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1 robacter aerogenes, Morganella morganii, and Citrobacter freundii.
2 using primers specific for the ampC gene of Citrobacter freundii.
3 lass C enzymes from Enterobacter cloacae and Citrobacter freundii.
4 e, Escherichia coli, Klebsiella oxytoca, and Citrobacter freundii.
7 Proteus mirabilis, 10 Citrobacter koseri, 9 Citrobacter freundii, 8 Klebsiella oxytoca, 5 Klebsiella
8 ll-free supernatants from Proteus mirabilis, Citrobacter freundii and Enterobacter agglomerans [cyclo
9 detected in carbapenem-resistant isolates of Citrobacter freundii and Klebsiella oxytoca recovered fr
11 tatively for Gram-negative Escherichia coli, Citrobacter freundii, and Enterobacter aerogenes, as wel
13 icant AmpC production (Enterobacter cloacae, Citrobacter freundii, and Klebsiella aerogenes only) or
14 aride produced by Salmonella enterica Typhi, Citrobacter freundii, and some soil bacteria belonging t
19 with colonization of the intestinal tract by Citrobacter freundii, Clostridium species, Enterobacter
22 e (WT) forms, such as the E. cloacae P99 and Citrobacter freundii enzymes, the ES GC1 beta-lactamase
24 stutzeri (GFB-2), Bacillus subtilis (GFB-3), Citrobacter freundii (GFB-4), and P. aeruginosa (GFB-5)
25 iae, Klebsiella oxytoca, Citrobacter koseri, Citrobacter freundii group, Enterobacter spp., and Serra
32 lle and propanediol utilization enzymes from Citrobacter freundii is fully functional when cloned in
33 he molecular interactions between AmpR (from Citrobacter freundii), its DNA operator, and repressor U
34 c inhibition was also observed in strains of Citrobacter freundii, Klebsiella pneumoniae, Enterobacte
35 xytoca (n = 8), Serratia marcescens (n = 6), Citrobacter freundii (n = 4), and Klebsiella aerogenes (
36 associated with PS biodegradation including Citrobacter freundii, Serratia marcescens, and Klebsiell
37 ve selectivity of these ligands for E. coli, Citrobacter freundii, Staphylococcus epidermidis were 10
38 lococcus aureus, Pseudomonas aeruginosa, and Citrobacter freundii to ensure the species specificity o
39 lococcus aureus, Pseudomonas aeruginosa, and Citrobacter freundii, to ensure the species-specificity
40 ophan indole-lyase and to wild type and Y71F Citrobacter freundii tyrosine phenol-lyase was investiga
42 five enterobacteria (Salmonella typhimurium, Citrobacter freundii, Yersinia enterocolitica, Serratia