157 related articles for article (PubMed ID: 17435251)
1. Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila.
Liu W; Gnanasambandam R; Benjamin J; Kaur G; Getman PB; Siegel AJ; Shortridge RD; Singh S
Genetics; 2007 Jun; 176(2):937-46. PubMed ID: 17435251
[TBL] [Abstract][Full Text] [Related]
2. Genetic mosaic analysis of a deleterious mitochondrial DNA mutation in Drosophila reveals novel aspects of mitochondrial regulation and function.
Chen Z; Qi Y; French S; Zhang G; Covian Garcia R; Balaban R; Xu H
Mol Biol Cell; 2015 Feb; 26(4):674-84. PubMed ID: 25501370
[TBL] [Abstract][Full Text] [Related]
3. Polyglutamine tract-binding protein-1 dysfunction induces cell death of neurons through mitochondrial stress.
Marubuchi S; Wada Y; Okuda T; Hara Y; Qi ML; Hoshino M; Nakagawa M; Kanazawa I; Okazawa H
J Neurochem; 2005 Nov; 95(3):858-70. PubMed ID: 16104847
[TBL] [Abstract][Full Text] [Related]
4. Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila.
Palladino MJ; Hadley TJ; Ganetzky B
Genetics; 2002 Jul; 161(3):1197-208. PubMed ID: 12136022
[TBL] [Abstract][Full Text] [Related]
5. Cytonuclear coadaptation in Drosophila: disruption of cytochrome c oxidase activity in backcross genotypes.
Sackton TB; Haney RA; Rand DM
Evolution; 2003 Oct; 57(10):2315-25. PubMed ID: 14628919
[TBL] [Abstract][Full Text] [Related]
6. wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death.
Gnerer JP; Kreber RA; Ganetzky B
Proc Natl Acad Sci U S A; 2006 Oct; 103(41):14987-93. PubMed ID: 17008404
[TBL] [Abstract][Full Text] [Related]
7. Human mitochondrial COX1 assembly into cytochrome c oxidase at a glance.
Dennerlein S; Rehling P
J Cell Sci; 2015 Mar; 128(5):833-7. PubMed ID: 25663696
[TBL] [Abstract][Full Text] [Related]
8. Increased mitochondrial cytochrome c levels and mitochondrial hyperpolarization precede camptothecin-induced apoptosis in Jurkat cells.
Sánchez-Alcázar JA; Ault JG; Khodjakov A; Schneider E
Cell Death Differ; 2000 Nov; 7(11):1090-100. PubMed ID: 11139283
[TBL] [Abstract][Full Text] [Related]
9. Combined expression of tau and the Harlequin mouse mutation leads to increased mitochondrial dysfunction, tau pathology and neurodegeneration.
Kulic L; Wollmer MA; Rhein V; Pagani L; Kuehnle K; Cattepoel S; Tracy J; Eckert A; Nitsch RM
Neurobiol Aging; 2011 Oct; 32(10):1827-38. PubMed ID: 19942317
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial function and content in pheochromocytoma/paraganglioma of succinate dehydrogenase mutation carriers.
Rapizzi E; Ercolino T; Canu L; Giaché V; Francalanci M; Pratesi C; Valeri A; Mannelli M
Endocr Relat Cancer; 2012 Jun; 19(3):261-9. PubMed ID: 22323561
[TBL] [Abstract][Full Text] [Related]
11. Early life benefits and later life costs of a two amino acid deletion in Drosophila simulans.
Ballard JW; Melvin RG
Evolution; 2011 May; 65(5):1400-12. PubMed ID: 21143473
[TBL] [Abstract][Full Text] [Related]
12. Identification and investigation of mitochondria lacking cytochrome c oxidase activity in axons.
Zambonin J; Engeham S; Campbell GR; Ziabreva I; Beadle NE; Taylor RW; Mahad DJ
J Neurosci Methods; 2010 Sep; 192(1):115-20. PubMed ID: 20659500
[TBL] [Abstract][Full Text] [Related]
13. The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura.
Farge G; Touraille S; Le Goff S; Petit N; Renoux M; Morel F; Alziari S
Eur J Biochem; 2002 Feb; 269(3):998-1005. PubMed ID: 11846802
[TBL] [Abstract][Full Text] [Related]
14. Activities of cytochrome c oxidase and citrate synthase in lymphocytes of obese and normal-weight subjects.
Capková M; Houstek J; Hansíková H; Hainer V; Kunesová M; Zeman J
Int J Obes Relat Metab Disord; 2002 Aug; 26(8):1110-7. PubMed ID: 12119577
[TBL] [Abstract][Full Text] [Related]
15. Females with a mutation in a nuclear-encoded mitochondrial protein pay a higher cost of survival than do males in Drosophila.
Melvin RG; Ballard JW
J Gerontol A Biol Sci Med Sci; 2011 Jul; 66(7):765-70. PubMed ID: 21498433
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene.
Debray FG; Seneca S; Gonce M; Vancampenhaut K; Bianchi E; Boemer F; Weekers L; Smet J; Van Coster R
Mitochondrion; 2014 Jul; 17():101-5. PubMed ID: 24956508
[TBL] [Abstract][Full Text] [Related]
17. Traumatic brain injury-induced changes in gene expression and functional activity of mitochondrial cytochrome C oxidase.
Harris LK; Black RT; Golden KM; Reeves TM; Povlishock JT; Phillips LL
J Neurotrauma; 2001 Oct; 18(10):993-1009. PubMed ID: 11686499
[TBL] [Abstract][Full Text] [Related]
18. Metabolic disruption in Drosophila bang-sensitive seizure mutants.
Fergestad T; Bostwick B; Ganetzky B
Genetics; 2006 Jul; 173(3):1357-64. PubMed ID: 16648587
[TBL] [Abstract][Full Text] [Related]
19. Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations.
Kovářová N; Cížková Vrbacká A; Pecina P; Stránecký V; Pronicka E; Kmoch S; Houštěk J
Biochim Biophys Acta; 2012 Jul; 1822(7):1114-24. PubMed ID: 22465034
[TBL] [Abstract][Full Text] [Related]
20. Progressive neurodegeneration in Drosophila: a model system.
Tschäpe JA; Bettencourt da Cruz A; Kretzschmar D
J Neural Transm Suppl; 2003; (65):51-62. PubMed ID: 12946048
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]