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Cited by 481

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells.

Open access
Hermonat, P L, Muzyczka, N·1984·Proceedings of the National Academy of Sciences

Abstract

Adeno-associated virus (AAV) is a human DNA virus that has a broad host range and can be grown both as an integrated provirus and as a lytic genome. These properties suggested that AAV may be useful as a mammalian transduction vector. To test this possibility, we have isolated a recombinant AAV viral stock in which the neomycin resistance gene was substituted for the AAV capsid genes. Using this recombinant stock, we have demonstrated that AAV can be used to transduce foreign DNA into human and murine tissue culture cells. In addition, we have demonstrated that, if the transductants are superinfected with a helper virus (adenovirus), the recombinant AAV genome is rescued from the proviral state and amplified to high copy number. These unique features of AAV vectors suggest that they may have a broad utility in the study of biological problems. Because AAV, itself, is nonpathogenic in both humans and animals, these vectors also may be useful for the purpose of gene therapy.

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Metadata

Authors
Hermonat, P. L., & Muzyczka, N.
Venue
Proceedings of the National Academy of Sciences
Published
1984-10
Volume
81
Issue
20
Pages
6466-6470
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2067189573
Cited by
481
References
3
FWCI
2.41
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells. https://app.cochat.ai/papers/10.1073/pnas.81.20.6466
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Hermonat, P. L., & Muzyczka, N. (1984). Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.81.20.6466

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.