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Julio Montoya

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Chemicals & Drugs

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Aleix Navarro-Sastre; Mónica Ruiz Pons; Frederic Tort; Maria Unceta; Maria Eugenia Yoldi; Paz Briones; Jaume Campistol; Jaume Colomer; Judit Garcia-Villoria; Ester López-Gallardo; Maria Jesús Martinez; Julio Montoya; Andrés Nascimento; Antonia Ribes
Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients.
David Pacheu-Grau; Aurora Gómez-Durán; Ester López-Gallardo; Julio Montoya; Eduardo Ruiz-Pesini
Read-through therapy for mitochondrial DNA nonsense mutations.
David Pacheu-Grau; Laura Pérez-Delgado; Jesus Fraile-Rodrigo; Covadonga Gómez-Díaz; Julio Montoya; Eduardo Ruiz-Pesini
Mitochondrial ribosome and Ménière's disease: a pilot study.

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All Publications

2012: Aleix Navarro-Sastre; Mónica Ruiz Pons; Frederic Tort; Maria Unceta; Maria Eugenia Yoldi; Paz Briones; Jaume Campistol; Jaume Colomer; Judit Garcia-Villoria; Ester López-Gallardo; Maria Jesús Martinez; Julio Montoya; Andrés Nascimento; Antonia Ribes
Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients.
Molecular genetics and metabolism 2012;107(3):409-15.
2012: David Pacheu-Grau; Aurora Gómez-Durán; Ester López-Gallardo; Julio Montoya; Eduardo Ruiz-Pesini
Read-through therapy for mitochondrial DNA nonsense mutations.
Drug discovery today 2012;17(19-20):1063-7.
2012: David Pacheu-Grau; Laura Pérez-Delgado; Jesus Fraile-Rodrigo; Covadonga Gómez-Díaz; Julio Montoya; Eduardo Ruiz-Pesini
Mitochondrial ribosome and Ménière's disease: a pilot study.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2012;269(8):2003-8.
2012: María del Mar O'Callaghan; Sonia Emperador; Isidre Ferrer; Angels Garcia-Cazorla; Diana Gonzaga; Cristina Jou; Ester López-Gallardo; Raquel Montero; Rafael Artuch; Paz Briones; Nuria Buján; Mercè Pineda; Eduardo Ruiz-Pesini; Julio Montoya
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.
Neurogenetics 2012;13(3):245-50.
2012: Aurora Gómez-Durán; Ester López-Gallardo; Manuel J López-Pérez; Iñigo Martínez-Romero; Julio Montoya; David Pacheu-Grau; Eduardo Ruiz-Pesini
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy.
Biochimica et biophysica acta 2012;1822(8):1216-22.
2011: David Pacheu-Grau; Tomàs Pinós; Antoni L Andreu; Aurora Gómez-Durán; Ester López-Gallardo; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
'Progress' renders detrimental an ancient mitochondrial DNA genetic variant.
Human molecular genetics 2011;20(21):4224-31.
2011: Ester López-Gallardo; Julio Montoya; Ruth Iceta; Eldris Iglesias; Eduardo Ruiz-Pesini
OXPHOS toxicogenomics and Parkinson's disease.
Mutation research 2011;728(3):98-106.
2011: Mireia Tondo; Sonia Emperador; Angels Garcia-Cazorla; Maria T Garcia-Silva; Ignácio Málaga; Elena Martin-Hernandez; Julio Montoya; Mar O'Callaghan; Aida Ormazabal; Merce Pineda; Eduardo Ruiz-Pesini; Mercedes Serrano; Rafael Artuch
Biochemical parameters to assess choroid plexus dysfunction in Kearns-Sayre syndrome patients.
Mitochondrion 2011;11(6):867-70.
2011: Francisco Cammarata-Scalisi; Gloria Da Silva; Sonia Emperador; Ester López-Gallardo; Nolis Camacho; Eduardo Ruiz-Pesini; Julio Montoya
[Pearson syndrome. Case report].
Investigación clínica 2011;52(3):261-7.
2011: María Pilar Bayona-Bafaluy; Ester López-Gallardo; Julio Montoya; Eduardo Ruiz-Pesini
Maternally inherited susceptibility to cancer.
Biochimica et biophysica acta 2011;1807(6):643-9.
2011: Aurora Gómez-Durán; David Pacheu-Grau; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
Mitochondrial pharma-Q-genomics: targeting the OXPHOS cytochrome b.
