A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3 von Sutherland, Megan S., Cumming, Anthony M., Bowman, Mackenzie, Bolton-Maggs, Paula H.B., Bowen, Derrick J., Collins, Peter W., Hay, Charles R.M., Will, Andrew M., Keeney, Stephen

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Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: Influence of glycosylation, proteolysis and gene mutations von Millar, Carolyn M., Riddell, Anne F., Brown, Simon A., Starke, Richard, Mackie, Ian, Bowen, Derrick J., Jenkins, P. Vincent, van Mourik, Jan A.

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Heterogeneous Detection of A-antigen on von Willebrand Factor Derived from Platelets, Endothelial Cells and Plasma von Brown, Simon A., Collins, Peter W., Bowen, Derrick J.

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Diagnosis of haemophilia in Pakistan: current picture von Khanum, Fatima, Collins, Peter, Bowen, Derrick J

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Survival of von Willebrand factor released following DDAVP in a type I von Willebrand disease cohort : Influence of glycosylation, proteolysis and gene mutations von MILLAR, Carolyn M, RIDDELL, Anne F, BROWN, Simon A, STARKE, Richard, MACKIE, Ian, BOWEN, Derrick J, JENKINS, P. Vincent, VAN MOURIK, Jan A

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Roles of promoter and 3′ untranslated motifs in expression of the human C5a receptor von Palmer, Elizabeth, Gray, Lisa C., Stott, Matthew, Bowen, Derrick J., van den Berg, Carmen W.

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Increased susceptibility of von Willebrand factor to proteolysis by ADAMTS13: should the multimer profile be normal or type 2A? von Bowen, Derrick J.

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Unleashing the long-distance PCR for detection of the intron 22 inversion of the factor VIII gene in severe haemophilia A von Bowen, Derrick J., Keeney, Stephen

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Factor VIIa Induced Release of von Willebrand Factor from Human Umbilical Vein Endothelial Cells by a Tyrosine Kinase Dependent Pathway von Brown, Simon A., Bowen, Derrick J., Hallett, Maurice B., Giddings, John C., Collins, Peter W.

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Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis von Carter, Kymberley, Bowen, Derrick J., McCune, C. Anne, Worwood, Mark

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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 proteoly... von Bowen, Derrick J., Collins, Peter W., Lester, Will, Cumming, Anthony M., Keeney, Steven, Grundy, Pamela, Enayat, Saad M., Bolton‐Maggs, Paula H. B., Keeling, David M., Khair, Kate, Campbell Tait, R., Wilde, Jonathon T., John Pasi, K., Hill, Frank G. H.

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Response to Langlois et al (LE 01059) von Carter, Kymberley, Bowen, Derrick J., Anne McCune, C., Worwood, Mark

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A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generators von Belli, Carolina, Bowen, Derrick J., Brasi, Carlos De, Larripa, Irene

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An Effective Route for the Isolation of Human Genetic Loci Exemplified Using the BglI Restriction Fragment Length Polymorphism of the Factor VIII Gene von Bowen, Derrick J.

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High concentrations of coagulation factor VIII and thrombosis: is the factor VIII‐binding domain of von Willebrand factor implicated? von Bowen, Derrick J., Maclean, Rhona M., Pellard, Sarah, Collins, Peter W.

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Identification and characterization of a novel gene encoding a SEREX antigen in chronic myeloid leukaemia von Rogers, Sarah A., Bowen, Derrick J., Ling, Min, Thomson, Peter, Wang, Zhiqing, Lim, Seah H.

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A new polymorphism in the human factor VIII gene : implications for linkage analysis in haemophilia A and for the evolution of int22h sequences von BOWEN, Derrick J, DE BRASI, Carlos D, LARRIPA, Irene B, COLLINS, Peter W

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von Willebrand factor: demographics of plasma protein level in a large blood donor cohort from South Wales in the United Kingdom von DAVIES, J. A., HATHAWAY, L. S., COLLINS, P. W., BOWEN, D. J.

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von Willebrand factor: evidence for variable clearance in vivo according to Y/C1584 phenotype and ABO blood group von DAVIES, J. A., COLLINS, P. W., HATHAWAY, L. S., BOWEN, D. J.

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Factor V Leiden and the common haemochromatosis mutation HFE C282Y: is there an association in familial venous thromboembolic disease? von MacLean, Rhona M., Feeney, Graham P., Bowley, Steven J., Bowen, Derrick J., Worwood, Mark, Collins, Peter W.

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