English   español  

Browsing by Author Martínez-Barricarte, Rubén

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 15 of 15
RightsPreviewIssue DateTitleAuthor(s)Type
openAccessJCI 123 (6) 2013-Óscar Llorca.pdf.jpgJun-2013C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulationTortajada, Agustín ; Yébenes, Hugo; Anter, Jauoad; García-Fernández, Jesús; Martínez-Barricarte, Rubén ; Llorca, Óscar ; Rodríguez de Córdoba, Santiago artículo
closedAccess5-Nov-2009Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndromeAbarrategui-Garrido, Cynthia; Martínez-Barricarte, Rubén ; López-Trascasa, Margarita; Rodríguez de Córdoba, Santiago ; Sánchez-Corral, Pilar artículo
openAccess1019338108.full.pdf.jpg9-May-2011Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease riskHeurich, Meike; Martínez-Barricarte, Rubén ; Francis, Nigel J.; Roberts, Dawn L.; Rodríguez de Córdoba, Santiago ; Morgan, B. Paul; Harris, Claire L.artículo
closedAccessrestringido.pdf.jpg2010Complement Factor H is expressed in adipose tissue in association with insulin resistanceMoreno-Navarrete, José M.; Martínez-Barricarte, Rubén ; Catalán, Victoria; Sabater, Mónica; Gómez-Ambrosi, Javier; Ortega, Francisco José; Ricart, Wifredo; Blüher, Mathias; Frühbeck, Gema; Rodríguez de Córdoba, Santiago ; Fernández-Real, José Manuelartículo
openAccessJCI43343 v1.pdf.jpg13-Sep-2010Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulationMartínez-Barricarte, Rubén ; Heurich, Meike; Valdés-Cañedo, Francisco; Vázquez-Martul, Eduardo; Torreira, Eva ; Montes, Tamara ; Tortajada, Agustín ; Pinto, Sheila ; López-Trascasa, Margarita; Morgan, B. Paul; Llorca, Óscar ; Harris, Claire L.; Rodríguez de Córdoba, Santiago artículo
openAccessTesis_Martínez-Barricarte_Rubén_2011.pdf.jpg2011Identificación y caracterización funcional de variantes genéticas de proteínas del complemento asociadas con patología.Martínez-Barricarte, Rubén tesis doctoral
closedAccessrestringido.pdf.jpg4-Sep-2010Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritisGale, Daniel P.; Goicoechea de Jorge, Elena ; Cook, H. Terence; Martínez-Barricarte, Rubén ; Hadjisavvas, Andreas; McLean, Adam G.; Pusey, Charles D.; Pierides, Alkis; Kyriacou, Kyriacos; Athanasiou, Yiannis; Voskarides, Konstantinos; Deltas, Constantinos; Palmer, Andrew; Fremeaux-Bacchi, Veronique; Rodríguez de Córdoba, Santiago ; Maxwell, Patrick H.; Pickering, Matthew C.artículo
closedAccessrestringido.pdf.jpgJan-2009Lack of association between polymorphisms in C4b-binding protein and atypical Haemolytic Uraemic Syndrome in the Spanish population (C4BPA and aHUS)Martínez-Barricarte, Rubén ; Goicoechea de Jorge, Elena ; Montes, Tamara ; Layana, Alfredo García; Rodríguez de Córdoba, Santiago artículo
openAccessES2399897B1.pdf.jpg4-Apr-2013Método para la predicción del riesgo de desarrollar la enfermedad de degeneración macular asociada a la edad en la población españolaRodríguez de Córdoba, Santiago ; Martínez-Barricarte, Rubén ; García-Layana, Alfredo; Fernández-Robredo, Patricia; Recalde, Sergio; Pérez-Pérez, Julián; Olavarrieta, Leticia; Viñuela, Antoniopatente
openAccess2012_Martinez-Barricarte et al_IOVS.pdf.jpg1-Mar-2012Relevance of complement factor H-related 1 (CFHR1) genotypes in age- related macular degeneration (AMD)Martínez-Barricarte, Rubén ; Recalde, Sergio; Fernández-Robredo, Patricia; Millán, Isabel; Olavarrieta, Leticia; Viñuela, Antonio; Pérez-Pérez, Julián; García-Layana, Alfredo; Rodríguez de Córdoba, Santiago artículo
openAccessspontaneous.pdf.jpg11-Jun-2007Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domainsPickering, Matthew C.; Goicoechea de Jorge, Elena ; Martínez-Barricarte, Rubén ; Recalde, Sergio; García-Layana, Alfredo; Rose, Kirsten L.; Moss, Jill; Walport, Mark J.; Cook, H. Terence; Rodríguez de Córdoba, Santiago ; Botto, Marinaartículo
openAccess2008_Martinez-Barricarte et al_JASN.pdf.jpgMar-2008The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndromeMartínez-Barricarte, Rubén ; Pianetti, Gaia; Gautard, Ruxandra; Misselwitz, Joachim; Strain, Lisa; Fremeaux-Bacchi, Veronique; Skerka, Christine; Zipfel, Peter F.; Goodship, Timothy H.J.; Noris, Marina; Remuzzi, Giuseppe; Rodríguez de Córdoba, Santiago artículo
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 ; Montes, Tamara ; Martínez-Barricarte, Rubén ; Morgan, B. Paul; Harris, Claire L.artículo
Molecular Microbiology _S. R. de Córdoba_2015.pdf.jpg2015The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndromeMartínez-Barricarte, Rubén ; López-Perrote, Andrés ; Tortajada, Agustín ; Pinto, Sheila ; Llorca, Óscar ; Rodríguez de Córdoba, Santiago artículo
openAccess2011_Alcorlo et al_PNAS.pdf.jpg9-Aug-2011Unique structure of iC3b resolved at a resolution of 24 A by 3D-electron microscopyAlcorlo, Martín ; Martínez-Barricarte, Rubén ; Fernández, Francisco J. ; Rodríguez-Gallego, César; Round, Adam; Vega, María Cristina ; Harris, Claire L.; Rodríguez de Córdoba, Santiago ; Llorca, Óscar artículo