A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease (Q35769219)

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scientific article published on December 1995

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Language	Label	Description	Also known as
English	A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease	scientific article published on December 1995

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

main subject

risk factor

0 references

coronary artery disease

1 reference

based on heuristic

inferred from title

author name string

Serrato M

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

Marian AJ

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

language of work or name

English

0 references

publication date

1 December 1995

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

published in

Journal of Clinical Investigation

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

volume

96

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

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10 August 2017

issue

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

page(s)

3005-3008

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stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

cites work

Human and rabbit paraoxonases: purification, cloning, sequencing, mapping and role of polymorphism in organophosphate detoxification

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Is paraoxonase related to atherosclerosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Genetic dissection of complex traits

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

The human serum paraoxonase/arylesterase polymorphism.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Distribution of paraoxon hydrolytic activity in the serum of patients after myocardial infarction.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Genetic susceptibility to atherosclerosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

Genetic polymorphism and interethnic variability of plasma paroxonase activity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

27 July 2018

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

25 September 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=186013

retrieved

15 November 2018

Paraoxonase prevents accumulation of lipoperoxides in low-density lipoprotein

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein polymorphisms fail to define risk of coronary artery disease. Results of a prospective, angiographically controlled study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of LDL apheresis on restenosis after angioplasty

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular variant of angiotensinogen gene is associated with coronary atherosclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein epsilon 4 is not a genetic risk factor for coronary artery disease or restenosis after percutaneous transluminal coronary angioplasty

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin-I converting enzyme genotype DD is a risk factor for coronary artery disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/8675673

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1172/JCI118373

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

PMC publication ID

186013

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

PubMed publication ID

8675673

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8675673

retrieved

10 August 2017

 

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