Publications (1184)

Ucar, A., Gupta, S. K., Fiedler, J., Erikci, E., Kardasinski, M., Batkai, S., Dangwal, S., Kumarswamy, R., Bang, C., Holzmann, A., Remke, J., Caprio, M., Jentzsch, C., Engelhardt, S., Geisendorf, S., Glas, C., Hofmann, T. G., Nessling, M., Richter, K., Schiffer, M., Carrier, L., Napp, L. C., Bauersachs, J., Chowdhury, K., Thum, T. :
The miRNA-212/132 family regulates both cardiac hypertrophy and cardiomyocyte autophagy Nat Commun, 2012 ; 3 : 1078
Castets, P., Lescure, A., Guicheney, P., Allamand, V. :
Selenoprotein N in skeletal muscle: from diseases to function J Mol Med (Berl), 2012 ; 90 (10) : 1095-1107
Herson, S., Hentati, F., Rigolet, A., Behin, A., Romero, N. B., Leturcq, F., Laforet, P., Maisonobe, T., Amouri, R., Haddad, H., Audit, M., Montus, M., Masurier, C., Gjata, B., Georger, C., Cherai, M., Carlier, P., Hogrel, J. Y., Herson, A., Allenbach, Y., Lemoine, F. M., Klatzmann, D., Sweeney, H. L., Mulligan, R. C., Eymard, B., Caizergues, D., Voit, T., Benveniste, O. :
A phase I trial of adeno-associated virus serotype 1-gamma-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C Brain, 2012 ; 135 (Pt 2) : 483-492
Ochala, J., Gokhin, D. S., Penisson-Besnier, I., Quijano-Roy, S., Monnier, N., Lunardi, J., Romero, N. B., Fowler, V. M. :
Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms Hum Mol Genet, 2012 ; 21 (20) : 4473-85
Wakeling, E. N., Joussemet, B., Costiou, P., Fanuel, D., Moullier, P., Barkats, M., Fyfe, J. C. :
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of SMA J Comp Neurol, 2012 ; 520 (8) : 1737-1750
Carlier, P. G. :
Skeletal muscle perfusion and oxygenation assessed by dynamic NMR imaging and spectroscopy Adv Exp Med Biol, 2011 ; 915 : 341-6
Hube, F., Velasco, G., Rollin, J., Furling, D., Francastel, C. :
Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiation Nucleic Acids Res, 2011 ; 39 (2) : 513-525
Pradat, P. F., Barani, A., Wanschitz, J., Dubourg, O., Lombes, A., Bigot, A., Mouly, V., Bruneteau, G., Salachas, F., Lenglet, T., Meininger, V., Butler-Browne, G. :
Abnormalities of satellite cells function in amyotrophic lateral sclerosis Amyotroph Lateral Scler, 2011 ; 12 (4) : 264-71
Dominguez, E., Marais, T., Chatauret, N., Benkhelifa-Ziyyat, S., Duque, S., Ravassard, P., Carcenac, R., Astord, S., Pereira de Moura, A., Voit, T., Barkats, M. :
Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice Hum Mol Genet, 2011 ; 20 (4) : 681-693
Leroux-Berger, M., Queguiner, I., Maciel, T. T., Ho, A., Relaix, F., Kempf, H. :
Pathological calcification of adult vascular smooth muscle cells differs upon their crest or mesodermal embryonic origin J Bone Miner Res, 2011 ; 26 (7) : 1543-53