ライフサイエンスコーパス: unstressed

1 xposure to novelty stress and the other left unstressed.

2 -independent, disappearing when the joint is unstressed.

3 The enhanced ubiquitin conjugation in unstressed A-T cells and attenuated ability of these cel

4 ummary, moderate activation of IKK2-NF-kB in unstressed adult mouse hepatocytes produces a cytoprotec

5 Unstressed adult Pitx2 homozygous mutant mice display va

6 t food deprivation, awake, unrestrained, and unstressed; all ICV infusion of L-NMMA or D-NMMA (contro

7 Transcripts of altered abundance in RNA from unstressed and 500 mm salt-shocked Mesembryanthemum crys

8 nd to bind the stress-gene promoters in both unstressed and heat-shocked cells but more strongly in t

9 fying DNA-binding proteins in the cytosol of unstressed and heat-shocked cells.

10 ardiography in mice under 1 of 2 conditions: unstressed and lightly anesthetized or restrained and aw

11 dentification of carbonylation sites on both unstressed and oxidized antibody bulk drug substances.

12 ESTs) expressed in leaves of ice plant under unstressed and salinity stressed conditions.

13 w (0.02-0.05 mumol g-1 fresh weight) in both unstressed and salinized conditions.

14 ase (PME) activity in roots and leaves under unstressed and salt stressed conditions.

15 te numbers in sections of inflamed skin from unstressed and stressed animals shows that stress induce

16 relevant analysis of the kidney in SCD under unstressed and stressed conditions.

17 ed by individual microRNAs will vary between unstressed and stressed conditions.

18 x fast removal and low compensation point in unstressed and stressed conditions.

19 ignaling pathways modulate GSH metabolism in unstressed and stressed cortical neurons.

20 e in an isoform-specific manner, both in the unstressed and stressed heart.

21 stem is related to the role of mTORC1 in the unstressed and stressed heart.

22 ombe under conditions of exponential growth (unstressed) and nitrogen starvation (nutritional stress)

23 libraries were constructed (Al stressed and unstressed), and a total of 1,194 and 774 ESTs were gene

24 ) autoreceptor expression reduced anxiety in unstressed animals but increased anxiety following inesc

25 X and induced increased expression of OPG in unstressed animals with PD.

26 hrelin can regulate negative emotionality in unstressed animals without altering appetite.

27 urobiological signals used to encode fear in unstressed animals, but rather by engaging distinct mech

28 In addition, in both stressed and unstressed animals, DOR activation decreases GABA(A)R cu

29 re sufficient to lower PPG mRNA in otherwise unstressed animals.

30 n performance (RI=58.2+/-4.1%) compared with unstressed animals.

31 xiety- and depression-like behaviors even in unstressed animals.

32 onstrated robust LTP comparable with that of unstressed animals.

33 effect on hedonic or open-field behavior in unstressed animals.

34 PT reduced alveolar bone loss in unstressed animals.

35 y enzyme limiting tocopherol biosynthesis in unstressed Arabidopsis leaves.

36 Brachial artery area, unstressed area, compliance, stress, strain, incremental

37 Unstressed beta1KOmdx mice were viable and had normal ca

38 These results indicate that unstressed binding affinity is not the only molecular pr

39 phrine (p = .001), suggesting an increase in unstressed blood volume at the lowest dose of norepineph

40 spectroscopy to probe the tensile strength, unstressed bond lifetime, and interaction energy between

41 When unstressed, both control and norleucine-substituted cell

42 t level of hsp110, with expression levels in unstressed brain being similar to the levels seen in hea

43 ulations were verified to be both viable and unstressed by evaluation of the transcriptional expressi

44 dc1, tdc2 expression was not detected in any unstressed Camptotheca tissues nor in developing seedlin

45 e the hypothalamic pituitary adrenal axis in unstressed CD-1 mice or have the abortive effects observ

46 90-containing HSF1 complex is present in the unstressed cell and dissociates during stress.

47 sed the basal level of system output only in unstressed cells and had little effect on the magnitude

48 to form complex with chaperon 14-3-3zeta in unstressed cells and mutation of 14-3-3zeta Ser-58 to As

49 maintenance of low levels of p53 and Mdm2 in unstressed cells and that inhibition of p53 ubiquitinati

50 scription factor Hsf1, which is monomeric in unstressed cells and upon activation trimerizes, and bin

51 ort hairpin (sh) RNAs had no overt effect on unstressed cells but inhibited the maintenance of G2 pha

52 sor pathway genes (p21 and p14ARF) in normal unstressed cells but is dissociated from both promoters

53 Swe1p is degraded during G2 in unstressed cells but is stabilized and accumulates follo

54 l proteins, which only sporadically arise in unstressed cells but strongly accumulate upon defective

55 hown to act as a transcriptional enhancer in unstressed cells by binding the transcription factor, pu

56 nhibitory functions of p53 are controlled in unstressed cells by rapid degradation of the p53 protein

57 that changes in nucleolin protein levels in unstressed cells cause parallel changes in the amount of

58 vacuolar and endosomal limiting membranes in unstressed cells in a manner that depended on its FYVE d

59 HSF1 is present in unstressed cells in an inactive monomeric form and becom

60 Increases in nucleolin levels in unstressed cells led to higher expression of p21(cip1/wa

61 Unstressed cells maintain p53 at low levels through regu

62 osphatase inhibitors to enzyme extracts from unstressed cells mimicked the effect of ER stress on GP

63 Protein aggregates do not accumulate in unstressed cells primarily because of the existence of c

64 The data suggest that unligated p53 in unstressed cells should be predominantly dimeric.

65 rrent understanding of sigmaB regulation, in unstressed cells the phosphorylated RsbV anti-anti-sigma

66 stress can be communicated from stressed to unstressed cells to elicit a remodeling response, and (i

67 The activity of this IRES in unstressed cells was approximately 6% the strength of th

68 omeric yeast frataxin (Yfh1) was detected in unstressed cells when mitochondrial iron uptake was main

69 Growth of SIK1 appears to be unchanged in unstressed cells, but hyphal extension rates are reduced

70 dly inhibits p53 transcriptional activity in unstressed cells, but SET-mediated repression is abolish

71 esults demonstrate that Mrr is a tetramer in unstressed cells, but shifts to a dimer after HP shock o

72 In unstressed cells, CBP/p300, HDM2 and p53 form a ternary

73 However, even in unstressed cells, DNA undergoes a plethora of spontaneou

74 e1p did not affect cell-cycle progression in unstressed cells, even when bud size was decreased by ov

75 al-stress-response activator is expressed in unstressed cells, illustrating a stress-response-control

76 2, and correspondingly p53 downregulation in unstressed cells, is accomplished by a specific isoform

77 In unstressed cells, low levels of eIF2alpha phosphorylatio

78 In unstressed cells, Nrf2 is maintained in the cytoplasm vi

79 In unstressed cells, p53 is maintained at a low level.

80 In unstressed cells, p53 is maintained at low levels and is

81 s substantial changes in mRNA translation in unstressed cells, particularly targeting the secretome.

82 In unstressed cells, the anti-proliferative effects of p53

83 In unstressed cells, the p53 tumor suppressor is highly uns

84 ins (hHR23A and B) regulate p53 stability in unstressed cells, the role of hHR23B in post-genotoxin r

85 In unstressed cells, the tumor suppressor p53 is maintained

86 In unstressed cells, the tumor suppressor protein p53 is pr

87 In unstressed cells, this association leads to increased hp

88 equent polyubiquitylation and degradation in unstressed cells, to a fate of activation via mitochondr

89 ring RNA to down-regulate endogenous MTBP in unstressed cells, we have found that MTBP significantly

90 d residues increased output 4- to 30-fold in unstressed cells, whereas substitutions at four nonconse

91 NA polymerase II (RNAP II) occupancy even in unstressed cells, with higher levels observed on cell cy

92 2-fold after 3 hours of stress compared with unstressed cells.

