In Vitro and In Vivo Tetracycline-Controlled Myogenic Conversion of NIH-3T3 Cells: Evidence of Programmed Cell Death after Muscle Cell Transplantation

Ex vivo gene therapy of Duchenne muscular dystrophy based on autologous transplantation of genetically modified myoblasts is limited by their premature senescence. MyoD-converted fibroblasts represent an alternative source of myogenic cells. In this study the forced MyoD-dependent conversion of muri...

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Hlavní autoři: Roberto Del Bo, Yvan Torrente, Stefania Corti, Maria Grazia D'angelo, Giacomo Pietro Comi, Gigliola Fagiolari, Sabrina Salani, Agata Cova, Federica Pisati, Maurizio Moggio, Carlo Ausenda, Guglielmo Scarlato, Nereo Bresolin
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publishing 2001-03-01
Edice:Cell Transplantation
On-line přístup:https://doi.org/10.3727/000000001783986855
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