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1 n organisms lacking a chromosomally mediated AmpC beta-lactamase.
2  1 nM inhibitor (compound 1) in complex with AmpC beta-lactamase.
3 o detect phenotypically isolates that harbor AmpC beta-lactamase.
4 llowing detection of the beta-lactam, of the AmpC beta-lactamase.
5 spectively against hits from docking against AmpC beta-lactamase.
6 ve infections caused by organisms expressing AmpC beta-lactamases.
7 extended-spectrum beta-lactamases (ESBL) and AmpC beta-lactamases.
8 sensitive and specific for detecting SHV and AmpC beta-lactamases.
9 btained only for isolates producing ESBLs or AmpC beta-lactamases.
10 ach compound in the library, docking against AmpC beta-lactamase (AmpC) and the D(4) dopamine recepto
11                                        Using AmpC beta-lactamase, an enzyme that is well-characterize
12 revalence of AMR organisms, particularly for AmpC beta-lactamase and methicillin-resistant Staphyloco
13 ere obtained for seven of eight producers of AmpC beta-lactamase and no ESBL producers.
14 g/ml were obtained for all strains producing AmpC beta-lactamase and only 1 of 33 strains producing E
15  correlate well for isolates containing both AmpC beta-lactamases and ESBLs.
16 um beta-lactamases (ESBLs), plasmid-mediated AmpC beta-lactamases and KPC carbapenemases in Enterobac
17 o be very potent inhibitors of the TEM-1 and AmpC beta-lactamases and less so against the class B met
18 sistent with production of both a TEM and an AmpC beta-lactamase, and representative isolates of seve
19 ectrum beta-lactamases (ESBLs), transferable AmpC beta-lactamases, and carbapenemases are associated
20  isolates) producing non-MBL carbapenemases, AmpC beta-lactamases, and extended-spectrum beta-lactama
21 f extended-spectrum beta-lactamases (ESBLs), AmpC beta-lactamases, and one or multiple carbapenemases
22 ted antibiotic-resistant proteins, including AmpC, beta-lactamase, and carO, in clinical resistant st
23                                              AmpC beta-lactamases are cephalosporinases that confer r
24 gative organisms expressing plasmid-mediated AmpC beta-lactamases are limited because these organisms
25                       Unlike ESBLs, however, AmpC beta-lactamases are not inhibited by clavulanic aci
26                                              AmpC beta-lactamases are related to the chromosomal enzy
27                                          For AmpC beta-lactamase, binding to aggregates of the small
28 MY-2 antibody was tested against a number of AmpC beta-lactamases by assaying known quantities of pur
29 e m-aminophenylboronic acid-Escherichia coli AmpC beta-lactamase complex to suggest modifications tha
30 tibiotic resistance genes, including a FOX-5 AmpC beta-lactamase encoded on a large IncA/C plasmid.
31 g family-specific ampC genes responsible for AmpC beta-lactamase expression in organisms with or with
32 deficient Q120L/Y150E variant of the class C AmpC beta-lactamase from Escherichia coli was solved at
33                            The structures of AmpC beta-lactamase from Escherichia coli, alone and in
34 ositive isolates were positive by PCR for an AmpC beta-lactamase gene.
35 n in organisms with or without a chromosomal AmpC beta-lactamase gene.
