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1 duals, dominated by the presence of modified octadecanoid acyl chains in phospho- and neutral lipids,
4 -isoleucine conjugate (JA-Ile) and (2) other octadecanoids are suppressed by microbe-associated molec
6 red in the def-1 mutant that is deficient in octadecanoid-based signaling of defensive proteinase inh
7 has been shown to be a significant source of octadecanoid biosynthesis, providing additional biosynth
8 oxyl groups located at carbons C9 and C13 of octadecanoids, C12 and C15 carbons of eicosanoids, and C
12 ously characterized ethylene response factor Octadecanoid derivative-Responsive Catharanthus APETALA2
13 ds include potent signaling molecules (e.g., octadecanoids, eicosanoids) that can exert essential fun
14 , summarize the phase-I metabolic pathway of octadecanoid formation in mammals, bacteria, and fungi,
16 y indicates that def1 plants are affected in octadecanoid metabolism between the synthesis of hydrope
19 olet light is blocked by an inhibitor of the octadecanoid pathway and it does not occur in a tomato m
20 an amplification loop that up-regulates the octadecanoid pathway and the synthesis of jasmonates to
22 t systemin induces PI expression through the octadecanoid pathway for jasmonic acid (JA) biosynthesis
23 ction of the phytohormone jasmonic acid, the octadecanoid pathway has been expanded to include produc
24 transgene that constitutively activates the octadecanoid pathway in a Def-1-dependent manner were hi
25 gh their cut stems with intermediates of the octadecanoid pathway indicates that def1 plants are affe
26 igosaccharide elicitors, indicating that the octadecanoid pathway is essential for the activation of
27 t line that is functionally deficient in the octadecanoid pathway is highly susceptible to attacks by
28 s generated at the attack sites activate the octadecanoid pathway via different recognition events to
29 gh substrate specificity and are part of the octadecanoid pathway which convert linolenic acid to the
30 c acid, synthesized from linolenic acid (the octadecanoid pathway), has been proposed to be part of a
32 les systemin perception to activation of the octadecanoid pathway, and that systemin acts at or near
33 tant (def-1), which has an impairment in the octadecanoid pathway, displayed a severe reduction in th
34 t JA, or a related compound derived from the octadecanoid pathway, may act as a transmissible wound s
35 acid and diethyldi-thiocarbamic acid) of the octadecanoid pathway, supporting a role for the pathway
36 ef1, a mutant tomato line having a defective octadecanoid pathway, the 48-kDa MBP kinase is activated
37 that is deficient in the biosynthesis of the octadecanoid pathway-derived signal, jasmonic acid (JA).
43 tandardized nomenclature, provide details of octadecanoid preparation and measurement, summarize the
44 is review, we summarize the current field of octadecanoids, propose standardized nomenclature, provid
46 es transcription of the genes YUC4, YUC8 and OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF (ORA)59 inde
47 nterestingly, in elp2, expression of WRKY33, OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59 (ORA59), a
48 RESPONSE FACTOR (ERF) transcription factors OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59 and ERF1 a
49 al activation experiments, we also show that OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59- and ERF1-
50 g ACC-induced APETALA2/ERFs, only ORA59 (for OCTADECANOID-RESPONSIVE ARABIDOPSIS APETALA2/ETHYLENE RE
51 xide synthase, which are associated with the octadecanoid signaling pathway and are expressed 0.5 to
53 ese findings indicate that activation of the octadecanoid signaling pathway promotes resistance of to
55 anding roles of prostaglandinE(2) in cancer, octadecanoid structures and nomenclature, complex forms