von Willebrand factor is a cofactor in complement regulation

A New Map of Glycosaminoglycan and C3b Binding Sites on Factor H

(2014) C. Q. Schmidt et al.   JOURNAL OF IMMUNOLOGY

Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome

(2013) S. Feng et al.   BLOOD

The interaction between factor H and VWF increases factor H cofactor activity and regulates VWF prothrombotic status

(2013) J. Rayes et al.   BLOOD

Complement and cytokine response in acute Thrombotic Thrombocytopenic Purpura

(2013) John-Paul Westwood et al.   BRITISH JOURNAL OF HAEMATOLOGY

Complement Activation Associated with ADAMTS13 Deficiency in Human and Murine Thrombotic Microangiopathy

(2013) R. Tati et al.   JOURNAL OF IMMUNOLOGY

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

(2013) F. Bu et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Assembly and Activation of Alternative Complement Components on Endothelial Cell-Anchored Ultra-Large Von Willebrand Factor Links Complement and Hemostasis-Thrombosis

(2013) Nancy A. Turner et al.   PLoS One

The Interaction between Factor H and Von Willebrand Factor

(2013) Shuju Feng et al.   PLoS One

Complement activation in thrombotic microangiopathies

(2012) Shuju Feng et al.   BRITISH JOURNAL OF HAEMATOLOGY

Complement Factor H–ligand interactions: Self-association, multivalency and dissociation constants

(2011) Stephen J. Perkins et al.   IMMUNOBIOLOGY

Thrombomodulin and its role in inflammation

(2011) Edward M. Conway   Seminars in Immunopathology

Endothelial cell ADAMTS-13 and VWF: production, release, and VWF string cleavage

(2009) N. A. Turner et al.   BLOOD