Beaulieu, D., Thebault, P., Pelletier, R., Chapdelaine, P., Tarnopolsky, M., Furling, D., Puymirat, J. :
Abnormal prostaglandin E2 production blocks myogenic differentiation in myotonic dystrophy
Neurobiol Dis, 2012 ; 45 (1) : 122-129
Publications (1184)
Eymard, B., Levy, N. :
Diagnostic strategy for limb-girdle muscular dystrophies Rev Neurol (Paris), 2012 ; 168 (12) : 919-926
Diagnostic strategy for limb-girdle muscular dystrophies Rev Neurol (Paris), 2012 ; 168 (12) : 919-926
Le Bihan, M C, Bigot, A, Skov Jensen, S, Dennis, J, Rogowska-Wrzesinska, A, Lainé, J, Gache, V, Furling, D, Norregaard Jensen, O, Voit; T, Mouly, V, Coulton, G R, Butler-Browne, G S :
In depth analysis of the secretome identifies three major independent pathways in differentiated myotubes J Proteomics, 2012 ; 77 : 344-356
In depth analysis of the secretome identifies three major independent pathways in differentiated myotubes J Proteomics, 2012 ; 77 : 344-356
Schlossarek, S., Schuermann, F., Geertz, B., Mearini, G., Eschenhagen, T., Carrier, L. :
Adrenergic stress reveals septal hypertrophy and proteasome impairment in heterozygous Mybpc3-targeted knock-in mice J Muscle Res Cell Motil, 2012 ; 33 : 5-15
Adrenergic stress reveals septal hypertrophy and proteasome impairment in heterozygous Mybpc3-targeted knock-in mice J Muscle Res Cell Motil, 2012 ; 33 : 5-15
Blumen, S. C., Astord, S., Robin, V., Vignaud, L., Toumi, N., Cieslik, A., Achiron, A., Carasso, R. L., Gurevich, M., Braverman, I., Blumen, N., Munich, A., Barkats, M., Viollet, L. :
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation Ann Neurol, 2012 ; 71 (4) : 509-19
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation Ann Neurol, 2012 ; 71 (4) : 509-19
Goyenvalle, A., Wright, J., Babbs, A., Wilkins, V., Garcia, L., Davies, K. E. :
Engineering Multiple U7snRNA Constructs to Induce Single and Multiexon-skipping for Duchenne Muscular Dystrophy Mol Ther, 2012 ; 20 (6) : 1212-1221
Engineering Multiple U7snRNA Constructs to Induce Single and Multiexon-skipping for Duchenne Muscular Dystrophy Mol Ther, 2012 ; 20 (6) : 1212-1221
Meune, C., Khouzami, L., Wahbi, K., Caramelle, P., Decostre, V., Bonne, G., Pecker, F. :
Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement Neuromuscul Disord, 2012 ; 22 (3) : 252-257
Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement Neuromuscul Disord, 2012 ; 22 (3) : 252-257
Vilquin, J. T. :
Converting pathological cells to therapeutic ones: an odyssey through pluripotency Mol Ther, 2012 ; 20 (11) : 2012-4
Converting pathological cells to therapeutic ones: an odyssey through pluripotency Mol Ther, 2012 ; 20 (11) : 2012-4
de Sousa, P. L., Vignaud, A., de Almeida Araujo, E. C., Carlier, P. G. :
Factors controlling T(2) mapping from partially spoiled SSFP sequence: Optimization for skeletal muscle characterization Magn Reson Med, 2012 ; 67 (5) : 1379-1390
Factors controlling T(2) mapping from partially spoiled SSFP sequence: Optimization for skeletal muscle characterization Magn Reson Med, 2012 ; 67 (5) : 1379-1390
Hogrel, J. Y., Decostre, V., Alberti, C., Canal, A., Ollivier, G., Josserand, E., Taouil, I., Simon, D. :
Stature is an essential predictor of muscle strength in children BMC Musculoskelet Disord, 2012 ; 13 (1) : 176
Stature is an essential predictor of muscle strength in children BMC Musculoskelet Disord, 2012 ; 13 (1) : 176