Drug discovery today 2011;16(5-6):176-80.
2011: Roberto Blanco; Elvira Mayordomo; Julio Montoya; Eduardo Ruiz-Pesini
Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge.
BMC bioinformatics 2011;12():174.
2011: Erika Fernández-Vizarra; José Antonio Enríquez; Acisclo Pérez-Martos; Julio Montoya; Patricio Fernández-Silva
Tissue-specific differences in mitochondrial activity and biogenesis.
Mitochondrion 2011;11(1):207-13.
2010: Francisco J Ascaso; Ester Lopez-Gallardo; Eduardo Del Prado; Eduardo Ruiz-Pesini; Julio Montoya
Macular lesion resembling adult-onset vitelliform macular dystrophy in Kearns-Sayre syndrome with multiple mtDNA deletions.
Clinical & experimental ophthalmology 2010;38(8):812-6.
2010: José Guevara-Campos; Lucía González-Guevara; Paz Briones; Ester López-Gallardo; Nuria Bulán; Eduardo Ruiz-Pesini; Denisse Ramnarine; Julio Montoya
Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain.
Investigación clínica 2010;51(3):423-31.
2010: David Pacheu-Grau; Aurora Gómez-Durán; Julio Montoya; Eduardo Ruiz-Pesini
Influence of mtDNA genetic variation on antibiotic therapy.
Pharmacogenomics 2010;11(9):1185-7.
2010: Aurora Gómez-Durán; David Pacheu-Grau; Ester López-Gallardo; Carmen Díez-Sánchez; Julio Montoya; Manuel J López-Pérez; Eduardo Ruiz-Pesini
Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.
Human molecular genetics 2010;19(17):3343-53.
2010: Ramon Martí; Andrés Nascimento; Jaume Colomer; Maria Carmen Lara; Ester López-Gallardo; Eduardo Ruiz-Pesini; Julio Montoya; Antoni L Andreu; Paz Briones; Mercè Pineda
Hearing loss in a patient with the myopathic form of mitochondrial DNA depletion syndrome and a novel mutation in the TK2 gene.
Pediatric research 2010;68(2):151-4.
2010: Mercedes Serrano; María Teresa García-Silva; Elena Martin-Hernandez; Maria del Mar O'Callaghan; Pilar Quijada; Ana Martinez-Aragón; Aida Ormazábal; Alberto Blázquez; Miguel A Martín; Paz Briones; Ester López-Gallardo; Eduardo Ruiz-Pesini; Julio Montoya; Rafael Artuch; Mercedes Pineda
Kearns-Sayre syndrome: cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features.
Mitochondrion 2010;10(5):429-32.
2010: Maria Dolores Herrero-Martín; Teresa Ayuso; Maria Teresa Tuñón; Miguel Angel Martín; Eduardo Ruiz-Pesini; Julio Montoya
A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation.
Journal of neurology, neurosurgery, and psychiatry 2010;81(4):471-2.
2010: Diana Martínez-Redondo; Ana Marcuello; José A Casajús; Ignacio Ara; Yahya Dahmani; Julio Montoya; Eduardo Ruiz-Pesini; Manuel J López-Pérez; Carmen Díez-Sánchez
Human mitochondrial haplogroup H: the highest VO2max consumer--is it a paradox?
Mitochondrion 2010;10(2):102-7.
2010: David Pacheu-Grau; Aurora Gómez-Durán; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
Mitochondrial pharmacogenomics: barcode for antibiotic therapy.
Drug discovery today 2010;15(1-2):33-9.
2009: Taha Rhouda; Diana Martínez-Redondo; Aurora Gómez-Durán; Noureddine Elmtili; Mouhamed Idaomar; Carmen Díez-Sánchez; Julio Montoya; Manuel J López-Pérez; Eduardo Ruiz-Pesini
Moroccan mitochondrial genetic background suggests prehistoric human migrations across the Gibraltar Strait.
Mitochondrion 2009;9(6):402-7.
2009: Ana Marcuello; Diana Martínez-Redondo; Yahya Dahmani; José L Terreros; Teresa Aragonés; José A Casajús; José M Echavarri; Julia Quílez; Julio Montoya; Manuel J López-Pérez; Carmen Díez-Sánchez
Steady exercise removes VO(2max) difference between mitochondrial genomic variants.
Mitochondrion 2009;9(5):326-30.
