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

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[29] Mitochondrial membrane potential monitored by JC-1 dye von Reers, Martin, Smiley, Stephen T., Mottola-Hartshorn, Cristina, Chen, Ann, Lin, Mei, Chen, Lan Bo

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MELAS Mutation in mtDNA Binding Site for Transcription Termination Factor Causes Defects in Protein Synthesis and in Respiration but no Change in Levels of Upstream and Downstream... von Chomyn, A., Martinuzzi, A., Yoneda, M., Daga, A., Hurko, O., Johns, D., Lai, S. T., Nonaka, I., Angelini, C., Attardi, G.

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[14] Isolation of highly purified mitochondria from Saccharomyces cerevisiae von Glick, Benjamin S., Pon, Liza A.

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MtDNA mutations in aging and apoptosis von 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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Marked Replicative Advantage of Human mtDNA Carrying a Point Mutation that Causes the MELAS Encephalomyopathy von Yoneda, Makoto, Chomyn, Anne, Martinuzzi, Andrea, Hurko, Orest, Attardi, Giuseppe

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

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Platelet-mediated transformation of mtDNA-less human cells: Analysis of phenotypic variability among clones from normal individuals-and complementation behavior of the tRNA[sup Lys... von Chomyn, A., Lai, S.T., Shakeley, R., Attardi, G., Bresolin, N., Scarlato, G.

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In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria von CHOMYN, A, MEOLA, G, BRESOLIN, N, LAI, S. T, SCARLATO, G, ATTARDI, G

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

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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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[7] Ubiquinol-cytochrome-c reductase from human and bovine mitochondria von Schägger, Hermann, Brandt, Ulrich, Gencic, Simonida, von Jagow, Gebhard

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[10] ATP synthase from Saccharomyces cerevisiae von Law, Ruby H.P., Manon, Stephen, Devenish, Rodney J., Nagley, Phillip

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59: Low Socioeconomic Status and Very Preterm Birth: A “Double Jeopardy” in Child Language Development von Chomyn, A, Reichert, A, Carroll, L, Qureshi, M, Toye, J

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Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR) von Helm, Mark, Florentz, Catherine, Chomyn, Anne, Attardi, Giuseppe

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

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[8] Cytochrome-c oxidase from Saccharomyces cerevisiae von Poyton, Robert O., Goehring, Bradley, Droste, Martin, Sevarino, Kevin A., Allen, Larry A., Zhao, Xiao-Jian

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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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[19] Mitochondrial receptor complex from Neurospora crassa and Saccharomyces cerevisiae von Alconada, Agustín, Gärtner, Frank, Hönlinger, Angelika, Kübrich, Michael, Pfanner, Nikolaus

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