Arimura, T., Onoue, K., Takahashi-Tanaka, Y., Ishikawa, T., Kuwahara, M., Setou, M., Shigenobu, S., Yamaguchi, K., Bertrand, A. T., Machida, N., Takayama, K., Fukusato, M., Tanaka, R., Somekawa, S., Nakano, T., Yamane, Y., Kuba, K., Imai, Y., Saito, Y., Bonne, G., Kimura, A. :
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations
Cardiovasc Res, 2013 ; 99 (3) : 382-94
Publications (1181)
Chort, A., Alves, S., Marinello, M., Dufresnois, B., Dornbierer, J. G., Tesson, C., Latouche, M., Baker, D. P., Barkats, M., El Hachimi, K. H., Ruberg, M., Janer, A., Stevanin, G., Brice, A., Sittler, A. :
Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice Brain, 2013 ; 136 (Pt 6) : 1732-1745
Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice Brain, 2013 ; 136 (Pt 6) : 1732-1745
Finsterer, J., Stollberger, C., Wahbi, K. :
Cardiomyopathy in neurological disorders Cardiovasc Pathol, 2013 ; 22 (5) : 389-400
Cardiomyopathy in neurological disorders Cardiovasc Pathol, 2013 ; 22 (5) : 389-400
Mayhew, A., Mazzone, E. S., Eagle, M., Duong, T., Ash, M., Decostre, V., Vandenhauwe, M., Klingels, K., Florence, J., Main, M., Bianco, F., Henrikson, E., Servais, L., Campion, G., Vroom, E., Ricotti, V., Goemans, N., McDonald, C., Mercuri, E. :
Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy Dev Med Child Neurol, 2013 ; 55 (11) : 1038-45
Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy Dev Med Child Neurol, 2013 ; 55 (11) : 1038-45
Aure, K., Dubourg, O., Jardel, C., Clarysse, L., Sternberg, D., Fournier, E., Laforet, P., Streichenberger, N., Petiot, P., Gervais-Bernard, H., Vial, C., Bedat-Millet, A. L., Drouin-Garraud, V., Bouillaud, F., Vandier, C., Fontaine, B., Lombes, A. :
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations Neurology, 2013 ; 81 (21) : 1810-8
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations Neurology, 2013 ; 81 (21) : 1810-8
Shichiji, M, Biancalana, V, Fardeau, M, Hogrel, J Y, Osawa, M, Laporte, J, Romero, N B :
Extensive morphological and immunohistochemical characterization in myotubular myopathy Brain Behavior, 2013 ; 3 (4) : 476-486
Extensive morphological and immunohistochemical characterization in myotubular myopathy Brain Behavior, 2013 ; 3 (4) : 476-486
Gedicke-Hornung, C., Behrens-Gawlik, V., Reischmann, S., Geertz, B., Stimpel, D., Weinberger, F., Schlossarek, S., Precigout, G., Braren, I., Eschenhagen, T., Mearini, G., Lorain, S., Voit, T., Dreyfus, P. A., Garcia, L., Carrier, L. :
Rescue of cardiomyopathy through U7snRNA-mediated exon skipping in Mybpc3-targeted knock-in mice EMBO Mol Med, 2013 ; 5 (7) : 1060-77
Rescue of cardiomyopathy through U7snRNA-mediated exon skipping in Mybpc3-targeted knock-in mice EMBO Mol Med, 2013 ; 5 (7) : 1060-77
Schirwis, E., Agbulut, O., Vadrot, N., Mouisel, E., Hourde, C., Bonnieu, A., Butler-Browne, G., Amthor, H., Ferry, A. :
The beneficial effect of myostatin deficiency on maximal muscle force and power is attenuated with age Exp Gerontol, 2013 ; 48 (2) : 183-190
The beneficial effect of myostatin deficiency on maximal muscle force and power is attenuated with age Exp Gerontol, 2013 ; 48 (2) : 183-190
Gil-Farina, I., Di Scala, M., Vanrell, L., Olague, C., Vales, A., High, K. A., Prieto, J., Mingozzi, F., Gonzalez-Aseguinolaza, G. :
IL12-mediated liver inflammation reduces the formation of AAV transcriptionally active forms but has no effect over preexisting AAV transgene expression PLoS ONE, 2013 ; 8 (7) : e67748
IL12-mediated liver inflammation reduces the formation of AAV transcriptionally active forms but has no effect over preexisting AAV transgene expression PLoS ONE, 2013 ; 8 (7) : e67748
Pannerec, A., Formicola, L., Besson, V., Marazzi, G., Sassoon, D. A. :
Defining skeletal muscle resident progenitors and their cell fate potentials Development, 2013 ; 140 (14) : 2879-2891
Defining skeletal muscle resident progenitors and their cell fate potentials Development, 2013 ; 140 (14) : 2879-2891