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Caspase-Independent Exposure of Aminophospholipids and Tyrosine Phosphorylation in Bicarbonate Responsive Human Sperm Cells

Biology of reproduction, 2003-06, Vol.68 (6), p.2122-2134

2003

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Unraveling the mysteries of phospholipid scrambling

Thrombosis and haemostasis, 2001-07, Vol.86 (1), p.266-275

2001

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Antileukemic roles of human phospholipid scramblase 1 gene, evidence from inducible PLSCR1-expressing leukemic cells

Oncogene, 2006-10, Vol.25 (50), p.6618-6627

2006

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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

The Journal of biological chemistry, 1989-10, Vol.264 (29), p.17049-17057

1989

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Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity

The Journal of biological chemistry, 1988-12, Vol.263 (34), p.18205-18212

1988

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Complement-Induced Vesiculation and Exposure of Membrane Prothrombinase Sites in Platelets of Paroxysmal Nocturnal Hemoglobinuria

Blood, 1993-08, Vol.82 (4), p.1192-1196

1993

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Stimulated secretion of endothelial von Willebrand factor is accompanied by rapid redistribution to the cell surface of the intracellular granule membrane protein GMP-140

The Journal of biological chemistry, 1989-05, Vol.264 (14), p.7768-7771

1989

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Effect of platelet activation on the conformation of the plasma membrane glycoprotein IIb-IIIa complex

The Journal of biological chemistry, 1991-04, Vol.266 (12), p.7345-7352

1991

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Platelet-derived microparticles express high affinity receptors for factor VIII

The Journal of biological chemistry, 1991-09, Vol.266 (26), p.17261-17268

1991

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Inhibition of homologous complement by CD59 is mediated by a species-selective recognition conferred through binding to C8 within C5b-8 or C9 within C5b-9

The Journal of immunology (1950), 1991-04, Vol.146 (7), p.2345-2351

1991

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Contribution of platelet microparticle formation and granule secretion to the transmembrane migration of phosphatidylserine

The Journal of biological chemistry, 1993-04, Vol.268 (10), p.7171-7178

1993

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Complement proteins C5b-9 induce vesiculation of the endothelial plasma membrane and expose catalytic surface for assembly of the prothrombinase enzyme complex

The Journal of biological chemistry, 1990-03, Vol.265 (7), p.3809-3814

1990

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The human complement regulatory protein CD59 binds to the alpha-chain of C8 and to the "b"domain of C9

The Journal of biological chemistry, 1992-07, Vol.267 (19), p.13675-13680

1992

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The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9

The Journal of immunology (1950), 1990-05, Vol.144 (9), p.3478-3483

1990

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Complement Proteins C5b-9 Induce Secretion of High Molecular Weight Multimers of Endothelial von Willebrand Factor and Translocation of Granule Membrane Protein GMP-140 to the Cell Surface

The Journal of biological chemistry, 1989-05, Vol.264 (15), p.9053-9060

1989

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Expression of proteins controlling transbilayer movement of plasma membrane phospholipids in the B lymphocytes from a patient with Scott syndrome

Blood, 1998-09, Vol.92 (5), p.1707-1712

1998

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Tramadol‐Warfarin Interaction

Pharmacotherapy, 1998-07, Vol.18 (4), p.871-873

1998

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Participation of Protein Kinases in Complement C5b-9–Induced Shedding of Platelet Plasma Membrane Vesicles

Blood, 1991-12, Vol.78 (11), p.2880-2886

1991

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Sphingomyelin Hydrolysis to Ceramide during the Execution Phase of Apoptosis Results from Phospholipid Scrambling and Alters Cell-Surface Morphology

The Journal of cell biology, 2000-07, Vol.150 (1), p.155-164

2000

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Overlapping But Nonidentical Binding Sites on CD2 for CD58 and a Second Ligand CD59

Science (American Association for the Advancement of Science), 1992-06, Vol.256 (5065), p.1805-1807

1992

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Regulatory control of complement on blood platelets. Modulation of platelet procoagulant responses by a membrane inhibitor of the C5b-9 complex

The Journal of biological chemistry, 1989-11, Vol.264 (32), p.19228-19235

1989

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Interaction between apolipoproteins A-I and A-II and the membrane attack complex of complement. Affinity of the apoproteins for polymeric C9

The Journal of biological chemistry, 1993-02, Vol.268 (5), p.3632-3638

1993

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Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids

The Journal of clinical investigation, 1997-05, Vol.99 (9), p.2232-2238

1997

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Molecular cloning of human plasma membrane phospholipid scramblase. A protein mediating transbilayer movement of plasma membrane phospholipids

The Journal of biological chemistry, 1997-07, Vol.272 (29), p.18240-18244

1997

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Regulation of glycoprotein IIb-IIIa receptor function studied with platelets permeabilized by the pore-forming complement proteins C5b-9

The Journal of biological chemistry, 1992-09, Vol.267 (26), p.18424-18431

1992

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Caspase-Independent Exposure of Aminophospholipids and Tyrosine Phosphorylation in Bicarbonate Responsive Human Sperm Cells

Unraveling the mysteries of phospholipid scrambling

Antileukemic roles of human phospholipid scramblase 1 gene, evidence from inducible PLSCR1-expressing leukemic cells

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

Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity

Complement-Induced Vesiculation and Exposure of Membrane Prothrombinase Sites in Platelets of Paroxysmal Nocturnal Hemoglobinuria

Stimulated secretion of endothelial von Willebrand factor is accompanied by rapid redistribution to the cell surface of the intracellular granule membrane protein GMP-140

Effect of platelet activation on the conformation of the plasma membrane glycoprotein IIb-IIIa complex

Platelet-derived microparticles express high affinity receptors for factor VIII

Inhibition of homologous complement by CD59 is mediated by a species-selective recognition conferred through binding to C8 within C5b-8 or C9 within C5b-9

Contribution of platelet microparticle formation and granule secretion to the transmembrane migration of phosphatidylserine

Complement proteins C5b-9 induce vesiculation of the endothelial plasma membrane and expose catalytic surface for assembly of the prothrombinase enzyme complex

The human complement regulatory protein CD59 binds to the alpha-chain of C8 and to the "b"domain of C9

The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9

Complement Proteins C5b-9 Induce Secretion of High Molecular Weight Multimers of Endothelial von Willebrand Factor and Translocation of Granule Membrane Protein GMP-140 to the Cell Surface

Expression of proteins controlling transbilayer movement of plasma membrane phospholipids in the B lymphocytes from a patient with Scott syndrome

Tramadol‐Warfarin Interaction

Participation of Protein Kinases in Complement C5b-9–Induced Shedding of Platelet Plasma Membrane Vesicles

Sphingomyelin Hydrolysis to Ceramide during the Execution Phase of Apoptosis Results from Phospholipid Scrambling and Alters Cell-Surface Morphology

Overlapping But Nonidentical Binding Sites on CD2 for CD58 and a Second Ligand CD59

Regulatory control of complement on blood platelets. Modulation of platelet procoagulant responses by a membrane inhibitor of the C5b-9 complex

Interaction between apolipoproteins A-I and A-II and the membrane attack complex of complement. Affinity of the apoproteins for polymeric C9

Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids

Molecular cloning of human plasma membrane phospholipid scramblase. A protein mediating transbilayer movement of plasma membrane phospholipids

Regulation of glycoprotein IIb-IIIa receptor function studied with platelets permeabilized by the pore-forming complement proteins C5b-9

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