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1 llowing detection of the beta-lactam, of the AmpC beta-lactamase.
2 n organisms lacking a chromosomally mediated AmpC beta-lactamase.
3 1 nM inhibitor (compound 1) in complex with AmpC beta-lactamase.
4 o detect phenotypically isolates that harbor AmpC beta-lactamase.
5 extended-spectrum beta-lactamases (ESBL) and AmpC beta-lactamases.
6 ve infections caused by organisms expressing AmpC beta-lactamases.
7 sensitive and specific for detecting SHV and AmpC beta-lactamases.
8 btained only for isolates producing ESBLs or AmpC beta-lactamases.
11 g/ml were obtained for all strains producing AmpC beta-lactamase and only 1 of 33 strains producing E
13 um beta-lactamases (ESBLs), plasmid-mediated AmpC beta-lactamases and KPC carbapenemases in Enterobac
14 o be very potent inhibitors of the TEM-1 and AmpC beta-lactamases and less so against the class B met
15 sistent with production of both a TEM and an AmpC beta-lactamase, and representative isolates of seve
16 ectrum beta-lactamases (ESBLs), transferable AmpC beta-lactamases, and carbapenemases are associated
17 isolates) producing non-MBL carbapenemases, AmpC beta-lactamases, and extended-spectrum beta-lactama
18 ted antibiotic-resistant proteins, including AmpC, beta-lactamase, and carO, in clinical resistant st
20 gative organisms expressing plasmid-mediated AmpC beta-lactamases are limited because these organisms
24 MY-2 antibody was tested against a number of AmpC beta-lactamases by assaying known quantities of pur
25 e m-aminophenylboronic acid-Escherichia coli AmpC beta-lactamase complex to suggest modifications tha
26 tibiotic resistance genes, including a FOX-5 AmpC beta-lactamase encoded on a large IncA/C plasmid.
27 g family-specific ampC genes responsible for AmpC beta-lactamase expression in organisms with or with
28 deficient Q120L/Y150E variant of the class C AmpC beta-lactamase from Escherichia coli was solved at
32 r the purpose of identifying family-specific AmpC beta-lactamase genes within gram-negative pathogens
36 eumoniae bloodstream isolates harbor ESBL or AmpC beta-lactamases, (ii). confirmatory tests are neces
37 a 1.07 A X-ray crystallographic structure of AmpC beta-lactamase in complex with a boronic acid deacy
38 ng frequency, the true rate of occurrence of AmpC beta-lactamases in Escherichia coli, Klebsiella pne
39 in all gram-negative isolates, transferable AmpC beta-lactamases in Klebsiella pneumoniae, and carba
40 ere evaluated for detecting plasmid-mediated AmpC beta-lactamases in Klebsiella spp., Escherichia col
41 nient means of detection of plasmid-mediated AmpC beta-lactamases in organisms lacking a chromosomall
45 boronic acid (BZB), a nanomolar inhibitor of AmpC beta-lactamase (K i = 27 nM), we have identified an
46 ither the class C Citrobacter freundii CMY-2 AmpC beta-lactamase nor the class A TEM-1 beta-lactamase
48 ae P99, Klebsiella pneumoniae ACT-1, and the AmpC beta-lactamases of Enterobacter aerogenes, Morganel
49 wn quantities of purified enzymes in ELISAs (AmpC beta-lactamases of M. morganii, C. freundii, E. col
50 x, and periplasmic degradation (catalyzed by AmpC beta-lactamase) of these two compounds, and correla
53 In patients with organisms hyperproducing AmpC beta-lactamases (positive by both methods), clinica
54 ity score matching of patients infected with AmpC beta-lactamase-positive organisms treated with cefe
57 spectrum beta-lactamase-producing organisms, AmpC beta-lactamase-producing organisms, carbapenem-resi
58 the treatment of invasive infections due to AmpC beta-lactamase-producing organisms, particularly wh
60 cloxacillin Etest to identify organisms with AmpC beta-lactamase production from February 2010 to Jan
61 vious microarray studies have shown that the AmpC beta-lactamase regulator AmpR, a member of the LysR
63 tion of organisms producing plasmid-mediated AmpC beta-lactamases, we evaluated the diagnostic utilit
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