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1 n the plasmid were selected according to the chloramphenicol resistance.
2 and > 50 compounds were tested for promoting chloramphenicol resistance.
3 n resistance developed both erythromycin and chloramphenicol resistance, and plasmid DNA isolated fro
4                                            A chloramphenicol resistance assay indicated that the hly
5 ml), 4/242 isolates tested were resistant to chloramphenicol (resistance breakpoint >/= 32 mug/ml), 1
6 Chlamydomonas reinhardtii, was replaced by a chloramphenicol resistance cartridge in the cyanobacteri
7 ylori rpoB-rpoC fusion gene with a non-polar chloramphenicol resistance cassette containing a new tra
8  various H. pylori strains by insertion of a chloramphenicol resistance cassette into lpxEHP and exam
9                                            A chloramphenicol resistance cassette was designed which,
10  constructed by replacing the P6 gene with a chloramphenicol resistance cassette.
11 oter, pOX38-tra719-traD411, which contains a chloramphenicol-resistance cassette in place of the kana
12 ng promoterless, terminatorless kanamycin or chloramphenicol resistance cassettes into the HindIII si
13  previously employed, using tetracycline and chloramphenicol resistance cassettes, and non-polar stra
14 individually engineered into a plasmid-borne chloramphenicol-resistance (cat) gene driven by the lac
15  orientations were disrupted by promoterless chloramphenicol resistance (Cm(r)) and kanamycin resista
16                                            A chloramphenicol-resistance (Cm(r)) reporter is used to s
17 oramphenicol acetyltransferase gene encoding chloramphenicol resistance (Cmr).
18 ying the ColE1 origin of replication and the chloramphenicol-resistance (CmR) gene to facilitate the
19 ene therapy by the addition of mitochondrial chloramphenicol resistance, conferred by a point mutatio
20 ed to clone and express the promoterless Tn9 chloramphenicol resistance gene (cat, CmR) in P. haemoly
21                             In contrast, the chloramphenicol resistance gene catII was more frequentl
22 or by introduction of both a kanamycin and a chloramphenicol resistance gene to produce a double muta
23                                            A chloramphenicol resistance gene, a modified lux operon f
24       WGS data revealed the integration of a chloramphenicol resistance gene, the deletion of the end
25 the fla operon promoter and a staphylococcal chloramphenicol resistance gene, was constructed to help
26 an IS605 derivative marked with a selectable chloramphenicol-resistance gene.
27                             The mechanism of chloramphenicol resistance in DT104 was determined by pr
28 RNA from a modified lac promoter resulted in chloramphenicol resistance in Escherichia coli.
29 ria and the inducible cmlA gene that confers chloramphenicol resistance in Pseudomonas spp.
30 ates recovered from the mice were tested for chloramphenicol resistance in vitro.
31 ac promoter or the cat start codon abolished chloramphenicol resistance, indicating that E. coli init
32  codon in the intergenic region, between the chloramphenicol resistance marker and ccsB, in frame wit
33 resulted in the introduction of a selectable chloramphenicol resistance marker into the chromosome.
34 containing transposon-based tetracycline and chloramphenicol resistance markers were combined to allo
35 gative bacteria and carries erythromycin and chloramphenicol resistance markers.
36 omycin resistance occurred in 132 (37%), and chloramphenicol resistance occurred in 33 (9%).
37        Bacteria with target genes expressing chloramphenicol resistance, penicillin resistance, or gy
38 r protein RepD encoded by the Staphylococcus chloramphenicol resistance plasmid pC221 stimulates the
39           The cmlA gene confers nonenzymatic chloramphenicol resistance via an efflux mechanism.
40                                              Chloramphenicol resistance was due in part to the dissem
41                           In filter matings, chloramphenicol resistance was observed to transfer from

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