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C0337: Molecular Characterization of Novel Protein C Mutations (p.Asp77Gly, p.Ala163Val and p.Ala163Glu) Causing Protein C Deficiency

Thrombosis research, 2014-05, Vol.133, p.S11-S11

2014

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Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A

Thrombosis and haemostasis, 2000-10, Vol.84 (4), p.595-600

2000

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Molecular mechanism of the interaction between activated factor XIII and its glutamine donor peptide substrate

Journal of thrombosis and haemostasis, 2009-04, Vol.7 (4), p.627-633

2009

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Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

Haematologica (Roma), 2008-02, Vol.93 (2), p.299-302

2008

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Anti‐factor V auto‐antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding

Journal of thrombosis and haemostasis, 2003-05, Vol.1 (5), p.943-949

2003

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Transformation of cellular factor XIII into an active zymogen transglutaminase in thrombin-stimulated platelets

Thrombosis and haemostasis, 1995-04, Vol.73 (4), p.702-705

1995

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Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

Blood, 2000-10, Vol.96 (7), p.2479-2486

2000

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TWO NOVEL MISSENSE MUTATIONS (THR233MET AND TRP308LEU) IN THE FACTOR X GENE AND THEIR FUNCTIONAL CONSEQUENCES IN A PATIENT WITH SEVERE FACTOR X DEFICIENCY

Journal of thrombosis and haemostasis, 2007-07, Vol.5, p.O-M-024-O-M-024

2007

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Factor XIII subunit B: a protein A binding protein

Journal of thrombosis and haemostasis, 2003-07, Vol.1, p.P0285-P0285

2003

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Activation of factor XIII in whole plasma: the influence of Val34Leu polymorphism

Journal of thrombosis and haemostasis, 2003-07, Vol.1, p.OC171-OC171

2003

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Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene

Blood, 2002-01, Vol.99 (2), p.702-705

2002

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The pool of fatty acids covalently bound to platelet proteins by thioester linkages can be altered by exogenously supplied fatty acids

Lipids, 1999-01, Vol.34 (S1Part3), p.S331-S337

1999

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Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteins

Thrombosis and haemostasis, 1997, Vol.77 (6), p.1068-1072

1997

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Promotion of the Crosslinking of Fibrin and α2-antiplasmin by Platelets

Thrombosis and haemostasis, 1996, Vol.75 (1), p.161-167

1996

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Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency : A splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA

Blood, 1997-02, Vol.89 (4), p.1279-1287

1997

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A simple, quick one-step ELISA assay for the determination of complex plasma factor XIII (A2B2)

Thrombosis and haemostasis, 2000-02, Vol.83 (2), p.268-273

2000

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Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

Blood, 2000-10, Vol.96 (7), p.2479-2486

2000

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Promotion of the crosslinking of fibrin and alpha 2-antiplasmin by platelets

Thrombosis and haemostasis, 1996-01, Vol.75 (1), p.161

1996

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Interleukin-6 in neuromyelitis optica spectrum disorder pathophysiology

Neurology : neuroimmunology & neuroinflammation, 2020-09, Vol.7 (5), p.e841-e841

2020

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The lack of aspirin resistance in patients with coronary artery disease

Journal of translational medicine, 2016-03, Vol.14 (73), p.74-74, Article 74

2016

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Synthesis and Structure−Activity Relationship of Small-Molecule Malonyl Coenzyme A Decarboxylase Inhibitors

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1517-1525

2006

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Behavior of hydrogen in an Ni3Al compound investigated by means of hydrogen microprint technique

Intermetallics, 2000-05, Vol.8 (5-6), p.599-603

2000

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Behavior of hydrogen in an Ni sub 3 Al compound investigated by means of hydrogen microprint technique

Intermetallics, 1999-06, Vol.8 (5-6), p.599-603

1999

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Behavior of Hydrogen in an Ni3Al Compound Investigated by means of Hydrogen Microprint Technique

Journal of the Japan Institute of Metals and Materials, 1999, Vol.63(5), pp.593-596

1999

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Behavior of hydrogen in an Ni sub 3 Al compound investigated by means of hydrogen microprint technique

Nihon Kinzoku Gakkai shi (1952), 1999-05, Vol.63 (5), p.593-596

1999

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C0337: Molecular Characterization of Novel Protein C Mutations (p.Asp77Gly, p.Ala163Val and p.Ala163Glu) Causing Protein C Deficiency

Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A

Molecular mechanism of the interaction between activated factor XIII and its glutamine donor peptide substrate

Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

Anti‐factor V auto‐antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding

Transformation of cellular factor XIII into an active zymogen transglutaminase in thrombin-stimulated platelets

Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

TWO NOVEL MISSENSE MUTATIONS (THR233MET AND TRP308LEU) IN THE FACTOR X GENE AND THEIR FUNCTIONAL CONSEQUENCES IN A PATIENT WITH SEVERE FACTOR X DEFICIENCY

Factor XIII subunit B: a protein A binding protein

Activation of factor XIII in whole plasma: the influence of Val34Leu polymorphism

Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene

The pool of fatty acids covalently bound to platelet proteins by thioester linkages can be altered by exogenously supplied fatty acids

Molecular mechanisms of mutations in factor XIII A-subunit deficiency: in vitro expression in COS-cells demonstrates intracellular degradation of the mutant proteins

Promotion of the Crosslinking of Fibrin and α2-antiplasmin by Platelets

Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency : A splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA

A simple, quick one-step ELISA assay for the determination of complex plasma factor XIII (A2B2)

Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

Promotion of the crosslinking of fibrin and alpha 2-antiplasmin by platelets

Interleukin-6 in neuromyelitis optica spectrum disorder pathophysiology

The lack of aspirin resistance in patients with coronary artery disease

Synthesis and Structure−Activity Relationship of Small-Molecule Malonyl Coenzyme A Decarboxylase Inhibitors

Behavior of hydrogen in an Ni3Al compound investigated by means of hydrogen microprint technique

Behavior of hydrogen in an Ni sub 3 Al compound investigated by means of hydrogen microprint technique

Behavior of Hydrogen in an Ni3Al Compound Investigated by means of Hydrogen Microprint Technique

Behavior of hydrogen in an Ni sub 3 Al compound investigated by means of hydrogen microprint technique

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