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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 2
2008 2
2009 3
2010 6
2011 5
2012 5
2013 2
2014 3
2015 5
2016 5
2017 2
2018 5
2019 2
2020 3
2021 1
2022 1
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48 results
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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. Among authors: lopez gallardo e. 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.
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy.
Bayona-Bafaluy MP, Iglesias E, López-Gallardo E, Emperador S, Pacheu-Grau D, Labarta L, Montoya J, Ruiz-Pesini E. Bayona-Bafaluy MP, et al. Among authors: lopez gallardo e. Mutat Res Rev Mutat Res. 2020 Oct-Dec;786:108334. doi: 10.1016/j.mrrev.2020.108334. Epub 2020 Aug 25. Mutat Res Rev Mutat Res. 2020. PMID: 33339579 Review.
OXPHOS toxicogenomics and Parkinson's disease.
López-Gallardo E, Iceta R, Iglesias E, Montoya J, Ruiz-Pesini E. López-Gallardo E, et al. Mutat Res. 2011 Nov-Dec;728(3):98-106. doi: 10.1016/j.mrrev.2011.06.004. Epub 2011 Jul 8. Mutat Res. 2011. PMID: 21763451 Review.
Maternally inherited susceptibility to cancer.
Bayona-Bafaluy MP, López-Gallardo E, Montoya J, Ruiz-Pesini E. Bayona-Bafaluy MP, et al. Among authors: lopez gallardo e. 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.
Diseases of the human mitochondrial oxidative phosphorylation system.
Montoya J, López-Gallardo E, Herrero-Martín MD, Martínez-Romero I, Gómez-Durán A, Pacheu D, Carreras M, Díez-Sánchez C, López-Pérez MJ, Ruiz-Pesini E. Montoya J, et al. Among authors: lopez gallardo e. Adv Exp Med Biol. 2009;652:47-67. doi: 10.1007/978-90-481-2813-6_5. Adv Exp Med Biol. 2009. PMID: 20225019 Review.
Mitochondrial DNA pathogenic mutations in multiple symmetric lipomatosis.
López-Gallardo E, Cammarata-Scalisi F, Emperador S, Hernández-Ainsa C, Habbane M, Vela-Sebastián A, Bayona-Bafaluy MP, Montoya J, Ruiz-Pesini E. López-Gallardo E, et al. Clin Genet. 2020 May;97(5):731-735. doi: 10.1111/cge.13701. Epub 2020 Jan 9. Clin Genet. 2020. PMID: 31912494
Ndufs4 related Leigh syndrome: A case report and review of the literature.
Ortigoza-Escobar JD, Oyarzabal A, Montero R, Artuch R, Jou C, Jiménez C, Gort L, Briones P, Muchart J, López-Gallardo E, Emperador S, Pesini ER, Montoya J, Pérez B, Rodríguez-Pombo P, Pérez-Dueñas B. Ortigoza-Escobar JD, et al. Among authors: lopez gallardo e. Mitochondrion. 2016 May;28:73-8. doi: 10.1016/j.mito.2016.04.001. Epub 2016 Apr 11. Mitochondrion. 2016. PMID: 27079373 Review.
Increasing mtDNA levels as therapy for mitochondrial optic neuropathies.
Ruiz-Pesini E, Emperador S, López-Gallardo E, Hernández-Ainsa C, Montoya J. Ruiz-Pesini E, et al. Among authors: lopez gallardo e. Drug Discov Today. 2018 Mar;23(3):493-498. doi: 10.1016/j.drudis.2018.01.031. Epub 2018 Jan 11. Drug Discov Today. 2018. PMID: 29337205
Mitochondrial antibiograms in personalized medicine.
Pacheu-Grau D, Gómez-Durán A, Iglesias E, López-Gallardo E, Montoya J, Ruiz-Pesini E. Pacheu-Grau D, et al. Among authors: lopez gallardo e. Hum Mol Genet. 2013 Mar 15;22(6):1132-9. doi: 10.1093/hmg/dds517. Epub 2012 Dec 7. Hum Mol Genet. 2013. PMID: 23223015
48 results