ライフサイエンスコーパス: pathogen resistance

1 spleen index, hematocrit, bacterial load and pathogen resistance).

2 nificant fitness costs often associated with pathogen resistance.

3 g roles in development, stress tolerance and pathogen resistance.

4 wild mice under selection for fecundity and pathogen resistance.

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

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

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

8 sensitive reactions involving cell death and pathogen resistance.

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

10 d peroxidation, response to heat stress, and pathogen resistance.

11 me, we identify candidate genes for pest and pathogen resistance.

12 as the hypersensitive response for microbial pathogen resistance.

13 ugh evidence shows that they may also confer pathogen resistance.

14 taneous improvement of crop productivity and pathogen resistance.

15 t regimens are hindered by host toxicity and pathogen resistance.

16 bee microbiome whose composition can affect pathogen resistance.

17 ing of sugar beet in the pursuit of improved pathogen resistance.

18 ical pro-inflammatory molecule necessary for pathogen resistance.

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

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

21 way shuts down SA biosynthesis and abrogates pathogen resistance.

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

23 phenotypes such as conditional sterility or pathogen resistance.

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

25 lists and specialists for different modes of pathogen resistance.

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

27 and neurological function, development, and pathogen resistance.

28 esponse, thereby avoiding the development of pathogen resistance.

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

30 nterfere with the host signaling involved in pathogen resistance.

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

32 ow compromised by an increasing incidence of pathogen resistance.

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

34 se (IPR), which is associated with increased pathogen resistance.

35 eeders in a colony has been shown to improve pathogen resistance.

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

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

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

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

40 of a correlation between the degree of plant pathogen resistance and grain nutritional content loss i

41 nt Ca(2+) accumulation in host cells, and to pathogen resistance and host cell death.

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

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

44 ry nervous system has been shown to regulate pathogen resistance and peripheral metabolic activity.

45 Pathogen resistance and safety concerns limit oral antib

46 might be further used as markers to improve pathogen resistance and storage properties.

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

48 fections elicit immune adaptations to enable pathogen resistance and/or tolerance and are associated

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

50 for studying fruit nutrient/quality traits, pathogen resistance, and environmental stress tolerance.

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

52 a(2+) influx, transcriptional reprogramming, pathogen resistance, and host cell death.

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

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

55 e pathways are engaged to mediate longevity, pathogen resistance, and xenobiotic detoxification in os

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

57 crop production; hence, plant genes encoding pathogen resistance are important tools for combating di

58 volved in the CO(2) -dependent regulation of pathogen resistance are largely unknown.

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

60 Genes involved in pathogen resistance are strongly enriched among these ca

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

62 ty that are essential for EDS1-PAD4-mediated pathogen resistance, but are dispensable for the PAD4-me

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

64 that SunTag-SDG2 can be employed to increase pathogen resistance by targeting the H3K4me3-dependent d

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

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

67 Pathogen resistance conferred by plant R genes of the nu

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

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

70 such as carbon sequestration, decomposition, pathogen resistance, etc., but quantitatively predicting

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

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

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

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

75 Pathogen resistance genes represent some of the most abu

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

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

78 The study of pathogen resistance genes, largely aided by mouse models

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

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

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

82 ctions in humans, but as with many bacterial pathogens, resistance has rendered a number of commonly

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

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

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

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

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

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

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

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

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

92 ecialized metabolites play a central role in pathogen resistance in maize (Zea mays) and other plants

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

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

95 sed to engineer SWEET mutants which modulate pathogen resistance in plants and its applications in th

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

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

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

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

100 that occurs autonomously, and which enhances pathogen resistance in vivo in A. thaliana, wild tomato

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

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

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

104 m ER stress and increased both longevity and pathogen resistance independent of canonical UPR(ER) act

105 Pathogen resistance is an ecologically important phenoty

106 The relative importance of pathogen resistance is higher in the tropics and that of

107 g to the present view on infectious diseases pathogen resistance is linked to human leukocyte antigen

108 Plant pathogen resistance is mediated by a large repertoire of

109 The mechanism of pathogen resistance is proposed to involve sequestration

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

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

112 ng histories and loci that may contribute to pathogen resistance, laying the groundwork for future ge

113 We observe an enrichment of pathogen resistance loci in selective sweeps associated

114 However, the degree to which pathogen resistance loci vary in effect across space and

115 , mechanisms of genome structural evolution, pathogen resistance, low-temperature tolerance, fertilit

116 ts to native plant ecology and suggests that pathogen resistance may be an important dimension of AMF

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

118 ly reduce treatment duration but also escape pathogen resistance mechanisms.

119 has become instrumental in uncovering novel pathogen resistance mechanisms.

120 ngly automated platforms to quickly identify pathogens, resistance mechanisms, and therapy options wi

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

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

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

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

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

126 Moreover, novel-pathogen resistance presented a much simpler genetic bas

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

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

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

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

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

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

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

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

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

136 ath glial hsf-1 overexpression also leads to pathogen resistance, suggesting a role for this signalin

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

138 le genetic (co)variance in immune assays and pathogen resistance, these genetic estimates differed ac

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

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

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

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

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

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

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

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

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

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

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

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

151 Therefore, whether AMF confer pathogen resistance to native (wild) plant species, and

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

153 xidation in the vte2 background and restores pathogen resistance to wild-type levels.

154 ve been offset by increases in Gram-negative pathogens' resistance to all empiric first-line antimicr

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

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

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

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

159 Pathogen resistance was independent of ARG acquisition v

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

161 , though no differences in bacterial load or pathogen resistance were noted.

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

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

164 nutrient acquisition, stress resilience, and pathogen resistance while strengthening ecosystem functi

165 ulates exclusively in the cytoplasm improved pathogen resistance without compromising plant growth.

166 1-1) mutant, which shows full restoration of pathogen resistance without the induction of SAR-associa

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