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Factor XI and contact activation as targets for antithrombotic therapy

Journal of thrombosis and haemostasis, 2015-08, Vol.13 (8), p.1383-1395

2015

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The intrinsic pathway of coagulation: a target for treating thromboembolic disease?

Journal of thrombosis and haemostasis, 2007-06, Vol.5 (6), p.1106-1112

2007

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Generation and characterization of aptamers targeting factor XIa

Thrombosis research, 2017-08, Vol.156, p.134-141

2017

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Evolution of the contact phase of vertebrate blood coagulation

Journal of thrombosis and haemostasis, 2008-11, Vol.6 (11), p.1876-1883

2008

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Structural and functional features of factor XI

Journal of thrombosis and haemostasis, 2009-07, Vol.7 (Suppl 1), p.75-78

2009

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Factor XII promotes blood coagulation independent of factor XI in the presence of long‐chain polyphosphates

Journal of thrombosis and haemostasis, 2013-07, Vol.11 (7), p.1341-1352

2013

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Factor IX binding to collagen

Journal of thrombosis and haemostasis, 2009-11, Vol.7 (11), p.1840-1842

GAILANI, D.

2009

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Factor XI promotes hemostasis in factor IX‐deficient mice

Journal of thrombosis and haemostasis, 2018-10, Vol.16 (10), p.2044-2049

2018

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Factor XI and pulmonary infections

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.519-521

2018

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Effects of factor IX or factor XI deficiency on ferric chloride‐induced carotid artery occlusion in mice

Journal of thrombosis and haemostasis, 2005-04, Vol.3 (4), p.695-702

2005

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Haemophilia A carriers experience reduced health-related quality of life

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-11, Vol.21 (6), p.761-765

2015

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Analysis of the factor XI variant Arg184Gly suggests a structural basis for factor IX binding to factor XIa

Journal of thrombosis and haemostasis, 2013-07, Vol.11 (7), p.1374-1384

2013

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Allosterism‐based simultaneous, dual anticoagulant and antiplatelet action: allosteric inhibitor targeting the glycoprotein Ibα‐binding and heparin‐binding site of thrombin

Journal of thrombosis and haemostasis, 2016-04, Vol.14 (4), p.828-838

2016

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Evidence for factor IX‐independent roles for factor XIa in blood coagulation

Journal of thrombosis and haemostasis, 2013-12, Vol.11 (12), p.2118-2127

2013

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Effects of factor XI deficiency on ferric chloride‐induced vena cava thrombosis in mice

Journal of thrombosis and haemostasis, 2006-09, Vol.4 (9), p.1982-1988

2006

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Factor XI anion‐binding sites are required for productive interactions with polyphosphate

Journal of thrombosis and haemostasis, 2013-11, Vol.11 (11), p.2020-2028

2013

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Laminin promotes coagulation and thrombus formation in a factor XII‐dependent manner

Journal of thrombosis and haemostasis, 2010-06, Vol.8 (6), p.1295-1301

2010

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Prolylcarboxypeptidase independently activates plasma prekallikrein (fletcher factor)

Current molecular medicine, 2014-01, Vol.14 (9), p.1173-1185

2014

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Differential Assessment of von Willebrand Factor Dysfunction in Durable Mechanical Circulatory Support: A Plead for Standardization

The Journal of heart and lung transplantation, 2016-04, Vol.35 (4), p.S150-S151

2016

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Haemophilia A carriers demonstrate pathological and radiological evidence of structural joint changes

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (6), p.e426-e429

2014

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Development of Coagulation Factor XII Antibodies for Inhibiting Vascular Device-Related Thrombosis

Cellular and molecular bioengineering, 2021-04, Vol.14 (2), p.161-175

2021

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Development of anti-factor XIII antibodies in a patient with hereditary factor XIII deficiency receiving therapy for chronic hepatitis C

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (6), p.e429-e432

2014

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Standard Dose Doxycycline Does Not Alter von Willebrand Factor Degradation in Patients with CF LVAD

The Journal of heart and lung transplantation, 2017-04, Vol.36 (4), p.S11-S11

2017

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Factor XII inhibition reduces thrombus formation in a primate thrombosis model

Blood, 2014-03, Vol.123 (11), p.1739-1746

2014

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C0459: Activated Factor XI Increases the Procoagulant Activity of the Extrinsic Pathway by Inactivating Tissue Factor Pathway Inhibitor

Thrombosis research, 2014-05, Vol.133, p.S6-S6

2014

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Factor XI and contact activation as targets for antithrombotic therapy

The intrinsic pathway of coagulation: a target for treating thromboembolic disease?

Generation and characterization of aptamers targeting factor XIa

Evolution of the contact phase of vertebrate blood coagulation

Structural and functional features of factor XI

Factor XII promotes blood coagulation independent of factor XI in the presence of long‐chain polyphosphates

Factor IX binding to collagen

Factor XI promotes hemostasis in factor IX‐deficient mice

Factor XI and pulmonary infections

Effects of factor IX or factor XI deficiency on ferric chloride‐induced carotid artery occlusion in mice

Haemophilia A carriers experience reduced health-related quality of life

Analysis of the factor XI variant Arg184Gly suggests a structural basis for factor IX binding to factor XIa

Allosterism‐based simultaneous, dual anticoagulant and antiplatelet action: allosteric inhibitor targeting the glycoprotein Ibα‐binding and heparin‐binding site of thrombin

Evidence for factor IX‐independent roles for factor XIa in blood coagulation

Effects of factor XI deficiency on ferric chloride‐induced vena cava thrombosis in mice

Factor XI anion‐binding sites are required for productive interactions with polyphosphate

Laminin promotes coagulation and thrombus formation in a factor XII‐dependent manner

Prolylcarboxypeptidase independently activates plasma prekallikrein (fletcher factor)

Differential Assessment of von Willebrand Factor Dysfunction in Durable Mechanical Circulatory Support: A Plead for Standardization

Haemophilia A carriers demonstrate pathological and radiological evidence of structural joint changes

Development of Coagulation Factor XII Antibodies for Inhibiting Vascular Device-Related Thrombosis

Development of anti-factor XIII antibodies in a patient with hereditary factor XIII deficiency receiving therapy for chronic hepatitis C

Standard Dose Doxycycline Does Not Alter von Willebrand Factor Degradation in Patients with CF LVAD

Factor XII inhibition reduces thrombus formation in a primate thrombosis model

C0459: Activated Factor XI Increases the Procoagulant Activity of the Extrinsic Pathway by Inactivating Tissue Factor Pathway Inhibitor

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