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EMBO Reports|June 14, 2022
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7BMichele Brischigliaro, Alfredo Cabrera-Orefice, Mattia Sturlese, et al.
Cell Metabolism|May 13, 2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial diseaseRaffaele Cerutti, Eija Pirinen, Costanza Lamperti, et al.
The Biochemical Journal|June 10, 2014
Complex IV-deficient Surf1(-/-) mice initiate mitochondrial stress responsesDaniel A Pulliam, Sathyaseelan S Deepa, Yuhong Liu, et al.
Brain : a Journal of Neurology|November 29, 2017
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational familyPeter J Kullar, Aurora Gomez-Duran, Payam A Gammage, et al.
Neurology|March 3, 2025
Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal SeizuresLuca Bergonzini, Sara Carli, Silvia Pelle, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2012
Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activitySathyaseelan S Deepa, Daniel Pulliam, Shauna Hill, et al.
Journal of Child Neurology|December 13, 2006
Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging reportEmilio Franzoni, Marjo S Van der Knaap, Alessandra Errani, et al.
FEBS Letters|October 11, 2022
Rapid fractionation of mitochondria from mouse liver and heart reveals in vivo metabolite compartmentationFay M Allen, Ana S H Costa, Anja V Gruszczyk, et al.
European Journal of Neurology|March 17, 2026
Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE-Like FeaturesGiuliana Capece, Luca Caumo, Sara Volta, et al.
Neuromuscular Disorders : NMD|July 7, 2007
A novel heteroplasmic tRNA(Ser(UCN)) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing lossElena Cardaioli, Paola Da Pozzo, Gian Nicola Gallus, et al.
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