2009: Ester López-Gallardo; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
CPEO and KSS differ in the percentage and location of the mtDNA deletion.
Mitochondrion 2009;9(5):314-7.
2009: Elena Domínguez-Garrido; Diana Martínez-Redondo; Carmen Martín-Ruiz; Aurora Gómez-Durán; Eduardo Ruiz-Pesini; Pilar Madero; Manuel Tamparillas; Julio Montoya; Thomas von Zglinicki; Carmen Díez-Sánchez; Manuel J López-Pérez
Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations.
Biogerontology 2009;10(4):435-42.
2009: Julio Montoya; Ester López-Gallardo; Carmen Díez-Sánchez; Manuel J López-Pérez; Eduardo Ruiz-Pesini
20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria.
Biochimica et biophysica acta 2009;1787(5):476-83.
2009: Ana Marcuello; Diana Martínez-Redondo; Yahya Dahmani; José A Casajús; Eduardo Ruiz-Pesini; Julio Montoya; Manuel J López-Pérez; Carmen Díez-Sánchez
Human mitochondrial variants influence on oxygen consumption.
Mitochondrion 2009;9(1):27-30.
2009: Julio Montoya; Ester López-Gallardo; María Dolores Herrero-Martín; Iñigo Martínez-Romero; Aurora Gómez-Durán; David Pacheu; Magdalena Carreras; Carmen Díez-Sánchez; Manuel J López-Pérez; Eduardo Ruiz-Pesini
Diseases of the human mitochondrial oxidative phosphorylation system.
Advances in experimental medicine and biology 2009;652():47-67.
2009: Ester López-Gallardo; Abelardo Solano; M D Herrero-Martín; I Martínez-Romero; M D Castaño-Pérez; Antoni L Andreu; Antonio Herrera; M J López-Pérez; Eduardo Ruiz-Pesini; Julio Montoya
NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein.
Journal of medical genetics 2009;46(1):64-7.
2008: Julio Montoya
[Giuseppe Attardi: mitochondrial genetic system and its influence in the study of the mitochondrial diseases].
Revista de neurologia 2008;47(9):483-7.
2008: Nuria Garrido; Acisclo Pérez-Martos; Mercedes Faro; José Manuel Lou-Bonafonte; Patricio Fernández-Silva; Manuel José López-Pérez; Julio Montoya; José Antonio Enríquez
Cisplatin-mediated impairment of mitochondrial DNA metabolism inversely correlates with glutathione levels.
The Biochemical journal 2008;414(1):93-102.
2008: María D Herrero-Martín; Mercedes Pineda; Paz Briones; Ester López-Gallardo; Magdalena Carreras; Mercedes Benac; Miguel Angel Idoate; Maria Antonia Vilaseca; Rafael Artuch; Manuel J López-Pérez; Eduardo Ruiz-Pesini; Julio Montoya
A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1).
Human mutation 2008;29(8):E112-22.
2008: Erika Fernández-Vizarra; José A Enriquez; Acisclo Pérez-Martos; Julio Montoya; Patricio Fernández-Silva
Mitochondrial gene expression is regulated at multiple levels and differentially in the heart and liver by thyroid hormones.
Current genetics 2008;54(1):13-22.
2008: Angels Garcia-Cazorla; Sofia Duarte; Mercedes Serrano; Andres Nascimento; Aida Ormazabal; Ines Carrilho; Paz Briones; Julio Montoya; Rafael Garesse; Pere Sala-Castellvi; Manuel Pineda; Rafael Artuch
Mitochondrial diseases mimicking neurotransmitter defects.
Mitochondrion 2008;8(3):273-8.
2008: Yahya Dahmani; Ana Marcuello; Carmen Díez-Sanchez; Eduardo Ruiz-Pesini; Julio Montoya; Manuel J López-Pérez
Association of human mitochondrial DNA variants with plasma LDL levels.
Mitochondrion 2008;8(3):247-53.
2008: Angels Garcia-Cazorla; E V Quadros; A Nascimento; M T Garcia-Silva; Paz Briones; Julio Montoya; A Ormazábal; Rafael Artuch; J M Sequeira; N Blau; J Arenas; Manuel Pineda; V T Ramaekers
Mitochondrial diseases associated with cerebral folate deficiency.
Neurology 2008;70(16):1360-2.
