Friedrich, F. W., Dilanian, G., Khattar, P., Juhr, D., Gueneau, L., Charron, P., Fressart, V., Vilquin, J. T., Isnard, R., Gouya, L., Richard, P., Hammoudi, N., Komajda, M., Bonne, G., Eschenhagen, T., Dubourg, O., Villard, E., Carrier, L. :
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity
Eur J Heart Fail, 2013 ; 15 (3) : 267-76
Publications (1181)
Vignier, N., Amor, F., Fogel, P., Duvallet, A., Poupiot, J., Charrier, S., Arock, M., Montus, M., Nelson, I., Richard, I., Carrier, L., Servais, L., Voit, T., Bonne, G., Israeli, D. :
Distinctive Serum miRNA Profile in Mouse Models of Striated Muscular Pathologies PLoS ONE, 2013 ; 8 (2) : e55281
Distinctive Serum miRNA Profile in Mouse Models of Striated Muscular Pathologies PLoS ONE, 2013 ; 8 (2) : e55281
Denard, J., Marolleau, B., Jenny, C., Rao, T. N., Fehling, H. J., Voit, T., Svinartchouk, F. :
C-reactive protein (CRP) is essential for efficient systemic transduction of recombinant adeno-associated virus vector 1 (rAAV-1) and rAAV-6 in mice J Virol, 2013 ; 87 (19) : 10784-91
C-reactive protein (CRP) is essential for efficient systemic transduction of recombinant adeno-associated virus vector 1 (rAAV-1) and rAAV-6 in mice J Virol, 2013 ; 87 (19) : 10784-91
Le Panse, R., Berrih-Aknin, S. :
Autoimmune myasthenia gravis: autoantibody mechanisms and new developments on immune regulation Curr Opin Neurol, 2013 ; 26 (5) : 569-76
Autoimmune myasthenia gravis: autoantibody mechanisms and new developments on immune regulation Curr Opin Neurol, 2013 ; 26 (5) : 569-76
Caruso, N., Herberth, B., Bartoli, M., Puppo, F., Dumonceaux, J., Zimmermann, A., Denadai, S., Lebosse, M., Roche, S., Geng, L., Magdinier, F., Attarian, S., Bernard, R., Maina, F., Levy, N., Helmbacher, F. :
Deregulation of the Protocadherin Gene FAT1 Alters Muscle Shapes: Implications for the Pathogenesis of Facioscapulohumeral Dystrophy PLoS Genet, 2013 ; 9 (6) : e1003550
Deregulation of the Protocadherin Gene FAT1 Alters Muscle Shapes: Implications for the Pathogenesis of Facioscapulohumeral Dystrophy PLoS Genet, 2013 ; 9 (6) : e1003550
Nebel, M., Schwoerer, A. P., Warszta, D., Siebrands, C. C., Limbrock, A. C., Swarbrick, J. M., Fliegert, R., Weber, K., Bruhn, S., Hohenegger, M., Geisler, A., Herich, L., Schlegel, S., Carrier, L., Eschenhagen, T., Potter, B. V., Ehmke, H., Guse, A. H. :
NAADP mediated calcium signalling and arrhythmias in the heart evoked by beta-adrenergic stimulation J Biol Chem, 2013 ; 288 (22) : 16017-16030
NAADP mediated calcium signalling and arrhythmias in the heart evoked by beta-adrenergic stimulation J Biol Chem, 2013 ; 288 (22) : 16017-16030
Benkhelifa-Ziyyat, S., Besse, A., Roda, M., Duque, S., Astord, S., Carcenac, R., Marais, T., Barkats, M. :
Intramuscular scAAV9-SMN Injection Mediates Widespread Gene Delivery to the Spinal Cord and Decreases Disease Severity in SMA Mice Mol Ther, 2013 ; 21 (2) : 282-90
Intramuscular scAAV9-SMN Injection Mediates Widespread Gene Delivery to the Spinal Cord and Decreases Disease Severity in SMA Mice Mol Ther, 2013 ; 21 (2) : 282-90
Willis, T. A., Hollingsworth, K. G., Coombs, A., Sveen, M. L., Andersen, S., Stojkovic, T., Eagle, M., Mayhew, A., de Sousa, P. L., Dewar, L., Morrow, J. M., Sinclair, C. D., Thornton, J. S., Bushby, K., Lochmuller, H., Hanna, M. G., Hogrel, J. Y., Carlier, P. G., Vissing, J., Straub, V. :
Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study PLoS ONE, 2013 ; 8 (8) : e70993
Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study PLoS ONE, 2013 ; 8 (8) : e70993
Popplewell, L., Koo, T., Leclerc, X., Duclert, A., Mamchaoui, K., Gouble, A., Mouly, V., Voit, T., Paques, F., Cedrone, F., Isman, O., Yanez-Munoz, R. J., Dickson, G. :
Gene correction of a duchenne muscular dystrophy mutation by meganuclease-enhanced exon knock-in Hum Gene Ther, 2013 ; 24 (7) : 692-701
Gene correction of a duchenne muscular dystrophy mutation by meganuclease-enhanced exon knock-in Hum Gene Ther, 2013 ; 24 (7) : 692-701
Le Hir, M., Goyenvalle, A., Peccate, C., Precigout, G., Davies, K. E., Voit, T., Garcia, L., Lorain, S. :
AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy Mol Ther, 2013 ; 21 (8) : 1551-1558
AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy Mol Ther, 2013 ; 21 (8) : 1551-1558
