ライフサイエンスコーパス: octadecanoid

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1 -isoleucine conjugate (JA-Ile) and (2) other octadecanoids are suppressed by microbe-associated molec

2 red in the def-1 mutant that is deficient in octadecanoid-based signaling of defensive proteinase inh

3 let radiation requires the activation of the octadecanoid defence signalling pathway.

4 X that may play a role as a component of the octadecanoid defense-signaling pathway.

5 Octadecanoid derivative-responsive AP2/ERF-domain transc

6 ously characterized ethylene response factor Octadecanoid derivative-Responsive Catharanthus APETALA2

7 The enzymatic reactions leading to octadecanoid lipid signaling intermediates in plants are

8 y indicates that def1 plants are affected in octadecanoid metabolism between the synthesis of hydrope

9 Taken together, these results show that octadecanoid metabolism plays an essential role in the t

10 enes that are normally activated through the octadecanoid pathway after wounding.

11 olet light is blocked by an inhibitor of the octadecanoid pathway and it does not occur in a tomato m

12 an amplification loop that up-regulates the octadecanoid pathway and the synthesis of jasmonates to

13 A mutant tomato line compromised in the octadecanoid pathway does not exhibit PG activity or H2O

14 t systemin induces PI expression through the octadecanoid pathway for jasmonic acid (JA) biosynthesis

15 transgene that constitutively activates the octadecanoid pathway in a Def-1-dependent manner were hi

16 gh their cut stems with intermediates of the octadecanoid pathway indicates that def1 plants are affe

17 igosaccharide elicitors, indicating that the octadecanoid pathway is essential for the activation of

18 t line that is functionally deficient in the octadecanoid pathway is highly susceptible to attacks by

19 s generated at the attack sites activate the octadecanoid pathway via different recognition events to

20 gh substrate specificity and are part of the octadecanoid pathway which convert linolenic acid to the

21 c acid, synthesized from linolenic acid (the octadecanoid pathway), has been proposed to be part of a

22 Inhibitors of the octadecanoid pathway, and a mutation that interrupts thi

23 les systemin perception to activation of the octadecanoid pathway, and that systemin acts at or near

24 tant (def-1), which has an impairment in the octadecanoid pathway, displayed a severe reduction in th

25 t JA, or a related compound derived from the octadecanoid pathway, may act as a transmissible wound s

26 acid and diethyldi-thiocarbamic acid) of the octadecanoid pathway, supporting a role for the pathway

27 ef1, a mutant tomato line having a defective octadecanoid pathway, the 48-kDa MBP kinase is activated

28 that is deficient in the biosynthesis of the octadecanoid pathway-derived signal, jasmonic acid (JA).

29 ransmissible signal that is derived from the octadecanoid pathway.

30 alicylic acid, which is known to inhibit the octadecanoid pathway.

31 r cut stems, as expected if they utilize the octadecanoid pathway.

32 which is derived from linolenic acid via the octadecanoid pathway.

33 todienoic acid and jasmonic acid through the octadecanoid pathway.

34 es transcription of the genes YUC4, YUC8 and OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF (ORA)59 inde

35 nterestingly, in elp2, expression of WRKY33, OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59 (ORA59), a

36 RESPONSE FACTOR (ERF) transcription factors OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59 and ERF1 a

37 al activation experiments, we also show that OCTADECANOID-RESPONSIVE ARABIDOPSIS AP2/ERF59- and ERF1-

38 g ACC-induced APETALA2/ERFs, only ORA59 (for OCTADECANOID-RESPONSIVE ARABIDOPSIS APETALA2/ETHYLENE RE

39 xide synthase, which are associated with the octadecanoid signaling pathway and are expressed 0.5 to

40 The octadecanoid signaling pathway has been shown to play an

41 ese findings indicate that activation of the octadecanoid signaling pathway promotes resistance of to

42 the generation of H2O2 requires a functional octadecanoid signaling pathway.

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