Publications by authors named "Colleen Notley"

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The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change.
Pamela A Christopherson, Nathalie Tijet, Sandra L Haberichter, Veronica H Flood, Justyne Ross, Colleen Notley

J Thromb Haemost· March 2024

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Mice possess a more limited natural antihuman factor VIII antibody repertoire than humans that is produced disproportionately by marginal zone B cells.
Matthew Cormier, Erin Burnett, Aomei Mo, Colleen Notley, Nathalie Tijet

J Thromb Haemost· January 2024

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Heterogeneity and reciprocity of FVIII and VWF expression, and the response to shear stress in cultured human endothelial cells.
Christine Hough, Colleen Notley, Aomei Mo, Barbara Videl, David Lillicrap

J Thromb Haemost· November 2022

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Stabilin-2 deficiency increases thrombotic burden and alters the composition of venous thrombi in a mouse model.
Alison Michels, Laura L Swystun, Courtney N Dwyer, Orla Rawley, Kate Nesbitt, Colleen Notley

J Thromb Haemost· October 2021

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Endothelial characteristics in healthy endothelial colony forming cells; generating a robust and valid ex vivo model for vascular disease.
Suzan de Boer, Mackenzie Bowman, Colleen Notley, Aomei Mo, Patricia Lima

J Thromb Haemost· October 2020

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The scavenger receptor SCARA5 is an endocytic receptor for von Willebrand factor expressed by littoral cells in the human spleen.
Laura L Swystun, Kenichi Ogiwara, Jesse D Lai, Juha R M Ojala, Orla Rawley, Colleen Notley

J Thromb Haemost· August 2019

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The endothelial lectin clearance receptor CLEC4M binds and internalizes factor VIII in a VWF-dependent and independent manner.
Laura L Swystun, Colleen Notley, Ilinca Georgescu, Jesse D Lai, Kate Nesbitt

J Thromb Haemost· April 2019

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The endothelial cell receptor stabilin-2 regulates VWF-FVIII complex half-life and immunogenicity.
Laura L Swystun, Jesse D Lai, Colleen Notley, Ilinca Georgescu, A Simonne Paine

J Clin Invest· August 2018

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Omental implantation of BOECs in hemophilia dogs results in circulating FVIII antigen and a complex immune response.
Margareth C Ozelo, Barbara Vidal, Christine Brown, Colleen Notley, Carol Hegadorn

Blood· June 2014

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The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels.
Natalia Rydz, Laura L Swystun, Colleen Notley, Andrew D Paterson, J Jacob Riches

Blood· June 2013

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Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models.
Cynthia M Pruss, Mia Golder, Andrea Bryant, Carol A Hegadorn, Erin Burnett, Colleen Notley

Blood· April 2011

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Frequency of platelet type versus type 2B von Willebrand disease. An international registry-based study.
Alexander Hamilton, Margareth Ozelo, Jayne Leggo, Colleen Notley, Hannah Brown

Thromb Haemost· March 2011

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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.
Maha Othman, Yvette Chirinian, Christine Brown, Colleen Notley, Nicholas Hickson

Blood· November 2010

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ADAMTS13 cleavage efficiency is altered by mutagenic and, to a lesser extent, polymorphic sequence changes in the A1 and A2 domains of von Willebrand factor.
Cynthia M Pruss, Colleen R P Notley, Carol A Hegadorn, Lee A O'Brien, David Lillicrap

Br J Haematol· November 2008

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The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.
Paula D James, Colleen Notley, Carol Hegadorn, Jayne Leggo, Angie Tuttle

Blood· January 2007

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Identification and functional characterization of a novel 27-bp deletion in the macroglycopeptide-coding region of the GPIBA gene resulting in platelet-type von Willebrand disease.
Maha Othman, Colleen Notley, Frances Louise Lavender, Helen White, Christopher D Byrne

Blood· June 2005

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Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor.
Christine Hough, Carla D Cuthbert, Colleen Notley, Christine Brown, Carol Hegadorn

Blood· February 2005

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A novel type 2A von Willebrand factor mutation located at the last nucleotide of exon 26 (3538G>A) causes skipping of 2 nonadjacent exons.
Paula D James, Lee A O'Brien, Carol A Hegadorn, Colleen R P Notley, Gary D Sinclair

Blood· November 2004

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Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease.
Lee A O'Brien, Paula D James, Maha Othman, Ergul Berber, Cherie Cameron, Colleen R P Notley

Blood· July 2003

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The canine factor VIII 3'-untranslated region and a concatemeric hepatocyte nuclear factor 1 regulatory element enhance factor VIII transgene expression in vivo.
Colleen Notley, Annie Killoran, Cherie Cameron, Kimberly Wynd, Christine Hough

Hum Gene Ther· September 2002

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Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophilia.
Christine Hough, Seiki Kamisue, Cherie Cameron, Colleen Notley, Shawn Tinlin

Thromb Haemost· April 2002

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