J. Montoya

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2018, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Cisplatin-mediated impairment of mitochondrial DNA metabolism inversely correlates with glutathione levels.

J. Enríquez, J. Montoya, P. Fernández-Silva, 2008, The Biochemical journal.

Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter

Pau Bernadó, Julio Montoya, H. Jacobs, 2011, Nature Structural &Molecular Biology.

Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain.

E. Ruiz-Pesini, J. Montoya, P. Briones, 2010, Investigacion clinica.

An international classification of inherited metabolic disorders (ICIMD)

Robert W. Taylor, A. Ballabio, E. Bertini, 2020, Journal of inherited metabolic disease.

Oxidative Phosphorylation Dysfunction Modifies the Cell Secretome

E. Ruiz-Pesini, M. Bayona-Bafaluy, Nuria Garrido-Pérez, 2020, International journal of molecular sciences.

Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience

E. Ruiz-Pesini, A. Ribes, J. Armstrong, 2018, Journal of Inherited Metabolic Disease.

Follow-up of folinic acid supplementation for patients with cerebral folate deficiency and Kearns-Sayre syndrome

E. Ruiz-Pesini, A. Ormazabal, R. Artuch, 2014, Orphanet Journal of Rare Diseases.

Mitochondrial DNA Content of Human Spermatozoa1

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2003, Biology of reproduction.

tRNA punctuation model of RNA processing in human mitochondria

Julio Montoya, J. Montoya, G. Attardi, 1981, Nature.

[Diseases of mitochondrial DNA].

J. Montoya, A. Solano, M. López-Pérez, 2000, Revista de neurologia.

Midline facial defect as a teratogenic effect of metronidazole.

Giuseppe Attardi, J. Montoya, D. Ojala, 1982 .

Mitochondrial DNA pathogenic mutations in multiple symmetric lipomatosis

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2019, Clinical genetics.

Human mtDNA haplogroups associated with high or reduced spermatozoa motility.

E. Ruiz-Pesini, J. Enríquez, J. Montoya, 2000, American journal of human genetics.

Variants Ala307Ala and Ser680Ser of 307 and 680 FSHr polymorphisms negatively influence on assisted reproductive techniques outcome and determine high probability of non-pregnancy in Caucasian patients

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2021, Journal of Assisted Reproduction and Genetics.

Highly efficient DNA synthesis in isolated mitochondria from rat liver.

J. Enríquez, J. Montoya, M. López-Pérez, 1994, Nucleic acids research.

Retrospective natural history of thymidine kinase 2 deficiency

Robert W. Taylor, S. Dimauro, P. Chinnery, 2018, Journal of Medical Genetics.

Xenobiotics that affect oxidative phosphorylation alter differentiation of human adipose-derived stem cells at concentrations that are found in human blood

J. Toivonen, E. Ruiz-Pesini, J. Montoya, 2015, Disease Models & Mechanisms.

DMM021774 1441..1455

J. Toivonen, E. Ruiz-Pesini, J. Montoya, 2015 .

Genetic causes of cerebral folate deficiency: clinical, biochemical and therapeutic aspects.

A. Ormazabal, R. Artuch, J. Montoya, 2012, Drug discovery today.

Brain pyrimidine nucleotide synthesis and Alzheimer disease

I. Ferrer, E. Ruiz-Pesini, M. Bayona-Bafaluy, 2019, Aging.

The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call

E. Ruiz-Pesini, R. Artuch, Miguel Ángel Martín, 2021, Genes.

Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy

F. Villarroya, S. Kalko, E. Ruiz-Pesini, 2020, Scientific Reports.

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies

L. de Meirleir, S. Kalko, E. Ruiz-Pesini, 2014, BMC Genomics.

Human Mitochondrial DNA: Particularities and Diseases

J. Montoya, S. Emperador, T. Rhouda, 2021, Biomedicines.

Kearns-Sayre syndrome: cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features.