2007: Francisco Javier Carod-Artal; MARÍA DOLORES HERRERO MARTÍN; Maria Carmen Lara; Ester López-Gallardo; Eduardo Ruiz-Pesini; Ramon Martí; Julio Montoya
Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007;14(5):581-5.
2007: R Delgado-Sánchez; A Zárate-Moysen; A Monsalvo-Reyes; MARÍA DOLORES HERRERO MARTÍN; Eduardo Ruiz-Pesini; Manuel J López-Pérez; Julio Montoya; J Francisco Montiel-Sosa
[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
Revista de neurologia 2007;44(1):18-22.
2006: Jordi P Guallar; Maya R Vilà; Ester López-Gallardo; Abelardo Solano; Joan Carles Domingo; Josep Gámez; Manuel Pineda; Jose Luis Capablo; Pere Domingo; Antoni L Andreu; Julio Montoya; Marta Giralt; Francesc Villarroya
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA.
Molecular genetics and metabolism 2006;89(3):283-5.
2006: Eduardo Ruiz-Pesini; Ester López-Gallardo; Yahya Dahmani; MARÍA DOLORES HERRERO MARTÍN; Abelardo Solano; Carmen Díez-Sánchez; Manuel J López-Pérez; Julio Montoya
[Diseases of the human mitochondrial oxidative phosphorylation system].
Revista de neurologia 2006;43(7):416-24.
2006: Francisco Javier Carod-Artal; E Lopez Gallardo; Abelardo Solano; Yahya Dahmani; MARÍA DOLORES HERRERO MARTÍN; Julio Montoya
[Mitochondrial DNA deletions in Kearns-Sayre syndrome].
Neurología (Barcelona, Spain) 2006;21(7):357-64.
2006: Julio Montoya; Manuel J López-Pérez; Eduardo Ruiz-Pesini
Mitochondrial DNA transcription and diseases: past, present and future.
Biochimica et biophysica acta 2006;1757(9-10):1179-89.
2006: Francisco Javier Carod-Artal; Ester López-Gallardo; Abelardo Solano; Yahya Dahmani; Eduardo Ruiz-Pesini; Julio Montoya
[Deletions of the mitochondrial DNA associated to chronic progressive external ophthalmoplegia with ragged-red fibers in 2 Brazilian patients].
Medicina clínica 2006;126(12):457-60.
2006: Francisco Montiel-Sosa; Eduardo Ruiz-Pesini; José Antonio Enríquez; Ana Marcuello; Carmen Díez-Sánchez; Julio Montoya; Douglas C Wallace; Manuel J López-Pérez
Differences of sperm motility in mitochondrial DNA haplogroup U sublineages.
Gene 2006;368():21-7.
2006: Manuel Pineda; Aida Ormazabal; Ester López-Gallardo; Andres Nascimento; Abelardo Solano; MARÍA DOLORES HERRERO MARTÍN; Maria Antonia Vilaseca; Paz Briones; Lourdes Ibáñez; Julio Montoya; Rafael Artuch
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion.
Annals of neurology 2006;59(2):394-8.
2005: Ricardo Gonzalo; Elena Garcia-Arumi; David Llige; Ramon Marti; Abelardo Solano; Julio Montoya; Joaquín Arenas; Antoni L Andreu
Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA.
FEBS letters 2005;579(30):6909-13.
2005: Marina Roberti; Patricio Fernandez-Silva; Paola Loguercio Polosa; Erika Fernandez-Vizarra; Francesco Bruni; Stefania Deceglie; Julio Montoya; Maria Nicola Gadaleta; Palmiro Cantatore
In vitro transcription termination activity of the Drosophila mitochondrial DNA-binding protein DmTTF.
Biochemical and biophysical research communications 2005;331(1):357-62.
2005: Raquel Montero; Rafael Artuch; Paz Briones; A Nascimento; Angels García-Cazorla; Maria Antonia Vilaseca; Plácido Navas; Julio Montoya; J A Sánchez-Alcázar; Manuel Pineda
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders.
BioFactors (Oxford, England) 2005;25(1-4):109-15.
2004: M Raspall-Chaure; Abelardo Solano; E Vázquez; A Macaya Ruiz; M del Toro Riera; A Cabezuelo-Briones; Julio Montoya; A Andreu; M Roig Quilis
[A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain].
Revista de neurologia 2004;39(12):1129-32.
2004: Ascensión Prieto-Martín; Julio Montoya; Francisco Martínez-Azorín
New DNA-binding activity of rat mitochondrial transcription termination factor (mTERF).