93 dt2)-dependent monoubiquitylation of PCNA in unstressed cells.

94 ling molecule generated by actively growing, unstressed cells.

95 on and the normally rapid turnover of p53 in unstressed cells.

96 nducible gene, is expressed at low levels in unstressed cells.

97 caused PKR activation and apoptosis, even in unstressed cells.

98 ributes to MDM2-dependent p53 homeostasis in unstressed cells.

99 H5B/C causes accumulation of Mdm2 and p53 in unstressed cells.

100 pathway for maintaining p53 at low levels in unstressed cells.

101 ed and then slowly returns to levels seen in unstressed cells.

102 resent in the RalBP1.HSF1 heterocomplexes in unstressed cells.

103 y 1 MDa complex with p53 in the cytoplasm of unstressed cells.

104 ases sigma(B) activity more than 400-fold in unstressed cells.

105 cessary to preserve the genomic stability of unstressed cells.

106 tion of p53, which regulates its turnover in unstressed cells.

107 p53 is present at low levels in unstressed cells.

108 reases its ubiquitination and degradation in unstressed cells.

109 ignificantly alter cell cycle progression in unstressed cells.

110 ing low, often undetectable levels of p53 in unstressed cells.

111 ffuse nucleoplasmic distribution, typical of unstressed cells.

112 PBS2 and STE11 localize to the cytoplasm of unstressed cells.

113 ressed, controls basal P-eIF2alpha levels in unstressed cells.

114 oxide-stressed cells greatly exceeds that of unstressed cells.

115 on and, in contrast to HSP26 is expressed in unstressed cells.

116 to ER stress without impacting viability of unstressed cells.

117 jor changes in translation or mRNA levels in unstressed cells.

118 ed13p mediates cyclin C nuclear retention in unstressed cells.

119 coordinated regulation, even in a subset of unstressed cells.

120 itting of assorted classical measurements of unstressed chromatin structure in solution.

121 bumin: 1) preferentially binds stressed over unstressed client proteins; 2) forms stable, soluble, hi

122 P60 protein resides in the ER membrane under unstressed condition and is cleaved in response to ER st

123 ng versus old male Sprague Dawley rats under unstressed conditions (1.3 +/- 0.2 versus 1.8 +/- 0.3 ng

124 to cyclin G1, can stabilize cyclin G1 under unstressed conditions and upon DNA damage, as well as in

125 3, BT474 cells exhibited activated p38 under unstressed conditions as well as activated Akt and MAPK.

126 gulated; Nrf2 expression is suppressed under unstressed conditions but strikingly induced under oxida

127 d localization of HSPs in either stressed or unstressed conditions has not been studied extensively i

128 essential regulator of ISC homeostasis under unstressed conditions in the posterior midgut.

129 Survival under unstressed conditions is due to cell type-specific autop

130 f p53 must be kept at a very low level under unstressed conditions to allow growth.

131 ritic spine density in the hippocampus under unstressed conditions, and their neuronal anatomy can re

132 Under unstressed conditions, BiP binds to bZIP28 as it binds t

133 In their unstressed conditions, both the sodB- and wild-type stra

134 Under unstressed conditions, cytochrome c mRNA is actively tra

135 ochondrial targeting domain (MTD), which, in unstressed conditions, is inhibited by intramolecular bi

136 Under unstressed conditions, msl2 msl3 seedlings exhibited sev

137 Under unstressed conditions, the modified Mcl1 is present at l

138 sses c-Jun-mediated AP-1 transcription under unstressed conditions, thereby preventing cells from und

139 utions to the stability of the monomer under unstressed conditions, we have used functional complemen

140 resses ABA signaling and stress responses in unstressed conditions, whereas ABA signaling represses T

141 e G3 sequences are largely folded even under unstressed conditions, while the less stable G2 sequence

142 predominantly occurs in the cytoplasm under unstressed conditions.

