Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors (Q84316586)

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scientific article published on 01 June 2011

Language	Label	Description	Also known as
English	Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors	scientific article published on 01 June 2011

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

coronary artery disease

1 reference

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inferred from title

Janina Stępińska

5

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Janina Stępińska

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Małgorzata Szperl

2

object named as

Małgorzata Szperl

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Marta Roszczynko

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Marta Roszczynko

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

author name string

Anna Konopka

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Walerian Piotrowski

3

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Europe PubMed Central

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3 February 2020

publication date

1 June 2011

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Molecular Diagnosis and Therapy

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

15

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

167-176

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21657802 AND SRC:MED&resulttype=core&format=json

3 February 2020

Interactions between gender and the angiotensin type 1 receptor gene polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

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inferred from PubMed ID database lookup

Parental history is an independent risk factor for coronary artery disease: the Framingham Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

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Angiotensinogen M235T polymorphism is associated with plasma angiotensinogen and cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family history of heart attack as an independent predictor of death due to cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship of reported parental history to the incidence of coronary heart disease in the Western Collaborative Group Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

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

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

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Predicting coronary heart disease in siblings--a multivariate assessment: the Framingham Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

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Angiotensin II type 1 receptor polymorphisms in the cardiovascular health study: relation to blood pressure, ethnicity, and cardiovascular events

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms of the renin-angiotensin system and angiographic extent and severity of coronary artery disease: the CORGENE study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between angiotensin II type I receptor polymorphism and resting hemodynamics in black and white youth

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen T174M and M235T gene polymorphisms are associated with the extent of coronary atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of the Angiotensinogen Gene to Essential Hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

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Pharmacogenetics of multigenic disease: heart disease as an example

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

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

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen mutations and risk for ischemic heart disease, myocardial infarction, and ischemic cerebrovascular disease. Six case-control studies from the Copenhagen City Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple molecular assay for the C1166 variant of the angiotensin II type 1 receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of renin-angiotensin agents in altering the natural history of type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin II type 1 receptor gene polymorphism in end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen gene M235T polymorphism and reduction in wall thickness in response to antihypertensive treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of gender and genetic variability on plasma angiotensin peptides.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotypic interactions of renin-angiotensin system genes in myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between polymorphisms in the renin-angiotensin system and nephropathy in type 2 diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21657802

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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