the role of paraoxonases in the pathogenesis of coronary artery disease: a systematic review Paraoxonase Gln-Arg(192) and Leu-Met(55) gene polymorphisms and enzyme activity in a population with a low rate of coronary heart disease Genetic analysis of Paraoxonase (PON1) locus reveals an increased frequency of Arg192 allele in centenarians The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in Taiwan. High expressor paraoxonase PON1 gene promoter polymorphisms are associated with reduced risk of vascular disease in younger coronary patients The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis Paraoxonase gene polymorphisms are associated with carotid arterial wall thickness in subjects with familial hypercholesterolemia Paraoxonase 1 status in the Thai population Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene. Paraoxonase-1 promoter haplotypes and serum paraoxonase: a predominant role for polymorphic position - 107, implicating the Sp1 transcription factor Relationship between Paraoxonase 1 (PON1) gene polymorphisms and susceptibility of stroke: a meta-analysis Lack of association between carotid intima-media thickness and paraoxonase gene polymorphism in non-insulin dependent diabetes mellitus Common paraoxonase gene variants, mortality risk and fatal cardiovascular events in elderly subjects Paraoxonase producing PON1 gene M/L55 polymorphism is related to autopsy-verified artery-wall atherosclerosis Both paraoxonase-1 genotype and activity do not predict the risk of future coronary artery disease; the EPIC-Norfolk Prospective Population Study The codon 55 polymorphism in the paraoxonase 1 gene is not associated with the risk of coronary heart disease in Asian Indians and Chinese Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease Serum paraoxonase is reduced in type 1 diabetic patients compared to non-diabetic, first degree relatives; influence on the ability of HDL to protect LDL from oxidation Interaction between smoking and PON2 Ser311Cys polymorphism as a determinant of the risk of myocardial infarction. Smoking is associated with reduced serum paraoxonase, antioxidants and increased oxidative stress in normolipidaemic acute myocardial infarct patients Relationship of age-related myocardial infarction risk and Gln/Arg 192 variants of the human paraoxonase1 gene: the REGICOR study The influence of renal function on the association of rs854560 polymorphism of paraoxonase 1 gene with long-term prognosis in patients after myocardial infarction Low serum paraoxonase: a risk factor for atherosclerotic disease? Differential effects of smoking on myocardial infarction risk according to the Gln/Arg 192 variants of the human paraoxonase gene Interaction effects between Paraoxonase 1 variants and cigarette smoking on risk of coronary heart disease in a Singaporean Chinese population Modulated serum activities and concentrations of paraoxonase in high density lipoprotein deficiency states. Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease Effects of paraoxonase 1 gene polymorphisms on heart diseases: Systematic review and meta-analysis of 64 case-control studies PON1-192 Phenotype and Genotype Assessments in 918 Subjects of the Stanislas Cohort Study The antioxidant function of high density lipoproteins: a new paradigm in atherosclerosis Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis

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