Traffic, polarity, and detergent solubility of a glycosylphosphatidylinositol-anchored protein after LDL-deprivation of MDCK cells.
about
GPI anchoring leads to sphingolipid-dependent retention of endocytosed proteins in the recycling endosomal compartment.Podocyte slit-diaphragm protein nephrin is linked to the actin cytoskeletonFunctional heterogeneity of Thy-1 membrane microdomains in rat basophilic leukemia cells.Evidence for budding of human immunodeficiency virus type 1 selectively from glycolipid-enriched membrane lipid rafts.Biochemical characterization of rotavirus receptors in MA104 cellsAbsence of direct delivery for single transmembrane apical proteins or their "Secretory" forms in polarized hepatic cells.The organizing potential of sphingolipids in intracellular membrane transport.Lipid metabolism and vesicle trafficking: more than just greasing the transport machinery.High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranesRafts: scale-dependent, active lipid organization at the cell surface.Distribution of a glycosylphosphatidylinositol-anchored protein at the apical surface of MDCK cells examined at a resolution of <100 A using imaging fluorescence resonance energy transferAcute cholesterol depletion inhibits clathrin-coated pit budding.Influenza virus morphogenesis and budding.Detergent-insoluble GPI-anchored proteins are apically sorted in fischer rat thyroid cells, but interference with cholesterol or sphingolipids differentially affects detergent insolubility and apical sorting.Anti-tetherin activities of HIV-1 Vpu and Ebola virus glycoprotein do not involve removal of tetherin from lipid rafts.Intra-Golgi protein transport depends on a cholesterol balance in the lipid membrane.Cytoplasmic signals mediate apical early endosomal targeting of endotubin in MDCK cells.N-Glycans mediate the apical sorting of a GPI-anchored, raft-associated protein in Madin-Darby canine kidney cells.Annexin XIIIb associates with lipid microdomains to function in apical delivery.Interaction of influenza virus haemagglutinin with sphingolipid-cholesterol membrane domains via its transmembrane domain.Signal transduction via glycosyl phosphatidylinositol-anchored proteins in T cells is inhibited by lowering cellular cholesterol.Cholesterol is required for surface transport of influenza virus hemagglutinin.Lipid raft disruption by cholesterol depletion enhances influenza A virus budding from MDCK cells.Effects of cholesterol depletion by cyclodextrin on the sphingolipid microdomains of the plasma membrane.Ras diffusion is sensitive to plasma membrane viscosity.Potentiation of Fas-mediated apoptosis by an engineered glycosylphosphatidylinositol-linked Fas.Variations in the effects on synthesis of amyloid beta protein in modulated autophagic conditions.Basic mechanisms of secretion: sorting into the regulated secretory pathway
P2860
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P2860
Traffic, polarity, and detergent solubility of a glycosylphosphatidylinositol-anchored protein after LDL-deprivation of MDCK cells.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@ast
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@en
type
label
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@ast
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@en
prefLabel
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@ast
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@en
P2860
P356
P1476
Traffic, polarity, and deterge ...... LDL-deprivation of MDCK cells.
@en
P2093
P2860
P304
P356
10.1083/JCB.133.6.1265
P407
P577
1996-06-01T00:00:00Z