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1 ants altered in JA synthesis and perception, allene oxide synthase and coi1-16B (for coronatine insen
2 he coral Capnella imbricata, form a being an allene oxide synthase and form b giving uncharacterized
3 indicating differing gene regulation of the allene oxide synthase and the newly identified catalase-
4 or the JA biosynthetic enzymes lipoxygenase, allene oxide synthase, and allene oxide cyclase were str
5 very similar to a cytochrome P450-containing allene oxide synthase, and DSA15 may be a fatty acid elo
6 resses linoleate 9R-dioxygenase (9R-DOX) and allene oxide synthase (AOS) activities in membrane fract
10 of the plant defensive response pathway, the allene oxide synthase (AOS) and hydroperoxide lyase (HPL
13 r to test whether or not a cytosol-localized allene oxide synthase (AOS) can promote JA biosynthesis,
14 onding 8 R-hydroperoxide, and the N-terminal allene oxide synthase (AOS) domain promotes the conversi
15 have expressed the separate lipoxygenase and allene oxide synthase (AOS) domains of the coral protein
18 f lipoxygenase 2 (LOX2) but had no effect on allene oxide synthase (AOS) or hydroperoxide lyase in wo
20 that NSAIDs act as competitive inhibitors of allene oxide synthase (AOS), the cytochrome P450 that in
21 efective in the JA biosynthetic gene CYP74A (allene oxide synthase, AOS) using reverse genetics scree
22 ombined, promote stomatal closure of ABA and allene oxide synthase biosynthetic mutants, albeit most
23 ly alter oxylipin profiles, particularly the allene oxide synthase branch of the oxylipin pathway, re
26 tion of 9S-hydroperoxylinoleic acid with the allene oxide synthase CYP74C3, a reported reaction that
28 enes encoding prosystemin, lipoxygenase, and allene oxide synthase, which are associated with the oct
29 g leaf senescence in Arabidopsis, except for allene oxide synthase, which is constitutively and highl
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