Gali Ramamoorthy, T., Laverny, G., Schlagowski, A. I., Zoll, J., Messaddeq, N., Bornert, J. M., Panza, S., Ferry, A., Geny, B., Metzger, D. :
The transcriptional coregulator PGC-1beta controls mitochondrial function and anti-oxidant defence in skeletal muscles
Nat Commun, 2015 ; 6 : 10210
Publications (1184)
Béhin, A., Tiberghien, D., Babonneau, M. L., Brocq, H., Michon, C. C., Gargiulo, M., Réveillère, C. :
Mise au point : Urgences psychiatriques et traitements psychotropes dans les maladies neuromusculaires Anesthésie & Réanimation, 2015 ; 1 (suppl 1) : 47-52
Mise au point : Urgences psychiatriques et traitements psychotropes dans les maladies neuromusculaires Anesthésie & Réanimation, 2015 ; 1 (suppl 1) : 47-52
Allenbach, Y, Guiguet, M, Rigolet, A, Marie, I, Hachulla, E, Drouot, L, Jouen, F, Jacquot, S, Mariampillai, K, Musset, L, Grenier, P, Devilliers, H, Hij, A, Boyer, O, Herson, S, Benveniste, O :
Efficacy of Rituximab in Refractory Inflammatory Myopathies Associated with Anti- Synthetase Auto-Antibodies: an Open-Label, Phase II Trial PLoS ONE, 2015 ; (SP) :
Efficacy of Rituximab in Refractory Inflammatory Myopathies Associated with Anti- Synthetase Auto-Antibodies: an Open-Label, Phase II Trial PLoS ONE, 2015 ; (SP) :
Maurer, M., Bougoin, S., Feferman, T., Frenkian, M., Bismuth, J., Mouly, V., Clairac, G., Tzartos, S., Fadel, E., Eymard, B., Fuchs, S., Souroujon, M. C., Berrih-Aknin, S. :
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
Meliani, A., Leborgne, C., Triffault, S., Jeanson-Leh, L., Veron, P., Mingozzi, F. :
Determination of anti-adeno-associated virus vector neutralizing antibody titer with an in vitro reporter system Hum Gene Ther Methods, 2015 ; 26 (2) : 45-53
Determination of anti-adeno-associated virus vector neutralizing antibody titer with an in vitro reporter system Hum Gene Ther Methods, 2015 ; 26 (2) : 45-53
Blondelle, J., Ohno, Y., Gache, V., Guyot, S., Storck, S., Blanchard-Gutton, N., Barthelemy, I., Walmsley, G., Rahier, A., Gadin, S., Maurer, M., Guillaud, L., Prola, A., Ferry, A., Aubin-Houzelstein, G., Demarquoy, J., Relaix, F., Piercy, R. J., Blot, S., Kihara, A., Tiret, L., Pilot-Storck, F. :
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth J Mol Cell Biol, 2015 ; 7 (5) : 429-40
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth J Mol Cell Biol, 2015 ; 7 (5) : 429-40
Yaou, R. B., De Sandre-Giovannoli, A., Leturcq, F., Levy, N., Bonne, G. :
Premiere reunion franco-italienne des laminopathies et autres pathologies liees a l’enveloppe nucleaire Med Sci (Paris), 2015 ; 31 Spec No 3 : 39-40
Premiere reunion franco-italienne des laminopathies et autres pathologies liees a l’enveloppe nucleaire Med Sci (Paris), 2015 ; 31 Spec No 3 : 39-40
Cacheux, M., Blum, A., Sebastien, M., Wozny, A. S., Brocard, J., Mamchaoui, K., Mouly, V., Roux-Buisson, N., Rendu, J., Monnier, N., Krivosic, R., Allen, P., Lacour, A., Lunardi, J., Faure, J., Marty, I. :
Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein J Neuromuscul Dis, 2015 ; 2 (4) : 421-432
Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein J Neuromuscul Dis, 2015 ; 2 (4) : 421-432
Chartier, A., Klein, P., Pierson, S., Barbezier, N., Gidaro, T., Casas, F., Carberry, S., Dowling, P., Maynadier, L., Bellec, M., Oloko, M., Jardel, C., Moritz, B., Dickson, G., Mouly, V., Ohlendieck, K., Butler-Browne, G., Trollet, C., Simonelig, M. :
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
Preisler, N., Laforet, P., Madsen, K. L., Prahm, K. P., Hedermann, G., Vissing, C. R., Galbo, H., Vissing, J. :
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III Neurology, 2015 ; 84 (17) : 1767-1771
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III Neurology, 2015 ; 84 (17) : 1767-1771
