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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| openAccess |  | 2016 | Generation of a human iPSC line from a patient with an optic atrophy 'plus' phenotype due to a mutation in the OPA1 gene | Galera, Teresa CSIC; Zurita Díaz, Francisco; Moreno-Izquierdo, Ana; Fraga, Mario F. CSIC ORCID; Fernández, Agustín F. CSIC ORCID; Ayuso, Carmen; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
| openAccess |  | 2016 | Generation of a human iPSC line from a patient with Leigh syndrome | Galera, Teresa CSIC; Zurita Díaz, Francisco; González Páramos, Cristina; Moreno-Izquierdo, Ana; Fraga, Mario F. CSIC ORCID; Fernández, Agustín F. CSIC ORCID; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
| openAccess |  | 2016 | Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene | Galera, Teresa CSIC; Zurita Díaz, Francisco; González Páramos, Cristina; Moreno-Izquierdo, Ana; Fraga, Mario F. CSIC ORCID; Fernández, Agustín F. CSIC ORCID; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
| openAccess |  | 2018 | Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup | Ortuño-Costela, María del Carmen; Moreno-Izquierdo, Ana; Garesse, Rafael CSIC ORCID; Gallardo, M. Esther CSIC ORCID | artículo |
| openAccess |  | 2022 | Generation of the first human in vitro model for McArdle disease based on iPSC Technology | Ortuño-Costela, María del Carmen; Cerrada, Victoria; Moreno-Izquierdo, Ana; García-Consuegra, Inés; Laberthonnière, Camille; Delourme, Mégane; Garesse, Rafael CSIC ORCID; Arenas, Joaquín; Fuster García, Carla; García García, Gema; Millán, José María; Magdinier, Frédérique; Gallardo, M. Esther CSIC ORCID | artículo |
| closedAccess |  | 2011 | Genetic basis of end-stage hypertrophic cardiomyopathy | García-Pavía, Pablo; Gallardo, M. Esther CSIC ORCID; Garesse, Rafael CSIC ORCID; Bornstein, Belén CSIC | artículo |
| closedAccess |  | 1999 | Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies | Gallardo, M. Esther CSIC ORCID; Lopez-Rios, Javier; Fernaud-Espinosa, Isabel CSIC ORCID; Granadino, Begoña CSIC ORCID ; Sanz, Raúl; Ramos, Carmen; Ayuso, Carmen; Seller, Mary J.; Brunner, Han G.; Bovolenta, Paola CSIC ORCID; Rodríguez de Córdoba, Santiago | artículo |
| closedAccess |  | 2014 | Glutamyl-tRNAGln amidotransferase is essential for mammalian mitochondrial translation in vivo | Echevarría, Lucía; Clemente, Paula; Hernández-Sierra, Rosana CSIC; Gallardo, M. Esther CSIC ORCID; Fernández-Moreno, Miguel Ángel CSIC ORCID; Garesse, Rafael CSIC ORCID | artículo |
| 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 |
