(Q46599027)

23 December 2017

title

Effect of the APOC3 Sst I SNP on fasting triglyceride levels in men heterozygous for the LPL P207L deficiency (English)

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23 December 2017

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Christophe Garenc

1

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23 December 2017

Charles Couillard

2

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23 December 2017

Nathalie Laflamme

3

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23 December 2017

François Cadelis

4

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23 December 2017

Claude Gagné

5

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23 December 2017

Patrick Couture

6

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23 December 2017

Pierre Julien

7

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23 December 2017

Jean Bergeron

8

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23 December 2017

publication date

1 October 2005

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23 December 2017

European Journal of Human Genetics

published in

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23 December 2017

volume

13

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23 December 2017

issue

10

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23 December 2017

page(s)

1159-1165

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23 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201469

exact match

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cites work

Molecular pathobiology of the human lipoprotein lipase gene

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Hyperinsulinemia and abdominal obesity affect the expression of hypertriglyceridemia in heterozygous familial lipoprotein lipase deficiency.

21 January 2018

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Role of ApoCs in lipoprotein metabolism: functional differences between ApoC1, ApoC2, and ApoC3

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Molecular mechanisms of type III hyperlipoproteinemia: The contribution of the carboxy-terminal domain of ApoE can account for the dyslipidemia that is associated with the E2/E2 phenotype

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Phospholipid and cholesteryl ester transfer are increased in lipoprotein lipase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Polymorphic markers in apolipoprotein C-III gene flanking regions and hypertriglyceridemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Effect of apoC-III gene polymorphisms on the lipoprotein-lipid profile of viscerally obese men.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Mode of action of peroxisome proliferators as hypolipidemic drugs. Suppression of apolipoprotein C-III.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Population prevalence of APOE, APOC3 and PPAR-? mutations associated to hypertriglyceridemia in French Canadians

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Polymorphisms in the insulin response element of APOC-III gene promoter influence the correlation between insulin and triglycerides or triglyceride-rich lipoproteins in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Apolipoprotein E polymorphism and atherosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Severe Hyperlipidemia in Apolipoprotein E2 Homozygotes Due to a Combined Effect of Hyperinsulinemia and an Sst I Polymorphism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Increase in plasma high-density lipoprotein concentration following complete androgen blockage in men with prostatic carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

[On a rapid determination of the cholesterol bound to the serum alpha- and beta-lipoproteins]

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Mismatch PCR: a rapid method to screen for the Pro207-->Leu mutation in the lipoprotein lipase (LPL) gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

DNA POLYMORPHISM ADJACENT TO HUMAN APOPROTEIN A-1 GENE: RELATION TO HYPERTRIGLYCERIDAEMIA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Apolipoprotein C-III gene variation and dyslipidaemia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Effect of lipoprotein lipase on binding of chylomicrons to LDL receptor-deficient Chinese hamster ovary cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201469

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201469

1 reference

23 December 2017

PubMed ID

16015281

1 reference

23 December 2017