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Mitochondrion|October 23, 2019
A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissuesLuísa Panadés-de Oliveira, Julio Montoya, Sonia Emperador, et al.Mitochondrion|June 19, 2008
Mitochondrial diseases mimicking neurotransmitter defectsAngels Garcia-Cazorla, Sofia Duarte, Mercedes Serrano, et al.Critical Care (London, England)|July 2, 2014
Higher platelet cytochrome oxidase specific activity in surviving than in non-surviving septic patientsLeonardo Lorente, María M Martín, Esther López-Gallardo, et al.Clinical & Experimental Ophthalmology|May 8, 2014
New MT-ND1 pathologic mutation for Leber hereditary optic neuropathyÍñigo Martínez-Romero, M Dolores Herrero-Martín, Laura Llobet, et al.International Journal of Molecular Sciences|May 14, 2020
Oxidative Phosphorylation Dysfunction Modifies the Cell SecretomeNuria Garrido-Pérez, Ana Vela-Sebastián, Ester López-Gallardo, et al.Human Molecular Genetics|January 30, 2003
An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNARebeca Acín-Pérez, María Pilar Bayona-Bafaluy, Marta Bueno, et al.European Journal of Human Genetics : EJHG|September 29, 2016
Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathySonia Emperador, M Pilar Bayona-Bafaluy, Ana Fernández-Marmiesse, et al.Advances in Experimental Medicine and Biology|March 13, 2010
Diseases of the human mitochondrial oxidative phosphorylation systemJulio Montoya, Ester López-Gallardo, María Dolores Herrero-Martín, et al.Mitochondrion|May 12, 2009
Steady exercise removes VO(2max) difference between mitochondrial genomic variantsAna Marcuello, Diana Martínez-Redondo, Yahya Dahmani, et al.Aging|September 28, 2019
Brain pyrimidine nucleotide synthesis and Alzheimer diseaseAlba Pesini, Eldris Iglesias, M Pilar Bayona-Bafaluy, et al.Pageof 16