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Santiago Rodriguez de Cordoba
Santiago Rodriguez de Cordoba
Centro de Investigaciones Biologicas Margarita Salas (CSIC)
Dirección de correo verificada de cib.csic.es
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
13059*2021
Genomic sequence of the pathogenic and allergenic filamentous fungus Aspergillus fumigatus
WC Nierman, A Pain, MJ Anderson, JR Wortman, HS Kim, J Arroyo, ...
Nature 438 (7071), 1151-1156, 2005
16622005
The human complement factor H: functional roles, genetic variations and disease associations
SR de Córdoba, J Esparza-Gordillo, EG de Jorge, M Lopez-Trascasa, ...
Molecular immunology 41 (4), 355-367, 2004
7472004
C3 glomerulopathy: consensus report
MC Pickering, VD D'agati, CM Nester, RJ Smith, M Haas, GB Appel, ...
Kidney international 84 (6), 1079-1089, 2013
6852013
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes”(KDIGO) Controversies Conference
THJ Goodship, HT Cook, F Fakhouri, FC Fervenza, V Frémeaux-Bacchi, ...
Kidney international 91 (3), 539-551, 2017
6432017
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
EG de Jorge, CL Harris, J Esparza-Gordillo, L Carreras, EA Arranz, ...
Proceedings of the National Academy of Sciences 104 (1), 240-245, 2007
5382007
Intracellular complement activation sustains T cell homeostasis and mediates effector differentiation
MK Liszewski, M Kolev, G Le Friec, M Leung, PG Bertram, AF Fara, ...
Immunity 39 (6), 1143-1157, 2013
5282013
Mechanism suppressing glycogen synthesis in neurons and its demise in progressive myoclonus epilepsy
D Vilchez, S Ros, D Cifuentes, L Pujadas, J Vallès, B García-Fojeda, ...
Nature neuroscience 10 (11), 1407-1413, 2007
4282007
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype
E Bresin, E Rurali, J Caprioli, P Sanchez-Corral, V Fremeaux-Bacchi, ...
Journal of the American Society of Nephrology 24 (3), 475-486, 2013
4142013
Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants
R Moreno-Loshuertos, R Acín-Pérez, P Fernández-Silva, N Movilla, ...
Nature genetics 38 (11), 1261-1268, 2006
3762006
Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H
SR De Córdoba, EG De Jorge
Clinical & Experimental Immunology 151 (1), 1-13, 2008
3752008
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
DP Gale, EG De Jorge, HT Cook, R Martinez-Barricarte, A Hadjisavvas, ...
The Lancet 376 (9743), 794-801, 2010
3712010
Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome
D Pérez-Caballero, C González-Rubio, ME Gallardo, M Vera, ...
The American Journal of Human Genetics 68 (2), 478-484, 2001
3532001
The molecular basis of alkaptonuria
JM Fernández-Cañón, B Granadino, DBV De Bernabé, M Renedo, ...
Nature genetics 14 (1), 19-24, 1996
3421996
Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains
MC Pickering, EG de Jorge, R Martinez-Barricarte, S Recalde, ...
The Journal of experimental medicine 204 (6), 1249-1256, 2007
3382007
Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32
J Esparza-Gordillo, EG Jorge, A Buil, LC Berges, M Lopez-Trascasa, ...
Human Molecular Genetics 14 (5), 703-712, 2005
3322005
New approaches to the treatment of dense deposit disease
RJH Smith, J Alexander, PN Barlow, M Botto, TL Cassavant, HT Cook, ...
Journal of the American Society of Nephrology 18 (9), 2447-2456, 2007
3272007
Atypical aHUS: state of the art
CM Nester, T Barbour, SR de Cordoba, MA Dragon-Durey, ...
Molecular immunology 67 (1), 31-42, 2015
3112015
C3 glomerulopathy—understanding a rare complement-driven renal disease
RJH Smith, GB Appel, AM Blom, HT Cook, VD D’Agati, F Fakhouri, ...
Nature reviews nephrology 15 (3), 129-143, 2019
2902019
Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome
P Sánchez-Corral, D Pérez-Caballero, O Huarte, AM Simckes, ...
The American Journal of Human Genetics 71 (6), 1285-1295, 2002
2722002
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