Fernandez-Vizarra E - Search Results

1

Inflammation causes remodeling of mitochondrial cytochrome c oxidase mediated by the bifunctional gene C15orf48.

Clayton SA, Daley KK, MacDonald L, Fernandez-Vizarra E, Bottegoni G, O'Neil JD, Major T, Griffin D, Zhuang Q, Adewoye AB, Woolcock K, Jones SW, Goodyear C, Elmesmari A, Filer A, Tennant DA, Alivernini S, Buckley CD, Pitceathly RDS, Kurowska-Stolarska M, Clark AR. Clayton SA, et al. Sci Adv. 2021 Dec 10;7(50):eabl5182. doi: 10.1126/sciadv.abl5182. Epub 2021 Dec 8. Sci Adv. 2021. PMID: 34878835 Free PMC article.

2

Two independent respiratory chains adapt OXPHOS performance to glycolytic switch.

Fernández-Vizarra E, López-Calcerrada S, Sierra-Magro A, Pérez-Pérez R, Formosa LE, Hock DH, Illescas M, Peñas A, Brischigliaro M, Ding S, Fearnley IM, Tzoulis C, Pitceathly RDS, Arenas J, Martín MA, Stroud DA, Zeviani M, Ryan MT, Ugalde C. Fernández-Vizarra E, et al. Cell Metab. 2022 Nov 1;34(11):1792-1808.e6. doi: 10.1016/j.cmet.2022.09.005. Epub 2022 Oct 4. Cell Metab. 2022. PMID: 36198313 Free article.

3

Emerging mechanisms in the redox regulation of mitochondrial cytochrome c oxidase assembly and function.

Povea-Cabello S, Brischigliaro M, Fernández-Vizarra E. Povea-Cabello S, et al. Among authors: fernandez vizarra e. Biochem Soc Trans. 2024 Apr 24;52(2):873-885. doi: 10.1042/BST20231183. Biochem Soc Trans. 2024. PMID: 38526156 Review.

4

Redox-Mediated Regulation of Mitochondrial Biogenesis, Dynamics, and Respiratory Chain Assembly in Yeast and Human Cells.

Geldon S, Fernández-Vizarra E, Tokatlidis K. Geldon S, et al. Front Cell Dev Biol. 2021 Sep 7;9:720656. doi: 10.3389/fcell.2021.720656. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34557489 Free PMC article. Review.

5

Mitochondrial Cytochrome c Oxidase Defects Alter Cellular Homeostasis of Transition Metals.

Brischigliaro M, Badocco D, Costa R, Viscomi C, Zeviani M, Pastore P, Fernández-Vizarra E. Brischigliaro M, et al. Front Cell Dev Biol. 2022 May 19;10:892069. doi: 10.3389/fcell.2022.892069. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35663391 Free PMC article.

6

Mitochondrial disorders of the OXPHOS system.

Fernandez-Vizarra E, Zeviani M. Fernandez-Vizarra E, et al. FEBS Lett. 2021 Apr;595(8):1062-1106. doi: 10.1002/1873-3468.13995. Epub 2020 Dec 18. FEBS Lett. 2021. PMID: 33159691 Free article. Review.

7

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. Martinez Lyons A, et al. J Med Genet. 2016 Dec;53(12):846-849. doi: 10.1136/jmedgenet-2016-104194. Epub 2016 Sep 28. J Med Genet. 2016. PMID: 27683825 Free PMC article.

8

Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA).

Fernandez-Vizarra E, Berardinelli A, Valente L, Tiranti V, Zeviani M. Fernandez-Vizarra E, et al. J Med Genet. 2007 Mar;44(3):173-80. doi: 10.1136/jmg.2006.045252. Epub 2006 Oct 20. J Med Genet. 2007. PMID: 17056637 Free PMC article.

9

Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy.

Fernandez-Vizarra E, Bugiani M, Goffrini P, Carrara F, Farina L, Procopio E, Donati A, Uziel G, Ferrero I, Zeviani M. Fernandez-Vizarra E, et al. Hum Mol Genet. 2007 May 15;16(10):1241-52. doi: 10.1093/hmg/ddm072. Epub 2007 Apr 2. Hum Mol Genet. 2007. PMID: 17403714

10

Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.

Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, Mereghetti P, D'Adamo P, Gasparini P, Zeviani M. Massa V, et al. Am J Hum Genet. 2008 Jun;82(6):1281-9. doi: 10.1016/j.ajhg.2008.05.002. Epub 2008 May 22. Am J Hum Genet. 2008. PMID: 18499082 Free PMC article.

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