| Year |
Citation |
Score |
| 2023 |
Caron-Godon CA, Della Vecchia S, Romano A, Doccini S, Dal Canto F, Pasquariello R, Rubegni A, Battini R, Santorelli FM, Glerum DM, Nesti C. Novel Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and . International Journal of Molecular Sciences. 24. PMID 38068960 DOI: 10.3390/ijms242316636 |
0.401 |
|
| 2011 |
Veniamin S, Sawatzky LG, Banting GS, Glerum DM. Characterization of the peroxide sensitivity of COX-deficient yeast strains reveals unexpected relationships between COX assembly proteins. Free Radical Biology & Medicine. 51: 1589-600. PMID 21821119 DOI: 10.1016/J.Freeradbiomed.2011.06.024 |
0.456 |
|
| 2008 |
Hsi G, Cullen LM, Macintyre G, Chen MM, Glerum DM, Cox DW. Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system. Human Mutation. 29: 491-501. PMID 18203200 DOI: 10.1002/Humu.20674 |
0.458 |
|
| 2006 |
Zee JM, Glerum DM. Defects in cytochrome oxidase assembly in humans: lessons from yeast. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 84: 859-69. PMID 17215873 DOI: 10.1139/o06-201 |
0.324 |
|
| 2006 |
Banting GS, Glerum DM. Mutational analysis of the Saccharomyces cerevisiae cytochrome c oxidase assembly protein Cox11p. Eukaryotic Cell. 5: 568-78. PMID 16524911 DOI: 10.1128/Ec.5.3.568-578.2006 |
0.536 |
|
| 2005 |
Taylor P, Manage DP, Helmle KE, Zheng Y, Glerum DM, Backhouse CJ. Analysis of mitochondrial DNA in microfluidic systems. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 822: 78-84. PMID 15990373 DOI: 10.1016/J.Jchromb.2005.05.025 |
0.4 |
|
| 2005 |
Williams JC, Sue C, Banting GB, Yang H, Glerum DM, Hendrickson WA, Schon EA. Crystal structure of human SCO1: Implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" protein Journal of Biological Chemistry. 280: 15202-15211. PMID 15659396 DOI: 10.1074/Jbc.M410705200 |
0.449 |
|
| 2004 |
Marriage BJ, Clandinin MT, Macdonald IM, Glerum DM. Cofactor treatment improves ATP synthetic capacity in patients with oxidative phosphorylation disorders. Molecular Genetics and Metabolism. 81: 263-72. PMID 15059613 DOI: 10.1016/J.Ymgme.2003.12.008 |
0.339 |
|
| 2004 |
Hsi G, Cullen LM, Glerum DM, Cox DW. Functional assessment of the carboxy-terminus of the Wilson disease copper-transporting ATPase, ATP7B Genomics. 83: 473-481. PMID 14962673 DOI: 10.1016/J.Ygeno.2003.08.022 |
0.486 |
|
| 2003 |
Marriage B, Clandinin MT, Glerum DM. Nutritional cofactor treatment in mitochondrial disorders. Journal of the American Dietetic Association. 103: 1029-38. PMID 12891154 DOI: 10.1016/S0002-8223(03)00476-0 |
0.404 |
|
| 2003 |
Punter FA, Glerum DM. Mutagenesis reveals a specific role for Cox17p in copper transport to cytochrome oxidase. The Journal of Biological Chemistry. 278: 30875-80. PMID 12788943 DOI: 10.1074/Jbc.M302358200 |
0.57 |
|
| 2003 |
Antonicka H, Mattman A, Carlson CG, Glerum DM, Hoffbuhr KC, Leary SC, Kennaway NG, Shoubridge EA. Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy. American Journal of Human Genetics. 72: 101-14. PMID 12474143 DOI: 10.1086/345489 |
0.498 |
|
| 2003 |
Carlson CG, Barrientos A, Tzagoloff A, Glerum DM. COX16 encodes a novel protein required for the assembly of cytochrome oxidase in Saccharomyces cerevisiae Journal of Biological Chemistry. 278: 3770-3775. PMID 12446688 DOI: 10.1074/Jbc.M209893200 |
0.549 |
|
| 2002 |
Leary SC, Hill BC, Lyons CN, Carlson CG, Michaud D, Kraft CS, Ko K, Glerum DM, Moyes CD. Chronic treatment with azide in situ leads to an irreversible loss of cytochrome c oxidase activity via holoenzyme dissociation. The Journal of Biological Chemistry. 277: 11321-8. PMID 11796734 DOI: 10.1074/Jbc.M112303200 |
0.429 |
|
| 2001 |
