Search Results - Perrine Castets
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Sustained Activation of mTORC1 in Skeletal Muscle Inhibits Constitutive and Starvation-Induced Autophagy and Causes a Severe, Late-Onset Myopathy by Perrine Castets, Shuo Lin, Nathalie Rion, Sabrina Di Fulvio, Klaas Romanino, Maitea Guridi, Stephan Frank, Lionel Tintignac, Michael Sinnreich, Markus A. Rüegg
Published 2013Artigo -
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Differential response of skeletal muscles to mTORC1 signaling during atrophy and hypertrophy by C. Florian Bentzinger, Shuo Lin, Klaas Romanino, Perrine Castets, Maitea Guridi, Serge Summermatter, Christoph Handschin, Lionel Tintignac, Michael N. Hall, Markus A. Rüegg
Published 2013Artigo -
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Rapamycin Attenuates the Progression of Tau Pathology in P301S Tau Transgenic Mice by Sefika Özcelik, Graham Fraser, Perrine Castets, Véronique Schaeffer, Zhiva Skachokova, Karin Breu, Florence Clavaguera, Michael Sinnreich, Ludwig Kappos, Michel Goedert, Markus Tolnay, David T. Winkler
Published 2013Artigo -
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Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I by Marielle Brockhoff, Nathalie Rion, Kathrin Chojnowska, Tatiana Wiktorowicz, Christopher Eickhorst, Beat Erne, Stephan Frank, C. Angelini, Denis Furling, Markus A. Rüegg, Michael Sinnreich, Perrine Castets
Published 2017Artigo -
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Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy by Mathieu Rederstorff, Perrine Castets, Sandrine Arbogast, Jeanne Lainé, Stéphane Vassilopoulos, Maud Beuvin, O. Dubourg, Alban Vignaud, Arnaud Ferry, Alain Krol, Valérie Allamand, Pascale Guicheney, Ana Ferreiro, Alain Lescure
Published 2011Artigo -
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mTORC1 and PKB/Akt control the muscle response to denervation by regulating autophagy and HDAC4 by Perrine Castets, Nathalie Rion, Marine Théodore, Denis Falcetta, Shuo Lin, Markus Reischl, Franziska Wild, Laurent Guérard, Christopher Eickhorst, Marielle Brockhoff, Maitea Guridi, Chikwendu Ibebunjo, Joseph Cruz, Michael Sinnreich, Rüdiger Rudolf, David J. Glass, Markus A. Rüegg
Published 2019Artigo -
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Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans by Erik Schoenmakers, Maura Agostini, Catherine Mitchell, Nadia Schoenmakers, Laura V. Papp, Odelia Rajanayagam, Raja Padidela, Lourdes Ceron‐Gutierrez, Rainer Döffinger, Claudia Prevosto, Jian’an Luan, Sergio Montaño, Jun Lu, Mireille Castanet, Nicholas J. Clemons, Matthijs Groeneveld, Perrine Castets, Mahsa Karbaschi, Sri W. Aitken, Adrian Dixon, Jane Williams, Irene Campi, Margaret Blount, H. Burton, Francesco Muntoni, Dominic G. O’Donovan, Andrew Dean, A Jane Warren, Charlotte Brierley, David Baguley, Pascale Guicheney, Rebecca C. Fitzgerald, Alasdair Coles, Hill Gaston, Pamela Todd, Arne Holmgren, Kum Kum Khanna, Marcus S. Cooke, Robert K. Semple, David Halsall, Nicholas J. Wareham, John W. R. Schwabe, L. Grasso, Paolo Beck‐Peccoz, Arthur Ogunko, Mehul Dattani, Mark Gurnell, Krishna Chatterjee
Published 2010Artigo
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