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Frontiers in Genetics|December 3, 2014
A novel mutation in TTC19 associated with isolated complex III deficiency, cerebellar hypoplasia, and bilateral basal ganglia lesionsLaura Melchionda, Nadirah S Damseh, Bassam Y Abu Libdeh, et al.
American Journal of Human Genetics|September 6, 2008
FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiencyDaniele Ghezzi, Ann Saada, Pio D'Adamo, et al.
Human Molecular Genetics|January 1, 2010
Sym1, the yeast ortholog of the MPV17 human disease protein, is a stress-induced bioenergetic and morphogenetic mitochondrial modulatorCristina Dallabona, René Massimiliano Marsano, Paola Arzuffi, et al.
The Journal of Biological Chemistry|May 11, 2018
Control of mitochondrial superoxide production by reverse electron transport at complex IEllen L Robb, Andrew R Hall, Tracy A Prime, et al.
Brain : a Journal of Neurology|April 20, 2010
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromesCharalampos Tzoulis, Gesche Neckelmann, Sverre J Mørk, et al.
Cerebellum (London, England)|November 29, 2022
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian PatientsFabiana Colucci, Marcella Neri, Fernanda Fortunato, et al.
Pharmacological Research|April 15, 2026
PPARγ activation by leriglitazone counteracts neurodegeneration and neuroinflammation in a disease-relevant mouse model of COASY dysfunctionChiara Cavestro, Floriana Cascone, Andrea Legati, et al.
Journal of Biological Engineering|March 6, 2023
Customized biofilm device for antibiofilm and antibacterial screening of newly developed nanostructured silver and zinc coatingsDaniele Ghezzi, Marco Boi, Enrico Sassoni, et al.
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