OXPHOS toxicogenomics and Parkinson's diseaseLOPEZ-GALLARDO, Ester; ICETA, Ruth; IGLESIAS, Eldris et al.Mutation research. Reviews in mutation research. 2011, Vol 728, Num 3, pp 98-106, issn 1383-5742, 9 p.Article

Read-through therapy for mitochondrial DNA nonsense mutationsPACHEU-GRAU, David; GOMEZ-DURAN, Aurora; LOPEZ-GALLARDO, Ester et al.Drug discovery today. 2012, Vol 17, Num 19-20, pp 1063-1067, issn 1359-6446, 5 p.Article

Effects of purifying and adaptive selection on regional variation in human mtDNARUIZ-PESINI, Eduardo; MISHMAR, Dan; BRANDON, Martin et al.Science (Washington, D.C.). 2004, Vol 303, Num 5655, pp 223-226, issn 0036-8075, 4 p.Article

Association between seminal plasma carnitine and sperm mitochondrial enzymatic activitiesRUIZ-PESINI, Eduardo; ALVAREZ, Enrique; ENRIQUEZ, José Antonio et al.International journal of andrology (Print). 2001, Vol 24, Num 6, pp 335-340, issn 0105-6263Article

Mitochondrial pharma-Q-genomics: Targeting the OXPHOS cytochrome bGOMEZ-DURAN, Aurora; PACHEU-GRAU, David; LOPEZ-PEREZ, Manuel J et al.Drug discovery today. 2011, Vol 16, Num 5-6, pp 176-180, issn 1359-6446, 5 p.Article

Mitochondrial pharmacogenomics: barcode for antibiotic therapyPACHEU-GRAU, David; GOMEZ-DURAN, Aurora; LOPEZ-PEREZ, Manuel J et al.Drug discovery today. 2010, Vol 15, Num 1-2, pp 33-39, issn 1359-6446, 7 p.Article

'Progress' renders detrimental an ancient mitochondrial DNA genetic variantPACHEU-GRAU, David; GOMEZ-DURAN, Aurora; LOPEZ-GALLARDO, Ester et al.Human molecular genetics (Print). 2011, Vol 20, Num 21, pp 4224-4231, issn 0964-6906, 8 p.Article

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial diseasePELLO, Rosa; MARTIN, Miguel A; SMEITINK, Jan A et al.Human molecular genetics (Print). 2008, Vol 17, Num 24, pp 4001-4011, issn 0964-6906, 11 p.Article

Mitochondrial DNA content of human spermatozoaDIEZ-SANCHEZ, Carmen; RUIZ-PESINI, Eduardo; LAPENA, Ana Cristina et al.Biology of reproduction. 2003, Vol 68, Num 1, pp 180-185, issn 0006-3363, 6 p.Article

Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 GeneMARTI, Ramon; NASCIMENTO, Andrés; COLOMER, Jaume et al.Pediatric research. 2010, Vol 68, Num 2, pp 151-154, issn 0031-3998, 4 p.Article

Mitochondrial DNA Haplogroups Influence Lipoatrophy After Highly Active Antiretroviral TherapyHENDRICKSON, Sher L; KINGSLEY, Lawrence A; RUIZ-PESINI, Eduardo et al.Journal of acquired immune deficiency syndromes (1999). 2009, Vol 51, Num 2, pp 111-116, issn 1525-4135, 6 p.Article

New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onsetMAR O'CALLAGHAN, Maria Del; EMPERADOR, Sonia; RUIZ-PESINI, Eduardo et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 245-250, issn 1364-6745, 6 p.Article

Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populationsDOMINGUEZ-GARRIDO, Elena; MARTINEZ-REDONDO, Diana; LOPEZ-PEREZ, Manuel J et al.Biogerontology (Dordrecht). 2009, Vol 10, Num 4, pp 435-442, issn 1389-5729, 8 p.Article

Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia- homocitrullinuria (HHH) syndromeCAMACHO, José A; MARDACH, Rebecca; RIOSECO-CAMACHO, Natalia et al.Pediatric research. 2006, Vol 60, Num 4, pp 423-429, issn 0031-3998, 7 p.Article

Platelet cytochrome c oxidase activity and quantity in septic patientsLORENTE, Leonardo; MARTIN, Maria M; HERNANDEZ, Miriram et al.Critical care medicine. 2011, Vol 39, Num 6, pp 1289-1294, issn 0090-3493, 6 p.Article

Mitochondrial DNA haplogroups influence AIDS progressionHENDRICKSON, Sher L; HUTCHESON, Holli B; WALLACE, Douglas C et al.AIDS (London). 2008, Vol 22, Num 18, pp 2429-2441, issn 0269-9370, 13 p.Article

Elevated male European and female African contributions to the genomes of African American individualsLIND, Joanne M; HUTCHESON-DILKS, Holli B; WILLIAMS, Scott M et al.Human genetics. 2007, Vol 120, Num 5, pp 713-722, issn 0340-6717, 10 p.Article