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Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) 2017 in Japan

International journal of hematology, 2017-07, Vol.106 (1), p.3-15

2017

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Studies of a microchip flow-chamber system to characterize whole blood thrombogenicity in healthy individuals

Thrombosis research, 2013-08, Vol.132 (2), p.263-270

2013

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Identification of ADAMTS13 peptide sequences binding to von Willebrand factor

Biochemical and biophysical research communications, 2010-01, Vol.391 (1), p.783-788

2010

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Structure and function of ADAMTS13, the recognition and cleavage of von Willebrand factor under blood flow

Nihon Kessen Shiketsu Gakkai shi, 2015, Vol.26 (4), p.433-438

MORIKI, Takanori

2015

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Monitoring ADAMTS13 Autoantibody Titer Using a Novel Quantitative Radioimmunoprecipitation Assay In Patients With Acquired Thrombotic Thrombocytopenic Purpura

Blood, 2013-11, Vol.122 (21), p.3561-3561

2013

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Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain

Journal of molecular biology, 2001-08, Vol.311 (5), p.1011-1026

2001

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Effects of VerifyNow P2Y12 test and CYP2C192 testing on clinical outcomes of patients with cardiovascular disease: A systematic review and meta-analysis

Platelets (Edinburgh), 2013-08, Vol.24 (5), p.352-361

2013

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Epitope analysis of autoantibodies to ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

Thrombosis research, 2011-08, Vol.128 (2), p.169-173

2011

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Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain11Edited by B. Holland

Journal of molecular biology, 2001-08, Vol.311 (5), p.1011-1026

2001

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Characterization of a Microchip Flow-Chamber System for the Analysis of Platelet Thrombus Formation Using Whole Blood Samples - Studies On Healthy Subjects

Blood, 2012-11, Vol.120 (21), p.1144-1144

2012

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Functional Analysis of a Peptide Sequence (Thr323 - Cys337) In ADAMTS13 Disintegrin-Like Domain Revealed Two Discontinuous Sequences Involved In the Interaction with VWF

Blood, 2010-11, Vol.116 (21), p.2200-2200

2010

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Identification of epitopes on ADAMTS13 recognized by a panel of monoclonal antibodies with functional or non-functional effects on catalytic activity

Thrombosis research, 2012-09, Vol.130 (3), p.e79-e83

2012

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Subcutaneous Preadipocytes Are Ideal Candidate To Produce A Large Number Of Functional Platelets In a Culture System

Blood, 2013-11, Vol.122 (21), p.3271-3271

2013

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Quantitative Analysis of the Domain-Specific Autoantibodies to ADAMTS13 in Patients with Acquired Thrombotic Thrombocytopenic Purpura

Blood, 2011-11, Vol.118 (21), p.1167-1167

2011

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Multiple Mapping of Peptide Sequences Recognized by Various Monoclonal Anti-ADAMTS13 Antibodies with Functional or Nonfunctional Effects On the Catalytic Activity

Blood, 2009-11, Vol.114 (22), p.3182-3182

2009

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Identification of ADAMTS13 Peptide Sequences Recognized by Autoantibodies in Patients with Acquired Thrombotic Thrombocytopenic Purpura

Blood, 2008-11, Vol.112 (11), p.2286-2286

2008

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Identification of ADAMTS13 Epitopes Required for Binding to von Willebrand Factor Using Lambda Phage Surface Display

Blood, 2007-11, Vol.110 (11), p.2707-2707

2007

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Rapid improvement of coagulopathy by all‐trans retinoic acid in acute promyelocytic leukemia

American journal of hematology, 1994-07, Vol.46 (3), p.184-188

1994

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Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency

Thrombosis research, 2005, Vol.115 (3), p.191-197

2005

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Acute promyelocytic leukemia developed in a patient with congenital antithrombin III deficiency

International journal of hematology, 1995, Vol.61 (1), p.39-42

1995

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Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency

Blood coagulation & fibrinolysis, 2004-07, Vol.15 (5), p.367-373

2004

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Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X

Blood coagulation & fibrinolysis, 2005-01, Vol.16 (1), p.9-16

2005

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Protein Domain Mapping by λ Phage Display: The Minimal Lactose-Binding Domain of Galectin-3

Biochemical and biophysical research communications, 1999-11, Vol.265 (2), p.291-296

1999

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A novel polymorphism, 70Leu/Phe, disrupts a consensus Leu residue within the leucine-rich repeat sequence of platelet glycoprotein Ibalpha

Thrombosis and haemostasis, 2002-05, Vol.87 (5), p.867

2002

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A Novel Polymorphism, 70Leu/Phe, Disrupts a Consensus Leu Residue within the Leucine-rich Repeat Sequence of Platelet Glycoprotein Ibα

Thrombosis and haemostasis, 2002, Vol.87 (5), p.867-872

2002

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Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) 2017 in Japan

Studies of a microchip flow-chamber system to characterize whole blood thrombogenicity in healthy individuals

Identification of ADAMTS13 peptide sequences binding to von Willebrand factor

Structure and function of ADAMTS13, the recognition and cleavage of von Willebrand factor under blood flow

Monitoring ADAMTS13 Autoantibody Titer Using a Novel Quantitative Radioimmunoprecipitation Assay In Patients With Acquired Thrombotic Thrombocytopenic Purpura

Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain

Effects of VerifyNow P2Y12 test and CYP2C192 testing on clinical outcomes of patients with cardiovascular disease: A systematic review and meta-analysis

Epitope analysis of autoantibodies to ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain11Edited by B. Holland

Characterization of a Microchip Flow-Chamber System for the Analysis of Platelet Thrombus Formation Using Whole Blood Samples - Studies On Healthy Subjects

Functional Analysis of a Peptide Sequence (Thr323 - Cys337) In ADAMTS13 Disintegrin-Like Domain Revealed Two Discontinuous Sequences Involved In the Interaction with VWF

Identification of epitopes on ADAMTS13 recognized by a panel of monoclonal antibodies with functional or non-functional effects on catalytic activity

Subcutaneous Preadipocytes Are Ideal Candidate To Produce A Large Number Of Functional Platelets In a Culture System

Quantitative Analysis of the Domain-Specific Autoantibodies to ADAMTS13 in Patients with Acquired Thrombotic Thrombocytopenic Purpura

Multiple Mapping of Peptide Sequences Recognized by Various Monoclonal Anti-ADAMTS13 Antibodies with Functional or Nonfunctional Effects On the Catalytic Activity

Identification of ADAMTS13 Peptide Sequences Recognized by Autoantibodies in Patients with Acquired Thrombotic Thrombocytopenic Purpura

Identification of ADAMTS13 Epitopes Required for Binding to von Willebrand Factor Using Lambda Phage Surface Display

Rapid improvement of coagulopathy by all‐trans retinoic acid in acute promyelocytic leukemia

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency

Acute promyelocytic leukemia developed in a patient with congenital antithrombin III deficiency

Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency

Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X

Protein Domain Mapping by λ Phage Display: The Minimal Lactose-Binding Domain of Galectin-3

A novel polymorphism, 70Leu/Phe, disrupts a consensus Leu residue within the leucine-rich repeat sequence of platelet glycoprotein Ibalpha

A Novel Polymorphism, 70Leu/Phe, Disrupts a Consensus Leu Residue within the Leucine-rich Repeat Sequence of Platelet Glycoprotein Ibα

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