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Life Science Alliance|October 20, 2022
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophyAi Vu Hong, Nathalie Bourg, Peggy Sanatine, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 25, 2025
Transgene-Induced Cardiotoxicity In High-Dose AAV Gene TransferAriane Biquand, Evelyne Gicquel, Jerome Poupiot, et al.
Human Molecular Genetics|March 24, 2017
AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expressionEvelyne Gicquel, Natacha Maizonnier, Steven J Foltz, et al.
Human Gene Therapy. Clinical Development|June 1, 2013
The phenotype of dysferlin-deficient mice is not rescued by adeno-associated virus-mediated transfer of anoctamin 5François Monjaret, Laurence Suel-Petat, Nathalie Bourg-Alibert, et al.
Human Molecular Genetics|February 7, 2008
Mannosidase I inhibition rescues the human alpha-sarcoglycan R77C recurrent mutationMarc Bartoli, Evelyne Gicquel, Laetitia Barrault, et al.
Skeletal Muscle|February 19, 2013
A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactomeGaëlle Blandin, Sylvie Marchand, Karine Charton, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 13, 2007
NF-kappaB-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2ABéatrice Benayoun, Stephen Baghdiguian, Alicia Lajmanovich, et al.
Nanomedicine (London, England)|June 10, 2014
Assessing dystrophies and other muscle diseases at the nanometer scale by atomic force microscopyRuthger W van Zwieten, Stefania Puttini, Małgorzata Lekka, et al.
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