Chuah, M. K., Petrus, I., De Bleser, P., Le Guiner, C., Gernoux, G., Adjali, O., Nair, N., Willems, J., Evens, H., Rincon, M. Y., Matrai, J., Di Matteo, M., Samara-Kuko, E., Yan, B., Acosta-Sanchez, A., Meliani, A., Cherel, G., Blouin, V., Christophe, O., Moullier, P., Mingozzi, F., Driessche, T. V. :
Liver-Specific Transcriptional Modules Identified by Genome-Wide in Silico Analysis Enable Efficient Gene Therapy in Mice and Non-Human Primates
Mol Ther, 2014 ; 22(9):1605-13 (9) : 1605-13
Publications (1181)
Gueugneau, M., Coudy-Gandilhon, C., Gourbeyre, O., Chambon, C., Combaret, L., Polge, C., Taillandier, D., Attaix, D., Friguet, B., Maier, A. B., Butler-Browne, G., Bechet, D. :
Proteomics of muscle chronological ageing in post-menopausal women BMC Genomics, 2014 ; 15 (1) : 1165
Proteomics of muscle chronological ageing in post-menopausal women BMC Genomics, 2014 ; 15 (1) : 1165
Punga, T., Le Panse, R., Andersson, M., Truffault, F., Berrih-Aknin, S., Punga, A. R. :
Circulating miRNAs in myasthenia gravis: miR-150-5p as a new potential biomarker Ann Clin Transl Neurol, 2014 ; 1 (1) : 49-58
Circulating miRNAs in myasthenia gravis: miR-150-5p as a new potential biomarker Ann Clin Transl Neurol, 2014 ; 1 (1) : 49-58
Zalc, A., Hayashi, S., Aurade, F., Brohl, D., Chang, T., Mademtzoglou, D., Mourikis, P., Yao, Z., Cao, Y., Birchmeier, C., Relaix, F. :
Antagonistic regulation of p57kip2 by Hes/Hey downstream of Notch signaling and muscle regulatory factors regulates skeletal muscle growth arrest Development, 2014 ; 141 (14) : 2780-90
Antagonistic regulation of p57kip2 by Hes/Hey downstream of Notch signaling and muscle regulatory factors regulates skeletal muscle growth arrest Development, 2014 ; 141 (14) : 2780-90
Gargiulo, M., Herson, A., Angeard, N. :
Informing a child about genetic disorders: the need to know and understand MĂ©d Ther PĂ©diatr, 2014 ; 17 (1) : 8-14
Informing a child about genetic disorders: the need to know and understand MĂ©d Ther PĂ©diatr, 2014 ; 17 (1) : 8-14
Benveniste, O. :
La myosite Ă inclusions Rev Med Interne, 2014 ; 35 (7) : 472-479
La myosite Ă inclusions Rev Med Interne, 2014 ; 35 (7) : 472-479
Dorboz, I., Coutelier, M., Bertrand, A. T., Caberg, J. H., Elmaleh-Berges, M., Laine, J., Stevanin, G., Bonne, G., Boespflug-Tanguy, O., Servais, L. :
Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1 Orphanet J Rare Dis, 2014 ; 9 (1) : 174
Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1 Orphanet J Rare Dis, 2014 ; 9 (1) : 174
Lefevre, G., Meyer, A., Launay, D., Machelart, I., DeBandt, M., Michaud, J., Tournadre, A., Godmer, P., Kahn, J. E., Behra-Marsac, A., Timsit, M. A., Schleinitz, N., Wendling, D., Melac-Ducamp, S., Boyer, P., Peretz, A., Lequerre, T., Richez, C., Stervinou-Wemeau, L., Morell-Dubois, S., Lambert, M., Dubucquoi, S., Wallaert, B., Benveniste, O., Flipo, R. M., Hatron, P. Y., Sibilia, J., Hachulla, E., Hervier, B., on behalf of the Club Rhumatismes, Inflammation :
Seronegative polyarthritis revealing antisynthetase syndrome: a multicentre study of 40 patients Rheumatology (Oxford), 2014 ; :
Seronegative polyarthritis revealing antisynthetase syndrome: a multicentre study of 40 patients Rheumatology (Oxford), 2014 ; :
Schwoerer, A. P., Neef, S., Broichhausen, I., Jacubeit, J., Tiburcy, M., Wagner, M., Biermann, D., Didie, M., Vettel, C., Maier, L. S., Zimmermann, W. H., Carrier, L., Eschenhagen, T., Volk, T., El-Armouche, A., Ehmke, H. :
Enhanced Ca(2)+ influx through cardiac L-type Ca(2)+ channels maintains the systolic Ca(2)+ transient in early cardiac atrophy induced by mechanical unloading Pflugers Arch, 2014 ; 465 (12) : 1763-73
Enhanced Ca(2)+ influx through cardiac L-type Ca(2)+ channels maintains the systolic Ca(2)+ transient in early cardiac atrophy induced by mechanical unloading Pflugers Arch, 2014 ; 465 (12) : 1763-73
Boizot, A., Talmat-Amar, Y., Morrogh, D., Kuntz, N. L., Halbert, C., Chabrol, B., Houlden, H., Stojkovic, T., Schulman, B. A., Rautenstrauss, B., Bomont, P. :
The instability of the BTB-KELCH protein Gigaxonin causes Giant Axonal Neuropathy and constitutes a new penetrant and specific diagnostic test Acta Neuropathol Commun, 2014 ; 2 (1) : 47
The instability of the BTB-KELCH protein Gigaxonin causes Giant Axonal Neuropathy and constitutes a new penetrant and specific diagnostic test Acta Neuropathol Commun, 2014 ; 2 (1) : 47