E. Ruiz-Pesini, A. Ormazabal, R. Artuch, 2010 .

International Workshop: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16–18 November 2016, Rome, Italy

M. Zeviani, H. Prokisch, M. Mancuso, 2017, Neuromuscular Disorders.

Regulation of mitochondrial transcription by mitochondrial transcription factor A

R. Wiesner, J. Montoya, A. Pérez-Martos, 1997, Molecular and Cellular Biochemistry.

Whole sequence of the mitochondrial DNA genome of Kearns Sayre Syndrome patients: Identification of deletions and variants.

E. Ruiz-Pesini, J. Montoya, S. Emperador, 2019, Gene.

Distinctive features of the 5′-terminal sequences of the human mitochondrial mRNAs

J. Montoya, G. Attardi, D. Ojala, 1981, Nature.

Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge

Roberto Blanco, Elvira Mayordomo, Eduardo Ruiz-Pesini, 2011, BMC Bioinformatics.

Analysis of polyadenylated RNA from brain synaptosomes and mitochondria

J. Montoya, P. Fernández-Silva, M. López-Pérez, 1990, Neurochemical Research.

RNA synthesis in isolated mitochondria from brain cortex, cerebellum and stem: evidence of different transcriptional rates.

J. Enríquez, J. Montoya, P. Fernández-Silva, 1993, The International journal of biochemistry.

Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome

E. Ruiz-Pesini, R. Artuch, J. Montoya, 2022, Disease models & mechanisms.

Steady exercise removes VO(2max) difference between mitochondrial genomic variants.

J. Montoya, M. López-Pérez, J. Casajús, 2009, Mitochondrion.

Human mitochondrial variants influence on oxygen consumption.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2009, Mitochondrion.

Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations

E. Ruiz-Pesini, T. Zglinicki, J. Montoya, 2009, Biogerontology.

Septic patients with mitochondrial DNA haplogroup JT have higher respiratory complex IV activity and survival rate.

E. Ruiz-Pesini, J. Montoya, J. Solé-Violán, 2016, Journal of critical care.

Survival and mitochondrial function in septic patients according to mitochondrial DNA haplogroup

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2012, Critical Care.

An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations

E. Ruiz-Pesini, M. Bayona-Bafaluy, Nuria Garrido-Pérez, 2015, Front. Genet..

Tissue-specific differences in mitochondrial activity and biogenesis.

J. Enríquez, J. Montoya, P. Fernández-Silva, 2011, Mitochondrion.

New MT‐ND1 pathologic mutation for Leber hereditary optic neuropathy

E. Ruiz-Pesini, J. Montoya, S. Emperador, 2014, Clinical & experimental ophthalmology.

Mechanism of mammalian mitochondrial DNA replication: import of mitochondrial transcription factor A into isolated mitochondria stimulates 7S DNA synthesis.

S. Gensler, J. Enríquez, R. Wiesner, 2001, Nucleic acids research.

Transient activation of mitochondrial translation regulates the expression of the mitochondrial genome during mammalian mitochondrial differentiation.

J. M. Izquierdo, J. Enríquez, J. Montoya, 1996, The Biochemical journal.

The synthesis of mRNA in isolated mitochondria can be maintained for several hours and is inhibited by high levels of ATP.

J. Enríquez, J. Montoya, P. Fernández-Silva, 1996, European journal of biochemistry.

In organello RNA synthesis system from mammalian liver and brain.

J. Enríquez, J. Montoya, M. López-Pérez, 1996, Methods in enzymology.

Specific increase of a mitochondrial RNA transcript in chronic ethanol‐fed rats

J. Enríquez, J. Montoya, P. Fernández-Silva, 1992, FEBS letters.

Saturation of the processing of newly synthesized rRNA in isolated brain mitochondria

J. Enríquez, J. Montoya, M. López-Pérez, 1991, FEBS letters.

Replication and Transcription of Mammalian Mitochondrial Dna

J. Enríquez, J. Montoya, P. Fernández-Silva, 2003, Experimental physiology.

Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA.

F. Villarroya, M. Pineda, J. Montoya, 2006, Molecular genetics and metabolism.

Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides

Elvira Mayordomo, Jorge Álvarez, Eduardo Ruiz-Pesini, 2017, BMC Bioinformatics.

