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Peer-reviewed veterinary case report

Viral Vectors for Gene Transfer.

Journal:
Current protocols in mouse biology
Year:
2018
Authors:
Chen, Yong Hong et al.
Affiliation:
The Children's Hospital of Philadelphia · United States

Abstract

Viral vectors are a promising tool for effective delivery of genetic material into cells. They take advantage of the natural ability of a virus to deliver a genetic payload into cells while being genetically modified such that their ability to replicate is crippled or removed. Here, an updated overview of routinely used viral vectors, including adeno-associated viruses (AAV), retroviruses/lentiviruses, and adenoviruses (Ads), is provided, as well as perspectives on their advantages and disadvantages in research and gene therapy. © 2018 by John Wiley & Sons, Inc.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/30485696/