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Journal Abstract Search

217 related items for PubMed ID: 8603914

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  • 3. Segregation of glucosylceramide and sphingomyelin occurs in the apical to basolateral transcytotic route in HepG2 cells.
    van IJzendoorn SC, Zegers MM, Kok JW, Hoekstra D.
    J Cell Biol; 1997 Apr 21; 137(2):347-57. PubMed ID: 9128247
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  • 4. Sorting of sphingolipids in epithelial (Madin-Darby canine kidney) cells.
    van Meer G, Stelzer EH, Wijnaendts-van-Resandt RW, Simons K.
    J Cell Biol; 1987 Oct 21; 105(4):1623-35. PubMed ID: 3667693
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  • 6. Epithelial sphingolipid sorting allows for extensive variation of the fatty acyl chain and the sphingosine backbone.
    van't Hof W, Silvius J, Wieland F, van Meer G.
    Biochem J; 1992 May 01; 283 ( Pt 3)(Pt 3):913-7. PubMed ID: 1590779
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  • 8. Epithelial sphingolipid sorting is insensitive to reorganization of the Golgi by nocodazole, but is abolished by monensin in MDCK cells and by brefeldin A in Caco-2 cells.
    van Meer G, van 't Hof W.
    J Cell Sci; 1993 Mar 01; 104 ( Pt 3)():833-42. PubMed ID: 8314877
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  • 9. Hierarchy of mechanisms involved in generating Na/K-ATPase polarity in MDCK epithelial cells.
    Mays RW, Siemers KA, Fritz BA, Lowe AW, van Meer G, Nelson WJ.
    J Cell Biol; 1995 Sep 01; 130(5):1105-15. PubMed ID: 7657695
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  • 11. Conversion of diacylglycerol to phosphatidylcholine on the basolateral surface of epithelial (Madin-Darby canine kidney) cells. Evidence for the reverse action of a sphingomyelin synthase.
    van Helvoort A, van't Hof W, Ritsema T, Sandra A, van Meer G.
    J Biol Chem; 1994 Jan 21; 269(3):1763-9. PubMed ID: 8294425
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  • 12. Trans-Golgi network and subapical compartment of HepG2 cells display different properties in sorting and exiting of sphingolipids.
    Maier O, Hoekstra D.
    J Biol Chem; 2003 Jan 03; 278(1):164-73. PubMed ID: 12407103
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  • 14. Fluorescent, short-chain C6-NBD-sphingomyelin, but not C6-NBD-glucosylceramide, is subject to extensive degradation in the plasma membrane: implications for signal transduction related to cell differentiation.
    Kok JW, Babia T, Klappe K, Hoekstra D.
    Biochem J; 1995 Aug 01; 309 ( Pt 3)(Pt 3):905-12. PubMed ID: 7639709
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  • 15. Sphingolipid transport from the trans-Golgi network to the apical surface in permeabilized MDCK cells.
    Kobayashi T, Pimplikar SW, Parton RG, Bhakdi S, Simons K.
    FEBS Lett; 1992 Apr 06; 300(3):227-31. PubMed ID: 1555649
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  • 17. Cholesterol-dependent increases in glucosylceramide synthase activity in Niemann-Pick disease type C model cells: Abnormal trafficking of endogenously formed ceramide metabolites by inhibition of the enzyme.
    Hashimoto N, Matsumoto I, Takahashi H, Ashikawa H, Nakamura H, Murayama T.
    Neuropharmacology; 2016 Nov 06; 110(Pt A):458-469. PubMed ID: 27539961
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  • 18. Rat liver dipeptidylpeptidase IV contains competing apical and basolateral targeting information.
    Weisz OA, Machamer CE, Hubbard AL.
    J Biol Chem; 1992 Nov 05; 267(31):22282-8. PubMed ID: 1358878
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  • 19. Apical and basolateral coated pits of MDCK cells differ in their rates of maturation into coated vesicles, but not in the ability to distinguish between mutant hemagglutinin proteins with different internalization signals.
    Naim HY, Dodds DT, Brewer CB, Roth MG.
    J Cell Biol; 1995 Jun 05; 129(5):1241-50. PubMed ID: 7775571
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  • 20. Intracellular translocation of fluorescent sphingolipids in cultured fibroblasts: endogenously synthesized sphingomyelin and glucocerebroside analogues pass through the Golgi apparatus en route to the plasma membrane.
    Lipsky NG, Pagano RE.
    J Cell Biol; 1985 Jan 05; 100(1):27-34. PubMed ID: 3965473
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