Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
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Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defectsGPIHBP1 is responsible for the entry of lipoprotein lipase into capillariesEvaluation and treatment of hypertriglyceridemia: an Endocrine Society clinical practice guidelineThe ANGPTL3-4-8 model, a molecular mechanism for triglyceride traffickingGlycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 and the intravascular processing of triglyceride-rich lipoproteinsHeterogeneity in the properties of mutant secreted lymphocyte antigen 6/urokinase receptor-related protein 1 (SLURP1) in Mal de MeledaInfluence of apolipoprotein A-V on the metabolic fate of triacylglycerolGenetic Variants Associated with Gestational Hypertriglyceridemia and PancreatitisOver-expression of human lipoprotein lipase in mouse mammary glands leads to reduction of milk triglyceride and delayed growth of suckling pupsTreatment options for hypertriglyceridemia: from risk reduction to pancreatitis.Multimerization of glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) and familial chylomicronemia from a serine-to-cysteine substitution in GPIHBP1 Ly6 domainChildhood-onset chylomicronaemia with reduced plasma lipoprotein lipase activity and mass: identification of a novel GPIHBP1 mutation.GPIHBP1 and the processing of triglyceride-rich lipoproteinsGPIHBP1, an endothelial cell transporter for lipoprotein lipase.Cholesterol intake modulates plasma triglyceride levels in glycosylphosphatidylinositol HDL-binding protein 1-deficient mice.Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia.Binding preferences for GPIHBP1, a glycosylphosphatidylinositol-anchored protein of capillary endothelial cellsEquivalent binding of wild-type lipoprotein lipase (LPL) and S447X-LPL to GPIHBP1, the endothelial cell LPL transporter.APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.Localization of lipoprotein lipase and GPIHBP1 in mouse pancreas: effects of diet and leptin deficiency.Genetic determinants of plasma triglyceridesMutations in lipoprotein lipase that block binding to the endothelial cell transporter GPIHBP1Assessing the role of the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) three-finger domain in binding lipoprotein lipaseIdentification and quantitative mRNA analysis of a novel splice variant of GPIHBP1 in dairy cattle.Evidence for Two Distinct Binding Sites for Lipoprotein Lipase on Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1).Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaDeletion of GPIHBP1 causing severe chylomicronemiaNew wrinkles in lipoprotein lipase biology.The acidic domain of the endothelial membrane protein GPIHBP1 stabilizes lipoprotein lipase activity by preventing unfolding of its catalytic domain.Biochemistry and pathophysiology of intravascular and intracellular lipolysis.The metabolism of triglyceride-rich lipoproteins revisited: new players, new insight.Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemiaEndothelium as a gatekeeper of fatty acid transport.A novel lipoprotein lipase gene missense mutation in Chinese patients with severe hypertriglyceridemia and pancreatitis.The complex genetic basis of plasma triglycerides.Chylomicronaemia--current diagnosis and future therapies.Mobility of "HSPG-bound" LPL explains how LPL is able to reach GPIHBP1 on capillaries.An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.GPIHBP1 and Plasma Triglyceride Metabolism.Angiopoietin-like 4 Modifies the Interactions between Lipoprotein Lipase and Its Endothelial Cell Transporter GPIHBP1.
P2860
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P2860
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@ast
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@en
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@nl
type
label
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@ast
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@en
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@nl
prefLabel
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@ast
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@en
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@nl
P2093
P2860
P50
P356
P1476
Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.
@en
P2093
Anna Lindberg
Anne P Beigneux
Brandon S J Davies
Elena Makoveichuk
Loren G Fong
Michael M Weinstein
Olle Hernell
Thomas Olivecrona
P2860
P304
P356
10.1194/JLR.M002717
P577
2009-12-21T00:00:00Z