Lagha, M., Sato, T., Regnault, B., Cumano, A. D., Zuniga, A., Licht, J., Relaix, F., Buckingham, M. :
Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo
BMC Genomics, 2010 ; 11 (1) : 696
Publications (1181)
Susman, R. D., Quijano-Roy, S., Yang, N., Webster, R., Clarke, N. F., Dowling, J., Kennerson, M., Nicholson, G., Biancalana, V., Ilkovski, B., Flanigan, K., Arbuckle, S., Malladi, C., Robinson, P., Vucic, S., Mayer, M., Romero, N. B., Urtizberea, J. A., Garcia-Bragado, F., Guicheney, P., Bitoun, M., Carlier, R. Y., North, K. N. :
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy Neuromuscul Disord, 2010 ; 20 (4) : 229-237
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy Neuromuscul Disord, 2010 ; 20 (4) : 229-237
Arbogast, S, Ferreiro, A :
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Durieux, A. C., Vignaud, A., Prudhon, B., Viou, M. T., Beuvin, M., Vassilopoulos, S., Fraysse, B., Ferry, A., Laine, J., Romero, N. B., Guicheney, P., Bitoun, M. :
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
Mearini, G., Gedicke, C., Schlossarek, S., Witt, C. C., Kramer, E., Cao, P., Gomes, M. D., Lecker, S. H., Labeit, S., Willis, M. S., Eschenhagen, T., Carrier, L. :
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Vuillerot, C., Girardot, F., Payan, C., Fermanian, J., Iwaz, J., De Lattre, C, Berard, C. :
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
Boerio, D., Creange, A., Hogrel, J. Y., Gueguen, A., Bertrand, D., Lefaucheur, J. P. :
Nerve excitability changes after intravenous immunoglobulin infusions in multifocal motor neuropathy and chronic inflammatory demyelinating neuropathy J Neurol Sci, 2010 ; 292 (1-2) : 63-71
Nerve excitability changes after intravenous immunoglobulin infusions in multifocal motor neuropathy and chronic inflammatory demyelinating neuropathy J Neurol Sci, 2010 ; 292 (1-2) : 63-71
Gilardeau, C :
Maladie de Charcot-Marie-Tooth (2Úme volet). Traitements Kiné Actualités, 2010 ; 1208 : 18-21
Maladie de Charcot-Marie-Tooth (2Úme volet). Traitements Kiné Actualités, 2010 ; 1208 : 18-21
Pietri-Rouxel, F., Gentil, C., Vassilopoulos, S., Baas, D., Mouisel, E., Ferry, A., Vignaud, A., Hourde, C., Marty, I., Schaeffer, L., Voit, T., Garcia, L. :
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis EMBO J, 2010 ; 29 (3) : 643-654
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis EMBO J, 2010 ; 29 (3) : 643-654
Claeys, K. G., Maisonobe, T., Bohm, J., Laporte, J., Hezode, M., Romero, N. B., Brochier, G., Bitoun, M., Carlier, R. Y., Stojkovic, T. :
Phenotype of a patient with recessive centronuclear myopathy and a novel bin1 mutation Neurology, 2010 ; 74 (6) : 519-521
Phenotype of a patient with recessive centronuclear myopathy and a novel bin1 mutation Neurology, 2010 ; 74 (6) : 519-521
