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I R Peake

Showing results (51-60 of 120) with videos related to

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British Journal of Haematology|June 1, 1979
An immunoradiometric assay for procoagulant factor VIII antigen: results in haemophilia, von Willebrand's disease and fetal plasma and serumI R Peake, A L Bloom, J C Giddings, et al.
Journal of Medical Genetics|November 1, 1988
Carrier detection through the use of abnormal deletion junction fragments in a case of haemophilia B involving complete deletion of the factor IX geneR J Matthews, I R Peake, A L Bloom, et al.
Thrombosis Research|January 1, 1979
High potency factor VIII concentrate: more effective than cryoprecipitate in a patient with von Willebrand's disease and inhibitorA L Bloom, I R Peake, R A Furlong, et al.
British Journal of Haematology|June 1, 1989
Defective propeptide processing and abnormal activation underlie the molecular pathology of factor IX Troed-y-RhiwM B Liddell, D P Lillicrap, I R Peake, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1996
A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII geneA C Goodeve, G Tagariello, A Chuansumrit, et al.
Thrombosis Research|May 1, 1978
Predominance of normal low molecular weight forms of factor VIII in "variant" von Willebrand's diseaseJ J Sixma, J Over, B N Bouma, et al.
Thrombosis Research|July 1, 1977
The characterization and synthesis of antigens related to factor VIII in vascular endotheliumS A Shearn, I R Peake, J C Giddings, et al.
British Journal of Haematology|October 1, 1990
Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequenceG R Standen, P Bignell, D J Bowen, et al.
Lancet (London, England)|September 8, 1990
Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reactionP Bignell, G R Standen, D J Bowen, et al.
Thrombosis and Haemostasis|May 24, 2000
Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin geneN J Beauchamp, M Makris, F E Preston, et al.
Pageof 12

Showing results (51-60 of 120) with videos related to

Sort By:
Pageof 12
British Journal of Haematology|June 1, 1979
An immunoradiometric assay for procoagulant factor VIII antigen: results in haemophilia, von Willebrand's disease and fetal plasma and serumI R Peake, A L Bloom, J C Giddings, et al.
Journal of Medical Genetics|November 1, 1988
Carrier detection through the use of abnormal deletion junction fragments in a case of haemophilia B involving complete deletion of the factor IX geneR J Matthews, I R Peake, A L Bloom, et al.
Thrombosis Research|January 1, 1979
High potency factor VIII concentrate: more effective than cryoprecipitate in a patient with von Willebrand's disease and inhibitorA L Bloom, I R Peake, R A Furlong, et al.
British Journal of Haematology|June 1, 1989
Defective propeptide processing and abnormal activation underlie the molecular pathology of factor IX Troed-y-RhiwM B Liddell, D P Lillicrap, I R Peake, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1996
A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII geneA C Goodeve, G Tagariello, A Chuansumrit, et al.
Thrombosis Research|May 1, 1978
Predominance of normal low molecular weight forms of factor VIII in "variant" von Willebrand's diseaseJ J Sixma, J Over, B N Bouma, et al.
Thrombosis Research|July 1, 1977
The characterization and synthesis of antigens related to factor VIII in vascular endotheliumS A Shearn, I R Peake, J C Giddings, et al.
British Journal of Haematology|October 1, 1990
Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequenceG R Standen, P Bignell, D J Bowen, et al.
Lancet (London, England)|September 8, 1990
Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reactionP Bignell, G R Standen, D J Bowen, et al.
Thrombosis and Haemostasis|May 24, 2000
Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin geneN J Beauchamp, M Makris, F E Preston, et al.
Pageof 12