Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia
Shapiro, Susan E., Phillips, Emma, Manning, Richard A., Morse, Colin V., Murden, Sherina L., Laffan, Michael A., Mumford, Andrew D.
Published in British journal of haematology (01.01.2013)
Published in British journal of haematology (01.01.2013)
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A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis
Mumford, Andrew D., Dawood, Ban B., Daly, Martina E., Murden, Sherina L., Williams, Michael D., Protty, Majd B., Spalton, Jennifer C., Wheatley, Mark, Mundell, Stuart J., Watson, Steve P.
Published in Blood (14.01.2010)
Published in Blood (14.01.2010)
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Partial deletion of the αC-domain in the Fibrinogen Perth variant is associated with thrombosis, increased clot strength and delayed fibrinolysis
Westbury, Sarah K, Duval, Cédric, Philippou, Helen, Brown, Rebecca, Lee, Kurtis R, Murden, Sherina L, Phillips, Emma, Reilly-Stitt, Christopher, Whalley, Daniel, Ariëns, Robert A, Mumford, Andrew D
Published in Thrombosis and haemostasis (01.12.2013)
Published in Thrombosis and haemostasis (01.12.2013)
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Low multiple electrode aggregometry platelet responses are not associated with non-synonymous variants in G-protein coupled receptor genes
Norman, Jane E, Lee, Kurtis R, Walker, Mary E, Murden, Sherina L, Harris, Jessica, Mundell, Stuart, J. Murphy, Gavin, Mumford, Andrew D
Published in Thrombosis research (01.10.2015)
Published in Thrombosis research (01.10.2015)
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Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
Jones, Matthew L, Murden, Sherina L, Brooks, Claire, Maloney, Viv, Manning, Richard A, Gilmour, Kimberly C, Bharadwaj, Vandana, de la Fuente, Josu, Chakravorty, Subarna, Mumford, Andrew D
Published in BMC genetics (04.04.2013)
Published in BMC genetics (04.04.2013)
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The protein C ω‐loop substitution Asn2Ile is associated with reduced protein C anticoagulant activity
Preston, Roger J. S., Morse, Colin, Murden, Sherina L., Brady, Sara Kate, O’Donnell, James S., Mumford, Andrew D.
Published in British journal of haematology (01.03.2009)
Published in British journal of haematology (01.03.2009)
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Journal Article
Disruption of AP3B1by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2
Jones, Matthew L, Murden, Sherina L, Brooks, Claire, Maloney, Viv, Manning, Richard A, Gilmour, Kimberly C, Bharadwaj, Vandana, de la Fuente, Josu, Chakravorty, Subarna, Mumford, Andrew D
Published in BMC medical genetics (04.04.2013)
Published in BMC medical genetics (04.04.2013)
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