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Journal Abstract Search

237 related items for PubMed ID: 9814689

  • 1. Regulatory mechanisms of transmembrane phospholipid distributions and pathophysiological implications of transbilayer lipid scrambling.
    Bevers EM, Comfurius P, Dekkers DW, Harmsma M, Zwaal RF.
    Lupus; 1998; 7 Suppl 2():S126-31. PubMed ID: 9814689
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  • 2. Regulatory mechanisms in maintenance and modulation of transmembrane lipid asymmetry: pathophysiological implications.
    Bevers EM, Comfurius P, Zwaal RF.
    Lupus; 1996 Oct; 5(5):480-7. PubMed ID: 8902787
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  • 6. Platelet membrane phospholipid asymmetry: from the characterization of a scramblase activity to the identification of an essential protein mutated in Scott syndrome.
    Lhermusier T, Chap H, Payrastre B.
    J Thromb Haemost; 2011 Oct; 9(10):1883-91. PubMed ID: 21958383
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  • 7. Impaired Ca2+-induced tyrosine phosphorylation and defective lipid scrambling in erythrocytes from a patient with Scott syndrome: a study using an inhibitor for scramblase that mimics the defect in Scott syndrome.
    Dekkers DW, Comfurius P, Vuist WM, Billheimer JT, Dicker I, Weiss HJ, Zwaal RF, Bevers EM.
    Blood; 1998 Mar 15; 91(6):2133-8. PubMed ID: 9490700
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  • 8. Unraveling the mysteries of phospholipid scrambling.
    Sims PJ, Wiedmer T.
    Thromb Haemost; 2001 Jul 15; 86(1):266-75. PubMed ID: 11487015
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  • 9. Mechanisms of phosphatidylserine exposure, a phagocyte recognition signal, on apoptotic T lymphocytes.
    Verhoven B, Schlegel RA, Williamson P.
    J Exp Med; 1995 Nov 01; 182(5):1597-601. PubMed ID: 7595231
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  • 10. Stimulated nonspecific transport of phospholipids results in elevated external appearance of phosphatidylserine in ras-transformed fibroblasts.
    Momchilova A, Ivanova L, Markovska T, Pankov R.
    Arch Biochem Biophys; 2000 Sep 15; 381(2):295-301. PubMed ID: 11032418
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  • 15. Phospholipid scramblase activation pathways in lymphocytes.
    Williamson P, Christie A, Kohlin T, Schlegel RA, Comfurius P, Harmsma M, Zwaal RF, Bevers EM.
    Biochemistry; 2001 Jul 10; 40(27):8065-72. PubMed ID: 11434775
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  • 16. Isolation of an erythrocyte membrane protein that mediates Ca2+-dependent transbilayer movement of phospholipid.
    Bassé F, Stout JG, Sims PJ, Wiedmer T.
    J Biol Chem; 1996 Jul 19; 271(29):17205-10. PubMed ID: 8663431
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  • 17. Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids.
    Stout JG, Bassé F, Luhm RA, Weiss HJ, Wiedmer T, Sims PJ.
    J Clin Invest; 1997 May 01; 99(9):2232-8. PubMed ID: 9151796
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  • 18. Scott syndrome, a bleeding disorder caused by defective scrambling of membrane phospholipids.
    Zwaal RF, Comfurius P, Bevers EM.
    Biochim Biophys Acta; 2004 Mar 22; 1636(2-3):119-28. PubMed ID: 15164759
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  • 19. Ca2+ sensitivity of phospholipid scrambling in human red cell ghosts.
    Woon LA, Holland JW, Kable EP, Roufogalis BD.
    Cell Calcium; 1999 Apr 22; 25(4):313-20. PubMed ID: 10456228
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  • 20. Appearance of phosphatidylserine on apoptotic cells requires calcium-mediated nonspecific flip-flop and is enhanced by loss of the aminophospholipid translocase.
    Bratton DL, Fadok VA, Richter DA, Kailey JM, Guthrie LA, Henson PM.
    J Biol Chem; 1997 Oct 17; 272(42):26159-65. PubMed ID: 9334182
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