Resultados de búsqueda - Peter A. Smethurst

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  1. 1
    Measurement of tissue transglutaminase activity in a permeabilized cell system: its regulation by Ca2+ and nucleotides

    Measurement of tissue transglutaminase activity in a permeabilized cell system: its regulation by Ca2+ and nucleotides por Peter A. Smethurst, Martin Griffin

    Publicado 1996
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  2. 2
    Alternatives to allogeneic platelet transfusion

    Alternatives to allogeneic platelet transfusion por Michael Desborough, Peter A. Smethurst, Lise J Estcourt, Simon Stanworth

    Publicado 2016
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  3. 3
    A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder

    A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder por Cédric Hermans, Christine Wittevrongel, Chantal Thys, Peter A. Smethurst, Chris Van Geet, Kathleen Freson

    Publicado 2009
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  4. 4
    Synergism between platelet collagen receptors defined using receptor-specific collagen-mimetic peptide substrata in flowing blood

    Synergism between platelet collagen receptors defined using receptor-specific collagen-mimetic peptide substrata in flowing blood por Nicholas Pugh, Anna M. C. Simpson, Peter A. Smethurst, Philip G. de Groot, Nicolas Raynal, Richard W. Farndale

    Publicado 2010
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  5. 5
    Identification of a major GpVI-binding locus in human type III collagen

    Identification of a major GpVI-binding locus in human type III collagen por Gavin E. Jarvis, Nicolas Raynal, Jonathan P. Langford, David J. Onley, A F Andrews, Peter A. Smethurst, Richard W. Farndale

    Publicado 2008
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  6. 6
    A 2-Step Mechanism of Arterial Thrombus Formation Induced by Human Atherosclerotic Plaques

    A 2-Step Mechanism of Arterial Thrombus Formation Induced by Human Atherosclerotic Plaques por Armin J. Reininger, Isabell Bernlochner, Sandra Penz, Catherine Ravanat, Peter A. Smethurst, Richard W. Farndale, Christian Gachet, Richard Brandl, Wolfgang Siess

    Publicado 2010
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  7. 7
    Integrin Activation State Determines Selectivity for Novel Recognition Sites in Fibrillar Collagens

    Integrin Activation State Determines Selectivity for Novel Recognition Sites in Fibrillar Collagens por Pia Siljander, Samir W. Hamaia, Anthony R. Peachey, David A. Slatter, Peter A. Smethurst, Willem H. Ouwehand, Christopher G. Knight, Richard W. Farndale

    Publicado 2004
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  8. 8
    Stored blood has compromised oxygen unloading kinetics that can be normalized with rejuvenation and predicted from corpuscular side-scatter

    Stored blood has compromised oxygen unloading kinetics that can be normalized with rejuvenation and predicted from corpuscular side-scatter por Killian Donovan, Athinoula Meli, Francesca Cendali, Kyung Chan Park, Rebecca Cardigan, Simon Stanworth, Stuart McKechnie, Angelo D’Alessandro, Peter A. Smethurst, Pawel Swietach

    Publicado 2021
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  9. 9
    Identification in Collagen Type I of an Integrin α2β1-binding Site Containing an Essential GER Sequence

    Identification in Collagen Type I of an Integrin α2β1-binding Site Containing an Essential GER Sequence por Christopher G. Knight, Laurence F. Morton, David J. Onley, Anthony R. Peachey, Anthea Messent, Peter A. Smethurst, Danny Tuckwell, Richard W. Farndale, Michael J. Barnes

    Publicado 1998
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  10. 10
    Metabolic reprogramming under hypoxic storage preserves faster oxygen unloading from stored red blood cells

    Metabolic reprogramming under hypoxic storage preserves faster oxygen unloading from stored red blood cells por Julija Rabcuka, Sławomir Błoński, Athinoula Meli, Samuel Sowemimo‐Coker, Damian Zaremba, Daniel Stephenson, Monika Dzieciątkowska, David Nerguizian, Rebecca Cardigan, Piotr M. Korczyk, Peter A. Smethurst, Angelo D’Alessandro, Pawel Swietach

    Publicado 2022
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  11. 11
    A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site

    A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site por Sylvia Nürnberg, Augusto Rendon, Peter A. Smethurst, Dirk S. Paul, Katrin Voß, Jonathan N. Thon, Heather Lloyd-Jones, Jennifer G. Sambrook, Marloes R. Tijssen, Joseph E. Italiano, Panos Deloukas, Berthold Göttgens, Nicole Soranzo, Willem H. Ouwehand

    Publicado 2012
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  12. 12
    The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression

    The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression por Lotta Joutsi‐Korhonen, Peter A. Smethurst, Angela Rankin, Elaine Gray, Martin J. W. IJsseldijk, Catherine M. Onley, Nicholas A. Watkins, Lorna M. Williamson, Alison H. Goodall, Philip G. de Groot, Richard W. Farndale, Willem H. Ouwehand

    Publicado 2003
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  13. 13
    Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators

    Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators por Marloes R. Tijssen, Ana Cvejic, Anagha Joshi, Rebecca Hannah, Rita Ferreira, Ariel Forrai, Dana C. Bellissimo, S. Oram, Peter A. Smethurst, Nicola K. Wilson, Xiaonan Wang, Katrin Ottersbach, Derek L. Stemple, Anthony R. Green, Willem H. Ouwehand, Berthold Göttgens

