(Q36503521)

14 August 2017

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title

Human genetics of variation in high-density lipoprotein cholesterol (English)

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14 August 2017

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Atif Qasim

1

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14 August 2017

Daniel J Rader

series ordinal

2

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14 August 2017

publication date

1 May 2006

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Current Atherosclerosis Reports

14 August 2017

published in

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14 August 2017

volume

8

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14 August 2017

issue

3

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14 August 2017

page(s)

198-205

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Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

14 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11883-006-0074-0

Molecular mechanisms of cholesteryl ester transfer protein deficiency in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-006-0074-0

Hepatic lipase deficiency. Clinical, biochemical, and molecular genetic characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-006-0074-0

Association between single-nucleotide polymorphisms in the endothelial lipase (LIPG) gene and high-density lipoprotein cholesterol levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-006-0074-0

Meta-analysis of genome-wide linkage studies for quantitative lipid traits in African Americans

21 January 2018

1 reference

12 December 2020

Hepatic lipase deficiency.

1 reference

12 December 2020

Overexpression of the HDL receptor SR-BI alters plasma HDL and bile cholesterol levels

1 reference

12 December 2020

Genetic cholesteryl ester transfer protein deficiency is extremely frequent in the Omagari area of Japan. Marked hyperalphalipoproteinemia caused by CETP gene mutation is not associated with longevity

1 reference

12 December 2020

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

1 reference

12 December 2020

Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation

1 reference

12 December 2020

Endothelial lipase is a major genetic determinant for high-density lipoprotein concentration, structure, and metabolism

1 reference

12 December 2020

Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans

1 reference

12 December 2020

The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes

1 reference

12 December 2020

A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the APOA2 gene and the APOA1C3A4 gene cluster

1 reference

12 December 2020

A targeted mutation in the murine gene encoding the high density lipoprotein (HDL) receptor scavenger receptor class B type I reveals its key role in HDL metabolism

1 reference

12 December 2020

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

1 reference

12 December 2020

Prevalence and phenotypic spectrum of cholesteryl ester transfer protein gene mutations in Japanese hyperalphalipoproteinemia

1 reference

12 December 2020

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

1 reference

12 December 2020

Apolipoprotein A-I deficiency with accumulated risk for CHD but no symptoms of CHD.

1 reference

12 December 2020

Inhibition of endothelial lipase causes increased HDL cholesterol levels in vivo

1 reference

12 December 2020

Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I

1 reference

12 December 2020

Targeted mutation reveals a central role for SR-BI in hepatic selective uptake of high density lipoprotein cholesterol

1 reference

12 December 2020

Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males

1 reference

12 December 2020

Genetics of variation in HDL cholesterol in humans and mice

1 reference

12 December 2020

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

1 reference

12 December 2020

High-density lipoprotein cholesterol as an independent risk factor in cardiovascular disease: assessing the data from Framingham to the Veterans Affairs High--Density Lipoprotein Intervention Trial

1 reference

12 December 2020

Association between a novel 11-base pair deletion mutation in the promoter region of the scavenger receptor class B type I gene and plasma HDL cholesterol levels in Taiwanese Chinese

1 reference

12 December 2020

Apolipoprotein A-I(Zavalla) (Leu159-->Pro): HDL cholesterol deficiency in a kindred associated with premature coronary artery disease

1 reference

12 December 2020

Activities of lipoprotein lipase and hepatic triglyceride lipase in postheparin plasma of patients with low concentrations of HDL cholesterol

1 reference

12 December 2020

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

1 reference

12 December 2020

Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol

1 reference

12 December 2020

HDL as a target in the treatment of atherosclerotic cardiovascular disease

1 reference

12 December 2020

Homozygous Tangier disease and cardiovascular disease

1 reference

12 December 2020

Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease

1 reference

12 December 2020

Familial apolipoprotein A-I, C-III, and A-IV deficiency and premature atherosclerosis due to deletion of a gene complex on chromosome 11

1 reference

12 December 2020

Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III)

1 reference

12 December 2020

A Low Prevalence of Coronary Heart Disease among Subjects with Increased High-Density Lipoprotein Cholesterol Levels, Including Those with Plasma Cholesteryl Ester Transfer Protein Deficiency

