Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
about
Familial apolipoprotein E deficiencySequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene.Cholesteryl ester accumulation in mouse peritoneal macrophages induced by beta-migrating very low density lipoproteins from patients with atypical dysbetalipoproteinemiaType III hyperlipoproteinemic phenotype in transgenic mice expressing dysfunctional apolipoprotein E.Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriersFamilial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigreeMolecular etiology of a dominant form of type III hyperlipoproteinemia caused by R142C substitution in apoE4Fat feeding in humans induces lipoproteins of density less than 1.006 that are enriched in apolipoprotein [a] and that cause lipid accumulation in macrophagesPre-beta-very low density lipoproteins as precursors of beta-very low density lipoproteins. A model for the pathogenesis of familial dysbetalipoproteinemia (type III hyperlipoproteinemia)Type III hyperlipoproteinemia associated with apolipoprotein E phenotype E3/3. Structure and genetics of an apolipoprotein E3 variantHigh receptor binding affinity of lipoproteins in atypical dysbetalipoproteinemia (type III hyperlipoproteinemia)A novel electrophoretic variant of human apolipoprotein E. Identification and characterization of apolipoprotein E1Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks.Apolipoprotein E2-Christchurch (136 Arg----Ser). New variant of human apolipoprotein E in a patient with type III hyperlipoproteinemiaDominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu).NMR studies of the low-density lipoprotein receptor-binding peptide of apolipoprotein E bound to dodecylphosphocholine micellesLipoproteins of special significance in atherosclerosis. Insights provided by studies of type III hyperlipoproteinemia.LDL receptor deficiency or apoE mutations prevent remnant clearance and induce hypertriglyceridemia in mice.Hypolipidemic and hyperlipidemic phenotypes in transgenic mice expressing human apolipoprotein E2.
P2860
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P2860
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
description
1983 nî lūn-bûn
@nan
1983 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1983 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1983年の論文
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1983年学术文章
@wuu
1983年学术文章
@zh-cn
1983年学术文章
@zh-hans
1983年学术文章
@zh-my
1983年学术文章
@zh-sg
1983年學術文章
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name
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@ast
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@en
type
label
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@ast
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@en
prefLabel
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@ast
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@en
P2093
P2860
P356
P1476
Atypical familial dysbetalipoproteinemia associated with apolipoprotein phenotype E3/3.
@en
P2093
P2860
P304
P356
10.1172/JCI110978
P407
P577
1983-07-01T00:00:00Z