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1 All participants received cephalexin.
2 coli elongated by growth in the presence of cephalexin.
3 eplication in the presence of rifampicin and cephalexin.
4 filament, as is found in cells treated with cephalexin.
5 3 orders of magnitude greater than that for cephalexin.
7 pants were randomly assigned to receive oral cephalexin, 500 mg, and metronidazole, 500 mg (n = 202 p
10 een for growth on the beta-lactam antibiotic cephalexin afforded a unique p-acrylamido-phenylalanine
11 us trimethoprim-sulfamethoxazole compared to cephalexin alone did not result in higher rates of clini
13 -lactam antibiotics ampicillin, amoxicillin, cephalexin and cefadroxil, the antineoplastics delta-ami
15 , double-blind clinical trial comparing oral cephalexin and metronidazole vs placebo for 48 hours fol
16 ng obese women who receive prophylactic oral cephalexin and metronidazole vs placebo for 48 hours fol
17 axis, a postoperative 48-hour course of oral cephalexin and metronidazole, compared with placebo, red
18 using low concentrations of the beta-lactams cephalexin and piperacillin to specifically inhibit FtsI
19 endence of k(cat)/K(m) for benzylpenicillin, cephalexin, and cefoxitin similarly indicated the import
21 d acylation of PBP3 with three beta-lactams (cephalexin, aztreonam, and piperacillin) in growing cell
22 ntly, when septal PG synthesis is blocked by cephalexin, both EnvC and NlpD are recruited to septal r
25 minopenicillins and aminocephalosporins (ie, cephalexin, cefaclor, and cefadroxil) of around 20%, as
26 tams, all subjects underwent skin tests with cephalexin, cefaclor, cefadroxil, cefuroxime, ceftriaxon
27 d polymer (MIP) for cephalosporin molecules (cephalexin (CFL) and cephapirin (CFP)), was prepared by
28 rect photolysis (t(1/2) = 0.7, 3.9 h), while cephalexin (CFX) and cephradine (CFD) were mainly transf
29 s, ampicillin (AMP), benzylpenicillin (PEG), cephalexin (CFX), cefazolin (CFL), cefoperazone (CFP), c
30 ural features of dileucine stereoisomers and cephalexin contributing to interaction with the dipeptid
32 addition of trimethoprim-sulfamethoxazole to cephalexin did not improve outcomes overall or by subgro
33 ional FtsZ rings assemble in the presence of cephalexin, even after several generations of growth.
34 served from milk components after elution of cephalexin from MIP, indicating selectivity and affinity
35 solid phase extraction (SPE) for recovery of cephalexin from spiked milk samples for further estimati
36 thoxazole group vs 165 (85.5%) of 193 in the cephalexin group (difference, -2.0%; 95% CI, -9.7% to 5.
37 thoxazole group vs 171 (69.0%) of 248 in the cephalexin group (difference, 7.3%; 95% CI, -1.0% to 15.
40 hydrolysis of cefoxitin, cephaloridine, and cephalexin indicate that an enzyme residue of apparent p
41 GFP localized to potential division sites in cephalexin-induced and ftsI mutant filaments, further su
44 tion was diagnosed in 13 women (6.4%) in the cephalexin-metronidazole group vs 31 women (15.4%) in th
46 . tuberculosis to DNA damaging agents, or to cephalexin, or growth of M. tuberculosis in macrophages
47 crogram of oxacillin per ml, 40 microgram of cephalexin per ml, or 2.5 microgram of methicillin per m
49 daily, for 7 days (n = 248 participants) or cephalexin plus placebo for 7 days (n = 248 participants
50 ts with uncomplicated cellulitis, the use of cephalexin plus trimethoprim-sulfamethoxazole compared t
51 ed in 189 (76.2%) of 248 participants in the cephalexin plus trimethoprim-sulfamethoxazole group vs 1
52 ed in 182 (83.5%) of 218 participants in the cephalexin plus trimethoprim-sulfamethoxazole group vs 1
54 d a clinically important difference favoring cephalexin plus trimethoprim-sulfamethoxazole, further r
55 Etest using BGA and Regan-Lowe agar without cephalexin (RL-C), and disk diffusion using BGA and RL-C
56 assemble in newborn cells in the presence of cephalexin, suggesting that newborn cells contain a site
60 Gliding movements of the leading poles of cephalexin-treated filamentous cells were observed but n
61 t septation, such as FtsZ overproduction and cephalexin treatment, induced growing cells to swell, bu
62 spitalization, recent skin infection, recent cephalexin use, and household S. aureus or MRSA fomite c
64 tem using isolated membranes, acylation with cephalexin was not impaired by depletion of FtsW or FtsN
65 Molecular imprinted polymer (MIP) against cephalexin was synthesized by co-polymerization of funct
66 be produced by treatment with the antibiotic cephalexin, which blocks cell division but allows cell g
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