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Thromb Haemost 1999; 81(02): 322-323
DOI: 10.1055/s-0037-1614469
DOI: 10.1055/s-0037-1614469
Letters to the Editor
Assessment of the Expression of Candidate Human Plasma Membrane Phospholipid Scramblase in Scott Syndrome Cells
Weitere Informationen
Publikationsverlauf
Received15. September 1998
Accepted26. Oktober 1998
Publikationsdatum:
08. Dezember 2017 (online)
* CRTH-CHRU, Nantes, France
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References
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- 3 Toti F, Satta N, Fressinaud E, Meyer D, Freyssinet JM. Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder. Blood 1996; 87: 1409-15.
- 4 Zhou Q, Zhao J, Stout JG, Luhm RA, Wiedmer T, Sims PJ. Molecular cloning of human plasma membrane phospholipid scramblase. J Biol Chem 1997; 272: 18240-4.
- 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 Zhao J, Zhou Q, Wiedmer T, Sims PJ. Level of expression of phospholipid scramblase regulates induced movement of phosphatidylserine to the cell surface. J Biol Chem 1998; 273: 6603-6.
- 7 Zhou Q, Sims PJ, Wiedmer T. Identity of a conserved motif phospholipid scramblase that is required for Ca2+-accelerated transbilayer movement of membrane phospholipids. Biochemistry 1998; 37: 2356-60.
- 8 Kasukabe T, Kobayashi H, Kaneko Y, Okabe-Kado J, Honma Y. Identity of human normal counterpart (MmTRA1b) of mouse leukemogenesiS-associated gene (MmTRA1a) product as plasma membrane phospholipid scramblase and chromosome mapping of the human MmTRA1b/phospholipid scramblase gene. Biochem Biophys Res Commun 1998; 249: 449-55.