    Publicado 2011
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  14. 14
    Identification of the primary collagen-binding surface on human glycoprotein VI by site-directed mutagenesis and by a blocking phage antibody

    Identification of the primary collagen-binding surface on human glycoprotein VI by site-directed mutagenesis and by a blocking phage antibody por Peter A. Smethurst, Lotta Joutsi‐Korhonen, Marie O’Connor, Erica Wilson, Nicola S. Jennings, Stephen F. Garner, Yanjun Zhang, Christopher G. Knight, Timothy R. Dafforn, Ashley M. Buckle, Martin J. W. IJsseldijk, Philip G. de Groot, Nicholas A. Watkins, Richard W. Farndale, Willem H. Ouwehand

    Publicado 2003
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  15. 15
    Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

    Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome por Cornelis A. Albers, Ana Cvejic, Rémi Favier, Evelien E. Bouwmans, Marie‐Christine Alessi, Paul Bertone, Gregory E. Jordan, Ross Kettleborough, Graham Kiddle, Myrto Kostadima, Randy J. Read, Botond Sipos, Suthesh Sivapalaratnam, Peter A. Smethurst, Jonathan Stephens, Katrin Voß, Alan T. Nurden, Augusto Rendon, Paquita Nurden, Willem H. Ouwehand

    Publicado 2011
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  16. 16
    Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

    Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome por Cornelis A. Albers, Dirk S. Paul, Harald Schulze, Kathleen Freson, Jonathan Stephens, Peter A. Smethurst, Jennifer D. Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone, Martijn H. Breuning, Najet Debili, Panos Deloukas, Rémi Favier, Janine Fiedler, Catherine M. Hobbs, Ni Huang, Matthew E. Hurles, Graham Kiddle, Ingrid P.C. Krapels, Paquita Nurden, Claudia Ruivenkamp, Jennifer G. Sambrook, Kenneth Smith, Derek L. Stemple, Gabriele Strauß, Chantal Thys, Chris Van Geet, Ruth Newbury‐Ecob, Willem H. Ouwehand, Cédric Ghevaert

    Publicado 2012
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  17. 17
    SMIM1 underlies the Vel blood group and influences red blood cell traits

    SMIM1 underlies the Vel blood group and influences red blood cell traits por Ana Cvejic, Lonneke Haer‐Wigman, Jonathan Stephens, Myrto Kostadima, Peter A. Smethurst, Mattia Frontini, Emile van den Akker, Paul Bertone, Ewa Bielczyk-Maczyńska, Samantha Farrow, Rudolf S.N. Fehrmann, Alan R. Gray, Masja de Haas, Vincent G. Haver, Gregory E. Jordan, Juha Karjalainen, Hindrik H. D. Kerstens, Graham Kiddle, Heather Lloyd-Jones, Malcolm Needs, Joyce Poole, Aïcha Ait Soussan, Augusto Rendon, Klaus Rieneck, Jennifer G. Sambrook, Hein Schepers, Herman H.W. Silljé, Botond Sipos, Dorine W. Swinkels, Asif U. Tamuri, Niek Verweij, Nicholas A. Watkins, Harm-Jan Westra, Derek L. Stemple, Lude Franke, Nicole Soranzo, Hendrik G. Stunnenberg, Nick Goldman, Pim van der Harst, C. Ellen van der Schoot, Willem H. Ouwehand, Cornelis A. Albers

    Publicado 2013
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  18. 18
    A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

    A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders por Ilenia Simeoni, Jonathan Stephens, Fengyuan Hu, Sri V. V. Deevi, Karyn Mégy, Tadbir K. Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J. A. Vries, Sarah K. Westbury, Daniel Greene, Sofia Papadia, Marie‐Christine Alessi, Antony Attwood, Matthias Ballmaier, Gareth Baynam, Emilsé Bermejo, Marta Bértoli, Paul F. Bray, Loredana Bury, Marco Cattaneo, Peter Collins, Louise C. Daugherty, Rémi Favier, Deborah L. French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cédric Ghevaert, Anne Goodeve, José A. Guerrero, Daniel J. Hampshire, Daniel P. Hart, Johan W. M. Heemskerk, Yvonne Henskens, Marian Hill, Nancy Hogg, Jennifer D. Jolley, Walter H.A. Kahr, Anne M. Kelly, Ron Kerr, Myrto Kostadima, Shinji Kunishima, Michele P. Lambert, Ri Liesner, José A. López, Rutendo Mapeta, Mary Mathias, Carolyn M. Millar, Amit Nathwani, Marguerite Neerman‐Arbez, Alan T. Nurden, Paquita Nurden, Maha Othman, Kathelijne Peerlinck, David J. Perry, Pawan Poudel, Pieter H. Reitsma, Matthew T. Rondina, Peter A. Smethurst, William Stevenson, Artur Szkotak, Salih Tuna, Chris Van Geet, Deborah Whitehorn, David A. Wilcox, Bin Zhang, Shoshana Revel‐Vilk, Paolo Gresele, Daniel B. Bellissimo, Christopher J. Penkett, Michael Laffan, Andrew Mumford, Augusto Rendon, Keith Gomez, Kathleen Freson, Willem H. Ouwehand, Ernest Turro

    Publicado 2016
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