Publications (1181)

Zyss, J., Behin, A., Couvert, P., Bouhour, F., Sassolas, A., Kolev, I., Denys, V., Vial, C., Lacour, A., Carrie, A., Stojkovic, T. :
Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease J Neurol, 2012 ; 259 (6) : 1222-1226
Bertrand, A. T., Renou, L., Papadopoulos, A., Beuvin, M., Lacene, E., Massart, C., Ottolenghi, C., Decostre, V., Maron, S., Schlossarek, S., Cattin, M. E., Carrier, L., Malissen, M., Arimura, T., Bonne, G. :
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death Hum Mol Genet, 2012 ; 21 (5) : 1037-48
Gayraud-Morel, B, Chrétien, F, Negroni, E, Jory, A, Sambasivan, R, Flamant, P, Soubigou, G, Coppée, J Y, Di Santo, J, Cumano, A, Mouly, V, Tajbakhsh, S :
Myf5 haploinsufficiency reveals distinct cell fate potentials for adult skeletal muscle stem cells J Cell Sci, 2012 ; 125 (Pt 7) : 1738-1749
Marsden, C. G., Wright, M. J., Carrier, L., Moroz, K., Rowan, B. G. :
Disseminated Breast Cancer Cells Acquire a Highly Malignant and Aggressive Metastatic Phenotype during Metastatic Latency in the Bone PLoS ONE, 2012 ; 7 (11) : e47587
Terrier, B., Geri, G., Chaara, W., Allenbach, Y., Rosenzwajg, M., Costedoat-Chalumeau, N., Fouret, P., Musset, L., Benveniste, O., Six, A., Klatzmann, D., Saadoun, D., Cacoub, P. :
IL-21 modulates Th1 and Th17 responses in giant cell arteritis Arthritis Rheum, 2012 ; 64 (6) : 2001-2011
Bouquet, F., Cossee, M., Behin, A., Deburgrave, N., Romero, N., Leturcq, F., Eymard, B. :
Miyoshi-like distal myopathy with mutations in anoctamin 5 gene Rev Neurol (Paris), 2012 ; 168 (2) : 135-141
Havis, E., Coumailleau, P., Bonnet, A., Bismuth, K., Bonnin, M. A., Johnson, R., Fan, C. M., Relaix, F., Shi, D. L., Duprez, D. :
Sim2 prevents entry into the myogenic program by repressing MyoD transcription during limb embryonic myogenesis Development, 2012 ; 139 (11) : 1910-1920
Nicolas, A., Lucchetti-Miganeh, C., Ben Yaou, R., Kaplan, J. C., Chelly, J., Leturcq, F., Barloy-Hubler, F., Le Rumeur, E. :
Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database Orphanet J Rare Dis, 2012 ; 7 (1) : 45
Wahbi, K., Meune, C., Porcher, R., Becane, H. M., Lazarus, A., Laforet, P., Stojkovic, T., Behin, A., Radvanyi-Hoffmann, H., Eymard, B., Duboc, D. :
Electrophysiological study with prophylactic pacing and survival in adults with myotonic dystrophy and conduction system disease JAMA, 2012 ; 307 (12) : 1292-1301
Baligand, C., Jouvion, G., Schackman, O., Gilson, H., Wary, C., Thissen, J. P., Carlier, P. G. :
Multiparametric functional NMR shows alterations associated with plasmid electrotransfer in mouse skeletal muscle J Gene Med, 2012 ; 14 (9-10) : 598-608