143 ether CK1 regulates p53 protein stability in unstressed conditions.

144 mal left ventricular mass and function under unstressed conditions.

145 l survival after x-irradiation but not under unstressed conditions.

146 g histology as those of wild-type mice under unstressed conditions.

147 and showed symptoms of ER stress even under unstressed conditions.

148 nt biomass growth determinant under natural, unstressed conditions.

149 bind BiP and is not retained in the ER under unstressed conditions.

150 required for normal vegetative growth under unstressed conditions.

151 required for OMV production under stress or unstressed conditions.

152 was lethal, impacting pollen viability under unstressed conditions.

153 ription factor, retaining it in the ER under unstressed conditions.

154 le, and its deletion was not oncogenic under unstressed conditions.

155 orepinephrine concentrations under baseline (unstressed) conditions.

156 some stimulation to oxidative damage in the unstressed control and stressed animals.

157 In unstressed control animals, the Lewis strain had lower D

158 hibited impaired LTP relative to slices from unstressed control animals, whereas hippocampal slices f

159 ergoing chronic social defeat stress or from unstressed control mice were isolated and adoptively tra

160 e intruder monkeys was compared with that of unstressed control monkeys.

161 n blood or striatal levels, as compared with unstressed control rats.

162 spectrometry and quantitated relative to an unstressed control.

163 alamic nuclei was higher in PRS rats than in unstressed controls, both under basal conditions and in

164 ffect of stress on lifetime ID compared with unstressed controls, undermining the prediction that str

165 s was significantly impaired relative to the unstressed controls, whereas conditioning in stressed ov

166 ere significantly impaired relative to their unstressed controls, whereas females administered the es

167 ion and activity returned to levels found in unstressed controls.

168 otic (ethanol, heat) stressors compared with unstressed controls.

169 nce of predator odor-paired context, or were unstressed Controls.

170 association was increased by comparison with unstressed controls.

171 fect the amplitude of temperature rhythms in unstressed controls.

172 m, hippocampus, and midbrain compared to the unstressed controls.

173 IE plants maintained high values similar to unstressed controls.

174 moters in stressed cells for comparison with unstressed counterparts.

175 Under basal, unstressed culture conditions, no change in the ATP : AD

176 igase MDM2, is critical for the viability of unstressed, cycling cells.

177 Treatment of unstressed detached leaves with ionomycin, a Ca(2+) iono

178 ABSTRACT: Satellite cell contribution to unstressed diaphragm is higher compared to hind limb mus

179 The CD44s-fibrin pair has a lower unstressed dissociation rate and a higher tensile streng

180 lasticity, and shear rate and found that the unstressed dissociation rate, k(r)(o), and the bond inte

181 lthough the probability of these openings in unstressed DNA is close to 10(-5), it increases sharply

182 with those receiving no cells or cells from unstressed donors.

183 energy associated with the disruption in the unstressed double helix, G(d).

184 ination, and L5 PN spine dynamics similar to unstressed EE mice.

185 unteracted by ethylene during development in unstressed environments.

186 mponent, oral keratinocytes, of stressed and unstressed EVPOMEs by measuring the release of vascular

187 Consistent with previous reports unstressed exercising mice demonstrated reduced acoustic

188 Control (unstressed) females had lower levels of estradiol and te

189 e a cDNA library for each by subtraction of "unstressed" from "stressed" cDNA and used DNA hybridizat

190 ing wheels were introduced into stressed and unstressed group-housed control cages.

191 that VBNC cells can exist stochastically in unstressed growing cultures, a finding that is character

192 in the kinase activity of JNK under normal, unstressed growth conditions indicating a dominant-negat

193 d epsilon(c) studies conducted in relatively unstressed growth conditions were used to determine the

194 Despite confining our analysis to relatively unstressed growth conditions, total incident solar radia

195 kinesis requires the UPR pathway even during unstressed growth conditions.

