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Browsing by Author Bornstein, Belén

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Showing results 1 to 18 of 18
Issue DateTitleAuthor(s)Type
2004A novel E2 box-GATA element modulates Cdc6 transcription during human cells polyploidizationVilaboa, Nuria; Bermejo, Rodrigo; Martinez, Pilar; Bornstein, Belén; Calés, CarmelaArtículo
2006Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish populationBlázquez, Alberto; Bornstein, Belén; Campos, Yolanda; Fernández-Moreno, Miguel Ángel; Garesse, Rafael; Arenas, Joaquín; Martín, Miguel A.Artículo
3-Dec-2008Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case reportMontero, Raquel; Sánchez-Alcázar, José Antonio; Gallardo, M. Esther; Bornstein, Belén; Rivera, Henry; Martín, Miguel A.; Navas, Plácido; Artuch, RafaelArtículo
1-May-2005Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) geneBornstein, Belén; Mas, José A.; Fernández-Moreno, Miguel Ángel; Martín, Miguel A.; Garesse, RafaelArtículo
2010Depleción del ácido desoxirribonucleico mitocondrial y mutaciones de POLG en un paciente con neuropatía sensorial atáxica, disartria y oftalmoplejíaPosada, Ignacio J.; Gallardo, M. Esther; Domínguez, Cristina; Rivera, Henry; Arenas, Joaquín; Martín, Miguel A.; Garesse, Rafael; Bornstein, BelénArtículo
2001Early onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA Cytochrome C oxidase II geneCampos, Yolanda; Fernández-Moreno, Miguel Ángel; Martín, Miguel A.; Bornstein, Belén; Garesse, Rafael; Arenas, JoaquínArtículo
2011Genetic basis of end-stage hypertrophic cardiomyopathyGarcía-Pavía, Pablo; Gallardo, M. Esther; Garesse, Rafael; Bornstein, BelénArtículo
2010Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic archRivera, Henry; Merinero, Begoña; Ruiz-Sala, Pedro; Bornstein, Belén; Gallardo, M. Esther; Garesse, Rafael; Ugarte, Magdalena; Martín, Miguel A.Artículo
2007Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicaseRivera, Henry; Blázquez, Alberto; Campos, Yolanda; Bornstein, Belén; Garesse, Rafael; Arenas, Joaquín; Martín, Miguel A.Artículo
2001Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL familyBornstein, Belén; Fernández-Moreno, Miguel Ángel; Martín, Miguel A.; Campos, Yolanda; Arenas, Joaquín; Garesse, RafaelArtículo
1998Mitochondrial gene expression and respiratory enzyme activities in cardiac diseasesBornstein, Belén; Ochoa, Pilar; Garesse, Rafael; Arenas, JoaquínArtículo
2012Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patientsGallardo, M. Esther; García-Pavía, Pablo; Chamorro-Garcia, Raquel; Domingo, Verónica; Garesse, Rafael; Bornstein, BelénArtículo
2012Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathiesArredondo, Juan J.; Gallardo, M. Esther; García-Pavía, Pablo; Domingo, Verónica; Bretón, Begoña; Martín, Miguel A.; Arenas, Joaquín; Cervera, Margarita; Garesse, Rafael; Bornstein, BelénArtículo
2008OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesAmati-Bonneau, Patrizia; Gallardo, M. Esther; Bornstein, Belén; Campos, Yolanda; Rivera, Henry; Martín, Miguel A.; Arenas, Joaquín; Garesse, Rafael; Carelli, ValerioArtículo
Mar-2003Reactive oxygen species mediate the down-regulation of mitochondrial transcripts and proteins by tumour necrosis factor-a in L929 cellsSánchez-Alcázar, José Antonio; Bornstein, Belén; Arenas, Joaquín; Garesse, Rafael; Navas, PlácidoArtículo
2002The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell linesBornstein, Belén; Mas, José A.; Fernández-Moreno, Miguel Ángel; Campos, Yolanda; Martín, Miguel A.; Arenas, Joaquín; Garesse, RafaelArtículo
2000The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genesFernández-Moreno, Miguel Ángel; Bornstein, Belén; Campos, Yolanda; Arenas, Joaquín; Garesse, RafaelArtículo
2000The pathophysiology of mitochondrial biogenesis: Towards four decades of mitochondrial DNA researchFernández-Moreno, Miguel Ángel; Bornstein, Belén; Petit, Nathalie; Garesse, RafaelArtículo

Showing results 1 to 18 of 18