Journal of biochemistry 2004;136(6):825-30.
2004: Abelardo Solano; Giovanna Russo; Ana Playán; Maria Parisi; Massimo DiPietro; Antonino Scuderi; Maddalena Palumbo; Marcella Renis; Manuel J López-Pérez; Antoni L Andreu; Julio Montoya
De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA.
Pediatric nephrology (Berlin, Germany) 2004;19(7):790-3.
2004: Manuel Pineda; Abelardo Solano; Rafael Artuch; Antoni L Andreu; Ana Playan; Maria Antonia Vilaseca; Jaume Colomer; Paz Briones; Jordi Casademont; Julio Montoya
Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA.
Pediatric research 2004;56(1):55-9.
2004: Manuel Pineda; A Playán Ariso; M J Alcaine-Villarroya; AM Vernet; A Serra-Castanera; Abelardo Solano; Maria Antonia Vilaseca; Rafael Artuch; Manuel J López-Pérez; M P Briones-Godino; A Andreu; Julio Montoya
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].
Revista de neurologia 2004;38(11):1023-7.
2004: Michelangelo Mancuso; Cristofol Vives-Bauza; Massimiliano Filosto; R Marti; Abelardo Solano; Julio Montoya; Josep Gamez; Salvatore DiMauro; Antoni L Andreu
A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome.
Journal of medical genetics 2004;41(6):e73.
2004: Katharina Maniura-Weber; Steffi Goffart; Heike L Garstka; Julio Montoya; Rudolf J Wiesner
Transient overexpression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mtDNA copy number in cultured cells.
Nucleic acids research 2004;32(20):6015-27.
2004: Ascensión Prieto-Martín; Julio Montoya; Francisco Martínez-Azorín
Phosphorylation of rat mitochondrial transcription termination factor (mTERF) is required for transcription termination but not for binding to DNA.
Nucleic acids research 2004;32(7):2059-68.
2003: Francisco Javier Carod-Artal; A Solano-Palacios; A Playán Ariso; I Viana-Brandi; Ester López-Gallardo; A Andreu; Manuel J López-Pérez; Julio Montoya
[A single deletion of mitochondrial DNA in a Brazilian patient with chronic progressive external ophthalmoplegia].
Revista de neurologia 2003;37(11):1029-31.
2003: Carmen Díez-Sánchez; Eduardo Ruiz-Pesini; Julio Montoya; Acisclo Pérez-Martos; José Antonio Enríquez; Manuel J López-Pérez
Mitochondria from ejaculated human spermatozoa do not synthesize proteins.
FEBS letters 2003;553(1-2):205-8.
2003: Abelardo Solano; Manuel Roig; Cristofol Vives-Bauza; Jose Hernandez-Peña; Elena Garcia-Arumi; Ana Playan; Manuel J Lopez-Perez; Antoni L Andreu; Julio Montoya
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene.
Annals of neurology 2003;54(4):527-30.
2003: Heike L Garstka; Wolfgang E Schmitt; Jeanette Schultz; Bettina Sogl; Barbara Silakowski; Acisclo Pérez-Martos; Julio Montoya; Rudolf J Wiesner
Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNA.
Nucleic acids research 2003;31(17):5039-47.
2003: Abelardo Solano; Josep Gámez; F J Carod; Manuel Pineda; Ana Playán; Ester López-Gallardo; Antoni L Andreu; Julio Montoya
Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA.
Journal of medical genetics 2003;40(7):e86.
2003: Rebeca Acín-Pérez; Maria Pilar Bayona-Bafaluy; Marta Bueno; Claudia Machicado; Patricio Fernández-Silva; Acisclo Pérez-Martos; Julio Montoya; Manuel J López-Pérez; javier sancho; José Antonio Enríquez
An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA.
Human molecular genetics 2003;12(3):329-39.
2003: Cristofol Vives-Bauza; Mireia Del Toro; Abelardo Solano; Julio Montoya; Antoni L Andreu; Manuel Roig
Genotype-phenotype correlation in the 5703G>A mutation in the tRNA(ASN) gene of mitochondrial DNA.
Journal of inherited metabolic disease 2003;26(5):507-8.
2003: Patricio Fernández-Silva; José A Enriquez; Julio Montoya
Replication and transcription of mammalian mitochondrial DNA.
Experimental physiology 2003;88(1):41-56.
