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Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results

PloS one, 2022-01, Vol.17 (1), p.e0262695-e0262695

2022

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Effect of ADAM28 on Carcinoma Cell Metastasis by Cleavage of von Willebrand Factor

JNCI : Journal of the National Cancer Institute, 2012-06, Vol.104 (12), p.906-922

2012

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Novel Antibody for the Treatment of Transthyretin Amyloidosis

The Journal of biological chemistry, 2016-11, Vol.291 (48), p.25096-25105

2016

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A novel monoclonal antibody cross-reactive with both human and mouse α9 integrin useful for therapy against rheumatoid arthritis

Journal of biochemistry (Tokyo), 2020-09, Vol.168 (3), p.231-241

2020

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A Novel Human Metalloprotease Synthesized in the Liver and Secreted into the Blood: Possibly, the von Willebrand Factor—Cleaving Protease?

Journal of biochemistry (Tokyo), 2001-10, Vol.130 (4), p.475-480

2001

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Mutations and Common Polymorphisms in ADAMTS13 Gene Responsible for von Willebrand Factor-Cleaving Protease Activity

Proceedings of the National Academy of Sciences - PNAS, 2002-09, Vol.99 (18), p.11902-11907

2002

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Pregnancy‐induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw–Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients

British journal of haematology, 2009-03, Vol.144 (5), p.742-754

2009

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ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage

Blood, 2003-11, Vol.102 (9), p.3232-3237

2003

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Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke

TH open : companion journal to thrombosis and haemostasis, 2023-10, Vol.7 (4), p.e294-e302

2023

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Serial Changes in von Willebrand Factor-Cleaving Protease (ADAMTS13) and Prognosis After Acute Myocardial Infarction

The American journal of cardiology, 2007-09, Vol.100 (5), p.758-763

2007

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ADAMTS13 unbound to larger von Willebrand factor multimers in cryosupernatant: implications for selection of plasma preparations for thrombotic thrombocytopenic purpura treatment

Transfusion (Philadelphia, Pa.), 2013-12, Vol.53 (12), p.3192-3202

2013

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Analysis on the Molecular Species and Concentration of Circulating ADAMTS13 in Blood

Journal of biochemistry (Tokyo), 2006, Vol.139 (1), p.147-154

2006

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Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage

The Kurume Medical Journal, 2016/07/31, Vol.63(1.2), pp.23-28

2019

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Contribution of ADAMTS13 to the better cell engraftment efficacy in mouse model of bone marrow transplantation

Haematologica (Roma), 2014-10, Vol.99 (10), p.e211-e213

2014

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Detection of von Willebrand factor-cleaving protease (ADAMTS-13) in human platelets

Biochemical and biophysical research communications, 2004-01, Vol.313 (1), p.212-216

2004

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The homozygous p.C1024R- ADAMTS13 gene mutation links to a late-onset phenotype of Upshaw-Schulman syndrome in Japan

Thrombosis and haemostasis, 2012, Vol.107 (5), p.1003-1005

2012

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Binding of von Willebrand factor cleaving protease ADAMTS13 to Lys-plasmin(ogen)

Journal of biochemistry (Tokyo), 2012-09, Vol.152 (3), p.251-258

2012

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ADAMTS-13 attenuates thrombus formation on type I collagen surface and disrupted plaques under flow conditions

Atherosclerosis, 2009-04, Vol.203 (2), p.409-416

2009

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Identification of Strain-specific Variants of Mouse Adamts13 Gene Encoding von Willebrand Factor-cleaving Protease

The Journal of biological chemistry, 2004-07, Vol.279 (29), p.30896-30903

2004

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Interplay between ADAMTS13 and von Willebrand factor in inherited and acquired thrombotic microangiopathies

Seminars in hematology, 2005, Vol.42 (1), p.56-62

2005

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Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan

Journal of thrombosis and haemostasis, 2011-07, Vol.9, p.283-301

2011

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Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease

PloS one, 2009-08, Vol.4 (8), p.e6506-e6506

2009

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Monte Carlo Sampling Method of Amino Acid Sequences Adaptable to Given Main-Chain Atoms in the Proteins

Journal of biochemistry (Tokyo), 2006-10, Vol.140 (4), p.543-552

2006

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Regulation of von Willebrand factor by ADAMTS13 ameliorates lipopolysaccharide-induced lung injury in mice

International journal of hematology, 2023-12, Vol.118 (6), p.699-710

2023

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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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Platelet surface receptor glycoprotein VI-dimer is overexpressed in stroke: The Glycoprotein VI in Stroke (GYPSIE) study results

Effect of ADAM28 on Carcinoma Cell Metastasis by Cleavage of von Willebrand Factor

Novel Antibody for the Treatment of Transthyretin Amyloidosis

A novel monoclonal antibody cross-reactive with both human and mouse α9 integrin useful for therapy against rheumatoid arthritis

A Novel Human Metalloprotease Synthesized in the Liver and Secreted into the Blood: Possibly, the von Willebrand Factor—Cleaving Protease?

Mutations and Common Polymorphisms in ADAMTS13 Gene Responsible for von Willebrand Factor-Cleaving Protease Activity

Pregnancy‐induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw–Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients

ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage

Platelet Receptor Glycoprotein VI-Dimer Is Overexpressed in Patients with Atrial Fibrillation at High Risk of Ischemic Stroke

Serial Changes in von Willebrand Factor-Cleaving Protease (ADAMTS13) and Prognosis After Acute Myocardial Infarction

ADAMTS13 unbound to larger von Willebrand factor multimers in cryosupernatant: implications for selection of plasma preparations for thrombotic thrombocytopenic purpura treatment

Analysis on the Molecular Species and Concentration of Circulating ADAMTS13 in Blood

Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage

Contribution of ADAMTS13 to the better cell engraftment efficacy in mouse model of bone marrow transplantation

Detection of von Willebrand factor-cleaving protease (ADAMTS-13) in human platelets

The homozygous p.C1024R- ADAMTS13 gene mutation links to a late-onset phenotype of Upshaw-Schulman syndrome in Japan

Binding of von Willebrand factor cleaving protease ADAMTS13 to Lys-plasmin(ogen)

ADAMTS-13 attenuates thrombus formation on type I collagen surface and disrupted plaques under flow conditions

Identification of Strain-specific Variants of Mouse Adamts13 Gene Encoding von Willebrand Factor-cleaving Protease

Interplay between ADAMTS13 and von Willebrand factor in inherited and acquired thrombotic microangiopathies

Natural history of Upshaw–Schulman syndrome based on ADAMTS13 gene analysis in Japan

Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease

Monte Carlo Sampling Method of Amino Acid Sequences Adaptable to Given Main-Chain Atoms in the Proteins

Regulation of von Willebrand factor by ADAMTS13 ameliorates lipopolysaccharide-induced lung injury in mice

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

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