Search Results - Christophe Hourde

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  1. 1

    Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle by Nathalie Didier, Christophe Hourdé, Helge Amthor, Giovanna Marazzi, David Sassoon

    Published in EMBO Molecular Medicine (2012-08-01)
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  2. 2

    Corrigendum to “Single Bout Exercise in Children with Juvenile Idiopathic Arthritis: Impact on Inflammatory Markers” by Emmanuelle Rochette, Pascale Duché, Christophe Hourdé, Bertrand Evrard, Bruno Pereira, Stéphane Echaubard, Etienne Merlin

    Published in Mediators of Inflammation (2018-01-01)
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  3. 3

    RIPK3‐mediated cell death is involved in DUX4‐mediated toxicity in facioscapulohumeral dystrophy by Virginie Mariot, Romain Joubert, Laura Le Gall, Eva Sidlauskaite, Christophe Hourde, William Duddy, Thomas Voit, Maximilien Bencze, Julie Dumonceaux

    Published in Journal of Cachexia, Sarcopenia and Muscle (2021-12-01)
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  4. 4

    Necroptosis mediates myofibre death in dystrophin-deficient mice by Jennifer E. Morgan, Alexandre Prola, Virginie Mariot, Veronica Pini, Jinhong Meng, Christophe Hourde, Julie Dumonceaux, Francesco Conti, Frederic Relaix, Francois-Jerôme Authier, Laurent Tiret, Francesco Muntoni, Maximilien Bencze

    Published in Nature Communications (2018-09-01)
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  5. 5

    Hypothalamic–pituitary–adrenal axis activation and glucocorticoid‐responsive gene expression in skeletal muscle and liver of Apc mice by Agnès Martin, Josiane Castells, Valentine Allibert, Andréa Emerit, Cindy Zolotoff, Victoire Cardot‐Ruffino, Yann S. Gallot, Barbara Vernus, Véronique Chauvet, Laurent Bartholin, Laurent Schaeffer, Anne‐Cécile Durieux, Christophe Hourdé, François B. Favier, Laetitia Mazelin, Damien Freyssenet

    Published in Journal of Cachexia, Sarcopenia and Muscle (2022-06-01)
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  6. 6

    Impaired adaptive response to mechanical overloading in dystrophic skeletal muscle. by Pierre Joanne, Christophe Hourdé, Julien Ochala, Yvain Caudéran, Fadia Medja, Alban Vignaud, Etienne Mouisel, Wahiba Hadj-Said, Ludovic Arandel, Luis Garcia, Aurélie Goyenvalle, Rémi Mounier, Daria Zibroba, Kei Sakamoto, Gillian Butler-Browne, Onnik Agbulut, Arnaud Ferry

    Published in PLoS ONE (2012-01-01)
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  7. 7

    Sex and genotype specificities of microvasculature and muscle remodeling in sub-Saharan sickle cell trait and disease by Léo Blervaque, Pablo Bartolucci, Manon Riccetti, Marion Ravelojaona, Angèle N. Merlet, Mathilde Noguer, Manon Rojo, Christophe Hourdé, Cyril Martin, Vincent Pialoux, Barnabas Gellen, Frédéric Galactéros, Samuel Oyono-Enguéllé, Léonard Féasson, Laurent A. Messonnier, Lucile Vincent, Clémence Bexon, Jérémy Delabre, Benjamin Chatel, Emeline Aufradet, Erica N Chirico, Patrice Thiriet, Etienne Audureau, Anoosha Habibi, Jean-Antoine Ribeil, Jean-Benoit Arlet, François Lionnet

    Published in Blood Advances (2025-09-01)
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  8. 8

    Activation of serum/glucocorticoid‐induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy by Eva Andres‐Mateos, Heinrich Brinkmeier, Tyesha N. Burks, Rebeca Mejias, Daniel C. Files, Martin Steinberger, Arshia Soleimani, Ruth Marx, Jessica L. Simmers, Benjamin Lin, Erika Finanger Hedderick, Tom G. Marr, Brian M. Lin, Christophe Hourdé, Leslie A. Leinwand, Dietmar Kuhl, Michael Föller, Silke Vogelsang, Ivan Hernandez‐Diaz, Dana K. Vaughan, Diego Alvarez de la Rosa, Florian Lang, Ronald D. Cohn

    Published in EMBO Molecular Medicine (2012-11-01)
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