ライフサイエンスコーパス: pathosystem

1 veral unique aspects of the leafroll disease pathosystem.

2 th which to describe many aspects of a plant pathosystem.

3 en sufficiently to prevent infection in this pathosystem.

4 and biologically relevant management of this pathosystem.

5 ular interactions that define the wheat-rust pathosystem.

6 enhances susceptibility in the investigated pathosystem.

7 g of these processes in a well-defined model pathosystem.

8 st resistance in the Arabidopsis-Pseudomonas pathosystem.

9 oxylipin cross-talk in the Aspergillus-seed pathosystem.

10 opted for RT-qPCR experiments involving this pathosystem.

11 ion in the Capsicum-Tobacco etch virus (TEV) pathosystem.

12 entified and characterized in numerous plant pathosystems.

13 ve been identified for even the best-studied pathosystems.

14 imal roguing schedule-are applicable to many pathosystems.

15 strategy may be widely used in Phytophthora pathosystems.

16 requires careful matching of antagonists to pathosystems.

17 ions, are rapid compared with other arboreal pathosystems.

18 fulvum and tomato, and related gene-for-gene pathosystems.

19 The complexity of forest pathosystems and the limitations of genetic analysis, ba

20 cation of this method to various Arabidopsis pathosystems and the wealth of available disease resista

21 s are studied as pathosystem components, and pathosystems are studied for their emergent properties.

22 (2) Agricultural plant pathosystems are the focus of research on endophyte dise

23 he information needed to manage a particular pathosystem at an acceptable financial risk; details of

24 Concepts and approaches developed in this pathosystem can guide future efforts when responding to

25 es and can be easily adapted to various crop pathosystems characterized by airborne inoculum.

26 gy in which virulence factors are studied as pathosystem components, and pathosystems are studied for

27 We show that in the pathosystem considered here, in general large stochastic

28 This naturally coevolving pathosystem contains an amazing level of genetic diversi

29 anipulation syndromes comprehensively within pathosystems, expanding the taxonomic and genetic breadt

30 phic pathogens and their hosts has generated pathosystems featuring extreme complexity and apparent r

31 This novel floral pathosystem for Arabidopsis appears to be highly represe

32 ve population and developed into an in vitro pathosystem for N. attenuata.

33 ys) with Colletotrichum graminicola, a model pathosystem for the study of hemibiotrophy.

34 This pathosystem has allowed us to exploit N. benthamiana as

35 The rice blast pathosystem has been the subject of intense interest in

36 vide evidence that this natural plant-fungus pathosystem has conditionally mutualistic features.

37 grees of disease control for a wide range of pathosystems, including crops with large plants, and pat

38 We first developed a pathosystem involving the infection of Arabidopsis acces

39 suggests that the Stagonospora nodorum-wheat pathosystem is controlled by host-selective toxins (HSTs

40 ilds on the notion that the S. nodorum-wheat pathosystem is largely based on multiple host-toxin inte

41 resistance in this endemic coevolved forest pathosystem is not exclusively polygenic.

42 r basis of gene-for-gene recognition in this pathosystem is the direct physical interaction of the Pt

43 evant tomato-Pseudomonas syringae pv. tomato pathosystem is widely used to explore and understand the

44 A genetically tractable model plant pathosystem, Pseudomonas syringae pv. tomato DC3000 on t

45 Within a specific pathosystem, refuge size can be estimated in experiments

46 tute of Allergy and Infectious Diseases, the Pathosystems Resource Integration Center (PATRIC) is a g

47 The PathoSystems Resource Integration Center (PATRIC) is one

48 The Pathosystems Resource Integration Center (PATRIC) is the

49 The Pathosystems Resource Integration Center (PATRIC) is the

50 ial virulence factor (VF) library in PATRIC (Pathosystems Resource Integration Center, www.patricbrc.

51 climate variables on infection rates, though pathosystem-specific characteristics make synthesis chal

52 logical functions with obvious roles in this pathosystem, such as biofilm formation, antibiotic metab

53 Here, we describe a novel pathosystem that consists of epitope-tagged Bs2-expressi

54 al importance of endophytes in natural plant pathosystems that are fundamental to biodiversity and co

55 apply high-throughput RNA sequencing to this pathosystem to identify genes whose expression changes s

56 We used an Arabidopsis/Pseudomonas syringae pathosystem to investigate the impact of pathogen-induce

57 ome sequence indicate the potential for this pathosystem to serve as a toxin-based, inverse gene-for-

58 To create a robust pathosystem to study AvrBsT immunity in Arabidopsis, the

59 We characterized a Medicago truncatula-ASR pathosystem to study molecular mechanisms of nonhost res

60 mbined with ecological studies in wild plant pathosystems to determine whether disease-modifying fung

61 the establishment of a new biotrophic model pathosystem: Ustilago bromivora and Brachypodium sp.

62 rticillium interactions, we have developed a pathosystem utilizing Arabidopsis thaliana and an isolat

63 r beet) cyst nematode (Heterodera schachtii) pathosystem, we have determined that the two Arabidopsis

64 Arabidopsis thaliana-Pseudomonas aeruginosa pathosystem, we provide evidence that SA acts directly o

65 ongbing (HLB) is the most destructive citrus pathosystem worldwide.

66 plant disease across a broad range of plant pathosystems, yet simultaneously reveals that complexity