ライフサイエンスコーパス: plant defence

1 numerous pyrrolizidine alkaloids involved in plant defence.

2 eir better-characterized role in suppressing plant defence.

3 which auxin signalling and miR393 influence plant defence.

4 ic basis for understanding priming events in plant defence.

5 gradation pathway plays an important role in plant defence.

6 wth, as required of an effective antifeedant plant defence.

7 d activity of respiratory metabolism to fuel plant defences.

8 eted effector proteins in the suppression of plant defences.

9 roduction of molecules that suppress induced plant defences.

10 We consider modern usage of fungicides and plant defence activators, assess the usefulness of biolo

11 ve shown the importance of ubiquitination in plant defence against a multitude of pathogens.

12 ing an involvement of SA in whitefly-derived plant defence against Agrobacterium.

13 s for a prime role of secondary compounds in plant defence against herbivores.

14 action which has been considered an indirect plant defence against herbivores.

15 However, despite its importance in plant defence against pathogens, SA biosynthesis is not

16 istance (R) genes are a crucial component in plant defence against pathogens.

17 In addition to their function in plant defence against pests and diseases above-ground, b

18 Salicylic acid (SA) mediates plant defences against pathogens, accumulating in both i

19 transfer proteins (LTP) play a major role in plant defence and are of particular interest due to thei

20 strategy in diverse host species to suppress plant defence and colonize plant tissue.

21 erturbed cell wall biosynthesis may activate plant defence and provide a rationale for the cie1 and t

22 rectly into plant cells, where they suppress plant defences and facilitate tissue invasion.

23 We propose that miR393 levels can fine-tune plant defences and prioritize resources.

24 ophic fungal pathogens simultaneously subdue plant defences and sequester host nutrients are poorly u

25 that plant chemistry plays a central role in plant defence, and the evolution of plant secondary chem

26 While plant defences are known to influence predator-prey inte

27 we propose criteria to classify inducers of plant defence as either MAMPs or microbe-induced molecul

28 iR863-3p silences two negative regulators of plant defence, atypical receptor-like pseudokinase1 (ARL

29 l nectar and protein bodies provide indirect plant defence by attracting natural enemies of herbivore

30 was undertaken to study the strengthening of plant defences by antioxidants.

31 Triterpenoids are widespread bioactive plant defence compounds with potential use as pharmaceut

32 The ability to evolve resistance to host-plant defences depends upon additive genetic variation i

33 which are thought to be helpless victims of plant defences elicited by their oral secretions.

34 Activation of local and systemic plant defences in response to pathogen attack involves d

35 the evolution of ontogenetic trajectories in plant defence, including developmental constraints, reso

36 rategies to counter constitutive and induced plant defences, including degradation of preformed antim

37 attenuates the transcriptional activation of plant defence independently of its protease activity.

38 The first is required early in plant defence, independently of PAD4.

39 ding to AtSR1 is required for suppression of plant defence, indicating a direct role for Ca(2+)/calmo

40 defence signaling pathways but their role in plant defence is less well studied.

41 ationships between herbivore performance and plant defence levels were typically linear, with varianc

42 hat the importance of secondary chemistry in plant defence may have been generally overstated in earl

43 ngly varied, and what might be elicited as a plant defence mechanism against a pathogen could promote

44 Here, we report the discovery of a novel plant defence mechanism resulting from an unusual symbio

45 e, no known roles in flower development, nor plant defence mechanisms against insects.

46 s are a class of products able to elicit the plant defence mechanisms against pathogens, incurring lo

47 leaves reduced canker formation and induced plant defence mechanisms.

48 vels were typically linear, with variance in plant defence not affecting herbivore performance via no

49 Plant defence often varies by orders of magnitude as pla

50 D4 are both required for accumulation of the plant defence-potentiating molecule, salicylic acid.

51 een was established for mutants in which the plant defence response is de-repressed.

52 Our evidence indicates that this plant defence response to certain wavelengths of ultravi

53 re known to act as priming agents, enhancing plant defence response to insects.

54 produce reactive oxygen species (ROS) in the plant defence response.

55 luminium might be to impair calcium-mediated plant defence responses against low pH.

56 ing the role of these hormones in modulating plant defence responses against various diseases and pes

57 -lyase (PAL), which has an important role in plant defence responses, and was purified.

58 essential and conserved primary mediator in plant defence responses, how Ca(2+) signals are sensed a

59 genes are regulated during the activation of plant defence responses, we are studying a group of path

60 bute to early basal and subsequent secondary plant defence responses.

61 tyrosine phosphatase activity that modulates plant defence responses.

62 ophthora proteins previously shown to elicit plant defence responses.

63 acid (SA), an endogenous signal involved in plant defence responses.

64 and peptide hormones are also implicated in plant defence signaling pathways but their role in plant

65 rains can influence infection and modify the plant defence signalling pathways.

66 ic rice pathogen Magnaporthe oryzae requires plant defence suppression to facilitate extensive biotro

67 and early signalling machinery to decoy the plants defence systems.

68 aintaining redox balance to avoid triggering plant defences that impact M. oryzae growth and BIC deve

69 calmodulin-activated transcription factor in plant defence, the present study reveals Ca(2+) signalli

70 immunity by affecting RNA metabolism and the plant defence transcriptome.

71 The function of NtCDPK2 in plant defence was investigated by employing virus-induce