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Addition of recommendations for the use of recombinant human thrombomodulin to the “Expert consensus for the treatment of disseminated intravascular coagulation in Japan”

Thrombosis research, 2014-10, Vol.134 (4), p.924-925

2014

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Aspirin resistance detected with aggregometry cannot be explained by cyclooxygenase activity: involvement of other signaling pathway(s) in cardiovascular events of aspirin‐treated patients

Journal of thrombosis and haemostasis, 2006-06, Vol.4 (6), p.1271-1278

2006

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Intra‐articular injection of mesenchymal stem cells expressing coagulation factor ameliorates hemophilic arthropathy in factor VIII‐deficient mice

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1802-1813

2012

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Production of functional coagulation factor VIII from iPSCs using a lentiviral vector

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.e40-e44

2014

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Induction of factor VIII‐specific unresponsiveness by intrathymic factor VIII injection in murine hemophilia A

Journal of thrombosis and haemostasis, 2009-05, Vol.7 (5), p.811-824

2009

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A classification of the fibrin network structures formed from the hereditary dysfibrinogens

Journal of thrombosis and haemostasis, 2006-08, Vol.4 (8), p.1738-1746

2006

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Immune response against serial infusion of factor VIII antigen through an implantable venous-access device system in haemophilia A mice

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e323-e330

2012

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Morphological assessment of the luminal surface of olfactory epithelium in mice deficient in tissue plasminogen activator following bulbectomy

Journal of laryngology and otology, 2012-11, Vol.126 (11), p.1114-1120

2012

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Induction of immune tolerance by neonatal intravenous injection of human factor VIII in murine hemophilia A

Journal of thrombosis and haemostasis, 2004-05, Vol.2 (5), p.754-762

2004

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Severe secondary deficiency of von Willebrand factor–cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: its correlation with development of renal failure

Blood, 2006-01, Vol.107 (2), p.528-534

2006

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Clinical evaluation of glycoPEGylated recombinant FVIII: Efficacy and safety in severe haemophilia A

Thrombosis and haemostasis, 2017, Vol.117 (2), p.252

2017

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Specific detection of human coagulation factor IX in cynomolgus macaques

Journal of thrombosis and haemostasis, 2004-02, Vol.2 (2), p.275-280

2004

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Recombinant adeno-associated virus vector-transduced vascular endothelial cells express the thrombomodulin transgene under the regulation of enhanced plasminogen activator inhibitor-1 promoter

Gene therapy, 2001-11, Vol.8 (22), p.1690-1697

2001

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Clinical features of 32 new Japanese cases with autoimmune haemorrha-philia due to anti-factor XIII antibodies

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-09, Vol.21 (5), p.653-658

2015

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Protein S–K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients

Blood, 2006-02, Vol.107 (4), p.1737-1738

2006

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Efficient expression of a transgene in platelets using simian immunodeficiency virus-based vector harboring glycoprotein Ibα promoter: in vivo model for platelet-targeting gene therapy

The FASEB journal, 2006-07, Vol.20 (9), p.1522-1524

2006

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Protection of Plasminogen Activator Inhibitor-1-Deficient Mice from Nasal Allergy

The Journal of immunology (1950), 2005-06, Vol.174 (12), p.8135-8143

2005

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As many as 12 cases with haemorrhagic acquired factor XIII deficiency due to its inhibitors were recently found in Japan

Thrombosis and haemostasis, 2011-05, Vol.105 (5), p.925

2011

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Inhibitors of Factor XIII/13 in older patients

Seminars in thrombosis and hemostasis, 2014-09, Vol.40 (6), p.704

Ichinose, Akitada

2014

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Role of the Kringle Domain in Plasminogen Activation with Staphylokinase

Journal of biochemistry (Tokyo), 1998-01, Vol.123 (1), p.71-77

1998

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Analysis of plasminogen conformational changes induced by monoclonal antibodies

Rinsho byori. The Japanese journal of clinical pathology, 1997-02, Vol.Suppl 104, p.170

1997

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A Battery of Monoclonal Antibodies That Induce Unique Conformations to Evolve Cryptic but Constitutive Functions of Plasminogen

Journal of biochemistry (Tokyo), 1997-02, Vol.121 (2), p.278-287

1997

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Hypofibrinogenemia caused by a nonsense mutation in the fibrinogen Bβ chain gene

Journal of thrombosis and haemostasis, 2003-11, Vol.1 (11), p.2356-2359

2003

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Thrombophilic dysfibrinogen Tokyo V with the amino acid substitution of γ Ala327Thr: formation of fragile but fibrinolysis-resistant fibrin clots and its relevance to arterial thromboembolism

Blood, 2004-04, Vol.103 (8), p.3045-3050

2004

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ORIGINAL ARTICLE: A classification of the fibrin network structures formed from the hereditary dysfibrinogens

Journal of thrombosis and haemostasis, 2006-08, Vol.4 (8), p.1738-1746

2006

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Addition of recommendations for the use of recombinant human thrombomodulin to the “Expert consensus for the treatment of disseminated intravascular coagulation in Japan”

Aspirin resistance detected with aggregometry cannot be explained by cyclooxygenase activity: involvement of other signaling pathway(s) in cardiovascular events of aspirin‐treated patients

Intra‐articular injection of mesenchymal stem cells expressing coagulation factor ameliorates hemophilic arthropathy in factor VIII‐deficient mice

Production of functional coagulation factor VIII from iPSCs using a lentiviral vector

Induction of factor VIII‐specific unresponsiveness by intrathymic factor VIII injection in murine hemophilia A

A classification of the fibrin network structures formed from the hereditary dysfibrinogens

Immune response against serial infusion of factor VIII antigen through an implantable venous-access device system in haemophilia A mice

Morphological assessment of the luminal surface of olfactory epithelium in mice deficient in tissue plasminogen activator following bulbectomy

Induction of immune tolerance by neonatal intravenous injection of human factor VIII in murine hemophilia A

Severe secondary deficiency of von Willebrand factor–cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: its correlation with development of renal failure

Clinical evaluation of glycoPEGylated recombinant FVIII: Efficacy and safety in severe haemophilia A

Specific detection of human coagulation factor IX in cynomolgus macaques

Recombinant adeno-associated virus vector-transduced vascular endothelial cells express the thrombomodulin transgene under the regulation of enhanced plasminogen activator inhibitor-1 promoter

Clinical features of 32 new Japanese cases with autoimmune haemorrha-philia due to anti-factor XIII antibodies

Protein S–K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients

Efficient expression of a transgene in platelets using simian immunodeficiency virus-based vector harboring glycoprotein Ibα promoter: in vivo model for platelet-targeting gene therapy

Protection of Plasminogen Activator Inhibitor-1-Deficient Mice from Nasal Allergy

As many as 12 cases with haemorrhagic acquired factor XIII deficiency due to its inhibitors were recently found in Japan

Inhibitors of Factor XIII/13 in older patients

Role of the Kringle Domain in Plasminogen Activation with Staphylokinase

Analysis of plasminogen conformational changes induced by monoclonal antibodies

A Battery of Monoclonal Antibodies That Induce Unique Conformations to Evolve Cryptic but Constitutive Functions of Plasminogen

Hypofibrinogenemia caused by a nonsense mutation in the fibrinogen Bβ chain gene

Thrombophilic dysfibrinogen Tokyo V with the amino acid substitution of γ Ala327Thr: formation of fragile but fibrinolysis-resistant fibrin clots and its relevance to arterial thromboembolism

ORIGINAL ARTICLE: A classification of the fibrin network structures formed from the hereditary dysfibrinogens

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