ライフサイエンスコーパス: osmotic stress

1 rrelates with increased levels of DoGs after osmotic stress.

2 lls under various frequencies of oscillating osmotic stress.

3 efective in the rapid mTORC1 inhibition upon osmotic stress.

4 wed hypersensitivity to both submergence and osmotic stress.

5 stress response to nutrient deprivation and osmotic stress.

6 hat are essential for the body's response to osmotic stress.

7 ants expressing AhCSD1 were more tolerant to osmotic stress.

8 in potato cell cultures gradually exposed to osmotic stress.

9 l system (HNS), wherein upregulation follows osmotic stress.

10 meric/knob regions of wild-type plants under osmotic stress.

11 ased volume when cells are subjected to hypo-osmotic stress.

12 ng protein required for a proper response to osmotic stress.

13 ting that FTT_0924 is required for resisting osmotic stress.

14 ycine betaine, an osmoprotectant used during osmotic stress.

15 in a pattern normally seen under drought or osmotic stress.

16 se valve that prevents cell lysis from acute osmotic stress.

17 laments in the bundles depend on the applied osmotic stress.

18 zed by bacteria to cope physiologically with osmotic stress.

19 e specifically phosphorylated in response to osmotic stress.

20 the occurrence of cell lysis caused by acute osmotic stress.

21 he nonequilibrium dynamics of vesicles under osmotic stress.

22 to function downstream of the perception of osmotic stress.

23 to that observed in plants under drought or osmotic stress.

24 on regulation and root growth in response to osmotic stress.

25 he cellular response to constitutive plastid osmotic stress.

26 e 3-kinase (PI3K) reduced OSR1 activation by osmotic stress.

27 ty to adjust DNA supercoiling in response to osmotic stress.

28 PknD substrate Rv0516c was highly induced by osmotic stress.

29 e block of lateral root (LR) formation under osmotic stress.

30 its expression, prominently change following osmotic stress.

31 ccessibility of DAG generated in response to osmotic stress.

32 s/remodelling proteins in DeltaBbGPCR3 after osmotic stress.

33 gically normal conditions, in the absence of osmotic stress.

34 n Cbc1 is important for yeast survival under osmotic stress.

35 and these zBves morphants were sensitive to osmotic stress.

36 tion of osmostress-protective proteins under osmotic stress.

37 ed in prokaryotes, stabilizing cells against osmotic stress.

38 d does not require exposure to extracellular osmotic stress.

39 nt transcription is activated in response to osmotic stress.

40 2 dynamics induced by glucose limitation and osmotic stress.

41 thway regulates cell survival in response to osmotic stress.

42 nduced genes in macrophages independently of osmotic stress.

43 ine betaine (GB), which confers tolerance to osmotic stress.

44 onsequence of proteostasis failure on severe osmotic stress.

45 i such as changes in membrane tension during osmotic stress.

46 ensis SurE exhibited increased resistance to osmotic stress.

47 wild type in culture media in the absence of osmotic stress.

48 line, and inositol 1,4,5-trisphosphate under osmotic stress.

49 phamide, culture with hydrogen peroxide, and osmotic stress.

50 ation with its inhibitory target Wee1 during osmotic stress.

51 y differential responses of PIN1 and PIN2 to osmotic stress.

52 heir utility to modulate plant resilience to osmotic stress.

53 r glycerol and trehalose accumulation during osmotic stress.

54 independently of both commensal microbes and osmotic stress.

55 sol and flagella in response to salinity and osmotic stress.

56 were differentially expressed in response to osmotic stress.

57 c intensities of water limitation imposed by osmotic stress.

58 to diverse environmental stressors, such as osmotic stress.

59 ompetent when challenged with severe heat or osmotic stress.

60 rp6 mutant exhibits anomalies in response to osmotic stress.

61 gulatory functions in the growth response to osmotic stress.

62 moss relies on other pathways to respond to osmotic stress.

63 (MAPK) network to retrigger with sequential osmotic stresses.

64 cell shape and is responsible for resisting osmotic stresses.

65 nd to hydrogen peroxide, but not to salt and osmotic stresses.