Direct and highly species-specific detection of pork meat and fat in meat products by PCR amplification of mitochondrial DNA.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2000, Journal of agricultural and food chemistry.

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene

J. Montoya, A. Solano, M. López-Pérez, 2003, Annals of neurology.

Oxidative phosphorylation inducers fight pathological angiogenesis.

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2019, Drug discovery today.

20 years of human mtDNA pathologic point mutations: carefully reading the pathogenicity criteria.

Eduardo Ruiz-Pesini, Julio Montoya, E. Ruiz-Pesini, 2009, Biochimica et biophysica acta.

Increasing mtDNA levels as therapy for mitochondrial optic neuropathies.

E. Ruiz-Pesini, J. Montoya, S. Emperador, 2018, Drug discovery today.

Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation

E. Ruiz-Pesini, J. Montoya, F. J. Carod-Artal, 2007, European journal of neurology.

'Progress' renders detrimental an ancient mitochondrial DNA genetic variant.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2011, Human molecular genetics.

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses

Robert W. Taylor, H. Hakonarson, Yiran Guo, 2018, Brain : a journal of neurology.

Monitoring mitochondrial translation in living cells

S. Jakobs, E. Fornasiero, S. Rizzoli, 2021, EMBO reports.

Macular lesion resembling adult‐onset vitelliform macular dystrophy in Kearns–Sayre syndrome with multiple mtDNA deletions

E. Ruiz-Pesini, J. Montoya, F. Ascaso, 2010, Clinical & experimental ophthalmology.

Phylogenetic analysis of mitochondrial DNA in a patient with Kearns–Sayre syndrome containing a novel 7629-bp deletion

E. Ruiz-Pesini, J. Montoya, M. D. Herrero, 2013, Mitochondrial DNA.

Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy.

E. Ruiz-Pesini, M. Bayona-Bafaluy, E. Iglesias, 2020, Mutation research.

mtDNA‐depleted U937 cells are sensitive to TNF and Fas‐mediated cytototxicity

A. Anel, J. Naval, J. Montoya, 1995, FEBS letters.

A small polyadenylated RNA (7 S RNA), containing a putative ribosome attachment site, maps near the origin of human mitochondrial DNA replication.

J. Montoya, S. Crews, G. Attardi, 1981, Journal of molecular biology.

FK506 affects mitochondrial protein synthesis and oxygen consumption in human cells

E. Coto, E. Ruiz-Pesini, J. Montoya, 2013, Cell Biology and Toxicology.

International Society for Pediatric and Adolescent Diabetes

V. Tillmann, D. Jacqmin, S. Bernasconi, 1998, Hormone Research in Paediatrics.

Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA

M. Pineda, J. Montoya, A. Solano, 2003, Journal of medical genetics.

Sea urchin mtDBP is a two-faced transcription termination factor with a biased polarity depending on the RNA polymerase.

J. Montoya, P. Fernández-Silva, M. Roberti, 2001, Nucleic acids research.

Identification and mapping of human mitochondrial genes.

J. Montoya, G. Attardi, D. Ojala, 1982, Birth defects original article series.

Mutation loads in different tissues from six pathogenic mtDNA point mutations.

E. Ruiz-Pesini, R. Artuch, M. Pineda, 2015, Mitochondrion.

Molecular Insights into Mitochondrial Protein Translocation and Human Disease

E. Ruiz-Pesini, J. Montoya, D. Pacheu-Grau, 2021, Genes.

Mitochondrial antibiograms in personalized medicine.

E. Ruiz-Pesini, E. Iglesias, J. Montoya, 2013, Human molecular genetics.

m.4216 T > C polymorphism in JT cluster determines a lower pregnancy rate in response to controlled ovarian stimulation treatment

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2023, Journal of Assisted Reproduction and Genetics.

Differences of sperm motility in mitochondrial DNA haplogroup U sublineages.

D. Wallace, E. Ruiz-Pesini, J. Enríquez, 2006, Gene.

Molecular characterization and cloning of sheep mitochondrial DNA

J. Montoya, P. Fernández-Silva, M. López-Pérez, 1992, Current Genetics.

Plasma coenzyme Q10 status is impaired in selected genetic conditions

Eduardo Ruiz-Pesini, Julio Montoya, Rafael Artuch, 2019, Scientific Reports.

