ORCA
Online Research @ Cardiff
Browse by Current Cardiff authors
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Number of items: 11.
Madrid-Gambin, Francisco, Föcking, Melanie, Sabherwal, Sophie, Heurich-Sevcenco, Meike, English, Jane A., O'Gorman, Aoife, Suvitaival, Tommi, Ahonen, Linda, Cannon, Mary, Lewis, Glynn, Mattila, Ismo, Scaife, Caitriona, Madden, Sean, Hyötyläinen, Tuulia, Orešič, Matej, Zammit, Stanley, Cagney, Gerard, Cotter, David R. and Brennan, Lorraine
2019.
Integrated lipidomics and proteomics point to early blood-based changes in childhood preceding later development of psychotic experiences: evidence from the Avon Longitudinal Study of Parents and Children.
Biological Psychiatry
86
(1)
, pp. 25-34.
10.1016/j.biopsych.2019.01.018
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Föcking, Melanie, Sabherwal, Sophie, Cates, Hannah M., Scaife, Caitriona, Dicker, Patrick, Hryniewiecka, Magdalena, Wynne, Kieran, Rutten, Bart P. F., Lewis, Glyn, Cannon, Mary, Nestler, Eric J., Heurich-Sevcenco, Meike, Cagney, Gerard, Zammit, Stanley and Cotter, David R.
2019.
Complement pathway changes at age 12 are associated with psychotic experiences at age 18 in a longitudinal population-based study: evidence for a role of stress.
Molecular Psychiatry
, -.
10.1038/s41380-018-0306-z
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| Slatter, David, Percy, Charles, Allen-Redpath, Keith, Gajsiewicz, J M, Brooks, N J, Clayton, Aled, Tyrrell, Victoria, Rosas, Marcela, Lauder, Sarah, Watson, Andrew, Dul, Maria, Garcia-Diaz, Y, Aldrovandi, MacEler, Heurich-Sevcenco, Meike, Hall, Judith, Morrissey, J H, Lacroix-Desmazes, P S, Delignat, S, Jenkins, P V, Collins, Peter and O'Donnell, Valerie 2018. Enzymatically-oxidized phospholipids restore thrombin generation in coagulation factor deficiencies. JCI Insight 3 (6) , e98459. 10.1172/jci.insight.98459 |
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| Heurich-Sevcenco, Meike, Preston, R.J.S., O'Donnell, Valerie Bridget, Morgan, Bryan Paul and Collins, Peter William 2016. Thrombomodulin enhances complement regulation through strong affinity interactions with factor H and C3b-Factor H complex. Thrombosis Research 145 , pp. 84-92. 10.1016/j.thromres.2016.07.017 |
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| Szakmany, Tamas and Heurich-Sevcenco, Meike 2015. Immunomodulation in sepsis - why blunting the response doesn't work? Journal of Infection 71 (2) , pp. 147-149. 10.1016/j.jinf.2015.04.019 |
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| Martínez-Barricarte, Rubén, Heurich-Sevcenco, Meike, López-Perrote, Andrés, Tortajada, Agustin, Pinto, Sheila, López-Trascasa, Margarita, Sánchez-Corral, Pilar, Morgan, Bryan Paul, Llorca, Oscar, Harris, Claire Louise and Rodríguez de Córdoba, Santiago 2015. The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome. Molecular Immunology 66 (2) , pp. 263-273. 10.1016/j.molimm.2015.03.248 |
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| Ruseva, M.M. and Heurich-Sevcenco, Meike 2014. Purification and characterization of human and mouse complement C3. In: Gadjeva, Mihaela ed. The Complement System: Methods and Protocols, Vol. 1100. Methods in Molecular Biology, Humana Press, pp. 75-91. (10.1007/978-1-62703-724-2_6) |
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| Heurich, Meike, Altintas, Zeynep and Tothill, Ibtisam 2013. Computational Design of Peptide Ligands for Ochratoxin A. Toxins 5 (6) , pp. 1202-1218. 10.3390/toxins5061202 |
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| Harris, Claire Louise, Heurich, Meike, Rodriguez de Cordoba, Santiago and Morgan, Bryan Paul 2012. The complotype: dictating risk for inflammation and infection. Trends in Immunology 33 (10) , pp. 513-521. 10.1016/j.it.2012.06.001 |
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| Heurich, Meike, Martinez-Barricarte, Ruben, Francis, Nigel, Roberts, Dawn L., Rodriguez de Cordoba, Santiago, Morgan, Bryan Paul and Harris, Claire Louise 2011. Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk. Proceedings of the National Academy of Sciences of the United States of America 108 (21) , pp. 8761-8766. 10.1073/pnas.1019338108 |
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| Martínez-Barricarte, Rubén, Heurich, Meike, Valdes-Cañedo, Francisco, Vazquez-Martul, Eduardo, Torreira, Eva, Montes, Tamara, Tortajada, Agustín, Pinto, Sheila, Lopez-Trascasa, Margarita, Morgan, Bryan Paul, Llorca, Oscar, Harris, Claire Louise and Rodríguez de Córdoba, Santiago 2010. Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. Journal of Clinical Investigation 120 (10) , pp. 3702-3712. 10.1172/JCI43343 |
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