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Items: 14


A mitochondrial CO2-adenylyl cyclase-cAMP signalosome controls yeast normoxic cytochrome c oxidase activity.

Hess KC, Liu J, Manfredi G, Mühlschlegel FA, Buck J, Levin LR, Barrientos A.

FASEB J. 2014 Oct;28(10):4369-80. doi: 10.1096/fj.14-252890. Epub 2014 Jul 1.


Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase.

Bourens M, Boulet A, Leary SC, Barrientos A.

Hum Mol Genet. 2014 Jun 1;23(11):2901-13. doi: 10.1093/hmg/ddu003. Epub 2014 Jan 8.


Investigation of cytocrom c oxidase gene subunits expression on the Multiple sclerosis.

Safavizadeh N, Rahmani SA, Zaefizadeh M.

Indian J Hum Genet. 2013 Jan;19(1):18-25. doi: 10.4103/0971-6866.112879.


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 22;288(12):8321-31. doi: 10.1074/jbc.M112.422220. Epub 2013 Jan 29.


Structure, function, and assembly of heme centers in mitochondrial respiratory complexes.

Kim HJ, Khalimonchuk O, Smith PM, Winge DR.

Biochim Biophys Acta. 2012 Sep;1823(9):1604-16. doi: 10.1016/j.bbamcr.2012.04.008. Epub 2012 Apr 24. Review.


Iterative orthology prediction uncovers new mitochondrial proteins and identifies C12orf62 as the human ortholog of COX14, a protein involved in the assembly of cytochrome c oxidase.

Szklarczyk R, Wanschers BF, Cuypers TD, Esseling JJ, Riemersma M, van den Brand MA, Gloerich J, Lasonder E, van den Heuvel LP, Nijtmans LG, Huynen MA.

Genome Biol. 2012 Feb 22;13(2):R12. doi: 10.1186/gb-2012-13-2-r12.


Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome.

Chabrol B, Martens K, Meulemans S, Cano A, Jaeken J, Matthijs G, Creemers JW.

BMJ Case Rep. 2009;2009. pii: bcr08.2008.0719. doi: 10.1136/bcr.08.2008.0719. Epub 2009 Feb 2.


A novel heme a insertion factor gene cotranscribes with the Thermus thermophilus cytochrome ba3 oxidase locus.

Werner C, Richter OM, Ludwig B.

J Bacteriol. 2010 Sep;192(18):4712-9. doi: 10.1128/JB.00548-10. Epub 2010 Jul 9.


Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2.

Yang H, Brosel S, Acin-Perez R, Slavkovich V, Nishino I, Khan R, Goldberg IJ, Graziano J, Manfredi G, Schon EA.

Hum Mol Genet. 2010 Jan 1;19(1):170-80. doi: 10.1093/hmg/ddp477. Epub .


Surf1, associated with Leigh syndrome in humans, is a heme-binding protein in bacterial oxidase biogenesis.

Bundschuh FA, Hannappel A, Anderka O, Ludwig B.

J Biol Chem. 2009 Sep 18;284(38):25735-41. doi: 10.1074/jbc.M109.040295. Epub 2009 Jul 22.


Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene.

Shteyer E, Saada A, Shaag A, Al-Hijawi FA, Kidess R, Revel-Vilk S, Elpeleg O.

Am J Hum Genet. 2009 Mar;84(3):412-7. doi: 10.1016/j.ajhg.2009.02.006. Epub 2009 Mar 5.


Trypanosoma brucei: differential requirement of membrane potential for import of proteins into mitochondria in two developmental stages.

Williams S, Saha L, Singha UK, Chaudhuri M.

Exp Parasitol. 2008 Mar;118(3):420-33. Epub 2007 Oct 15.

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