Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease (Q46121100)

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scientific article published on 14 February 2009

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English	Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease	scientific article published on 14 February 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Association of genetic variants in Methylenetetrahydrofolate Reductase and Paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

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1 reference

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author name string

Makbule Aydin

1

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Cahide Gokkusu

2

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Elif Ozkok

3

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Feti Tulubas

4

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Yesim Unlucerci

5

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Burak Pamukcu

6

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Zeynep Ozbek

7

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Berrin Umman

8

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

language of work or name

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publication date

14 February 2009

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Europe PubMed Central

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19 December 2017

http://europepmc.org/abstract/MED/19219535

Molecular and Cellular Biochemistry

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

325

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PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

1-2

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

199-208

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

Homocysteine and stroke: evidence on a causal link from mendelian randomisation

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

Paraoxonase PON1 polymorphism leu-Met54 is associated with carotid atherosclerosis: results of the Austrian Stroke Prevention Study

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

Non-random reflections on health services research

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

A polymorphism of the paraoxonase gene associated with variation in plasma lipoproteins in a genetic isolate.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

Theodore Cooper Memorial Lecture. Hypertension and the pathogenesis of atherosclerosis. Oxidative stress and the mediation of arterial inflammatory response: a new perspective

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

Genetic polymorphism of paraoxonase and the risk of coronary heart disease

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

C-reactive protein in ischemic stroke: an independent prognostic factor.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-009-0038-0

21 January 2018

Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medical therapies and invasive treatments for coronary artery disease by body mass: the "obesity paradox" in the Get With The Guidelines database

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Randomized controlled trial of homocysteine-lowering vitamin treatment in elderly patients with vascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined impact of matrix metalloproteinase-3 and paraoxonase 1 55/192 gene variants on coronary artery disease in Turkish patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between plasma homocysteine and vitamin status in the Framingham study population. Impact of folic acid fortification

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gln-Arg192 polymorphism of human paraoxonase gene is not associated with coronary artery disease in italian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High performance liquid chromatography method for rapid and accurate determination of homocysteine in plasma and serum

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calcium-dependent human serum homocysteine thiolactone hydrolase. A protective mechanism against protein N-homocysteinylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two types of seizures in homocysteine thiolactone-treated adult rats, behavioral and electroencephalographic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine-thiolactone and S-nitroso-homocysteine mediate incorporation of homocysteine into protein in humans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lowering blood homocysteine with folic acid based supplements: meta-analysis of randomised trials. Homocysteine Lowering Trialists' Collaboration

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine level and coronary heart disease incidence: a systematic review and meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G1793A polymorphisms in the methylene-tetrahydrofolate gene: effect of folic acid on homocysteine levels.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine thiolactone and protein homocysteinylation in human endothelial cells: implications for atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blood levels of homocysteine and increased risks of cardiovascular disease: causal or casual?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine: the Rubik's cube of cardiovascular risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heart disease and stroke statistics--2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of fibrinogen, C-reactive protein, albumin, or leukocyte count with coronary heart disease: meta-analyses of prospective studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum total homocysteine concentrations in the third National Health and Nutrition Examination Survey (1991-1994): population reference ranges and contribution of vitamin status to high serum concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two alleles of the human paraoxonase gene produce different amounts of mRNA. An explanation for differences in serum concentrations of paraoxonase associated with the (Leu-Met54) polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gln-Arg192 polymorphism of paraoxonase and coronary heart disease in type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase 192 Gln/Arg gene polymorphism, coronary artery disease, and myocardial infarction in type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The paraoxonase promoter polymorphism (-107)T>C is not associated with carotid intima-media thickness in Sicilian hypercholesterolemic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and its effects on in-stent restenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine, folic acid and coronary artery disease: possible impact on prognosis and therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inflammation and atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MTHFR Gene polymorphisms, B-vitamins and hyperhomocystinemia in young and middle-aged acute myocardial infarction patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of simvastatin therapy on paraoxonase activity and related lipoproteins in familial hypercholesterolemic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase (PON1) deficiency is associated with increased macrophage oxidative stress: studies in PON1-knockout mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The correlation of homocysteine-thiolactonase activity of the paraoxonase (PON1) protein with coronary heart disease status

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma homocysteine as a risk factor for dementia and Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atherosclerosis — An Inflammatory Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of folic acid and nitric oxide synthase inhibition on coronary flow and oxidative stress markers in isolated rat heart

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase status in coronary heart disease: are activity and concentration more important than genotype?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid high-performance liquid chromatographic assay for total homocysteine levels in human serum

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-nutrient interactions in one-carbon metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase 55 and 192 polymorphism and its relationship to serum paraoxonase activity and serum lipids in Turkish patients with non-insulin dependent diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The TT genotype of the methylenetetrahydrofolate reductase C677T gene polymorphism is associated with the extent of coronary atherosclerosis in patients at high risk for coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Interaction between MTHFR 677 C→T Genotype and Folate Status Is a Determinant of Coronary Atherosclerosis Risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia, paraoxonase activity and risk of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The determination of homocysteine-thiolactone in human plasma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 192 Arg Variant of the Human Paraoxonase (HUMPONA) Gene Polymorphism Is Associated With an Increased Risk for Coronary Artery Disease in the Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and classification of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219535

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11010-009-0038-0

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219535

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