66 rane-permeating peptides, and mechanical and osmotic stresses.

67 sponse-dependent growth and development with osmotic stresses.

68 sitivity to cell wall-damaging agents and to osmotic stresses.

69 transcription of osmU is induced 23-fold by osmotic stress (0.3 M NaCl).

70 and promote cross talk with a branch of the osmotic stress/ABA signaling pathway.

71 Interestingly, various osmotic stress/abscisic acid (ABA)-inducible genes were

72 a and Alternaria brassisicola Both PAMPs and osmotic stress activate some of the same MPKs in Arabido

73 Analysis of tobacco (Nicotiana tabacum) Osmotic Stress-Activated Protein Kinase activity in toba

74 SnRK2.4 is the closest homolog of tobacco Osmotic Stress-Activated Protein Kinase in Arabidopsis (

75 ver, CurT deficiency enhances sensitivity to osmotic stress, adding a level of complexity to CurT fun

76 E2sca operon transcription was induced under osmotic stress, along with the ClpP proteinase genes.

77 iana), At5g59220, is a negative regulator of osmotic stress and ABA signaling and that this function

78 bition prevents cell swelling in response to osmotic stress and ameliorates post-ischemic brain swell

79 d SakA::GFP translocated to the nucleus upon osmotic stress and cell wall damage, with SakA::GFP show

80 ost bacteria rely on their cell wall to bear osmotic stress and determine cell shape.

81 e EnvZ/OmpR two-component system responds to osmotic stress and regulates expression of outer membran

82 atory volume decrease capability during hypo-osmotic stress and this ability is impaired in TgVP1 nul

83 The schA was transcriptionally regulated by osmotic stress and this response was dependent on SakA a

84 the stk deletion mutant is more sensitive to osmotic stress and to penicillin than the wild type.

85 response and causes hypersensitivity to salt/osmotic stress and to the glycosylation inhibitor tunica

86 ironmental challenges including salt stress, osmotic stress and water deficit.

87 had higher germination rates under salt and osmotic stresses and in the presence of ethylene substra

88 Moreover, our osmotic stressing and D2O-H2O exchange experiments demon

89 del system, mammalian cells under reversible osmotic stress, and a recently introduced Forster resona

90 utant lines exhibit sensitivity to salinity, osmotic stress, and abscisic acid treatment at the seedl

91 channel kinetics, differences in response to osmotic stress, and altered membrane protein trafficking

92 responds similarly to glucose limitation and osmotic stress, and its pulsatile translocation is large

93 using nuclear RNA-Seq, comparing heat shock, osmotic stress, and oxidative stress in NIH 3T3 mouse fi

94 ttl4 mutants show reduced root growth under osmotic stress, and the analysis of double and triple mu

95 physiological and developmental responses to osmotic stress, and those with clear combined phenotypes

96 a sko1Delta/Delta mutant strain subjected to osmotic stress, and we utilized gene sequence enrichment

97 The main response is related to osmotic stress, and we were also able to detect novel re

98 conferred tolerance to anoxia, oxidative and osmotic stresses, and enhanced the sensitivity to abscis

99 nonlamellar-forming lipids, detergents, and osmotic stress are all explained by the FSM.

100 al rat kidney (NRK) epithelial cell layer to osmotic stress are studied by both conventional and long

101 These results identify osmotic stress as a potent protein aggregation stimuli i

102 rom its previously characterized response to osmotic stress, as the two conditions cause different tr

103 Osmotic stress associated with drought or salinity is a

104 amy3 bam1 plants close their stomata under osmotic stress at similar rates as the wild type but fai

105 We postulate that ApoL1 initiates osmotic stress at the plasma membrane, which sensitizes

106 We observed mitochondrial fission during osmotic stress, but blocking fission did not affect AMPK

107 -independent stress responses increase under osmotic stress, but cytokinin responses are only slightl

108 ans and mammalian cell culture, we show that osmotic stress, but not other proteotoxic stressors, ind

109 However, it introduces the detrimental osmotic stress by adding and removing high contents of c

110 in the open channel state in the absence of osmotic stress by binding to its C-terminal cytoplasmic

111 cells have effective mechanisms to cope with osmotic stress by engaging various adaptation responses.

