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P V Jenkins

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

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Thrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.
Thrombosis and Haemostasis|August 26, 2000
Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factorL Hilbert, P V Jenkins, C Gaucher, et al.
British Journal of Haematology|November 25, 2000
The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophiliaK J Pasi, C A Sabin, P V Jenkins, et al.
International Journal of Obstetric Anesthesia|July 16, 2022
A description of the coagulopathy characteristics in amniotic fluid embolism: a case reportC Oliver, J Freyer, M Murdoch, et al.
Blood|October 1, 1994
Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counselingP V Jenkins, P W Collins, E Goldman, et al.
Thrombosis and Haemostasis|August 26, 2000
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiencyF Peyvandi, P V Jenkins, P M Mannucci, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2008
Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effectP V Jenkins, H Egan, C Keenan, et al.
Thrombosis and Haemostasis|January 12, 2001
Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiencyS Akhavan, P M Mannucci, M Lak, et al.
Thrombosis and Haemostasis|January 12, 2001
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modellingI C Nitu-Whalley, A Riddell, C A Lee, et al.
Blood|July 27, 2001
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand diseaseM S Enayat, A M Guilliatt, G K Surdhar, et al.
Pageof 3

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

Sort By:
Pageof 3
Thrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.
Thrombosis and Haemostasis|August 26, 2000
Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factorL Hilbert, P V Jenkins, C Gaucher, et al.
British Journal of Haematology|November 25, 2000
The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophiliaK J Pasi, C A Sabin, P V Jenkins, et al.
International Journal of Obstetric Anesthesia|July 16, 2022
A description of the coagulopathy characteristics in amniotic fluid embolism: a case reportC Oliver, J Freyer, M Murdoch, et al.
Blood|October 1, 1994
Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counselingP V Jenkins, P W Collins, E Goldman, et al.
Thrombosis and Haemostasis|August 26, 2000
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiencyF Peyvandi, P V Jenkins, P M Mannucci, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2008
Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effectP V Jenkins, H Egan, C Keenan, et al.
Thrombosis and Haemostasis|January 12, 2001
Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiencyS Akhavan, P M Mannucci, M Lak, et al.
Thrombosis and Haemostasis|January 12, 2001
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modellingI C Nitu-Whalley, A Riddell, C A Lee, et al.
Blood|July 27, 2001
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand diseaseM S Enayat, A M Guilliatt, G K Surdhar, et al.
Pageof 3