Works by Rodríguez de Córdoba, Santiago

Results: 56

Eculizumab Modifies Outcomes in Adults with Atypical Hemolytic Uremic Syndrome with Acute Kidney Injury.

Published in:

2018

By:

Cao, Mercedes;
Leite, Bruna N.;
Ferreiro, Tamara;
Calvo, María;
Fernández, Constantino;
Alonso, Ángel;
Rodriguez, Alejandro;
Salvador, Pilar;
Seijo, Rocío;
Pita, Salvador;
Arjona, Emilia;
Rodríguez de Córdoba, Santiago;
Valdés Cañedo, Francisco;
Leite, Bruna N;
Rodríguez de Córdoba, Santiago;
Valdés Cañedo, Francisco

Publication type:

journal article

Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation.

Published in:

2010

By:

Martínez-Barricarte, Rubén;
Heurich, Meike;
Valdes-Cañedo, Francisco;
Vazquez-Martul, Eduardo;
Torreira, Eva;
Montes, Tamara;
Tortajada, Agustín;
Pinto, Sheila;
Lopez-Trascasa, Margarita;
Morgan, B. Paul;
Llorca, Oscar;
Harris, Claire L.;
de Córdoba, Santiago Rodríguez;
Martínez-Barricarte, Rubén;
Valdes-Cañedo, Francisco;
Tortajada, Agustín;
Rodríguez de Córdoba, Santiago

Publication type:

journal article

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.

Published in:

2007

By:

Saunders, Rebecca E.;
Abarrategui-Garrido, Cynthia;
Frémeaux-Bacchi, Véronique;
Goicoechea de Jorge, Elena;
Goodship, Timothy H.J.;
López Trascasa, Margarita;
Noris, Marina;
Ponce Castro, Isabel Maria;
Remuzzi, Giuseppe;
Rodríguez de Córdoba, Santiago;
Sánchez-Corral, Pilar;
Skerka, Christine;
Zipfel, Peter F.;
Perkins, Stephen J.

Publication type:

Other

m.6267G>A: a recurrent mutation in the human mitochondrial DNA that reduces cytochrome c oxidase activity and is associated with tumors.

Published in:

Human Mutation, 2006, v. 27, n. 6, p. 575, doi. 10.1002/humu.20338

By:

Gallardo, M. Esther;
Moreno-Loshuertos, Raquel;
López, Celia;
Casqueiro, Mercedes;
Silva, Javier;
Bonilla, Felix;
de Córdoba, Santiago Rodríguez;
Enríquez, José Antonio

Publication type:

Article

Corrigendum: High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3 <sup>*</sup> B.

Published in:

2020

By:

Pouw, Richard B.;
Gómez Delgado, Irene;
López Lera, Alberto;
Rodríguez de Córdoba, Santiago;
Wouters, Diana;
Kuijpers, Taco W.;
Sánchez-Corral, Pilar

Publication type:

Correction Notice

Blocking Complement Factor B Activation Reduces Renal Injury and Inflammation in a Rat Brain Death Model.

Published in:

Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02528

By:

Jager, Neeltina M.;
van Zanden, Judith E.;
Subías, Marta;
Leuvenink, Henri G. D.;
Daha, Mohamed R.;
Rodríguez de Córdoba, Santiago;
Poppelaars, Felix;
Seelen, Marc A.

Publication type:

Article

Factor H-related protein 1 promotes complement-mediated opsonization of Pseudomonas aeruginosa.

Published in:

Frontiers in Cellular & Infection Microbiology, 2024, p. 01, doi. 10.3389/fcimb.2024.1328185

By:

González-Alsina, Alex;
Martín-Merinero, Héctor;
Mateu-Borrás, Margalida;
Verd, María;
Doménech-Sánchez, Antonio;
Goldberg, Joanna B.;
de Córdoba, Santiago Rodríguez;
Albertí, Sebastián

Publication type:

Article

Characteristics, management and outcomes of atypical haemolytic uraemic syndrome in kidney transplant patients: a retrospective national study.

