ライフサイエンスコーパス: osmotic stress

1 to growth inhibition and hypersensitivity to osmotic stress.

2 he nonequilibrium dynamics of vesicles under osmotic stress.

3 2 dynamics induced by glucose limitation and osmotic stress.

4 onsequence of proteostasis failure on severe osmotic stress.

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

6 heir utility to modulate plant resilience to osmotic stress.

7 r glycerol and trehalose accumulation during osmotic stress.

8 independently of both commensal microbes and osmotic stress.

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

10 were differentially expressed in response to osmotic stress.

11 c intensities of water limitation imposed by osmotic stress.

12 to diverse environmental stressors, such as osmotic stress.

13 ompetent when challenged with severe heat or osmotic stress.

14 gulatory functions in the growth response to osmotic stress.

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

16 rrelates with increased levels of DoGs after osmotic stress.

17 lls under various frequencies of oscillating osmotic stress.

18 efective in the rapid mTORC1 inhibition upon osmotic stress.

19 wed hypersensitivity to both submergence and osmotic stress.

20 stress response to nutrient deprivation and osmotic stress.

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

22 in potato cell cultures gradually exposed to osmotic stress.

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

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

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

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

27 ting that FTT_0924 is required for resisting osmotic stress.

28 ycine betaine, an osmoprotectant used during osmotic stress.

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

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

31 zed by bacteria to cope physiologically with osmotic stress.

32 e specifically phosphorylated in response to osmotic stress.

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

34 to function downstream of the perception of osmotic stress.

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

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

37 he cellular response to constitutive plastid osmotic stress.

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

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

40 PknD substrate Rv0516c was highly induced by osmotic stress.

41 its expression, prominently change following osmotic stress.

42 ccessibility of DAG generated in response to osmotic stress.

43 s/remodelling proteins in DeltaBbGPCR3 after osmotic stress.

44 activating the Hippo pathway in response to osmotic stress.

45 pression and ABA accumulation in response to osmotic stress.

46 tional reprogramming in response to heat and osmotic stress.

47 resistance to abscisic acid and tolerance to osmotic stress.

48 l strength to maintain cell shape and resist osmotic stress.

49 itivity of endotube mutants to oxidative and osmotic stress.

50 cartilage cells under mechanical loading or osmotic stress.

51 en gel decreased with higher levels of hyper-osmotic stress.

52 e valve discharging cytoplasmic solutes upon osmotic stress.

53 or signaling the transcriptional response to osmotic stress.

54 cate and cluster to the pores in response to osmotic stress.

55 e valve discharging cytoplasmic solutes upon osmotic stress.

56 or reprograming the transcriptome to counter osmotic stress.

57 development as part of the plant response to osmotic stress.

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

59 ation with its inhibitory target Wee1 during osmotic stress.

60 rp6 mutant exhibits anomalies in response to osmotic stress.

61 ants expressing AhCSD1 were more tolerant to osmotic stress.

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

63 cell shape and is responsible for resisting osmotic stresses.

64 sponse-dependent growth and development with osmotic stresses.

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

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

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

68 induced the ESR in response to oxidative and osmotic stresses.

69 onditions, but is induced upon starvation or osmotic stresses.

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 that this M3K clade is required for ABA- and osmotic-stress-activation of SnRK2 kinases, enabling rob

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

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

76 osmotic stress and are central components in osmotic stress and abscisic acid (ABA) signaling pathway

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

78 sion mutants showed increased sensitivity to osmotic stress and anoxia, surprisingly we found that th

79 kinase 2s (SnRK2s) are quickly activated by osmotic stress and are central components in osmotic str

80 B2, B3 and B4 RAFs are quickly activated by osmotic stress and are required for phosphorylation and

81 s was detected under nitrogen starvation and osmotic stress and can be inhibited by sulfide.

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

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

84 e mutant plants by reducing water loss under osmotic stress and drought conditions.

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

86 messenger c-di-AMP in cellular adjustment to osmotic stress and the role of osmotic forces in the lif

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

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

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

90 ltaFolvam7 mutant is insensitive to salt and osmotic stresses and hypersensitive to cell wall stresso

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

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

93 expression and splicing of genes involved in osmotic-stress and ABA responses, light signaling, and m

94 ding drought and salinity, trigger a complex osmotic-stress and abscisic acid (ABA) signal transducti

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

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

97 conditions that induce proteotoxic, salt and osmotic stress, and also accumulated several proteasome

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

99 component systems (TCSs), capsule synthesis, osmotic stress, and DNA-damage response, among other cat

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

101 iofilm formation, antibiotic susceptibility, osmotic stress, and outer membrane vesicle (OMV) product

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

103 a mutant to heat shock, nutrient limitation, osmotic stress, and oxidative treatment using cell growt

104 rsenic, were dispensable for the response to osmotic stress, and promoted the nuclear localization of

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

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

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

108 cellular responses to mechanical stimuli and osmotic stresses, and it also guides multiple biological

109 onding to environmental water deficiency and osmotic stresses are essential for the growth, developme

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

111 families of Raf-like kinases (RAFs) in early osmotic stress as well as ABA signaling in Arabidopsis t

112 to activate the Hippo pathway in response to osmotic stress, as measured by LATS and YAP phosphorylat

