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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.
5 plication and was most similar to the parABS bacteriophage P1 and P7 system.
6 over, lox, while studying the maintenance of bacteriophage P1 as a stable plasmid.
7                        The RepA protein from bacteriophage P1 binds DNA to initiate replication.
8 ombinase of yeast and the Cre recombinase of bacteriophage P1 both belong to the lambda-integrase (In
9        The Hot (homolog of theta) protein of bacteriophage P1 can substitute for the Escherichia coli
10                       The Cre-recombinase of bacteriophage P1 catalyses site-specific recombination b
11 g a rapid method generally applicable to all bacteriophage P1 clones containing large DNA inserts.
12        We isolated and characterized genomic bacteriophage P1 clones encoding the mouse gastrin-relea
13 ast and bacterial artificial chromosomes and bacteriophage P1 clones spanning the approximately 300-k
14 ed bacterial artificial chromosome (BAC) and bacteriophage P1 clones to fill gaps.
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
17                                              Bacteriophage P1 Cre recombinase fused to the secretion
18          We report here the development of a bacteriophage P1 Cre recombinase-based system to monitor
19                                          The bacteriophage P1 Cre/loxP site-specific recombination sy
20                                          The bacteriophage P1 Cre/loxP system has become a powerful t
21                         Here, we developed a bacteriophage P1-derived Cre/loxP recombination system i
22        For example, the Cre recombinase from bacteriophage P1 efficiently carries out recombination a
23 tructure of epsilon in complex with HOT, the bacteriophage P1-encoded homolog of , at 2.1 A resolutio
24                                          The bacteriophage P1-encoded Ref protein enhances RecA-depen
25              The plasmid addiction module of bacteriophage P1 encodes two proteins, Doc, a toxin that
26  (homolog of umuD) is, however, found on the bacteriophage P1 genome.
27 chromosomal localization of the BRS-3 genes, bacteriophage P1 genomic clones, harboring the genes for
28 n of the gene was isolated after screening a bacteriophage P1 genomic library.
29                   The Cre DNA recombinase of bacteriophage P1 has become a useful tool for genomic ma
30                   The Cre DNA recombinase of bacteriophage P1 has become a useful tool for precise ge
31      In recent years, the Cre integrase from bacteriophage P1 has become an essential tool for condit
32                                   Cre-lox of bacteriophage P1 has become one of the most widely used
33                     The cre-loxP system from bacteriophage P1 has been used in transgenic animals to
34                 We conclude, therefore, that bacteriophage P1 HumD is a functional homolog of the Umu
35  using the Cre-lox recombination system from bacteriophage P1 in vivo.
36               The Cre recombinase (Cre) from bacteriophage P1 is an important tool for genetic engine
37                 The possible role of hot for bacteriophage P1 is discussed.
38 s required for transcriptional activation of bacteriophage P1 late promoters.
39 spectinomycin resistance cassette flanked by bacteriophage P1 loxP sites oriented as direct repeats w
40 termined structure of the theta homolog from bacteriophage P1, named HOT, we constructed a homology m
41                           The Doc toxin from bacteriophage P1 (of the phd-doc toxin-antitoxin system)
42 eractions of ClpAP with the model substrate, bacteriophage P1 protein, RepA.
43                         Cre recombinase from bacteriophage P1 recognizes a 34-bp recombination site,
44 y Cre recombinase/LoxP sequence derived from bacteriophage P1 recombination (Cre/LoxP).
45                                          The bacteriophage P1 recombination enhancement function (Ref
46 r Cre recombinase/LoxP sequence derived from bacteriophage P1 recombination suppressed CAF activation
47                                          The bacteriophage P1 Ref (recombination enhancement function
48  ATP-dependent molecular chaperone, remodels bacteriophage P1 RepA dimers into monomers, thereby acti
49 naJ and DnaK with a known natural substrate, bacteriophage P1 RepA protein.
50 e sequence logo for DNA binding sites of the bacteriophage P1 replication protein RepA shows unusuall
51       Transgene coplacement makes use of the bacteriophage P1 system of Cre/loxP site-specific recomb
52    The utility of promoters regulated by the bacteriophage P1 temperature-sensitive C1 repressor was
53  Cre mediated site-specific recombination in bacteriophage P1, the Cre-lox system of recombination ha
54  lacking type 1 fimbriae, was constructed by bacteriophage P1 transduction of the fim region of the E
55  can be transferred into chromosomes by: (i) bacteriophage P1 transduction; and (ii) transformation o
56 ipulation of genomic inserts cloned into the bacteriophage P1 vector is hindered by the large size of
57                         The Lyz endolysin of bacteriophage P1 was found to cause lysis of the host wi
58  proteins of the plasmid addiction system of bacteriophage P1 were purified as a complex.