A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia. - Wikidata - wikimedia - TriplyDB

A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia.

A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia.

http://www.wikidata.org/entity/Q34386536

about

Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.Genetics of LDL particle heterogeneity: from genetic epidemiology to DNA-based variations.Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia.Metabolic pathogenesis of familial combined hyperlipidaemia with emphasis on insulin resistance, adipose tissue metabolism and free fatty acids.

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P2860

A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia.

http://www.wikidata.org/entity/Q34386536

description

1998 nî lūn-bûn

@nan

1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@ast

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@en

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@nl

type

label

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@ast

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@en

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@nl

prefLabel

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@ast

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@en

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@nl

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American Journal of Human Genetics

P1476

A common genetic mechanism det ...... ilial combined hyperlipidemia.

@en

P2093

Bredie SJ

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Demacker PN

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Juo SH

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Kiemeney LA

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Stalenhoef AF

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P2860

Banting lecture 1988. Role of insulin resistance in human disease

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia.

A genetic model for control of hypertriglyceridemia and apolipoprotein B levels in the Johns Hopkins colony of St. Thomas Hospital rabbits.

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

Both inherited susceptibility and environmental exposure determine the low-density lipoprotein-subfraction pattern distribution in healthy Dutch families.

Bias of the contribution of single-locus effects to the variance of a quantitative trait.

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

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

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

Immunonephelometric assay of human apolipoprotein AI.

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586-594

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scholarly article

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10.1086/301962

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2

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63

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1998-08-01T00:00:00Z

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13600772

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9683593

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