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Journal Abstract Search

177 related items for PubMed ID: 9716599

  • 21. Transbilayer phospholipid movements in ABCA1-deficient cells.
    Williamson P, Halleck MS, Malowitz J, Ng S, Fan X, Krahling S, Remaley AT, Schlegel RA.
    PLoS One; 2007 Aug 15; 2(8):e729. PubMed ID: 17710129
    [Abstract] [Full Text] [Related]

  • 22. Phosphatidylserine exposure during apoptosis is a cell-type-specific event and does not correlate with plasma membrane phospholipid scramblase expression.
    Fadeel B, Gleiss B, Högstrand K, Chandra J, Wiedmer T, Sims PJ, Henter JI, Orrenius S, Samali A.
    Biochem Biophys Res Commun; 1999 Dec 20; 266(2):504-11. PubMed ID: 10600532
    [Abstract] [Full Text] [Related]

  • 23. Lipid translocation across the plasma membrane of mammalian cells.
    Bevers EM, Comfurius P, Dekkers DW, Zwaal RF.
    Biochim Biophys Acta; 1999 Aug 18; 1439(3):317-30. PubMed ID: 10446420
    [Abstract] [Full Text] [Related]

  • 24. Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalization.
    Toti F, Schindler V, Riou JF, Lombard-Platet G, Fressinaud E, Meyer D, Uzan A, Le Pecq JB, Mandel JL, Freyssinet JM.
    Biochem Biophys Res Commun; 1997 Dec 18; 241(2):548-52. PubMed ID: 9425308
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Significance of capacitative Ca2+ entry in the regulation of phosphatidylserine expression at the surface of stimulated cells.
    Martínez MC, Martin S, Toti F, Fressinaud E, Dachary-Prigent J, Meyer D, Freyssinet JM.
    Biochemistry; 1999 Aug 03; 38(31):10092-8. PubMed ID: 10433717
    [Abstract] [Full Text] [Related]

  • 27. A TMEM16F point mutation causes an absence of canine platelet TMEM16F and ineffective activation and death-induced phospholipid scrambling.
    Brooks MB, Catalfamo JL, MacNguyen R, Tim D, Fancher S, McCardle JA.
    J Thromb Haemost; 2015 Dec 03; 13(12):2240-52. PubMed ID: 26414452
    [Abstract] [Full Text] [Related]

  • 28. Normal hemostasis but defective hematopoietic response to growth factors in mice deficient in phospholipid scramblase 1.
    Zhou Q, Zhao J, Wiedmer T, Sims PJ.
    Blood; 2002 Jun 01; 99(11):4030-8. PubMed ID: 12010804
    [Abstract] [Full Text] [Related]

  • 29. Calcium-dependent phospholipid scrambling by TMEM16F.
    Suzuki J, Umeda M, Sims PJ, Nagata S.
    Nature; 2010 Dec 09; 468(7325):834-8. PubMed ID: 21107324
    [Abstract] [Full Text] [Related]

  • 30. 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
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. Phospholipid flip-flop and phospholipid scramblase 1 (PLSCR1) co-localize to uropod rafts in formylated Met-Leu-Phe-stimulated neutrophils.
    Frasch SC, Henson PM, Nagaosa K, Fessler MB, Borregaard N, Bratton DL.
    J Biol Chem; 2004 Apr 23; 279(17):17625-33. PubMed ID: 14766753
    [Abstract] [Full Text] [Related]

  • 33. Regulation of phospholipid scramblase activity during apoptosis and cell activation by protein kinase Cdelta.
    Frasch SC, Henson PM, Kailey JM, Richter DA, Janes MS, Fadok VA, Bratton DL.
    J Biol Chem; 2000 Jul 28; 275(30):23065-73. PubMed ID: 10770950
    [Abstract] [Full Text] [Related]

  • 34. Contribution of platelet microparticle formation and granule secretion to the transmembrane migration of phosphatidylserine.
    Chang CP, Zhao J, Wiedmer T, Sims PJ.
    J Biol Chem; 1993 Apr 05; 268(10):7171-8. PubMed ID: 8463253
    [Abstract] [Full Text] [Related]

  • 35. Store-mediated calcium entry in the regulation of phosphatidylserine exposure in blood cells from Scott patients.
    Munnix IC, Harmsma M, Giddings JC, Collins PW, Feijge MA, Comfurius P, Heemskerk JW, Bevers EM.
    Thromb Haemost; 2003 Apr 05; 89(4):687-95. PubMed ID: 12669124
    [Abstract] [Full Text] [Related]

  • 36. The complex of phosphatidylinositol 4,5-bisphosphate and calcium ions is not responsible for Ca2+-induced loss of phospholipid asymmetry in the human erythrocyte: a study in Scott syndrome, a disorder of calcium-induced phospholipid scrambling.
    Bevers EM, Wiedmer T, Comfurius P, Zhao J, Smeets EF, Schlegel RA, Schroit AJ, Weiss HJ, Williamson P, Zwaal RF, Sims PJ.
    Blood; 1995 Sep 01; 86(5):1983-91. PubMed ID: 7655025
    [Abstract] [Full Text] [Related]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder.
    Toti F, Satta N, Fressinaud E, Meyer D, Freyssinet JM.
    Blood; 1996 Feb 15; 87(4):1409-15. PubMed ID: 8608230
    [Abstract] [Full Text] [Related]

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  • 40. Transbilayer motion of spin-labelled phospholipids in the plasma membrane of epididymal and ejaculated ram spermatozoa.
    Müller K, Müller P, Herrmann A.
    J Reprod Fertil; 1997 Sep 15; 111(1):81-9. PubMed ID: 9370971
    [Abstract] [Full Text] [Related]

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