Vuillaumier-Barrot, S., Quijano-Roy, S., Bouchet-Seraphin, C., Maugenre, S., Peudenier, S., Van den Bergh, P., Marcorelles, P., Avila-Smirnow, D., Chelbi, M., Romero, N. B., Carlier, P., Estournet, B., Guicheney, P., Seta, N. :
Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype
Neuromuscul Disord, 2009 ; 19 (3) : 182-188
Publications (1181)
Daubas, P., Crist, C. G., Bajard, L., Relaix, F., Pecnard, E., Rocancourt, D., Buckingham, M. :
The regulatory mechanisms that underlie inappropriate transcription of the myogenic determination gene Myf5 in the central nervous system Dev Biol, 2009 ; 327 (1) : 71-82
The regulatory mechanisms that underlie inappropriate transcription of the myogenic determination gene Myf5 in the central nervous system Dev Biol, 2009 ; 327 (1) : 71-82
Kahn, J, Shwartz, Y, Blitz, E, Krief, S, Sharir, A, Breitel, D. A, Rattenbach, R, Relaix, F, Maire, P, Rountree, R.B, Kingsley, D.M, Zelzer, E :
Muscle contraction is necessary to maintain joint progenitor cell fate Dev Cell, 2009 ; 16 (5) : 734-743
Muscle contraction is necessary to maintain joint progenitor cell fate Dev Cell, 2009 ; 16 (5) : 734-743
Park, Y. E., Hayashi, Y. K., Bonne, G., Arimura, T., Noguchi, S., Nonaka, I., Nishino, I. :
Autophagic degradation of nuclear components in mammalian cells Autophagy, 2009 ; 5 (6) : 795-804
Autophagic degradation of nuclear components in mammalian cells Autophagy, 2009 ; 5 (6) : 795-804
Bevilacqua, J. A., Bitoun, M., Biancalana, V., Oldfors, A., Stoltenburg, G., Claeys, K. G., Lacene, E., Brochier, G., Manere, L., Laforet, P., Eymard, B., Guicheney, P., Fardeau, M., Romero, N. B. :
« Necklace » fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy Acta Neuropathol, 2009 ; 117 (3) : 283-91
« Necklace » fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy Acta Neuropathol, 2009 ; 117 (3) : 283-91
Duque, S., Joussemet, B., Riviere, C., Marais, T., Dubreil, L., Douar, A. M., Fyfe, J., Moullier, P., Colle, M. A., Barkats, M. :
Intravenous Administration of Self-complementary AAV9 Enables Transgene Delivery to Adult Motor Neurons Mol Ther, 2009 ; 17 (7) : 1187-1196
Intravenous Administration of Self-complementary AAV9 Enables Transgene Delivery to Adult Motor Neurons Mol Ther, 2009 ; 17 (7) : 1187-1196
Lievens, I., Fournier, E., Viala, K., Maisonobe, T., Bouche, P., Leger, J. M. :
Neuropathie motrice multifocale: existe-t-il une alteration de la conduction sensitive au long cours? Une etude retrospective chez 21 patients. Rev Neurol (Paris), 2009 ; 165 (3) : 243-8
Neuropathie motrice multifocale: existe-t-il une alteration de la conduction sensitive au long cours? Une etude retrospective chez 21 patients. Rev Neurol (Paris), 2009 ; 165 (3) : 243-8
Schussler, O., Coirault, C., Louis-Tisserand, M., Al-Chare, W., Oliviero, P., Menard, C., Michelot, R., Bochet, P., Salomon, D. R., Chachques, J. C., Carpentier, A., Lecarpentier, Y. :
Use of arginine-glycine-aspartic acid adhesion peptides coupled with a new collagen scaffold to engineer a myocardium-like tissue graft Nat Clin Pract Cardiovasc Med, 2009 ; 6 (3) : 240-9
Use of arginine-glycine-aspartic acid adhesion peptides coupled with a new collagen scaffold to engineer a myocardium-like tissue graft Nat Clin Pract Cardiovasc Med, 2009 ; 6 (3) : 240-9
Chaouch, S., Mouly, V., Goyenvalle, A., Vulin, A., Mamchaoui, K., Negroni, E., Di Santo, J., Butler-Browne, G., Torrente, Y., Garcia, L., Furling, D. :
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon skipping approach to restore dystrophin in DMD cells Hum Gene Ther, 2009 ; 20 (7) : 784-790
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon skipping approach to restore dystrophin in DMD cells Hum Gene Ther, 2009 ; 20 (7) : 784-790
Gueneau, L., Bertrand, A. T., Jais, J. P., Salih, M. A., Stojkovic, T., Wehnert, M., Hoeltzenbein, M., Spuler, S., Saitoh, S., Verschueren, A., Tranchant, C., Beuvin, M., Lacene, E., Romero, N. B., Heath, S., Zelenika, D., Voit, T., Eymard, B., Ben Yaou, R., Bonne, G. :
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy Am J Hum Genet, 2009 ; 85 (3) : 338-53
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy Am J Hum Genet, 2009 ; 85 (3) : 338-53
