Mostrando resultados 10 a 27 de 27
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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| closedAccess |  | 2001 | Early onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA Cytochrome C oxidase II gene | Campos, Yolanda; Fernández-Moreno, Miguel Ángel CSIC ORCID; Martín, Miguel A.; Bornstein, Belén CSIC; Garesse, Rafael CSIC ORCID; Arenas, Joaquín | artículo |
| closedAccess |  | 1994 | Effects of thyroid hormone deiodination on regulation of thyroid axis in undernourished rats | Pascual-Leone, Ana María; Aláez, C. CSIC; Calvo, Rosa M. CSIC; Martín, Miguel A.; Obregón, María Jesús CSIC ORCID | artículo |
| openAccess |  | 2017 | Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease | Ortuño-Costela, María del Carmen; Rodríguez-Mancera, Nathalie; García-López, Marta; Zurita Díaz, Francisco; Moreno-Izquierdo, Ana; Lucia, Alejandro; Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
| openAccess |  | 2016 | Functional characterization of three concomitant MtDNA LHON mutations shows no synergistic effect on mitochondrial activity | Cruz-Bermúdez, Alberto CSIC ORCID; Vicente-Blanco, Ramiro J. CSIC; Hernández-Sierra, Rosana CSIC; Blázquez, Alberto; Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Fernández-Moreno, Miguel Ángel CSIC ORCID | artículo |
| closedAccess |  | 2005 | Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE | Blázquez, Alberto; Martín, Miguel A.; Campos, Yolanda; Garesse, Rafael CSIC ORCID; Bautista, José M.; Arenas, Joaquín | artículo |
| closedAccess |  | 2001 | Influence of type II 5' deiodinase on TSH content in diabetic rats | Aláez, C. CSIC; Calvo, Rosa M. CSIC; Obregón, María Jesús CSIC ORCID ; Escrivá, Fernando; Martín, Miguel A.; Pascual-Leone, Ana María | artículo |
| closedAccess |  | 2005 | Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene | Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Campos, Yolanda; Arenas, Joaquín | artículo |
| openAccess |  | dic-2022 | Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment? | Villarreal-Salazar, M.; Santalla, A.; Real-Martínez, A.; Nogales-Gadea, G.; Valenzuela, P. L.; Fiuza-Luces, C.; Andreu, Antoni L.; Rodríguez-Aguilera, Juan Carlos CSIC ORCID; Martín, Miguel A.; Arenas, Joaquín; Vissing, J.; Lucía, A.; Krag, T. O.; Pinós, T. | artículo |
| closedAccess |  | 2007 | Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicase | Rivera, Henry; Blázquez, Alberto; Campos, Yolanda; Bornstein, Belén CSIC; Garesse, Rafael CSIC ORCID; Arenas, Joaquín; Martín, Miguel A. | artículo |
| openAccess |  | 2020 | Mitochondrial dysfunction and calcium dysregulation in Leigh syndrome induced pluripotent stem cell derived neurons | Galera‐Monge, Teresa; Zurita Díaz, Francisco; Canals, Isaac; Grønning Hansen, Marita; Rufián-Vázquez, Laura; Ehinger, Johannes K.; Elmér, Eskil; Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Ahlenius, Henrik; Gallardo, M. Esther CSIC ORCID | artículo |
| closedAccess |  | 2001 | Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family | Bornstein, Belén CSIC; Fernández-Moreno, Miguel Ángel CSIC ORCID; Martín, Miguel A.; Campos, Yolanda; Arenas, Joaquín; Garesse, Rafael CSIC ORCID | artículo |
| closedAccess |  | 2012 | Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathies | Arredondo, Juan J. CSIC; Gallardo, M. Esther CSIC ORCID; García-Pavía, Pablo; Domingo, Verónica; Martín, Miguel A.; Arenas, Joaquín; Cervera, Margarita CSIC; Garesse, Rafael CSIC ORCID; Bornstein, Belén CSIC | artículo |
| openAccess |  | 2008 | OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes | Amati-Bonneau, Patrizia; Gallardo, M. Esther CSIC ORCID; Bornstein, Belén CSIC; Campos, Yolanda; Rivera, Henry; Martín, Miguel A.; Arenas, Joaquín; Garesse, Rafael CSIC ORCID; Carelli, Valerio | artículo |
| closedAccess |  | 2016 | Pharmacogenetics and pharmacogenomics as tools in cancer therapy | Rodríguez-Vicente, Ana Eugenia; Lumbreras, Eva CSIC ORCID; Hernández, Jesús M. CSIC ORCID ; Martín, Miguel A.; Calles, Antonio; López-Otín, Carlos CSIC ORCID; Martín Algarra, Salvador; Paéz, David; Taron, Miquel | artículo |
| closedAccess |  | 2016 | Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders | Yubero, Delia; Montero, Raquel; Martín, Miguel A.; Rodríguez-Aguilera, Juan Carlos CSIC ORCID; Navas, Plácido CSIC ORCID; Artuch, Rafael; García-Cazorla, Angels; Rivas Infante, Eloy; Cascajo Almenara, M. V. CSIC ORCID; Alcázar-Fabra, María CSIC ORCID; Brea-Calvo, Gloria CSIC ORCID | artículo |
| closedAccess |  | 2002 | The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines | Bornstein, Belén CSIC; Mas, José A.; Fernández-Moreno, Miguel Ángel CSIC ORCID; Campos, Yolanda; Martín, Miguel A.; Arenas, Joaquín; Garesse, Rafael CSIC ORCID | artículo |
| closedAccess |  | 2013 | The evolving landscape of protein kinases in breast cancer: clinical implications | Ocaña, Alberto; Amir, Eitan; Seruga, Bostjan; Martín, Miguel A.; Pandiella, Atanasio CSIC ORCID CVN | artículo |
| closedAccess |  | 2001 | Thyroid hormone regulates oxidative phosphorylation in the cerebral cortex and striatum of neonatal rats | Martínez, Bienvenida; Martín, Miguel A.; Arenas, Joaquín; Pérez Castillo, Ana CSIC ORCID; Santos, Ángel | artículo |
