Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ester Tobías"'
Autor:
Sergio Barroso, Mariona Guitart-Mampel, Francesc Josep García-García, Judith Cantó-Santos, Laura Valls-Roca, Félix Andújar-Sánchez, Adrià Vilaseca-Capel, Ester Tobías, Angela Arias-Dimas, Tania Quesada-López, Rafael Artuch, Francesc Villarroya, Marta Giralt, Esteban Martínez, Ester Lozano, Glòria Garrabou
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8418 (2024)
This study aimed to comprehensively assess the metabolic, mitochondrial, and inflammatory effects of first-line efavirenz, emtricitabine, and tenofovir disoproxil fumarate (EFV/FTC/TDF) single-tablet regimen (STR) relative to untreated asymptomatic H
Externí odkaz:
https://doaj.org/article/aed86b621cc948c9be25c1225e368177
Autor:
Judith Cantó‐Santos, Laura Valls‐Roca, Ester Tobías, Francesc Josep García‐García, Mariona Guitart‐Mampel, Anna Esteve‐Codina, Beatriz Martín‐Mur, Mercedes Casado, Rafael Artuch, Estel Solsona‐Vilarrasa, José Carlos Fernandez‐Checa, Carmen García‐Ruiz, Carles Rentero, Carlos Enrich, Pedro J. Moreno‐Lozano, José César Milisenda, Francesc Cardellach, Josep M. Grau‐Junyent, Glòria Garrabou
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 14, Iss 2, Pp 964-977 (2023)
Abstract Background Inclusion body myositis (IBM) is an inflammatory myopathy clinically characterized by proximal and distal muscle weakness, with inflammatory infiltrates, rimmed vacuoles and mitochondrial changes in muscle histopathology. There is
Externí odkaz:
https://doaj.org/article/0f82886d569447a682acbe705f05bfcc
Autor:
Judith Cantó-Santos, Laura Valls-Roca, Ester Tobías, Clara Oliva, Francesc Josep García-García, Mariona Guitart-Mampel, Félix Andújar-Sánchez, Anna Esteve-Codina, Beatriz Martín-Mur, Joan Padrosa, Raquel Aránega, Pedro J. Moreno-Lozano, José César Milisenda, Rafael Artuch, Josep M. Grau-Junyent, Glòria Garrabou
Publikováno v:
Antioxidants, Vol 12, Iss 8, p 1639 (2023)
Inclusion body myositis (IBM) is an acquired inflammatory myopathy affecting proximal and distal muscles that leads to weakness in patients over 50. It is diagnosed based on clinical and histological findings in muscle related to inflammation, degene
Externí odkaz:
https://doaj.org/article/0544446c413446e08d5fb26deb02142b
Autor:
Noura Abdalla, Ester Tobías-Baraja, Alejandro Gonzalez, Gloria Garrabou, Gustavo Egea, Victoria Campuzano
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10071 (2023)
Williams–Beuren syndrome (WBS) is a rare neurodevelopmental disorder that, together with a rather characteristic neurocognitive profile, presents a strong cardiovascular phenotype. The cardiovascular features of WBS are mainly related to a gene dos
Externí odkaz:
https://doaj.org/article/6d1ae4da82b840238b68390a5418a854
Autor:
Ingrid González-Casacuberta, Dolores Vilas, Claustre Pont-Sunyer, Ester Tobías, Judith Cantó-Santos, Laura Valls-Roca, Francesc Josep García-García, Glòria Garrabou, Josep Maria Grau-Junyent, Maria Josep Martí, Francesc Cardellach, Constanza Morén
Publikováno v:
PLoS ONE, Vol 17, Iss 3 (2022)
Neurodegenerative diseases, such as Parkinson’s disease, are heterogeneous disorders with a multifactorial nature involving impaired bioenergetics. Stem-regenerative medicine and bioenergetics have been proposed as promising therapeutic targets in
Externí odkaz:
https://doaj.org/article/c50fb249254043e3997e8d8e11b21890
Autor:
Nuria Bujan, Constanza Morén, Francesc J. García-García, Alberto Blázquez, Clara Carnicer, Ana Belén Cortés, Cristina González, Ester López-Gallardo, Ester Lozano, Sonia Moliner, Laura Gort, Ester Tobías, Aitor Delmiro, Miguel Ángel Martin, Miguel Ángel Fernández-Moreno, Eduardo Ruiz-Pesini, Elena Garcia-Arumí, Juan Carlos Rodríguez-Aguilera, Glòria Garrabou
Publikováno v:
Antioxidants, Vol 11, Iss 4, p 741 (2022)
The quantification of mitochondrial respiratory chain (MRC) enzymatic activities is essential for diagnosis of a wide range of mitochondrial diseases, ranging from inherited defects to secondary dysfunctions. MRC lesion is frequently linked to extend
Externí odkaz:
https://doaj.org/article/d0611c0ec08947eb8c86d361cf171d51
Autor:
Maria Bañó, Constanza Morén, Sergio Barroso, Diana Luz Juárez, Mariona Guitart-Mampel, Ingrid González-Casacuberta, Judith Canto-Santos, Ester Lozano, Agathe León, Enric Pedrol, Òscar Miró, Ester Tobías, Josep Mallolas, Jhon F. Rojas, Francesc Cardellach, Esteban Martínez, Gloria Garrabou
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Background: Mitochondrial genome has been used across multiple fields in research, diagnosis, and toxicogenomics. Several compounds damage mitochondrial DNA (mtDNA), including biological and therapeutic agents like the human immunodeficiency virus (H
Externí odkaz:
https://doaj.org/article/742f6e2c08eb40bea0a5c226c37accaf
Autor:
Diana Luz Juárez-Flores, Mario Ezquerra, ïngrid Gonzàlez-Casacuberta, Aida Ormazabal, Constanza Morén, Eduardo Tolosa, Raquel Fucho, Mariona Guitart-Mampel, Mercedes Casado, Francesc Valldeoriola, Joan de la Torre-Lara, Esteban Muñoz, Ester Tobías, Yaroslau Compta, Francesc Josep García-García, Carmen García-Ruiz, Jose Carlos Fernandez-Checa, Maria José Martí, Josep Maria Grau, Francesc Cardellach, Rafael Artuch, Rubén Fernández-Santiago, Glòria Garrabou
Publikováno v:
Antioxidants, Vol 9, Iss 11, p 1063 (2020)
Idiopathic Parkinson’s disease (iPD) and type 2 diabetes mellitus (T2DM) are chronic, multisystemic, and degenerative diseases associated with aging, with eventual epidemiological co-morbidity and overlap in molecular basis. This study aims to expl
Externí odkaz:
https://doaj.org/article/16b6809826044832a91b3dac74fed192
Autor:
Campuzano, Noura Abdalla, Ester Tobías-Baraja, Alejandro Gonzalez, Gloria Garrabou, Gustavo Egea, Victoria
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 12; Pages: 10071
Williams–Beuren syndrome (WBS) is a rare neurodevelopmental disorder that, together with a rather characteristic neurocognitive profile, presents a strong cardiovascular phenotype. The cardiovascular features of WBS are mainly related to a gene dos
Autor:
Noura Abdalla, Ester Tobías-Baraja, Alejandro Gonzalez, Gloria Garrabou, Gustavo Egea, Victoria Campuzano
SummaryWilliams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder that, together with a rather characteristic neurocognitive profile, presents a strong cardiovascular phenotype. The cardiovascular features of WBS are mainly related to a gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b633d488465fa7bf816e617d6cd0f52
https://doi.org/10.1101/2023.05.15.540778
https://doi.org/10.1101/2023.05.15.540778