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1 e for growth (50 microgram/ml [77 microM] on agar medium).
2 tin-exposed yeast since it failed to grow on agar medium.
3 op around individual donors during mating on agar medium.
4 loids, however, showed marked penetration of agar medium.
5 so highly induced by root penetration of the agar medium.
6 ed, homogenized, and cultured in tryptic soy agar medium.
7 or would these cells form colonies in a soft-agar medium.
8 stitutive swarmer cells and swarm on minimal agar medium.
9 cent, since they could not be subcultured on agar medium.
10 ants with altered swarming abilities in soft agar medium.
11 umptive colonies were subcultured on Gelatin Agar medium.
12 ureus genome that altered hemolysis on blood agar medium.
13 ae, LSUPB201, also produced toxoflavin on LB agar medium.
14 nfected with these strains and overlaid with agar-medium.
15 ained from the samples using Simmons citrate agar medium and characterised by antimicrobial susceptib
16 strains produced rough-surfaced cultures on agar medium and demonstrated a propensity to form pseudo
17 Both mutants displayed a growth defect on agar medium and hypersensitivity to sodium dodecyl sulfa
19 ction occurred in seedlings exposed to water-agar medium and in roots, related luminescence responses
20 cted anaerobically, plated on enriched blood agar medium, and incubated at 35 degrees C for 5 to 7 da
21 35000 grown in liquid medium, grown on solid agar medium, and isolated from lesions of H. ducreyi-inf
22 These samples were cultured on cetrimide agar medium, and isolates were epidemiologically charact
27 ur current method of direct plating on blood agar medium containing neomycin and nalidixic acid (NNA)
28 me Les Grottes, France) is a new chromogenic agar medium designed to enable the isolation of staphylo
29 is thaliana (L.) Heynh. plants were grown in agar medium during 6 or 11 d of spaceflight exposure on
30 and evaluation of MRSA ID, a new chromogenic agar medium for the specific isolation and identificatio
32 verse microbiota using a semiselective blood agar medium incorporating nalidixic acid and sulfamethaz
33 Moreover, the expression of zapA on nutrient agar medium is co-ordinately regulated in concert with t
36 mis bacterial colonies grown on low-nutrient agar medium mutually inhibit growth through secretion of
37 died revertants, selected on lactose minimal agar medium, of the Escherichia coli lacZam strain that
43 is end, we evaluated a prototype chromogenic agar medium (VRE-BMX; bioMerieux, Marcy l'Etoile, France
44 Herbicidal effects were reversed when the agar medium was supplemented with AMP, but not IMP or GM
45 trast, dig1 dig2 cells constitutively invade agar medium, whereas a dig1 dig2 ste12 triple mutant doe
46 performed using a liquid medium and a solid agar medium with an incubation period of up to 60 days.