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1 and oxidase positive, and it is sensitive to cephalothin.
2 sensitive to nalidixic acid but resistant to cephalothin.
3    Our first model suggests that this chiral cephalothin analogue adopts a novel conformation in the
4 intermediate with (i) the meta-carboxyphenyl cephalothin analogue and (ii) the carbapenems, imipenem
5  In antimicrobial susceptibility tests, this cephalothin analogue lowered the ceftazidime and cefotax
6         In the boronic acid series, a chiral cephalothin analogue with a meta-carboxyphenyl moiety co
7 sidered two beta-lactam antibiotics, namely, cephalothin and aztreonam, belonging to two different su
8 nicillin, ampicillin, and the cephalosporins cephalothin and cefotaxime.
9                          The permeability of cephalothin and cephaloridine in A. baumannii was decrea
10 thermore, the outer membrane permeability to cephalothin and cephaloridine, measured in intact cells,
11 nic acid transition state analogs that mimic cephalothin and found substitutions at Arg-244 markedly
12  of acyl-enzyme intermediates formed between cephalothin and the dd-peptidase of Streptomyces sp. R61
13 xhibiting enhanced hydrolysis of nitrocefin, cephalothin, and cefotaxime relative to IMP-1.
14 educed nitrate to nitrite, were resistant to cephalothin, and exhibited intermediate susceptibility t
15 s combined was more than 20% for ampicillin, cephalothin, and sulfamethoxazole in each year studied.
16 hatase, and was resistant to nalidixic acid, cephalothin, and trimethoprim-sulfamethoxazole.
17 actam antibiotics (penicillin G, ampicillin, cephalothin, cefaclor, cefuroxime, cefoperazone, and cef
18                         For other compounds (cephalothin, cefamandole, and cephaloridine) that showed
19 -four of 49 isolates (49%) were sensitive to cephalothin, cefazolin, and cefuroxime.
20 that cefazolin is a more accurate proxy than cephalothin for uncomplicated urinary tract infections (
21 K(i) value for cefotaxime as an inhibitor of cephalothin hydrolysis is 27 nM.
22 imethoprim-sulfamethoxazole, ampicillin, and cephalothin increased significantly among uropathogens c
23        The thiol intermediate generated from cephalothin is a slow binding inhibitor.
24 mical analyses, testing of susceptibility to cephalothin, lysis by a Hafnia-specific phage, and ampli
25 demonstrate that other beta-lactams, such as cephalothin, meropenem, and penicillin G, proceed throug
26 cefazolin (P = 0.02), cefotetan (P = 0.006), cephalothin (P<0.0001), clindamycin (P = 0.04), erythrom
27                               Traditionally, cephalothin susceptibility results were used to predict
28 ates combined to ampicillin (P<.002), and to cephalothin, trimethoprim, and trimethoprim-sulfamethoxa
29 nt complexes of the beta-lactamase substrate cephalothin were determined by X-ray crystallography.
30 vieae, the MICs of penicillin and, possibly, cephalothin were higher than for L. lactis, and unlike L
31 ) by 50-70% against "good" substrates (i.e., cephalothin) while increasing k(cat)/K(m) against "poor"