227 related articles for article (PubMed ID: 11595737)
1. In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I.
D'Aurelio M; Pallotti F; Barrientos A; Gajewski CD; Kwong JQ; Bruno C; Beal MF; Manfredi G
J Biol Chem; 2001 Dec; 276(50):46925-32. PubMed ID: 11595737
[TBL] [Abstract][Full Text] [Related]
2. A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.
Bruno C; Martinuzzi A; Tang Y; Andreu AL; Pallotti F; Bonilla E; Shanske S; Fu J; Sue CM; Angelini C; DiMauro S; Manfredi G
Am J Hum Genet; 1999 Sep; 65(3):611-20. PubMed ID: 10441567
[TBL] [Abstract][Full Text] [Related]
3. Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.
Jesina P; Tesarová M; Fornůsková D; Vojtísková A; Pecina P; Kaplanová V; Hansíková H; Zeman J; Houstek J
Biochem J; 2004 Nov; 383(Pt. 3):561-71. PubMed ID: 15265003
[TBL] [Abstract][Full Text] [Related]
4. A pathogenic 15-base pair deletion in mitochondrial DNA-encoded cytochrome c oxidase subunit III results in the absence of functional cytochrome c oxidase.
Hoffbuhr KC; Davidson E; Filiano BA; Davidson M; Kennaway NG; King MP
J Biol Chem; 2000 May; 275(18):13994-4003. PubMed ID: 10788526
[TBL] [Abstract][Full Text] [Related]
5. A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome.
Tiranti V; Corona P; Greco M; Taanman JW; Carrara F; Lamantea E; Nijtmans L; Uziel G; Zeviani M
Hum Mol Genet; 2000 Nov; 9(18):2733-42. PubMed ID: 11063732
[TBL] [Abstract][Full Text] [Related]
6. The subunit composition and function of mammalian cytochrome c oxidase.
Kadenbach B; Hüttemann M
Mitochondrion; 2015 Sep; 24():64-76. PubMed ID: 26190566
[TBL] [Abstract][Full Text] [Related]
7. m.6267G>A: a recurrent mutation in the human mitochondrial DNA that reduces cytochrome c oxidase activity and is associated with tumors.
Gallardo ME; Moreno-Loshuertos R; López C; Casqueiro M; Silva J; Bonilla F; Rodríguez de Córdoba S; Enríquez JA
Hum Mutat; 2006 Jun; 27(6):575-82. PubMed ID: 16671096
[TBL] [Abstract][Full Text] [Related]
8. Cytochrome c oxidase subunit IV is essential for assembly and respiratory function of the enzyme complex.
Li Y; Park JS; Deng JH; Bai Y
J Bioenerg Biomembr; 2006 Dec; 38(5-6):283-91. PubMed ID: 17091399
[TBL] [Abstract][Full Text] [Related]
9. Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines.
Dey R; Barrientos A; Moraes CT
J Biol Chem; 2000 Oct; 275(40):31520-7. PubMed ID: 10908562
[TBL] [Abstract][Full Text] [Related]
10. Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.
Kenney MC; Chwa M; Atilano SR; Falatoonzadeh P; Ramirez C; Malik D; Tarek M; Del Carpio JC; Nesburn AB; Boyer DS; Kuppermann BD; Vawter MP; Jazwinski SM; Miceli MV; Wallace DC; Udar N
Biochim Biophys Acta; 2014 Feb; 1842(2):208-19. PubMed ID: 24200652
[TBL] [Abstract][Full Text] [Related]
11. A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy.
Rahman S; Taanman JW; Cooper JM; Nelson I; Hargreaves I; Meunier B; Hanna MG; García JJ; Capaldi RA; Lake BD; Leonard JV; Schapira AH
Am J Hum Genet; 1999 Oct; 65(4):1030-9. PubMed ID: 10486321
[TBL] [Abstract][Full Text] [Related]
12. Metabolic consequences of a novel missense mutation of the mtDNA CO I gene.
Varlamov DA; Kudin AP; Vielhaber S; Schröder R; Sassen R; Becker A; Kunz D; Haug K; Rebstock J; Heils A; Elger CE; Kunz WS
Hum Mol Genet; 2002 Aug; 11(16):1797-805. PubMed ID: 12140182
[TBL] [Abstract][Full Text] [Related]
13. In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.
Villani G; Attardi G
Proc Natl Acad Sci U S A; 1997 Feb; 94(4):1166-71. PubMed ID: 9037024
[TBL] [Abstract][Full Text] [Related]
14. Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.
Hanna MG; Nelson IP; Rahman S; Lane RJ; Land J; Heales S; Cooper MJ; Schapira AH; Morgan-Hughes JA; Wood NW
Am J Hum Genet; 1998 Jul; 63(1):29-36. PubMed ID: 9634511
[TBL] [Abstract][Full Text] [Related]
15. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants.
Tiranti V; Munaro M; Sandonà D; Lamantea E; Rimoldi M; DiDonato S; Bisson R; Zeviani M
Hum Mol Genet; 1995 Nov; 4(11):2017-23. PubMed ID: 8589677
[TBL] [Abstract][Full Text] [Related]
16. Increased transcription of mitochondrial genes for Complex I in human platelets during ageing.
Merlo Pich M; Raule N; Catani L; Fagioli ME; Faenza I; Cocco L; Lenaz G
FEBS Lett; 2004 Jan; 558(1-3):19-22. PubMed ID: 14759509
[TBL] [Abstract][Full Text] [Related]
17. Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.
Manfredi G; Fu J; Ojaimi J; Sadlock JE; Kwong JQ; Guy J; Schon EA
Nat Genet; 2002 Apr; 30(4):394-9. PubMed ID: 11925565
[TBL] [Abstract][Full Text] [Related]
18. An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.
Clark KM; Taylor RW; Johnson MA; Chinnery PF; Chrzanowska-Lightowlers ZM; Andrews RM; Nelson IP; Wood NW; Lamont PJ; Hanna MG; Lightowlers RN; Turnbull DM
Am J Hum Genet; 1999 May; 64(5):1330-9. PubMed ID: 10205264
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I.
Kollberg G; Moslemi AR; Lindberg C; Holme E; Oldfors A
J Neuropathol Exp Neurol; 2005 Feb; 64(2):123-8. PubMed ID: 15751226
[TBL] [Abstract][Full Text] [Related]
20. Effects of anoxia and the mitochondrion on expression of aerobic nuclear COX genes in yeast: evidence for a signaling pathway from the mitochondrial genome to the nucleus.
Dagsgaard C; Taylor LE; O'Brien KM; Poyton RO
J Biol Chem; 2001 Mar; 276(10):7593-601. PubMed ID: 11099503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
