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1 o mechanical strength, water conduction, and plant defence.
2 s, in this case, as indispensable players in plant defence.
3 numerous pyrrolizidine alkaloids involved in plant defence.
4 eir better-characterized role in suppressing plant defence.
5  which auxin signalling and miR393 influence plant defence.
6 ic basis for understanding priming events in plant defence.
7 gradation pathway plays an important role in plant defence.
8 wth, as required of an effective antifeedant plant defence.
9 ces in understanding molecular mechanisms of plant defence.
10 d activity of respiratory metabolism to fuel plant defences.
11 eted effector proteins in the suppression of plant defences.
12 roduction of molecules that suppress induced plant defences.
13 xins are thought to have cracked the code of plant defences.
14   We consider modern usage of fungicides and plant defence activators, assess the usefulness of biolo
15 robiome was enriched in pathways involved in plant defence activities; the conventional orchard micro
16 ve shown the importance of ubiquitination in plant defence against a multitude of pathogens.
17 ing an involvement of SA in whitefly-derived plant defence against Agrobacterium.
18 e for mobile host and pathogen small RNAs in plant defence against eukaryotic pathogens.
19 action which has been considered an indirect plant defence against herbivores.
20 s for a prime role of secondary compounds in plant defence against herbivores.
21           However, despite its importance in plant defence against pathogens, SA biosynthesis is not
22 monic acid (JA) often play distinct roles in plant defence against pathogens.
23 istance (R) genes are a crucial component in plant defence against pathogens.
24 emerged as an important mechanism underlying plant defence against pathogens.
25             In addition to their function in plant defence against pests and diseases above-ground, b
26   Although the role of MYC2 in orchestrating plant defences against pathogens is well established, it
27                 Salicylic acid (SA) mediates plant defences against pathogens, accumulating in both i
28                        COs can also activate plant defence, although there are scarce data about CO p
29                         They are integral to plant defence and adaptation.
30 transfer proteins (LTP) play a major role in plant defence and are of particular interest due to thei
31 strategy in diverse host species to suppress plant defence and colonize plant tissue.
32 erturbed cell wall biosynthesis may activate plant defence and provide a rationale for the cie1 and t
33 tially expressed, including some involved in plant defences and auxin signalling.
34 rectly into plant cells, where they suppress plant defences and facilitate tissue invasion.
35  We propose that miR393 levels can fine-tune plant defences and prioritize resources.
36 ophic fungal pathogens simultaneously subdue plant defences and sequester host nutrients are poorly u
37 that plant chemistry plays a central role in plant defence, and the evolution of plant secondary chem
38                                        While plant defences are known to influence predator-prey inte
39  we propose criteria to classify inducers of plant defence as either MAMPs or microbe-induced molecul
40 iR863-3p silences two negative regulators of plant defence, atypical receptor-like pseudokinase1 (ARL
41 l nectar and protein bodies provide indirect plant defence by attracting natural enemies of herbivore
42 was undertaken to study the strengthening of plant defences by antioxidants.
43 key mechanistic link underlying CMN-mediated plant defence communication.
44      Further research on the biosynthesis of plant defence compounds in different tissues, their toxi
45       Triterpenoids are widespread bioactive plant defence compounds with potential use as pharmaceut
46     The ability to evolve resistance to host-plant defences depends upon additive genetic variation i
47  repressed genes encoded proteins related to plant defence (e.g. a putative probenazole inducible pro
48  which are thought to be helpless victims of plant defences elicited by their oral secretions.
49 econdary metabolism, and an up-regulation of plant defence genes associated with induced systemic res
50 Production of salicylic acid (SA), a central plant defence hormone(1-3), is particularly vulnerable t
51 r knowledge gap in the biosynthesis of a key plant defence hormone, establishing a foundation for new
52             Activation of local and systemic plant defences in response to pathogen attack involves d
53 appears to be involved in the suppression of plant defences in response to the fungal symbiont.
54 the evolution of ontogenetic trajectories in plant defence, including developmental constraints, reso
55 rategies to counter constitutive and induced plant defences, including degradation of preformed antim
56 attenuates the transcriptional activation of plant defence independently of its protease activity.