36   Screening a deep mutant library of the bla(ampC) beta-lactamase gene of Escherichia coli, we identi
37 r the purpose of identifying family-specific AmpC beta-lactamase genes within gram-negative pathogens
38                             Plasmid-mediated AmpC beta-lactamases have been associated with false in
39                       Plasmid-mediated CMY-2 AmpC beta-lactamases have been identified in Salmonella
40             Six families of plasmid-mediated AmpC beta-lactamases have been identified, but no phenot
41 eumoniae bloodstream isolates harbor ESBL or AmpC beta-lactamases, (ii). confirmatory tests are neces
42 a 1.07 A X-ray crystallographic structure of AmpC beta-lactamase in complex with a boronic acid deacy
43 ng frequency, the true rate of occurrence of AmpC beta-lactamases in Escherichia coli, Klebsiella pne
44  in all gram-negative isolates, transferable AmpC beta-lactamases in Klebsiella pneumoniae, and carba
45 ere evaluated for detecting plasmid-mediated AmpC beta-lactamases in Klebsiella spp., Escherichia col
46 nient means of detection of plasmid-mediated AmpC beta-lactamases in organisms lacking a chromosomall
47                The diagnostic utility of the AmpC beta-lactamase inhibitors LN-2-128, 48-1220, and Sy
48           In particular, derepression of the AmpC beta-lactamase is a common mechanism of beta-lactam
49          Inducible expression of chromosomal AmpC beta-lactamase is a major cause of beta-lactam anti
50 boronic acid (BZB), a nanomolar inhibitor of AmpC beta-lactamase (K i = 27 nM), we have identified an
51                 Understanding the nuances of AmpC beta-lactamase-mediated resistance can be challengi
52 ither the class C Citrobacter freundii CMY-2 AmpC beta-lactamase nor the class A TEM-1 beta-lactamase
53 ta-lactam antibiotics induce the chromosomal ampC beta-lactamase of many gram-negative bacteria.
54 ae P99, Klebsiella pneumoniae ACT-1, and the AmpC beta-lactamases of Enterobacter aerogenes, Morganel
55 wn quantities of purified enzymes in ELISAs (AmpC beta-lactamases of M. morganii, C. freundii, E. col
56 x, and periplasmic degradation (catalyzed by AmpC beta-lactamase) of these two compounds, and correla
57 m beta-lactamase (ESBL) and plasmid-mediated AmpC beta-lactamase (pAmpC) genes.
58 f Klebsiella spp. producing plasmid-mediated AmpC beta-lactamases (pAmpCs) was evaluated.
59    In patients with organisms hyperproducing AmpC beta-lactamases (positive by both methods), clinica
60 ity score matching of patients infected with AmpC beta-lactamase-positive organisms treated with cefe
61  extended-spectrum beta-lactamase (ESBL) and AmpC beta-lactamase producers.
62        Lastly, we report the presence of the AmpC beta-lactamase producing gene (CITM) in 4.56% and 3
63 ctamase-producing Enterobacterales (ESBL-E), AmpC beta- lactamase-producing Enterobacterales (AmpC-E)
64      Here, guidance is provided for treating AmpC beta-lactamase-producing Enterobacterales (AmpC-E),
65 ctamase producing Enterobacterales (ESBL-E), AmpC beta-lactamase-producing Enterobacterales (AmpC-E),
66      Serratia marcescens is an opportunistic AmpC beta-lactamase-producing Enterobacterales associate
67 eam infections or pneumonia due to wild-type AmpC beta-lactamase-producing Enterobacterales, species
68                                              AmpC beta-lactamase-producing organisms are associated w
69 spectrum beta-lactamase-producing organisms, AmpC beta-lactamase-producing organisms, carbapenem-resi
70  the treatment of invasive infections due to AmpC beta-lactamase-producing organisms, particularly wh
71 eria, 96 (24%) had confirmed infections with AmpC beta-lactamase-producing organisms.
72 cloxacillin Etest to identify organisms with AmpC beta-lactamase production from February 2010 to Jan
73 vious microarray studies have shown that the AmpC beta-lactamase regulator AmpR, a member of the LysR
74  did not recognize TEM-1, K-1, OXA-1, or any AmpC beta-lactamase tested.
75 tion of organisms producing plasmid-mediated AmpC beta-lactamases, we evaluated the diagnostic utilit
76                                 Transferable AmpC beta-lactamases were detected in 3.3% of K. pneumon
77                    Although plasmid-mediated AmpC beta-lactamases were first reported in the late 198
78                                              AmpC beta-lactamases were initially more dominant in Nor
79 , organisms producing ESBLs and transferable AmpC beta-lactamases were widespread.