Browsing by Author Fourcade, Stéphane
Showing results 20 to 24 of 24
< previous
Issue Date | Title | Author(s) |
---|---|---|
1-Mar-2018 | SIRT2 in age-related neurodegenerative disorders | Fourcade, Stéphane; Outeiro, Tiago F.; Pujol Onofre, Aurora |
23-May-2023 | Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity | Planas Serra, Laura; Launay, Nathalie; Goicoechea, Leire; Heron, Bénédicte; Jou, Cristina; Juliá Palacios, Natalia; Ruiz, Montserrat; Fourcade, Stéphane; Casasnovas Pons, Carlos; Torre, Carolina de la; Gelot, Antoinette; Marsal, Maria; Loza Álvarez, Pablo; García Cazorla, Àngels; Fatemi, Ali; Ferrer, Isidro (Ferrer Abizanda); Portero Otin, Manuel; Area Gómez, Estela; Pujol Onofre, Aurora |
Feb-2017 | Tauroursodeoxycholic bile acid arrests axonal degeneration by inhibiting the unfolded protein response in X-linked adrenoleukodystrophy | Launay, Nathalie; Ruiz, Montserrat; Grau, Laia; Ortega González, Fco. Javier; Ilieva, Ekaterina V.; Martínez, Juan José; Galea, Elena; Ferrer, Isidro (Ferrer Abizanda); Knecht, Erwin; Pujol Onofre, Aurora; Fourcade, Stéphane |
1-Feb-2020 | The peroxisomal fatty acid transporter ABCD1/PMP-4 is required in the C. elegans hypodermis for axonal maintenance: A worm model for adrenoleukodystrophy | Coppa, Andrea; Guha, Sanjib; Fourcade, Stéphane; Parameswaran, Janani; Ruiz, Montserrat; Moser, Ann B.; Schlüter, Agatha; Murphy, Michael P.; Lizcano, José Miguel; Miranda Vizuete, Antonio; Dalfó Capella, Esther; Pujol Onofre, Aurora |
14-Oct-2020 | The Value of Mouse Models of Rare Diseases: A Spanish Experience | Murillo Cuesta, Silvia; Artuch Iriberri, Rafael; Asensio, Fernando; Villa, Pedro de la; Dierssen, Mara; Enriquez, Jose Antonio; Fillat i Fonts, Cristina; Fourcade, Stéphane; Ibánez, Borja; Montoliu, Lluis; Oliver, Eduardo; Pujol Onofre, Aurora; Salido, Eduardo; Vallejo, Mario; Varela Nieto, Isabel; Working Group on Animal Models of Rare Diseases; Networking Center for Rare Diseases (CIBERER) |