(Q28609419)

3 February 2017

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Europe PubMed Central

title

Genetic determinants of plasma triglycerides: impact of rare and common mutations (English)

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3 February 2017

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P. J. Talmud

1

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3 February 2017

publication date

1 May 2001

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Current Atherosclerosis Reports

3 February 2017

published in

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3 February 2017

volume

3

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3 February 2017

issue

3

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3 February 2017

page(s)

191–199

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

3 February 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11883-001-0061-4

The Asp9 Asn mutation in the lipoprotein lipase gene is associated with increased progression of coronary atherosclerosis. REGRESS Study Group, Interuniversity Cardiology Institute, Utrecht, The Netherlands. Regression Growth Evaluation Statin Study

21 January 2018

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A common mutation in the lipoprotein lipase gene promoter, -93T/G, is associated with lower plasma triglyceride levels and increased promoter activity in vitro

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11883-001-0061-4

Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase gene

21 January 2018

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Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function

21 January 2018

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ApoCIII gene variants modulate postprandial response to both glucose and fat tolerance tests.

21 January 2018

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Common genetic variation in the promoter of the human apo CIII gene abolishes regulation by insulin and may contribute to hypertriglyceridemia

21 January 2018

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12 December 2020

A common Hpa I RFLP of apolipoprotein C-I increases gene transcription and exhibits an ethnically distinct pattern of linkage disequilibrium with the alleles of apolipoprotein E.

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Plasma triglyceride level is a risk factor for cardiovascular disease independent of high-density lipoprotein cholesterol level: a meta-analysis of population-based prospective studies.

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Modulation of plasma triglyceride levels by apoE phenotype: a meta-analysis

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Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women.

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Relationship of glucose intolerance to coronary risk in Afro-Caribbeans compared with Europeans

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Substitution of asparagine for aspartic acid at residue 9 (D9N) of lipoprotein lipase markedly augments risk of ischaemic heart disease in male smokers.

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Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice. Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes

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A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians

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Remnant lipoprotein metabolism: key pathways involving cell-surface heparan sulfate proteoglycans and apolipoprotein E

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Association between the LPL-D9N mutation in the lipoprotein lipase gene and plasma lipid traits in myocardial infarction survivors from the ECTIM study

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Overexpression of apolipoprotein CII causes hypertriglyceridemia in transgenic mice

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Lipoprotein lipase mutations, plasma lipids and lipoproteins, and risk of ischemic heart disease. A meta-analysis

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Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells

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The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease

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12 December 2020

Modulation of lipoprotein lipase activity by apolipoproteins. Effect of apolipoprotein C-III

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Type III hyperlipoproteinemic phenotype in transgenic mice expressing dysfunctional apolipoprotein E.

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Variation at the apo AI/CIII/AIV gene complex is associated with elevated plasma levels of apo CIII

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Alteration of lipid profiles in plasma of transgenic mice expressing human lipoprotein lipase.

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Targeted disruption of the apolipoprotein C-III gene in mice results in hypotriglyceridemia and protection from postprandial hypertriglyceridemia

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

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The insulin resistance syndrome and postprandial lipid intolerance in smokers.

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Mechanism of hypertriglyceridemia in human apolipoprotein (apo) CIII transgenic mice. Diminished very low density lipoprotein fractional catabolic rate associated with increased apo CIII and reduced apo E on the particles

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Increased response to cholesterol feeding in apolipoprotein C1-deficient mice

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Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein

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Apolipoprotein C-III gene variation and dyslipidaemia

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Interaction of the lipoprotein lipase asparagine 291-->serine mutation with body mass index determines elevated plasma triacylglycerol concentrations: a study in hyperlipidemic subjects, myocardial infarction survivors, and healthy adults.

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Evidence for the role of hepatic endothelial lipase in the metabolism of plasma high density lipoprotein2 in man.

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The multifunctional role of hormone-sensitive lipase in lipid metabolism

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Characterization of the lipid-binding properties and lipoprotein lipase inhibition of a novel apolipoprotein C-III variant Ala23Thr

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12 December 2020

Induced mutant mouse lines that express lipoprotein lipase in cardiac muscle, but not in skeletal muscle and adipose tissue, have normal plasma triglyceride and high-density lipoprotein-cholesterol levels

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12 December 2020

Black-white differences in postprandial triglyceride response and postheparin lipoprotein lipase and hepatic triglyceride lipase among young men.

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12 December 2020

Contribution of apolipoprotein C-III gene variants to determination of triglyceride levels and interaction with smoking in middle-aged men

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Combined hyperlipidemia in transgenic mice overexpressing human apolipoprotein Cl

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

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Familial lipoprotein lipase (LPL) deficiency: A catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy

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Triglyceride lipases and atherosclerosis.

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Atherogenic, dense low-density lipoproteins. Pathophysiology and new therapeutic approaches

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Apolipoprotein C-I modulates the interaction of apolipoprotein E with beta-migrating very low density lipoproteins (beta-VLDL) and inhibits binding of beta-VLDL to low density lipoprotein receptor-related protein

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12 December 2020

10.1007/S11883-001-0061-4

Identifiers

DOI

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Dimensions Publication ID

1040841320

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