Denard, J., Beley, C., Kotin, R., Lai-Kuen, R., Blot, S., Leh, H., Asokan, A., Samulski, R. J., Moullier, P., Voit, T., Garcia, L., Svinartchouk, F. :
Human galectin 3 binding protein interacts with recombinant adeno-associated virus type 6
J Virol, 2012 ; 86 (12) : 6620-6631
Publications (1181)
Hoogaars, W., Mouisel, E., Pasternack, A., Hulmi, J. J., Relizani, K., Schuelke, M., Schirwis, E., Garcia, L., Ritvos, O., Ferry, A., t Hoen, P. A., Amthor, H. :
Combined effect of AAV-U7-induced dystrophin exon skipping and soluble activin type IIB receptor in mdx mice Hum Gene Ther, 2012 ; 23 (12) : 1269-79
Combined effect of AAV-U7-induced dystrophin exon skipping and soluble activin type IIB receptor in mdx mice Hum Gene Ther, 2012 ; 23 (12) : 1269-79
Preisler, N., Laforet, P., Madsen, K. L., Hansen, R. S., Lukacs, Z., Orngreen, M. C., Lacour, A., Vissing, J. :
Fat and carbohydrate metabolism during exercise in late-onset Pompe disease Mol Genet Metab, 2012 ; 107 (3) : 462-468
Fat and carbohydrate metabolism during exercise in late-onset Pompe disease Mol Genet Metab, 2012 ; 107 (3) : 462-468
Willer, T., Lee, H., Lommel, M., Yoshida-Moriguchi, T., de Bernabe, D. B., Venzke, D., Cirak, S., Schachter, H., Vajsar, J., Voit, T., Muntoni, F., Loder, A. S., Dobyns, W. B., Winder, T. L., Strahl, S., Mathews, K. D., Nelson, S. F., Moore, S. A., Campbell, K. P. :
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Nat Genet, 2012 ; 44 (5) : 575-580
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Nat Genet, 2012 ; 44 (5) : 575-580
BĂ©hin, A, LĂ©ger, J M :
Quand recourir Ă la Commission permanente des permis de conduire ? Neurologie Pratique, 2012 ; 80 : 9-10
Quand recourir Ă la Commission permanente des permis de conduire ? Neurologie Pratique, 2012 ; 80 : 9-10
Fraysse, B, Weinberger, F, Bardswell, S, Cuello, F, Vignier, N, Geertz, B, Starbatty, J, KrÀmer, E, Coirault, C, Eschenhagen, T, Kentish, J C, Avkiran, M, Carrier, L :
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice J Mol Cell Cardiol, 2012 ; 52 : 1299-1307
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice J Mol Cell Cardiol, 2012 ; 52 : 1299-1307
Ledoux, I., Laforet, P., Wary, C., Carlier, P. G., Hogrel, J. Y. :
Explorations de lâintolĂ©rance musculaire Ă lâeffort de lâenfant Arch Pediatr, 2012 ; 19 (6 S1) : H107-H108
Explorations de lâintolĂ©rance musculaire Ă lâeffort de lâenfant Arch Pediatr, 2012 ; 19 (6 S1) : H107-H108
Schoindre, Y., Terrier, B., Kahn, J. E., Saadoun, D., Souberbielle, J. C., Benveniste, O., Amoura, Z., Piette, J. C., Cacoub, P., Costedoat-Chalumeau, N. :
Vitamine D et auto-immunité. PremiÚre partie : aspects fondamentaux. Rev Med Interne, 2012 ; 33 (2) : 80-6
Vitamine D et auto-immunité. PremiÚre partie : aspects fondamentaux. Rev Med Interne, 2012 ; 33 (2) : 80-6
Bohm, J., Biancalana, V., Dechene, E. T., Bitoun, M., Pierson, C. R., Schaefer, E., Karasoy, H., Dempsey, M. A., Klein, F., Dondaine, N., Kretz, C., Haumesser, N., Poirson, C., Toussaint, A., Greenleaf, R. S., Barger, M. A., Mahoney, L. J., Kang, P. B., Zanoteli, E., Vissing, J., Witting, N., Echaniz-Laguna, A., Wallgren-Pettersson, C., Dowling, J., Merlini, L., Oldfors, A., Bomme Ousager, L., Melki, J., Krause, A., Jern, C., Oliveira, A. S., Petit, F., Jacquette, A., Chaussenot, A., Mowat, D., Leheup, B., Cristofano, M., Poza Aldea, J. J., Michel, F., Furby, A., Llona, J. E., Van Coster, R., Bertini, E., Urtizberea, J. A., Drouin-Garraud, V., Beroud, C., Prudhon, B., Bedford, M., Mathews, K., Erby, L. A., Smith, S. A., Roggenbuck, J., Crowe, C. A., Brennan Spitale, A., Johal, S. C., Amato, A. A., Demmer, L. A., Jonas, J., Darras, B. T., Bird, T. D., Laurino, M., Welt, S. I., Trotter, C., Guicheney, P., Das, S., Mandel, J. L., Beggs, A. H., Laporte, J. :
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy Hum Mutat, 2012 ; 33 (6) : 949-59
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy Hum Mutat, 2012 ; 33 (6) : 949-59
Guerci, A., Lahoute, C., Hebrard, S., Collard, L., Graindorge, D., Favier, M., Cagnard, N., Batonnet-Pichon, S., Precigout, G., Garcia, L., Tuil, D., Daegelen, D., Sotiropoulos, A. :
Srf-dependent paracrine signals produced by myofibers control satellite cell-mediated skeletal muscle hypertrophy Cell Metab, 2012 ; 15 (1) : 25-37
Srf-dependent paracrine signals produced by myofibers control satellite cell-mediated skeletal muscle hypertrophy Cell Metab, 2012 ; 15 (1) : 25-37
