Mostrando resultados 1 a 20 de 21
Siguiente >
| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| openAccess |  | 2004 | A novel E2 box-GATA element modulates Cdc6 transcription during human cells polyploidization | Vilaboa, Nuria; Bermejo, Rodrigo CSIC ORCID CVN ; Martínez, Pilar; Bornstein, Belén CSIC; Calés, Carmela CSIC ORCID | artículo |
| closedAccess |  | 2006 | Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population | Blázquez, Alberto; Bornstein, Belén CSIC; Campos, Yolanda; Fernández-Moreno, Miguel Ángel CSIC ORCID; Garesse, Rafael CSIC ORCID; Arenas, Joaquín; Martín, Miguel A. | artículo |
| openAccess |  | 2013 | Cardiac dysfunction in mitochondrial disease. Clinical and molecular features | García-Pavía, Pablo; Blázquez, Alberto; Martín, Miguel A.; Garesse, Rafael CSIC ORCID; Bornstein, Belén CSIC; Gallardo, M. Esther CSIC ORCID | artículo |
| closedAccess |  | 3-dic-2008 | Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report | Montero, Raquel; Sánchez-Alcázar, José Antonio CSIC ORCID ; Gallardo, M. Esther CSIC ORCID; Bornstein, Belén CSIC; Rivera, Henry; Martín, Miguel A.; Navas, Plácido CSIC ORCID; Artuch, Rafael | artículo |
| closedAccess |  | 1-may-2005 | Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene | Bornstein, Belén CSIC; Mas, José A.; Fernández-Moreno, Miguel Ángel CSIC ORCID; Martín, Miguel A.; Garesse, Rafael CSIC ORCID | 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 |  | 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 |  | 2013 | Leigh syndrome and the mitochondrial m.13513G>A mutation: Expanding the clinical spectrum | Bornstein, Belén CSIC; Munell, Francina | 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 |  | 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 |
| 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 |  | 1998 | Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases | Bornstein, Belén CSIC; Ochoa, Pilar CSIC; Garesse, Rafael CSIC ORCID; Arenas, Joaquín | 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 |  | mar-2003 | Reactive oxygen species mediate the down-regulation of mitochondrial transcripts and proteins by tumour necrosis factor-a in L929 cells | Sánchez-Alcázar, José Antonio CSIC ORCID ; Schneider, Erasmus; Hernández-Muñoz, Inmaculada; Ruiz-Cabello, Jesús; Siles, Eva; Torre, Paz de la; Bornstein, Belén CSIC; Brea-Calvo, Gloria CSIC ORCID; Arenas, Joaquín; Garesse, Rafael CSIC ORCID; Solís-Herruzo, José A.; Knox, Alan J.; Navas, Plácido 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 |  | 2000 | The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes | Fernández-Moreno, Miguel Ángel CSIC ORCID; Bornstein, Belén CSIC; Campos, Yolanda; Arenas, Joaquín; Garesse, Rafael CSIC ORCID | artículo |
| closedAccess |  | 2000 | The pathophysiology of mitochondrial biogenesis: Towards four decades of mitochondrial DNA research | Fernández-Moreno, Miguel Ángel CSIC ORCID; Bornstein, Belén CSIC; Petit, Nathalie; Garesse, Rafael CSIC ORCID | artículo |
