Mostrando resultados 29 a 45 de 45
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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | 2016 | iPSCs, a future tool for therapeutic intervention in mitochondrial disorders: pros and cons | Galera, Teresa CSIC; Zurita Díaz, Francisco; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
openAccess | | 2016 | IPSCs, a promising tool to restore muscle atrophy | Pareja-Galeano, Helios; Sanchis-Gomar, Fabian; Emanuele, Enzo; Gallardo, M. Esther CSIC ORCID; Lucia, Alejandro | artículo |
openAccess | | 2016 | IPSCs-based anti-aging therapies: Recent discoveries and future challenges | Pareja-Galeano, Helios; Sanchis-Gomar, Fabian; Pérez, Laura M.; Emanuele, Enzo; Lucia, Alejandro; Gálvez, Beatriz G.; Gallardo, M. Esther CSIC ORCID | artículo |
openAccess | | jun-2019 | iPSCs: A powerful tool for skeletal muscle tissue engineering | Ortuño-Costela, María del Carmen; García‐López, Marta; Cerrada, Victoria; Gallardo, M. Esther CSIC ORCID | artículo |
openAccess | | 2006 | m.6267G > A: A recurrent mutation in the human mitochondrial DNA that reduces cytochrome C oxidase activity and is associated with tumors | Gallardo, M. Esther CSIC ORCID; Moreno-Loshuertos, Raquel; López, Cecilia I.; Casqueiro, Mercedes CSIC; Silva, Javier; Bonilla, Félix; Rodríguez de Córdoba, Santiago ; Enríquez, José Antonio | artículo |
closedAccess | | 2010 | Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch | Rivera, Henry; Merinero, Begoña CSIC; Ruiz-Sala, Pedro; Bornstein, Belén CSIC; Gallardo, M. Esther CSIC ORCID; Garesse, Rafael CSIC ORCID; Ugarte, Magdalena CSIC ; Martín, Miguel Ángel | artículo |
closedAccess | | 2010 | MidA is a putative methyltransferase that is required for mitochondrial complex I function | Carilla-Latorre, Sergio CSIC; Gallardo, M. Esther CSIC ORCID; Calvo-Garrido, Javier CSIC; Garesse, Rafael CSIC ORCID; Escalante, Ricardo CSIC ORCID | artículo |
closedAccess | | 2011 | Mitochondrial DNA replication in health and disease | Gallardo, M. Esther CSIC ORCID; Clemente, Paula; Echevarría, Lucía; Peralta, Susana; Garesse, Rafael CSIC ORCID | capítulo de libro |
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 | | 2012 | Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patients | Gallardo, M. Esther CSIC ORCID; García-Pavía, Pablo; Chamorro-Garcia, Raquel; Domingo, Verónica; Garesse, Rafael CSIC ORCID; Bornstein, Belén CSIC | 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 | | may-2007 | Reply to "Reactive oxygen species and the segregation of mtDNA sequence variants | Enríquez, José Antonio; Moreno-Loshuertos, Raquel; Acín-Pérez, Rebeca; Movilla, Nieves; Gallardo, M. Esther CSIC ORCID; Rodríguez de Córdoba, Santiago ; Pérez-Martos, Acisclo; Fernández-Silva, Patricio | artículo |
openAccess | | 2016 | Reprogramming for cardiac regeneration-strategies for innovation | Sanchis-Gomar, Fabian; Galera, Teresa CSIC; Lucia, Alejandro; Gallardo, M. Esther CSIC ORCID | artículo |
closedAccess | | feb-2001 | The molecular basis of 3-methylcrotonylglycinuria, a disorder of the leucine catabolism | Gallardo, M. Esther CSIC ORCID; Desviat, Lourdes R. CSIC ORCID; Rodríguez, José M.; Esparza-Gordillo, Jorge CSIC; Pérez-Cerdá, Celia; Pérez, Belén CSIC ORCID; Rodríguez-Pombo, Pilar CSIC ORCID; Navarrete, Olga; Sanz, Raúl; Morton, D.Holmes; Criado-García, Olga CSIC ORCID ; Gibson, K.Michael; Le, Thuy P.; Ribes, Antonia; Rodríguez de Córdoba, Santiago ; Ugarte, Magdalena CSIC ; Peñalva, Miguel Ángel CSIC ORCID | artículo |
closedAccess | | nov-2019 | The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant-load dependent way | Galera‐Monge, Teresa; Zurita Díaz, Francisco; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
openAccess | | 2014 | The thyroid hormone receptor β induces DNA damage and premature senescence | Zambrano, Alberto CSIC ORCID; García-Carpizo, Verónica CSIC; Gallardo, M. Esther CSIC ORCID; Villamuera, Raquel CSIC ORCID; Gómez-Ferrería, María Ana CSIC; Pascual, Ángel CSIC; Buisine, Nicolas; Sachs, Laurent M.; Garesse, Rafael CSIC ORCID; Aranda, Ana CSIC ORCID | artículo |