ライフサイエンスコーパス: pathogen resistance

1 ritical roles in inflammation, immunity, and pathogen resistance.

2 sensitive reactions involving cell death and pathogen resistance.

3 g that toxicity of PAP can be separated from pathogen resistance.

4 development, and for understanding long-term pathogen resistance.

5 phenotypes such as conditional sterility or pathogen resistance.

6 C. albicans infection and were required for pathogen resistance.

7 lists and specialists for different modes of pathogen resistance.

8 een the microbiota and the host that impacts pathogen resistance.

9 and neurological function, development, and pathogen resistance.

10 esponse, thereby avoiding the development of pathogen resistance.

11 sor in the thymus but play distinct roles in pathogen resistance.

12 nterfere with the host signaling involved in pathogen resistance.

13 d ethylene (ET) signaling and is involved in pathogen resistance.

14 ow compromised by an increasing incidence of pathogen resistance.

15 scence in GPA-infested plants as well as for pathogen resistance.

16 nding stem cell biology and the evolution of pathogen resistance.

17 gnaling, by an unknown mechanism, leading to pathogen resistance.

18 wild mice under selection for fecundity and pathogen resistance.

19 t of a natural selection probably related to pathogen resistance.

20 rance or how this relates to SA signaling in pathogen resistance.

21 way shuts down SA biosynthesis and abrogates pathogen resistance.

22 d signal transduction, stress responses, and pathogen resistance.

23 and identify a candidate gene, Intracellular pathogen resistance 1 (Ipr1), within the sst1 locus.

24 cation in genetic engineering for increasing pathogen resistance across diverse plant families.

25 n enhanced hypersensitive response, elevated pathogen resistance against both virulent and avirulent

26 nergy in macrophages, which is important for pathogen resistance and immune homeostasis.

27 ity, suggesting that the interaction between pathogen resistance and Ni tolerance and hyperaccumulati

28 nship between the fitness costs of immunity, pathogen resistance and the strength of an immune respon

29 ty to a family of plant proteins involved in pathogen resistance, and because mutations in Card15, en

30 ts, plays important roles in cell expansion, pathogen resistance, and heavy-metal stress tolerance in

31 eviously been considered to be a strategy of pathogen resistance, and the general occurrence of leaf

32 of plant photosynthesis, water homeostasis, pathogen resistance, and ultimately yield.

33 We found that sterility and pathogen resistance are highly correlated and that resis

34 innate effector functions that mediate this pathogen resistance are largely unknown.

35 Within corals, superoxide may contribute to pathogen resistance but also bleaching, the loss of esse

36 Our results show that the inhibition of pathogen resistance by let-7 involves downstream heteroc

37 pathogen virulence and that the mechanism of pathogen resistance can determine the direction of virul

38 netic knockdown of autophagy genes abrogates pathogen resistance conferred by a loss-of-function muta

39 Pathogen resistance conferred by plant R genes of the nu

40 suggest that S. maltophilia JCMS evades the pathogen resistance conferred by the loss of DAF-2/16 pa

41 gainst pathogen attack, we analyzed enhanced pathogen resistance (epr) mutants obtained from a forwar

42 d as an activator of SAR gene expression and pathogen resistance, followed by assays for resistance t

43 ariation in MTI correlated with the level of pathogen resistance for each genotype.

44 hod that enables discovery and annotation of pathogen resistance gene family members in plant genome

45 As such, this is an example of a pathogen resistance gene that has evolved to underlie tw

46 Pathogen resistance genes represent some of the most abu

47 basis for developing drive systems to spread pathogen resistance genes through vector mosquito popula

48 re being a ten times higher mutation rate in pathogen resistance genes, expected to be under positive

49 oxifying genes, stress resistance genes, and pathogen resistance genes.

50 gh PR1 and PDF1.2 but probably through other pathogen-resistance genes or pathways as well.

51 y within plant genes that function to detect pathogens (resistance genes) counteracts changing struct

52 very limited number of molecular markers for pathogen resistance have been validated in conifer speci

53 rk implicated insulin signaling in mediating pathogen resistance in a manner dependent on the transcr

54 We anticipate that the study of pathogen resistance in C. elegans will continue to provi

55 on of diverse stress signals contributing to pathogen resistance in C. elegans.

56 nsulin-like pathway modulates both aging and pathogen resistance in Caenorhabditis elegans.

57 egun to define the molecular determinants of pathogen resistance in Caenorhabditis elegans.

58 Moreover, enhanced pathogen resistance in crowded locusts is associated wit

59 intracellular bacterial pathogen and mediate pathogen resistance in long-lived mutant nematodes.

