Enfermedades metabólicas hereditarias y enfermedades musculares
Publicaciones destacadas
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Integrated Multi-Omics Analysis for Inferring Molecular Players in Inclusion Body Myositis
Cantó-Santos, J; Valls-Roca, L; Tobías, E; Oliva, C; García-García, FJ;(...)Moreno-Lozano, PJ; Milisenda, JC; Artuch, R; Grau-Junyent, JM; Garrabou, G.Referencia:Antioxidants 2023.
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Functional Evidence of <i>CCDC186</i> as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations
Arrabal, L; Muñoz-Pujol, G; Martínez, IM; Gort, L; García-Villoria, J;Roldán, S; Tort, F; Ribes, A.Referencia:International Journal Of Molecular Sciences 2023.
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Unravelling inclusion body myositis using a patient-derived fibroblast model
Cantó-Santos, J; Valls-Roca, L; Tobías, E; García-García, FJ; Guitart-Mampel, M;(...)Moreno-Lozano, PJ; Milisenda, JC; Cardellach, F; Grau-Junyent, JM; Garrabou, G.Referencia:Journal Of Cachexia Sarcopenia And Muscle 2023.
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Transcriptional derepression of CHD4/NuRD-regulated genes in the muscle of patients with dermatomyositis and anti-Mi2 autoantibodies
Pinal-Fernandez I; Milisenda JC; Pak K; Muñoz-Braceras S; Casal-Dominguez M;(...)Christopher-Stine L; Lloyd TE; Grau-Junyent JM; Selva-O'Callaghan A; Mammen AL.Referencia:Annals Of The Rheumatic Diseases 2023.
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Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases
Bullich, G; Matalonga, L; Pujadas, M; Papakonstantinou, A; Piscia, D;(...)Macaya, A; Palau, F; Ribes, A; Perez-Jurado, LA; Beltran, S.Referencia:Journal Of Molecular Diagnostics 2022.
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Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects
Bujan, N; Morén, C; García-García, FJ; Blázquez, A; Carnicer, C;(...)Fernández-Moreno, MA; Ruiz-Pesini, E; Garcia-Arumí, E; Rodríguez-Aguilera, JC; Garrabou, G.Referencia:Antioxidants 2022.
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Progressive endothelial cell damage in correlation with sepsis severity
Fernández, S; Palomo, M; Molina, P; Díaz-Ricart, M; Escolar, G;(...)Torramade-Moix, S; Rovira, M; Carreras, E; Nicolás, JM; Castro, P.Referencia:Journal Of Thrombosis And Haemostasis 2021.
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The protective effect of fibroblast growth factor-21 in alcoholic cardiomyopathy: a role in protecting cardiac mitochondrial function
Ferrer-Curriu, G; Guitart-Mampel, M; Rupérez, C; Zamora, M; Crispi, F;Villarroya, F; Fernández-Solà, J; Garrabou, G; Planavila, A.Referencia:Journal Of Pathology 2021.
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Physiopathological Bases of the Disease Caused by HACE1 Mutations: Alterations in Autophagy, Mitophagy and Oxidative Stress Response
Ugarteburu, Olatz; Sanchez-Viles, Marta; Ramos, Julio; Barcos-Rodriguez, Tamara; Garrabou, Gloria;Garcia-Villoria, Judit; Ribes, Antonia; Tort, Frederic.Referencia:Journal Of Clinical Medicine 2020.
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Mutations in TIMM50 cause severe mitochondrial dysfunction by targeting key aspects of mitochondrial physiology.
Tort, Frederic; Ugarteburu, Olatz; Texido, Laura; Gea-Sorli, Sabrina; Garcia-Villoria, Judit;(...)Cardellach, Francesc; Wanders, Ronald J A; Fillat, Cristina; Teresa Garcia-Silva, Maria; Ribes, Antonia.Referencia:Human Mutation 2019.