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1 fluid were quantified fluorimetrically using oxytetracycline.
2 compared by staining with alizarin red S and oxytetracycline.
3 d more potent than the commercial antibiotic oxytetracycline.
4 e key precursor anhydrotetracycline 3 during oxytetracycline 1 biosynthesis has been previously chara
5 oderate improvement were: minocycline versus oxytetracycline -1.2% (unadjusted 95% CI -13.3 to 10.9);
6 ned erythromycin and benzoyl peroxide versus oxytetracycline 11.1% (-0.7 to 22.9) and versus minocycl
7 575 tetracycline aglycon 8 parallels that of oxytetracycline 4 and diverges after the assembly of 4-k
8 3.5% (-15.2 to 8.2); benzoyl peroxide versus oxytetracycline 5.0% (-7.0 to 17.0), versus minocycline
10 (3), minocycline (4), chlortetracycline (5), oxytetracycline (6), and doxycycline (7) were biotransfo
12 combinations are similar in efficacy to oral oxytetracycline and minocycline and are not affected by
13 the feeding of milk replacer medicated with oxytetracycline and neomycin to preweaned calves reduced
15 Just one clam sample showed the presence of oxytetracycline at a concentration slightly higher than
16 entified the minimum set of enzymes from the oxytetracycline biosynthetic pathway that is required to
17 yS, which are enzymes in the mithramycin and oxytetracycline biosynthetic pathways, respectively.
19 ory concentrations (MIC) were determined for oxytetracycline, danofloxacin and tulathromycin against
20 y were to determine the effector kinetics of oxytetracycline, danofloxacin and tulathromycin against
22 lower in serum than in artificial medium for oxytetracycline, danofloxacin and tulathromycin, respect
24 , dicloxacillin, enrofloxacin, tetracycline, oxytetracycline, erythromycin, spinosad, cyclo-1,3,5,7-t
29 cin, florfenicol, gentamicin, oxolinic acid, oxytetracycline, ormetoprim-sulfadimethoxine, and trimet
30 flow assay (LFA) was developed to screen the oxytetracycline (OTC) antibiotics residues in milk sampl
31 esent a new method for specific detection of oxytetracycline (OTC) at nanomolar concentrations based
35 plexation of Fe(II) with tetracycline (TTC), oxytetracycline (OTC), or chlorotetracycline (CTC) could
36 se) rendered S. cerevisiae hypersensitive to oxytetracycline (OTC): a sod1Delta mutant exhibited a >9
37 r(2)) were 0.997, 0.992, 0.994 and 0.998 for oxytetracycline (OXI), tetracycline (TC), chlortetracycl
38 oof of concept, this approach was applied to oxytetracycline (OXY), one of the antibiotics frequently
39 n 72 (55%) of 131 participants assigned oral oxytetracycline plus topical placebo, 70 (54%) of 130 as
41 ing use of calf milk replacer medicated with oxytetracycline results in increased tetracycline suscep
45 ive isolation and clean-up of tetracyclines (oxytetracycline, tetracycline, epi-chlorotetracycline, c
48 lly believed that foot trimming with topical oxytetracycline was the better treatment, changed to ent
50 ichlorobenzylamine, phenyltrimethylammonium, oxytetracycline) with two aluminosilicate clay minerals
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