60 AtJAZ genes and measured stomata opening and pathogen resistance in loss- and gain-of-function mutant

61 eins include key regulators of apoptosis and pathogen resistance in mammals and plants.

62 putatively adaptive variants associated with pathogen resistance in modern Europeans were already pre

63 -LRR/LRR immune receptor gene regulation and pathogen resistance in Solanaceae.

64 ated signal transduction pathway and confers pathogen resistance in the absence of ribosome binding,

65 ation in cuticular colour has been linked to pathogen resistance in this species and in several other

66 genes that could be manipulated to engineer pathogen resistance in vector populations.

67 ungicides results in a synergistic effect on pathogen resistance in wild-type plants and an additive

68 These mechanisms of pathogen resistance, in turn, affect the microbiota comp

69 nal transduction components are required for pathogen resistance, including a Toll/IL-1 receptor doma

70 Pathogen resistance is an ecologically important phenoty

71 Plant pathogen resistance is mediated by a large repertoire of

72 The mechanism of pathogen resistance is proposed to involve sequestration

73 CRK13-conferred pathogen resistance is salicylic acid-dependent.

74 We show that the mechanism of NPR-1-mediated pathogen resistance is through oxygen-dependent behavior

75 is similar to molecules involved in natural pathogen resistance mechanisms in plants and mammals.

76 ments these resistance defects and increases pathogen resistance of wild-type plants.

77 al antibodies, to engineer antibody-mediated pathogen resistance or to alter the plant phenotype by i

78 These include signaling molecules for the pathogen resistance pathway and enzymes required for cel

79 e kinase (MAPKKK) homologs of human MEKK1 in pathogen-resistance pathways.

80 pression after elf18 treatment and display a pathogen resistance phenotype.

81 s of innate and adaptive immunity, including pathogen resistance, production of type I interferon, an

82 Pathogen resistance (R) genes of the NBS-LRR class (for

83 signal in planta during either the wound or pathogen resistance response.

84 eport on the effect of FC on a gene-for-gene pathogen-resistance response and show that FC applicatio

85 APK regulation of plant development and / or pathogen resistance responses.

86 Major early regulators of pathogen-resistance responses, including EDS1, PAD4, RAR

87 the identification of two genes required for pathogen resistance: sek-1, which encodes a mitogen-acti

88 al processes, including growth architecture, pathogen resistance, stomata-mediated leaf-air gas excha

89 er integrity, with a variety of functions in pathogen resistance such as mucus layer modifications an

90 lated with the characteristic development of pathogen resistance that occurs in fruits during ripenin

91 Because HLA polymorphism is crucial for pathogen resistance, this may manifest as a frequency-de

92 pathogen suppression of PTI and reestablish pathogen resistance through effector-triggered immunity

93 , a homolog of mammalian MKP7, also regulate pathogen resistance through the modulation of PMK-1 acti

94 d family transcription factor DAF-16 confers pathogen resistance through the regulation of genes that

95 The increasing threat of pathogen resistance to antibiotics requires the developm

96 ower-middle-income countries, but increasing pathogen resistance to antimicrobials threatens to roll

97 inst a broad spectrum of pathogens, restores pathogen resistance to Atelp2 mutant plants.

98 tore pathogenesis-related gene expression or pathogen resistance to basal levels in the low-18:1-cont

99 logy of distribution systems have found that pathogen resistance to chlorination is affected by micro

100 llenge to human health that is heightened by pathogen resistance to current therapeutic agents.

101 ic side effects, patient non-compliance, and pathogen resistance to existing therapies.

102 increasingly curtailed by the development of pathogen resistance to many key fungicides, the lack of

103 e that provides long-lasting, broad-spectrum pathogen resistance to uninfected systemic leaves follow

104 Across a range of pathogens, resistance to chemotherapy is a growing probl

105 y molecular markers that co-segregate with a pathogen resistance trait of interest.

106 Despite their enhanced pathogen resistance, ttm2 plants did not display constit

107 abidopsis, can trigger immune signalling and pathogen resistance via the flagellin receptor kinase FL

108 Such a behavioral strategy could evolve if pathogen resistance were heritable.

109 ise, we observed that both MTI variation and pathogen resistance were quantitatively inherited.

110 mutants were found to be defective in basal pathogen resistance, whereas induced resistance was unaf

111 1-1) mutant, which shows full restoration of pathogen resistance without the induction of SAR-associa

112 up-regulation of numerous genes involved in pathogen resistance, wounding, and cell wall biogenesis.