Published in:

Clinical Kidney Journal, 2021, v. 14, n. 4, p. 1173, doi. 10.1093/ckj/sfaa096

By:

Portoles, José;
Huerta, Ana;
Arjona, Emilia;
Gavela, Eva;
Agüera, Marisa;
Jiménez, Carlos;
Cavero, Teresa;
Marrero, Domingo;
Córdoba, Santiago Rodríguez de;
Diekmann, Fritz;
Investigators, Matrix

Publication type:

Article

Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease.

Published in:

Clinical Kidney Journal, 2012, v. 5, n. 2, p. 133, doi. 10.1093/ckj/sfs002

By:

Nozal, Pilar;
Strobel, Stefanie;
Ibernon, Meritxell;
López, Dolores;
Sánchez-Corral, Pilar;
Rodríguez de Córdoba, Santiago;
Józsi, Mihály;
López-Trascasa, Margarita

Publication type:

Article

Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 12, p. 946, doi. 10.1038/sj.ejhg.5200571

By:

Gómez-Garre, Pilar;
Sanz, Yolanda;
de Córdoba, Santiago Rodríguez;
Serratosa, José M

Publication type:

Article

Riñón, hipertensión y activación del complemento. En búsqueda de nuevas dianas terapéuticas.

Published in:

Nefrologia, 2019, v. 39, n. 2, p. 111, doi. 10.1016/j.nefro.2018.10.002

By:

Rodríguez de Córdoba, Santiago;
Espinosa Hernández, Mario

Publication type:

Article

Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso.

Published in:

Nefrologia, 2015, v. 35, n. 5, p. 421, doi. 10.1016/j.nefro.2015.07.005

By:

Campistol, Josep M.;
Arias, Manuel;
Ariceta, Gema;
Blasco, Miguel;
Espinosa, Laura;
Espinosa, Mario;
Grinyó, Josep M.;
Macía, Manuel;
Mendizábal, Santiago;
Praga, Manuel;
Román, Elena;
Torra, Roser;
Valdés, Francisco;
Vilalta, Ramón;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso.

Published in:

Nefrologia, 2013, v. 33, n. 1, p. 27, doi. 10.3265/Nefrologia.pre2012.Nov.11781

By:

Campistol, Josep M.;
Arias, Manuel;
Ariceta, Gema;
Blasco, Miguel;
Espinosa, Mario;
Grinyó, Josep M.;
Praga, Manuel;
Torra, Roser;
Vilalta, Ramón;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Role of factor H-related protein 3 in Pseudomonas aeruginosa bloodstream infections.

Published in:

Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1449003

By:

González-Alsina, Alex;
Martín-Merinero, Héctor;
Mateu-Borrás, Margalida;
Verd, María;
Doménech-Sánchez, Antonio;
Goldberg, Joanna B.;
Rodríguez de Córdoba, Santiago;
Albertí, Sebastián

Publication type:

Article

The crystal structure of iC3b-CR3 αI reveals a modular recognition of the main opsonin iC3b by the CR3 integrin receptor.

Published in:

Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29580-2

By:

Fernández, Francisco J.;
Santos-López, Jorge;
Martínez-Barricarte, Rubén;
Querol-García, Javier;
Martín-Merinero, Héctor;
Navas-Yuste, Sergio;
Savko, Martin;
Shepard, William E.;
Rodríguez de Córdoba, Santiago;
Vega, M. Cristina

Publication type:

Article

Increased Endoplasmic Reticulum Stress and Decreased Proteasomal Function in Lafora Disease Models Lacking the Phosphatase Laforin.

Published in:

PLoS ONE, 2009, v. 4, n. 6, p. 1, doi. 10.1371/journal.pone.0005907

By:

Vernia, Santiago;
Rubio, Teresa;
Heredia, Miguel;
de Córdoba, Santiago Rodríguez;
Sanz, Pascual

Publication type:

Article

High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B.