Biochemical parameters to assess choroid plexus dysfunction in Kearns-Sayre syndrome patients.

E. Ruiz-Pesini, A. Ormazabal, R. Artuch, 2011, Mitochondrion.

Lower mitochondrial dysfunction in survivor septic patients with mitochondrial DNA haplogroup JT.

E. Ruiz-Pesini, J. Montoya, J. Solé-Violán, 2017, Enfermedades infecciosas y microbiologia clinica.

Defining the Substrate Spectrum of the TIM22 Complex Identifies Pyruvate Carrier Subunits as Unconventional Cargos

B. Warscheid, P. Rehling, J. Montoya, 2020, Current Biology.

OXPHOS, pyrimidine nucleotides, and Alzheimer's disease: a pharmacogenomics approach.

E. Ruiz-Pesini, M. Bayona-Bafaluy, E. Iglesias, 2014, Journal of Alzheimer's disease : JAD.

Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy

Robert W. Taylor, A. Torkamani, E. Ruiz-Pesini, 2018, Human molecular genetics.

Mitochondrial DNA transcription and diseases: past, present and future.

Eduardo Ruiz-Pesini, Julio Montoya, E. Ruiz-Pesini, 2006, Biochimica et biophysica acta.

A study on the human mitochondrial RNA polymerase activity points to existence of a transcription factor B‐like protein

J. Montoya, A. Prieto-Martín, F. Martínez-Azorín, 2001, FEBS letters.

Infectious stress triggers a POLG-related mitochondrial disease

E. Ruiz-Pesini, R. Artuch, M. Bayona-Bafaluy, 2019, neurogenetics.

Phosphorylation of rat mitochondrial transcription termination factor (mTERF) is required for transcription termination but not for binding to DNA.

J. Montoya, A. Prieto-Martín, F. Martínez-Azorín, 2004, Nucleic acids research.

A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities

M D Ugarte, A Adin, P. Navas, 2016, Scientific Reports.

Mitochondrial ribosome and Ménière’s disease: a pilot study

E. Ruiz-Pesini, J. Montoya, J. Fraile-Rodrigo, 2012, European Archives of Oto-Rhino-Laryngology.

Prenatal exposure to oxidative phosphorylation xenobiotics and late-onset Parkinson disease

E. Ruiz-Pesini, M. Bayona-Bafaluy, Nuria Garrido-Pérez, 2018, Ageing Research Reviews.

Lower mitochondrial dysfunction in survivor septic patients with mitochondrial DNA haplogroup JT

E. Ruiz-Pesini, J. Montoya, J. Solé-Violán, 2018, Enfermedades infecciosas y microbiologia clinica (English ed.).

Higher platelet cytochrome oxidase specific activity in surviving than in non-surviving septic patients

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2014, Critical Care.

Severe Septic Patients with Mitochondrial DNA Haplogroup JT Show Higher Survival Rates: A Prospective, Multicenter, Observational Study

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2013, PloS one.

Platelet cytochrome c oxidase activity and quantity in septic patients*

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2011, Critical care medicine.

Mitochondrial m.13513G>A Point Mutation in ND5 in a 16-Year-Old Man with Leber Hereditary Optic Neuropathy Detected by Next-Generation Sequencing

E. Ruiz-Pesini, J. Montoya, E. García-Arumí, 2019, Journal of Pediatric Genetics.

Screening for nuclear genetic defects in the ATP synthase‐associated genes TMEM70, ATP12 and ATP5E in patients with 3‐methylglutaconic aciduria

F. Tort, A. Ribes, W. Lissens, 2011, Clinical genetics.

Free radicals‐mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA

J. Arenas, J. Montoya, A. Solano, 2005, FEBS letters.

Mitochondrial Genetic Background May Impact Statins Side Effects and Atherosclerosis Development in Familial Hypercholesterolemia

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2022, International journal of molecular sciences.

Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy

E. Ruiz-Pesini, R. Artuch, M. Pineda, 2016, European Journal of Human Genetics.

Diseases of the human mitochondrial oxidative phosphorylation system.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2009, Advances in experimental medicine and biology.

[Genetic diseases of the mitochondrial DNA in humans].

J. Montoya, A. Solano, M. López-Pérez, 2001, Salud publica de Mexico.

Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother.

X. Estivill, A. Rötig, J. Montoya, 1994, Human molecular genetics.

[Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].

R. Barrena, J. Montoya, E. Marta, 2006, Neurologia.

[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].

J. Montoya, A. Solano, A. Andreu, 2004, Revista de neurologia.

Mitochondrial diseases mimicking neurotransmitter defects.

S. Duarte, A. Ormazabal, R. Artuch, 2008, Mitochondrion.

Decrease of oxidative phosphorylation system function in severe septic patients.

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2015, Journal of critical care.

Ketogenic treatment reduces the percentage of a LHON heteroplasmic mutation and increases mtDNA amount of a LHON homoplasmic mutation

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2019, Orphanet Journal of Rare Diseases.

Oxidative phosphorylation system and cell culture media.

E. Ruiz-Pesini, M. Bayona-Bafaluy, J. Montoya, 2021, Trends in cell biology.

The Decrease in Mitochondrial DNA Mutation Load Parallels Visual Recovery in a Leber Hereditary Optic Neuropathy Patient

E. Ruiz-Pesini, R. Artuch, M. Bayona-Bafaluy, 2018, Front. Neurosci..

Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers.

V. Petruzzella, E. Ruiz-Pesini, J. Montoya, 2016, Brain : a journal of neurology.

A novel mutation in the mitochondrial MTND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues.

E. Ruiz-Pesini, J. Arenas, Miguel Ángel Martín, 2019, Mitochondrion.

High Mitochondrial DNA Copy Number Is a Protective Factor From Vision Loss in Heteroplasmic Leber's Hereditary Optic Neuropathy (LHON).

V. Petruzzella, J. Montoya, S. Emperador, 2017, Investigative ophthalmology & visual science.

Mitochondrial lineages distribution in the Spanish population: anticipating association studies

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2006 .

A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT‐CO1)

E. Ruiz-Pesini, R. Artuch, M. Pineda, 2008, Human mutation.

A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation

E. Ruiz-Pesini, Miguel Ángel Martín, J. Montoya, 2010, Journal of Neurology Neurosurgery & Psychiatry.

Nucleotide sequence of the sheep mitochondrial DNA D-loop and its flanking tRNA genes

R. Zardoya, J. Montoya, M. López-Pérez, 1995, Current Genetics.

Sequence analysis and precise mapping of the 3' ends of HeLa cell mitochondrial ribosomal RNAs.

J. Montoya, G. Attardi, D. Dubin, 1982, Journal of molecular biology.

Machine learning classifier for identification of damaging missense mutations exclusive to human mitochondrial DNA-encoded polypeptides

E. Ruiz-Pesini, J. Montoya, A. Martín-Navarro, 2017, BMC Bioinformatics.

Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutation

E. Ruiz-Pesini, J. Montoya, S. Emperador, 2022, Clinical Genetics.

[Mitochondrial DNA deletions in Kearns-Sayre syndrome].

J. Montoya, A. Solano, F. J. Carod-Artal, 2006, Neurologia.

Mitochondria from ejaculated human spermatozoa do not synthesize proteins

E. Ruiz-Pesini, J. Enríquez, J. Montoya, 2003, FEBS letters.

Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases.

E. Ruiz-Pesini, R. Artuch, J. Montoya, 2021, Clinical chemistry.

New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset

E. Ruiz-Pesini, R. Artuch, M. Pineda, 2012, neurogenetics.

Influence of mtDNA genetic variation on antibiotic therapy.

E. Ruiz-Pesini, J. Montoya, A. Gomez-Duran, 2010, Pharmacogenomics.

[Aspects of neuropathy in mitochondrial diseases].

