Publications (1181)

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
Biancalana, V., Beggs, A. H., Das, S., Jungbluth, H., Kress, W., Nishino, I., North, K., Romero, N. B., Laporte, J. :
Clinical utility gene card for: Centronuclear and myotubular myopathies Eur J Hum Genet, 2012 ; 20 :
Geier, C, Schultze-Bahr, E, Bonne, G. :
Guiding the molecular diagnosis of hypertrophic cardiomyopathy J Thorac Cardiovasc Surg, 2012 ; 143 (5) : 1234
Marston, S., Copeland, O., Gehmlich, K., Schlossarek, S., Carrrier, L. :
How do MYBPC3 mutations cause hypertrophic cardiomyopathy? J Muscle Res Cell Motil, 2012 ; 33 : 75-80
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
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
Rigolet, A., Musset, L., Dubourg, O., Maisonobe, T., Grenier, P., Charuel, J. L., Behin, A., Herson, S., Amoura, Z., Benveniste, O. :
Inflammatory myopathies with anti-ku antibodies: a prognosis dependent on associated lung disease Medicine (Baltimore), 2012 ; 91 (2) : 95-102
Dowling, J. J., Arbogast, S., Hur, J., Nelson, D. D., McEvoy, A., Waugh, T., Marty, I., Lunardi, J., Brooks, S. V., Kuwada, J. Y., Ferreiro, A. :
Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy Brain, 2012 ; 135 (Pt 4) : 1115-1127