Procoagulant Expression in Platelets and Defects Leading to Clinical Disorders
- 1 December 1999
- journal article
- review article
- Published by Wolters Kluwer Health in Arteriosclerosis, Thrombosis, and Vascular Biology
- Vol. 19 (12) , 2841-2846
- https://doi.org/10.1161/01.atv.19.12.2841
Abstract
—Hemostasis is a result of interactions between fibrillar structures in the damaged vessel wall, soluble components in plasma, and cellular elements in blood represented mainly by platelets...Keywords
This publication has 44 references indexed in Scilit:
- Identity of a Conserved Motif in Phospholipid Scramblase That Is Required for Ca2+-Accelerated Transbilayer Movement of Membrane PhospholipidsBiochemistry, 1998
- Aminophospholipid exposure, microvesiculation and abnormal protein tyrosine phosphorylation in the platelets of a patient with Scott syndrome: a study using physiologic agonists and local anaestheticsBritish Journal of Haematology, 1997
- Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids.Journal of Clinical Investigation, 1997
- Effector Cell Protease Receptor-1, a Platelet Activation-dependent Membrane Protein, Regulates Prothrombinase-catalyzed Thrombin GenerationJournal of Biological Chemistry, 1997
- Activation of Receptor-operated Cation Channels via P2X1 Not P2T Purinoceptors in Human PlateletsJournal of Biological Chemistry, 1996
- Reconstitution of Phospholipid Scramblase Activity from Human Blood PlateletsBiochemistry, 1996
- Calcium involvement in aminophospholipid exposure and microparticle formation during platelet activation: A study using Ca2+-ATPase inhibitorsBiochemistry, 1995
- Platelet procoagulant activity: physiological significance and mechanisms of exposureBlood Reviews, 1991
- Platelet receptor-mediated factor X activation by factor IXa. High-affinity factor IXa receptors induced by factor VIII are deficient on platelets in Scott syndrome.Journal of Clinical Investigation, 1989
- Platelet prothrombin converting activity in hereditary disorders of platelet functionBritish Journal of Haematology, 1986