(Q81944118)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18779834%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia (English)

1 reference

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13 January 2020

1 reference

5

Salim Yusuf

1 reference

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13 January 2020

author name string

Jian Wang

1

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13 January 2020

Matthew R Ban

2

1 reference

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13 January 2020

Brooke A Kennedy

3

1 reference

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13 January 2020

Sonia Anand

4

1 reference

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13 January 2020

Murray W Huff

6

1 reference

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13 January 2020

Rebecca L Pollex

7

1 reference

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13 January 2020

Robert A Hegele

8

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13 January 2020

publication date

9 September 2008

1 reference

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Nature Clinical Practice Cardiovascular Medicine

13 January 2020

published in

1 reference

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13 January 2020

volume

5

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13 January 2020

issue

11

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13 January 2020

page(s)

730-737

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The metabolic syndrome: a practical guide to origins and treatment: Part II.

13 January 2020

cites work

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7 January 2021

Triglycerides and the Risk of Coronary Heart Disease

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7 January 2021

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7 January 2021

Hypertriglyceridemia: its etiology, effects and treatment

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7 January 2021

Gene:environment interaction in lipid metabolism and effect on coronary heart disease risk

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7 January 2021

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

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7 January 2021

Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular disease

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7 January 2021

Apolipoprotein E in hyperlipidemia

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7 January 2021

An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing

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7 January 2021

APOA5 and triglyceride metabolism, lesson from human APOA5 deficiency

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7 January 2021

Rare APOA5 mutations--clinical consequences, metabolic and functional effects: an ENID review

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7 January 2021

Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels

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7 January 2021

Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglycerides

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7 January 2021

Determination of the functionality of common APOA5 polymorphisms

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7 January 2021

Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

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7 January 2021

Elevated serum C-reactive protein and free fatty acids among nondiabetic carriers of missense mutations in the gene encoding lamin A/C (LMNA) with partial lipodystrophy

1 reference

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7 January 2021

Multiplex ligation-dependent probe amplification of LDLR enhances molecular diagnosis of familial hypercholesterolemia

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7 January 2021

Low density lipoprotein receptor (LDLR) gene mutations in Canadian subjects with familial hypercholesterolemia, but not of French descent

1 reference

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7 January 2021

Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia

1 reference

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7 January 2021

Relation of high-density lipoprotein cholesterol and triglycerides to incidence of atherosclerotic coronary artery disease (the PROCAM experience). Prospective Cardiovascular Münster study

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7 January 2021

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

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7 January 2021

Polymorphisms in the apolipoprotein A5 (APOA5) gene and type III hyperlipidemia

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7 January 2021

Uptake of type III hypertriglyceridemic VLDL by macrophages is enhanced by oxidation, especially after remnant formation

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7 January 2021

Basic local alignment search tool

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7 January 2021

A comparison of bayesian methods for haplotype reconstruction from population genotype data

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https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

In vivo characterization of human APOA5 haplotypes

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Detection of missense mutations in the genes for lipoprotein lipase and hepatic triglyceride lipase in patients with dyslipidemia undergoing coronary angiography

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Patients With ApoE3 Deficiency (E2/2, E3/2, and E4/2) Who Manifest With Hyperlipidemia Have Increased Frequency of an Asn 291→Ser Mutation in the Human LPL Gene

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Dysbetalipoproteinemia in a kindred with hypobetalipoproteinemia due to mutations in the genes for ApoB (ApoB-70.5) and ApoE (ApoE2).

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Hyperlipidemia in patients with apolipoprotein E 2/2 phenotype: apolipoprotein A5 S19W mutation as a cofactor

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Hypertriglyceridemia: interaction between APOE and APOAV variants.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Apolipoprotein A5 S19W may play a role in dysbetalipoproteinemia in patients with the Apo E2/E2 genotype

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Plasma apoAV levels are markedly elevated in severe hypertriglyceridemia and positively correlated with the APOA5 S19W polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1326

7 January 2021

Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia

1 reference

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7 January 2021

Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)

1 reference

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7 January 2021

Identifiers

DOI

10.1038/NCPCARDIO1326

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18779834%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference