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Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors

For gene therapy of inherited diseases, targeted integration/gene repair through homologous recombination (HR) between exogenous and chromosomal DNA would be an ideal strategy to avoid potentially serious problems of random integration such as cellular transformation and gene silencing. Efficient se...

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Main Authors: Ohbayashi, Fumi, Balamotis, Michael A., Kishimoto, Atsuhiro, Aizawa, Emi, Diaz, Arturo, Hasty, Paul, Graham, Frank L., Caskey, C. Thomas, Mitani, Kohnosuke
פורמט: Artigo
שפה:Inglês
יצא לאור: National Academy of Sciences 2005
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גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1224662/
https://ncbi.nlm.nih.gov/pubmed/16174752
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0506598102
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