Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle von Boyer, Olivier, Butler-Browne, Gillian, Chinoy, Hector, Cossu, Giulio, Galli, Francesco, Lilleker, James B, Magli, Alessandro, Mouly, Vincent, Perlingeiro, Rita C R, Previtali, Stefano C, Sampaolesi, Maurilio, Smeets, Hubert, Schoewel-Wolf, Verena, Spuler, Simone, Torrente, Yvan, Van Tienen, Florence

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Autologous Transplantation of Muscle-Derived CD133+ Stem Cells in Duchenne Muscle Patients von Torrente, Y., Belicchi, M., Marchesi, C., D'antona, G., Cogiamanian, F., Pisati, F., Gavina, M., Giordano, R., Tonlorenzi, R., Fagiolari, G., Lamperti, C., Porretti, L., Lopa, R., Sampaolesi, M., Vicentini, L., Grimoldi, N., Tiberio, F., Songa, V., Baratta, P., Prelle, A., Forzenigo, L., Guglieri, M., Pansarasa, O., Rinaldi, C., Mouly, V., Butler-Browne, G. S., Comi, G. P., Biondetti, P., Moggio, M., Gaini, S. M., Stocchetti, N., Priori, A., D'angelo, M. G., Turconi, A., Bottinelli, R., Cossu, G., Rebulla, P., Bresolin, N.

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Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy von Díaz-Manera, J, Touvier, T, Dellavalle, A, Tonlorenzi, R, Tedesco, F S, Messina, G, Meregalli, M, Navarro, C, Perani, L, Bonfanti, C, Illa, I, Torrente, Y, Cossu, G

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Necdin enhances muscle reconstitution of dystrophic muscle by vessel-associated progenitors, by promoting cell survival and myogenic differentiation von Pessina, P, Conti, V, Tonlorenzi, R, Touvier, T, Meneveri, R, Cossu, G, Brunelli, S

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03P Modulation of the cyclin inhibitor p27 can ameliorate muscular dystrophy in LAMA2-RD von Bonaccorso, R., Porrello, E., Tonlorenzi, R., Previtali, S.

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Combined cell and gene therapy to treat merosin deficient congenital muscular dystrophy von Velardo, D, Domi, T, Porrello, E, Capotondo, A, Biffi, A, Tonlorenzi, R, Takeda, S, Amadio, S, Ruegg, M, Previtali, S

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Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells von Benedetti, S, Hoshiya, H, Ragazzi, M, Uno, N, Kazuki, Y, Ferrari, G, Tonlorenzi, R, Lombardo, A, Mouly, V, Naldini, L, Messina, G, Oshimura, M, Cossu, G, Tedesco, F

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Inflammatory and alternatively activated human macrophages attract vessel-associated stem cells, relying on separate HMGB1- and MMP-9-dependent pathways von Lolmede, Karine, Campana, Lara, Vezzoli, Michela, Bosurgi, Lidia, Tonlorenzi, Rossana, Clementi, Emilio, Bianchi, Marco E., Cossu, Giulio, Manfredi, Angelo A., Brunelli, Silvia, Rovere‐Querini, Patrizia

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Extracellular HMGB1, a Signal of Tissue Damage, Induces Mesoangioblast Migration and Proliferation von Palumbo, Roberta, Sampaolesi, Maurilio, De Marchis, Francesco, Tonlorenzi, Rossana, Colombetti, Sara, Mondino, Anna, Cossu, Giulio, Bianchi, Marco E.

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Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle von Torrente, Yvan, Belicchi, Marzia, Sampaolesi, Maurilio, Pisati, Federica, Meregalli, Mirella, D’Antona, Giuseppe, Tonlorenzi, Rossana, Porretti, Laura, Gavina, Manuela, Mamchaoui, Kamel, Pellegrino, Maria Antonietta, Furling, Denis, Mouly, Vincent, Butler-Browne, Gillian S., Bottinelli, Roberto, Cossu, Giulio, Bresolin, Nereo

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Cell Therapy of α-Sarcoglycan Null Dystrophic Mice through Intra-Arterial Delivery of Mesoangioblasts von Sampaolesi, Maurilio, Torrente, Yvan, Innocenzi, Anna, Tonlorenzi, Rossana, D'Antona, Giuseppe, Pellegrino, M. Antonietta, Barresi, Rita, Bresolin, Nereo, M. Cabriella Cusella De Angelis, Campbell, Kevin P., Bottinelli, Roberto, Cossu, Giulio

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Jab1 in the pathogenesis of Merosin deficient congenital muscular dystrophy (MDC1A) von Velardo, D., Porrello, E., Tonlorenzi, R., Lorenzetti, I., Pardi, R., Goldhamer, D., Previtali, S.

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P.33 - Jab1 in the pathogenesis of Merosin deficient congenital muscular dystrophy (MDC1A) von Velardo, D., Porrello, E., Tonlorenzi, R., Lorenzetti, I., Pardi, R., Goldhamer, D., Previtali, S.

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Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR) von Meloni, I, Vitelli, F, Pucci, L, Lowry, R B, Tonlorenzi, R, Rossi, E, Ventura, M, Rizzoni, G, Kashtan, C E, Pober, B, Renieri, A

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G.P.281 - Combined cell and gene therapy to treat merosin deficient congenital muscular dystrophy von Velardo, D., Domi, T., Porrello, E., Capotondo, A., Biffi, A., Tonlorenzi, R., Takeda, S., Amadio, S., Ruegg, M., Previtali, S.

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G.P.218 - Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells von Benedetti, S., Hoshiya, H., Ragazzi, M., Uno, N., Kazuki, Y., Ferrari, G., Tonlorenzi, R., Lombardo, A., Mouly, V., Naldini, L., Messina, G., Oshimura, M., Cossu, G., Tedesco, F.

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Msx2 and Necdin Combined Activities Are Required for Smooth Muscle Differentiation in Mesoangioblast Stem Cells von Brunelli, Silvia, Tagliafico, Enrico, De Angelis, Fernanda G, Tonlorenzi, Rossana, Baesso, Silvia, Ferrari, Sergio, Niinobe, Michio, Yoshikawa, Kazuaki, Schwartz, Robert J, Bozzoni, Irene, Ferrari, Stefano, Cossu, Giulio

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A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome von BROWN, C. J, BALLABIO, A, RUPERT, J. L, LAFRENIERE, R. G, GROMPE, M, TONLORENZI, R, WILLARD, H. F

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules von FRANCO, B, GUIOLI, S, BROWN, C. J, WILLARD, H. F, LAWRENCE, C, GRAZIELLA PERSICO, M, CAMERINO, G, BALLABIO, A, PRAGLIOLA, A, INCERTI, B, BARDONI, B, TONLORENZI, R, CARROZZO, R, MEASTRINI, E, PIERETTI, M, TAILLON-MILLER, P

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Characterization of a murine gene expressed from the inactive X chromosome von BORSANI, G, TONLORENZI, R, WILLARD, H. F, AVNER, P, SALLABIO, A, CHRISTINE SIMMLER, M, DANDOLO, L, ARNAUD, D, CAPRA, V, GROMPE, M, PIZZUTI, A, MUZNY, D, LAWRENCE, C

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