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1 eir coupling at C3 glucuronic acid site with dodecylamine.
2 , l-valine, or a non-GR-dependent germinant, dodecylamine.
3 r, germinate with Ca(2+)-dipicolinic acid or dodecylamine.
4 ype spores with the GR-independent germinant dodecylamine.
5 ermination with nutrients, and probably with dodecylamine.
6 zite CTSe nanocrystals were synthesized with dodecylamine and 1-dodecanethiol as coordinating solvent
7 -type spores with the nonnutrient germinants dodecylamine and a 1:1 chelate of Ca2+ and dipicolinic a
9 2+) and dipicolinic acid (DPA), but not with dodecylamine, and the defect was prior to DPA release in
11 1), which was suitable for determinations of dodecylamine at levels typically present in fully formul
12 normally with nutrients and even better with dodecylamine but not with a 1:1 chelate of Ca(2+) and di
13 tion of CaDPA release with both l-valine and dodecylamine but not with faster CaDPA release once this
14 ductivity of films of octylamine (C8NH2)- or dodecylamine (C12NH2)-coated Pd, PdAg, and PdAu MPCs inc
18 s subtilis spores by the cationic surfactant dodecylamine exhibited a pH optimum of approximately 9 a
19 temperature sensitive in DPA release during dodecylamine germination as well as in lysozyme germinat
21 elease) times were relatively similar during dodecylamine germination of spores of the five strains.
22 bout fourfold faster than DPA release during dodecylamine germination of wild-type spores and was inh
24 a 1:1 chelate of Ca2+ and dipicolinic acid, dodecylamine, lysozyme in hypertonic medium, a pressure
25 e surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn(2
29 mixture of Ca2+ and dipicolinic acid or with dodecylamine was normal, as was the spontaneous germinat