(Q54364291)

English

Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease. (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

2

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Asad Vaisi-Raygani

1

object named as

Asad Vaisi-Raygani

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

author name string

Haidar Tavilani

3

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Hadiss Vaisi-Raygani

4

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

A Kiani

5

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

M Aminian

6

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

E Shakiba

7

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Y Shakiba

8

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Tayebeh Pourmotabbed

9

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

publication date

17 June 2011

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

Molecular Biology Reports

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

39

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

3

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

2723-2731

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

https://scigraph.springernature.com/pub.10.1007/s11033-011-1027-4

0 references

Serum butyrylcholinesterase activity and phenotype associations with lipid profile in stroke patients

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Association of homocysteine thiolactonase activity and PON1 polymorphisms with the severity of acute coronary syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

The angiotensin converting enzyme D allele is an independent risk factor for early onset coronary artery disease.

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Association between apolipoprotein E polymorphism and serum lipid and apolipoprotein levels with Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

The relationship between paraoxonase1-192 polymorphism and activity with coronary artery disease

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

LDL oxidation by arterial wall macrophages depends on the oxidative status in the lipoprotein and in the cells: role of prooxidants vs. antioxidants

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Paraoxonase-gene polymorphisms associated with coronary heart disease: support for the oxidative damage hypothesis?

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions. A possible peroxidative role for paraoxonase

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Angiotensin-converting enzyme gene polymorphism and allele frequencies in the Lebanese population: prevalence and review of the literature

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Angiotensin converting enzyme DD genotype not associated with increased risk of coronary artery disease in the Iranian population.

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Paraoxonase and coronary heart disease

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11033-011-1027-4

21 January 2018

Paraoxonases: structure, gene polymorphism & role in coronary artery disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin converting enzyme I/D, angiotensinogen M235T and AT1-R A/C1166 gene polymorphisms in patients with acromegaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and epidemiological characteristics of juvenile myocardial infarction in Italy: the GISSI experience.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coronary artery disease risk in Chinese type 2 diabetics: is there a role for paraxonase 1 gene (Q192R) polymorphism?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renin-angiotensin system gene polymorphisms and premature coronary heart disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of coronary artery disease risk factors in Iran: a population based survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between apolipoprotein E polymorphism and coronary artery disease in the Kermanshah population in Iran

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The frequency of factor V Leiden mutation, ACE gene polymorphism, serum ACE activity and response to ACE inhibitor and angiotensin II receptor antagonist drugs in Iranians type II diabetic patients with microalbuminuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and functional diversity of paraoxonases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin I converting enzyme, angiotensin II type 1 receptor and angiotensinogen polymorphisms and early myocardial infarction in Turkish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does paraoxonase play a role in susceptibility to cardiovascular disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

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/21681430

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/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between apolipoprotein ε4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased angiotensin-converting enzyme activity in coronary artery specimens from patients with acute coronary syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DD genotype of ace gene I/D polymorphism is associated in a turkish study population with osteoarthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presence of apolipoprotein ε4 and ε2 alleles augments the risk of coronary artery disease in type 2 diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: association with early coronary disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of the human serum paraoxonase 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Butyrylcholinesterase K variant and the APOE-ε4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synergistic effects of angiotensin-converting enzyme and angiotensin-II type 1 receptor gene polymorphisms on risk of myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin-converting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common paraoxonase gene variants, mortality risk and fatal cardiovascular events in elderly subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase gene polymorphism in Japanese subjects with coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of angiotensin-converting enzyme gene insertion/deletion polymorphism with metabolic syndrome in Iranians with type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

1 reference

https://pubmed.ncbi.nlm.nih.gov/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 192Arg 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/21681430

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11033-011-1027-4

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/21681430

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