Christine Brown

发表

Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.

D. Lillicrap, Z. Başlar, M. Ozbil, 2017, Blood transfusion = Trasfusione del sangue.

The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.

L. O'Brien, J. Leggo, M. Othman, 2007, Blood.

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study

A. Paterson, L. O'Brien, J. Leggo, 2006, Journal of thrombosis and haemostasis : JTH.

Analysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation.

B. Nieswandt, D. Lillicrap, Kate Sponagle, 2014, Blood.

THROMBOSIS AND HEMOSTASIS Analysis of the role of von Willebrand factor , platelet glycoprotein VI-, and a 2 b 1-mediated collagen binding in thrombus formation

B. Nieswandt, D. Lillicrap, Kate Sponagle, 2014 .

Genetic determinants of VWF clearance and FVIII-binding modify FVIII pharmacokinetics in pediatric hemophilia A patients.

V. Blanchette, M. Carcao, W. Hopman, 2019, Blood.

Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter

L. O'Brien, D. Lillicrap, C. Hough, 2008, Journal of thrombosis and haemostasis : JTH.

Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor.

D. Lillicrap, C. Hough, C. Notley, 2005, Blood.

Cell type – specific regulation of von Willebrand factor expression by the E 4 BP 4 transcriptional repressor

D. Lillicrap, C. Hough, C. Notley, 2005 .

Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease.

D. Hampshire, M. Othman, A. Parker, 2010, Blood.

Molecular coevolution of coagulation factor VIII and von Willebrand factor.

E. Gaucher, H. Spencer, C. Doering, 2021, Blood advances.

Shear stress and platelet‐induced tensile forces regulate ADAMTS13‐localization within the platelet thrombus

D. Lillicrap, C. Hough, J. Mewburn, 2019, Research and practice in thrombosis and haemostasis.

Comprehensive analysis of the role of von Willebrand factor and platelet glycoprotein VI-and α 2 β 1-mediated collagen binding in thrombus formation

B. Nieswandt, D. Lillicrap, Kate Sponagle, 2014 .

The genetics of Canadian type 3 von Willebrand disease: further evidence for co‐dominant inheritance of mutant alleles

V. Blanchette, J. Leggo, P. James, 2013, Journal of thrombosis and haemostasis : JTH.

Omental implantation of BOECs in hemophilia dogs results in circulating FVIII antigen and a complex immune response.

M. Ozelo, V. Arruda, A. Winterborn, 2014, Blood.