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Janice M Staber

Showing results (11-20 of 22) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|July 23, 2016
Endothelial Cell-Derived von Willebrand Factor Is the Major Determinant That Mediates von Willebrand Factor-Dependent Acute Ischemic Stroke by Promoting Postischemic Thrombo-InflammationNirav Dhanesha, Prem Prakash, Prakash Doddapattar, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 20, 2018
Endothelial Cell-Derived Von Willebrand Factor, But Not Platelet-Derived, Promotes Atherosclerosis in Apolipoprotein E-Deficient MicePrakash Doddapattar, Nirav Dhanesha, Mehul R Chorawala, et al.
Blood Vessels, Thrombosis & Hemostasis|June 8, 2026
Cost comparison of efanesoctocog alfa vs conventional factor VIII therapies for major surgeries in patients with severe hemophilia AJanice M Staber, Alix Arnaud, Ion Agirrezabal, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 13, 2017
ADAMTS13 Retards Progression of Diabetic Nephropathy by Inhibiting Intrarenal Thrombosis in MiceNirav Dhanesha, Prakash Doddapattar, Mehul R Chorawala, et al.
American Journal of Hematology|October 6, 2023
Trends in dedicated care for females with bleeding disorders within U.S. hemophilia treatment centersAllison P Wheeler, Ming Y Lim, Patricia S Huguelet, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
A Hyperactive Transposase Promotes Persistent Gene Transfer of a piggyBac DNA TransposonErin R Burnight, Janice M Staber, Pavel Korsakov, et al.
Advances in Therapy|March 26, 2026
A New Risk-Based Scoring Approach to Individualize Prophylaxis in Patients with Hemophilia A: Results from the PREDICT StudyDoris V Quon, Miguel Escobar, Lisa Boggio, et al.
The New England Journal of Medicine|September 9, 2020
BIVV001 Fusion Protein as Factor VIII Replacement Therapy for Hemophilia ABarbara A Konkle, Amy D Shapiro, Doris V Quon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 12, 2025
Safety and Effectiveness of Emicizumab in People With Haemophilia A Enrolled in the ATHN 7 Haemophilia Natural History StudyTyler W Buckner, Shannon L Carpenter, Nabil Daoud, et al.
American Journal of Hematology|May 19, 2020
Laboratory misdiagnosis of von Willebrand disease in post-menarchal females: A multi-center studyJulie Jaffray, Janice M Staber, Jemily Malvar, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Arteriosclerosis, Thrombosis, and Vascular Biology|July 23, 2016
Endothelial Cell-Derived von Willebrand Factor Is the Major Determinant That Mediates von Willebrand Factor-Dependent Acute Ischemic Stroke by Promoting Postischemic Thrombo-InflammationNirav Dhanesha, Prem Prakash, Prakash Doddapattar, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 20, 2018
Endothelial Cell-Derived Von Willebrand Factor, But Not Platelet-Derived, Promotes Atherosclerosis in Apolipoprotein E-Deficient MicePrakash Doddapattar, Nirav Dhanesha, Mehul R Chorawala, et al.
Blood Vessels, Thrombosis & Hemostasis|June 8, 2026
Cost comparison of efanesoctocog alfa vs conventional factor VIII therapies for major surgeries in patients with severe hemophilia AJanice M Staber, Alix Arnaud, Ion Agirrezabal, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 13, 2017
ADAMTS13 Retards Progression of Diabetic Nephropathy by Inhibiting Intrarenal Thrombosis in MiceNirav Dhanesha, Prakash Doddapattar, Mehul R Chorawala, et al.
American Journal of Hematology|October 6, 2023
Trends in dedicated care for females with bleeding disorders within U.S. hemophilia treatment centersAllison P Wheeler, Ming Y Lim, Patricia S Huguelet, et al.
Molecular Therapy. Nucleic Acids|January 25, 2013
A Hyperactive Transposase Promotes Persistent Gene Transfer of a piggyBac DNA TransposonErin R Burnight, Janice M Staber, Pavel Korsakov, et al.
Advances in Therapy|March 26, 2026
A New Risk-Based Scoring Approach to Individualize Prophylaxis in Patients with Hemophilia A: Results from the PREDICT StudyDoris V Quon, Miguel Escobar, Lisa Boggio, et al.
The New England Journal of Medicine|September 9, 2020
BIVV001 Fusion Protein as Factor VIII Replacement Therapy for Hemophilia ABarbara A Konkle, Amy D Shapiro, Doris V Quon, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 12, 2025
Safety and Effectiveness of Emicizumab in People With Haemophilia A Enrolled in the ATHN 7 Haemophilia Natural History StudyTyler W Buckner, Shannon L Carpenter, Nabil Daoud, et al.
American Journal of Hematology|May 19, 2020
Laboratory misdiagnosis of von Willebrand disease in post-menarchal females: A multi-center studyJulie Jaffray, Janice M Staber, Jemily Malvar, et al.
Pageof 3