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Martina E. Daly
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Journal Articles

Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

e-blood
Marie Lordkipanidzé, Gillian C. Lowe, Nicholas S. Kirkby, Melissa V. Chan, Martina H. Lundberg, Neil V. Morgan, Danai Bem, Shaista P. Nisar, Vincenzo C. Leo, Matthew L. Jones, Stuart J. Mundell, Martina E. Daly, Andrew D. Mumford, Timothy D. Warner, Steve P. Watson
Journal: Blood
Blood (2014) 123 (8): e11–e22.
https://doi.org/10.1182/blood-2013-08-520387
Published: 2014
Includes: Supplemental data
Journal Articles

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

Brief Report
Jacqueline Stockley, Neil V. Morgan, Danai Bem, Gillian C. Lowe, Marie Lordkipanidzé, Ban Dawood, Michael A. Simpson, Kirsty Macfarlane, Kevin Horner, Vincenzo C. Leo, Katherine Talks, Jayashree Motwani, Jonathan T. Wilde, Peter W. Collins, Michael Makris, Steve P. Watson, Martina E. Daly
Journal: Blood
Blood (2013) 122 (25): 4090–4093.
https://doi.org/10.1182/blood-2013-06-506873
Published: 2013
Includes: Supplemental data
Journal Articles

Functional Variations In Genes Encoding Platelet G-Protein Coupled Receptors In Unselected and Platelet Function Disorder Populations

Jane E Norman, Matthew L Jones, Neil V Morgan, Jacqui Stockley, Martina E Daly, Stuart J Mundell, Steve P Watson, Andrew D Mumford, UK GAPP study group
Journal: Blood
Blood (2013) 122 (21): 3511.
https://doi.org/10.1182/blood.V122.21.3511.3511
Published: 2013
Journal Articles

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Clinical Trials & Observations
Ban B. Dawood, Gillian C. Lowe, Marie Lordkipanidzé, Danai Bem, Martina E. Daly, Mike Makris, Andrew Mumford, Jonathan T. Wilde, Steve P. Watson
Journal: Blood
Blood (2012) 120 (25): 5041–5049.
https://doi.org/10.1182/blood-2012-07-444281
Published: 2012
Includes: Supplemental data
Journal Articles

An intact PDZ motif is essential for correct P2Y 12 purinoceptor traffic in human platelets

Shaista Nisar, Martina E. Daly, Augusto B. Federici, Andrea Artoni, Andrew D. Mumford, Stephen P. Watson, Stuart J. Mundell
Journal: Blood
Blood (2011) 118 (20): 5641–5651.
https://doi.org/10.1182/blood-2011-02-336826
Published: 2011
Includes: Supplemental data
Journal Articles

A novel thromboxane A 2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis

Andrew D. Mumford, Ban B. Dawood, Martina E. Daly, Sherina L. Murden, Michael D. Williams, Majd B. Protty, Jennifer C. Spalton, Mark Wheatley, Stuart J. Mundell, Steve P. Watson
Journal: Blood
Blood (2010) 115 (2): 363–369.
https://doi.org/10.1182/blood-2009-08-236976
Published: 2010
Journal Articles

Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

Brief Report
Martina E. Daly, Ban B. Dawood, William A. Lester, Ian R. Peake, Francesco Rodeghiero, Anne C. Goodeve, Michael Makris, Jonathan T. Wilde, Andrew D. Mumford, Stephen P. Watson, Stuart J. Mundell
Journal: Blood
Blood (2009) 113 (17): 4110–4113.
https://doi.org/10.1182/blood-2008-11-190850
Published: 2009
Journal Articles

Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease–causing variants of von Willebrand factor

Grégoire Michaux, Lindsay J. Hewlett, Sarah L. Messenger, Anne C. Goodeve, Ian R. Peake, Martina E. Daly, Daniel F. Cutler
Journal: Blood
Blood (2003) 102 (7): 2452–2458.
https://doi.org/10.1182/blood-2003-02-0599
Published: 2003
Journal Articles

A novel von Willebrand disease–causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion

Simon Allen, Adel M. Abuzenadah, Joanna Hinks, Joanna L. Blagg, Turkiz Gursel, Jørgen Ingerslev, Anne C. Goodeve, Ian R. Peake, Martina E. Daly
Journal: Blood
Blood (2000) 96 (2): 560–568.
https://doi.org/10.1182/blood.V96.2.560
Published: 2000
Journal Articles

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

Michael Makris, Michael Leach, Nick J. Beauchamp, Martina E. Daly, Peter C. Cooper, Kingsley K. Hampton, Pauline Bayliss, Ian R. Peake, George J. Miller, F. Eric Preston
Journal: Blood
Blood (2000) 95 (6): 1935–1941.
https://doi.org/10.1182/blood.V95.6.1935
Published: 2000
Journal Articles

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Simon Allen, Adel M. Abuzenadah, Joanna L. Blagg, Joanna Hinks, I. Mandy Nesbitt, Anne C. Goodeve, Turkiz Gursel, Jørgen Ingerslev, Ian R. Peake, Martina E. Daly
Journal: Blood
Blood (2000) 95 (6): 2000–2007.
https://doi.org/10.1182/blood.V95.6.2000
Published: 2000