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Rodríguez de Córdoba, Santiago

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Firma en Digital.CSIC (*)
Rodríguez de Córdoba, Santiago
 
Centro o Instituto
CSIC - Centro de Investigaciones Biologicas Margarita Salas (CIB)
 
Departamento
Biomedicina Molecular
 
Especialización
Patología Molecular/Genética del Complemento
 
Email
srdecordoba@cib.csic.es
 
ORCID
 
WoS ResearcherID - Publons
 
Scopus AuthorID
 

Publications

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Autor:  Martínez-Barricarte, Rubén

Resultados 1-13 de 13.

DerechosPreviewFecha Public.TítuloAutor(es)Tipo
1openAccessJCI 123 (6) 2013-Óscar Llorca.pdf.jpgjun-2013C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulationTortajada, Agustín CSIC ORCID; Yébenes, Hugo CSIC ORCID; Anter, Jaouad CSIC; García-Fernández, Jesús CSIC ; Martínez-Barricarte, Rubén CSIC; Llorca, Óscar CSIC ORCID; Rodríguez de Córdoba, Santiago artículo
2closedAccess5-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 CSIC; López-Trascasa, Margarita; Rodríguez de Córdoba, Santiago ; Sánchez-Corral, Pilar CSIC ORCIDartículo
3openAccess1019338108.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 CSIC; Francis, Nigel J.; Roberts, Dawn L.; Rodríguez de Córdoba, Santiago ; Morgan, B. Paul; Harris, Claire L.artículo
4closedAccessrestringido.pdf.jpg2010Complement Factor H is expressed in adipose tissue in association with insulin resistanceMoreno-Navarrete, José Maria; Martínez-Barricarte, Rubén CSIC; Catalán, Victoria; Sabater, Mónica; Gómez-Ambrosi, Javier; Ortega, Francisco J.; Ricart, Wifredo; Blüher, Mathias; Frühbeck, Gema; Rodríguez de Córdoba, Santiago ; Fernández-Real, José Manuelartículo
5openAccessJCI43343 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 CSIC; Heurich, Meike; Valdés-Cañedo, Francisco; Vázquez-Martul, Eduardo; Torreira, Eva CSIC; Montes, Tamara CSIC; Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; López-Trascasa, Margarita; Morgan, B. Paul; Llorca, Óscar CSIC ORCID; Harris, Claire L.; Rodríguez de Córdoba, Santiago artículo
6closedAccessrestringido.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 CSIC ORCID; Cook, H. Terence; Martínez-Barricarte, Rubén CSIC; 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
7closedAccessrestringido.pdf.jpgene-2009Lack of association between polymorphisms in C4b-binding protein and atypical Haemolytic Uraemic Syndrome in the Spanish population (C4BPA and aHUS)Martínez-Barricarte, Rubén CSIC; Goicoechea de Jorge, Elena CSIC ORCID; Montes, Tamara CSIC; Layana, Alfredo García; Rodríguez de Córdoba, Santiago artículo
8openAccess2012_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 CSIC; Recalde, Sergio; Fernández-Robredo, Patricia; Millán, Isabel; Olavarrieta, Leticia CSIC; Viñuela, Antonio; Pérez-Pérez, Julián; García-Layana, Alfredo; Rodríguez de Córdoba, Santiago artículo
9openAccessspontaneous.pdf.jpg11-jun-2007Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domainsPickering, Matthew C.; Goicoechea de Jorge, Elena CSIC ORCID; Martínez-Barricarte, Rubén CSIC; Recalde, Sergio; García-Layana, Alfredo; Rose, Kirsten L.; Moss, Jill; Walport, Mark J.; Cook, H. Terence; Rodríguez de Córdoba, Santiago ; Botto, Marinaartículo
10openAccess2008_Martinez-Barricarte et al_JASN.pdf.jpgmar-2008The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndromeMartínez-Barricarte, Rubén CSIC; 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
11openAccessNature Communications_Fernández_2022.pdf.jpg12-abr-2022The crystal structure of iC3b-CR3 αI reveals a modular recognition of the main opsonin iC3b by the CR3 integrin receptorFernández, Francisco J. CSIC ORCID; Santos-López, Jorge CSIC; Martínez-Barricarte, Rubén CSIC; Querol-García, Javier CSIC ORCID; Martín Merinero, Héctor CSIC ORCID; Navas-Yuste, Sergio CSIC; Savko, Martin; Shepard, William E.; Rodríguez de Córdoba, Santiago ; Vega, María Cristina CSIC ORCID artículo
12Molecular 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 CSIC; López-Perrote, Andrés CSIC ORCID; Tortajada, Agustín CSIC ORCID; Pinto, Sheila CSIC; Llorca, Óscar CSIC ORCID; Rodríguez de Córdoba, Santiago artículo
13openAccess2011_Alcorlo et al_PNAS.pdf.jpg9-ago-2011Unique structure of iC3b resolved at a resolution of 24 A by 3D-electron microscopyAlcorlo, Martín; Martínez-Barricarte, Rubén CSIC; Fernández, Francisco J. CSIC ORCID; Rodríguez-Gallego, César CSIC; Round, Adam; Vega, María Cristina CSIC ORCID ; Harris, Claire L.; Rodríguez de Córdoba, Santiago ; Llorca, Óscar CSIC ORCIDartículo