112 cotransporters, is activated in response to osmotic stress by WNK family members, and is largely ass

113 conditions, whereas application of transient osmotic stress can trigger activation of Ca(2+) sparks t

114 , such as temperature, oxidative stress, and osmotic stress, can also damage proteins, it is not know

115 Here, we show that osmotic stress caused by decreasing the osmolarity in ha

116 a well-documented physiological response to osmotic stress caused by drought or salinity.

117 Osmotic stress caused by drought, salt or cold decreases

118 During osmotic stress, Cdr1 exited cortical nodes and localized

119 exhibited a defect in volume recovery under osmotic stress conditions in vitro, underscoring the rel

120 reveals that ABA regulates root growth under osmotic stress conditions via an interacting hormonal ne

121 ackground during growth under non-stress and osmotic stress conditions, but upregulated under oxidati

122 es, in the cytosol, and in the nucleus under osmotic stress conditions.

123 proXWV, which enhances growth recovery under osmotic stress conditions.

124 Structurally, we find that mild osmotic stress corresponding roughly to a pressure of 3.

125 Using osmotic stress coupled with x-ray scattering, we have in

126 m as well as genes involved in oxidative and osmotic stress, defense responses, anaerobic respiration

127 Although mild osmotic stress deforms caveolae and alters interactions

128 tly reduced; inhibition of root growth under osmotic stress does not require ethylene signalling, but

129 the vector, is subjected to nutritional and osmotic stresses during its development.

130 is workflow we demonstrated that heat shock, osmotic stress, endoplasmic reticulum stress, oxidative

131 onstrated the induction of genes involved in osmotic stress, energy production and conversion, membra

132 Accordingly, dehydration induced by osmotic stress enhanced the interaction of the congeners

133 Multiple rounds of osmotic stress followed by recovery of cells in normal m

134 l TAK1 activation upon stimulation with IL-1/osmotic stress, for downstream activation of nuclear fac

135 In response to osmotic stress, global translation is inhibited, but the

136 In the absence of osmotic stress, group 1 ACQOS contributes to bacterial r

137 tecting cells from death in response to hypo-osmotic stress, heat shock, and other stimuli.

138 Unlike ALG, PEG resists osmotic stress, hence we generated hybrid microcapsules

139 ding reactive oxygen species, cytokines, and osmotic stress; however, a molecular understanding of ho

140 ve mRNAs are transcriptionally induced after osmotic stress in cbc1Delta cells, but their rapid assoc

141 result from transcriptional readthrough upon osmotic stress in human cells.

142 We show that osmotic stress in N. crassa induced the phosphorylation

143 dity and NaCl in guard cells and to NaCl and osmotic stress in roots and ABA transport from the hypoc

144 lt in significant susceptibility to elevated osmotic stress in the bacterial pathogen Listeria monocy

145 ted glucose concentrations and the resultant osmotic stress in the developing embryo and fetus.

146 multiple environmental conditions including osmotic stress in the fission yeast Schizosaccharomyces

147 This excess glutamine leads to osmotic stress in these cells.

148 e determination and cellular integrity under osmotic stress in virtually all bacteria.

149 an abnormal blood-brain barrier response to osmotic stress in vivo.

150 RC2-Gad8 also occurs in response to ionic or osmotic stress, in a manner dependent on the cAMP/PKA an

151 everal hallmarks of drought or environmental osmotic stress, including solute accumulation, elevated

152 btain a global view of molecular response to osmotic stresses, including the non-coding portion of ge

153 upon exposure to lysozyme treatment and hypo-osmotic stress, indicating a contribution of the S-layer

154 Osmotic stress induced a robust increase in tyrosine pho

155 By contrast, hypo-osmotic stress induced a series of repetitive Ca(2+) ele

156 a population of cells that were resistant to osmotic stress induced apoptosis.

