Items where authors include "Watson, S.P."

Article

Xu, R.-G. orcid.org/0000-0003-0774-112X, Tiede, C. orcid.org/0000-0003-0280-4005, Calabrese, A.N. orcid.org/0000-0003-2437-7761 et al. (13 more authors) (2024) Affimer reagents as tool molecules to modulate platelet GPVI-ligand interactions and specifically bind GPVI dimer. Blood Advances, 8 (15). pp. 3917-3928. ISSN 2473-9529

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Jones, M.L., Norman, J.E., Morgan, N.V. et al. (9 more authors) (2016) Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors. THROMBOSIS AND HAEMOSTASIS, 113 (4). pp. 826-837. ISSN 0340-6245

Stockley, J., Nisar, S.P., Leo, V.C. et al. (9 more authors) (2015) Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease. PLoS ONE, 10 (12). e0143913. ISSN 1932-6203

Fletcher, S.J., Johnson, B., Lowe, G.C. et al. (12 more authors) (2015) SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. Journal of Clinical Investigation, 125 (9). 3600 - 3605. ISSN 0021-9738

Leo, V.C., Morgan, N.V., Bem, D. et al. (9 more authors) (2015) Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders. Journal of Thrombosis and Haemostasis, 13 (4). pp. 643-650. ISSN 1538-7933

Conference or Workshop Item

Xu, R.-G. orcid.org/0000-0003-0774-112X, Cheah, L.T., Adams, L. et al. (9 more authors) (2021) Affimers modulate GPVI interactions with collagen/fibrinogen and GPVI-mediated platelet aggregation. In: 29th Congress of the International Society on Thrombosis and Haemostasis, 17-21 Jul 2021, Philadephia (USA), Virtual.