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The European Respiratory Journal. Supplement|April 1, 1991
Immunoregulation of asthma: control of T-lymphocyte activation in the respiratory tractP G Holt, C McMenamin, M A Schon-Hegrad, et al.
American Journal of Human Genetics|August 2, 2002
Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndromeSara Shanske, Yingying Tang, Michio Hirano, et al.
Scientific Reports|November 27, 2015
Diverse Roles of Axonemal Dyneins in Drosophila Auditory Neuron Function and Mechanical Amplification in HearingSomdatta Karak, Julie S Jacobs, Maike Kittelmann, 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.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Chronic ER Stress Disrupts Mitochondrial-Associated ER Membrane Integrity in Corneal Endothelial CellsStephanie Lee, Stefan Y Kim, H Orhan Akman, et al.
The Biochemical Journal|August 25, 2004
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutationsFrancesco Pallotti, Alessandra Baracca, Evelyn Hernandez-Rosa, et al.
Neurobiology of Disease|January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brainGuomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Archives of Neurology|May 22, 2002
Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann diseaseLeonardo Salviati, Sabrina Sacconi, Minerva M Rasalan, et al.
Iscience|September 22, 2018
Three-Dimensional Analysis of Mitochondrial Crista Ultrastructure in a Patient with Leigh Syndrome by In Situ Cryoelectron TomographyStephanie E Siegmund, Robert Grassucci, Stephen D Carter, et al.
The EMBO Journal|July 21, 2016
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variabilityEster Perales-Clemente, Alexandra N Cook, Jared M Evans, et al.
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