ライフサイエンスコーパス: abiotic stress

1 neity among cell types in the response to an abiotic stress.

2 iculture, and for better managing biotic and abiotic stress.

3 re involved in plant responses to biotic and abiotic stress.

4 response against herbivores, pathogens, and abiotic stress.

5 morphogenesis and defense against biotic and abiotic stress.

6 s implicated in pathogen defense, biotic and abiotic stress.

7 n of the IAA5 and IAA19 genes in response to abiotic stress.

8 , defense against pathogens, and response to abiotic stress.

9 role in the acclimation process of plants to abiotic stress.

10 ne organization and protein structure during abiotic stress.

11 gulating stomatal aperture during biotic and abiotic stress.

12 onditions, demonstrating a role for auxin in abiotic stress.

13 nd oxygen levels, is characteristic for this abiotic stress.

14 longation, seed germination, and response to abiotic stress.

15 in mediating rapid systemic signaling during abiotic stress.

16 lant development and responses to biotic and abiotic stress.

17 has been scarcely studied in the context of abiotic stress.

18 the plants to protect them against biotic or abiotic stress.

19 athways that control responses to biotic and abiotic stress.

20 iable estimates of this trait in response to abiotic stress.

21 integration during the response of plants to abiotic stress.

22 xpression patterns in response to biotic and abiotic stress.

23 ntial for plant survival under conditions of abiotic stress.

24 e response genes in the absence of biotic or abiotic stress.

25 plants as well as in fortifying them against abiotic stress.

26 l benefits for crop resistance to biotic and abiotic stress.

27 play an important role in plant tolerance of abiotic stress.

28 e outer surface of plants against biotic and abiotic stresses.

29 on and elongation, and response to different abiotic stresses.

30 h and reproduction under combined biotic and abiotic stresses.

31 lines were more susceptible to ABA and other abiotic stresses.

32 that can tolerate a wide range of biotic and abiotic stresses.

33 bly confer enhanced tolerance to postharvest abiotic stresses.

34 as previously demonstrated to be involved in abiotic stresses.

35 eration, or for cells to cope with biotic or abiotic stresses.

36 lay important roles in plant development and abiotic stresses.

37 chromatin dynamics induced by cold or other abiotic stresses.

38 differential expression of genes involved in abiotic stresses.

39 ival under flooding stress, as well as other abiotic stresses.

40 eeds, leaves, and roots exposed to different abiotic stresses.

41 ted molecular patterns (MAMPs) or with other abiotic stresses.

42 3 and 8 were majorly regulated in biotic and abiotic stresses.

43 and activates its expression under different abiotic stresses.

44 athway regulates plant responses to multiple abiotic stresses.

45 mone transport or defense against biotic and abiotic stresses.

46 l to engineer plants against both biotic and abiotic stresses.

47 ion in the alleviation of diverse biotic and abiotic stresses.

48 pensates for growth rate reduction caused by abiotic stresses.

49 a protective barrier against many biotic and abiotic stresses.

50 cotiana benthamiana and confers tolerance to abiotic stresses.

51 ion productivity and tolerance of biotic and abiotic stresses.

52 impending challenges from specific biotic or abiotic stresses.

53 fits and protecting hosts against biotic and abiotic stresses.

54 have suggested roles mainly in tolerance to abiotic stresses.

55 proteins perceive and respond to biotic and abiotic stresses.

56 seed coat permeability and susceptibility to abiotic stresses.

57 plays a critical role in plant tolerance to abiotic stresses.

58 responsible for maize molecular response to abiotic stresses.

59 lopmental stages and tolerance of biotic and abiotic stresses.

60 th, development, and responses to biotic and abiotic stresses.

61 ically confronted by simultaneous biotic and abiotic stresses.

62 global interest because of its tolerance to abiotic stresses.

63 nt are continuously challenged by biotic and abiotic stresses.

64 scence, and in plant responses to biotic and abiotic stresses.

65 as increase in tolerance against biotic and abiotic stresses.

66 es whose expression is strongly regulated by abiotic stresses.

67 insights into the functional consequences of abiotic stresses.

68 va is especially vulnerable to pathogens and abiotic stresses.

69 bscisic acid-a plant hormone associated with abiotic stresses.

70 canonical poly(A) site choice in response to abiotic stresses.

71 environmental factors, including biotic and abiotic stresses.

72 nt, hormone response, response to biotic and abiotic stresses.

73 nment and survive a combination of different abiotic stresses.

74 rovide wider protection from combinations of abiotic stresses.

75 signalling cascade in response to biotic and abiotic stresses.

76 thogens and to increase tolerance to various abiotic stresses.

