Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Christophe Hourde"'
Autor:
Emmanuelle Rochette, Pascale Duché, Christophe Hourdé, Bertrand Evrard, Bruno Pereira, Stéphane Echaubard, Etienne Merlin
Publikováno v:
Mediators of Inflammation, Vol 2018 (2018)
Externí odkaz:
https://doaj.org/article/2b3ee273a3cd4587b13986f4cfdac3e9
Autor:
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
Publikováno v:
EMBO Molecular Medicine, Vol 5, Iss 1, Pp 80-91 (2012)
Abstract Maintaining skeletal muscle mass is essential for general health and prevention of disease progression in various neuromuscular conditions. Currently, no treatments are available to prevent progressive loss of muscle mass in any of these con
Externí odkaz:
https://doaj.org/article/c7e7ee667b3842f2970220ef68ddfecc
Publikováno v:
EMBO Molecular Medicine, Vol 4, Iss 9, Pp 910-923 (2012)
Abstract Muscle wasting is a major cause of morbidity in the elderly. Ku80 is required for DNA double strand repair and is implicated in telomere maintenance. Complete loss‐of‐function leads to reduced post‐natal growth and severe progeria in m
Externí odkaz:
https://doaj.org/article/4c250d45ea5d47ea86aec0c77b9ecf74
Autor:
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 Sakamato, Gillian Butler-Browne, Onnik Agbulut, Arnaud Ferry
Publikováno v:
PLoS ONE, Vol 8, Iss 6 (2013)
Externí odkaz:
https://doaj.org/article/9b229a225b854d358d35081040de604d
Autor:
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
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35346 (2012)
Dystrophin contributes to force transmission and has a protein-scaffolding role for a variety of signaling complexes in skeletal muscle. In the present study, we tested the hypothesis that the muscle adaptive response following mechanical overloading
Externí odkaz:
https://doaj.org/article/f9ff90c6c49547609d7f97fb4652c55d
Autor:
Virginie Mariot, Romain Joubert, Laura Le Gall, Eva Sidlauskaite, Christophe Hourde, William Duddy, Thomas Voit, Maximilien Bencze, Julie Dumonceaux
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 6, Pp 2079-2090 (2021)
Abstract Background Facioscapulohumeral dystrophy (FSHD) is caused by mutations leading to the aberrant expression of the DUX4 transcription factor in muscles. DUX4 was proposed to induce cell death, but the involvement of different death pathways is
Externí odkaz:
https://doaj.org/article/28d75bc156bf4a87a01d22b7bad629e6
Autor:
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
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Muscular dystrophies are characterised by extensive myofibre cell death. Here Morgan et al. show that RIPK3-mediated necroptosis contributes to myofibre cell death in Duchenne muscular dystrophy, and that RIPK3 deletion protects dystrophic mice again
Externí odkaz:
https://doaj.org/article/e3702b52675e4cdd82568be2bf38a982
Autor:
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
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-1 (2018)
The original version of this article contained an error in Fig. 3. In panel c, the labels ‘mdx’ and ‘mdx Ripk3-/-‘ were inadvertently inverted. This has now been corrected in the PDF and HTML versions of the Article.
Externí odkaz:
https://doaj.org/article/bc571b2b1d674f85a50ecedc8287b7c3
Akademický článek
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Autor:
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
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 13, Iss 3, Pp 1686-1703 (2022)
Abstract Background Cancer patients at advanced stages experience a severe depletion of skeletal muscle compartment together with a decrease in muscle function, known as cancer cachexia. Cachexia contributes to reducing quality of life, treatment eff
Externí odkaz:
https://doaj.org/article/7f4c031da44d40ad8a2fdd254a02185b