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Adenoviral vectors for improved gene delivery to the inner ear

An important requirement for gene therapy in the inner ear is to achieve efficient gene delivery without damaging residual inner ear function. This can be achieved by delivering a high concentration of vector in a minimal volume. Adenovectors are well suited to meet these requirements since high qua...

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Hlavní autoři: Praetorius, Mark, Brough, Douglas E., Hsu, Chi, Plinkert, Peter K., Staecker, Hinrich
Médium: Artigo
Jazyk:Inglês
Vydáno: 2008
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2679534/
https://ncbi.nlm.nih.gov/pubmed/19105978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.heares.2008.11.009
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