(Q37835397)

PubMed publication ID

21291740

24 August 2017

title

Clinical presentation, laboratory values, and coronary heart disease risk in marked high-density lipoprotein-deficiency states (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

1 reference

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coronary artery disease

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6

Ernst J Schaefer

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

author name string

Raul D Santos

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

Bela F Asztalos

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

Lilton R C Martinez

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

Marcio H Miname

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

Eliana Polisecki

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

language of work or name

English

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publication date

13 June 2008

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PubMed publication ID

21291740

Journal of Clinical Lipidology

24 August 2017

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

issue

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

page(s)

237-247

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

Compound heterozygosity for an apolipoprotein A1 gene promoter mutation and a structural nonsense mutation with apolipoprotein A1 deficiency

13 May 2020

cites work

1 reference

12 December 2020

An inherited polymorphism in the human apolipoprotein A-I gene locus related to the development of atherosclerosis

1 reference

12 December 2020

Case report: retinopathy and neuropathy associated with complete apolipoprotein A-I deficiency

1 reference

12 December 2020

Familial apolipoprotein A-I and C-III deficiency, variant II.

1 reference

12 December 2020

Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindreds

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

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

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

Effect of blood high density lipoprotein cholesterol concentration on fecal steroid excretion in humans

1 reference

12 December 2020

Ocular Manifestations of Familial High-Density Lipoprotein Deficiency (Tangier Disease)

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

Apolipoprotein B metabolism in subjects with deficiency of apolipoproteins CIII and AI. Evidence that apolipoprotein CIII inhibits catabolism of triglyceride-rich lipoproteins by lipoprotein lipase in vivo

1 reference

12 December 2020

Diabetes, plasma insulin, and cardiovascular disease: subgroup analysis from the Department of Veterans Affairs high-density lipoprotein intervention trial (VA-HIT).

1 reference

12 December 2020

Deficiency of apolipoproteins A-I and C-III and severe coronary heart disease

1 reference

12 December 2020

The pathology of Tangier disease. A light and electron microscopic study

1 reference

12 December 2020

Plasma-triglycerides in regulation of H.D.L.-cholesterol levels

1 reference

12 December 2020

Lipoprotein abnormalities in primary biliary cirrhosis. Association with hepatic lipase inhibition as well as altered cholesterol esterification.

1 reference

12 December 2020

The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families

1 reference

12 December 2020

Apolipoprotein A-I(Milano) and apolipoprotein A-I(Paris) exhibit an antioxidant activity distinct from that of wild-type apolipoprotein A-I.

1 reference

12 December 2020

Neuropathy in Tangier disease. Alpha-Lipoprotein deficiency manifesting as familial recurrent neuropathy and intestinal lipid storage.

1 reference

12 December 2020

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

1 reference

12 December 2020

Homozygous Tangier disease and cardiovascular disease

1 reference

12 December 2020

Familial hypoalphalipoproteinemia in premature coronary artery disease

1 reference

12 December 2020

Change in alpha1 HDL concentration predicts progression in coronary artery stenosis

1 reference

12 December 2020

Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency

1 reference

12 December 2020

A novel two nucleotide deletion in the apolipoprotein A-I gene, apoA-I Shinbashi, associated with high density lipoprotein deficiency, corneal opacities, planar xanthomas, and premature coronary artery disease

1 reference

12 December 2020

Cellular cholesterol efflux in heterozygotes for tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle size

1 reference

12 December 2020

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency

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

Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group

1 reference

12 December 2020

Role of LCAT in HDL remodeling: investigation of LCAT deficiency states

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12 December 2020

Subpopulations of high density lipoproteins in homozygous and heterozygous Tangier disease

1 reference

12 December 2020

Relation of gemfibrozil treatment and lipid levels with major coronary events: VA-HIT: a randomized controlled trial

1 reference

12 December 2020

Molecular cloning of the human ATP-binding cassette transporter 1 (hABC1): evidence for sterol-dependent regulation in macrophages.

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

Familial lipoprotein disorders in patients with premature coronary artery disease

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12 December 2020

High-density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants of the Framingham Offspring Study

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12 December 2020

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

1 reference

12 December 2020

Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease

1 reference

12 December 2020

Effect of apolipoprotein activators on the specificity of lecithin:cholesterol acyltransferase: determination of cholesteryl esters formed in A-I/C-III deficiency

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12 December 2020

Severe acquired (secondary) high-density lipoprotein deficiency

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12 December 2020

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

1 reference

12 December 2020

Prevalence of risk factors in men with premature coronary artery disease

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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

Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency

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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

Familial apolipoprotein AI and apolipoprotein CIII deficiency. Subclass distribution, composition, and morphology of lipoproteins in a disorder associated with premature atherosclerosis

1 reference

12 December 2020

Value of high-density lipoprotein (HDL) subpopulations in predicting recurrent cardiovascular events in the Veterans Affairs HDL Intervention Trial

1 reference

12 December 2020

DNA inversion within the apolipoproteins AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosis

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12 December 2020

Characterization of apoA- and apoB-containing lipoprotein particles in a variant of familial apoA-I deficiency with planar xanthoma: the metabolic significance of LP-A-II particles

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12 December 2020

Differential effects of HDL subpopulations on cellular ABCA1- and SR-BI-mediated cholesterol efflux

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12 December 2020

Cholesterol and apolipoprotein B metabolism in Tangier disease

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12 December 2020

HDL-mediated efflux of intracellular cholesterol is impaired in fibroblasts from Tangier disease patients

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12 December 2020

Isolation and Characterization of an Abnormal High Density Lipoprotein in Tangier Disease

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12 December 2020

10.1016/J.JACL.2008.06.002

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6942923&resulttype=core&format=json

13 May 2020

PubMed publication ID

21291740

1 reference