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E G Tuddenham

Showing results (81-90 of 167) with videos related to

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Thrombosis and Haemostasis|July 1, 1997
Inherited factor X deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
Nature|April 1, 1985
Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneJ Gitschier, D Drayna, E G Tuddenham, et al.
Journal of Thrombosis and Haemostasis : JTH|June 16, 2010
Enhanced thrombin generation in patients with cirrhosis-induced coagulopathyA Gatt, A Riddell, V Calvaruso, et al.
Nature|October 24, 1985
Distribution of factor VIII mRNA and antigen in human liver and other tissuesK L Wion, D Kelly, J A Summerfield, et al.
Thrombosis and Haemostasis|May 1, 1997
High prevalence of elevated factor VIII levels in patients referred for thrombophilia screening: role of increased synthesis and relationship to the acute phase reactionJ O'Donnell, E G Tuddenham, R Manning, et al.
Haemostasis|May 1, 1995
Factor VIIShinjo: a dysfunctional factor VII variant homozygous for the substitution Gln for Arg at position 79O Takamiya, S Abe, A Yoshioka, et al.
Thrombosis and Haemostasis|July 1, 1997
Inherited factor VII deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
Biochemistry|July 30, 1985
Purification of human factor VIII:C and its characterization by Western blotting using monoclonal antibodiesF Rotblat, D P O'Brien, F J O'Brien, et al.
British Journal of Haematology|June 1, 1993
A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.
Blood|May 1, 1993
Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndromeS D Wright, K Michaelides, D J Johnson, et al.
Pageof 17

Showing results (81-90 of 167) with videos related to

Sort By:
Pageof 17
Thrombosis and Haemostasis|July 1, 1997
Inherited factor X deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
Nature|April 1, 1985
Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneJ Gitschier, D Drayna, E G Tuddenham, et al.
Journal of Thrombosis and Haemostasis : JTH|June 16, 2010
Enhanced thrombin generation in patients with cirrhosis-induced coagulopathyA Gatt, A Riddell, V Calvaruso, et al.
Nature|October 24, 1985
Distribution of factor VIII mRNA and antigen in human liver and other tissuesK L Wion, D Kelly, J A Summerfield, et al.
Thrombosis and Haemostasis|May 1, 1997
High prevalence of elevated factor VIII levels in patients referred for thrombophilia screening: role of increased synthesis and relationship to the acute phase reactionJ O'Donnell, E G Tuddenham, R Manning, et al.
Haemostasis|May 1, 1995
Factor VIIShinjo: a dysfunctional factor VII variant homozygous for the substitution Gln for Arg at position 79O Takamiya, S Abe, A Yoshioka, et al.
Thrombosis and Haemostasis|July 1, 1997
Inherited factor VII deficiency: molecular genetics and pathophysiologyD N Cooper, D S Millar, A Wacey, et al.
Biochemistry|July 30, 1985
Purification of human factor VIII:C and its characterization by Western blotting using monoclonal antibodiesF Rotblat, D P O'Brien, F J O'Brien, et al.
British Journal of Haematology|June 1, 1993
A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiencyA I Wacey, S Pemberton, D N Cooper, et al.
Blood|May 1, 1993
Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndromeS D Wright, K Michaelides, D J Johnson, et al.
Pageof 17