Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Journal of Thrombosis and Haemostasis : JTH|March 5, 2026
Recommendation to adopt the Type 1C VWD nomenclature into the classification of von Willebrand disease: Communication from the ISTH SSC Subcommittee on von Willebrand Factor (VWF)Christopher J Ng, Ross I Baker, Michelle Lavin, et al.
Blood|January 19, 2006
P-selectin binds to the D'-D3 domains of von Willebrand factor in Weibel-Palade bodiesGrégoire Michaux, Timothy J Pullen, Sandra L Haberichter, et al.
Blood|March 26, 2010
The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWFSandra L Haberichter, Ulrich Budde, Tobias Obser, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 18, 2002
The von Willebrand factor propeptide (VWFpp) traffics an unrelated protein to storageSandra L Haberichter, Mary A Jozwiak, Jonathan B Rosenberg, et al.
Thrombosis Research|August 18, 2016
Mutations in the D'D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWFTara C White-Adams, Christopher J Ng, Paula M Jacobi, et al.
Developmental Cell|February 7, 2006
The physiological function of von Willebrand's factor depends on its tubular storage in endothelial Weibel-Palade bodiesGrégoire Michaux, Kate B Abbitt, Lucy M Collinson, et al.
Journal of Thrombosis and Haemostasis : JTH|October 13, 2020
Laboratory variability in the diagnosis of type 2 VWD variantsStefanie DiGiandomenico, Pamela A Christopherson, Sandra L Haberichter, et al.
Research and Practice in Thrombosis and Haemostasis|November 16, 2022
Ristocetin dependent cofactor activity in von Willebrand disease diagnosis: Limitations of relying on a single measurePamela A Christopherson, Sandra L Haberichter, Veronica H Flood, et al.
Blood Advances|September 2, 2020
von Willebrand factor variant D1472H has no effect in mice with humanized VWF-platelet interactionsHannah K Lohmeier, Tricia L Slobodianuk, Sachiko Kanaji, et al.
Blood|March 21, 2012
Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storagePaula M Jacobi, Joan Cox Gill, Veronica H Flood, et al.
Pageof 6