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DerechosPreviewFecha Public.TítuloAutor(es)Tipo
openAccess2011_Rodriguez de Cordoba et al_Biochim Biophys_completo.pdf.jpgene-2011Lessons from functional and structural analyses of disease-associated genetic variants in the complement alternative pathwayRodríguez de Córdoba, Santiago ; Harris, Claire L.; Morgan, B. Paul; Llorca, Óscar CSIC ORCIDartículo
closedAccessrestringido.pdf.jpgmay-2008Measurement of factor H variants in plasma using variant-specific monoclonal antibodies: application to assessing risk of age-related macular degenerationHakobyan, Svetlana; Harris, Claire L.; Tortajada, Agustín CSIC ORCID; Goicoechea de Jorge, Elena CSIC ORCID; García-Layana, Alfredo; Fernández-Robredo, Patricia; Rodríguez de Córdoba, Santiago ; Morgan, B. Paulartículo
closedAccessaccesoRestringido.pdf.jpg1-nov-2012Sensitive and specific assays for C3 nephritic factors permit dissection of mechanisms underlying complement dysregulationPaixao-Cavalcante, Danielle; López-Trascasa, Margarita; Skattum, Lillemor; Giclas, Patricia C.; Goodship, Timothy H.J.; Rodríguez de Córdoba, Santiago ; Truedsson, Lennart; Morgan, B. Paul; Harris, Claire L.artículo
openAccess10.1016j.it.2012.06.001.pdf.jpgjul-2012The complotype: dictating risk for inflamation and infectionHarris, Claire L.; Heurich, Meike; Rodríguez de Córdoba, Santiago ; Morgan, B. Paulartículo
openAccess2009_Tortajada et al_Hum Mol Genet.pdf.jpg15-sep-2009The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activityTortajada, Agustín CSIC ORCID; Montes, Tamara CSIC; Martínez-Barricarte, Rubén CSIC; Morgan, B. Paul; Harris, Claire L.artículo
closedAccessrestringido.pdf.jpgoct-2010Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical Hemolytic Uremic SyndromeHakobyan, Svetlana; Tortajada, Agustín CSIC ORCID; Harris, Claire L.; Rodríguez de Córdoba, Santiago ; Morgan, B. Paulartículo
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