Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
about
Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiencyApolipoprotein CIISt. Michael. Familial apolipoprotein CII deficiency associated with premature vascular diseaseApolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patientsIsolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CIIStructure of apolipoprotein C-IIToronto, a nonfunctional human apolipoproteinA nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiencyNo severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency allelesMonascus purpureus-fermented Thai glutinous rice reduces blood and hepatic cholesterol and hepatic steatosis concentrations in diet-induced hypercholesterolemic rats.New mutants of apolipoprotein E associated with atherosclerotic diseases but not to type III hyperlipoproteinemia.Molecular studies on primary lipoprotein lipase (LPL) deficiency. One base deletion (G916) in exon 5 of LPL gene causes no detectable LPL protein due to the absence of LPL mRNA transcript.Human apolipoprotein C-II: complete nucleic acid sequence of preapolipoprotein C-II.Hydroxysafflor yellow A alleviates myocardial ischemia/reperfusion in hyperlipidemic animals through the suppression of TLR4 signalingA deletion of one nucleotide results in functional deficiency of apolipoprotein CII (apo CII Toronto).Diet alters performance and transcription patterns in Oedaleus asiaticus (Orthoptera: Acrididae) grasshoppersLipoprotein lipase with a defect in lipid interface recognition in a case with type I hyperlipidaemia.Kinetic analysis of apolipoproteins in postprandial hypertriglyceridaemia rabbits.Heterozygous apolipoprotein C-II deficiency: lipoprotein and apoprotein phenotype and RsaI restriction enzyme polymorphism in the Apo C-IIPadova kindred.Apolipoprotein C-II deficiency syndrome due to apo C-IIHamburg: clinical and biochemical features and HphI restriction enzyme polymorphism.
P2860
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P2860
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
description
1979 nî lūn-bûn
@nan
1979 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@ast
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@en
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@nl
type
label
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@ast
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@en
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@nl
prefLabel
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@ast
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@en
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@nl
P2093
P1433
P1476
Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency.
@en
P2093
P356
10.1016/0021-9150(79)90106-0
P577
1979-09-01T00:00:00Z