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P Lollar

Showing results (61-70 of 76) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 11, 2017
A discontinuous autoinhibitory module masks the A1 domain of von Willebrand factorW Deng, Y Wang, S A Druzak, et al.
Journal of Thrombosis and Haemostasis : JTH|December 22, 2006
The humoral response to human factor VIII in hemophilia A miceJ F Healey, E T Parker, R T Barrow, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 23, 2014
Lack of recombinant factor VIII B-domain induces phospholipid vesicle aggregation: implications for the immunogenicity of factor VIIIK Grushin, J Miller, D Dalm, et al.
The Journal of Biological Chemistry|June 20, 1998
Changing residue 338 in human factor IX from arginine to alanine causes an increase in catalytic activityJ Chang, J Jin, P Lollar, et al.
Blood|September 18, 1997
Loss of tolerance to exogenous and endogenous factor VIII in a mild hemophilia A patient with an Arg593 to Cys mutationA R Thompson, M E Murphy, M Liu, et al.
The Journal of Biological Chemistry|June 16, 1995
Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIIIJ F Healey, I M Lubin, H Nakai, et al.
Blood|November 10, 1998
Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIIIJ F Healey, R T Barrow, H M Tamim, et al.
Journal of Thrombosis and Haemostasis : JTH|July 28, 2018
Delimiting the autoinhibitory module of von Willebrand factorW Deng, K M Voos, J K Colucci, et al.
The Journal of Clinical Investigation|June 1, 1994
Inhibition of human factor VIIIa by anti-A2 subunit antibodiesP Lollar, E T Parker, J E Curtis, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 18, 2015
Porcine recombinant factor VIII (Obizur; OBI-1; BAX801): product characteristics and preclinical profileD Lillicrap, A Schiviz, C Apostol, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Journal of Thrombosis and Haemostasis : JTH|July 11, 2017
A discontinuous autoinhibitory module masks the A1 domain of von Willebrand factorW Deng, Y Wang, S A Druzak, et al.
Journal of Thrombosis and Haemostasis : JTH|December 22, 2006
The humoral response to human factor VIII in hemophilia A miceJ F Healey, E T Parker, R T Barrow, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 23, 2014
Lack of recombinant factor VIII B-domain induces phospholipid vesicle aggregation: implications for the immunogenicity of factor VIIIK Grushin, J Miller, D Dalm, et al.
The Journal of Biological Chemistry|June 20, 1998
Changing residue 338 in human factor IX from arginine to alanine causes an increase in catalytic activityJ Chang, J Jin, P Lollar, et al.
Blood|September 18, 1997
Loss of tolerance to exogenous and endogenous factor VIII in a mild hemophilia A patient with an Arg593 to Cys mutationA R Thompson, M E Murphy, M Liu, et al.
The Journal of Biological Chemistry|June 16, 1995
Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIIIJ F Healey, I M Lubin, H Nakai, et al.
Blood|November 10, 1998
Residues Glu2181-Val2243 contain a major determinant of the inhibitory epitope in the C2 domain of human factor VIIIJ F Healey, R T Barrow, H M Tamim, et al.
Journal of Thrombosis and Haemostasis : JTH|July 28, 2018
Delimiting the autoinhibitory module of von Willebrand factorW Deng, K M Voos, J K Colucci, et al.
The Journal of Clinical Investigation|June 1, 1994
Inhibition of human factor VIIIa by anti-A2 subunit antibodiesP Lollar, E T Parker, J E Curtis, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 18, 2015
Porcine recombinant factor VIII (Obizur; OBI-1; BAX801): product characteristics and preclinical profileD Lillicrap, A Schiviz, C Apostol, et al.
Pageof 8