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Emanueli, C, Shearn, AIU, Laftah, A, Fiorentino, F, Reeves, BC, Beltrami, C, Mumford, A, Clayton, A, Gurney, M, Shantikumar, S & Angelini, GD, 2016, ‘Coronary Artery-Bypass-Graft Surgery Increases the Plasma Concentration of Exosomes Carrying a Cargo of Cardiac MicroRNAs: An Example of Exosome Trafficking Out of the Human Heart with Potential for Cardiac Biomarker Discovery’. PLoS ONE, vol 11. Westbury, SK & Mumford, AD, 2016, ‘Genomics of platelet disorders’. Haemophilia, vol 22., pp. 20-24 Burley, K, Whyte, CS, Westbury, SK, Walker, M, Stirrups, KE, Turro, E, BioResource, N, Chapman, OG, Reilly-Stitt, C, Mutch, NJ & Mumford, AD, 2016, ‘Altered fibrinolysis in autosomal dominant thrombomodulin-associated coagulopathy’. Blood. Simeoni, I, Stephens, JC, Hu, F, Deevi, SVV, Megy, K, Bariana, TK, Lentaigne, C, Schulman, S, Sivapalaratnam, S, Vries, MJA, Westbury, SK, Greene, D, Papadia, S, Alessi, M-C, Attwood, AP, Ballmaier, M, Baynam, G, Bermejo, E, Bertoli, M, Bray, PF, Bury, L, Cattaneo, M, Collins, P, Daugherty, LC, Favier, R, French, DL, Furie, B, Gattens, M, Germeshausen, M, Ghevaert, C, Goodeve, A, Guerrero, J, Hampshire, DJ, Hart, DP, Heemskerk, JWM, Henskens, YMC, Hill, M, Hogg, N, Jolley, JD, Kahr, WH & others 2016, ‘A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders’. Blood, vol 127., pp. 2791-2803 Aungraheeta, R, Conibear, A, Butler, M, Kelly, E, Nylander, S, Mumford, A & Mundell, S, 2016, ‘Inverse agonism at the P2Y12 receptor and ENT1 transporter blockade contribute to platelet inhibition by ticagrelor’. Blood. Stritt, S, Nurden, P, Turro, E, Greene, D, Jansen, SB, Westbury, SK, Petersen, R, Astle, WJ, Marlin, S, Bariana, TK, Kostadima, M, Lentaigne, C, Maiwald, S, Papadia, S, Kelly, AM, Stephens, JC, Penkett, CJ, Ashford, S, Tuna, S, Austin, S, Bakchoul, T, Collins, P, Favier, R, Lambert, MP, Mathias, M, Millar, CM, Mapeta, R, Perry, DJ, Schulman, S, Simeoni, I, Thys, C, Consortium, B-B, Gomez, K, Erber, WN, Stirrups, K, Rendon, A, Bradley, JR, van Geet, C, Raymond, FL, Laffan, MA & others 2016, ‘A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss’. Blood, vol 127., pp. 2903-2914 Johnson, B, Lowe, GC, Futterer, J, Lordkipanidze', M, MacDonald, D, Simpson, MA, Guiu', IS, Drake, S, Bem, D, Leo, V, Fletcher, SJ, Dawood, B, Rivera, J, Allsup, D, Biss, T, Bolton-Maggs, PHB, Collins, P, Curry, N, Grimley, C, James, B, Makris, M, Motwani, J, Pavord, S, Talks, K, Thachil, J, Wilde, J, Williams, M, Harrison, P, Gissen, P, Mundell, S, Mumford, A, Daly, ME, Watson, SP, Morgan, NV & , 2016, ‘Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects’. Haematologica. Norman, JE, Cunningham, MR, Jones, ML, Walker, ME, Westbury, SK, Sessions, RB, Mundell, SJ & Mumford, AD, 2016, ‘Protease-Activated Receptor 4 Variant p.Tyr157Cys Reduces Platelet Functional Responses and Alters Receptor Trafficking’. Arteriosclerosis, Thrombosis and Vascular Biology, vol 36., pp. 952-960 Turro, E, Greene, D, Wijgaerts, A, Thys, C, Lentaigne, C, Bariana, TK, Westbury, SK, Kelly, AM, Selleslag, D, Stephens, JC, Papadia, S, Simeoni, I, Penkett, CJ, Ashford, S, Attwood, A, Austin, S, Bakchoul, T, Collins, P, Deevi, SVV, Favier, R, Kostadima, M, Lambert, MP, Mathias, M, Millar, CM, Peerlinck, K, Perry, DJ, Schulman, S, Whitehorn, D, Wittevrongel, C, , De Maeyer, M, Rendon, A, Gomez, K, Erber, WN, Mumford, AD, Nurden, P, Stirrups, K, Bradley, JR, Raymond, FL, Laffan, MA & others 2016, ‘A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies’. Science Translational Medicine, vol 8. Engert, A, Mumford, AD & Toye, AM, 2016, ‘The European Hematology Association Roadmap For European Hematology Research: A Consensus Document’. Haematologica, vol 101., pp. 115-208