Julio Montoya
Affiliations: | University of Zaragoza, Zaragoza, Aragón, Spain |
Area:
Mitochondrial biogenesisGoogle:
"Julio Montoya"
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Publications
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| Habbane M, Montoya J, Rhouda T, et al. (2021) Human Mitochondrial DNA: Particularities and Diseases. Biomedicines. 9 |
| Yousefi R, Fornasiero EF, Cyganek L, et al. (2021) Monitoring mitochondrial translation in living cells. Embo Reports. e51635 |
| López-Gallardo E, Cammarata-Scalisi F, Emperador S, et al. (2020) Mitochondrial DNA Pathogenic Mutations in Multiple Symmetric Lipomatosis. Clinical Genetics |
| Saldaña-Martínez A, Muñoz ML, Pérez-Ramírez G, et al. (2018) Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants. Gene. 688: 171-181 |
| Pacheu-Grau D, Callegari S, Emperador S, et al. (2018) Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy. Human Molecular Genetics. 27: 4135-4144 |
| Moncada PA, Budvytiene I, Ho DY, et al. (2013) Utility of DNA sequencing for direct identification of invasive fungi from fresh and formalin-fixed specimens. American Journal of Clinical Pathology. 140: 203-8 |
| Montiel-Sosa JF, Herrero MD, Munoz Mde L, et al. (2013) Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion. Mitochondrial Dna. 24: 420-31 |
| Pacheu-Grau D, Gómez-Durán A, Iglesias E, et al. (2013) Mitochondrial antibiograms in personalized medicine. Human Molecular Genetics. 22: 1132-9 |
| Gómez-Durán A, Pacheu-Grau D, Martínez-Romero I, et al. (2012) Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Biochimica Et Biophysica Acta. 1822: 1216-22 |
| Rubio-Cosials A, Sidow JF, Jiménez-Menéndez N, et al. (2011) Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter. Nature Structural & Molecular Biology. 18: 1281-9 |