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P V Jenkins

Showing results (1-10 of 22) with videos related to

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Methods in Molecular Medicine|February 23, 2011
Screening for Candidate Mutations Causing von Willebrand's Disease (vWD)P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Inversion mutation analysis in hemophilia a by restriction enzyme analysis and southern blottingC Ononye, P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Detection of mutations causing hemophilia a using an in vitro coupled transcription and translation systemC Ononye, P V Jenkins
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Factor VIII and von Willebrand factor interaction: biological, clinical and therapeutic importanceV Terraube, J S O'Donnell, P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Multiplex PCR for Detection of the Prothrombin 3'-UTR (G20210A) Polymorphism and the Factor V Leiden MutationG Mellars, P V Jenkins, D J Perry
Blood|April 16, 1998
Molecular modeling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's diseaseP V Jenkins, K J Pasi, S J Perkins
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Carrier detection and prenatal diagnosis by intron 22 inversion analysis of the factor VIII geneC Ononye, P V Jenkins, E Goldman, et al.
Journal of Thrombosis and Haemostasis : JTH|March 11, 2004
Clustered basic residues within segment 484-510 of the factor VIIIa A2 subunit contribute to the catalytic efficiency for factor Xa generationP V Jenkins, J L Dill, Q Zhou, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 13, 2010
Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancyR Gilmore, S Harmon, C Gannon, et al.
British Journal of Haematology|February 26, 2000
Type 1 von Willebrand disease - a clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding historyI C Nitu-Whalley, C A Lee, A Griffioen, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Methods in Molecular Medicine|February 23, 2011
Screening for Candidate Mutations Causing von Willebrand's Disease (vWD)P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Inversion mutation analysis in hemophilia a by restriction enzyme analysis and southern blottingC Ononye, P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Detection of mutations causing hemophilia a using an in vitro coupled transcription and translation systemC Ononye, P V Jenkins
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Factor VIII and von Willebrand factor interaction: biological, clinical and therapeutic importanceV Terraube, J S O'Donnell, P V Jenkins
Methods in Molecular Medicine|February 23, 2011
Multiplex PCR for Detection of the Prothrombin 3'-UTR (G20210A) Polymorphism and the Factor V Leiden MutationG Mellars, P V Jenkins, D J Perry
Blood|April 16, 1998
Molecular modeling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's diseaseP V Jenkins, K J Pasi, S J Perkins
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Carrier detection and prenatal diagnosis by intron 22 inversion analysis of the factor VIII geneC Ononye, P V Jenkins, E Goldman, et al.
Journal of Thrombosis and Haemostasis : JTH|March 11, 2004
Clustered basic residues within segment 484-510 of the factor VIIIa A2 subunit contribute to the catalytic efficiency for factor Xa generationP V Jenkins, J L Dill, Q Zhou, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 13, 2010
Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancyR Gilmore, S Harmon, C Gannon, et al.
British Journal of Haematology|February 26, 2000
Type 1 von Willebrand disease - a clinical retrospective study of the diagnosis, the influence of the ABO blood group and the role of the bleeding historyI C Nitu-Whalley, C A Lee, A Griffioen, et al.
Pageof 3