77 imilarly regulated by different hormones and abiotic stresses.

78 lant responses to a wide range of biotic and abiotic stresses.

79 rtant for plant responses to both biotic and abiotic stresses.

80 tegies for obtaining nutrients and resisting abiotic stresses.

81 decreased fitness under combined biotic and abiotic stresses.

82 crop yield has always been impaired through abiotic stresses.

83 r sessile habit and combat biotic as well as abiotic stresses.

84 h reduce oxidative damage during extremes of abiotic stress, a pattern that would be expected to ampl

85 ting new insights into effectors that target abiotic stress adaptation pathways, tampering with key f

86 tained due to a trade-off between biotic and abiotic stress adaptation.

87 uction is challenged by different biotic and abiotic stresses, among which downy mildew (DM) is a sev

88 lated categories of holm oak are enriched in abiotic stress and chromatin assembly.

89 teractions can buffer plant communities from abiotic stress and consumer pressure caused by climatic

90 ones that orchestrates the plant response to abiotic stress and drive changes in transcriptomic, meta

91 al interactions occurring under simultaneous abiotic stress and herbivory.

92 effects on ER morphology of drug treatments, abiotic stress and over-expression of ER tubule-shaping

93 fected splicing efficiency were enriched for abiotic stress and signaling-related functions.

94 Both abiotic stress and species interactions can limit popula

95 ing a putative regulatory connection between abiotic stress and the circadian clock.

96 te, no systematic screening of lncRNAs under abiotic stress and their regulatory roles in cassava has

97 onal cross-talk modulates plant responses to abiotic stresses and defenses against insect herbivores

98 showed unequal contributions in response to abiotic stresses and development, which may aid wheat ad

99 plants from pathogens, promotes tolerance to abiotic stresses and fortifies cells to withstand the fo

100 nut crops worldwide, is highly adaptable to abiotic stresses and is tolerant to drought and salt str

101 in various organs, as well as in response to abiotic stresses and various hormone treatments.

102 sociated with leaf expansion, independent of abiotic stress, and another that is drought induced.

103 abundance was increased significantly during abiotic stress, and characterization of mutant lines rev

104 tes may contribute to mulberry fitness under abiotic stress, and it provides a foundation for the dev

105 intensity of habitat disturbance, degree of abiotic stress, and methods of trait characterization.

106 plants are activated by developmental cues, abiotic stress, and pathogen infection.

107 tudies revealed that in response to a single abiotic stress, applied to a single leaf, plants mount a

108 Abiotic stresses are main limiting factors for agricultu

109 Traditional evaluation of crop biotic and abiotic stresses are time-consuming and labor-intensive

110 espiration or as a consequence of biotic and abiotic stress as well as in the initiation of senescenc

111 exploitation of plant microRNAs induced with abiotic stress, as a tool for bio-enrichment with pharma

112 ply for protection of spores from biotic and abiotic stresses but also for spore structural developme

113 ctively defend themselves against biotic and abiotic stresses by synthesizing diverse secondary metab

114 insects and numerous microbial pathogens and abiotic stresses caused by adverse climatic conditions.

115 Frost stress is one of the major abiotic stresses causing seedling death and yield reduct

116 distinct from nitrogen starvation and other abiotic stresses commonly used to induce oil accumulatio

117 and OsSIZ1-overexpressing plants under every abiotic stress condition tested.

118 s a key phytohormone produced in response to abiotic stress conditions and is an activator of abiotic

119 ed by an ethylene treatment and that several abiotic stress conditions could stimulate cell elongatio

120 ioides) plants were subjected to four common abiotic stress conditions individually: high soil salini

121 that auxin-mediated growth inhibition under abiotic stress conditions is one of the developmental an

122 Improving crop tolerance to abiotic stress conditions requires a deep understanding

123 Each year, abiotic stress conditions such as drought, heat, salinit

124 accretion of reactive oxygen species during abiotic stress conditions.

125 d gene could improve plant performance under abiotic stress conditions.

126 e tested in roots and leaves under different abiotic stress conditions.

127 tyl esters accumulate in higher levels under abiotic stress conditions.

128 es a high proportion of beta-carotene during abiotic stress conditions.

129 will become increasingly compounded by harsh abiotic stress conditions.

130 Drought is the main abiotic stress constraining sugarcane production.

131 rammed cell death in development, biotic and abiotic stresses, damage-induced immune response, and re

132 With increased risk from abiotic stresses due to climate variability, it is imper

133 ed to a combination of two or more different abiotic stresses, each potentially triggering its own st

134 xify ROS, ROS is beneficial to plants during abiotic stress enabling them to adjust their metabolism

135 Rapidly communicating the perception of an abiotic stress event, wounding or pathogen infection, fr

136 s of plants, protecting them from biotic and abiotic stress factors.