196 sed superoxide dismutase-encoding gene under unstressed growth conditions.

197 nts indicate that manganese is essential for unstressed growth in some bacterial species, but is requ

198 suggesting a requirement for the metal under unstressed growth.

199 3 REs within the promoter of the p21 gene in unstressed HCT116 colon carcinoma cells are localized wi

200 Of 37 direct targets of miR-133a defined in unstressed hearts (fold change >/=25%, false discovery r

201 We found that unstressed Hippo-deficient adult mouse cardiomyocytes re

202 exposure increased expression relative to an unstressed homecage control group, but expression did no

203 Notably, unstressed HSCs lacking Hif-1alpha efficiently self-rene

204 Chk2 from unstressed human cells is largely monomeric and inactive

205 in the natural world where both stressed and unstressed individuals are both hermaphrodite.

206 ressor by increasing investment in sperm and unstressed individuals should invest solely in embryos.

207 heir resources entirely to male function and unstressed individuals will increase their allocation to

208 Unstressed k(off) values based on the Bell model were 2.

209 ome of PGs from chloroplasts of stressed and unstressed leaves of Arabidopsis (Arabidopsis thaliana)

210 chemic diastolic dysfunction by reducing the unstressed left ventricular end-diastolic volume.

211 that tissue maintaining hexose levels at an "unstressed" level, and at lower ABA levels, which was co

212 The amounts of both compounds return to the unstressed levels by 20 min after the temperature shift.

213 teins.Clusterin also binds to many different unstressed ligands including the cell surface receptor l

214 ding sites for LRP-2, stressed proteins, and unstressed ligands, respectively, and (ii) the binding s

215 ns in drought-exposed lineages compared with unstressed lineages.

216 icle emitted more conditioned responses than unstressed males.

217 gh throughput, purity, and recovery of live, unstressed mammalian cells.

218 essed approximately 70% less bcl-2 mRNA than unstressed mice after ischemia.

219 aneous development of retinal vasculature of unstressed mice and in the dramatically decreased angiog

220 Unstressed mice demonstrated recognition of the novel ob

221 rentially expressed between the stressed and unstressed mice was conducted.

222 In WT mice after CRS and in unstressed mice with a BDNF loss-of-function allele (BDN

223 f Bnip3 increased cardiomyocyte apoptosis in unstressed mice, causing progressive LV dilation and dim

224 In unstressed mice, forced expression of hMCIP1 resulted in

225 but neither process affected fear memory in unstressed mice.

226 he drug-paired chamber over the responses of unstressed mice.

227 y, and perhaps other factors may protect the unstressed mouse from the types of abnormalities that mi

228 In unstressed mouse hearts with a 30-fold increase in proca

229 ase) activity in cultured cardiomyocytes and unstressed mouse hearts.

230 ed its phosphorylation state in stressed and unstressed mouse hearts.

231 Finally, treatment of unstressed msl2 msl3 plants with exogenous ABA elicited

232 Unstressed mutant larvae show similar defects in transcr

233 by almost twofold relative to motions in the unstressed network.

234 assays have been developed to determine the unstressed (no-force) 2-D affinity but fail to disclose

235 an equivalent SS protein basis) in attached, unstressed nodules.

236 pN and a preexponential factor, or apparent unstressed off rate, of approximately 1/s.

237 to withstand forces up to 175 pN and had an unstressed off-rate of 0.20 s(-1).

238 on carcinomas approached 125 pN, whereas the unstressed off-rate was 2.78 s(-1).

239 ons (referred to as LL and LH for maternally unstressed offspring, assigned in low and high density,

240 ons (referred to as LL and LH for maternally unstressed offspring, assigned in low and high density,

241 ween maternally density-stressed and density-unstressed offspring.

242 c brains and in the mitochondrial lysates of unstressed old NEIL1-deficient mice.

243 Unstressed or dark-stressed wild-type plants were resist

244 normal start site; this site is not used in unstressed or heat-stressed tissues.