2003: Carmen Díez-Sánchez; Eduardo Ruiz-Pesini; Ana Cristina Lapeña; Julio Montoya; Acisclo Pérez-Martos; José Antonio Enríquez; Manuel J López-Pérez
Mitochondrial DNA content of human spermatozoa.
Biology of reproduction 2003;68(1):180-5.
2003: Kurenai Tanji; Josep Gamez; Carlos Cervera; Fermín Mearin; Arantxa Ortega; Javier de la Torre; Julio Montoya; Antoni L Andreu; Salvatore DiMauro; Eduardo Bonilla
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction.
Acta neuropathologica 2003;105(1):69-75.
2002: Ana Playán; A Solano-Palacios; JB González de la Rosa; JM Merino Arribas; Antoni L Andreu; Manuel J López-Pérez; Julio Montoya
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)].
Revista de neurologia 2002;34(12):1124-6.
2001: P Fernandez-Silva; Paola Loguercio Polosa; Marina Roberti; Barbara Di Ponzio; Maria Nicola Gadaleta; Julio Montoya; Palmiro Cantatore
Sea urchin mtDBP is a two-faced transcription termination factor with a biased polarity depending on the RNA polymerase.
Nucleic acids research 2001;29(22):4736-43.
2001: Cristofol Vives-Bauza; Josep Gamez; Manuel Roig; Paz Briones; Carlos Cervera; Abelardo Solano; Julio Montoya; Antoni L Andreu
Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene.
Annals of medicine 2001;33(7):493-6.
2001: S Gensler; K Weber; W E Schmitt; Acisclo Pérez-Martos; José A Enriquez; Julio Montoya; Rudolf J Wiesner
Mechanism of mammalian mitochondrial DNA replication: import of mitochondrial transcription factor A into isolated mitochondria stimulates 7S DNA synthesis.
Nucleic acids research 2001;29(17):3657-63.
2001: Ascensión Prieto-Martín; Julio Montoya; Francisco Martínez-Azorín
A study on the human mitochondrial RNA polymerase activity points to existence of a transcription factor B-like protein.
FEBS letters 2001;503(1):51-5.
2001: Abelardo Solano; Ana Playán; Manuel J López-Pérez; Julio Montoya
[Genetic diseases of the mitochondrial DNA in humans].
Salud pública de México 2001;43(2):151-61.
2000: Maya R Vilà; Josep Gámez; Abelardo Solano; Ana Playán; Simón Schwartz; F M Santorelli; Carlos Cervera; C Casali; Julio Montoya; Francesc Villarroya
Uncoupling protein-1 mRNA expression in lipomas from patients bearing pathogenic mitochondrial DNA mutations.
Biochemical and biophysical research communications 2000;278(3):800-2.
2000: L Coelho-Miranda; Ana Playan; Rafael Artuch; Maria Antonia Vilaseca; Jaume Colomer; Paz Briones; J Coll-Cantí; Joan Conill; Anna Sans; A López de Munain; Abelardo Solano; MJ Alcaine; Julio Montoya; Manuel Pineda
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].
Revista de neurologia 2000;31(9):804-11.
2000: J Asín; Acisclo Pérez-Martos; Patricio Fernández-Silva; Julio Montoya; Antoni L Andreu
Iron(II) induces changes in the conformation of mammalian mitochondrial DNA resulting in a reduction of its transcriptional rate.
FEBS letters 2000;480(2-3):161-4.
2000: Eduardo Ruiz-Pesini; Ana Cristina Lapeña; Carmen Díez-Sánchez; Acisclo Pérez-Martos; Julio Montoya; E Alvarez; M Díaz; A Urriés; L Montoro; Manuel J López-Pérez; José Antonio Enríquez
Human mtDNA haplogroups associated with high or reduced spermatozoa motility.
American journal of human genetics 2000;67(3):682-96.
2000: Julio Montoya; Ana Playán; Abelardo Solano; MJ Alcaine; Manuel J López-Pérez; Acisclo Pérez-Martos
[Diseases of mitochondrial DNA].
Revista de neurologia 2000;31(4):324-33.
2000: Rafael Artuch; Catrina Colomé; Ana Playán; MJ Alcaine; Paz Briones; Julio Montoya; Maria Antonia Vilaseca; Manuel Pineda
Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases.
Clinical biochemistry 2000;33(6):481-5.
