(Q30652148)

English

Recent Advances in Molecular Genetics of Cardiovascular Disorders - Implications for Atherosclerosis and Diseases of Cellular Lipid Metabolism

scientific article

Recent advances in molecular genetics of cardiovascular disorders. Implications for atherosclerosis and diseases of cellular lipid metabolism.

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scholarly article

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

Recent Advances in Molecular Genetics of Cardiovascular Disorders - Implications for Atherosclerosis and Diseases of Cellular Lipid Metabolism (English)

1 reference

Europe PubMed Central

25 June 2017

Recent advances in molecular genetics of cardiovascular disorders. Implications for atherosclerosis and diseases of cellular lipid metabolism (English)

1 reference

Europe PubMed Central

6 July 2017

atherosclerosis

1 reference

based on heuristic

inferred from title

author name string

Gerd Schmitz

1

1 reference

Europe PubMed Central

25 June 2017

Charalampos Aslanidis

2

1 reference

Europe PubMed Central

25 June 2017

Karl J Lackner

3

1 reference

Europe PubMed Central

25 June 2017

Schmitz G

1

1 reference

Europe PubMed Central

6 July 2017

Aslanidis C

2

1 reference

Europe PubMed Central

6 July 2017

Lackner KJ

3

1 reference

Europe PubMed Central

6 July 2017

publication date

1 January 1998

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

Pathology Oncology Research

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

4

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

153-161

1 reference

Europe PubMed Central

25 June 2017

152-160

1 reference

Europe PubMed Central

6 July 2017

2

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

1 reference

https://api.crossref.org/works/10.1007%2FBF02904710

21 January 2018

Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham study.

1 reference

https://api.crossref.org/works/10.1007%2FBF02904710

21 January 2018

Genetic determinants of atherosclerosis-related dyslipidemias and their clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is familial combined hyperlipidaemia a genetic disorder of adipose tissue?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoprotein(a) and risks of cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes in Australian aborigines: impact of the western diet and life style

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preliminary report: genetic variation in the human stromelysin promoter is associated with progression of coronary atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of the apolipoprotein B signal peptide (ins/del) and XbaI polymorphisms on plasma lipid responses to dietary change

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E-selectin polymorphism and atherosclerosis: an association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Life style and genes--the key factors for diabetes and the metabolic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoprotein(a) is an independent risk factor for myocardial infarction at a young age

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic associations with human longevity at the APOE and ACE loci.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics: cardiac disease and risk-related genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of the apolipoprotein E gene and severity of coronary artery disease defined by angiography

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen gene and hypertension in Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

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/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PIA1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke, and venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of polymorphisms in the renin-angiotensin system and in E-selectin of patients with early severe coronary heart disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common thrombomodulin amino acid dimorphism is associated with myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoprotein metabolism in the macrophage: implications for cholesterol deposition in atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

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/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-environment interaction in the determination of levels of haemostatic variables involved in thrombosis and fibrinolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma Ip(a) concentration is inversely correlated with the ratio of Kringle IV/Kringle V encoding domains in the apo(a) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The peroxisome proliferator-activated receptor-gamma is a negative regulator of macrophage activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association analysis of CA repeat polymorphism of the endothelial nitric oxide synthase gene with essential hypertension in Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevance

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenesis of atherosclerosis: a perspective for the 1990s

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mysteries of lipoprotein(a)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two variants of extracellular-superoxide dismutase: relationship to cardiovascular risk factors in an unselected middle-aged population

1 reference

https://pubmed.ncbi.nlm.nih.gov/9654602

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02904710

2 references

Europe PubMed Central

25 June 2017

Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

25 June 2017

1 reference

Europe PubMed Central

6 July 2017

Springer Nature article ID

10.1007/bf02904710

0 references

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