Assessing the role of the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) three-finger domain in binding lipoprotein lipase
about
Glycosylphosphatidylinositol-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 triacylglycerolPalmoplantar keratoderma along with neuromuscular and metabolic phenotypes in Slurp1-deficient miceMultimerization of glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) and familial chylomicronemia from a serine-to-cysteine substitution in GPIHBP1 Ly6 domainGPIHBP1, an endothelial cell transporter for lipoprotein lipase.High-resolution imaging of dietary lipids in cells and tissues by NanoSIMS analysis.Identification 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).Chylomicronemia mutations yield new insights into interactions between lipoprotein lipase and GPIHBP1New 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.Monoclonal antibodies that bind to the Ly6 domain of GPIHBP1 abolish the binding of LPL.An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.GPIHBP1 and Plasma Triglyceride Metabolism.Angiopoietin-like 4 promotes intracellular degradation of lipoprotein lipase in adipocytes.Functional validation of GPIHBP1 and identification of a functional mutation in GPIHBP1 for milk fat traits in dairy cattleGPIHBP1 missense mutations often cause multimerization of GPIHBP1 and thereby prevent lipoprotein lipase binding.Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia.Lipoprotein lipase reaches the capillary lumen in chickens despite an apparent absence of GPIHBP1.Mutating a conserved cysteine in GPIHBP1 reduces amounts of GPIHBP1 in capillaries and abolishes LPL binding.GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia.
P2860
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P2860
Assessing the role of the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) three-finger domain in binding lipoprotein lipase
description
2011 nî lūn-bûn
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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年論文
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2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
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name
Assessing the role of the glyc ...... in binding lipoprotein lipase
@ast
Assessing the role of the glyc ...... in binding lipoprotein lipase
@en
type
label
Assessing the role of the glyc ...... in binding lipoprotein lipase
@ast
Assessing the role of the glyc ...... in binding lipoprotein lipase
@en
prefLabel
Assessing the role of the glyc ...... in binding lipoprotein lipase
@ast
Assessing the role of the glyc ...... in binding lipoprotein lipase
@en
P2093
P2860
P356
P1476
Assessing the role of the glyc ...... in binding lipoprotein lipase
@en
P2093
André Bensadoun
Anne P Beigneux
Clive R Pullinger
Constance V Voss
Jenny Chen
Loren G Fong
Michael M Weinstein
Shelly Tat
P2860
P304
19735-19743
P356
10.1074/JBC.M111.242024
P407
P577
2011-04-07T00:00:00Z