Disruption of Fusion Results in Mitochondrial Heterogeneity and Dysfunction von Chen, Hsiuchen, Chomyn, Anne, Chan, David C.

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Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations von Chen, Hsiuchen, Vermulst, Marc, Wang, Yun E., Chomyn, Anne, Prolla, Tomas A., McCaffery, J. Michael, Chan, David C.

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MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases von Hashimoto, Masami, Bacman, Sandra R, Peralta, Susana, Falk, Marni J, Chomyn, Anne, Chan, David C, Williams, Sion L, Moraes, Carlos T

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Decreased reactive oxygen species production in cells with mitochondrial haplogroups associated with longevity von Chen, Ai, Raule, Nicola, Chomyn, Anne, Attardi, Giuseppe

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Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology von Duvezin-Caubet, Stéphane, Jagasia, Ravi, Wagener, Johannes, Hofmann, Sabine, Trifunovic, Aleksandra, Hansson, Anna, Chomyn, Anne, Bauer, Matthias F., Attardi, Giuseppe, Larsson, Nils-Göran, Neupert, Walter, Reichert, Andreas S.

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Identification of a Novel Mitochondrial Complex Containing Mitofusin 2 and Stomatin-like Protein 2 von Hájek, Petr, Chomyn, Anne, Attardi, Giuseppe

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[18] In vivo labeling and analysis of human mitochondrial translation products von Chomyn, Anne

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MtDNA mutations in aging and apoptosis von Chomyn, Anne, Attardi, Giuseppe

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Respiration and Growth Defects in Transmitochondrial Cell Lines Carrying the 11778 Mutation Associated with Leber's Hereditary Optic Neuropathy von Hofhaus, G, Johns, D R, Hurko, O, Attardi, G, Chomyn, A

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Mitochondrial Outer Membrane Permeability Change and Hypersensitivity to Digitonin Early in Staurosporine-induced Apoptosis von Duan, Shili, Hájek, Petr, Lin, Catherine, Shin, Soo Kyung, Attardi, Giuseppe, Chomyn, Anne

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Mitochondrial genetic control of assembly and function of complex I in mammalian cells von Chomyn, A

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The Myoclonic Epilepsy and Ragged-Red Fiber Mutation Provides New Insights into Human Mitochondrial Function and Genetics von Chomyn, Anne

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[29] Platelet-mediated transformation of human mitochondrial DNA-less cells von Chomyn, Anne

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URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase Subunit von Chomyn, Anne, Michael W. J. Cleeter, Ragan, C. Ian, Riley, Marcia, Doolittle, Russell F., Attardi, Giuseppe

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mitoTALENs as DNA editing tools for mitochondrial diseases von Bacman, Sandra R., Hashimoto, Masami, Peralta, Susana, Falk, Marni J., Chomyn, Anne, Chan, David C., Williams, Sion L., Moraes, Carlos T.

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Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase von Chomyn, Anne, Mariottini, Paolo, Cleeter, Michael W. J., Ragan, C. Ian, Matsuno-Yagi, Akemi, Hatefi, Youssef, Doolittle, Russell F., Attardi, Giuseppe

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MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination von Enriquez, J A, Chomyn, A, Attardi, G

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Lack of Complex I Activity in Human Cells Carrying a Mutation in MtDNA-encoded ND4 Subunit Is Corrected by theSaccharomyces cerevisiae NADH-Quinone Oxidoreductase (NDI1) Gene von Bai, Yidong, Hájek, Petr, Chomyn, Anne, Chan, Elisa, Seo, Byoung Boo, Matsuno-Yagi, Akemi, Yagi, Takao, Attardi, Giuseppe

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The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency... von Chomyn, Anne, Enriquez, José Antonio, Micol, Vicente, Fernandez-Silva, Patricio, Attardi, Giuseppe

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Lack of complex I activity in human cells carrying a mutation in MtDNA-encoded ND4 subunit is corrected by the Saccharomyces cerevisiae NADH-quinone oxidoreductase (NDI1) gene von Bai, Y, Hájek, P, Chomyn, A, Chan, E, Seo, B B, Matsuno-Yagi, A, Yagi, T, Attardi, G

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