245 odels are strictly valid on average only for unstressed or overwound DNA up to P-DNA formation.

246 Adult unstressed or PRS rats were treated daily with either ag

247 The mice were either left unstressed or were subjected to an air blower for 5 h/d,

248 mplicate roles for manganese in key steps in unstressed oxidative metabolism in B. japonicum.

249 Furthermore, adding purified cyclin C to unstressed permeabilized MEF cultures induced complete m

250 io is maintained under conditions of normal (unstressed) photosynthesis, implying a continuously enga

251 In the unstressed plant, the extA gene is only expressed in the

252 anscript, Rip1, was of very low abundance in unstressed plants and was strongly induced by stress.

253 reasing ARGdc activity by up to 10-fold over unstressed plants with a corresponding increase in putre

254 igible level of constitutive iox emission in unstressed plants, and in plants treated with high O3.

255 t exclusively in emerging secondary roots in unstressed plants, but is primarily expressed in the roo

256 but did not alter the glutathione content in unstressed plants, which supports the idea that the glut

257 , but is constitutively active in anthers of unstressed plants.

258 ow water potential while having no effect on unstressed plants.

259 e solute proline without negative effects on unstressed plants.

260 prevent activation of the stress response in unstressed plants.

261 ted as soft, thermal fluctuations even in an unstressed portion of network were expected to be many t

262 The task was completed in both an ideal unstressed posture and an uncomfortable, stressed elevat

263 ase or Raf kinase can increase GSH levels in unstressed primary rat neurons through the same ERK/c-My

264 ine, cadaverine, and N8-acetylspermidine, in unstressed proliferating cells, or of N1-acetylspermidin

265 tor of cellular redox state, is increased in unstressed puf3Delta cells but remains lower under stres

266 in the conscious, chronically catheterized, unstressed rat to investigate whether NO interacts with

267 etrodotoxin produced thermal hyperalgesia in unstressed rats and blocked the anti-hyperalgesic effect

268 Glucocorticoid administration to unstressed rats is sufficient to cause decrements in PPG

269 ioning of fatty acids in the liver of awake, unstressed rats was studied using selective labelling of

270 ude that ARC controls body energy balance in unstressed rats, possibly by alphaMSH input to PVN, and

271 was compared with that of a control group of unstressed rats.

272 al neurons were observed compared to control unstressed rats.

273 between active and passive stress-coping and unstressed rats.

274 reduce tissue breakdown resulting from PD in unstressed rats.

275 he slope and intercept of the plot yield the unstressed reverse reaction rate, k(r)(o), and a paramet

276 In unstressed rodents, endogenous peripheral acyl-ghrelin r

277 ance liquid chromatography studies show that unstressed sac9 mutants accumulate elevated levels of Pt

278 re expressed at a noticeably higher level in unstressed salt cress plants and are induced rapidly und

279 ndistinguishable from stressed sedentary and unstressed sedentary controls on each anxiety measure.

280 owing mCPP administration when compared with unstressed sedentary controls.

281 d leaf solute content and water relations in unstressed soil-grown plants.

282 trate a heightened HPA stress profile in the unstressed state.

283 2ird1) that is expressed in the cytoplasm of unstressed tenocytes translocated into the nucleus upon

284 tole, when the mitral leaflets are slack and unstressed, the leaflets appear markedly thickened in pa

285 ) kinase pathway during cell wall stress and unstressed vegetative growth.

286 sed emitted fewer conditioned responses than unstressed vehicle controls.

287 antitative shotgun proteomics, we found that unstressed vipp1 mutant cells accumulate 14 to 20% less

288 In cardiac myocytes isolated from unstressed wild-type and GRK2KO hearts, myocyte contract

289 We identified that in the unstressed wild-type male gamete containing pollen of fl

290 ite scavenger activities in dark-stressed or unstressed wild-type plants, while expression of the sul

291 1-3, more H1-3 is bound to chromatin than in unstressed wild-type plants.