Mingozzi, F., Chen, Y., Edmonson, S. C., Zhou, S., Thurlings, R. M., Tak, P. P., High, K. A., Vervoordeldonk, M. J. :
Prevalence and pharmacological modulation of humoral immunity to AAV vectors in gene transfer to synovial tissue
Gene Ther, 2013 ; 20 (4) : 417-24
Publications (1181)
Gertel-Lapter, S., Mizrachi, K., Berrih-Aknin, S., Fuchs, S., Souroujon, M. C. :
Impairment of regulatory T cells in myasthenia gravis: Studies in an experimental model Autoimmun Rev, 2013 ; 12 (9) : 894-903
Impairment of regulatory T cells in myasthenia gravis: Studies in an experimental model Autoimmun Rev, 2013 ; 12 (9) : 894-903
Mingozzi, F., Anguela, X. M., Pavani, G., Chen, Y., Davidson, R. J., Hui, D. J., Yazicioglu, M., Elkouby, L., Hinderer, C. J., Faella, A., Howard, C., Tai, A., Podsakoff, G. M., Zhou, S., Basner-Tschakarjan, E., Wright, J. F., High, K. A. :
Overcoming preexisting humoral immunity to AAV using capsid decoys Sci Transl Med, 2013 ; 5 (194) : 194ra92
Overcoming preexisting humoral immunity to AAV using capsid decoys Sci Transl Med, 2013 ; 5 (194) : 194ra92
Gauthier, M., Marteyn, A., Denis, J. A., Cailleret, M., Giraud-Triboult, K., Aubert, S., Lecuyer, C., Marie, J., Furling, D., Vernet, R., Yanguas, C., Baldeschi, C., Pietu, G., Peschanski, M., Martinat, C. :
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1 Hum Mol Genet, 2013 ; 22 (25) : 5188-98
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1 Hum Mol Genet, 2013 ; 22 (25) : 5188-98
Baraibar, M. A., Gueugneau, M., Duguez, S., Butler-Browne, G., Bechet, D., Friguet, B. :
Expression and modification proteomics during skeletal muscle ageing Biogerontology, 2013 ; 4 (3) : 339-352
Expression and modification proteomics during skeletal muscle ageing Biogerontology, 2013 ; 4 (3) : 339-352
Moraux, A., Canal, A., Ollivier, G., Ledoux, I., Doppler, V., Payan, C., Hogrel, J. Y. :
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years BMC Musculoskelet Disord, 2013 ; 14 : 104
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years BMC Musculoskelet Disord, 2013 ; 14 : 104
Desdouits, M., Cassar, O., Maisonobe, T., Desrames, A., Aouba, A., Hermine, O., Mikol, J., Polivka, M., Penisson-Besnier, I., Marcorelles, P., Zagnoli, F., Papo, T., Lacour, A., Amoura, Z., Haroche, J., Cherin, P., Teixeira, A., Benveniste, O., Herson, S., Morin, A. S., Mortreux, F., Wattel, E., Huerre, M., Cumont, M. C., Martin-Latil, S., Butler-Browne, G., Gout, O., Taylor, G., Gessain, A., Ozden, S., Ceccaldi, P. E. :
HTLV-1-associated inflammatory myopathies: Low proviral load and moderate inflammation in 13 patients from West Indies and West Africa J Clin Virol, 2013 ; 57 (1) : 70-76
HTLV-1-associated inflammatory myopathies: Low proviral load and moderate inflammation in 13 patients from West Indies and West Africa J Clin Virol, 2013 ; 57 (1) : 70-76
Weiss, J. M., Cufi, P., Le Panse, R., Berrih-Aknin, S. :
The thymus in autoimmune Myasthenia Gravis: Paradigm for a tertiary lymphoid organ Rev Neurol (Paris), 2013 ; 169 (8-9) : 640-649
The thymus in autoimmune Myasthenia Gravis: Paradigm for a tertiary lymphoid organ Rev Neurol (Paris), 2013 ; 169 (8-9) : 640-649
Rokach, O., Ullrich, N. D., Rausch, M., Mouly, V., Zhou, H., Muntoni, F., Zorzato, F., Treves, S. :
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization Biochem J, 2013 ; 455 (2) : 169-77
Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization Biochem J, 2013 ; 455 (2) : 169-77
Bohm, J., Leshinsky-Silver, E., Vassilopoulos, S., Le Gras, S., Lerman-Sagie, T., Ginzberg, M., Jost, B., Lev, D., Laporte, J. :
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation Acta Neuropathol, 2012 ; 124 (4) : 575-581
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation Acta Neuropathol, 2012 ; 124 (4) : 575-581
