(Q34386695)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

atherosclerosis

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

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based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

familial combined hyperlipidemia

1 reference

based on heuristic

inferred from title

Jerome I Rotter

7

object named as

J I Rotter

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Europe PubMed Central

PubMed publication ID

1 August 2017

3

object named as

R M Cantor

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Europe PubMed Central

PubMed publication ID

1 August 2017

Aldons Jake Lusis

8

object named as

A J Lusis

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Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

H Allayee

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

B E Aouizerat

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

G M Dallinga-Thie

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

R M Krauss

5

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Europe PubMed Central

PubMed publication ID

1 August 2017

C D Lanning

6

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Europe PubMed Central

PubMed publication ID

1 August 2017

T W de Bruin

9

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Europe PubMed Central

PubMed publication ID

1 August 2017

language of work or name

0 references

publication date

1 August 1998

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

1 August 2017

63

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Europe PubMed Central

PubMed publication ID

1 August 2017

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

577-585

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Europe PubMed Central

PubMed publication ID

1 August 2017

Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

Decreased HDL cholesterol levels but normal lipid absorption, growth, and feeding behavior in apolipoprotein A-IV knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

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=1377323

6 July 2018

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=1377323

6 July 2018

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=1377323

6 July 2018

A method for constructing radiation hybrid maps of whole genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 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=1377323

6 July 2018

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=1377323

6 July 2018

Association of coronary atherosclerosis with hyperapobetalipoproteinemia [increased protein but normal cholesterol levels in human plasma low density (beta) lipoproteins]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

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=1377323

6 July 2018

Low-Density Lipoprotein Subclass Patterns and Risk of Myocardial Infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

Inheritance of low-density lipoprotein subclass patterns: results of complex segregation analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

A more powerful robust sib-pair test of linkage for quantitative traits.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

Manganous superoxide dismutase is essential for cellular resistance to cytotoxicity of tumor necrosis factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

Dinucleotide repeat polymorphism at the 3' end of the LDL receptor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

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=1377323

6 July 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=1377323

6 July 2018

Linkage of atherogenic lipoprotein phenotype to the low density lipoprotein receptor locus on the short arm of chromosome 19

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

Variations in oxidative susceptibility among six low density lipoprotein subfractions of differing density and particle size

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 2018

An amino acid exchange in exon I of the human lecithin: cholesterol acyltransferase (LCAT) gene is associated with fish eye disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

6 July 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=1377323

27 October 2018

Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377323

27 October 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

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/9683614

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/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma lipid transfer proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nondenaturing polyacrylamide gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

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/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced susceptibility to in vitro oxidation of the dense low density lipoprotein subfraction in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of exon 15 missense mutation (442D:G) in cholesteryl ester transfer protein gene in hyperalphalipoproteinemic Japanese subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The atherogenic lipoprotein phenotype is not caused by a mutation in the coding region of the low density lipoprotein receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9683614

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

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