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SDF-1α/CXCR4 Signaling in Lipid Rafts Induces Platelet Aggregation via PI3 Kinase-Dependent Akt Phosphorylation

PloS one, 2017-01, Vol.12 (1), p.e0169609-e0169609

2017

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Integrin-Dependent Transient Density Increase in Detergent-Resistant Membrane Rafts in Platelets Activated by Thrombin

Biomedicines, 2024-01, Vol.12 (1), p.69

2024

Volltextzugriff (PDF)

Inhibitor development, safety and efficacy of Advate® among previously treated patients with hemophilia A in a postmarketing surveillance in Japan

International journal of hematology, 2019-03, Vol.109 (3), p.336-345

2019

Volltextzugriff (PDF)

Inhibitor development, safety, and efficacy of Advate® in previously untreated patients with hemophilia A in a postmarketing surveillance in Japan

International journal of hematology, 2019-01, Vol.109 (1), p.70-78

2019

Volltextzugriff (PDF)

Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations

International journal of hematology, 2017-11, Vol.106 (5), p.704-710

2017

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Perioperative safety and hemostatic efficacy of Advate® in patients with hemophilia A in a postmarketing surveillance in Japan

International journal of hematology, 2018-07, Vol.108 (1), p.22-29

2018

Volltextzugriff (PDF)

Involvement of glycoprotein VI in platelet thrombus formation on both collagen and von Willebrand factor surfaces under flow conditions

Circulation (New York, N.Y.), 2002-07, Vol.106 (2), p.266-272

2002

Volltextzugriff (PDF)

Collagen-stimulated Activation of Syk but Not c-Src Is Severely Compromised in Human Platelets Lacking Membrane Glycoprotein VI

The Journal of biological chemistry, 1997-01, Vol.272 (1), p.63-68

1997

Volltextzugriff (PDF)

Clot retraction is mediated by factor XIII-dependent fibrin-αIIbβ3-myosin axis in platelet sphingomyelin-rich membrane rafts

Blood, 2013-11, Vol.122 (19), p.3340-3348

2013

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Distribution of F8 Gene Mutations in 81 Inhibitor-Free, Severe Hemophilia a Patients with Full Exposure to FVIII

Blood, 2014-12, Vol.124 (21), p.1527-1527

2014

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Convenience Comparison Study of Reconstitution Devices for the Blood Coagulation Factor VIII Products Rurioctocog Alfa Pegol and Antihemophilic Factor (Recombinant)

International journal of general medicine, 2020-01, Vol.13, p.1469-1476

2020

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Five novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis

International journal of hematology, 2003-07, Vol.78 (1), p.79-83

2003

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SDF-1[alpha]/CXCR4 Signaling in Lipid Rafts Induces Platelet Aggregation via PI3 Kinase-Dependent Akt Phosphorylation.(Research Article)

PloS one, 2017-01, Vol.12 (1), p.e0169609

2017

Volltextzugriff (PDF)

Correction to: Inhibitor development, safety, and efficacy of Advate® in previously untreated patients with hemophilia A in a postmarketing surveillance in Japan

International journal of hematology, 2019-02, Vol.109 (2), p.241-241

2019

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Two double heterozygous mutations in the F7 gene show different manifestations

British journal of haematology, 2002-12, Vol.119 (4), p.1052-1058

2002

Volltextzugriff (PDF)

A Novel Association of Fc Receptor γ-Chain with Glycoprotein VI and Their Co-expression as a Collagen Receptor in Human Platelets

The Journal of biological chemistry, 1997-09, Vol.272 (38), p.23528-23531

1997

Volltextzugriff (PDF)

Clinical trial to investigate the pharmacokinetics, pharmacodynamics, safety, and efficacy of recombinant factor VIIa in Japanese patients with hemophilia with inhibitors

International journal of hematology, 2001-06, Vol.73 (4), p.517-525

2001

Volltextzugriff (PDF)

Correction to: Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations

International journal of hematology, 2018, Vol.107 (1), p.123-124

2018

Volltextzugriff (PDF)

Novel Bernard-Soulier syndrome variants caused by compound heterozygous mutations (case I) or a cytoplasmic tail truncation (case II) of GPIbα

Thrombosis research, 2013-04, Vol.131 (4), p.e160-e167

2013

Volltextzugriff (PDF)

Coagulopathy with autoantibodies to blood-clotting factors: overview and laboratory diagnosis

Rinsho byori. The Japanese journal of clinical pathology, 2004-02, Vol.52 (2), p.178

Arai, Morio

2004

Volltextzugriff (PDF)