157 Our result suggests that reducing osmotic stress induced by vitrification could improve th

158 Osmotic stress induced hyperphosphorylation of the mitot

159 eas hyper-ionic, -reductive, -oxidative, or -osmotic stress induced much less.

160 Using fluorescent biosensors, we found that osmotic stress induced the formation of PI(4,5)P2 cluste

161 Osmotic stress induced the release of IL-33 from explant

162 ynchronous Ca(2+) oscillation contributes to osmotic stress-induced Ca(2+) increase in seedlings.

163 ity and attenuate endoplasmic reticulum- and osmotic stress-induced cell death.

164 son of the results and discrimination of the osmotic stress-induced effects in different parts of the

165 [Ca(2+)](i) mediate osmotic stress-induced JNK activation and subsequent c-S

166 lular calcium concentration ([Ca(2+)](i)) in osmotic stress-induced JNK activation and tight junction

167 Osmotic stress-induced JNK2 activation was abolished by

168 en demonstrated in the pheromone-induced and osmotic stress-induced MAPK pathways in yeast and in the

169 Osmotic stress-induced polyQ aggregates could be disting

170 acellular Ca(2+) depletion partially reduced osmotic stress-induced rise in [Ca(2+)](i), whereas thap

171 reduced IAA levels and did not display high osmotic stress-induced root architecture changes.

172 [Ca(2+)](i) play a role in the mechanism of osmotic stress-induced tight junction disruption in an i

173 Osmotic stress-induced tight junction disruption was att

174 ted release of ER Ca(2+) also contributes to osmotic stress-induced tight junction disruption.

175 Osmotic stress induces changes in gibberellin metabolism

176 In nematodes, osmotic stress induces massive protein aggregation coupl

177 Our results show that osmotic stress induces transient energy stress, and AMPK

178 at sites of polarized growth during intense osmotic stress; inhibition of calcineurin-activated gene

179 ntial vanilloid 4 (TRPV4) channel translates osmotic stress into ion flux.

180 The response of lipid bilayers to osmotic stress is an important part of cellular function

181 Our results reveal that osmotic stress is associated with the induction of devel

182 irement for Ca(2+) signalling in response to osmotic stress is conserved between land plants and gree

183 Cellular response to osmotic stress is critical for survival and involves vol

184 s unclear whether this local MPS response to osmotic stress is important to systemic blood pressure c

185 Kernel abortion resulting from osmotic stress is not from a lack of carbohydrate reserv

186 Ssp2-pT189 during osmotic stress is transient and leads to transient regul

187 Activated under conditions of high osmotic stress, it interacts with other HOG pathway prot

188 GlcNAcylation of TAB1 is induced by IL-1 and osmotic stress, known inducers of the TAK1 signalling ca

189 Osmotic stress, known to increase PI3,5P2 levels, did no

190 activation tuned activation of MEKK1 during osmotic stress, leading to junction dissociation and cel

191 res energy sensing by AMPK heterotrimer, and osmotic stress leads to decreased intracellular ATP leve

192 The mutant suffered from oxidative and osmotic stress, macronutrient limitation, and an energy

193 t not CA3 neurons following ischemia reveals osmotic stress may be a key factor in delayed neurodegen

194 Osmotic stress measurements were performed with proteoli

195 terstrand repulsion free energy derived from osmotic stress measurements, which constitutes the major

196 ise-induced adaptation, caloric restriction, osmotic stress, mechanical stress, immune response, and

197 ere, we have defined the genomic response to osmotic stress mediated by transcription factor Sko1.

198 Using small-angle x-ray scattering and osmotic stress methods, we investigated the structure of

199 he miR167a complementary site and under high osmotic stress miR167a levels decreased, whereas IAR3 mR

200 in can rescue root growth and meristem size; osmotic stress modulates auxin transporter levels and lo

201 responses of Msn2 to glucose limitation and osmotic stress observed in vivo and found that a positiv

202 In contrast, abscisic acid treatment or osmotic stress of P. patens does not activate MPK4a or a

203 We examine the effect of osmotic stress on abscisic acid (ABA), cytokinin and eth

204 Previously, we studied the effects of osmotic stress on dividing leaf cells in Arabidopsis (Ar

205 atB gene was strongly induced in response to osmotic stress or desiccation.

