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Derrick J Bowen

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Thrombosis and Haemostasis|June 27, 2002
Heterogeneous detection of A-antigen on von Willebrand factor derived from platelets, endothelial cells and plasmaSimon A Brown, Peter W Collins, Derrick J Bowen
British Journal of Haematology|July 9, 2003
Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysisKymberley Carter, Derrick J Bowen, C Anne McCune, et al.
British Journal of Haematology|August 4, 2004
A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generatorsCarolina Belli, Derrick J Bowen, Carlos De Brasi, et al.
Journal of Human Genetics|May 29, 2002
The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human malesCarlos D De Brasi, Derrick J Bowen, Peter W Collins, et al.
British Journal of Haematology|October 3, 2002
Identification and characterization of a novel gene encoding a SEREX antigen in chronic myeloid leukaemiaSarah A Rogers, Derrick J Bowen, Min Ling, et al.
Molecular Immunology|May 22, 2012
Roles of promoter and 3' untranslated motifs in expression of the human C5a receptorElizabeth Palmer, Lisa C Gray, Matthew Stott, et al.
Thrombosis and Haemostasis|June 27, 2002
Factor VIIa induced release of von Willebrand factor from human umbilical vein endothelial cells by a tyrosine kinase dependent pathwaySimon A Brown, Derrick J Bowen, Maurice B Hallett, et al.
Thrombosis and Haemostasis|May 2, 2008
Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycosylation, proteolysis and gene mutationsCarolyn M Millar, Anne F Riddell, Simon A Brown, et al.
Blood|April 18, 2009
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, et al.
British Journal of Haematology|March 10, 2005
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotypeDerrick J Bowen, Peter W Collins, Will Lester, et al.
Pageof 1

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

Sort By:
Pageof 1
Thrombosis and Haemostasis|June 27, 2002
Heterogeneous detection of A-antigen on von Willebrand factor derived from platelets, endothelial cells and plasmaSimon A Brown, Peter W Collins, Derrick J Bowen
British Journal of Haematology|July 9, 2003
Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysisKymberley Carter, Derrick J Bowen, C Anne McCune, et al.
British Journal of Haematology|August 4, 2004
A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generatorsCarolina Belli, Derrick J Bowen, Carlos De Brasi, et al.
Journal of Human Genetics|May 29, 2002
The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human malesCarlos D De Brasi, Derrick J Bowen, Peter W Collins, et al.
British Journal of Haematology|October 3, 2002
Identification and characterization of a novel gene encoding a SEREX antigen in chronic myeloid leukaemiaSarah A Rogers, Derrick J Bowen, Min Ling, et al.
Molecular Immunology|May 22, 2012
Roles of promoter and 3' untranslated motifs in expression of the human C5a receptorElizabeth Palmer, Lisa C Gray, Matthew Stott, et al.
Thrombosis and Haemostasis|June 27, 2002
Factor VIIa induced release of von Willebrand factor from human umbilical vein endothelial cells by a tyrosine kinase dependent pathwaySimon A Brown, Derrick J Bowen, Maurice B Hallett, et al.
Thrombosis and Haemostasis|May 2, 2008
Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycosylation, proteolysis and gene mutationsCarolyn M Millar, Anne F Riddell, Simon A Brown, et al.
Blood|April 18, 2009
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3Megan S Sutherland, Anthony M Cumming, Mackenzie Bowman, et al.
British Journal of Haematology|March 10, 2005
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotypeDerrick J Bowen, Peter W Collins, Will Lester, et al.
Pageof 1