Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains.
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Structural requirements for the recruitment of Gaa1 into a functional glycosylphosphatidylinositol transamidase complexHuman PIG-U and yeast Cdc91p are the fifth subunit of GPI transamidase that attaches GPI-anchors to proteinsBiochemical and morphological changes in endothelial cells in response to hypoxic interstitial edema.Lipid raft: A floating island of death or survivalYeast ARV1 is required for efficient delivery of an early GPI intermediate to the first mannosyltransferase during GPI assembly and controls lipid flow from the endoplasmic reticulum.The tetraspan protein EMP2 modulates the surface expression of caveolins and glycosylphosphatidyl inositol-linked proteinsHeparanase induces Akt phosphorylation via a lipid raft receptorArachidonic acid release from mammalian cells transfected with human groups IIA and X secreted phospholipase A(2) occurs predominantly during the secretory process and with the involvement of cytosolic phospholipase A(2)-alpha.Diabodies targeting epithelial membrane protein 2 reduce tumorigenicity of human endometrial cancer cell linesAnnexin 2 promotes the formation of lipid microdomains required for calcium-regulated exocytosis of dense-core vesicles.Differential sorting and fate of endocytosed GPI-anchored proteins.Initial steps of Shigella infection depend on the cholesterol/sphingolipid raft-mediated CD44-IpaB interactionQuantitative proteomics of caveolin-1-regulated proteins: characterization of polymerase i and transcript release factor/CAVIN-1 IN endothelial cellsRafts can trigger contact-mediated secretion of bacterial effectors via a lipid-based mechanism.Sensitivity of polarized epithelial cells to the pore-forming toxin aerolysin.Myelin associated glycoprotein cross-linking triggers its partitioning into lipid rafts, specific signaling events and cytoskeletal rearrangements in oligodendrocytes.Membrane dynamics, cholesterol homeostasis, and Alzheimer's disease.Impaired FcεRI stability, signaling, and effector functions in murine mast cells lacking glycosylphosphatidylinositol-anchored proteins.Lipid rafts: heterogeneity on the high seas.Interaction with caveolin-1 modulates G protein coupling of mouse β3-adrenoceptor.Glycosylphosphatidylinositol anchors regulate glycosphingolipid levels.Membranes: a meeting point for lipids, proteins and therapiesSignificance of glycosylphosphatidylinositol-anchored protein enrichment in lipid rafts for the control of autoimmunity.Peroxisome dependency of alkyl-containing GPI-anchor biosynthesis in the endoplasmic reticulum.Entry of the lymphogranuloma venereum strain of Chlamydia trachomatis into host cells involves cholesterol-rich membrane domains.Ceramide function in the brain: when a slight tilt is enough.Requirement of N-glycan on GPI-anchored proteins for efficient binding of aerolysin but not Clostridium septicum alpha-toxin.Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.The role of cholesterol in UV light B-induced apoptosisAfa/Dr diffusely adhering Escherichia coli infection in T84 cell monolayers induces increased neutrophil transepithelial migration, which in turn promotes cytokine-dependent upregulation of decay-accelerating factor (CD55), the receptor for Afa/Dr aCaveolin mediates rapid glucocorticoid effects and couples glucocorticoid action to the antiproliferative program.A GPI-anchored co-receptor for tissue factor pathway inhibitor controls its intracellular trafficking and cell surface expression.Glycosylphosphatidylinositol-anchored proteins regulate transforming growth factor-beta signaling in human keratinocytes.Involvement of a Golgi-resident GPI-anchored protein in maintenance of the Golgi structure.Heliothis virescens and Manduca sexta lipid rafts are involved in Cry1A toxin binding to the midgut epithelium and subsequent pore formation.Domain architecture of the smooth-muscle plasma membrane: regulation by annexins.Association of Helicobacter pylori vacuolating toxin (VacA) with lipid rafts.Compositional changes in lipid microdomains of air-blood barrier plasma membranes in pulmonary interstitial edema.The NK1 receptor localizes to the plasma membrane microdomains, and its activation is dependent on lipid raft integrity.The glycan core of GPI-anchored proteins modulates aerolysin binding but is not sufficient: the polypeptide moiety is required for the toxin-receptor interaction.
P2860
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P2860
Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains.
@en
type
label
Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains.
@en
prefLabel
Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains.
@en
P2860
P50
P356
P1476
Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains
@en
P2093
Kinoshita T
Kobayashi T
P2860
P304
30729-30736
P356
10.1074/JBC.M102039200
P407
P577
2001-06-13T00:00:00Z