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Spatial Propagation and Localization of Blood Coagulation Are Regulated by Intrinsic and Protein C Pathways, Respectively

Biophysical journal, 2006-03, Vol.90 (5), p.1489-1500

2006

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apoE isoform binding properties of the VLDL receptor reveal marked differences from LRP and the LDL receptor

Journal of lipid research, 2005-08, Vol.46 (8), p.1721-1731

2005

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Identification of a protein S-interactive site within the A2 domain of the factor VIII heavy chain

Thrombosis and haemostasis, 2009-10, Vol.102 (4), p.645-655

2009

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Factor VIII bypasses CD91/LRP for endocytosis by dendritic cells leading to T-cell activation

Haematologica (Roma), 2008-01, Vol.93 (1), p.83-89

2008

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Identification of a plasmin-interactive site within the A2 domain of the factor VIII heavy chain

Biochimica et biophysica acta, 2008-05, Vol.1784 (5), p.753-763

2008

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Identification of Plasmin-interactive Sites in the Light Chain of Factor VIII Responsible for Proteolytic Cleavage at Lys36

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.6934-6945

2009

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Localization of the low-density lipoprotein receptor-related protein regions involved in binding to the A2 domain of coagulation factor VIII

Thrombosis and haemostasis, 2007-12, Vol.98 (6), p.1170-1181

2007

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Kinetics of Factor X activation by the membrane-bound complex of Factor IXa and Factor VIIIa

Biochemical journal, 2004-08, Vol.381 (Pt 3), p.779-794

2004

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Intrinsic pathway of blood coagulation contributes to thrombogenicity of atherosclerotic plaque

Blood, 2002-06, Vol.99 (12), p.4475-4485

2002

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A novel mechanism of factor VIII protection by von Willebrand factor from activated protein C–catalyzed inactivation

Blood, 2002-06, Vol.99 (11), p.3993-3998

2002

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Role of the B domain in proteolytic inactivation of activated coagulation factor VIII by activated protein C and activated factor X

Blood coagulation & fibrinolysis, 2006-07, Vol.17 (5), p.379-388

2006

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Hemophilia A mutations within the factor VIII A2-A3 subunit interface destabilize factor VIIIa and cause one-stage/two-stage activity discrepancy

Thrombosis and haemostasis, 2002-11, Vol.88 (5), p.781-787

2002

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Epitope mapping of polyclonal clotting factor VIII-inhibitory antibodies using phage display

Thrombosis and haemostasis, 2004-03, Vol.91 (3), p.619-625

2004

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Effect of factor VIII on tissue factor-initiated spatial clot growth

Thrombosis and haemostasis, 2003-02, Vol.89 (2), p.235-242

2003

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The Acidic Region of the Factor VIII Light Chain and the C2 Domain Together Form the High Affinity Binding Site for von Willebrand Factor

The Journal of biological chemistry, 1997-07, Vol.272 (29), p.18007-18014

1997

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Role of the Low Density Lipoprotein-related Protein Receptor in Mediation of Factor VIII Catabolism

The Journal of biological chemistry, 1999-12, Vol.274 (53), p.37685-37692

1999

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Inhibitors in hemophilia A: advances in elucidation of inhibitory mechanisms and in inhibitor management with bypassing agents

Seminars in thrombosis and hemostasis, 2009-11, Vol.35 (8), p.735-751

2009

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Protein S down‐regulates factor Xase activity independent of activated protein C: specific binding of factor VIII(a) to protein S inhibits interactions with factor IXa

British journal of haematology, 2008-11, Vol.143 (3), p.409-420

2008

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In Hemophilia A and Autoantibody Inhibitor Patients: The Factor VIII A2 Domain and Light Chain Are Most Immunogenic

Thrombosis research, 2001-03, Vol.101 (5), p.377-385

2001

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Gene therapy for hemophilia A. Friend or foe?

