Bayona-Bafaluy MP - Search Results

1

Prenatal exposure to oxidative phosphorylation xenobiotics and late-onset Parkinson disease.

Iglesias E, Pesini A, Garrido-Pérez N, Meade P, Bayona-Bafaluy MP, Montoya J, Ruiz-Pesini E. Iglesias E, et al. Ageing Res Rev. 2018 Aug;45:24-32. doi: 10.1016/j.arr.2018.04.006. Epub 2018 Apr 22. Ageing Res Rev. 2018. PMID: 29689408 Review.

2

An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA.

Acín-Pérez R, Bayona-Bafaluy MP, Bueno M, Machicado C, Fernández-Silva P, Pérez-Martos A, Montoya J, López-Pérez MJ, Sancho J, Enríquez JA. Acín-Pérez R, et al. Hum Mol Genet. 2003 Feb 1;12(3):329-39. doi: 10.1093/hmg/ddg021. Hum Mol Genet. 2003. PMID: 12554686

3

Maternally inherited susceptibility to cancer.

Bayona-Bafaluy MP, López-Gallardo E, Montoya J, Ruiz-Pesini E. Bayona-Bafaluy MP, et al. Biochim Biophys Acta. 2011 Jun;1807(6):643-9. doi: 10.1016/j.bbabio.2010.08.004. Epub 2010 Aug 21. Biochim Biophys Acta. 2011. PMID: 20732295 Free article. Review.

4

OXPHOS, pyrimidine nucleotides, and Alzheimer's disease: a pharmacogenomics approach.

Pesini A, Iglesias E, Garrido N, Bayona-Bafaluy MP, Montoya J, Ruiz-Pesini E. Pesini A, et al. J Alzheimers Dis. 2014;42(1):87-96. doi: 10.3233/JAD-140384. J Alzheimers Dis. 2014. PMID: 25024340

5

An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.

Emperador S, Pacheu-Grau D, Bayona-Bafaluy MP, Garrido-Pérez N, Martín-Navarro A, López-Pérez MJ, Montoya J, Ruiz-Pesini E. Emperador S, et al. Front Genet. 2015 Jan 14;5:469. doi: 10.3389/fgene.2014.00469. eCollection 2014. Front Genet. 2015. PMID: 25642242 Free PMC article.

6

Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy.

Emperador S, Bayona-Bafaluy MP, Fernández-Marmiesse A, Pineda M, Felgueroso B, López-Gallardo E, Artuch R, Roca I, Ruiz-Pesini E, Couce ML, Montoya J. Emperador S, et al. Eur J Hum Genet. 2016 Jan;25(1):153-156. doi: 10.1038/ejhg.2016.124. Epub 2016 Sep 28. Eur J Hum Genet. 2016. PMID: 27677415 Free PMC article.

7

Pharmacologic concentrations of linezolid modify oxidative phosphorylation function and adipocyte secretome.

Llobet L, Bayona-Bafaluy MP, Pacheu-Grau D, Torres-Pérez E, Arbones-Mainar JM, Navarro MÁ, Gómez-Díaz C, Montoya J, López-Gallardo E, Ruiz-Pesini E. Llobet L, et al. Redox Biol. 2017 Oct;13:244-254. doi: 10.1016/j.redox.2017.05.026. Epub 2017 May 31. Redox Biol. 2017. PMID: 28600981 Free PMC article.

8

The Decrease in Mitochondrial DNA Mutation Load Parallels Visual Recovery in a Leber Hereditary Optic Neuropathy Patient.

Emperador S, Vidal M, Hernández-Ainsa C, Ruiz-Ruiz C, Woods D, Morales-Becerra A, Arruga J, Artuch R, López-Gallardo E, Bayona-Bafaluy MP, Montoya J, Ruiz-Pesini E. Emperador S, et al. Front Neurosci. 2018 Feb 9;12:61. doi: 10.3389/fnins.2018.00061. eCollection 2018. Front Neurosci. 2018. PMID: 29479304 Free PMC article.

9

Food derived respiratory complex I inhibitors modify the effect of Leber hereditary optic neuropathy mutations.

López-Gallardo E, Emperador S, Hernández-Ainsa C, Montoya J, Bayona-Bafaluy MP, Ruiz-Pesini E. López-Gallardo E, et al. Food Chem Toxicol. 2018 Oct;120:89-97. doi: 10.1016/j.fct.2018.07.014. Epub 2018 Jul 6. Food Chem Toxicol. 2018. PMID: 29991444

10

Mutations in the mitochondrial complex I assembly factor NDUFAF6 cause isolated bilateral striatal necrosis and progressive dystonia in childhood.

Baide-Mairena H, Gaudó P, Marti-Sánchez L, Emperador S, Sánchez-Montanez A, Alonso-Luengo O, Correa M, Grau AM, Ortigoza-Escobar JD, Artuch R, Vázquez E, Del Toro M, Garrido-Pérez N, Ruiz-Pesini E, Montoya J, Bayona-Bafaluy MP, Pérez-Dueñas B. Baide-Mairena H, et al. Mol Genet Metab. 2019 Mar;126(3):250-258. doi: 10.1016/j.ymgme.2019.01.001. Epub 2019 Jan 5. Mol Genet Metab. 2019. PMID: 30642748 Review.

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