Barros MH, Carlson CG, Glerum DM, Tzagoloff A. Involvement of mitochondrial ferredoxin and Cox15p in hydroxylation of heme O Febs Letters. 492: 133-138. PMID 11248251 DOI: 10.1016/S0014-5793(01)02249-9 |
0.413 |
|
| 2000 |
Punter FA, Adams DL, Glerum DM. Characterization and localization of human COX17, a gene involved in mitochondrial copper transport. Human Genetics. 107: 69-74. PMID 10982038 DOI: 10.1007/S004390000339 |
0.565 |
|
| 2000 |
Dickinson EK, Adams DL, Schon EA, Glerum DM. A human SCO2 mutation helps define the role of Sco1p in the cytochrome oxidase assembly pathway. The Journal of Biological Chemistry. 275: 26780-5. PMID 10854440 DOI: 10.1074/Jbc.M004032200 |
0.527 |
|
| 1999 |
Papadopoulou LC, Sue CM, Davidson MM, Tanji K, Nishino I, Sadlock JE, Krishna S, Walker W, Selby J, Glerum DM, Coster RV, Lyon G, Scalais E, Lebel R, Kaplan P, et al. Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nature Genetics. 23: 333-7. PMID 10545952 DOI: 10.1038/15513 |
0.441 |
|
| 1998 |
Glerum DM, Tzagoloff A. Affinity purification of yeast cytochrome oxidase with biotinylated subunits 4, 5, or 6 Analytical Biochemistry. 260: 38-43. PMID 9648650 DOI: 10.1006/abio.1998.2683 |
0.379 |
|
| 1997 |
Beers J, Glerum DM, Tzagoloff A. Purification, characterization, and localization of yeast Cox17p, a mitochondrial copper shuttle Journal of Biological Chemistry. 272: 33191-33196. PMID 9407107 DOI: 10.1074/Jbc.272.52.33191 |
0.435 |
|
| 1997 |
Glerum DM, Tzagoloff A. Submitochondrial distributions and stabilities of subunits 4, 5, and 6 of yeast cytochrome oxidase in assembly defective mutants Febs Letters. 412: 410-414. PMID 9276437 DOI: 10.1016/S0014-5793(97)00799-0 |
0.334 |
|
| 1997 |
Glerum DM, Muroff I, Jin C, Tzagoloff A. COX15 codes for a mitochondrial protein essential for the assembly of yeast cytochrome oxidase Journal of Biological Chemistry. 272: 19088-19094. PMID 9228094 DOI: 10.1074/Jbc.272.30.19088 |
0.487 |
|
| 1997 |
Mashkevich G, Repetto B, Glerum DM, Jin C, Tzagoloff A. SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration Journal of Biological Chemistry. 272: 14356-14364. PMID 9162072 DOI: 10.1074/Jbc.272.22.14356 |
0.474 |
|
| 1997 |
Amaravadi R, Glerum DM, Tzagoloff A. Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment Human Genetics. 99: 329-333. PMID 9050918 DOI: 10.1007/s004390050367 |
0.468 |
|
| 1996 |
Glerum DM, Shtanko A, Tzagoloff A, Gorman N, Sinclair PR. Cloning and identification of HEM14, the yeast gene for mitochondrial protoporphyrinogen oxidase Yeast. 12: 1421-1425. PMID 8948097 DOI: 10.1002/(Sici)1097-0061(199611)12:14<1421::Aid-Yea38>3.0.Co;2-W |
0.436 |
|
| 1996 |
Tzagoloff A, Jang J, Glerum DM, Wu M. FLX1 codes for a carrier protein involved in maintaining a proper balance of flavin nucleotides in yeast mitochondria Journal of Biological Chemistry. 271: 7392-7397. PMID 8631763 DOI: 10.1074/Jbc.271.13.7392 |
0.431 |
|
| 1995 |
Wu M, Repetto B, Glerum DM, Tzagoloff A. Cloning and characterization of FAD1, the structural gene for flavin adenine dinucleotide synthetase of Saccharomyces cerevisiae Molecular and Cellular Biology. 15: 264-271. PMID 7799934 DOI: 10.1128/Mcb.15.1.264 |
0.431 |
|
| 1994 |
Glerum DM, Tzagoloff A. Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant Proceedings of the National Academy of Sciences of the United States of America. 91: 8452-8456. PMID 8078902 |
0.407 |
|
| 1988 |
Glerum DM, Yanamura W, Capaldi RA, Robinson BH. Characterization of cytochrome-c oxidase mutants in human fibroblasts. Febs Letters. 236: 100-4. PMID 2841159 DOI: 10.1016/0014-5793(88)80293-X |
0.316 |
|
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