Search Results - "Goubin, H"

P.20.12 Gene therapy of Duchenne Muscular Dystrophy using rAAV vectors: Patterns of dystrophin expression and histological improvements by Cherel, Y, Guiner, C. Le, Guigand, L, Dutilleul, M, Larcher, T, Goubin, H, Fraysse, B, Deschamps, J.Y, Montus, M, Servais, L, Voit, T, Moullier, P

“…Duchenne Muscular Dystrophy (DMD) is caused by mutations in the gene encoding dystrophin. About 60% of the affected boys are treatable by exon skipping, i.e…”
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G.P.92 by Servais, L, Le Guiner, C, Montus, M, Cherel, Y, Francois, V, Thibaud, J.L, Wary, C, Matot, B, Larche, T, Guigand, L, Dutilleul, M, Goubin, H, Deschamps, J.Y, Domenger, C, Allais, M, Le Duff, J, Devaux, M, Jaulin, N, Guilbaud, M, Adjali, O, Latournerie, V, Veron, P, Boutin, S, Leborgne, C, Desgue, D, Moullec, S, Barnay-Toutain, F, Riviere, C, Delaunay, N, Bonne, G, Masurier, C, Hogrel, J.Y, Carlier, P, Moullier, P, Voit, T

“…We have previously demonstrated that a recombinant adeno-associated virus vector, serotype 8 (rAAV8) carrying a modified U7snRNA sequence promoting exon…”
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G.P.92 : Persistence and stability at 6 months of AAV genome and dystrophin expression in GRMD dogs after forelimb delivery of a recombinant AAV carrying an exon skipping sequence by Servais, L., Le Guiner, C., Montus, M., Cherel, Y., Francois, V., Thibaud, J.L., Wary, C., Matot, B., Larche, T., Guigand, L., Dutilleul, M., Goubin, H., Deschamps, J.Y., Domenger, C., Allais, M., Le Duff, J., Devaux, M., Jaulin, N., Guilbaud, M., Adjali, O., Latournerie, V., Veron, P., Boutin, S., Leborgne, C., Desgue, D., Moullec, S., Barnay-Toutain, F., Riviere, C., Delaunay, N., Bonne, G., Masurier, C., Hogrel, J.Y., Carlier, P., Moullier, P., Voit, T.

“…We have previously demonstrated that a recombinant adeno-associated virus vector, serotype 8 (rAAV8) carrying a modified U7snRNA sequence promoting exon…”
Get full text