Systematic reviews: causes of non-adherence to P2Y12 inhibitors in acute coronary syndromes and response to intervention

por Johnston, Nina, Weinman, John, Ashworth, Lucy, Smethurst, Peter, El Khoury, Jad, Moloney, Clare
Publicado 2016

Identification of a major GpVI-binding locus in human type III collagen

por Jarvis, Gavin E., Raynal, Nicolas, Langford, Jonathan P., Onley, David J., Andrews, Allen, Smethurst, Peter A., Farndale, Richard W.
Publicado 2008

Stored blood has compromised oxygen unloading kinetics that can be normalized with rejuvenation and predicted from corpuscular side-scatter

por Donovan, Killian, Meli, Athinoula, Cendali, Francesca, Park, Kyung Chan, Cardigan, Rebecca, Stanworth, Simon, McKechnie, Stuart, D’Alessandro, Angelo, Smethurst, Peter A., Swietach, Pawel
Publicado 2021

Metabolic reprogramming under hypoxic storage preserves faster oxygen unloading from stored red blood cells

por Rabcuka, Julija, Blonski, Slawomir, Meli, Athinoula, Sowemimo-Coker, Samuel, Zaremba, Damian, Stephenson, Daniel, Dzieciatkowska, Monika, Nerguizian, David, Cardigan, Rebecca, Korczyk, Piotr M., Smethurst, Peter A., D’Alessandro, Angelo, Swietach, Pawel
Publicado 2022

Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators

por Tijssen, Marloes R., Cvejic, Ana, Joshi, Anagha, Hannah, Rebecca L., Ferreira, Rita, Forrai, Ariel, Bellissimo, Dana C., Oram, S. Helen, Smethurst, Peter A., Wilson, Nicola K., Wang, Xiaonan, Ottersbach, Katrin, Stemple, Derek L., Green, Anthony R., Ouwehand, Willem H., Göttgens, Berthold
Publicado 2011

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

por Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Publicado 2011

Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR

por Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Christel, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric
Publicado 2012