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

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

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

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

117 wn for its role in mediating the response to osmotic stress, but it is also activated by various mech

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

119 ess mechanisms that permit the perception of osmotic stress by bacterial cells and provide an overvie

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

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

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

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

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

125 Osmotic stress caused by drought, salt or cold decreases

126 During osmotic stress, Cdr1 exited cortical nodes and localized

127 lation of human BRAFV600E.By showing that in osmotic stress conditions hBRAFV600E can rescue the grow

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

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

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

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

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

133 Strawberry crop is very sensitive to osmotic stress conditions.

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

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

136 Although mild osmotic stress deforms caveolae and alters interactions

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

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

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

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

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

142 While hyper-osmotic stress had no major impact on the transporters o

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

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

145 Cytokinin-induced growth inhibition and osmotic stress hypersensitivity were rescued by treatmen

146 ition, the bon mutants are hypersensitive to osmotic stress in growth inhibition.

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

148 diesterase (GAP) that promotes resistance to osmotic stress in M. xanthus.

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

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

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

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

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

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

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

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

157 The pkd2 mutant cells show signs of osmotic stress, including temporary shrinking, paused tu

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

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

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

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

162 Osmotic stress induced hyperphosphorylation of the mitot

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

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

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

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

167 lix docking to the SDD1 promoter, leading to osmotic stress-induced Ca(2+)/CaM-dependent activation (

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

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

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

171 Osmotic stress-induced SG formation and TDP-43 ubiquityl

172 ABA sensitivity and strongly impaired rapid osmotic-stress-induced SnRK2 activation.

173 Osmotic stress induces diverse responses in plants inclu

174 In nematodes, osmotic stress induces massive protein aggregation coupl

175 Mechanistically, osmotic stress induces PI(4,5)P(2) plasma membrane enric

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 ins has been established and evaluated using osmotic stress management in the Gram-positive model bac

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

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

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

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

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

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

197 plasmic vacuolization, possibly resulting in osmotic stress; no accumulation of multiple kinetoplasts

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

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

200 acids for parasite metabolism and preventing osmotic stress of this organelle.

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

202 ment with pharmacological agents that induce osmotic stress on lysosomes.

203 rofluidic model to study the impact of hyper-osmotic stress on the migration, proliferation and ion c

204 Therefore, the effects of hyper-osmotic stress on two transporters, aquaporin 5 (AQP5) a

205 udy provides evidence on the impact of hyper-osmotic stress on various aspects of metastatic cell pro

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

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

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

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

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 and is widely synthesized by bacteria as an osmotic stress protectant.

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

214 phile properties, for example, resistance to osmotic stress, reactive oxygen species, pH, and UV expo

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

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

217 Activation during osmotic stress requires energy sensing by AMPK heterotri

218 critical role of the bacterial cell wall for osmotic stress resistance.

219 with distinct temporal patterns in our yeast osmotic stress response and axolotl limb regeneration ca

220 e as a starting point for future research on osmotic stress response and help develop better strategi

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 We chose the bacterial osmotic stress response model to determine genomic featu

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

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

227 In the osmotic stress response, the signal is sensed upstream a

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

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

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

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

232 ndings indicate that NLR signaling represses osmotic stress responses and that BON proteins suppress

233 eins suppress NLR signaling to enable global osmotic stress responses in plants.

234 found that the defects of the bon mutants in osmotic stress responses were suppressed by mutations in

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

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

237 (BON) proteins are critical for all of these osmotic stress responses.

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

239 (2020) show that cell volume changes upon osmotic stress result in rapid and reversible condensati

240 Osmotic stress resulted in higher concentrations of sucr

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

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

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

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

245 Osmotic stress reveals a higher volume/surface ratio of

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

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

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

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

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

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

252 on of SnRK2 kinases, enabling robust ABA and osmotic stress signal transduction.

253 ents required for SnRK2 activation and early osmotic stress signaling are still unknown.

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 by a rapid, largely unknown, ABA-independent osmotic-stress signalling pathway.

257 Osmotic stress significantly affects density and volume,

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

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

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

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

262 Osmotic stress stimulated an increase in PKA activity an

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

264 Osmotic stress stimuli modulate auxin responses by affec

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

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

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

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

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

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

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

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

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

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

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

278 trihelix transrepressor directly transduces osmotic stress to repress stomatal development to improv

279 of RAFs reveal critical roles of the RAFs in osmotic stress tolerance and ABA responses as well as in

280 4D, and that RPL4 loss-of-function increases osmotic stress tolerance and decreases sensitivity to cy

281 tein synthesis negatively impacts growth and osmotic stress tolerance and explain some of the adverse

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 gnaling, protein synthesis, plant growth and osmotic stress tolerance.

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

286 cell migration and proliferation upon hyper-osmotic stress treatment, with similar responses between

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

288 ression signature that is suggestive of hypo-osmotic stress, using a strategy that enables the observ

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

290 Furthermore, bacterial resistance to osmotic stress was markedly reduced when lon-1 was inact

291 II medium, resistance of the lon-2 mutant to osmotic stress was markedly reduced.

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

293 Transcriptional responses to oxidative and osmotic stresses were assessed using microarray and reve

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

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

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

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 ion in turgor buffering, the amelioration of osmotic stress, wounding-induced sieve tube occlusion, a