206 suppressed by conditions that reduce plastid osmotic stress or inhibition of ABA biosynthesis.

207 involved in stress response (e.g., to salt, osmotic stress or water deprivation) were the most relat

208 cation of Glc, Fru, or Suc, as well as cold, osmotic stress, or low nitrogen, provoke the down-regula

209 om in planta cells and from cells exposed to osmotic stress, oxidative stress, and iron and nitrogen

210 water deficit, dehydration, salt, and other osmotic stresses point towards direct and indirect molec

211 To protect the body from osmotic stress, posterior pituitary-projecting, vasopres

212 o co-localized with PI(4,5)P2 clusters under osmotic stress, providing a molecular link between these

213 Osmotic stress rapidly induced c-Src activation, which w

214 ral sediments altered the crab's response to osmotic stress regardless of plastic concentration added

215 erm-free zebrafish embryo model to show that osmotic stress regulates the activation of immunity and

216 Activation during osmotic stress requires energy sensing by AMPK heterotri

217 However, osmotic stress resistance mutants, which genetically act

218 wn on NaCl or mannitol, suggesting a role in osmotic stress resistance.

219 The osmotic stress resistant cells developed a RVI response,

220 Interestingly, these osmotic stress resistant cells showed no increase in ant

221 entral energy metabolism that influences the osmotic stress response and stomatal closure.

222 quired for transcriptional activation of the osmotic stress response genes betIBA-proXWV.

223 al role in transcriptional regulation of the osmotic stress response in bacteria.

224 e first time, that CaTLP1 may be involved in osmotic stress response in plants.

225 We applied our method to extend pathways in osmotic stress response in yeast and identified several

226 verify several of these predictions for the osmotic stress response network.

227 e models of transcriptional dynamics for the osmotic stress response pathway in Saccharomyces cerevis

228 ance mutants, which genetically activate the osmotic stress response, strongly inhibited the formatio

229 ight into cellular processes involved in the osmotic stress response.

230 n medium with salt, urea failed to stimulate osmotic stress response.

231 the dynamic protein-DNA interactions during osmotic stress response.

232 ther, our real time-qPCR results showed that osmotic stress-response genes that are dependent on the

233 nrichment mapping to identify Sko1-dependent osmotic stress-response genes.

234 functional redundancy, their contribution to osmotic stress responses remained unclear.

235 es a role for PIAL1 and 2 in salt stress and osmotic stress responses, whereas under standard conditi

236 r (AtWRKY15) modulates plant growth and salt/osmotic stress responses.

237 ates the DNA synthesis, independently of the osmotic stress responses.

238 so activates the expression of a plethora of osmotic stress-responsive genes, including the well-know

239 Osmotic stress resulted in higher concentrations of sucr

240 Activation of betaine catabolism at high osmotic stress resulted, in part, from induction of gbdR

241 show that the origin of this process is the osmotic stress resulting from the presence of salt impur

242 This loss in Galphaq/Cav1 association due to osmotic stress results in a significant reduction of Gal

243 Cell swelling induced by hypo-osmotic stress results in activation of volume-regulated

244 Osmotic stress reveals a higher volume/surface ratio of

245 ng pathway and that subjecting cells to hypo-osmotic stress reverses this enhancement.

246 . thaliana resulted in improved tolerance to osmotic stress, salinity and drought stress in addition

247 genetic screens for altered sensitivities to osmotic stress seem to function downstream of the percep

248 tes to plant defense to bacterial pathogens, osmotic stress sensitivity, and cellular responses and t

249 he buried water molecules by imposing a high osmotic stress should accelerate the rate of recovery, w

250 y3 bam1 double mutants are hypersensitive to osmotic stress, showing impaired root growth.

251 ritical functions of the SnRK2s in mediating osmotic stress signaling and tolerance.

252 gent and conserved aspects of Sko1-dependent osmotic stress signaling.

253 suggesting that the kinases are involved in osmotic stress signaling.

