Mostrando resultados 9 a 21 de 21
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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
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 |
closedAccess | | 2015 | Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction | González-López, Esther; Bornstein, Belén CSIC; García-Pavía, Pablo | artículo |