R. Artuch, M. Pineda, J. Montoya, 2000, Revista de neurologia.

De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA

J. Montoya, A. Solano, M. López-Pérez, 2004, Pediatric Nephrology.

Gamma‐aminobutyric acid levels in cerebrospinal fluid in neuropaediatric disorders

D. Cuadras, R. Artuch, J. Montoya, 2018, Developmental medicine and child neurology.

Association of human mitochondrial DNA variants with plasma LDL levels.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2008, Mitochondrion.

A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome

S. Dimauro, M. Mancuso, M. Filosto, 2004, Journal of Medical Genetics.

Muscle Involvement in a Large Cohort of Pediatric Patients with Genetic Diagnosis of Mitochondrial Disease

F. Tort, P. Navas, E. Ruiz-Pesini, 2019, Journal of clinical medicine.

Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers

V. Petruzzella, J. Montoya, S. Emperador, 2018, BMC Research Notes.

"…the number of people at risk for developing toxic side effects after therapy with translation-targeted antibiotics may be substantial."

J. Montoya, A. Gomez-Duran, D. Pacheu-Grau, 2010 .

New DNA-binding activity of rat mitochondrial transcription termination factor (mTERF).

J. Montoya, A. Prieto-Martín, F. Martínez-Azorín, 2004, Journal of biochemistry.

Iron(II) induces changes in the conformation of mammalian mitochondrial DNA resulting in a reduction of its transcriptional rate

J. Montoya, P. Fernández-Silva, A. Andreu, 2000, FEBS letters.

A simple procedure for recovering the denaturing effect of methylmercury in agarose gel electrophoresis.

J. Enríquez, J. Montoya, P. Fernández-Silva, 1992, BioTechniques.

Human liver mitochondrial RNA synthesized in isolated organelles

J. Montoya, M. López-Pérez, A. Andreu, 1996 .

Analysis of the transcription products of the rainbow trout (Oncorynchus mykiss) liver mitochondrial genome: detection of novel mitochondrial transcripts

R. Zardoya, J. Montoya, A. Pérez-Martos, 1995, Current Genetics.

Analysis of polyadenylated RNA from human heart mitochondria

J. Montoya, M. Villalta, 1991, Current Genetics.

Analysis of human mitochondrial RNA.

J. Montoya, G. Attardi, 1983, Methods in enzymology.

[41] Analysis of human mitochondrial RNA

J. Montoya, G. Attardi, 1983 .

Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome

E. Ruiz-Pesini, R. Artuch, M. Bayona-Bafaluy, 2020, Frontiers in Genetics.

Infectious stress triggers a POLG-related mitochondrial disease

E. Ruiz-Pesini, R. Artuch, M. Bayona-Bafaluy, 2019, neurogenetics.

Mitochondrial genetic variability of North Morocco population

E. Ruiz-Pesini, J. Montoya, T. Rhouda, 2006 .

Human mitochondrial mTERF wraps around DNA through a left-handed superhelical tandem repeat

Pau Bernadó, Isabel Usón, Julio Montoya, 2010, Nature Structural &Molecular Biology.

Read-through therapy for mitochondrial DNA nonsense mutations.

E. Ruiz-Pesini, J. Montoya, A. Gomez-Duran, 2012, Drug discovery today.

Plasma coenzyme Q10 status is impaired in selected genetic conditions

P. Navas, E. Ruiz-Pesini, R. Artuch, 2019, Scientific Reports.

Mitochondrial pharma-Q-genomics: targeting the OXPHOS cytochrome b.

E. Ruiz-Pesini, J. Montoya, M. López-Pérez, 2011, Drug discovery today.

Platelet cytochrome c oxidase activity and quantity in septic patients*

E. Ruiz-Pesini, J. Montoya, J. Blanquer, 2011, Critical care medicine.

OXPHOS, pyrimidine nucleotides, and Alzheimer's disease: a pharmacogenomics approach.

M. Bayona-Bafaluy, E. Iglesias, J. Montoya, 2014, Journal of Alzheimer's disease : JAD.

Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis.

A. Zorzano, Á. Díaz-Ramos, J. Montoya, 2016, Clinical science.

Organization and Expression of Genetic Information in Human Mitochondrial DNA

Giuseppe Attardi, J. Montoya, S. Crews, 1981 .