Search research articles
Contact Us
Filters
Showing results (111-120 of 216) with videos related to
Page
of 22
Sort By:
Blood
|
September 27, 2003
Helper-dependent adenoviral vectors mediate therapeutic factor VIII expression for several months with minimal accompanying toxicity in a canine model of severe hemophilia A
Brian D Brown, Chang Xin Shi, Sandra Powell, et al.
Blood
|
October 23, 2004
Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor
Christine Hough, Carla D Cuthbert, Colleen Notley, et al.
The Lancet. Haematology
|
November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implications
Omid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 29, 2019
Challenges in diagnosis of von Willebrand disease in the presence of combined mutations of different genes
Tiago Nava, Evemie Dubé, Julie Gauthier, et al.
British Journal of Haematology
|
November 7, 2008
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, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 21, 2021
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, et al.
Blood
|
September 26, 2008
Anti-CD3 prevents factor VIII inhibitor development in hemophilia A mice by a regulatory CD4+CD25+-dependent mechanism and by shifting cytokine production to favor a Th1 response
Braden Waters, Mohammad Qadura, Erin Burnett, et al.
Blood
|
May 5, 2009
Recombinant and plasma-derived factor VIII products induce distinct splenic cytokine microenvironments in hemophilia A mice
Mohammad Qadura, Braden Waters, Erin Burnett, et al.
Blood
|
February 12, 2005
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, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 15, 2024
The history of women and hemophilia: a narrative review of evolving beliefs and testing practices
Megan Chaigneau, Mackenzie Bowman, Pamela Wilton, et al.
Page
of 22
Search research articles
Search
Showing results (111-120 of 216) with videos related to
Sort By:
Page
of 22
Blood
|
September 27, 2003
Helper-dependent adenoviral vectors mediate therapeutic factor VIII expression for several months with minimal accompanying toxicity in a canine model of severe hemophilia A
Brian D Brown, Chang Xin Shi, Sandra Powell, et al.
Blood
|
October 23, 2004
Cell type-specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor
Christine Hough, Carla D Cuthbert, Colleen Notley, et al.
The Lancet. Haematology
|
November 5, 2025
Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implications
Omid Seidizadeh, Ferdows Atiq, Nathan T Connell, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
January 29, 2019
Challenges in diagnosis of von Willebrand disease in the presence of combined mutations of different genes
Tiago Nava, Evemie Dubé, Julie Gauthier, et al.
British Journal of Haematology
|
November 7, 2008
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, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 21, 2021
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, et al.
Blood
|
September 26, 2008
Anti-CD3 prevents factor VIII inhibitor development in hemophilia A mice by a regulatory CD4+CD25+-dependent mechanism and by shifting cytokine production to favor a Th1 response
Braden Waters, Mohammad Qadura, Erin Burnett, et al.
Blood
|
May 5, 2009
Recombinant and plasma-derived factor VIII products induce distinct splenic cytokine microenvironments in hemophilia A mice
Mohammad Qadura, Braden Waters, Erin Burnett, et al.
Blood
|
February 12, 2005
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, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 15, 2024
The history of women and hemophilia: a narrative review of evolving beliefs and testing practices
Megan Chaigneau, Mackenzie Bowman, Pamela Wilton, et al.
Page
of 22