2000: J Francisco Montiel-Sosa; Eduardo Ruiz-Pesini; Julio Montoya; Pedro Roncalés; Manuel J López-Pérez; Acisclo Pérez-Martos
Direct and highly species-specific detection of pork meat and fat in meat products by PCR amplification of mitochondrial DNA.
Journal of agricultural and food chemistry 2000;48(7):2829-32.
2000: Jaume Colomer; C Iturriaga; M Bestué; Rafael Artuch; Paz Briones; Julio Montoya; Maria Antonia Vilaseca; Manuel Pineda
[Aspects of neuropathy in mitochondrial diseases].
Revista de neurologia 2000;30(12):1117-21.
2000: M Rodríguez-Hernández; M Hirano; T Arrieta; Z Lestayo; R Estrada; R Santiesteban; R Guerra-Badía; J Galarraga; J Gutierres; E Hechevarría; A Andreu; Julio Montoya; S DiMauro
[Molecular studies in Cuban patients with progressive external ophthalmoplegia].
Revista de neurologia 2000;30(11):1001-5.
2000: Julio Montoya; Ana Playán; MJ Alcaine; Abelardo Solano; Patricio Fernández-Silva; José Antonio Enríquez
[Recent advances in genetics of epilepsy. Genetic of mitochondrial epilepsy].
Revista de neurologia 2000;30(4):330-2.
2000: Isabel Lorda-Sanchez; P J Garcia-Ruiz; Marta Rodriguez de Alba; Julio Montoya; Ana Playan; J L Sarasa; Maria Jose Trujillo; Raul Sanz; Carmen Ramos; Carmen Ayuso
A MELAS phenotype and a paternal inherited inversion of chromosome 10 in a female patient.
Genetic counseling (Geneva, Switzerland) 2000;11(3):261-5.
1999: José Antonio Enríquez; P Fernández-Sílva; Julio Montoya
Autonomous regulation in mammalian mitochondrial DNA transcription.
Biological chemistry 1999;380(7-8):737-47.
1999: José Antonio Enríquez; Patricio Fernández-Silva; N Garrido-Pérez; Manuel J López-Pérez; Acisclo Pérez-Martos; Julio Montoya
Direct regulation of mitochondrial RNA synthesis by thyroid hormone.
Molecular and cellular biology 1999;19(1):657-70.
1998: J A Rábano; Ana Playan; F Guirado; Julio Montoya; A Baldellou; J López Pisón
[Acute presentation of leukodystrophy due to mitochondrial cytopathology and multiple deletions of mitochondrial DNA].
Revista de neurologia 1998;27(160):1005-7.
1998: Antoni L Andreu; MA Arbos; A Perez-Martos; M J Lopez-Perez; J Asin; N Lopez; Julio Montoya; Simón Schwartz
Reduced mitochondrial DNA transcription in senescent rat heart.
Biochemical and biophysical research communications 1998;252(3):577-81.
1998: Eduardo Ruiz-Pesini; C Diez; Ana Cristina Lapeña; Acisclo Pérez-Martos; Julio Montoya; E Alvarez; Joaquín Arenas; Manuel J López-Pérez
Correlation of sperm motility with mitochondrial enzymatic activities.
Clinical chemistry 1998;44(8 Pt 1):1616-20.
1998: Josep Gámez; Ana Playán; Antoni L Andreu; Claudio Bruno; Carmen Navarro; Carlos Cervera; M A Arbós; Simón Schwartz; José A Enriquez; Julio Montoya
Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA.
Neurology 1998;51(1):258-60.
1998: Belén Bornstein; José Antonio Enríquez; Julio Montoya; Rafael Garesse
[Studies of pathogenicity and characterization of molecular phenotype caused by mutations in human mitochondrial DNA].
Revista de neurologia 1998;26 Suppl 1():S36-43.
1998: José Antonio Enríquez; Francisco Martínez-Azorín; Rafael Garesse; Manuel J López-Pérez; Acisclo Pérez-Martos; Belén Bornstein; Julio Montoya
[Human mitochondrial genetic system].
Revista de neurologia 1998;26 Suppl 1():S21-6.
1998: Rafael Artuch; C Pavía; Ana Playán; Maria Antonia Vilaseca; Jaume Colomer; Carme Valls; M Rissech; M A González; A Pou; Paz Briones; Julio Montoya; Manuel Pineda
Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome.
Hormone research 1998;50(2):99-104.
