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1 Cre is a site-specific recombinase from bacteriophage P1.
2 tance of F-plasmids and the prophage form of bacteriophage P1.
3 reported to be essential for lytic growth of bacteriophage P1.
4 ologs have also been found in the genomes of bacteriophage P1 and of certain conjugative plasmids.
8 ombinase of yeast and the Cre recombinase of bacteriophage P1 both belong to the lambda-integrase (In
11 g a rapid method generally applicable to all bacteriophage P1 clones containing large DNA inserts.
13 ast and bacterial artificial chromosomes and bacteriophage P1 clones spanning the approximately 300-k
15 acquisition of sequence from clones such as bacteriophage P1 clones, cosmids, or yeast artificial ch
16 transcribed sequences in this region using a bacteriophage P1 contig containing 700 kb of DNA surroun
22 tructure of epsilon in complex with HOT, the bacteriophage P1-encoded homolog of , at 2.1 A resolutio
26 chromosomal localization of the BRS-3 genes, bacteriophage P1 genomic clones, harboring the genes for
38 spectinomycin resistance cassette flanked by bacteriophage P1 loxP sites oriented as direct repeats w
39 termined structure of the theta homolog from bacteriophage P1, named HOT, we constructed a homology m
45 ATP-dependent molecular chaperone, remodels bacteriophage P1 RepA dimers into monomers, thereby acti
47 e sequence logo for DNA binding sites of the bacteriophage P1 replication protein RepA shows unusuall
49 The utility of promoters regulated by the bacteriophage P1 temperature-sensitive C1 repressor was
50 Cre mediated site-specific recombination in bacteriophage P1, the Cre-lox system of recombination ha
51 lacking type 1 fimbriae, was constructed by bacteriophage P1 transduction of the fim region of the E
52 can be transferred into chromosomes by: (i) bacteriophage P1 transduction; and (ii) transformation o
53 ipulation of genomic inserts cloned into the bacteriophage P1 vector is hindered by the large size of
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