L. Swystun

发表

D. Lillicrap, L. Swystun, 2016, Circulation research.

Protective effects of activated protein C in sepsis

P. Liaw, L. Toltl, L. Swystun, 2008, Thrombosis and Haemostasis.

The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance.

D. Hampshire, J. Goudemand, C. Halldén, 2018, Blood advances.

The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels.

A. Paterson, R. Montgomery, P. James, 2013, Blood.

Modulation of Hemostatic Pathways by Breast Cancer Chemotherapy Agents

L. Swystun, 2011 .

The chemotherapy metabolite acrolein upregulates thrombin generation and impairs the protein C anticoagulant pathway in animal‐based and cell‐based models

P. Liaw, M. Levine, L. Swystun, 2011, Journal of thrombosis and haemostasis : JTH.

Chemotherapeutic agents doxorubicin and epirubicin induce a procoagulant phenotype on endothelial cells and blood monocytes

P. Liaw, L. Swystun, L. Shin, 2009, Journal of thrombosis and haemostasis : JTH.

Effects of the chemotherapeutic agent doxorubicin on the protein C anticoagulant pathway

P. Liaw, L. Swystun, L. Shin, 2006, Molecular Cancer Therapeutics.

Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A population

W. Hopman, D. Lillicrap, I. Pabinger, 2020, Journal of thrombosis and haemostasis : JTH.

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

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

Genetic regulation of plasma von Willebrand factor levels in health and disease

D. Lillicrap, L. Swystun, 2018, Journal of thrombosis and haemostasis : JTH.

How much do we really know about von Willebrand disease?

D. Lillicrap, L. Swystun, 2016, Current opinion in hematology.

Stabilin‐2 deficiency increases thrombotic burden and alters the composition of venous thrombi in a mouse model

D. Lillicrap, C. Notley, L. Swystun, 2021, Journal of thrombosis and haemostasis : JTH.

The scavenger receptor SCARA5 is an endocytic receptor for von Willebrand factor expressed by littoral cells in the human spleen

K. Tryggvason, D. Lillicrap, J. Lai, 2019, Journal of thrombosis and haemostasis : JTH.

Using genetic diagnostics in hemophilia and von Willebrand disease.

P. James, L. Swystun, 2015, Hematology. American Society of Hematology. Education Program.

Dalteparin low molecular weight heparin (LMWH) in ovarian cancer: a phase II randomized study.

P. Liaw, L. Elit, M. Levine, 2012, Thrombosis research.

Histones link inflammation and thrombosis through the induction of Weibel–Palade body exocytosis

P. Liaw, P. James, D. Lillicrap, 2016, Journal of thrombosis and haemostasis : JTH.

Abnormal von Willebrand factor secretion, factor VIII stabilization and thrombus dynamics in type 2N von Willebrand disease mice

D. Lillicrap, J. Mewburn, C. Notley, 2017, Journal of thrombosis and haemostasis : JTH.

N-linked glycosylation modulates the immunogenicity of recombinant human factor VIII in hemophilia A mice

J. Dennis, D. Lillicrap, J. Lai, 2018, Haematologica.

Kaiso regulates Znf131-mediated transcriptional activation.

J. Daniel, C. Nordgaard, L. Swystun, 2010, Experimental cell research.

Extracellular Histones Increase Tissue Factor Activity and Enhance Thrombin Generation by Human Blood Monocytes

D. Dwivedi, T. Gould, A. Fox-Robichaud, 2016, Shock.

Breast cancer chemotherapy induces the release of cell‐free DNA, a novel procoagulant stimulus

P. Liaw, L. Swystun, S. Mukherjee, 2011, Journal of thrombosis and haemostasis : JTH.

Early cellular interactions and immune transcriptome profiles in human factor VIII‐exposed hemophilia A mice

J. Voorberg, A. V. van Velzen, D. Lillicrap, 2018, Journal of thrombosis and haemostasis : JTH.

Genetic diagnosis in hemophilia and von Willebrand disease.

P. James, L. Swystun, 2017, Blood reviews.

FVIII stabilization: VWF D'D3 will do.

D. Lillicrap, L. Swystun, 2014, Blood.

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.

The endothelial lectin clearance receptor CLEC4M binds and internalizes factor VIII in a VWF‐dependent and independent manner

P. James, D. Lillicrap, J. Lai, 2019, Journal of thrombosis and haemostasis : JTH.

The role of leukocytes in thrombosis.

P. Liaw, L. Swystun, 2016, Blood.

Prognostic utility and characterization of cell-free DNA in patients with severe sepsis

D. Cook, J. Pogue, D. Dwivedi, 2012, Critical Care.

Lung cancer chemotherapy agents increase procoagulant activity via protein disulfide isomerase-dependent tissue factor decryption

P. Liaw, S. Kuruvilla, L. Swystun, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Neutrophil Extracellular Traps Promote Thrombin Generation Through Platelet-Dependent and Platelet-Independent Mechanisms

D. Dwivedi, T. Gould, S. Mai, 2014, Arteriosclerosis, thrombosis, and vascular biology.

Activation of protein C and thrombin activable fibrinolysis inhibitor on cultured human endothelial cells

P. Liaw, J. Weitz, P. Kim, 2016, Journal of thrombosis and haemostasis : JTH.

Current Understanding of Inherited Modifiers of FVIII Pharmacokinetic Variation

D. Lillicrap, L. Swystun, 2023, Pharmacogenomics and personalized medicine.

The Endothelial Lectin Receptor CLEC4M Internalizes Factor VIII and Von Willebrand Factor Via a Clathrin-Coated Pit-Dependent Mechanism

P. James, D. Lillicrap, C. Notley, 2013 .

Impact of Chemotherapy on Thrombin Generation and on the Protein C Pathway in Breast Cancer Patients

N. Mackman, P. Liaw, M. Levine, 2011, Pathophysiology of Haemostasis and Thrombosis.

von Willebrand Factor Is a Critical Mediator of Deep Vein Thrombosis in a Mouse Model of Diet-Induced Obesity

P. Lenting, D. Lillicrap, J. Mewburn, 2020, Arteriosclerosis, thrombosis, and vascular biology.

The endothelial cell receptor stabilin-2 regulates VWF-FVIII complex half-life and immunogenicity

S. Goerdt, R. Montgomery, P. James, 2018, The Journal of clinical investigation.

Abstract 569: Neutrophil Extracellular Traps Promote Thrombin Generation Through Platelet-Dependent and -Independent Mechanisms

D. Dwivedi, T. Gould, P. Liaw, 2014, Arteriosclerosis, Thrombosis, and Vascular Biology.

The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assays

S. Susen, J. Goudemand, J. Gauthier, 2020, Haemophilia : the official journal of the World Federation of Hemophilia.

Exome Sequencing Studies Identify Mutations in STAB2 As a Genetic Risk for Venous Thromboembolic Disease

D. Goldstein, Jun Z. Li, P. Reitsma, 2017 .

The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels.

D. Lillicrap, Kate Sponagle, N. Rydz, 2013, Blood.

Dalteparin low molecular weight heparin (LMWH) in ovarian cancer: a phase II randomized study.

P. Liaw, L. Elit, M. Levine, 2012, Thrombosis research.