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A new pathway in the generation of defective retrovirus DNA.

We used a retrovirus shuttle vector to make molecular clones of circular viral DNA from infected cells. One-third of the molecules examined had deletions that started within or near the U5 domain of the long terminal repeat (LTR) region and extended a variable distance toward the gag gene. We presen...

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Dettagli Bibliografici
Pubblicato in:J Virol
Autori principali: Olsen, J C, Swanstrom, R
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Microbiology (ASM) 1985
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Accesso online:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC252648/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4068144/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.56.3.779-789.1985
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