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Unrecognized blood clotting factors

International journal of hematology, 2021-06, Vol.113 (6), p.785-788

2021

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Advances in the understanding of MYH9 disorders

Current opinion in hematology, 2010-09, Vol.17 (5), p.405-410

2010

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TUBB1 mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopenia

European journal of haematology, 2014-04, Vol.92 (4), p.276-282

2014

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Brief history of the Asiatic International Society of Hematology: our roots of international cooperation with Asian countries

International journal of hematology, 2018-12, Vol.108 (6), p.566-570

2018

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ACTN1 Mutations Cause Congenital Macrothrombocytopenia

American journal of human genetics, 2013-03, Vol.92 (3), p.431-438

2013

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Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance

The New England journal of medicine, 2012-06, Vol.366 (25), p.2390-2396

2012

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Mechanism of constitutive activation of FLT3 with internal tandem duplication in the juxtamembrane domain

Oncogene, 2002-04, Vol.21 (16), p.2555-2563

2002

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The Japan Marrow Donor Program, 25 years of experience in achieving 20,000 bone marrow transplantations: organization structure, activity, and financial basis

Bone marrow transplantation (Basingstoke), 2018-05, Vol.53 (5), p.609-616

2018

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Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice

Nagoya journal of medical science, 2021-02, Vol.83 (1), p.75-86

2021

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Recombinant human soluble thrombomodulin (thrombomodulin alfa) to treat disseminated intravascular coagulation in solid tumors: results of a one-arm prospective trial

International journal of clinical oncology, 2015-08, Vol.20 (4), p.821-828

2015

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Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents

British journal of haematology, 2014-06, Vol.165 (6), p.885-887

2014

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Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

Blood, 2008-03, Vol.111 (6), p.3015-3023

2008

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Historical hematology: May–Hegglin anomaly

American journal of hematology, 2008-04, Vol.83 (4), p.304-306

2008

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Combined medialis pedis and medial plantar fasciocutaneous flaps for coverage of soft tissue defects of multiple adjacent fingers

Microsurgery, 2014-09, Vol.34 (6), p.454-458

2014

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Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability

PloS one, 2013-08, Vol.8 (8), p.e71187-e71187

2013

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Molecular mechanisms of syndecan-4 upregulation by TNF-α in the endothelium-like EAhy926 cells

Journal of biochemistry (Tokyo), 2013-07, Vol.154 (1), p.41-50

2013

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Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines

Oncogene, 2000-02, Vol.19 (5), p.624-631

2000

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Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion

Pediatrics international, 2013-08, Vol.55 (4), p.434-437

2013

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Effects of thrombomodulin alfa on hemostatic parameters in disseminated intravascular coagulation: Post hoc analysis of a phase 3 randomized controlled trial

Research and practice in thrombosis and haemostasis, 2020-10, Vol.4 (7), p.1141-1149

2020

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Altered interaction of HDAC5 with GATA-1 during MEL cell differentiation

Oncogene, 2003-12, Vol.22 (57), p.9176-9184

2003

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Divergent Fracture–Dislocation of the Hamatometacarpal Joint: Case Report

The Journal of hand surgery (American ed.), 2011, Vol.36 (1), p.47-51

2011

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Up-regulation of costimulatory/adhesion molecules by histone deacetylase inhibitors in acute myeloid leukemia cells

Blood, 2000-12, Vol.96 (12), p.3847-3856

2000

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Studies on Fletcher trait and Fitzgerald trait. A rare chance to disclose body's defense reactions against injury

Thrombosis and haemostasis, 2010-11, Vol.104 (5), p.867

Saito, Hidehiko

2010

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Nuclear Targeting by the Growth Factor Midkine

Molecular and Cellular Biology, 2002-10, Vol.22 (19), p.6788-6796

2002

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Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations

Laboratory investigation, 2003-01, Vol.83 (1), p.115-122

2003

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Unrecognized blood clotting factors

Advances in the understanding of MYH9 disorders

TUBB1 mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopenia

Brief history of the Asiatic International Society of Hematology: our roots of international cooperation with Asian countries

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance

Mechanism of constitutive activation of FLT3 with internal tandem duplication in the juxtamembrane domain

The Japan Marrow Donor Program, 25 years of experience in achieving 20,000 bone marrow transplantations: organization structure, activity, and financial basis

Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice

Recombinant human soluble thrombomodulin (thrombomodulin alfa) to treat disseminated intravascular coagulation in solid tumors: results of a one-arm prospective trial

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

Historical hematology: May–Hegglin anomaly

Combined medialis pedis and medial plantar fasciocutaneous flaps for coverage of soft tissue defects of multiple adjacent fingers

Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability

Molecular mechanisms of syndecan-4 upregulation by TNF-α in the endothelium-like EAhy926 cells

Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines

Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion

Effects of thrombomodulin alfa on hemostatic parameters in disseminated intravascular coagulation: Post hoc analysis of a phase 3 randomized controlled trial

Altered interaction of HDAC5 with GATA-1 during MEL cell differentiation

Divergent Fracture–Dislocation of the Hamatometacarpal Joint: Case Report

Up-regulation of costimulatory/adhesion molecules by histone deacetylase inhibitors in acute myeloid leukemia cells

Studies on Fletcher trait and Fitzgerald trait. A rare chance to disclose body's defense reactions against injury

Nuclear Targeting by the Growth Factor Midkine

Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations

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