Published in:

Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00848

By:

Pouw, Richard B.;
Gómez Delgado, Irene;
López Lera, Alberto;
Rodríguez de Córdoba, Santiago;
Wouters, Diana;
Kuijpers, Taco W.;
Sánchez-Corral, Pilar

Publication type:

Article

Functional and structural characterization of four mouse monoclonal antibodies to complement C3 with potential therapeutic and diagnostic applications.

Published in:

European Journal of Immunology, 2017, v. 47, n. 3, p. 504, doi. 10.1002/eji.201646758

By:

Subías Hidalgo, Marta;
Yébenes, Hugo;
Rodríguez‐Gallego, César;
Martín‐Ambrosio, Adrián;
Domínguez, Mercedes;
Tortajada, Agustin;
Rodríguez de Córdoba, Santiago;
Llorca, Oscar

Publication type:

Article

The phosphatase activity of laforin is dispensable to rescue Epm2a−/− mice from Lafora disease.

Published in:

Brain: A Journal of Neurology, 2014, v. 137, n. 3, p. 806, doi. 10.1093/brain/awt353

By:

Gayarre, Javier;
Duran-Trío, Lara;
Criado Garcia, Olga;
Aguado, Carmen;
Juana-López, Lucia;
Crespo, Inmaculada;
Knecht, Erwin;
Bovolenta, Paola;
Rodríguez de Córdoba, Santiago

Publication type:

Article

C3 glomerulopathy--associated CFHR1 mutation alters FHR oligomerization and complement regulation.

Published in:

Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 2434, doi. 10.1172/JCI68280

By:

Tortajada, Agustín;
Yébenes, Hugo;
Abarrategui-Garrido, Cynthia;
Anter, Jaouad;
García-Fernández, Jesús M.;
Martínez-Barricarte, Rubén;
Alba-Domínguez, María;
Malik, Talat H.;
Bedoya, Rafael;
Pérez, Rocío Cabrera;
Trascasa, Margarita López;
Pickering, Matthew C.;
Harris, Claire L.;
Sánchez-Corral, Pilar;
Llorca, Oscar;
de Córdoba, Santiago Rodríguez

Publication type:

Article

C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation.

Published in:

2013

By:

Tortajada, Agustín;
Yébenes, Hugo;
Abarrategui-Garrido, Cynthia;
Anter, Jaouad;
García-Fernández, Jesús M;
Martínez-Barricarte, Rubén;
Alba-Domínguez, María;
Malik, Talat H;
Bedoya, Rafael;
Cabrera Pérez, Rocío;
López Trascasa, Margarita;
Pickering, Matthew C;
Harris, Claire L;
Sánchez-Corral, Pilar;
Llorca, Oscar;
Rodríguez de Córdoba, Santiago

Publication type:

journal article

C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation.

Published in:

Journal of Clinical Investigation, 2013, v. 123, n. 6, p. 2334, doi. 10.1172/JCI68280

By:

Tortajada, Agustín;
Yébenes, Hugo;
Abarrategui-Garrido, Cynthia;
Anter, Jaouad;
García-Fernández, Jesús M.;
Martínez-Barricarte, Rubén;
Alba-Domínguez, María;
Pickering, Matthew C.;
Harris, Claire L.;
Sánchez-Corral, Pilar;
Llorca, Oscar;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Mechanism suppressing glycogen synthesis in neurons and its demise in progressive myoclonus epilepsy.

Published in:

Nature Neuroscience, 2007, v. 10, n. 11, p. 1407, doi. 10.1038/nn1998

By:

Vilchez, David;
Ros, Susana;
Cifuentes, Daniel;
Pujadas, Lluís;
Vallès, Jordi;
García-Fojeda, Belén;
Criado-García, Olga;
Fernández-Sánchez, Elena;
Medraño-Fernández, Iria;
Domínguez, Jorge;
García-Rocha, Mar;
Soriano, Eduardo;
de Córdoba, Santiago Rodríguez;
Guinovart, Joan J.

Publication type:

Article

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).

