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

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The endothelial cell receptor stabilin-2 regulates VWF-FVIII complex half-life and immunogenicity von Swystun, Laura L, Lai, Jesse D, Notley, Colleen, Georgescu, Ilinca, Paine, A Simonne, Mewburn, Jeff, Nesbitt, Kate, Schledzewski, Kai, Géraud, Cyrill, Kzhyshkowska, Julia, Goerdt, Sergij, Hopman, Wilma, Montgomery, Robert R, James, Paula D, Lillicrap, David

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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 von Rydz, Natalia, Swystun, Laura L., Notley, Colleen, Paterson, Andrew D., Riches, J. Jacob, Sponagle, Kate, Boonyawat, Boonchai, Montgomery, Robert R., James, Paula D., Lillicrap, David

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Endothelial characteristics in healthy endothelial colony forming cells; generating a robust and valid ex vivo model for vascular disease von Boer, Suzan, Bowman, Mackenzie, Notley, Colleen, Mo, Aomei, Lima, Patricia, Jong, Annika, Dirven, Richard, Weijers, Ester, Lillicrap, David, James, Paula, Eikenboom, Jeroen

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The scavenger receptor SCARA5 is an endocytic receptor for von Willebrand factor expressed by littoral cells in the human spleen von Swystun, Laura L., Ogiwara, Kenichi, Lai, Jesse D., Ojala, Juha R. M., Rawley, Orla, Lassalle, Fanny, Notley, Colleen, Rengby, Olle, Michels, Alison, Nesbitt, Kate, Tryggvason, Karl, Lillicrap, David

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The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study von James, Paula D., Notley, Colleen, Hegadorn, Carol, Leggo, Jayne, Tuttle, Angie, Tinlin, Shawn, Brown, Christine, Andrews, Chandler, Labelle, Andrea, Chirinian, Yvette, O'Brien, Lee, Othman, Maha, Rivard, Georges, Rapson, Dilys, Hough, Christine, Lillicrap, David

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Omental implantation of BOECs in hemophilia dogs results in circulating FVIII antigen and a complex immune response von Ozelo, Margareth C., Vidal, Barbara, Brown, Christine, Notley, Colleen, Hegadorn, Carol, Webster, Sandra, Harpell, Lori, Ahlin, James, Winterborn, Andrew, Handforth, Janine, Arruda, Valder R., Hough, Christine, Lillicrap, David

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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 von Pruss, Cynthia M., Notley, Colleen R. P., Hegadorn, Carol A., O’Brien, Lee A., Lillicrap, David

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Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models von Pruss, Cynthia M., Golder, Mia, Bryant, Andrea, Hegadorn, Carol A., Burnett, Erin, Laverty, Kimberly, Sponagle, Kate, Dhala, Aly, Notley, Colleen, Haberichter, Sandra, Lillicrap, David

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Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease von O'Brien, Lee A., James, Paula D., Othman, Maha, Berber, Ergul, Cameron, Cherie, Notley, ColleenR.P., Hegadorn, Carol A., Sutherland, Jeffrey J., Hough, Christine, Rivard, Georges E., O'Shaunessey, Denise, Lillicrap, David

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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 von Othman, Maha, Notley, Colleen, Lavender, Frances Louise, White, Helen, Byrne, Christopher D., Lillicrap, David, O'Shaughnessy, Denise Frances

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

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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 von James, Paula D., O'Brien, Lee A., Hegadorn, Carol A., Notley, Colleen R.P., Sinclair, Gary D., Hough, Christine, Poon, Man-Chiu, Lillicrap, David

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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 von Cormier, Matthew, Burnett, Erin, Mo, Aomei, Notley, Colleen, Tijet, Nathalie, Christie-Holmes, Natasha, Hough, Christine, Lillicrap, David

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Mice possess a more limited natural anti-human Factor VIII antibody repertoire than humans that is produced disproportionately by marginal zone B cells von Cormier, Matthew, Burnett, Erin, Mo, Aomei, Notley, Colleen, Tijet, Nathalie, Christie-Holmes, Natasha, Hough, Christine, Lillicrap, David

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Frequency of Platelet type versus Type 2B von Willebrand Disease von Hamilton, Alexander, Ozelo, Margareth, Leggo, Jayne, Notley, Colleen, Brown, Hannah, Pablo Frontroth, Juan, Angelillo-Scherrer, Anne, Baghaei, Fariba, Enayat, Said M., Favaloro, Emmanuel, Lillicrap, David, Othman, Maha

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Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia... von Gallo-Penn, Angela M., Shirley, Pamela S., Andrews, Julie L., Tinlin, Shawn, Webster, Sandy, Cameron, Cherie, Hough, Christine, Notley, Colleen, Lillicrap, David, Kaleko, Michael, Connelly, Sheila

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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... von Hough, Christine, Kamisue, Seiki, Cameron, Cherie, Notley, Colleen, Tinlin, Shawn, Giles, Alan, Lillicrap, David

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

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The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change von Christopherson, Pamela A., Tijet, Nathalie, Haberichter, Sandra L., Flood, Veronica H., Ross, Justyne, Notley, Colleen, Rawley, Orla, Montgomery, Robert R., James, Paula D., Lillicrap, David

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