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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 plasma
Simon 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 analysis
Kymberley 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 generators
Carolina 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 males
Carlos 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 leukaemia
Sarah 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 receptor
Elizabeth 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 pathway
Simon 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 mutations
Carolyn 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 3
Megan 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 phenotype
Derrick J Bowen, Peter W Collins, Will Lester, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Thrombosis and Haemostasis
|
June 27, 2002
Heterogeneous detection of A-antigen on von Willebrand factor derived from platelets, endothelial cells and plasma
Simon 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 analysis
Kymberley 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 generators
Carolina 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 males
Carlos 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 leukaemia
Sarah 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 receptor
Elizabeth 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 pathway
Simon 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 mutations
Carolyn 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 3
Megan 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 phenotype
Derrick J Bowen, Peter W Collins, Will Lester, et al.
Page
of 1