The RNase P Associated with HeLa Cell Mitochondria Contains an Essential RNA Component Identical in Sequence to That of the Nuclear RNase P von Puranam, Ram S., Attardi, Giuseppe

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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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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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Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells von King, M.P., Attardi, G.

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Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within di... von YONEDA, M, MIYATAKE, T, ATTARDI, G

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Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase von Hofhaus, Götz, Attardi, Giuseppe

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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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Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for Replication von Michikawa, Yuichi, Mazzucchelli, Franca, Bresolin, Nereo, Scarlato, Guglielmo, Attardi, Giuseppe

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Discovery of a Major D-Loop Replication Origin Reveals Two Modes of Human mtDNA Synthesis von Fish, Jennifer, Raule, Nicola, Attardi, Giuseppe

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Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and... von van den Ouweland, J M, Maechler, P, Wollheim, C B, Attardi, G, Maassen, J A

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Lack of assembly of mitochondrial DNA‐encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene produ... von Hofhaus, G., Attardi, G.

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Termination Factor-Mediated DNA Loop between Termination and Initiation Sites Drives Mitochondrial rRNA Synthesis von Martin, Miguel, Cho, Jaehyoung, Cesare, Anthony J., Griffith, Jack D., Attardi, Giuseppe

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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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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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Molecular characterization of the transcription termination factor from human mitochondria von DAGA, A, MICOL, V, HESS, D, AEBERSOLD, R, ATTARDI, G

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Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant von Walker, D.W, Hájek, P, Muffat, J, Knoepfle, D, Cornelison, S, Attardi, G, Benzer, S

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In vivo control of respiration by cytochrome c oxidase in human cells von Villani, Gaetano, Attardi, Giuseppe

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Differential regulation of expression of the multiple ADP/ATP translocase genes in human cells von LUNARDI, J, ATTARDI, G

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[27] Isolation of human cell lines lacking mitochondrial DNA von King, Michael P., Attardi, Giuseppe

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