Langhans, C., Weber-Carstens, S., Schmidt, F., Hamati, J., Kny, M., Zhu, X., Wollersheim, T., Koch, S., Krebs, M., Schulz, H., Lodka, D., Saar, K., Labeit, S., Spies, C., Hubner, N., Spranger, J., Spuler, S., Boschmann, M., Dittmar, G., Butler-Browne, G., Mouly, V., Fielitz, J. :
Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy
PLoS ONE, 2014 ; 9 (3) : e92048
Publications (1181)
Mearini, G, Stimpel, D, Geertz, B, Weinberger, F, Krämer, E, Schlossarek, S, Mourot-Filiatre, J, Stöhr, A, Dutsch, A, Wijnker, P J M, Braren, I, Katus, H A, Müller, O J, Voit, T, Eschenhagen, T, Carrier, L. :
Mybpc3 gene therapy for neonatal cardiomyopathy enableslongterm disease prevention in mice Nat Commun, 2014 ; 5 : 5515
Mybpc3 gene therapy for neonatal cardiomyopathy enableslongterm disease prevention in mice Nat Commun, 2014 ; 5 : 5515
Tegtmeyer, L. C., Rust, S., van Scherpenzeel, M., Ng, B. G., Losfeld, M. E., Timal, S., Raymond, K., He, P., Ichikawa, M., Veltman, J., Huijben, K., Shin, Y. S., Sharma, V., Adamowicz, M., Lammens, M., Reunert, J., Witten, A., Schrapers, E., Matthijs, G., Jaeken, J., Rymen, D., Stojkovic, T., Laforet, P., Petit, F., Aumaitre, O., Czarnowska, E., Piraud, M., Podskarbi, T., Stanley, C. A., Matalon, R., Burda, P., Seyyedi, S., Debus, V., Socha, P., Sykut-Cegielska, J., van Spronsen, F., de Meirleir, L., Vajro, P., DeClue, T., Ficicioglu, C., Wada, Y., Wevers, R. A., Vanderschaeghe, D., Callewaert, N., Fingerhut, R., van Schaftingen, E., Freeze, H. H., Morava, E., Lefeber, D. J., Marquardt, T. :
Multiple phenotypes in phosphoglucomutase 1 deficiency N Engl J Med, 2014 ; 370 (6) : 533-42
Multiple phenotypes in phosphoglucomutase 1 deficiency N Engl J Med, 2014 ; 370 (6) : 533-42
Bohm, J., Biancalana, V., Malfatti, E., Dondaine, N., Koch, C., Vasli, N., Kress, W., Strittmatter, M., Taratuto, A. L., Gonorazky, H., Laforet, P., Maisonobe, T., Olive, M., Gonzalez-Mera, L., Fardeau, M., Carriere, N., Clavelou, P., Eymard, B., Bitoun, M., Rendu, J., Faure, J., Weis, J., Mandel, J. L., Romero, N. B., Laporte, J. :
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations Brain, 2014 ; 137 (Pt 12) : 3160-70
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations Brain, 2014 ; 137 (Pt 12) : 3160-70
Ferreboeuf, M., Mariot, V., Furling, D., Butler-Browne, G., Mouly, V., Dumonceaux, J. :
Nuclear protein spreading: implication for pathophysiology of neuromuscular diseases Hum Mol Genet, 2014 ; 23 (15) : 4125-4133
Nuclear protein spreading: implication for pathophysiology of neuromuscular diseases Hum Mol Genet, 2014 ; 23 (15) : 4125-4133
Possidonio, A. C., Soares, C. P., Portilho, D. M., Midlej, V., Benchimol, M., Butler-Browne, G., Costa, M. L., Mermelstein, C. :
Differences in the expression and distribution of flotillin-2 in chick, mice and human muscle cells PLoS ONE, 2014 ; 9 (8) : e103990
Differences in the expression and distribution of flotillin-2 in chick, mice and human muscle cells PLoS ONE, 2014 ; 9 (8) : e103990
Yuen, M., Sandaradura, S. A., Dowling, J. J., Kostyukova, A. S., Moroz, N., Quinlan, K. G., Lehtokari, V. L., Ravenscroft, G., Todd, E. J., Ceyhan-Birsoy, O., Gokhin, D. S., Maluenda, J., Lek, M., Nolent, F., Pappas, C. T., Novak, S. M., D'Amico, A., Malfatti, E., Thomas, B. P., Gabriel, S. B., Gupta, N., Daly, M. J., Ilkovski, B., Houweling, P. J., Davidson, A. E., Swanson, L. C., Brownstein, C. A., Gupta, V. A., Medne, L., Shannon, P., Martin, N., Bick, D. P., Flisberg, A., Holmberg, E., Van den Bergh, P., Lapunzina, P., Waddell, L. B., Sloboda, D. D., Bertini, E., Chitayat, D., Telfer, W. R., Laquerriere, A., Gregorio, C. C., Ottenheijm, C. A., Bonnemann, C. G., Pelin, K., Beggs, A. H., Hayashi, Y. K., Romero, N. B., Laing, N. G., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V. M., MacArthur, D. G., North, K. N., Clarke, N. F. :
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy J Clin Invest, 2014 ; 124 (11) : 4693-4708
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy J Clin Invest, 2014 ; 124 (11) : 4693-4708
Aouizerate, J., De Antonio, M., Bassez, G., Gherardi, R. K., Berenbaum, F., Guillevin, L., Berezne, A., Valeyre, D., Maisonobe, T., Dubourg, O., Cosnes, A., Benveniste, O., Authier, F. J. :
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathy Acta Neuropathol Commun, 2014 ; 2 : 154
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathy Acta Neuropathol Commun, 2014 ; 2 : 154
Chatzifrangkeskou, M., Bonne, G., Muchir, A. :
Nuclear envelope and striated muscle diseases Curr Opin Cell Biol, 2014 ; 32C : 1-6
Nuclear envelope and striated muscle diseases Curr Opin Cell Biol, 2014 ; 32C : 1-6
Gradolatto, A., Nazzal, D., Truffault, F., Bismuth, J., Fadel, E., Foti, M., Berrih-Aknin, S. :
Both Treg cells and Tconv cells are defective in the Myasthenia gravis thymus: Roles of IL-17 and TNF-alpha J Autoimmun, 2014 ; 52 : 53-63
Both Treg cells and Tconv cells are defective in the Myasthenia gravis thymus: Roles of IL-17 and TNF-alpha J Autoimmun, 2014 ; 52 : 53-63
