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182 related items for PubMed ID: 9490700
1. 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 [Abstract] [Full Text] [Related]
2. 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]
3. 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 [Abstract] [Full Text] [Related]
12. Collagen but not fibrinogen surfaces induce bleb formation, exposure of phosphatidylserine, and procoagulant activity of adherent platelets: evidence for regulation by protein tyrosine kinase-dependent Ca2+ responses. Heemskerk JW, Vuist WM, Feijge MA, Reutelingsperger CP, Lindhout T. Blood; 1997 Oct 01; 90(7):2615-25. PubMed ID: 9326228 [Abstract] [Full Text] [Related]
13. 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]