Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2 , a COX assembly gene von Schon, Eric A, Papadopoulou, Lefkothea C, Sue, Carolyn M, Davidson, Mercy M, Tanji, Kurenai, Nishino, Ichizo, Sadlock, James E, Krishna, Sindu, Walker, Winsome, Selby, Jeanette, Glerum, D. Moira, Coster, Rudy Van, Lyon, Gilles, Scalais, Emmanuel, Lebel, Roger, Kaplan, Paige, Shanske, Sara, De Vivo, Darryl C, Bonilla, Eduardo, Hirano, Michio, DiMauro, Salvatore

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Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment von AMARAVADI, R, GLERUM, D. M, TZAGOLOFF, A

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Isolation of a Human cDNA for Heme A:Farnesyltransferase by Functional Complementation of a Yeast cox10 Mutant von Glerum, D. Moira, Tzagoloff, Alexander

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Characterization of COX17, a Yeast Gene Involved in Copper Metabolism and Assembly of Cytochrome Oxidase von Glerum, D M, Shtanko, A, Tzagoloff, A

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Purification, Characterization, and Localization of Yeast Cox17p, a Mitochondrial Copper Shuttle von Beers, John, Glerum, D. Moira, Tzagoloff, Alexander

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SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper Recruitment Defect in Saccharomyces cerevisiae von Glerum, D. Moira, Shtanko, Andrey, Tzagoloff, Alexander

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Frontal analysis on a microchip von BACKHOUSE, C. J, CRABTREE, H. J, GLERUM, D. M

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Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O von Barros, Mario H., Carlson, Christopher G., Glerum, D.Moira, Tzagoloff, Alexander

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Cloning and characterization of FAD1, the structural gene for flavin adenine dinucleotide synthetase of Saccharomyces cerevisiae von Wu, Mian, Repetto, Barbara, Glerum, D. Moira, Tzagoloff, Alexander

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Mutagenesis Reveals a Specific Role for Cox17p in Copper Transport to Cytochrome Oxidase von Punter, Fiona A., Glerum, D.Moira

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Chronic Treatment with Azide in Situ Leads to an Irreversible Loss of Cytochrome c Oxidase Activity via Holoenzyme Dissociation von Leary, Scot C., Hill, Bruce C., Lyons, Carrie N., Carlson, Christopher G., Michaud, Denise, Kraft, Claudia S., Ko, Kenton, Glerum, D. Moira, Moyes, Christopher D.

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A human SCO2 mutation helps define the role of Sco1p in the cytochrome oxidase assembly pathway von Dickinson, E K, Adams, D L, Schon, E A, Glerum, D M

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SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration von Mashkevich, G, Repetto, B, Glerum, D M, Jin, C, Tzagoloff, A

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COX15 Codes for a Mitochondrial Protein Essential for the Assembly of Yeast Cytochrome Oxidase von Glerum, D. Moira, Muroff, Ivor, Jin, Can, Tzagoloff, Alexander

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COX16 Encodes a Novel Protein Required for the Assembly of Cytochrome Oxidase in Saccharomyces cerevisiae von Carlson, Christopher G., Barrientos, Antoni, Tzagoloff, Alexander, Glerum, D. Moira

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FLX1 Codes for a Carrier Protein Involved in Maintaining a Proper Balance of Flavin Nucleotides in Yeast Mitochondria (∗) von Tzagoloff, Alexander, Jang, Jeanne, Glerum, D. Moira, Wu, Mian

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Submitochondrial distributions and stabilities of subunits 4, 5, and 6 of yeast cytochrome oxidase in assembly defective mutants von Glerum, D.Moira, Tzagoloff, Alexander

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Sample purification on a microfluidic device von Footz, Tim, Wunsam, Sybille, Kulak, Stephen, Crabtree, H. John, Glerum, D. Moira, Backhouse, Christopher J.

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The use of lymphocytes to screen for oxidative phosphorylation disorders von Marriage, Barbara J, Thomas Clandinin, M, MacDonald, Ian M, Moira Glerum, D

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Characterization and localization of human COX17, a gene involved in mitochondrial copper transport von PUNTER, F. A, ADAMS, D. L, GLERUM, D. M

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