Published in:

Human Molecular Genetics, 1999, v. 8, n. 2, p. 345, doi. 10.1093/hmg/8.2.345

By:

Serratosa, José M.;
Gómez-Garre, Pilar;
Gallardo, Ma Esther;
Anta, Berta;
Beltrán-Valero de Bernabé, Daniel;
Lindhout, Dick;
Augustijn, Paul B.;
Tassinari, Carlo A.;
Malafosse, Roberto Michelucci6, Alain;
Topcu, Meral;
Grid, Djamel;
Dravet, Charlotte;
Berkovic, Samuel F.;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation.

Published in:

Kidney International, 2012, v. 82, n. 10, p. 1084, doi. 10.1038/ki.2012.250

By:

Paixão-Cavalcante, Danielle;
López-Trascasa, Margarita;
Skattum, Lillemor;
Giclas, Patricia C;
Goodship, Timothy H;
de Córdoba, Santiago Rodríguez;
Truedsson, Lennart;
Morgan, B Paul;
Harris, Claire L

Publication type:

Article

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance.

Published in:

2012

By:

Tortajada A;
Pinto S;
Martínez-Ara J;
López-Trascasa M;
Sánchez-Corral P;
de Córdoba SR;
Tortajada, Agustín;
Pinto, Sheila;
Martínez-Ara, Jorge;
López-Trascasa, Margarita;
Sánchez-Corral, Pilar;
de Córdoba, Santiago Rodríguez

Publication type:

journal article

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance.

Published in:

Kidney International, 2012, v. 81, n. 1, p. 56, doi. 10.1038/ki.2011.291

By:

Tortajada, Agustín;
Pinto, Sheila;
Martínez-Ara, Jorge;
López-Trascasa, Margarita;
Sánchez-Corral, Pilar;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Genetic and environmental factors influencing the human factor H plasma levels.

Published in:

Immunogenetics, 2004, v. 56, n. 2, p. 77, doi. 10.1007/s00251-004-0660-7

By:

Esparza-Gordillo, Jorge;
Soria, José Manuel;
Buil, Alfonso;
Almasy, Laura;
Blangero, John;
Fontcuberta, Jordi;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families.

Published in:

Immunogenetics, 2003, v. 54, n. 12, p. 862, doi. 10.1007/s00251-003-0537-1

By:

Esparza-Gordillo, Jorge;
Soria, José Manuel;
Buil, Alfonso;
Souto, Joan Carles;
Almasy, Laura;
Blangero, John;
Fontcuberta, Jordi;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Functional and structural characterization of mouse Factor H-related B protein unveils a novel dimerization domain shared by FHR-B and FH.

Published in:

Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1522651

By:

Martín-Ambrosio Doménech, Adrián;
González Sanz, Silvia;
Márquez Tirado, Bárbara;
Juana-López, Lucia;
Goicoechea de Jorge, Elena;
Rodríguez de Córdoba, Santiago;
Martín Merinero, Héctor

Publication type:

Article

Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevance.

Published in:

Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2024.1527016

By:

Rodríguez de Córdoba, Santiago;
Reparaz, Andrea;
Sanchez, Daniel;
Pinto, Sheila;
Juana Lopez, Lucia;
Martin Merinero, Héctor;
Calvete, Iria;
Perez-Perez, Julian;
Jellison, Sydney S.;
Zhang, Yuzhou;
Smith, Richard J. H.;
Moreno, Inmaculada;
Dominguez, Mercedes

Publication type:

Article

Laforin, the most common protein mutated in Lafora disease, regulates autophagy.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 14, p. 2867, doi. 10.1093/hmg/ddq190

By:

Aguado, Carmen;
Sarkar, Sovan;
Korolchuk, Viktor I.;
Criado, Olga;
Vernia, Santiago;
Boya, Patricia;
Sanz, Pascual;
de Córdoba, Santiago Rodríguez;
Knecht, Erwin;
Rubinsztein, David C.

