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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| openAccess | | 23-abr-2021 | Datasets related to a study aimed to identify genetic markers of CDA by subphenotypes associated with cardiotoxicity | Gómez-Vecino, Aurora CSIC; Corchado Cobos, Roberto CSIC ORCID; Blanco-Gómez, Adrián CSIC ORCID; Castillo, Sonia CSIC ORCID; García-Sancha, Natalia CSIC ORCID; Martin-Garcia, Ana; Prieto, Carlos CSIC ORCID ; Ruiz-Pinto, Sara; Pita, Guillermo; Velasco-Ruiz, Alejandro; Patino-Alonso, María Carmen; Galindo-Villardón, Purificación; Linarejos Vera-Pedrosa, María; Jalife, José; Macías de Plasencia, Guillermo; Castellanos-Martín, Andrés CSIC ORCID; Sáez-Freire, María del Mar; Mendiburu-Eliçabe, Marina CSIC ORCID; Fraile, Susana CSIC; Rodrigues Teixeira, Telmo; García-Macías, Carmen CSIC ORCID CVN; Galvis-Jiménez, Julie Milena; García-Sánchez, Asunción; Isidoro-García, María; Fuentes, Manuel CSIC ORCID ; García-Cenador, Begoña; García-Criado, Francisco Javier; García, Juan L. CSIC ORCID CVN ; Hernández-García, María Ángeles; Cruz, Juan Jesús CSIC ORCID; Rodríguez-Sánchez, César Augusto; Martín-Ruiz, Alejandro; Pérez-López, Estefanía; Pérez-Martínez, Antonio; Gutiérrez-Larraya, Federico; Cartón, Antonio J.; García-Saenz, José Ángel; Patiño-García, Ana; Martín, Miguel A.; Alonso Gordoa, Teresa; Vulsteke, Christof; Croes, Lieselot; Hatse, Sigrid; Van Brussel, Thomas; Lambrechts, Diether; Wildiers, Hans; Holgado-Madruga, M.; González-Neira, Ana; Sánchez, Pedro L.; Pérez-Losada, J. CSIC ORCID | dataset |
| openAccess |  | 18-ene-2018 | Defects in the mitochondrial-tRNA modification enzymes MTO1 and GTPBP3 promote different metabolic reprogramming through a HIF-PPARγ-UCP2-AMPK axis | Boutoual, Rachid; Meseguer, Salvador CSIC ORCID; Villarroya, Magda; Martín-Hernández, Elena; Errami, Mohammed; Martín, Miguel A.; Casado, Marta CSIC ORCID ; Armengod, M.-Eugenia | artículo |
| closedAccess |  | 2010 | Depleción del ácido desoxirribonucleico mitocondrial y mutaciones de POLG en un paciente con neuropatía sensorial atáxica, disartria y oftalmoplejía | Posada, Ignacio J.; Gallardo, M. Esther CSIC ORCID; Domínguez, Cristina; Rivera, Henry; Arenas, Joaquín; Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Bornstein, Belén CSIC | artículo |
| 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 |