1 reference

12 December 2020

THE INHERITANCE OF HIGH DENSITY LIPOPROTEIN DEFICIENCY (TANGIER DISEASE)

1 reference

12 December 2020

Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene

1 reference

12 December 2020

New insights into the regulation of HDL metabolism and reverse cholesterol transport

1 reference

12 December 2020

Plasma apolipoprotein A-1 absence associated with a marked reduction of high density lipoproteins and premature coronary artery disease

1 reference

12 December 2020

Natural genetic variation as a tool in understanding the role of CETP in lipid levels and disease

1 reference

12 December 2020

Coronary heart disease prevalence and other clinical features in familial high-density lipoprotein deficiency (Tangier disease)

1 reference

12 December 2020

Hepatic lipase: new insights from genetic and metabolic studies

1 reference

12 December 2020

Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population

1 reference

12 December 2020

Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia

1 reference

12 December 2020

Endothelial lipase is a major determinant of HDL level

1 reference

12 December 2020

Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins

1 reference

12 December 2020

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

1 reference

12 December 2020

Apolipoprotein A-I deficiency. Biochemical and metabolic characteristics

1 reference

12 December 2020

Apolipoprotein A-I(Milano): current perspectives

1 reference

12 December 2020

Identification of genetic variants in endothelial lipase in persons with elevated high-density lipoprotein cholesterol

1 reference

12 December 2020

A major locus influencing plasma high-density lipoprotein cholesterol levels in the San Antonio Family Heart Study. Segregation and linkage analyses

1 reference

12 December 2020

In vivo metabolism of a mutant form of apolipoprotein A-I, apo A-IMilano, associated with familial hypoalphalipoproteinemia

1 reference

12 December 2020

Atherosclerotic disease in marked hyperalphalipoproteinemia. Combined reduction of cholesteryl ester transfer protein and hepatic triglyceride lipase

1 reference

12 December 2020

Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease

1 reference

12 December 2020

Effect of recombinant ApoA-I Milano on coronary atherosclerosis in patients with acute coronary syndromes: a randomized controlled trial

1 reference

12 December 2020

The replacement of arginine by cysteine at residue 151 in apolipoprotein A-I produces a phenotype similar to that of apolipoprotein A-IMilano

1 reference

12 December 2020

Inhibition of cholesteryl ester transfer protein activity: a new therapeutic approach to raising high-density lipoprotein

1 reference

12 December 2020

A novel endothelial-derived lipase that modulates HDL metabolism

1 reference

12 December 2020

A mutation in the human apolipoprotein A-I gene. Dominant effect on the level and characteristics of plasma high density lipoproteins

1 reference

12 December 2020

A prospective study of HDL-C and cholesteryl ester transfer protein gene mutations and the risk of coronary heart disease in the elderly

1 reference

12 December 2020

Evidence for a gene influencing high-density lipoprotein cholesterol on chromosome 4q31.21.

1 reference

12 December 2020

Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the li

1 reference

12 December 2020

A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians

1 reference

12 December 2020

Metabolism of High-Density Lipoprotein Apolipoproteins in Tangier Disease

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12 December 2020

Increased catabolic rate of low density lipoproteins in humans with cholesteryl ester transfer protein deficiency

1 reference

12 December 2020

Familial deficiency of apolipoproteins A-I and C-III and precocious coronary-artery disease

1 reference

12 December 2020

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

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12 December 2020

Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency

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12 December 2020

Delayed catabolism of high density lipoprotein apolipoproteins A-I and A-II in human cholesteryl ester transfer protein deficiency

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12 December 2020

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

1 reference

12 December 2020

Evidence of linkage of familial hypoalphalipoproteinemia to a novel locus on chromosome 11q23.

1 reference

12 December 2020

In vivo metabolism of a mutant apolipoprotein, apoA-IIowa, associated with hypoalphalipoproteinemia and hereditary systemic amyloidosis

1 reference

12 December 2020

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol

1 reference

12 December 2020

10.1007/S11883-006-0074-0

Identifiers

DOI

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release_x4ugsvf2ofggzcpimvzyxj6icy

14 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/x4ugsvf2ofggzcpimvzyxj6icy

24 November 2022

mapped directly with Wikidata item

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