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Activated protein C resistance in the Japanese population due to homozygosity for the factor V R2 haplotype

International journal of hematology, 2010-04, Vol.91 (3), p.549-550

2010

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Defining the Factor Xa-binding Site on Factor Va by Site-directed Glycosylation

The Journal of biological chemistry, 2002-12, Vol.277 (51), p.50022-50029

2002

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Human Ryudocan from Endothelium-like Cells Binds Basic Fibroblast Growth Factor, Midkine, and Tissue Factor Pathway Inhibitor (∗)

The Journal of biological chemistry, 1996-03, Vol.271 (10), p.5914-5920

1996

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Establishment of a stroma-dependent human acute myelomonocytic leukemia cell line, NAMO-2, with FLT3 tandem duplication

International journal of hematology, 2006-11, Vol.84 (4), p.328-336

2006

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The Gene for Human Protein Z Is Localized to Chromosome 13 at Band q34 and Is Coded by Eight Regular Exons and One Alternative Exon

Biochemistry (Easton), 1998-05, Vol.37 (19), p.6838-6846

1998

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Structural Requirements of Anticoagulant Protein S for Its Binding to the Complement Regulator C4b-binding Protein

The Journal of biological chemistry, 2002-04, Vol.277 (17), p.15099-15106

2002

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Common mutation of plasminogen detected in three Asian populations by an amplification refractory mutation system and rapid automated capillary electrophoresis

Thrombosis and haemostasis, 1999-10, Vol.82 (4), p.1342-1346

1999

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The carboxyl-terminal region of protein C is essential for its secretion

Blood, 1998-05, Vol.91 (10), p.3784-3791

1998

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In vitro characterisation of two naturally occurring mutations in the thrombin-sensitive region of anticoagulant protein S

Thrombosis and haemostasis, 1999-12, Vol.82 (6), p.1627-1633

1999

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Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively

Thrombosis and haemostasis, 1998-03, Vol.79 (3), p.486-490

1998

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Severe factor VII deficiency caused by a novel mutation His348 to Gln in the catalytic domain

Thrombosis and haemostasis, 2000, Vol.83 (2), p.239-243

2000

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Molecular Cloning, Genomic Organization, Promoter Activity, and Tissue-Specific Expression of the Mouse Ryudocan Gene

Journal of biochemistry (Tokyo), 1997-07, Vol.122 (1), p.17-24

1997

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Presence of two plasminogen alleles in normal populations

Thrombosis and haemostasis, 1998-01, Vol.79 (1), p.150-154

1998

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A novel splice site mutation in intron C of PROS1 leads to markedly reduced mutant mRNA level, absence of thrombin-sensitive region, and impaired secretion and cofactor activity of mutant protein S

Thrombosis research, 2010-05, Vol.125 (5), p.e246-e250

2010

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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The Carboxyl-Terminal Region of Protein C Is Essential for Its Secretion

Blood, 1998-05, Vol.91 (10), p.3784-3791

1998

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Structural organization and promoter activity of the human ryudocan gene

Journal of biochemistry (Tokyo), 1996-05, Vol.119 (5), p.979-984

1996

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The D2194G mutation is responsible for increased levels of FV1 in carriers of the factor V R2 haplotype

Thrombosis and haemostasis, 2010-10, Vol.104 (4), p.860-861

2010

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibb mutations

European journal of haematology, 2006-12, Vol.77 (6), p.501-512

2006

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Molecular basis of quantitative factor V deficiency associated with factor V R2 haplotype

Blood, 2002-10, Vol.100 (7), p.2515-2521

2002

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Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized

Blood, 2003-08, Vol.102 (4), p.1316-1322

2003

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Identification of protein Sα gene mutations including four novel mutations in eight unrelated patients with protein S deficiency

British journal of haematology, 2004-07, Vol.126 (2), p.219-225

2004

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Analysis for heterozygosity of protein S mRNA : application to genetic screening and family studies in hereditary protein S deficiency

International journal of hematology, 1996-08, Vol.64 (2), p.119-125

1996

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Homozygous type IIC von Willebrand's disease

International journal of hematology, 1996-04, Vol.63 (3), p.243

1996

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Activated protein C resistance in the Japanese population due to homozygosity for the factor V R2 haplotype

Defining the Factor Xa-binding Site on Factor Va by Site-directed Glycosylation

Human Ryudocan from Endothelium-like Cells Binds Basic Fibroblast Growth Factor, Midkine, and Tissue Factor Pathway Inhibitor (∗)

Establishment of a stroma-dependent human acute myelomonocytic leukemia cell line, NAMO-2, with FLT3 tandem duplication

The Gene for Human Protein Z Is Localized to Chromosome 13 at Band q34 and Is Coded by Eight Regular Exons and One Alternative Exon

Structural Requirements of Anticoagulant Protein S for Its Binding to the Complement Regulator C4b-binding Protein

Common mutation of plasminogen detected in three Asian populations by an amplification refractory mutation system and rapid automated capillary electrophoresis

The carboxyl-terminal region of protein C is essential for its secretion

In vitro characterisation of two naturally occurring mutations in the thrombin-sensitive region of anticoagulant protein S

Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively

Severe factor VII deficiency caused by a novel mutation His348 to Gln in the catalytic domain

Molecular Cloning, Genomic Organization, Promoter Activity, and Tissue-Specific Expression of the Mouse Ryudocan Gene

Presence of two plasminogen alleles in normal populations

A novel splice site mutation in intron C of PROS1 leads to markedly reduced mutant mRNA level, absence of thrombin-sensitive region, and impaired secretion and cofactor activity of mutant protein S

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations

The Carboxyl-Terminal Region of Protein C Is Essential for Its Secretion

Structural organization and promoter activity of the human ryudocan gene

The D2194G mutation is responsible for increased levels of FV1 in carriers of the factor V R2 haplotype

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations

Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibb mutations

Molecular basis of quantitative factor V deficiency associated with factor V R2 haplotype

Factor V New Brunswick: Ala221Val associated with FV deficiency reproduced in vitro and functionally characterized

Identification of protein Sα gene mutations including four novel mutations in eight unrelated patients with protein S deficiency

Analysis for heterozygosity of protein S mRNA : application to genetic screening and family studies in hereditary protein S deficiency

Homozygous type IIC von Willebrand's disease

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