Amthor, H., Hoogaars, W. M. :
Interference with Myostatin/ActRIIB Signaling as a Therapeutic Strategy for Duchenne Muscular Dystrophy
Curr Gene Ther, 2012 ; 12 (3) : 245-259
Publications (1184)
Didier, N., Hourde, C., Amthor, H., Marazzi, G., Sassoon, D. :
Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle EMBO Mol Med, 2012 ; 4 (9) : 910-23
Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle EMBO Mol Med, 2012 ; 4 (9) : 910-23
Huguet, A, Medja, F, Nicole, A, Vignaud, A, Guiraud-Dogan, C, Ferry, A, Decostre, V, Hogrel, J Y, Metzger, F, Hoeflich, A, Baraibar, M, Gomes-Pereira, M, Puymirat, J, Bassez, G, Furling, D, Munnich, A, Gourdon, G :
Molecular, physiological and motor performance defects in DMSXL mice carrying >1000 CTG repeats from the human DM1 locus PLoS Genet, 2012 ; 8 (11) : e1003043
Molecular, physiological and motor performance defects in DMSXL mice carrying >1000 CTG repeats from the human DM1 locus PLoS Genet, 2012 ; 8 (11) : e1003043
Preisler, N., Orngreen, M. C., Echaniz-Laguna, A., Laforet, P., Lonsdorfer-Wolf, E., Doutreleau, S., Geny, B., Akman, H. O., Dimauro, S., Vissing, J. :
Muscle phosphorylase kinase deficiency: A neutral metabolic variant or a disease? Neurology, 2012 ; 78 (4) : 265-8
Muscle phosphorylase kinase deficiency: A neutral metabolic variant or a disease? Neurology, 2012 ; 78 (4) : 265-8
Yger, M., Stojkovic, T., Tardieu, S., Maisonobe, T., Brice, A., Echaniz-Laguna, A., Alembik, Y., Girard, S., Cazeneuve, C., Leguern, E., Dubourg, O. :
Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C J Peripher Nerv Syst, 2012 ; 17 (1) : 112-122
Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C J Peripher Nerv Syst, 2012 ; 17 (1) : 112-122
Benchaouir, R., Goyenvalle, A. :
Splicing Modulation Mediated by Small Nuclear RNAs as Therapeutic Approaches for Muscular Dystrophies Curr Gene Ther, 2012 ; 12 (3) : 179-191
Splicing Modulation Mediated by Small Nuclear RNAs as Therapeutic Approaches for Muscular Dystrophies Curr Gene Ther, 2012 ; 12 (3) : 179-191
Friedrich, F. W., Carrier, L. :
Genetics of hypertrophic and dilated cardiomyopathy Curr Pharm Biotechnol, 2012 ; 13 (13) : 2467-76
Genetics of hypertrophic and dilated cardiomyopathy Curr Pharm Biotechnol, 2012 ; 13 (13) : 2467-76
Li, K., Hogrel, J. Y., Duchene, J., Hewson, D. J. :
Analysis of fatigue and tremor during sustained maximal grip contractions using Hilbert-Huang Transformation Med Eng Phys, 2012 ; 34 (7) : 832-840
Analysis of fatigue and tremor during sustained maximal grip contractions using Hilbert-Huang Transformation Med Eng Phys, 2012 ; 34 (7) : 832-840
Shevchuk, A. I., Novak, P., Taylor, M., Diakonov, I. A., Ziyadeh-Isleem, A., Bitoun, M., Guicheney, P., Lab, M. J., Gorelik, J., Merrifield, C. J., Klenerman, D., Korchev, Y. E. :
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopy J Cell Biol, 2012 ; 197 (4) : 499-508
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopy J Cell Biol, 2012 ; 197 (4) : 499-508
Bohm, J., Leshinsky-Silver, E., Vassilopoulos, S., Le Gras, S., Lerman-Sagie, T., Ginzberg, M., Jost, B., Lev, D., Laporte, J. :
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation Acta Neuropathol, 2012 ; 124 (4) : 575-581
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation Acta Neuropathol, 2012 ; 124 (4) : 575-581
