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1  to digestible carbohydrate (P:C) ratios, or allelochemical.
2 xpression are resistant to nicotine, a plant allelochemical.
3  officinalis and further characterized as an allelochemical.
4 lved in detoxifying both pesticide and plant allelochemicals.
5  than the expected additive value of the two allelochemicals.
6 e induction of CYP321A1 by either of the two allelochemicals.
7 ing induction of CYP321A1 by both of the two allelochemicals.
8 green alga Chlorodesmis fastigiata as potent allelochemicals.
9 actone diterpenoids as both phytoalexins and allelochemicals.
10 or through interference by the production of allelochemicals.
11 e momilactones are constantly synthesized as allelochemicals.
12 mizing the harmful effects of ingested plant allelochemicals.
13 rest invader that produces known anti-fungal allelochemicals.
14 ane-related diterpenoids as phytoalexins and allelochemicals.
15  clusters involved in the biosynthesis of an allelochemical 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-
16       To decipher the molecular basis of the allelochemical activity of MDCA, we evaluated the effect
17  little is known about the direct effects of allelochemical addition on bacterial and fungal communit
18                              The response of allelochemicals affecting insect performance varies unde
19 ot placement patterns were mediated by wheat allelochemicals and (-)-loliolide signaling of neighbor
20  in response to the challenge by potato leaf allelochemicals and imidacloprid.
21 fferences in the selective regime imposed by allelochemicals and insecticides may account for the rel
22 examining plant transcriptional responses to allelochemicals and other environmental toxins and provi
23 nes transcriptionally regulated by hostplant allelochemicals and provide insights into the process by
24 cant role in the detoxification of hostplant allelochemicals and synthetic insecticides in Lepidopter
25 sed to exogenous toxins (microbial products, allelochemicals, and agrochemicals), cell survival is co
26 networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woo
27   Insect herbivores also regularly encounter allelochemicals as they eat, and recent work indicates t
28 n. gambiae females and the role root exudate allelochemicals could play on anopheline bionomics, with
29                         Here, we report that allelochemicals derived from the common class of cyclic
30 ed unigenes involved in biotransformation of allelochemicals, digestion of plant cell walls and trans
31                                          The allelochemical DIMBOA gene cluster is activated in respo
32 wide investigation of microbial mediation of allelochemical effects on plant performance by testing h
33 h a repertoire of cues, but the influence of allelochemicals, especially root phytochemicals in modul
34 eat, and recent work indicates the effect an allelochemical has on nutrient regulation, and insect he
35 re generated by both signaling chemicals and allelochemicals in allelopathic plant-plant interactions
36 tions to detoxification, especially of plant allelochemicals in phytophagous insects, and resistance
37                                        These allelochemicals inhibit histone deacetylases both in vit
38 lutionary association with genes involved in allelochemical metabolism.
39 ting elements mediating the induction of the allelochemical-metabolizing CYP321A1 from the generalist
40 ctionally more diverse, two counterdefensive allelochemical-metabolizing cytochrome P450 proteins, CY
41           Benzoxazolin-2(3H)-one (BOA) is an allelochemical most commonly associated with monocot spe
42 nal genes after the addition of the dominant allelochemical native to this habitat.
43                           The representative allelochemicals of the tested hostplants significantly (
44 n defence below-ground, where they can exert allelochemical or antimicrobial activities.
45 y called 'semiochemicals', 'infochemicals', 'allelochemicals' or 'pheromones'.
46 tly damage corals by transfer of hydrophobic allelochemicals present on algal surfaces.
47 hin insects because of stress and prooxidant allelochemicals produced by host plants in response to h
48  (14-year) field experiment, we show that an allelochemical-producing invader affects plants through
49 In particular, (-)-loliolide triggered wheat allelochemical production that altered root growth and p
50 cessary to follow the qualitative changes of allelochemicals production at different developmental st
51  suggest that local effects are generated by allelochemical rather than physical mechanisms.
52 e to a broad range of structurally different allelochemicals remains largely unknown.
53  whether this is accomplished by having more allelochemical-response elements or the similar number o
54                 Co-administration of the two allelochemicals resulted in an induction fold that is si
55 rmore, plant performance was mediated by the allelochemical-selected microbiome, with allelopathic in
56  and fungal communities or the potential for allelochemical-selected microbiomes to mediate plant per
57 ed to be involved in the biosynthesis of the allelochemical sorgoleone.
58  enzymes involved in the biosynthesis of the allelochemical sorgoleone.
59 ese results suggest that naturally-occurring allelochemicals such as nicotine are the initial driving
60 arthropod-induced plant proteins and defense allelochemicals synthesized by resistance gene products.
61  induced the production and release of wheat allelochemicals that modulated root placement patterns.
62 s of the roles of glycosylated norisoprenoid allelochemicals, the physiological functions of apocarot
63               Plants produce a wide range of allelochemicals to defend against herbivore attack, and
64 le species such as Arabidopsis thaliana, the allelochemical triggers a wave of reactive oxygen specie
65 rspecific competitors invest more in a toxic allelochemical under common conditions.
66 ly more diverse common elements although the allelochemical-unique elements also play a role.
67 e CYP28 cytochrome P450s by toxic host-plant allelochemicals (up to 11.5-fold) and phenobarbital (up
68 ody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 a
69 toxin and flavone, two structurally distinct allelochemicals with very different encounter rate by th
70 aldrin), whereas CYP6B1 metabolizes only two allelochemicals (xanthotoxin and flavone) and one insect
71 r aryl hydrocarbons (benzo[alpha]pyrene) and allelochemicals (xanthotoxin).
72 tabolizes six biosynthetically diverse plant allelochemicals (xanthotoxin, quercetin, flavone, chloro