1997: Julio Montoya; A Perez-Martos; Heike L Garstka; Rudolf J Wiesner
Regulation of mitochondrial transcription by mitochondrial transcription factor A.
Molecular and cellular biochemistry 1997;174(1-2):227-30.
1996: L K Ostronoff; José M Izquierdo; José Antonio Enríquez; Julio Montoya; José M Cuezva
Transient activation of mitochondrial translation regulates the expression of the mitochondrial genome during mammalian mitochondrial differentiation.
The Biochemical journal 1996;316 ( Pt 1)():183-91.
1996: José Antonio Enríquez; P Fernández-Silva; Acisclo Pérez-Martos; Manuel J López-Pérez; Julio Montoya
The synthesis of mRNA in isolated mitochondria can be maintained for several hours and is inhibited by high levels of ATP.
European journal of biochemistry / FEBS 1996;237(3):601-10.
1996: José Antonio Enríquez; Acisclo Pérez-Martos; Manuel J López-Pérez; Julio Montoya
In organello RNA synthesis system from mammalian liver and brain.
Methods in enzymology 1996;264():50-7.
1995: Susana Gamen; Alberto Anel; Julio Montoya; I Marzo; Andrés Piñeiro; Javier Naval
mtDNA-depleted U937 cells are sensitive to TNF and Fas-mediated cytotoxicity.
FEBS letters 1995;376(1-2):15-8.
1995: R Zardoya; M Villalta; Manuel J López-Pérez; Amando Garrido-Pertierra; Julio Montoya; José M Bautista
Nucleotide sequence of the sheep mitochondrial DNA D-loop and its flanking tRNA genes.
Current genetics 1995;28(1):94-6.
1995: R Zardoya; Acisclo Pérez-Martos; José M Bautista; Julio Montoya
Analysis of the transcription products of the rainbow trout (Oncorynchus mykiss) liver mitochondrial genome: detection of novel mitochondrial transcripts.
Current genetics 1995;28(1):67-70.
1994: Jordi Casademont; Antoni Barrientos; F Cardellach; A Rötig; Josep M Grau; Julio Montoya; B Beltrán; F Cervantes; Ciril Rozman; Xavier Estivill
Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother.
Human molecular genetics 1994;3(11):1945-9.
1994: José Antonio Enríquez; J Ramos; Acisclo Pérez-Martos; Manuel J López-Pérez; Julio Montoya
Highly efficient DNA synthesis in isolated mitochondria from rat liver.
Nucleic acids research 1994;22(10):1861-5.
1993: José Antonio Enríquez; Acisclo Pérez-Martos; P Fernández-Silva; Manuel J López-Pérez; Julio Montoya
RNA synthesis in isolated mitochondria from brain cortex, cerebellum and stem: evidence of different transcriptional rates.
The International journal of biochemistry 1993;25(12):1951-6.
1992: José Antonio Enríquez; Acisclo Pérez-Martos; P Fernández-Silva; Manuel J López-Pérez; Julio Montoya
Specific increase of a mitochondrial RNA transcript in chronic ethanol-fed rats.
FEBS letters 1992;304(2-3):285-8.
1992: P Fernández-Silva; J A Enriquez; Julio Montoya
A simple procedure for recovering the denaturing effect of methylmercury in agarose gel electrophoresis.
BioTechniques 1992;12(4):480-2.
1992: M Villalta; P Fernández-Silva; B Beltrán; L Enguita; Manuel J López-Pérez; Julio Montoya
Molecular characterization and cloning of sheep mitochondrial DNA.
Current genetics 1992;21(3):235-40.
1991: V Corbaton; M T Muiño; P Fernández-Silva; Manuel J López-Pérez; Julio Montoya
Estimation of the chloramphenicol and cycloheximide inhibition of protein synthesis in brain cholinergic synaptosomes.
Brain research 1991;543(2):351-3.
1991: J A Enriquez; Manuel J López-Pérez; Julio Montoya
Saturation of the processing of newly synthesized rRNA in isolated brain mitochondria.
FEBS letters 1991;280(1):32-6.
1991: M Villalta; Julio Montoya
Analysis of polyadenylated RNA from human heart mitochondria.
Current genetics 1991;19(2):119-20.
1990: V Corbatón; P Fernández-Silva; Manuel J López-Pérez; Julio Montoya
Analysis of polyadenylated RNA from brain synaptosomes and mitochondria.
Neurochemical research 1990;15(7):711-7.