137 stem can be manipulated to impose biotic and abiotic stresses for testing how microbial inoculants in

138 th biotic stress from pathogen infection and abiotic stress from drought, is important both for under

139 associated with suppression of ABA-inducible abiotic stress genes.

140 ainst pathogen infections, pest attacks, and abiotic stresses has advanced, the exact mechanism(s) by

141 ealize that the roles of B vitamins in plant abiotic stress have had minimal attention in the literat

142 veness, acclimation, and memory of plants to abiotic stress holds substantive potential for improving

143 ication in the alleviation of the effects of abiotic stresses; however, its role in mitigating Buta t

144 Abiotic stresses impact negatively on plant growth, prof

145 review recent studies on the role of ROS in abiotic stress in plants, and propose that different abi

146 Tolerance of abiotic stress in woody plants is known to be constraine

147 Epmbf1 was induced by a number of abiotic stresses in E. pusillum and transgenic yeast, an

148 characteristics and tolerance to biotic and abiotic stresses in hexaploid wheat can be drastically i

149 f ARFs in conferring tolerance to biotic and abiotic stresses in plant species.

150 th, development, and responses to biotic and abiotic stresses in plants, likely via their interaction

151 ator of defense responses against biotic and abiotic stresses in plants.

152 ptional regulation in mediating responses to abiotic stresses in Sorghum.

153 in fruit development as well as responses to abiotic stresses in strawberry.

154 s of peanut (Arachis hypogaea) to biotic and abiotic stresses include the synthesis of prenylated sti

155 H. mephisto can thrive under conditions of abiotic stress including heat and minimal oxygen, where

156 d these accessions to an array of biotic and abiotic stresses including heat, ER stress-inducing chem

157 umulated transcripts functionally related to abiotic stress, including oxidative stress, as well as i

158 Abiotic stresses, including drought and salinity, trigge

159 st developments in the perception of various abiotic stresses, including drought, salinity, flooding,

160 Because of the focus on abiotic stress-induced elRs in recent decades, biotic st

161 FINGER OF ARABIDOPSIS THALIANA12 (ZAT12), an abiotic stress-induced transcription factor.

162 in addition to tolerance against a range of abiotic stress inducers.

163 notyping pipeline for the genetic studies of abiotic stress iron deficiency chlorosis (IDC) of soybea

164 Its accumulation in ssadh mutants and during abiotic stresses is a response to avoid the SSA induced

165 The protective function of melanin in abiotic stresses is well documented.

166 ENPs) and trace elements (a common source of abiotic stress) is critical to gaining insights into the

167 thought to be required for the tolerance of abiotic stress, is not required for high rates of photos

168 Interestingly, abiotic stresses led to the re-directing of transcriptio

169 chia coli or Saccharomyces cerevisiae for an abiotic stress-low temperature.

170 During abiotic stress, MG levels accumulate to toxic levels in

171 e report for the first time that, similar to abiotic stresses, MG levels increase during biotic stres

172 ated at the transcription level by different abiotic stresses, namely salt and drought stress, until

173 ss five locations worldwide, we tested three abiotic stresses, nitrogen deficiency, drought and salin

174 s include the significant upregulation under abiotic stress of several expanded ICE-L gene families,

175 Perception of biotic and abiotic stresses often leads to stomatal closure in plan

176 ormative system for dissecting the impact of abiotic stress on peroxisome proliferation because it is

177 ws for confirmatory diagnostic of biotic and abiotic stresses on plants.

178 compounds in olive leaves and the effect of abiotic stresses on their synthesis, this study evaluate

179 heir specialized metabolites in responses to abiotic stress or biotic stress factors like pathogens a

180 eta-Glucosidases are known to play a role in abiotic stresses, particularly dehydration through absci

181 search to improve the understanding of plant abiotic stress perception.

182 Despite this abiotic stress, plantlets survived.

183 In response to abiotic stresses, plants produce the hormone abscisic ac

184 tes the expression of XIW1, and both ABA and abiotic stresses promote XIW1 accumulation in the nucleu

185 Manipulation of a single abiotic stress-related gene could improve plant performa

186 While the abiotic stress-related hormone abscisic acid (ABA) is kn

187 loit genetic diversity to improve biotic and abiotic stress resistance and oil production, while also

188 her caused by climate change, enhancement of abiotic stress resistance in crops is increasingly urgen

189 tic stress conditions and is an activator of abiotic stress resistance mechanisms and a regulator dur

190 enhanced nutrition, disease suppression and abiotic stress resistance, and have potential to contrib

191 y adaptive loci related mainly to biotic and abiotic stress resistance.

