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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 19, 2024
Muscle type-specific effects of bilateral abobotulinumtoxinA injection on muscle growth and contractile function in spastic miceCintia Rivares, Alban Vignaud, Wendy Noort, et al.
Neuromuscular Disorders : NMD|March 30, 2010
Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin-proteasome pathwayAlban Vignaud, Arnaud Ferry, Aline Huguet, et al.
Neuromuscular Disorders : NMD|October 22, 2013
Longitudinal in vivo muscle function analysis of the DMSXL mouse model of myotonic dystrophy type 1Valérie Decostre, Alban Vignaud, Béatrice Matot, et al.
European Journal of Applied Physiology|January 27, 2010
Skeletal muscle telomere length in healthy, experienced, endurance runnersDale E Rae, Alban Vignaud, Gillian S Butler-Browne, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 3, 2016
Phosphatidylinositol 3-kinase inhibition restores Ca2+ release defects and prolongs survival in myotubularin-deficient miceCandice Kutchukian, Mirella Lo Scrudato, Yves Tourneur, et al.
Muscle & Nerve|May 15, 2012
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophyIsabelle Desguerre, Ludovic Arnold, Alban Vignaud, et al.
Molecular Therapy. Methods & Clinical Development|May 1, 2018
Preclinical Development of a Lentiviral Vector for Gene Therapy of X-Linked Severe Combined ImmunodeficiencyValentina Poletti, Sabine Charrier, Guillaume Corre, et al.
The EMBO Journal|December 25, 2009
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesisFrance Piétri-Rouxel, Christel Gentil, Stéphane Vassilopoulos, et al.
Molecular Therapy. Methods & Clinical Development|September 22, 2016
Efficacy and biodistribution analysis of intracerebroventricular administration of an optimized scAAV9-SMN1 vector in a mouse model of spinal muscular atrophyNicole Armbruster, Annalisa Lattanzi, Matthieu Jeavons, et al.
Human Molecular Genetics|December 5, 2009
Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe diseaseGaelle Douillard-Guilloux, Nina Raben, Shoichi Takikita, et al.
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