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

Year Number of Results
1990 1
2003 2
2006 5
2007 1
2008 2
2009 4
2010 6
2011 7
2012 6
2013 3
2014 4
2015 5
2016 5
2017 2
2018 5
2019 2
2020 3
2022 7
2024 1

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67 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.
Pathological Features in Paediatric Patients with TK2 Deficiency.
Jou C, Nascimento A, Codina A, Montoya J, López-Gallardo E, Emperador S, Ruiz-Pesini E, Montero R, Natera-de Benito D, Ortez CI, Marquez J, Zelaya MV, Gutierrez-Mata A, Badosa C, Carrera-García L, Expósito-Escudero J, Roldán M, Camara Y, Marti R, Ferrer I, Jimenez-Mallebrera C, Artuch R. Jou C, et al. Among authors: lopez gallardo e. Int J Mol Sci. 2022 Sep 20;23(19):11002. doi: 10.3390/ijms231911002. Int J Mol Sci. 2022. PMID: 36232299 Free PMC article.
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.
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.
Palmitic acid control of ciliogenesis modulates insulin signaling in hypothalamic neurons through an autophagy-dependent mechanism.
Ávalos Y, Hernández-Cáceres MP, Lagos P, Pinto-Nuñez D, Rivera P, Burgos P, Díaz-Castro F, Joy-Immediato M, Venegas-Zamora L, Lopez-Gallardo E, Kretschmar C, Batista-Gonzalez A, Cifuentes-Araneda F, Toledo-Valenzuela L, Rodriguez-Peña M, Espinoza-Caicedo J, Perez-Leighton C, Bertocchi C, Cerda M, Troncoso R, Parra V, Budini M, Burgos PV, Criollo A, Morselli E. Ávalos Y, et al. Among authors: lopez gallardo e. Cell Death Dis. 2022 Jul 28;13(7):659. doi: 10.1038/s41419-022-05109-9. Cell Death Dis. 2022. PMID: 35902579 Free PMC article.
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.
Mitochondrial E3 ubiquitin ligase 1 (MUL1) as a novel therapeutic target for diseases associated with mitochondrial dysfunction.
Calle X, Garrido-Moreno V, Lopez-Gallardo E, Norambuena-Soto I, Martínez D, Peñaloza-Otárola A, Troncossi A, Guerrero-Moncayo A, Ortega A, Maracaja-Coutinho V, Parra V, Chiong M, Lavandero S. Calle X, et al. Among authors: lopez gallardo e. IUBMB Life. 2022 Sep;74(9):850-865. doi: 10.1002/iub.2657. Epub 2022 Jun 21. IUBMB Life. 2022. PMID: 35638168 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
67 results