Browsing by Author Colomer Oferil, Jaume
Showing results 1 to 7 of 7
Issue Date | Title | Author(s) |
---|---|---|
22-Feb-2010 | Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissue | Raymond, Frederic; Métairon, Sylviane; Kussmann, Martin; Colomer Oferil, Jaume; Nascimento, Andrés; Mormeneo, Emma; García Martínez, Celia; Gómez Foix, Anna Maria |
11-Oct-2013 | Gene expression profiling identifies molecular pathways associated with collagen VI deficiency and provides novel therapeutic targets | Paco Mercader, Sonia; Kalko, Susana; Jou, Cristina; Rodríguez, María Angeles; Corbera, Joan; Muntoni, Francesco; Feng, Lucy; Rivas, Eloy; Torner Rubies, Ferran; Gualandi, Francesca; Gomez-Foix, Anna M.; Ferrer, Anna; Ortez, Carlos Ignacio; Nascimento, Andrés; Colomer Oferil, Jaume; Jiménez Mallebrera, Cecilia |
23-Mar-2015 | Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations | Brito, Sara; Thompson, Kyle; Campistol Plana, Jaume; Colomer Oferil, Jaume; Hardy, Steven A.; Langping, He; Fernández Marmiesse, Ana; Palacios, Lourdes; Jou, Cristina; Jiménez Mallebrera, Cecilia; Armstrong i Morón, Judith; Montero Sánchez, Raquel; Artuch Iriberri, Rafael; Tischner, Christin; Wenz, Tina; McFarland, Robert; Taylor, Robert W. |
12-Jan-2012 | PGC-1α induces mitochondrial and myokine transcriptional programs and lipid droplet and glycogen accumulation in cultured human skeletal muscle cells | Mormeneo, Emma; Jiménez Mallebrera, Cecilia; Palomer Tarridas, Francesc Xavier; De Nigris, Valeria; Vázquez Carrera, Manuel; Orozco, Anna; Nascimento, Andrés; Colomer Oferil, Jaume; Lerín Martínez, Carlos; Gómez Foix, Anna Maria |
23-Oct-2012 | Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy | Juan Mateu, Jonàs; Rodríguez, Maria José; Nascimento, Andrés; Jiménez Mallebrera, Cecilia; González Quereda, Lidia; Rivas, Eloy; Paradas, Carmen; Madruga, Marcos; Sánchez Ayaso, Pedro; Jou, Cristina; González Mera, Laura; Munell Casadesús, Francina; Roig Quilis, Manuel; Rabasa, Maria; Hernández Lain, Aurelio; Díaz Manera, Jordi; Gallardo, Eduard; Pascual Calvet, Jordi; Verdura, Edgard; Colomer Oferil, Jaume; Baiget Bastús, Montserrat; Olivé i Plana, Montserrat; Gallano, Pia |
15-Sep-2017 | Síndromes Miasténicos Congénitos en Población Española: Caracterización Clínica, Genética y de su Respuesta Terapéutica | Natera de Benito, Daniel |
1-Feb-2014 | Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies | Kalko, Susana; Paco Mercader, Sonia; Jou, Cristina; Rodríguez, María Angeles; Meznaric, Marija; Rogac, Mihael; Jekovec-Vrhovsek, Maja; Sciacco, Monica; Moggio, Maurizio; Fagiolari, Gigliola; De Paepe, Boel; De Meirleir, Linda; Ferrer, Isidro (Ferrer Abizanda); Roig Quilis, Manuel; Munell Casadesús, Francina; Montoya, Julio; López Gallardo, Ester; Ruiz Pesini, Eduardo; Artuch Iriberri, Rafael; Montero Sánchez, Raquel; Torner Rubies, Ferran; Nascimento, Andrés; Ortez, Carlos Ignacio; Colomer Oferil, Jaume; Jiménez Mallebrera, Cecilia |