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R Tonlorenzi

Showing results (1-10 of 10) with videos related to

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European Journal of Human Genetics : EJHG|March 27, 1999
Spectrum of mutations in fucosidosisP J Willems, H C Seo, P Coucke, et al.
Cell Death and Differentiation|November 19, 2011
Necdin enhances muscle reconstitution of dystrophic muscle by vessel-associated progenitors, by promoting cell survival and myogenic differentiationP Pessina, V Conti, R Tonlorenzi, et al.
Archives Italiennes De Biologie|August 16, 2005
Cell therapy of primary myopathiesM Sampaolesi, S Biressi, R Tonlorenzi, et al.
Nature|January 3, 1991
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeC J Brown, A Ballabio, J L Rupert, et al.
Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.
The EMBO Journal|May 15, 1997
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressorG Meroni, A Reymond, M Alcalay, et al.
Cell Death & Disease|March 3, 2011
Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathyJ Díaz-Manera, T Touvier, A Dellavalle, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
Nature|October 10, 1991
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding moleculesB Franco, S Guioli, A Pragliola, et al.
Cell Transplantation|October 5, 2007
Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patientsY Torrente, M Belicchi, C Marchesi, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|March 27, 1999
Spectrum of mutations in fucosidosisP J Willems, H C Seo, P Coucke, et al.
Cell Death and Differentiation|November 19, 2011
Necdin enhances muscle reconstitution of dystrophic muscle by vessel-associated progenitors, by promoting cell survival and myogenic differentiationP Pessina, V Conti, R Tonlorenzi, et al.
Archives Italiennes De Biologie|August 16, 2005
Cell therapy of primary myopathiesM Sampaolesi, S Biressi, R Tonlorenzi, et al.
Nature|January 3, 1991
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeC J Brown, A Ballabio, J L Rupert, et al.
Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.
The EMBO Journal|May 15, 1997
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressorG Meroni, A Reymond, M Alcalay, et al.
Cell Death & Disease|March 3, 2011
Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathyJ Díaz-Manera, T Touvier, A Dellavalle, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
Nature|October 10, 1991
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding moleculesB Franco, S Guioli, A Pragliola, et al.
Cell Transplantation|October 5, 2007
Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patientsY Torrente, M Belicchi, C Marchesi, et al.
Pageof 1