254 Environmental water deficiency triggers an osmotic stress signalling cascade, which induces short-t

255 abolic responses that differ from short-term osmotic stress signalling.

256 Osmotic stress significantly affects density and volume,

257 uction in cellular volume, induced by severe osmotic stress, slows down the dynamics of several signa

258 sordered (Ld) domains, we performed detailed osmotic stress small-angle x-ray scattering experiments

259 cooperation of MVA and MEP reprogrammed upon osmotic stress (sorbitol treatment) in Arabidopsis (Arab

260 During osmotic stress, starch is degraded in the light by stres

261 Osmotic stress stimulated an increase in PKA activity an

262 Here, we discovered that osmotic stress stimulates a signaling network in Mycobac

263 Osmotic stress stimuli modulate auxin responses by affec

264 CD4c was up-regulated by wounding, heat, and osmotic stress, suggesting an involvement of its apocaro

265 ein kinase 2 (SnRK2) family are activated by osmotic stress, suggesting that the kinases are involved

266 mline- and DAF-9/DAF-12-dependent shrinking, osmotic stress susceptibility, and subsequent life-span

267 The intense osmotic stress sustained by brain cells is believed to b

268 Prolonged endoplasmic reticulum and osmotic stress synergistically activate the stress-induc

269 nd ornithine peptides are measured using the osmotic stress technique coupled with X-ray scattering.

270 itu, we measured the hydration parameters by osmotic stress techniques and modeled them as linear fun

271 chA DeltampkC mutants were more sensitive to osmotic stress than the corresponding parental strains.

272 vely growing leaves after sudden exposure to osmotic stress that mimics mild drought.

273 Under osmotic stress, the filaments formed two-dimensional hex

274 During osmotic stress, the internal pH is above the threshold,

275 lta mutants, translation drops sharply under osmotic stress, the subsequent reinitiation of translati

276 Thr(101) position in mediating adaptation to osmotic stress, thereby verifying biological relevance o

277 When subjected to a hypo-osmotic stress, these cells show faster volume recovery

278 DoGs are inducible by osmotic stress through an IP3 receptor signaling-depende

279 Rv0516c, and SigF that enables adaptation to osmotic stress through cell wall remodeling and virulenc

280 he activity of BAM1 and AMY3 in leaves under osmotic stress through the AREB/ABF-SnRK2 kinase-signali

281 liana mutant exhibiting constitutive plastid osmotic stress to investigate the molecular and genetic

282 revealed unique protein families involved in osmotic stress tolerance and saccharide metabolism that

283 ts a novel strategy to significantly improve osmotic stress tolerance of E. coli.

284 nd the founder member, TTL1, is required for osmotic stress tolerance.

285 -inducible gene expression and freezing- and osmotic-stress tolerance.

286 acteria maintain an acidic cytoplasm and the osmotic stress transcription factor OmpR is required for

287 temperatures, freeze tolerance, dehydration, osmotic stress, ultraviolet radiation and other forms of

288 Osmotic stress was applied to maize (Zea mays) B73 by ir

289 Tight junction disruption by osmotic stress was blocked by tyrosine kinase inhibitors

290 diffraction experiments in combination with osmotic stress we found, in agreement with previous stud

291 Airway epithelial responses to wounding and osmotic stress were assessed in primary airway epithelia

292 ransport sites that helps overcome issues of osmotic stress when attempting to provide enough materia

293 High affinity binding is destabilized by osmotic stress, whereas low affinity binding is insensit

294 re frequently linked to shifts in soil pH or osmotic stress, which can independently affect microbial

295 mponents out of the OS may protect rods from osmotic stress, which could be especially harmful in dis

296 utants exhibit increased cell survival after osmotic stress, while coordinate overexpression of lovK

297 tion lines are dwarfed and hypersensitive to osmotic stress, while the growth of erf5erf6 loss-of-fun

298 ular and genetic pathways connecting plastid osmotic stress with cell differentiation at the shoot ap

299 apid off/on switch in response to increasing osmotic stress, with almost constant expression rates an

300 stem for the study of organellar response to osmotic stress within the context of the cell.