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Contact System: A Vascular Biology Modulator With Anticoagulant, Profibrinolytic, Antiadhesive, and Proinflammatory Attributes

Blood, 1997-11, Vol.90 (10), p.3819-3843

1997

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Cleaved high-molecular-weight kininogen and its domain 5 inhibit migration and invasion of human prostate cancer cells through the epidermal growth factor receptor pathway

Oncogene, 2009-07, Vol.28 (30), p.2756-2765

2009

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Domain 5 of high molecular weight kininogen (kininostatin) down-regulates endothelial cell proliferation and migration and inhibits angiogenesis

Blood, 2000-01, Vol.95 (2), p.543-550

2000

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Biologic activities of the contact factors in vivo--potentiation of hypotension, inflammation, and fibrinolysis, and inhibition of cell adhesion, angiogenesis and thrombosis

Thrombosis and haemostasis, 1999-12, Vol.82 (6), p.1568-1577

Colman, R W

1999

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Two faces of high‐molecular‐weight kininogen (HK) in angiogenesis: bradykinin turns it on and cleaved HK (HKa) turns it off

Journal of thrombosis and haemostasis, 2005-04, Vol.3 (4), p.670-676

2005

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Identification of Interaction Sites of Cyclic Nucleotide Phosphodiesterase Type 3A with Milrinone and Cilostazol Using Molecular Modeling and Site-Directed Mutagenesis

Molecular pharmacology, 2002-09, Vol.62 (3), p.514-520

2002

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Differential regulation of human platelet responses by cGMP inhibited and stimulated cAMP phosphodiesterases

Thrombosis and haemostasis, 2002-05, Vol.87 (5), p.873-879

2002

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Binding of high molecular weight kininogen to human endothelial cells is mediated via a site within domains 2 and 3 of the urokinase receptor

The Journal of clinical investigation, 1997-09, Vol.100 (6), p.1481-1487

1997

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Inhibition of angiogenesis by antibody blocking the action of proangiogenic high‐molecular‐weight kininogen

Journal of thrombosis and haemostasis, 2003-01, Vol.1 (1), p.164-170

2003

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Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass

Circulation (New York, N.Y.), 1996-06, Vol.93 (11), p.2014-2018

1996

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Different mechanisms define the antiadhesive function of high molecular weight kininogen in integrin- and urokinase receptor-dependent interactions

Blood, 2000-07, Vol.96 (2), p.514-522

2000

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Interaction of high-molecular-weight kininogen with endothelial cell binding proteins suPAR, gC1qR and cytokeratin 1 determined by surface plasmon resonance (BiaCore)

Thrombosis and haemostasis, 2011-06, Vol.105 (6), p.1053-1059

2011

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Kallikrein–kinin system in inflammatory bowel diseases: Intestinal involvement and correlation with the degree of tissue inflammation

Digestive and liver disease, 2005-09, Vol.37 (9), p.665-673

2005

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Interactions between bradykinin (BK) and cell adhesion molecule (CAM) expression in peptidoglycan‐polysaccharide (PG‐PS)‐induced arthritis

The FASEB journal, 2004-05, Vol.18 (7), p.887-889

2004

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Role of the Light Chain of High Molecular Weight Kininogen in Adhesion, Cell-Associated Proteolysis and Angiogenesis

Biological chemistry, 2001-01, Vol.382 (1), p.65-70

Colman, R W

2001

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Fine mapping of the sequences in domain 5 of high molecular weight kininogen (HK) interacting with heparin and zinc

Journal of thrombosis and haemostasis, 2003-08, Vol.1 (8), p.1791-1798

2003

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Regulation of angiogenesis by the kallikrein-kinin system

Current pharmaceutical design, 2006-07, Vol.12 (21), p.2599-2607

Colman, Robert W

2006

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Clopidogrel inhibits the binding of ADP analogues to the receptor mediating inhibition of platelet adenylate cyclase

Arteriosclerosis and thrombosis, 1992-04, Vol.12 (4), p.430-436

1992

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Human factor XII (Hageman factor) autoactivation by dextran sulfate. Circular dichroism, fluorescence, and ultraviolet difference spectroscopic studies

The Journal of biological chemistry, 1992-09, Vol.267 (27), p.19691-19697

1992

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High molecular weight kininogen binds to Mac-1 on neutrophils by its heavy chain (domain 3) and its light chain (domain 5)

