(Q37364446)

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Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes

scientific article published on March 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1 reference

based on heuristic

inferred from title

Jerome I Rotter

3

object named as

J I Rotter

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

4

object named as

R M Cantor

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Aldons Jake Lusis

6

object named as

A J Lusis

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

G M Dallinga-Thie

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

M van Linde-Sibenius Trip

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

X Bu

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

T W de Bruin

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

1 March 1997

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

99

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

953-961

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Inherited susceptibility determines the distribution of dense low-density lipoprotein subfraction profiles in familial combined hyperlipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Multilocus genetic determinants of LDL particle size in coronary artery disease families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Familial combined hyperlipidaemia: 1973-1991

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Pedigree and sib-pair linkage analysis suggest the apolipoprotein B gene is not the major gene influencing plasma apolipoprotein B levels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

6 September 2017

Molecular genetics of coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

14 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

28 September 2017

Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

28 September 2017

Polymorphism in the promoter region of the apolipoprotein AI gene associated with differences in apolipoprotein AI levels: the European Atherosclerosis Research Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

Complex Segregation Analysis of Hypertriglyceridemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

DNA polymorphisms in the apolipoprotein C-III and insulin genes and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

Familial combined hyperlipidaemia: Use of stable isotopes to demonstrate overproduction of very low‐density lipoprotein apolipoprotein B by the liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

Familial combined hyperlipidemia and abnormal lipoprotein lipase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

26 June 2018

Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507903

2 September 2018

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://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic markers in the apo AI-CIII-AIV gene cluster for combined hyperlipidemia, hypertriglyceridemia, and predisposition to atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between genetic variation at the APO AI-CIII-AIV gene cluster and familial combined hyperlipidaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The investigation of linkage between a quantitative trait and a marker locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex segregation analysis of hyperlipidemia in a Seattle sample

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in the apolipoprotein AI-CIII-AIV gene cluster and coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G to A substitution in the promoter region of the apolipoprotein AI gene is associated with elevated serum apolipoprotein AI and high density lipoprotein cholesterol concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human apolipoprotein A-I gene promoter polymorphism: association with hyperalphalipoproteinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus Relationships with lipids, apolipoproteins, and premature coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the apolipoprotein (apo) AI-CIII-AIV gene cluster: detection of genetic variation determining plasma apo AI, apo CIII and apo AIV concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9062353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI119260

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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