Publication type:

Article

The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 18, p. 3452, doi. 10.1093/hmg/ddp289

By:

Tortajada, Agustín;
Montes, Tamara;
Martı́nez-Barricarte, Rubén;
Morgan, B. Paul;
Harris, Claire L.;
de Córdoba, Santiago Rodríguez

Publication type:

Article

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 8, p. 1107, doi. 10.1093/hmg/ddi099

By:

Esparza-Gordillo, Jorge;
Goicoechea de Jorge, Elena;
Buil, Alfonso;
Berges, Luis Carreras;
López-Trascasa, Margarita;
Sánchez-Corral, Pilar;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 5, p. 703, doi. 10.1093/hmg/ddi066

By:

Esparza-Gordillo, Jorge;
Jorge, Elena Goicoechea de;
Buil, Alfonso;
Berges, Luis Carreras;
López-Trascasa, Margarita;
Sánchez-Corral, Pilar;
Córdoba, Santiago Rodríguez de

Publication type:

Article

Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 23, p. 3161, doi. 10.1093/hmg/ddg340

By:

Fernández-Sánchez, Maria Elena;
Criado-García, Olga;
Heath, Karen E.;
García-Fojeda, Belén;
Medraño-Fernández, Iria;
Gomez-Garre, Pilar;
Sanz, Pascual;
Serratosa, José María;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Crystal structure of human homogentisate dioxygenase.

Published in:

Nature Structural Biology, 2000, v. 7, n. 7, p. 542

By:

Titus, Greg P.;
Mueller, Heather A.;
Burgner, John;
Rodríguez de Córdoba, Santiago;
Peñalva, Miguel A.;
Timm, David E.

Publication type:

Article

Genetic variability shapes the alternative pathway complement activity and predisposition to complement‐related diseases.

Published in:

Immunological Reviews, 2023, v. 313, n. 1, p. 71, doi. 10.1111/imr.13131

By:

Rodríguez de Córdoba, Santiago

Publication type:

Article

The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report.

Published in:

Frontiers in Immunology, 2020, v. 11, p. 1, doi. 10.3389/fimmu.2020.01348

By:

Lumbreras, Javier;
Subias, Marta;
Espinosa, Natalia;
Ferrer, Juana María;
Arjona, Emilia;
Rodríguez de Córdoba, Santiago

Publication type:

Article

The role of the complement system in Shiga toxin-associated hemolytic uremic syndrome.

Published in:

Pediatric Nephrology, 2025, v. 40, n. 5, p. 1711, doi. 10.1007/s00467-024-06629-6

By:

Bocanegra, Victoria;
Luna, Mariana;
Costantino, Valeria V.;
Lorenzo, Andrea F. Gil;
Marino, Raul;
Miatello, Roberto;
Cacciamani, Valeria;
Benardon, M. Eugenia;
Godoy, Clara Pott;
Pinto, Sheila;
de Córdoba, Santiago Rodríguez;
Vallés, Patricia G.

Publication type:

Article

Eculizumab in dense-deposit disease after renal transplantation.

Published in:

2014

By:

Sánchez-Moreno, Ana;
De la Cerda, Francisco;
Cabrera, Rocío;
Fijo, Julia;
López-Trascasa, Margarita;
Bedoya, Rafael;
Rodríguez de Córdoba, Santiago;
Ybot-González, Patricia

Publication type:

Report

Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease.

Published in:

EMBO Molecular Medicine, 2017, v. 9, n. 7, p. 906, doi. 10.15252/emmm.201707608

By:

Nitschke, Felix;
Sullivan, Mitchell A;
Wang, Peixiang;
Zhao, Xiaochu;
Chown, Erin E;
Perri, Ami M;
Israelian, Lori;
Juana‐López, Lucia;
Bovolenta, Paola;
Rodríguez de Córdoba, Santiago;
Steup, Martin;
Minassian, Berge A

Publication type:

Article

Erratum to: Knecht E, Criado-García O, Aguado C, Gayarre J, Duran-Trio L, Garcia-Cabrero AM, et al. Malin knockout mice support a primary role of autophagy in the pathogenesis of Lafora disease. Autophagy 2012; 8:701-3.