A Gln747→Pro Substitution in the IIb Subunit Is Responsible for a Moderate IIbβ3Deficiency in Glanzmann Thrombasthenia

Blood, 1998-10, Vol.92 (8), p.2750-2758

1998

Volltextzugriff (PDF)

A Gln747→Pro Substitution in the IIb Subunit Is Responsible for a Moderate IIbβ3Deficiency in Glanzmann Thrombasthenia

Blood, 1998-10, Vol.92 (8), p.2750-2758

1998

Volltextzugriff (PDF)

BIACORETM, a System for Biomolecular Interaction Analysis Using Surface Plasmon Resonance: The Technique and its Applications to Research on Hemostasis and Thrombosis

Japanese Journal of Thrombosis and Hemostasis, 1997/10/01, Vol.8(5), pp.397-405

ARAI, Morio

1997

Volltextzugriff (PDF)

A naturally occurring Tyr143HisαIIb mutation abolishes αIIbβ3 function for soluble ligands but retains its ability for mediating cell adhesion and clot retraction: comparison with other mutations causing ligand-binding defects

Blood, 2003-05, Vol.101 (9), p.3485-3491

2003

Volltextzugriff (PDF)

Influences of strenuous exercise (triathlon) on blood coagulation and fibrinolytic system

Thrombosis research, 1990-02, Vol.57 (3), p.465-471

1990

Volltextzugriff (PDF)

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SDF-1α/CXCR4 Signaling in Lipid Rafts Induces Platelet Aggregation via PI3 Kinase-Dependent Akt Phosphorylation

Integrin-Dependent Transient Density Increase in Detergent-Resistant Membrane Rafts in Platelets Activated by Thrombin

Inhibitor development, safety and efficacy of Advate® among previously treated patients with hemophilia A in a postmarketing surveillance in Japan

Inhibitor development, safety, and efficacy of Advate® in previously untreated patients with hemophilia A in a postmarketing surveillance in Japan

Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations

Perioperative safety and hemostatic efficacy of Advate® in patients with hemophilia A in a postmarketing surveillance in Japan

Involvement of glycoprotein VI in platelet thrombus formation on both collagen and von Willebrand factor surfaces under flow conditions

Collagen-stimulated Activation of Syk but Not c-Src Is Severely Compromised in Human Platelets Lacking Membrane Glycoprotein VI

Clot retraction is mediated by factor XIII-dependent fibrin-αIIbβ3-myosin axis in platelet sphingomyelin-rich membrane rafts

Distribution of F8 Gene Mutations in 81 Inhibitor-Free, Severe Hemophilia a Patients with Full Exposure to FVIII

Convenience Comparison Study of Reconstitution Devices for the Blood Coagulation Factor VIII Products Rurioctocog Alfa Pegol and Antihemophilic Factor (Recombinant)

Five novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis

SDF-1[alpha]/CXCR4 Signaling in Lipid Rafts Induces Platelet Aggregation via PI3 Kinase-Dependent Akt Phosphorylation.(Research Article)

Correction to: Inhibitor development, safety, and efficacy of Advate® in previously untreated patients with hemophilia A in a postmarketing surveillance in Japan

Two double heterozygous mutations in the F7 gene show different manifestations

A Novel Association of Fc Receptor γ-Chain with Glycoprotein VI and Their Co-expression as a Collagen Receptor in Human Platelets

Clinical trial to investigate the pharmacokinetics, pharmacodynamics, safety, and efficacy of recombinant factor VIIa in Japanese patients with hemophilia with inhibitors

Correction to: Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations

Novel Bernard-Soulier syndrome variants caused by compound heterozygous mutations (case I) or a cytoplasmic tail truncation (case II) of GPIbα

Coagulopathy with autoantibodies to blood-clotting factors: overview and laboratory diagnosis

A Gln747→Pro Substitution in the IIb Subunit Is Responsible for a Moderate IIbβ3Deficiency in Glanzmann Thrombasthenia

A Gln747→Pro Substitution in the IIb Subunit Is Responsible for a Moderate IIbβ3Deficiency in Glanzmann Thrombasthenia

BIACORETM, a System for Biomolecular Interaction Analysis Using Surface Plasmon Resonance: The Technique and its Applications to Research on Hemostasis and Thrombosis

A naturally occurring Tyr143HisαIIb mutation abolishes αIIbβ3 function for soluble ligands but retains its ability for mediating cell adhesion and clot retraction: comparison with other mutations causing ligand-binding defects

Influences of strenuous exercise (triathlon) on blood coagulation and fibrinolytic system

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