ライフサイエンスコーパス: allelochemical

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 or through interference by the production of allelochemicals.

9 green alga Chlorodesmis fastigiata as potent allelochemicals.

10 actone diterpenoids as both phytoalexins and allelochemicals.

11 e momilactones are constantly synthesized as allelochemicals.

12 actone diterpenoids as both phytoalexins and allelochemicals.

13 mizing the harmful effects of ingested plant allelochemicals.

14 rest invader that produces known anti-fungal allelochemicals.

15 ane-related diterpenoids as phytoalexins and allelochemicals.

16 clusters involved in the biosynthesis of an allelochemical 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-

17 To decipher the molecular basis of the allelochemical activity of MDCA, we evaluated the effect

18 The response of allelochemicals affecting insect performance varies unde

19 in response to the challenge by potato leaf allelochemicals and imidacloprid.

20 fferences in the selective regime imposed by allelochemicals and insecticides may account for the rel

21 examining plant transcriptional responses to allelochemicals and other environmental toxins and provi

22 nes transcriptionally regulated by hostplant allelochemicals and provide insights into the process by

23 cant role in the detoxification of hostplant allelochemicals and synthetic insecticides in Lepidopter

24 sed to exogenous toxins (microbial products, allelochemicals, and agrochemicals), cell survival is co

25 networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woo

26 Insect herbivores also regularly encounter allelochemicals as they eat, and recent work indicates t

27 Here, we report that allelochemicals derived from the common class of cyclic

28 The allelochemical DIMBOA gene cluster is activated in respo

29 eat, and recent work indicates the effect an allelochemical has on nutrient regulation, and insect he

30 tions to detoxification, especially of plant allelochemicals in phytophagous insects, and resistance

31 These allelochemicals inhibit histone deacetylases both in vit

32 lutionary association with genes involved in allelochemical metabolism.

33 ting elements mediating the induction of the allelochemical-metabolizing CYP321A1 from the generalist

34 ctionally more diverse, two counterdefensive allelochemical-metabolizing cytochrome P450 proteins, CY

35 Benzoxazolin-2(3H)-one (BOA) is an allelochemical most commonly associated with monocot spe

36 The representative allelochemicals of the tested hostplants significantly (

37 n defence below-ground, where they can exert allelochemical or antimicrobial activities.

38 tly damage corals by transfer of hydrophobic allelochemicals present on algal surfaces.

39 hin insects because of stress and prooxidant allelochemicals produced by host plants in response to h

40 cessary to follow the qualitative changes of allelochemicals production at different developmental st

41 suggest that local effects are generated by allelochemical rather than physical mechanisms.

42 e to a broad range of structurally different allelochemicals remains largely unknown.

43 whether this is accomplished by having more allelochemical-response elements or the similar number o

44 Co-administration of the two allelochemicals resulted in an induction fold that is si

45 ed to be involved in the biosynthesis of the allelochemical sorgoleone.

46 enzymes involved in the biosynthesis of the allelochemical sorgoleone.

47 ese results suggest that naturally-occurring allelochemicals such as nicotine are the initial driving

48 arthropod-induced plant proteins and defense allelochemicals synthesized by resistance gene products.

49 Plants produce a wide range of allelochemicals to defend against herbivore attack, and

50 le species such as Arabidopsis thaliana, the allelochemical triggers a wave of reactive oxygen specie

51 rspecific competitors invest more in a toxic allelochemical under common conditions.

52 ly more diverse common elements although the allelochemical-unique elements also play a role.

53 e CYP28 cytochrome P450s by toxic host-plant allelochemicals (up to 11.5-fold) and phenobarbital (up

54 ody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 a

55 toxin and flavone, two structurally distinct allelochemicals with very different encounter rate by th

56 aldrin), whereas CYP6B1 metabolizes only two allelochemicals (xanthotoxin and flavone) and one insect

57 r aryl hydrocarbons (benzo[alpha]pyrene) and allelochemicals (xanthotoxin).

58 tabolizes six biosynthetically diverse plant allelochemicals (xanthotoxin, quercetin, flavone, chloro