About: Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion

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About: Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 1981

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1981 (uk) artículu científicu espublizáu en febreru de 1981 (ast) scientific article published on 01 February 1981 (en) im Februar 1981 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q71541866-5A04C4C2-23CE-429B-B6B1-4DC11C23EFEF
publication date	1981-02-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q71541866-047BF721-8828-4C2F-94DC-2EA57BD3E651 wds:Q71541866-18F34368-76B3-46A3-9392-379E40A29336 wds:Q71541866-33A77042-870F-4B32-9D87-9BB967D22749 wds:Q71541866-7ED34DFD-12E0-4846-A512-F7FDC64ECED9 wds:Q71541866-B3086FD0-9051-4595-BD56-A9E7F9F3ACFC wds:Q71541866-B75EE0A6-FEB1-4186-864C-A0D3BA5B2DE1 wds:Q71541866-E64F7F3C-0266-43E7-A318-50960F93513C
author name string	P Alaupovic N E Miller J D Brunzell B Lewis J Slack S N Rao N Noble
rdfs:label	Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (en) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (nl) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (sq)
skos:prefLabel	Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (en) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (nl) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (sq)
name	Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (en) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (nl) Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (sq)
title	wds:Q71541866-63C3B2B5-EF84-49C6-A87E-EBE52AFDE52F
title	Familial apolipoprotein CII deficiency: plasma lipoproteins and apolipoproteins in heterozygous and homozygous subjects and the effects of plasma infusion (en)
page(s)	wds:Q71541866-AB5D51AE-ED08-4FC1-915E-65B2DF9572F2
page(s)	69-76
instance of	wds:Q71541866-E2482E3D-B2CC-4B15-BF46-18AB044F9EEA
instance of	scholarly article
main subject	wds:Q71541866-AD012D30-3CFF-4D02-8744-DE99B0B43006 wds:Q71541866-BCC5B275-F2D0-4674-8614-A8761561C16E
main subject	homozygosity heterozygosity
PubMed ID	wds:Q71541866-89E14EF3-B680-4661-9016-D820C9B55C6C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6783432
PubMed ID	6783432
published in	wds:Q71541866-4705B9F1-2C5F-44CC-9EB6-CBF763ADCEAB
published in	European Journal of Clinical Investigation
issue	wds:Q71541866-0AE97829-8265-456E-87E7-494E1ECF4768
volume	wds:Q71541866-10969431-95EB-41D6-927A-7A0F162D1B84
issue	1
volume	11
DOI	wds:Q71541866-42328B60-64C8-4B89-ABE1-71A5CF2B1C4F
DOI	http://dx.doi.org/10.1111/J.1365-2362.1981.TB01768.X
DOI	10.1111/J.1365-2362.1981.TB01768.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71541866
is cites work of	Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19 Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man Chromosomal localization of the human apoprotein ci gene and of a polymorphic apoprotein AII gene Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiency Apolipoprotein CIISt. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients Human plasma apolipoprotein C-II: total solid-phase synthesis and chemical and biological characterization Structure of apolipoprotein C-IIToronto, a nonfunctional human apolipoprotein A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiency Apolipoprotein C-II deficiency: Identification of a structural variant apoC-IIPadova Analysis of the apoC-II gene in apoC-II deficient patients The familial chylomicronemia syndrome Human apolipoprotein C-II: complete nucleic acid sequence of preapolipoprotein C-II. The localization of the gene for apolipoprotein C-II to chromosome 19 Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII Mechanism of hypertriglyceridemia in human apolipoprotein (apo) CIII transgenic mice. Diminished very low density lipoprotein fractional catabolic rate associated with increased apo CIII and reduced apo E on the particles Abnormalities in very low, low and high density lipoproteins in hypertriglyceridemia. Reversal toward normal with bezafibrate treatment Localization of genes encoding apolipoproteins CI, CII, and E to the p13----cen region of human chromosome 19. Hypertriglyceridaemia due to genetic defects in lipoprotein lipase and apolipoprotein C-II Enzymes involved in triglyceride hydrolysis A novel type hypertriglyceridemia observed in FLS mice The role of exercise training in the therapy of hyperlipoproteinemia. Defective metabolism of hypertriglyceridemic low density lipoprotein in cultured human skin fibroblasts. Normalization with bezafibrate therapy Effects of heparin infusion on plasma lipoproteins in subjects with lipoprotein lipase deficiency. Evidence for a role of hepatic endothelial lipase in the metabolism of high-density lipoprotein subfractions in man Lipoproteins and lipoprotein metabolism. A dynamic evaluation of the plasma fat transport system Human immunoglobulin G stimulates human adipocyte lipogenesis A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis. Apo C-II deficiency type Bari A deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto). The role of apoproteins in disorders of lipoprotein metabolism Lipoprotein lipase: Mechanism of action and role in lipoprotein metabolism Genes and nutrition in the regulation of human lipoprotein metabolism Apolipoproteins in lipid transport, an impressionist view [Apolipoproteinopathies] Familial lipoprotein lipase deficiency: abnormal lipoproteins and defective metabolism of low density lipoproteins in cultured human skin fibroblasts Studies on an apolipoprotein C-II variant occurring in Caucasians Classification of primary dyslipoproteinemias.
is cites work of	wds:Q24618630-99A8E8BB-EC09-41B0-9E8E-76FA62918A1E wds:Q24620852-4C5B420D-A0BA-4411-900E-16631F07A26A wds:Q28286373-08A85CD0-1623-4354-9438-FA09E54565A3 wds:Q24595943-F85D6E82-7516-4C2B-BD73-9DC6928245E3 wds:Q44594566-2BA0C3E6-C5D6-469C-A404-682A80C88545 wds:Q36992958-E2F3F978-AB46-4F92-BCC5-916D1C0DA11D wds:Q68446482-D633547E-7E81-4A42-B860-1B5673256758 wds:Q24561514-8F9F0A65-6B9D-4C10-93D5-448951ED9329

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