57               The first is required early in plant defence, independently of PAD4.
58 ding to AtSR1 is required for suppression of plant defence, indicating a direct role for Ca(2+)/calmo
59 defence signaling pathways but their role in plant defence is less well studied.
60 ationships between herbivore performance and plant defence levels were typically linear, with varianc
61 hat the importance of secondary chemistry in plant defence may have been generally overstated in earl
62 ngly varied, and what might be elicited as a plant defence mechanism against a pathogen could promote
63     Here, we report the discovery of a novel plant defence mechanism resulting from an unusual symbio
64 esting that in addition to its function as a plant defence mechanism, DNA methylation could have a ro
65                                         Host plant defence mechanisms (resistance and tolerance) and
66 e, no known roles in flower development, nor plant defence mechanisms against insects.
67 s are a class of products able to elicit the plant defence mechanisms against pathogens, incurring lo
68 offering a foundation for future research in plant defence mechanisms and environmental interactions.
69 o determine whether its competition-mediated plant defence mechanisms effect on wheat grain quality,
70  leaves reduced canker formation and induced plant defence mechanisms.
71 rimacy of how herbivore host recognition and plant defences mediate whether novel host interactions w
72 rom Mexican maize fields can cope with these plant defence metabolites, but the results also indicate
73 acity of herbivore natural enemies to resist plant defence metabolites.
74                                         This plant defence molecule has strong antibiotic properties.
75 vels were typically linear, with variance in plant defence not affecting herbivore performance via no
76                                              Plant defence often varies by orders of magnitude as pla
77 D4 are both required for accumulation of the plant defence-potentiating molecule, salicylic acid.
78  first linkages reported among trade-offs in plant defences related to the intensity of herbivory, al
79 for the resource availability hypothesis and plant defence research.
80 te (MeSA) is a plant metabolite that induces plant defence resistance and an odorous volatile compoun
81  findings suggest that coilin is involved in plant defence, responding to TRV infection by recognitio
82 D-box RNA helicase and played vital roles in plant defence response against salinity stress.
83 een was established for mutants in which the plant defence response is de-repressed.
84             Our evidence indicates that this plant defence response to certain wavelengths of ultravi
85 re known to act as priming agents, enhancing plant defence response to insects.
86 rrier properties of the cell wall inducing a plant defence response, which results in the production
87 produce reactive oxygen species (ROS) in the plant defence response.
88 luminium might be to impair calcium-mediated plant defence responses against low pH.
89 ing the role of these hormones in modulating plant defence responses against various diseases and pes
90 recently emerged as pivotal to co-ordinating plant defence responses and as a target of plant pathoge
91 d and balanced intracellular redox system in plant defence responses to biotic and abiotic stresses a
92 -lyase (PAL), which has an important role in plant defence responses, and was purified.
93  essential and conserved primary mediator in plant defence responses, how Ca(2+) signals are sensed a
94 genes are regulated during the activation of plant defence responses, we are studying a group of path
95 r the mechanisms of insect herbivore-induced plant defence responses.
96 bute to early basal and subsequent secondary plant defence responses.
97 tyrosine phosphatase activity that modulates plant defence responses.
98 o be a key transcriptional regulator in some plant defence responses.
99 ophthora proteins previously shown to elicit plant defence responses.
100  acid (SA), an endogenous signal involved in plant defence responses.
101  and peptide hormones are also implicated in plant defence signaling pathways but their role in plant
102 ombination of actions including induction of plant defence signalling callose deposition and the stre
103 rains can influence infection and modify the plant defence signalling pathways.
104                         Here, we investigate plant defence signalling with a focus on salicylic acid
105 elicitor and other genes implicated in early plant defence signalling.
106 ic rice pathogen Magnaporthe oryzae requires plant defence suppression to facilitate extensive biotro
107  and early signalling machinery to decoy the plants defence systems.
108 aintaining redox balance to avoid triggering plant defences that impact M. oryzae growth and BIC deve
109 calmodulin-activated transcription factor in plant defence, the present study reveals Ca(2+) signalli
110 r initiates signalling pathways that enhance plant defences to UV-B damage, mitigating the effects of
111 immunity by affecting RNA metabolism and the plant defence transcriptome.
112                   The function of NtCDPK2 in plant defence was investigated by employing virus-induce
113                            Unlike many other plant defences, where diet specialisation often helps he

 
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