Crocini, C., Arimura, T., Reischmann, S., Eder, A., Braren, I., Hansen, A., Eschenhagen, T., Kimura, A., Carrier, L. :
Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue
Basic Res Cardiol, 2013 ; 108 (3) : 349
Publications (1184)
Bohm, J., Chevessier, F., De Paula, A. M., Koch, C., Attarian, S., Feger, C., Hantai, D., Laforet, P., Ghorab, K., Vallat, J. M., Fardeau, M., Figarella-Branger, D., Pouget, J., Romero, N. B., Koch, M., Ebel, C., Levy, N., Krahn, M., Eymard, B., Bartoli, M., Laporte, J. :
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy Am J Hum Genet, 2013 ; 92 (2) : 271-8
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy Am J Hum Genet, 2013 ; 92 (2) : 271-8
Prevel, N., Allenbach, Y., Klatzmann, D., Salomon, B., Benveniste, O. :
Beneficial role of rapamycin in experimental autoimmune myositis PLoS ONE, 2013 ; 8 (11) : e74450
Beneficial role of rapamycin in experimental autoimmune myositis PLoS ONE, 2013 ; 8 (11) : e74450
Butler-Browne, G., McPhee, J., Mouly, V., Ottavi, A. :
Understanding and combating age-related muscle weakness: MYOAGE challenge Biogerontology, 2013 ; 14 (3) : 229-30
Understanding and combating age-related muscle weakness: MYOAGE challenge Biogerontology, 2013 ; 14 (3) : 229-30
Ousterout, D. G., Perez-Pinera, P., Thakore, P. I., Kabadi, A. M., Brown, M. T., Qin, X., Fedrigo, O., Mouly, V., Tremblay, J. P., Gersbach, C. A. :
Reading Frame Correction by Targeted Genome Editing Restores Dystrophin Expression in Cells From Duchenne Muscular Dystrophy Patients Mol Ther, 2013 ; 21 (9) : 1718-26
Reading Frame Correction by Targeted Genome Editing Restores Dystrophin Expression in Cells From Duchenne Muscular Dystrophy Patients Mol Ther, 2013 ; 21 (9) : 1718-26
Joanne, P., Chourbagi, O., Hourde, C., Ferry, A., Butler-Browne, G., Vicart, P., Dumonceaux, J., Agbulut, O. :
Viral-mediated expression of desmin mutants to create mouse models of myofibrillar myopathy Skelet Muscle, 2013 ; 3 (1) : 4
Viral-mediated expression of desmin mutants to create mouse models of myofibrillar myopathy Skelet Muscle, 2013 ; 3 (1) : 4
Houdayer, F., Gargiulo, M., Frischmann, M., Labalme, A., Decullier, E., Cordier, M. P., Dupuis-Girod, S., Lesca, G., Till, M., Sanlaville, D., Edery, P., Rossi, M. :
The psychological impact of cryptic chromosomal abnormalities diagnosis announcement Eur J Med Genet, 2013 ; 56 (11) : 585-590
The psychological impact of cryptic chromosomal abnormalities diagnosis announcement Eur J Med Genet, 2013 ; 56 (11) : 585-590
Eymard, B., Hantai, D., Estournet, B. :
Congenital myasthenic syndromes Handb Clin Neurol, 2013 ; 113 : 1469-80
Congenital myasthenic syndromes Handb Clin Neurol, 2013 ; 113 : 1469-80
Brinas, L., Vassilopoulos, S., Bonne, G., Guicheney, P., Bitoun, M. :
Role of dynamin 2 in the disassembly of focal adhesions J Mol Med (Berl), 2013 ; 91 (7) : 803-9
Role of dynamin 2 in the disassembly of focal adhesions J Mol Med (Berl), 2013 ; 91 (7) : 803-9
Gargiulo, M, Scelles, R :
Famille et handicap : mutations dans les pratiques Dialogue, 2013 ; 200 : 85-96
Famille et handicap : mutations dans les pratiques Dialogue, 2013 ; 200 : 85-96
