Sobre el grupo


Investigador Principal

Eduardo Ruiz Pesini, María Pilar Bayona Bafaluy

Equipo

Ainoa Pueyo Franco, Aldara Mainé Rodrigo, Ana Vela Sebastián, Celia Aladrén Herrer, David Pacheu Grau, Elena De Tomás Mateo, Erika María Fernández-Vizarra Bailey, Ester López Gallardo, Javier Sanz Pons, José Lorenzo Labarta Monzón, Nuria Garrido Pérez, Patricia Meade Huerta, Sonia Emperador Ortiz.

ARAID

Universidad de Zaragoza

Líneas de Investigación


Enfermedades del sistema de fosforilación oxidativa

Farmacogenética mitocondrial

Publicaciones más relevantes


Vela Sebastián A, Bayona Bafaluy M, Pacheu Grau D. ISR pathway contribution to tissue specificity of mitochondrial diseases. TRENDS IN ENDOCRINOLOGY AND METABOLISM. 10.1016/j.tem.2024.05.001. Q-1. F.I-12,6

Jiménez Salvador I, Meade Huerta P, Iglesias Huerta E, Bayona Bafaluy M, Ruiz Pesini E. Developmental origins of Parkinson disease: Improving the rodent models. AGEING RESEARCH REVIEWS. 10.1016/j.arr.2023.101880. Q-1. F.I-12,4

Bayona Bafaluy M, Garrido Pérez N, Meade Huerta P, Iglesias Huerta E, Jiménez Salvador I, Montoya Villarroya J, Martinez-Cue C, Ruiz Pesini E. Down syndrome is an oxidative phosphorylation disorder Redox Biology. 10.1016/j.redox.2021.101871. Q-1. F.I-11,9

Gaudó Pardo P, De Tomás Mateo E, Garrido Pérez N, Santana A, Ruiz Pesini E, Montoya Villarroya J, Bayona Bafaluy M. "ATAD3C regulates ATAD3A assembly and function in the mitochondrial membrane" FREE RADICAL BIOLOGY AND MEDICINE. 10.1016/j.freeradbiomed.2023.12.006. Q-1. F.I-8,2

Yousefi R, Cruz-Zaragoza L, Valpadashi A, Hansohn C, Dahal D, Richter-Dennerlein R, Rizzoli S, Urlaub H, Rehling P, Pacheu Grau D. A microscopy-based screen identifies cellular kinases modulating mitochondrial translation. Cell Reports. 10.1016/j.celrep.2024.115143. Q-1. F.I-6,9

Trifunov S, Paredes-Fuentes A, Badosa C, Codina A, Montoya Villarroya J, Ruiz Pesini E, Jou C, Garrabou G, Grau-Junyent J, Yubero D, Montero R, Muchart J, Ortigoza-Escobar J, O'Callaghan M, Nascimento A, Catala A, Garcia-Cazorla A, Jimenez-Mallebrera C, Artuch R. Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases CLINICAL CHEMISTRY. 10.1093/clinchem/hvab091. Q-1. F.I-6,3

Yousefi R, Fornasiero E, Cyganek L, Montoya Villarroya J, Jakobs S, Rizzoli S, Rehling P, Pacheu-Grau D. Monitoring mitochondrial translation in living cells EMBO REPORTS. 10.15252/embr.202051635. Q-1. F.I-6,2

Sanclemente T, Carazo A, Silvestre-Munoz T, Montoya J, Ruiz Pesini E, Puzo J, Pacheu Grau D. Assessment of CoQ10 Dietary Intake in a Mediterranean Cohort of Familial Hypercholesterolemia Patients: A Pilot Study Nutrients. 10.3390/nu17223512. Q-1. F.I-5

Ruiz Pesini E, Bayona Bafaluy M, Sanclemente T, Puzo Foncillas J, Montoya Villarroya J, Pacheu Grau D. Mitochondrial Genetic Background May Impact Statins Side Effects and  Atherosclerosis Development in Familial Hypercholesterolemia. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 10.3390/ijms24010471. Q-1. F.I-4,9

Jou C, Nascimento A, Codina A, Montoya Villarroya J, López Gallardo E, Emperador Ortiz S, Ruiz Pesini E, Montero R, Natera-de Benito D, Ortez C, Marquez J, Zelaya M, Gutierrez-Mata A, Badosa C, Carrera-García L, Expósito-Escudero J, Roldán M, Camara Y, Marti R, Ferrer Cerón I, Jimenez-Mallebrera C, Artuch R. Pathological Features in Paediatric Patients with TK2 Deficiency. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 10.3390/ijms231911002. Q-1. F.I-4,9

Otra Actividad


Proyectos


 

Título Expediente Investigador Principal Duración Importe Financiador
Oxidative phosphorylation genetic disorders: pathological mechanisms and therapeutic approachesPI21/00229Eduardo Ruiz Pesini01/01/2022 - 30/06/2025203280Instituto de Salud Carlos III