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Efficient Double-Strand Break-Stimulated Recombination Promoted by the General Recombination Systems of Phages λ and P22

To examine bacteriophage recombination in vivo, independent of such other processes as replication and packaging, substituted λ phages bearing restriction site polymorphisms were employed in a direct physical assay. Bacteria were infected with two phage variants; DNA was extracted from the infected...

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Main Authors: Poteete, A. R., Fenton, A. C.
Formato: Artigo
Idioma:Inglês
Publicado: 1993
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1205569/
https://ncbi.nlm.nih.gov/pubmed/8104156
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