192 protein structure and function of biotic and abiotic stress-resistance genes, and QTLs could shed lig

193 al processes, yet it has also been linked to abiotic stress response in a less defined manner.

194 unknown link between histone chaperones and abiotic stress response in plants.

195 like kinase (CrRLK1L) and others involved in abiotic stress response.

196 mRNA isoforms is an important feature of the abiotic stress response.

197 volved in the plant defense response and the abiotic stress response.

198 ole in plant flowering, seed development and abiotic stress response.

199 ection, in some cases promoting diversity in abiotic stress response.

200 one abscisic acid and a component of a major abiotic stress-response pathway, to promote disease susc

201 nowledge on how hormonal signaling regulates abiotic stress responses and defenses against insects, a

202 ets, controls the balance between biotic and abiotic stress responses and is a master regulator of pl

203 transcription factors (TFs) are involved in abiotic stress responses and plant development.

204 The biotic and abiotic stress responses are conferred by series of gene

205 we provide genetic evidence that biotic and abiotic stress responses are differentially prioritized

206 lly redundant functions in the regulation of abiotic stress responses but have opposite functions to

207 iated lincRNAs play important roles in plant abiotic stress responses but lincRNAs and TE-lincRNAs mi

208 ors induced, in a similar manner, biotic and abiotic stress responses by the coordinated activation o

209 sidering the dimension of time in studies on abiotic stress responses in Arabidopsis.

210 heir possible roles in mediating hormone and abiotic stress responses in cassava.

211 te pathogen effectors that induce biotic and abiotic stress responses in the plant, as a first step t

212 r, the biological functions of CDK8 in plant abiotic stress responses remain largely unexplored.

213 Furthermore, we show that ERFVIIs enhance abiotic stress responses via physical and genetic intera

214 lants, G-proteins affect multiple biotic and abiotic stress responses, as well as many developmental

215 oxygen species are key players in biotic and abiotic stress responses, but there is no consensus on w

216 in kinase-2s (SnRK2s) are critical for plant abiotic stress responses, including abscisic acid (ABA)

217 eed yield, organ size regulation, biotic and abiotic stress responses, symbiosis, and nitrogen use ef

218 isregulation of genes involved in biotic and abiotic stress responses, the most prominent one being t

219 , catalytic activity, cellular processes and abiotic stress responses.

220 ars to control both cell fate regulators and abiotic stress responses.

221 enriched in proteins involved in biotic and abiotic stress responses.

222 rotenoids, functions in seed germination and abiotic stress responses.

223 is and photosynthesis, and (3) activation of abiotic stress responses.

224 toperiodic control of flowering, growth, and abiotic stress responses.

225 OsHOX24, a member of HD-ZIP I subfamily, in abiotic stress responses.

226 e plays vital roles in plant development and abiotic stress responses; however, little is known about

227 all defense while simultaneously suppressing abiotic stress-responsive genes.

228 the variability in transcriptome response to abiotic stress, RNA sequencing was performed using 14-da

229 lFG3 is well-adapted to different biotic and abiotic stress situations imposed by extreme conditions

230 s in the defense mechanism against different abiotic-stress situations.

231 known to increase plant tolerance to several abiotic stresses, specifically those from dry and salty

232 Furthermore, abiotic stresses such as dark and ultraviolet C irradiat

233 s may require novel approaches to overcoming abiotic stresses such as drought and salinity as well as

234 est attack and exhibit enhanced tolerance to abiotic stresses such as drought, low temperature, or me

235 maintaining fitness in the face of long-term abiotic stresses such as drought.

236 Abiotic stresses such as water deficit, salt, and heat a

237 stress in plants, and propose that different abiotic stresses, such as drought, heat, salinity and hi

238 tal role in plant response and adaptation to abiotic stresses, such as drought, high salinity and low

239 Abiotic stresses, such as high salinity and drought, blu

240 and its uptake by plants is affected by many abiotic stresses, such as salinity, cold, heat, and drou

241 el for the study of higher plant response to abiotic stresses, survive in the desert ecosystem charac

242 Heat stress is a critical abiotic stress that reduces the yield and quality of flo

243 Low temperature is a seasonal abiotic stress that restricts native plant ranges and cr

244 Drought is a major abiotic stress that threatens global food security.

245 Plants are exposed to recurring biotic and abiotic stresses that can, in extreme situations, lead t

246 rt of a larger global response of Sorghum to abiotic stresses that involves the re-direction of trans

247 This is particularly true under abiotic stresses that lead to the accumulation of reacti

248 rly and late phases of the plant response to abiotic stress, the key role of respiratory burst oxidas

249 Plants respond to abiotic stress through a variety of physiological, bioch

250 characterization of CsBGlu12 and its role in abiotic stress through ROS scavenging.

