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1 n that in the case of a simply mixed colloid-bacterial suspension.
2 tivation activity retained after washing the bacterial suspension.
3 esence of available complex carbohydrates in bacterial suspension.
4 lated intranasally with the initial doses of bacterial suspension.
5 ) in solution when adding humic acid (HA) to bacterial suspensions.
6 ting of self-propelled particles, like dense bacterial suspensions.
7 on the membrane surface and its exposure to bacterial suspensions.
8 0-fold less active, respectively, than whole bacterial suspensions.
9 le systems, which are representative of some bacterial suspensions, a hitherto unknown static structu
10 ficantly longer than in mice challenged with bacterial suspensions alone but also required prolonged
12 metastomal flaps regulate the flow of dense bacterial suspensions and exclude excessively large part
13 eir ability to recover Brucella DNA from PBS bacterial suspensions and from swab specimens and, thus,
16 ial suspensions were consistently present in bacterial suspensions of buffer/tryptic soy broth (posit
18 stant strains) and the H37Rv strain by using bacterial suspensions prepared directly from solid media
19 lts and cryoprotectant (e.g., glycerol) from bacterial suspensions, the significant osmotic pressures
22 the expression of thymosin beta-10, whereas bacterial suspensions upregulated thymosin beta-10 expre
23 A combined ultrasound and ozone treatment of bacterial suspensions using a commercial system affords
25 on interactions between single stimulus and bacterial suspension, we emphasize on compounding effect
26 iomarkers from direct MALDI analysis of pure bacterial suspensions were consistently present in bacte
29 bacterial cells per microwire in 1000 CFU/mL bacterial suspensions when the electric field generated
30 esulted in superior levels of detection from bacterial suspensions, while the MasterPure kit and MagN
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