Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00035024.xml
Download PDF
Thromb Haemost 2004; 91(02): 412-415
DOI: 10.1055/s-0037-1613744
DOI: 10.1055/s-0037-1613744
Letters to the Editor
Characterisation of lymphocyte responses to Ca2+ in Scott syndrome
Further Information
Publication History
Received
01 July 2003
Accepted after resubmission
18 August 2003
Publication Date:
15 December 2017 (online)
-
References
- 1 Weiss HJ, Vicic WJ, Lages BA. etal Isolated deficiency of platelet procoagulant activity. Am J Med 1979; 67: 206-13.
- 2 Gilbert GE, Arena AA. Activation of the factor Villa-factor IXa enzyme complex of blood coagulation by membranes containing phosphatidyl-L-serine. J Biol Chem 1996; 271: 11120-5.
- 3 Toti F, Satta N, Fressinaud E. et al. Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder. Blood 1996; 87: 1409-15.
- 4 Weiss HJ, Lages B. Family studies in Scott syndrome. Blood 1997; 87: 475-6.
- 5 Zhou Q, Sims PJ, Wiedmer T. Expression of proteins controlling transbilayer movement of plasma membrane phospholipids in the B lymphocytes from a patient with Scott syndrome. Blood 1998; 92: 1707-12.
- 6 Stout JG, Basse F, Luhm RA. et al. Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids. J Clin Invest 1997; 99: 2232-8.
- 7 Martinez MC, Martin S, Toti F. et al. Significance of capacitative Ca2+ entry in the regulation of phosphatidylserine expression at the surface of stimulated cells. Biochemistry..
- 8 Munnix IC, Harmsma M, Giddings JC. et al. Store-mediated calcium entry in the regulation of phosphatidylserine exposure in blood cells from Scott patients. Thromb Haemost 2003; 89: 687-95.
- 9 Parry DH, Giddings JC, Bloom AL. Familial haemostatic defect associated with reduced prothrombin consumption. Br J Haematol 1980; 44: 323-34.
- 10 Kojima H, Newton-Nash D, Weiss HJ. et al. Production and characterization of transformed B-lymphocytes expressing the membrane defect of Scott syndrome. J Clin Invest 1994; 94: 2237-44.
- 11 Elliott JI, Higgins CF. IKCa1 activity is required for cell shrinkage, phosphatidylserine translocation and death in T lymphocyte apoptosis. EMBO Reports 2002; 04: 189-94.
- 12 Sims PJ, Wiedmer T, Esmon CT. et al. Assembly of the platelet prothrombinase complex is linked to vesiculation of the platelet plasma membrane. Studies in Scott syndrome: an isolated defect in platelet procoagulant activity. J Biol Chem 1989; 264: 17049-57.