251 Plants need to cope with biotic and abiotic stress through well-coordinated cell-to-cell com

252 We propose that plants sense multiple abiotic stresses through the Cys-Arg/N-end rule pathway

253 bscisic acid (ABA) is induced in response to abiotic stress to mediate plant acclimation to environme

254 ysis reveals a fundamental trade-off between abiotic stress tolerance and competitive ability, whereb

255 acid (ABA) is a plant hormone that mediates abiotic stress tolerance and regulates growth and develo

256 The roles of Tre6P in abiotic stress tolerance and stomatal regulation are als

257 ly discovered agonists for manipulating crop abiotic stress tolerance and water use.

258 c acid (ABA) is a key phytohormone promoting abiotic stress tolerance as well as developmental proces

259 Plants lacking PBS3 exhibited enhanced abiotic stress tolerance at the cost of decreased fitnes

260 st time, show that the BjERD4 is involved in abiotic stress tolerance besides offering new clues abou

261 ifying capabilities, confers dual biotic and abiotic stress tolerance in model plant Nicotiana tabacu

262 A detailed understanding of abiotic stress tolerance in plants is essential to provi

263 erved role of this gene in drought and other abiotic stress tolerance in several plant species.

264 zobacteria (PGPR) have been shown to improve abiotic stress tolerance in several plants.

265 ility of Bacillus velezensis 5113 to mediate abiotic stress tolerance in wheat.

266 One of four genes involved in generalized abiotic stress tolerance increased with ambient N deposi

267 so far the contribution of Ara metabolism to abiotic stress tolerance is still poorly understood.

268 the ERF-VII protein family) by examining the abiotic stress tolerance of an ERF74 overexpression line

269 Our analyses indicate an important abiotic stress tolerance strategy in several eudicots, w

270 2 phosphorylation plays an important role in abiotic stress tolerance that likely serves as a univers

271 evelopment, hormone signaling and biotic and abiotic stress tolerance through coordination of transcr

272 e fungal endophytes often confers biotic and abiotic stress tolerance to their hosts.

273 nding the genetic and physiological basis of abiotic stress tolerance under field conditions is key t

274 ression of AVP1 and OsSIZ1 in Arabidopsis on abiotic stress tolerance were studied.

275 ncing plant growth, nutrient use efficiency, abiotic stress tolerance, and disease resistance-into ag

276 nal network revealed mechanism of biotic and abiotic stress tolerance, energy conservation and photop

277 eness of the role of the phytobiome in plant abiotic stress tolerance, led us to sequence the transcr

278 astid MSH1 depletion results in variegation, abiotic stress tolerance, variable growth rate, and dela

279 f crop traits, including disease resistance, abiotic stress tolerance, yield, nutritional quality and

280 protein arginine methyltransferase vital to abiotic stress tolerance.

281 nctional traits, change within the limits of abiotic stress tolerance.

282 t performance and may also impact biotic and abiotic stress tolerance.

283 N-glycosylation, cell wall biosynthesis, and abiotic stress tolerance.

284 n among plant immunity, leaf microbiota, and abiotic stress tolerance.

285 all major theories about trade-offs between abiotic stress tolerances, providing a unified trade-off

286 es, plant immunity, signaling in response to abiotic stress, transporters, biosynthesis of cells wall

287 Abiotic stress treatments incited changes in poly(A) sit

288 creased expression in response to biotic and abiotic stress treatments suggestive of a role in adapta

289 ts from single cell gene expression and from abiotic stress treatments.

290 Abiotic stress triggers an ABA signal transduction casca

291 The early response to abiotic stress typically involves induction of genes inv

292 h, 24 h, 48 h, 1 week and 4 weeks) after an abiotic stress (US) was imposed on in vitro potato expla

293 would alter their tolerance to a subsequent abiotic stress, we further subjected individuals to heat

294 ific features in transcriptional response to abiotic stress were detected.

295 ilies in B. distachyon, wheat and rice under abiotic stresses were investigated by next-generation se

296 Drought and salinity are the major abiotic stresses which adversely affect the growth and p

297 tantly exposed to a wide range of biotic and abiotic stresses which they must defend themselves again

298 altered levels of expression in response to abiotic stress, which requires concerted action of both

299 promote plant growth and confer tolerance to abiotic stress, which suggests common principles underpi

300 ellular transcriptional response pathways to abiotic stress, while reducing the dimensions in gene-or