Population
Adenovirus vectors (preclinical model)
Design
Preclinical
Authors
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Supports retargeted adenoviral vectors in animal models; leaves open translation to human gene therapy.
A novel platform combining genetic and chemical modifications of adenovirus capsids enables flexible and efficient retargeting of viral vectors, with potential applications in clinical gene therapy and vaccination.
Kreppel et al. (2005) studied this question.
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