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Journal Abstract Search

287 related items for PubMed ID: 9151796

  • 1. 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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  • 3. 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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  • 4. 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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  • 10. 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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  • 11. Production and characterization of transformed B-lymphocytes expressing the membrane defect of Scott syndrome.
    Kojima H, Newton-Nash D, Weiss HJ, Zhao J, Sims PJ, Wiedmer T.
    J Clin Invest; 1994 Dec 10; 94(6):2237-44. PubMed ID: 7989579
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  • 12. Facilitated phosphatidylserine (PS) flip-flop and thrombin activation using a synthetic PS scramblase.
    Boon JM, Lambert TN, Sisson AL, Davis AP, Smith BD.
    J Am Chem Soc; 2003 Jul 09; 125(27):8195-201. PubMed ID: 12837089
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  • 13. Influence of erythrocyte shape on the rate of Ca2+-induced scrambling of phosphatidylserine.
    Wolfs JL, Comfurius P, Bevers EM, Zwaal RF.
    Mol Membr Biol; 2003 Jul 09; 20(1):83-91. PubMed ID: 12745928
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  • 14. Roles and regulation of phospholipid scramblases.
    Kodigepalli KM, Bowers K, Sharp A, Nanjundan M.
    FEBS Lett; 2015 Jan 02; 589(1):3-14. PubMed ID: 25479087
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  • 15. 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 02; 9(10):1883-91. PubMed ID: 21958383
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  • 17. Reconstitution of phospholipid scramblase activity from human blood platelets.
    Comfurius P, Williamson P, Smeets EF, Schlegel RA, Bevers EM, Zwaal RF.
    Biochemistry; 1996 Jun 18; 35(24):7631-4. PubMed ID: 8672463
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  • 20. Defective Ca(2+)-induced microvesiculation and deficient expression of procoagulant activity in erythrocytes from a patient with a bleeding disorder: a study of the red blood cells of Scott syndrome.
    Bevers EM, Wiedmer T, Comfurius P, Shattil SJ, Weiss HJ, Zwaal RF, Sims PJ.
    Blood; 1992 Jan 15; 79(2):380-8. PubMed ID: 1730083
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