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Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency.
Tiranti V, Hoertnagel K, Carrozzo R, Galimberti C, Munaro M, Granatiero M, Zelante L, Gasparini P, Marzella R, Rocchi M, Bayona-Bafaluy MP, Enriquez JA, Uziel G, Bertini E, Dionisi-Vici C, Franco B, Meitinger T, Zeviani M. Tiranti V, et al. Am J Hum Genet. 1998 Dec;63(6):1609-21. doi: 10.1086/302150. Am J Hum Genet. 1998. PMID: 9837813 Free PMC article.
Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly.
Perales-Clemente E, Fernández-Vizarra E, Acín-Pérez R, Movilla N, Bayona-Bafaluy MP, Moreno-Loshuertos R, Pérez-Martos A, Fernández-Silva P, Enríquez JA. Perales-Clemente E, et al. Mol Cell Biol. 2010 Jun;30(12):3038-47. doi: 10.1128/MCB.00025-10. Epub 2010 Apr 12. Mol Cell Biol. 2010. PMID: 20385768 Free PMC article.
A genome-wide shRNA screen for new OxPhos related genes.
Bayona-Bafaluy MP, Sánchez-Cabo F, Fernández-Silva P, Pérez-Martos A, Enríquez JA. Bayona-Bafaluy MP, et al. Mitochondrion. 2011 May;11(3):467-75. doi: 10.1016/j.mito.2011.01.007. Epub 2011 Feb 1. Mitochondrion. 2011. PMID: 21292037
Revisiting the mouse mitochondrial DNA sequence.
Bayona-Bafaluy MP, Acín-Pérez R, Mullikin JC, Park JS, Moreno-Loshuertos R, Hu P, Pérez-Martos A, Fernández-Silva P, Bai Y, Enríquez JA. Bayona-Bafaluy MP, et al. Nucleic Acids Res. 2003 Sep 15;31(18):5349-55. doi: 10.1093/nar/gkg739. Nucleic Acids Res. 2003. PMID: 12954771 Free PMC article.
37 results