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1 ratia marcescens, Staphylococcus aureus, and Stenotrophomonas maltophilia).
2 structure of PabB from the emerging pathogen Stenotrophomonas maltophilia.
3 n Xylella fastidiosa and the human pathogen, Stenotrophomonas maltophilia.
4 he extensively drug resistant human pathogen Stenotrophomonas maltophilia.
5 talyzed by the dizinc L1 beta-lactamase from Stenotrophomonas maltophilia.
6 ermentative gram-negative bacilli, including Stenotrophomonas maltophilia.
7 nterocolitica O9, Escherichia hermannii, and Stenotrophomonas maltophilia.
8 ureus [3 methicillin-resistant S. aureus], 2 Stenotrophomonas maltophilia, 1 Klebsiella pneumoniae) a
9 losoxidans (33%), and finally, pan-resistant Stenotrophomonas maltophilia (20%).
10 scens (5.5%), Enterobacter aerogenes (4.4%), Stenotrophomonas maltophilia (4.3%), Proteus mirabilis (
11 mobacter xylosoxidans (100%) followed by MDR Stenotrophomonas maltophilia (46%), MDR Achromobacter xy
12 Staphylococcal aureus, Burkholderia cepacia, Stenotrophomonas maltophilia, Achromobacter xylosoxidans
13      We sequence 552 genomes of the pathogen Stenotrophomonas maltophilia across 23 sites of the lung
14 acter baumannii, Pseudomonas aeruginosa, and Stenotrophomonas maltophilia--all major threats to our c
15 s uncommon, occurring in 2 patients with MDR Stenotrophomonas maltophilia and 2 patients with MDR Ach
16                                              Stenotrophomonas maltophilia and Achromobacter (Alcalige
17 (LUV) and to kill the Gram negative bacteria Stenotrophomonas maltophilia and Escherichia coli.
18 coccus spp., and the opportunistic pathogens Stenotrophomonas maltophilia and Ochrobactrum anthropi w
19  reviewed for Achromobacter xylosoxidans and Stenotrophomonas maltophilia and their antibiotic suscep
20 ction of tobramycin-resistant P. aeruginosa, Stenotrophomonas maltophilia, and Achromobacter xylosoxi
21 s, Aeromonas caviae, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, and Enterococcus sp.
22 Klebsiella pneumoniae, Enterobacter cloacae, Stenotrophomonas maltophilia, and the Burkholderia cepac
23    Standard microbiology references describe Stenotrophomonas maltophilia as oxidase negative and var
24 significantly, an extensively drug-resistant Stenotrophomonas maltophilia clinical isolate expressing
25 ta-lactamase from the opportunistic pathogen Stenotrophomonas maltophilia has been determined at 1.7
26                                              Stenotrophomonas maltophilia has recently emerged as an
27 patients with Achromobacter xylosoxidans and Stenotrophomonas maltophilia have similar posttransplant
28               Metallo-beta-lactamase L1 from Stenotrophomonas maltophilia is a dinuclear Zn(II) enzym
29                                              Stenotrophomonas maltophilia is a Gram-negative bacteriu
30                                              Stenotrophomonas maltophilia is a gram-negative bacteriu
31                                              Stenotrophomonas maltophilia is a multiple-antibiotic-re
32                                              Stenotrophomonas maltophilia is a ubiquitous bacterium a
33                                              Stenotrophomonas maltophilia is an emerging opportunisti
34                                              Stenotrophomonas maltophilia is an emerging, opportunist
35                  The Gram-negative bacterium Stenotrophomonas maltophilia is increasingly identified
36           The L1 metallo-beta-lactamase from Stenotrophomonas maltophilia is unique among this class
37 pan-resistant Achromobacter xylosoxidans and Stenotrophomonas maltophilia, is poorly characterized.
38 seobacterium meningosepticum isolates, and 1 Stenotrophomonas maltophilia isolate) producing IMP-1, I
39  26 Acinetobacter baumannii isolates, and 11 Stenotrophomonas maltophilia isolates.
40 , Escherichia coli, Serratia marcescens, and Stenotrophomonas maltophilia isolates.
41 rized a polysaccharide lyase (Smlt1473) from Stenotrophomonas maltophilia k279a, which exhibited sign
42 c mechanism of beta-lactam hydrolysis by the Stenotrophomonas maltophilia L1 metallo-beta-lactamase.
43 ese were found to be P. aeruginosa (n = 10), Stenotrophomonas maltophilia (n = 1), and Burkholderia c
44 nt Stenotrophomonas maltophilia (n = 5), MDR Stenotrophomonas maltophilia (n = 26), and CF patients w
45 s mirabilis (n = 3), Serratia spp. (n = 10), Stenotrophomonas maltophilia (n = 43), Sphingobacterium
46 obacter xylosoxidans (n = 15), pan-resistant Stenotrophomonas maltophilia (n = 5), MDR Stenotrophomon
47 patients without Achromobacter xylosoxidans, Stenotrophomonas maltophilia or Bulkholderia cenocepacia
48  increase isolation of Burkholderia cepacia, Stenotrophomonas maltophilia, or Alcaligenes xylosoxidan
49 smid pB10 was shown to be highly unstable in Stenotrophomonas maltophilia P21 and Pseudomonas putida
50                    To achieve the objective, Stenotrophomonas maltophilia strain ZL1 was used as a mo
51 rains, 5 Alcaligenes xylosoxidans strains, 5 Stenotrophomonas maltophilia strains, and 5 Pseudomonas
52 trains, 10 Pseudomonas aeruginosa strains, 8 Stenotrophomonas maltophilia strains, and 9 isolates bel
53                        With the exception of Stenotrophomonas maltophilia, these organisms are infreq
54 chromosomal carbapenemases are restricted to Stenotrophomonas maltophilia, to a few Bacteroides fragi
55 ionella pneumophila, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Vibrio cholerae, and Yersi
56 3 of [corrected] 35 home-use nebulizers, and Stenotrophomonas maltophilia was isolated from 4 of 35 h
57                                              Stenotrophomonas maltophilia was isolated from the respi
58 trocefin with metallo-beta-lactamase L1 from Stenotrophomonas maltophilia was studied using rapid-sca
59                                              Stenotrophomonas maltophilia WR-C is capable of forming

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