191 related articles for article (PubMed ID: 25604084)
1. Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature.
Ostergaard E; Weraarpachai W; Ravn K; Born AP; Jønson L; Duno M; Wibrand F; Shoubridge EA; Vissing J
J Med Genet; 2015 Mar; 52(3):203-7. PubMed ID: 25604084
[TBL] [Abstract][Full Text] [Related]
2. Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.
Weraarpachai W; Sasarman F; Nishimura T; Antonicka H; Auré K; Rötig A; Lombès A; Shoubridge EA
Am J Hum Genet; 2012 Jan; 90(1):142-51. PubMed ID: 22243966
[TBL] [Abstract][Full Text] [Related]
3. Coa3 and Cox14 are essential for negative feedback regulation of COX1 translation in mitochondria.
Mick DU; Vukotic M; Piechura H; Meyer HE; Warscheid B; Deckers M; Rehling P
J Cell Biol; 2010 Oct; 191(1):141-54. PubMed ID: 20876281
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A
Bourens M; Barrientos A
EMBO Rep; 2017 Mar; 18(3):477-494. PubMed ID: 28082314
[TBL] [Abstract][Full Text] [Related]
6. Cox25 teams up with Mss51, Ssc1, and Cox14 to regulate mitochondrial cytochrome c oxidase subunit 1 expression and assembly in Saccharomyces cerevisiae.
Fontanesi F; Clemente P; Barrientos A
J Biol Chem; 2011 Jan; 286(1):555-66. PubMed ID: 21068384
[TBL] [Abstract][Full Text] [Related]
7. hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria.
Clemente P; Peralta S; Cruz-Bermudez A; Echevarría L; Fontanesi F; Barrientos A; Fernandez-Moreno MA; Garesse R
J Biol Chem; 2013 Mar; 288(12):8321-8331. PubMed ID: 23362268
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein.
Richter-Dennerlein R; Oeljeklaus S; Lorenzi I; Ronsör C; Bareth B; Schendzielorz AB; Wang C; Warscheid B; Rehling P; Dennerlein S
Cell; 2016 Oct; 167(2):471-483.e10. PubMed ID: 27693358
[TBL] [Abstract][Full Text] [Related]
9. A Novel Function of Pet54 in Regulation of Cox1 Synthesis in Saccharomyces cerevisiae Mitochondria.
Mayorga JP; Camacho-Villasana Y; Shingú-Vázquez M; García-Villegas R; Zamudio-Ochoa A; García-Guerrero AE; Hernández G; Pérez-Martínez X
J Biol Chem; 2016 Apr; 291(17):9343-55. PubMed ID: 26929411
[TBL] [Abstract][Full Text] [Related]
10. Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects.
Kovářová N; Pecina P; Nůsková H; Vrbacký M; Zeviani M; Mráček T; Viscomi C; Houštěk J
Biochim Biophys Acta; 2016 Apr; 1862(4):705-715. PubMed ID: 26804654
[TBL] [Abstract][Full Text] [Related]
11. LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.
Oláhová M; Hardy SA; Hall J; Yarham JW; Haack TB; Wilson WC; Alston CL; He L; Aznauryan E; Brown RM; Brown GK; Morris AA; Mundy H; Broomfield A; Barbosa IA; Simpson MA; Deshpande C; Moeslinger D; Koch J; Stettner GM; Bonnen PE; Prokisch H; Lightowlers RN; McFarland R; Chrzanowska-Lightowlers ZM; Taylor RW
Brain; 2015 Dec; 138(Pt 12):3503-19. PubMed ID: 26510951
[TBL] [Abstract][Full Text] [Related]
12. COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency.
Martinez Lyons A; Ardissone A; Reyes A; Robinson AJ; Moroni I; Ghezzi D; Fernandez-Vizarra E; Zeviani M
J Med Genet; 2016 Dec; 53(12):846-849. PubMed ID: 27683825
[TBL] [Abstract][Full Text] [Related]
13. An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.
Janer A; Antonicka H; Lalonde E; Nishimura T; Sasarman F; Brown GK; Brown RM; Majewski J; Shoubridge EA
Am J Hum Genet; 2012 Oct; 91(4):737-43. PubMed ID: 23022098
[TBL] [Abstract][Full Text] [Related]
14. CCDC90A (MCUR1) is a cytochrome c oxidase assembly factor and not a regulator of the mitochondrial calcium uniporter.
Paupe V; Prudent J; Dassa EP; Rendon OZ; Shoubridge EA
Cell Metab; 2015 Jan; 21(1):109-16. PubMed ID: 25565209
[TBL] [Abstract][Full Text] [Related]
15. An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.
Hinttala R; Sasarman F; Nishimura T; Antonicka H; Brunel-Guitton C; Schwartzentruber J; Fahiminiya S; Majewski J; Faubert D; Ostergaard E; Smeitink JA; Shoubridge EA
Hum Mol Genet; 2015 Jul; 24(14):4103-13. PubMed ID: 25911677
[TBL] [Abstract][Full Text] [Related]
16. Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.
Dong HL; Ma Y; Yu H; Wei Q; Li JQ; Liu GL; Li HF; Chen L; Chen DF; Bai G; Wu ZY
Brain; 2021 Sep; 144(8):2457-2470. PubMed ID: 33751098
[TBL] [Abstract][Full Text] [Related]
17. A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy.
Ronchi D; Garbellini M; Magri F; Menni F; Meneri M; Bedeschi MF; Dilena R; Cecchetti V; Picciolli I; Furlan F; Polimeni V; Salani S; Pezzoli L; Fortunato F; Bellini M; Piga D; Ripolone M; Zanotti S; Napoli L; Ciscato P; Sciacco M; Mangili G; Mosca F; Corti S; Iascone M; Comi GP
Eur J Hum Genet; 2023 Dec; 31(12):1414-1420. PubMed ID: 37468577
[TBL] [Abstract][Full Text] [Related]
18. Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1.
Stiburek L; Vesela K; Hansikova H; Pecina P; Tesarova M; Cerna L; Houstek J; Zeman J
Biochem J; 2005 Dec; 392(Pt 3):625-32. PubMed ID: 16083427
[TBL] [Abstract][Full Text] [Related]
19. COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthood.
Pitceathly RD; Taanman JW; Rahman S; Meunier B; Sadowski M; Cirak S; Hargreaves I; Land JM; Nanji T; Polke JM; Woodward CE; Sweeney MG; Solanki S; Foley AR; Hurles ME; Stalker J; Blake J; Holton JL; Phadke R; Muntoni F; Reilly MM; Hanna MG;
JAMA Neurol; 2013 Dec; 70(12):1556-61. PubMed ID: 24100867
[TBL] [Abstract][Full Text] [Related]
20. A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.
Szklarczyk R; Wanschers BF; Nijtmans LG; Rodenburg RJ; Zschocke J; Dikow N; van den Brand MA; Hendriks-Franssen MG; Gilissen C; Veltman JA; Nooteboom M; Koopman WJ; Willems PH; Smeitink JA; Huynen MA; van den Heuvel LP
Hum Mol Genet; 2013 Feb; 22(4):656-67. PubMed ID: 23125284
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
