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1 ype spores with the GR-independent germinant dodecylamine.
2 r, germinate with Ca(2+)-dipicolinic acid or dodecylamine.
3 ermination with nutrients, and probably with dodecylamine.
4 , l-valine, or a non-GR-dependent germinant, dodecylamine.
5 zite CTSe nanocrystals were synthesized with dodecylamine and 1-dodecanethiol as coordinating solvent
6 -type spores with the nonnutrient germinants dodecylamine and a 1:1 chelate of Ca2+ and dipicolinic a
8 2+) and dipicolinic acid (DPA), but not with dodecylamine, and the defect was prior to DPA release in
10 1), which was suitable for determinations of dodecylamine at levels typically present in fully formul
11 normally with nutrients and even better with dodecylamine but not with a 1:1 chelate of Ca(2+) and di
12 tion of CaDPA release with both l-valine and dodecylamine but not with faster CaDPA release once this
13 ductivity of films of octylamine (C8NH2)- or dodecylamine (C12NH2)-coated Pd, PdAg, and PdAu MPCs inc
17 s subtilis spores by the cationic surfactant dodecylamine exhibited a pH optimum of approximately 9 a
18 temperature sensitive in DPA release during dodecylamine germination as well as in lysozyme germinat
20 elease) times were relatively similar during dodecylamine germination of spores of the five strains.
21 bout fourfold faster than DPA release during dodecylamine germination of wild-type spores and was inh
23 a 1:1 chelate of Ca2+ and dipicolinic acid, dodecylamine, lysozyme in hypertonic medium, a pressure
24 e surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn(2
28 mixture of Ca2+ and dipicolinic acid or with dodecylamine was normal, as was the spontaneous germinat
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