(Q50851387)

English

The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in Taiwan.

scientific article published in December 1998

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scholarly article

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7 December 2019

The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in Taiwan (English)

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7 December 2019

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

4

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7 December 2019

author name string

Y L Ko

1

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7 December 2019

Y S Ko

2

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7 December 2019

S M Wang

3

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7 December 2019

C J Chang

5

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7 December 2019

P H Chu

6

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7 December 2019

N J Cheng

7

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7 December 2019

W J Chen

8

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7 December 2019

C W Chiang

9

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7 December 2019

Y S Lee

10

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7 December 2019

publication date

1 December 1998

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7 December 2019

Atherosclerosis

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7 December 2019

141

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7 December 2019

2

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7 December 2019

259-264

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7 December 2019

Genetic susceptibility to death from coronary heart disease in a study of twins

1 reference

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7 January 2021

Genetic susceptibility to atherosclerosis

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7 January 2021

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction

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7 January 2021

Association of angiotensinogen gene T235 variant with increased risk of coronary heart disease

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7 January 2021

Alcohol intake modulates the effect of a polymorphism of the cholesteryl ester transfer protein gene on plasma high density lipoprotein and the risk of myocardial infarction

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7 January 2021

Apolipoprotein A-I gene polymorphism associated with premature coronary artery disease and familial hypoalphalipoproteinemia

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7 January 2021

Genetic polymorphisms of apolipoprotein C-III and insulin in survivors of myocardial infarction

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7 January 2021

Polymorphisms in the lipoprotein lipase gene and their associations with plasma lipid concentrations in 40-year-old Danish men.

1 reference

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7 January 2021

Beta fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study. Etude Cas-Temoins sur l'Infarctus du Myocarde

1 reference

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7 January 2021

A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis.

1 reference

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7 January 2021

Protective effect of high density lipoprotein associated paraoxonase. Inhibition of the biological activity of minimally oxidized low density lipoprotein

1 reference

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7 January 2021

Protection of low-density lipoprotein against oxidative modification by high-density lipoprotein associated paraoxonase

1 reference

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7 January 2021

The oxidation hypothesis of atherosclerosis

1 reference

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7 January 2021

Effect of platelet activating factor-acetylhydrolase on the formation and action of minimally oxidized low density lipoprotein

1 reference

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7 January 2021

Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2898%2900179-8

7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus

1 reference

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7 January 2021

The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns

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7 January 2021

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

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7 January 2021

Paraoxonase gene polymorphism in Japanese subjects with coronary heart disease

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7 January 2021

The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individuals

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7 January 2021

Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese

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7 January 2021

Angiotensinogen and angiotensin-I converting enzyme gene polymorphisms and the risk of coronary artery disease in Chinese

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7 January 2021

Genetic polymorphism of paraoxonase and the risk of coronary heart disease.

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7 January 2021

Influence of serum paraoxonase polymorphism on serum lipids and apolipoproteins

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7 January 2021

Multiple Genetic Determinants of Variation of Plasma Lipoproteins in Alberta Hutterites

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7 January 2021

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

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7 January 2021

Paraoxonase genotypes, lipoprotein lipase activity, and HDL.

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7 January 2021

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