1984
Analysis of the γδ res site Sites required for site-specific recombination and gene expression
Wells R, Grindley N. Analysis of the γδ res site Sites required for site-specific recombination and gene expression. Journal Of Molecular Biology 1984, 179: 667-687. PMID: 6094833, DOI: 10.1016/0022-2836(84)90161-x.Peer-Reviewed Original Research
1983
Construction of a plasmid that overproduces the large proteolytic fragment (Klenow fragment) of DNA polymerase I of Escherichia coli.
Joyce C, Grindley N. Construction of a plasmid that overproduces the large proteolytic fragment (Klenow fragment) of DNA polymerase I of Escherichia coli. Proceedings Of The National Academy Of Sciences Of The United States Of America 1983, 80: 1830-1834. PMID: 6340110, PMCID: PMC393703, DOI: 10.1073/pnas.80.7.1830.Peer-Reviewed Original ResearchConceptsDNA polymerase IOverproducing strainPolymerase IGene fusion techniquesLarge proteolytic fragmentCellular proteinsLac promoterGene fragmentsProtein structurePhage lambdaLeftward promoterEscherichia coliCarboxyl terminalPolymerase fragmentProteolytic fragmentsKlenow fragmentPromoterPlasmidPurification procedureFragmentsOverproductionExpressionI. MoreoverMechanistic studiesCloning
1982
Identification of two genes immediately downstream from the polA gene of Escherichia coli
Joyce C, Grindley N. Identification of two genes immediately downstream from the polA gene of Escherichia coli. Journal Of Bacteriology 1982, 152: 1211-1219. PMID: 6183253, PMCID: PMC221628, DOI: 10.1128/jb.152.3.1211-1219.1982.Peer-Reviewed Original Research
1978
IS1 insertion generates duplication of a nine base pair sequence at its target site
Grindley N. IS1 insertion generates duplication of a nine base pair sequence at its target site. Cell 1978, 13: 419-426. PMID: 350412, DOI: 10.1016/0092-8674(78)90316-1.Peer-Reviewed Original Research