Wray, D. W., Nishiyama, S. K., Monnet, A., Wary, C., Duteil, S. S., Carlier, P. G., Richardson, R. S. :
Antioxidants and aging: NMR-based evidence of improved skeletal muscle perfusion and energetics
Am J Physiol Heart Circ Physiol, 2009 ; 297 (5) : H1870-5
Publications (1184)
Claeys, K. G., van der Ven, P. F., Behin, A., Stojkovic, T., Eymard, B., Dubourg, O., Laforet, P., Faulkner, G., Richard, P., Vicart, P., Romero, N. B., Stoltenburg, G., Udd, B., Fardeau, M., Voit, T., Furst, D. O. :
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Acta Neuropathol, 2009 ; 117 (3) : 293-307
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Acta Neuropathol, 2009 ; 117 (3) : 293-307
Krahn, M., Borges, A., Navarro, C., Schuit, R., Stojkovic, T., Torrente, Y., Wein, N., Pecheux, C., Levy, N. :
Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR Genet Test Mol Biomarkers, 2009 ; 13 (4) : 439-442
Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR Genet Test Mol Biomarkers, 2009 ; 13 (4) : 439-442
Relaix, F., Marcelle, C. :
Muscle stem cells Curr Opin Cell Biol, 2009 ; 21 (6) : 748-53
Muscle stem cells Curr Opin Cell Biol, 2009 ; 21 (6) : 748-53
Amthor, H., Otto, A., Vulin, A., Rochat, A., Dumonceaux, J., Garcia, L., Mouisel, E., Hourde, C., Macharia, R., Friedrichs, M., Relaix, F., Zammit, P. S., Matsakas, A., Patel, K., Partridge, T. :
Muscle hypertrophy driven by myostatin blockade does not require stem/precursor-cell activity Proc Natl Acad Sci U S A, 2009 ; 106 (18) : 7479-84
Muscle hypertrophy driven by myostatin blockade does not require stem/precursor-cell activity Proc Natl Acad Sci U S A, 2009 ; 106 (18) : 7479-84
Djouadi, F., Lecarpentier, Y., Hebert, J. L., Charron, P., Bastin, J., Coirault, C. :
A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy Cardiovasc Res, 2009 ; 84 (1) : 83-90
A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy Cardiovasc Res, 2009 ; 84 (1) : 83-90
Marmursztejn, J., Vignaux, O., Cohen, P., Guilpain, P., Pagnoux, C., Gouya, H., Mouthon, L., Legmann, P., Duboc, D., Guillevin, L. :
Impact of cardiac magnetic resonance imaging for assessment of Churg-Strauss syndrome: a cross-sectional study in 20 patients Clin Exp Rheumatol, 2009 ; 27 (1 Suppl 52) : S70-6
Impact of cardiac magnetic resonance imaging for assessment of Churg-Strauss syndrome: a cross-sectional study in 20 patients Clin Exp Rheumatol, 2009 ; 27 (1 Suppl 52) : S70-6
Tuffery-Giraud, S, Béroud, C, Leturcq, F, Ben Yaou, R, Hamroun, D, Michel-Calemard, L, Moizard, M P, Bernard, R, Cossée, M, Boisseau, P, Blayau, M, Creveaux, I, Guiochon-Mantel, A, de Martinville, B, Philippe, C, Monnier, N, Bieth, E, Khau van Kien, P, Desmet, F O, Humbertclaude, V, Kaplan, J C, Chelly, J, Claustres, M :
Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase Human Mutation, 2009 ; 30 (934-945) :
Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase Human Mutation, 2009 ; 30 (934-945) :
Bitoun, M., Durieux, A. C., Prudhon, B., Bevilacqua, J. A., Herledan, A., Sakanyan, V., Urtizberea, A., Cartier, L., Romero, N. B., Guicheney, P. :
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis Hum Mutat, 2009 ; 30 (10) : 1419-1427
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis Hum Mutat, 2009 ; 30 (10) : 1419-1427
Friedrich, F. W., Bausero, P., Sun, Y., Treszl, A., Kramer, E., Juhr, D., Richard, P., Wegscheider, K., Schwartz, K., Brito, D., Arbustini, E., Waldenstrom, A., Isnard, R., Komajda, M., Eschenhagen, T., Carrier, L. :
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy Eur Heart J, 2009 ; 30 (13) : 1648-55
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy Eur Heart J, 2009 ; 30 (13) : 1648-55
