Kandalla, P. K., Goldspink, G., Butler-Browne, G., Mouly, V. :
Mechano Growth Factor E peptide (MGF-E), derived from an isoform of IGF-1, activates human muscle progenitor cells and induces an increase in their fusion potential at different ages
Mech Ageing Dev, 2011 ; 132 (4) : 154-62
Publications (1184)
Rau, F., Freyermuth, F., Fugier, C., Villemin, J. P., Fischer, M. C., Jost, B., Dembele, D., Gourdon, G., Nicole, A., Duboc, D., Wahbi, K., Day, J. W., Fujimura, H., Takahashi, M. P., Auboeuf, D., Dreumont, N., Furling, D., Charlet-Berguerand, N. :
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy Nat Struct Mol Biol, 2011 ; 18 (7) : 840-5
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy Nat Struct Mol Biol, 2011 ; 18 (7) : 840-5
Dubourg, O., Maisonobe, T., Behin, A., Suominen, T., Raheem, O., Penttila, S., Parton, M., Eymard, B., Dahl, A., Udd, B. :
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient J Neurol, 2011 ; 258 (6) : 1157-1163
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient J Neurol, 2011 ; 258 (6) : 1157-1163
Li, K, Hewson, DJ, DuchĂȘne, J, Hogrel, J Y :
Recurrence quantification analysis of sustained sub-maximal grip contractions in patients with various metabolic muscle disorders Biomed Sig Proc Control, 2011 ; 6 (1) : 70-76
Recurrence quantification analysis of sustained sub-maximal grip contractions in patients with various metabolic muscle disorders Biomed Sig Proc Control, 2011 ; 6 (1) : 70-76
Sylvius, N., Bonne, G., Straatman, K., Reddy, T., Gant, T. W., Shackleton, S. :
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy FASEB J, 2011 ; 25 (11) : 3966-78
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy FASEB J, 2011 ; 25 (11) : 3966-78
Carrier, L, Schlossarek, S, Willis, M, Eschenhagen, T :
Ubiquitin-proteasome system nonsense-mediated mRNA decay in hypertrophic cardiomyopathy Cardiovasc Res, 2010 ; 85 (2) : 330-338
Ubiquitin-proteasome system nonsense-mediated mRNA decay in hypertrophic cardiomyopathy Cardiovasc Res, 2010 ; 85 (2) : 330-338
Knoblauch, H., Geier, C., Adams, S., Budde, B., Rudolph, A., Zacharias, U., Schulz-Menger, J., Spuler, A., Ben Yaou, R., Nurnberg, P., Voit, T., Bonne, G., Spuler, S. :
Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation Ann Neurol, 2010 ; 67 (1) : 136-40
Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation Ann Neurol, 2010 ; 67 (1) : 136-40
Schessl, J., Columbus, A., Hu, Y., Zou, Y., Voit, T., Goebel, H. H., Bonnemann, C. G. :
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1 Neuropediatrics, 2010 ; 41 (1) : 43-6
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1 Neuropediatrics, 2010 ; 41 (1) : 43-6
Douillard-Guilloux, G., Raben, N., Takikita, S., Ferry, A., Vignaud, A., Guillet-Deniau, I., Favier, M., Thurberg, B. L., Roach, P. J., Caillaud, C., Richard, E. :
Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe disease Hum Mol Genet, 2010 ; 19 (4) : 684-96
Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe disease Hum Mol Genet, 2010 ; 19 (4) : 684-96
Lorain, S, Peccate, C, Le Hir, M, Garcia, L :
Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts PLoS ONE, 2010 ; 5 (5) : e10894
Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts PLoS ONE, 2010 ; 5 (5) : e10894