Published in:

Autophagy, 2012, v. 8, n. 7, p. 1163, doi. 10.4161/auto.21428

By:

Knecht, Erwin;
Criado-García, Olga;
Aguado, Carmen;
Gayarre, Javier;
Duran-Trio, Lara;
Garcia-Cabrero, Ana M.;
Vernia, Santiago;
San Millán, Beatriz;
Heredia, Miguel;
Romá-Mateo, Carlos;
Mouron, Silvana;
Juana-López, Lucía;
Dominguez, Mercedes;
Navarro, Carmen;
Serratosa, Jose M.;
Sanchez, Marina;
Sanz, Pascual;
Bovolenta, Paola;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Impaired autophagy in Lafora disease.

Published in:

Autophagy, 2010, v. 6, n. 7, p. 991, doi. 10.4161/auto.6.7.13308

By:

Knecht, Erwin;
Aguado, Carmen;
Sarkar, Sovan;
Korolchuk, Viktor I.;
Criado-García, Olga;
Vernia, Santiago;
Boya, Patricia;
Sanz, Pascual;
de Córdoba, Santiago Rodríguez;
Rubinsztein, David C.

Publication type:

Article

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation.

Published in:

BMC Nephrology, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12882-015-0032-6

By:

Nozal, Pilar;
Garrido, Sofía;
Martínez-Ara, Jorge;
Picazo, María Luz;
Yébenes, Laura;
Álvarez-Doforno, Rita;
Pinto, Sheila;
de Córdoba, Santiago Rodríguez;
López-Trascasa, Margarita

Publication type:

Article

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation.

Published in:

2015

By:

Nozal, Pilar;
Garrido, Sofía;
Martínez-Ara, Jorge;
Picazo, María Luz;
Yébenes, Laura;
Alvarez-Doforno, Rita;
Pinto, Sheila;
de Córdoba, Santiago Rodríguez;
López-Trascasa, Margarita;
Álvarez-Doforno, Rita

Publication type:

journal article

Assessment of the interaction of human complement regulatory proteins with group A Streptococcus. Identification of a high-affinity group A Streptococcus binding site in FHL-1.

Published in:

European Journal of Immunology, 2000, v. 30, n. 4, p. 1243, doi. 10.1002/(SICI)1521-4141(200004)30:4<1243::AID-IMMU1243>3.0.CO;2-D

By:

Pérez-Caballero, David;
Albertí, Sebastian;
Vivanco, Fernando;
Sánchez-Corral, Pilar;
Rodríguez de Córdoba, Santiago

Publication type:

Article

Structural insights on complement activation.

Published in:

FEBS Journal, 2015, v. 282, n. 20, p. 3883, doi. 10.1111/febs.13399

By:

Alcorlo, Martín;
López‐Perrote, Andrés;
Delgado, Sandra;
Yébenes, Hugo;
Subías, Marta;
Rodríguez‐Gallego, César;
Rodríguez de Córdoba, Santiago;
Llorca, Oscar

Publication type:

Article

Crystal Structure of Glyceraldehyde-3-Phosphate Dehydrogenase from the Gram-Positive Bacterial Pathogen A vaginae, an Immunoevasive Factor that Interacts with the Human C5a Anaphylatoxin.

Published in:

Frontiers in Microbiology, 2017, v. 8, p. 1, doi. 10.3389/fmicb.2017.00541

By:

Querol-García, Javier;
Fernández, Francisco J.;
Marin, Ana V.;
Gómez, Sara;
Fullà, Daniel;
Melchor-Tafur, Cecilia;
Franco-Hidalgo, Virginia;
Albertí, Sebastián;
Juanhuix, Jordi;
Córdoba, Santiago Rodríguez de;
Regueiro, José R.;
Vega, M. Cristina

Publication type:

Article

How novel structures inform understanding of complement function.

Published in:

Seminars in Immunopathology, 2018, v. 40, n. 1, p. 3, doi. 10.1007/s00281-017-0643-z

By:

de Jorge, Elena Goicoechea;
Yebenes, Hugo;
Serna, Marina;
Tortajada, Agustín;
Llorca, Oscar;
de Córdoba, Santiago Rodríguez

Publication type:

Article