Cristina Ugalde
Cristina Ugalde
Principal Investigator, Hospital Doce de Octubre Research Institute i+12 (Madrid, Spain)
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Mitochondrial complex I plays an essential role in human respirasome assembly
D Moreno-Lastres, F Fontanesi, I García-Consuegra, MA Martín, J Arenas, ...
Cell metabolism 15 (3), 324-335, 2012
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency
C Ugalde, RJRJ Janssen, LP van den Heuvel, JAM Smeitink, ...
Human molecular genetics 13 (6), 659-667, 2004
Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies
C Ugalde, R Vogel, R Huijbens, B van den Heuvel, J Smeitink, L Nijtmans
Human molecular genetics 13 (20), 2461-2472, 2004
Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency
MJH Coenen, H Antonicka, C Ugalde, F Sasarman, R Rossi, JA Heister, ...
New England Journal of Medicine 351 (20), 2080-2086, 2004
Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease
R Pello, MA Martín, V Carelli, LG Nijtmans, A Achilli, M Pala, A Torroni, ...
Human molecular genetics 17 (24), 4001-4011, 2008
Human mitochondrial complex I assembly is mediated by NDUFAF1
RO Vogel, RJRJ Janssen, C Ugalde, M Grovenstein, RJ Huijbens, ...
The FEBS journal 272 (20), 5317-5326, 2005
Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced.
M Calleja, P Pena, C Ugalde, C Ferreiro, R Marco, R Garesse
Journal of Biological Chemistry 268 (25), 18891-18897, 1993
Mitochondrial respiratory chain dysfunction: implications in neurodegeneration
M Morán, D Moreno-Lastres, L Marín-Buera, J Arenas, MA Martín, ...
Free Radical Biology and Medicine 53 (3), 595-609, 2012
X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy
D Fernandez‐Moreira, C Ugalde, R Smeets, RJT Rodenburg, ...
Annals of neurology 61 (1), 73-83, 2007
Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene
C Ugalde, RH Triepels, MJH Coenen, LP Van Den Heuvel, R Smeets, ...
Annals of Neurology: Official Journal of the American Neurological …, 2003
Cytoplasmic gelsolin increases mitochondrial activity and reduces Aβ burden in a mouse model of Alzheimer's disease
D Antequera, T Vargas, C Ugalde, C Spuch, JA Molina, I Ferrer, ...
Neurobiology of disease 36 (1), 42-50, 2009
Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh syndrome
C Ugalde, R Hinttala, S Timal, R Smeets, RJT Rodenburg, J Uusimaa, ...
Molecular genetics and metabolism 90 (1), 10-14, 2007
Aβ accumulation in choroid plexus is associated with mitochondrial-induced apoptosis
T Vargas, C Ugalde, C Spuch, D Antequera, MJ Morán, MA Martín, ...
Neurobiology of aging 31 (9), 1569-1581, 2010
Mitochondrial bioenergetics and dynamics interplay in complex I-deficient fibroblasts
M Moran, H Rivera, M Sánchez-Aragó, A Blázquez, B Merinero, C Ugalde, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1802 (5), 443-453, 2010
Cell biological consequences of mitochondrial NADH: ubiquinone oxidoreductase deficiency
JAM Smeitink, LWPJ van den Heuvel, WJH Koopman, LGJ Nijtmans, ...
Current neurovascular research 1 (1), 29-40, 2004
Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency
M Morán, L Marín‐Buera, MC Gil‐Borlado, H Rivera, A Blázquez, ...
Human mutation 31 (8), 930-941, 2010
Microgravity effects on Drosophila melanogaster behavior and aging. Implications of the IML-2 experiment
A Benguría, E Grande, E De Juan, C Ugalde, J Miquel, R Garesse, ...
Journal of biotechnology 47 (2-3), 191-201, 1996
COX7A2L is a mitochondrial complex III binding protein that stabilizes the III2+ IV supercomplex without affecting respirasome formation
R Pérez-Pérez, T Lobo-Jarne, D Milenkovic, A Mourier, A Bratic, ...
Cell reports 16 (9), 2387-2398, 2016
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene
MJH Coenen, LP van den Heuvel, C Ugalde, M ten Brinke, LGJ Nijtmans, ...
Annals of Neurology: Official Journal of the American Neurological …, 2004
Complex I assembly: a puzzling problem
R Vogel, L Nijtmans, C Ugalde, L van den Heuvel, J Smeitink
Current opinion in neurology 17 (2), 179-186, 2004
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