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Self-complementary AAV Virus (scAAV) Safe and Long-term Gene Transfer in the Trabecular Meshwork of Living Rats and Monkeys

PURPOSE. AAV vectors produce stable transgene expression and elicit low immune response in many tissues. AAVs have been the vectors of choice for gene therapy for the eye, in particular the retina. scAAVs are modified AAVs that bypass the required second-strand DNA synthesis to achieve transcription...

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Detalhes bibliográficos
Main Authors: Buie, LaKisha K., Rasmussen, Carol A., Porterfield, Eric C., Ramgolam, Vinod S., Choi, Vivian W., Markovic-Plese, Silva, Samulski, Richard J., Kaufman, Paul L., Borrás, Teresa
Formato: Artigo
Idioma:Inglês
Publicado em: Association for Research in Vision and Ophthalmology, Inc. 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2869048/
https://ncbi.nlm.nih.gov/pubmed/19684004
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.09-3847
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