Blood coagulation & fibrinolysis, 2009-09, Vol.20 (6), p.395-399

2009

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Cell Surface Heparan Sulfate Proteoglycans Participate in Factor VIII Catabolism Mediated by Low Density Lipoprotein Receptor-related Protein

The Journal of biological chemistry, 2001-04, Vol.276 (15), p.11970-11979

2001

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Identification of Plasmin-interactive Sites in the Light Chain of Factor VIII Responsible for Proteolytic Cleavage at Lys

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.6934-6945

2009

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Human factor VIII inhibitor alloantibodies with a C2 epitope inhibit factor Xa-catalyzed factor VIII activation: a new anti-factor VIII inhibitory mechanism

Thrombosis and haemostasis, 2002-03, Vol.87 (3), p.459-465

2002

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Hemophilia A mutations associated with 1-stage/2-stage activity discrepancy disrupt protein-protein interactions within the triplicated A domains of thrombin-activated factor VIIIa

Blood, 2001-02, Vol.97 (3), p.685-691

2001

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Development of a Peptidomimetic Ligand for Efficient Isolation and Purification of Factor VIII via Affinity Chromatography

Journal of medicinal chemistry, 2007-09, Vol.50 (18), p.4329-4339

2007

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Spatial Propagation and Localization of Blood Coagulation Are Regulated by Intrinsic and Protein C Pathways, Respectively

apoE isoform binding properties of the VLDL receptor reveal marked differences from LRP and the LDL receptor

Identification of a protein S-interactive site within the A2 domain of the factor VIII heavy chain

Factor VIII bypasses CD91/LRP for endocytosis by dendritic cells leading to T-cell activation

Identification of a plasmin-interactive site within the A2 domain of the factor VIII heavy chain

Identification of Plasmin-interactive Sites in the Light Chain of Factor VIII Responsible for Proteolytic Cleavage at Lys36

Localization of the low-density lipoprotein receptor-related protein regions involved in binding to the A2 domain of coagulation factor VIII

Kinetics of Factor X activation by the membrane-bound complex of Factor IXa and Factor VIIIa

Intrinsic pathway of blood coagulation contributes to thrombogenicity of atherosclerotic plaque

A novel mechanism of factor VIII protection by von Willebrand factor from activated protein C–catalyzed inactivation

Role of the B domain in proteolytic inactivation of activated coagulation factor VIII by activated protein C and activated factor X

Hemophilia A mutations within the factor VIII A2-A3 subunit interface destabilize factor VIIIa and cause one-stage/two-stage activity discrepancy

Epitope mapping of polyclonal clotting factor VIII-inhibitory antibodies using phage display

Effect of factor VIII on tissue factor-initiated spatial clot growth

The Acidic Region of the Factor VIII Light Chain and the C2 Domain Together Form the High Affinity Binding Site for von Willebrand Factor

Role of the Low Density Lipoprotein-related Protein Receptor in Mediation of Factor VIII Catabolism

Inhibitors in hemophilia A: advances in elucidation of inhibitory mechanisms and in inhibitor management with bypassing agents

Protein S down‐regulates factor Xase activity independent of activated protein C: specific binding of factor VIII(a) to protein S inhibits interactions with factor IXa

In Hemophilia A and Autoantibody Inhibitor Patients: The Factor VIII A2 Domain and Light Chain Are Most Immunogenic

Gene therapy for hemophilia A. Friend or foe?

Cell Surface Heparan Sulfate Proteoglycans Participate in Factor VIII Catabolism Mediated by Low Density Lipoprotein Receptor-related Protein

Identification of Plasmin-interactive Sites in the Light Chain of Factor VIII Responsible for Proteolytic Cleavage at Lys

Human factor VIII inhibitor alloantibodies with a C2 epitope inhibit factor Xa-catalyzed factor VIII activation: a new anti-factor VIII inhibitory mechanism

Hemophilia A mutations associated with 1-stage/2-stage activity discrepancy disrupt protein-protein interactions within the triplicated A domains of thrombin-activated factor VIIIa

Development of a Peptidomimetic Ligand for Efficient Isolation and Purification of Factor VIII via Affinity Chromatography

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