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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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Detalles Bibliográficos
Publicado en:J Virol
Principais autores: Olsen, J C, Swanstrom, R
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Microbiology (ASM) 1985
Assuntos:
Acceso en liña: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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