The Journal of biological chemistry, 1994-07, Vol.269 (30), p.19307-19312

1994

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Kallikrein-kininogen system activation and bradykinin (B2) receptors in indomethacin induced enterocolitis in genetically susceptible Lewis rats

Gut, 1998-09, Vol.43 (3), p.365-374

1998

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Surface-bound heparin fails to reduce thrombin formation during clinical cardiopulmonary bypass

The Journal of thoracic and cardiovascular surgery, 1996, Vol.111 (1), p.1-12

1996

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Cleaved high molecular weight kininogen inhibits tube formation of endothelial progenitor cells via suppression of matrix metalloproteinase 2

Journal of thrombosis and haemostasis, 2010-01, Vol.8 (1), p.185-193

2010

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Tissue Factor Is Expressed on Monocytes During Simulated Extracorporeal Circulation

Circulation research, 1993-05, Vol.72 (5), p.1075-1081

1993

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Aprotinin inhibits the contact, neutrophil, and platelet activation systems during simulated extracorporeal perfusion

The Journal of thoracic and cardiovascular surgery, 1993-07, Vol.106 (1), p.1-10

1993

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Contact System: A Vascular Biology Modulator With Anticoagulant, Profibrinolytic, Antiadhesive, and Proinflammatory Attributes

Cleaved high-molecular-weight kininogen and its domain 5 inhibit migration and invasion of human prostate cancer cells through the epidermal growth factor receptor pathway

Domain 5 of high molecular weight kininogen (kininostatin) down-regulates endothelial cell proliferation and migration and inhibits angiogenesis

Biologic activities of the contact factors in vivo--potentiation of hypotension, inflammation, and fibrinolysis, and inhibition of cell adhesion, angiogenesis and thrombosis

Two faces of high‐molecular‐weight kininogen (HK) in angiogenesis: bradykinin turns it on and cleaved HK (HKa) turns it off

Identification of Interaction Sites of Cyclic Nucleotide Phosphodiesterase Type 3A with Milrinone and Cilostazol Using Molecular Modeling and Site-Directed Mutagenesis

Differential regulation of human platelet responses by cGMP inhibited and stimulated cAMP phosphodiesterases

Binding of high molecular weight kininogen to human endothelial cells is mediated via a site within domains 2 and 3 of the urokinase receptor

Inhibition of angiogenesis by antibody blocking the action of proangiogenic high‐molecular‐weight kininogen

Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass

Different mechanisms define the antiadhesive function of high molecular weight kininogen in integrin- and urokinase receptor-dependent interactions

Interaction of high-molecular-weight kininogen with endothelial cell binding proteins suPAR, gC1qR and cytokeratin 1 determined by surface plasmon resonance (BiaCore)

Kallikrein–kinin system in inflammatory bowel diseases: Intestinal involvement and correlation with the degree of tissue inflammation

Interactions between bradykinin (BK) and cell adhesion molecule (CAM) expression in peptidoglycan‐polysaccharide (PG‐PS)‐induced arthritis

Role of the Light Chain of High Molecular Weight Kininogen in Adhesion, Cell-Associated Proteolysis and Angiogenesis

Fine mapping of the sequences in domain 5 of high molecular weight kininogen (HK) interacting with heparin and zinc

Regulation of angiogenesis by the kallikrein-kinin system

Clopidogrel inhibits the binding of ADP analogues to the receptor mediating inhibition of platelet adenylate cyclase

Human factor XII (Hageman factor) autoactivation by dextran sulfate. Circular dichroism, fluorescence, and ultraviolet difference spectroscopic studies

High molecular weight kininogen binds to Mac-1 on neutrophils by its heavy chain (domain 3) and its light chain (domain 5)

Kallikrein-kininogen system activation and bradykinin (B2) receptors in indomethacin induced enterocolitis in genetically susceptible Lewis rats

Surface-bound heparin fails to reduce thrombin formation during clinical cardiopulmonary bypass

Cleaved high molecular weight kininogen inhibits tube formation of endothelial progenitor cells via suppression of matrix metalloproteinase 2

Tissue Factor Is Expressed on Monocytes During Simulated Extracorporeal Circulation

Aprotinin inhibits the contact, neutrophil, and platelet activation systems during simulated extracorporeal perfusion

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