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Year Number of Results
1999 1
2014 1
2015 1
2018 1
2019 5
2020 3
2021 1
2023 1
2024 1

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Page 1
Oxidative Phosphorylation Dysfunction Modifies the Cell Secretome.
Garrido-Pérez N, Vela-Sebastián A, López-Gallardo E, Emperador S, Iglesias E, Meade P, Jiménez-Mallebrera C, Montoya J, Bayona-Bafaluy MP, Ruiz-Pesini E. Garrido-Pérez N, et al. Int J Mol Sci. 2020 May 10;21(9):3374. doi: 10.3390/ijms21093374. Int J Mol Sci. 2020. PMID: 32397676 Free PMC article. Review.
Down syndrome is an oxidative phosphorylation disorder.
Bayona-Bafaluy MP, Garrido-Pérez N, Meade P, Iglesias E, Jiménez-Salvador I, Montoya J, Martínez-Cué C, Ruiz-Pesini E. Bayona-Bafaluy MP, et al. Among authors: garrido perez n. Redox Biol. 2021 May;41:101871. doi: 10.1016/j.redox.2021.101871. Epub 2021 Jan 22. Redox Biol. 2021. PMID: 33540295 Free PMC article.
Infectious stress triggers a POLG-related mitochondrial disease.
Gaudó P, Emperador S, Garrido-Pérez N, Ruiz-Pesini E, Yubero D, García-Cazorla A, Artuch R, Montoya J, Bayona-Bafaluy MP. Gaudó P, et al. Among authors: garrido perez n. Neurogenetics. 2020 Jan;21(1):19-27. doi: 10.1007/s10048-019-00593-2. Epub 2019 Oct 26. Neurogenetics. 2020. PMID: 31655921
Brain pyrimidine nucleotide synthesis and Alzheimer disease.
Pesini A, Iglesias E, Bayona-Bafaluy MP, Garrido-Pérez N, Meade P, Gaudó P, Jiménez-Salvador I, Andrés-Benito P, Montoya J, Ferrer I, Pesini P, Ruiz-Pesini E. Pesini A, et al. Among authors: garrido perez n. Aging (Albany NY). 2019 Sep 27;11(19):8433-8462. doi: 10.18632/aging.102328. Epub 2019 Sep 27. Aging (Albany NY). 2019. PMID: 31560653 Free PMC article.
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. Among authors: garrido perez n. 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.
"ATAD3C regulates ATAD3A assembly and function in the mitochondrial membrane".
Gaudó P, de Tomás-Mateo E, Garrido-Pérez N, Santana A, Ruiz-Pesini E, Montoya J, Bayona-Bafaluy P. Gaudó P, et al. Among authors: garrido perez n. Free Radic Biol Med. 2024 Feb 1;211:114-126. doi: 10.1016/j.freeradbiomed.2023.12.006. Epub 2023 Dec 12. Free Radic Biol Med. 2024. PMID: 38092275 Free article.
Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome.
Emperador S, Garrido-Pérez N, Amezcua-Gil J, Gaudó P, Andrés-Sanz JA, Yubero D, Fernández-Marmiesse A, O'Callaghan MM, Ortigoza-Escobar JD, Iriondo M, Ruiz-Pesini E, García-Cazorla A, Gil-Campos M, Artuch R, Montoya J, Bayona-Bafaluy MP. Emperador S, et al. Among authors: garrido perez n. Front Genet. 2020 Jan 8;10:1300. doi: 10.3389/fgene.2019.01300. eCollection 2019. Front Genet. 2020. PMID: 31969900 Free PMC article.
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. Among authors: garrido perez n. Front Genet. 2015 Jan 14;5:469. doi: 10.3389/fgene.2014.00469. eCollection 2014. Front Genet. 2015. PMID: 25642242 Free PMC article.
11 results