(Q74106098)

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The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia

scientific article published on 01 August 2000

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scholarly article

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9 November 2019

The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10924721%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

familial combined hyperlipidemia

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based on heuristic

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M J Hoffer

1

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9 November 2019

H Snieder

2

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9 November 2019

S J Bredie

3

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9 November 2019

P N Demacker

4

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9 November 2019

J J Kastelein

5

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9 November 2019

R R Frants

6

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9 November 2019

A F Stalenhoef

7

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9 November 2019

publication date

1 August 2000

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9 November 2019

Atherosclerosis

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9 November 2019

151

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9 November 2019

2

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9 November 2019

443-450

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9 November 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Inheritance of combined hyperlipoproteinemia: evidence for a new lipoprotein phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Very low density lipoprotein overproduction in genetic forms of hypertriglyceridaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Very low density lipoprotein triglyceride metabolism in relatives of hypertriglyceridemic probands. Evidence for genetic control of triglyceride removal

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Stable isotopes show a direct relation between VLDL apoB overproduction and serum triglyceride levels and indicate a metabolically and biochemically coherent basis for familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Integrated regulation of very low density lipoprotein triglyceride and apolipoprotein-B kinetics in man: Normolipemic subjects, familial hypertriglyceridemia and familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

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/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjects.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Codon 54 polymorphism of the human intestinal fatty acid binding protein 2 gene is associated with dyslipidemias but not with insulin resistance in patients with familial combined hyperlipidemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Two novel apolipoprotein A-IV variants in individuals with familial combined hyperlipidemia and diminished levels of lipoprotein lipase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Human hepatic lipase mutations and polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Extensions to pedigree analysis. III. Variance components by the scoring method

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Genetic influence on cytokine production and fatal meningococcal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Association of variation in hepatic lipase activity with promoter variation in the hepatic lipase gene. The LOCAT Study Invsestigators

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900428-1

7 January 2021

Identifiers

10.1016/S0021-9150(99)00428-1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10924721%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10924721%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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