ライフサイエンスコーパス: unstressed

1 -independent, disappearing when the joint is unstressed.

2 xposure to novelty stress and the other left 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 relevant analysis of the kidney in SCD under unstressed and stressed conditions.

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

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

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

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

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

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

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

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

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

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

26 PRQ occurs at low frequency in unstressed animals, but is more frequent in animals that

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 onstrated robust LTP comparable with that of unstressed animals.

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

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

34 PT reduced alveolar bone loss in unstressed animals.

35 In unstressed Arabidopsis (Arabidopsis thaliana) leaves, al

36 y enzyme limiting tocopherol biosynthesis in unstressed Arabidopsis leaves.

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

38 Unstressed beta1KOmdx mice were viable and had normal ca

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

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

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

42 When unstressed, both control and norleucine-substituted cell

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

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

45 exhibit larger relaxation times than in the unstressed case.

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

47 ther and how cells restrain CtIP activity in unstressed cells and activate CtIP when needed.

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

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

50 e immunity to HSV-1 is normally repressed in unstressed cells and repression appears to be determined

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

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

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

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

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

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

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

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

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

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

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

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

63 Unstressed cells maintain p53 at low levels through regu

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

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

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

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

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

69 L3MBTL2 associates with the CHOP promoter in unstressed cells to repress CHOP induction but dissociat

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

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

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

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

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

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

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

77 In unstressed cells, eIF4A, eIF4B, and Ded1 primarily targe

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

79 y resumes in stressed cells or is ongoing in unstressed cells, excess Rpt subunits are recognized by

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

81 2, and correspondingly p53 downregulation in unstressed cells, is accomplished by a specific isoform

82 In unstressed cells, low levels of eIF2alpha phosphorylatio

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

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

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

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

87 In unstressed cells, Polkappa is continually transported ou

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

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

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

91 In unstressed cells, the tumor suppressor p53 is maintained

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

93 In unstressed cells, this association leads to increased hp

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

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

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

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

98 The two forms can also be detected in unstressed cells.

99 2-fold after 3 hours of stress compared with unstressed cells.

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

101 ling molecule generated by actively growing, unstressed cells.

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

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

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

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

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

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

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

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

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

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

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

113 p53 is present at low levels in unstressed cells.

114 reases its ubiquitination and degradation in unstressed cells.

115 ignificantly alter cell cycle progression in unstressed cells.

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

117 ffuse nucleoplasmic distribution, typical of unstressed cells.

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

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

120 cessary to preserve the genomic stability of unstressed cells.

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

122 to ER stress without impacting viability of unstressed cells.

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

124 ed13p mediates cyclin C nuclear retention in unstressed cells.

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

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

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

128 d SPS (58-60 postnatal days; n = 14), or (3) unstressed conditions (n = 8).

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

130 3, BT474 cells exhibited activated p38 under unstressed conditions as well as activated Akt and MAPK.

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

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

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

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

135 of CHK1 are maintained under physiological, unstressed conditions is not well understood.

136 Even when normal during unstressed conditions such as rest, hemodynamics classic

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

138 ss responses in plants, also functions under unstressed conditions to support normal development.

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

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

141 Under unstressed conditions, cytochrome c mRNA is actively tra

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

143 Under unstressed conditions, msl2 msl3 seedlings exhibited sev

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

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

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

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

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

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 predominantly occurs in the cytoplasm under unstressed conditions.

156 ether CK1 regulates p53 protein stability in unstressed conditions.

157 mal left ventricular mass and function under unstressed conditions.

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

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

160 ession in these neurons both in stressed and unstressed conditions.

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

162 nt biomass growth determinant under natural, unstressed conditions.

163 orepinephrine concentrations under baseline (unstressed) conditions.

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

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

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

167 ontal cortex) of susceptible, resilient, and unstressed control mice.

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

169 spectrometry and quantitated relative to an unstressed control.

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

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

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

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

174 association was increased by comparison with unstressed controls.

175 fect the amplitude of temperature rhythms in unstressed controls.

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

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

178 IE plants maintained high values similar to unstressed controls.

179 moters in stressed cells for comparison with unstressed counterparts.

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

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

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

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

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

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

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

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

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

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

190 unteracted by ethylene during development in unstressed environments.

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

192 Consistent with previous reports unstressed exercising mice demonstrated reduced acoustic

193 onist/OTR-Gi agonist, has the same effect in unstressed females.

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

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

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

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

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

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

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

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

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

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

204 suggesting a requirement for the metal under unstressed growth.

205 3 REs within the promoter of the p21 gene in unstressed HCT116 colon carcinoma cells are localized wi

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

207 ontrast to AMPK activities during stress, in unstressed hearts, AICAR induced a mild activation of Ak

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

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

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

211 Chk2 from unstressed human cells is largely monomeric and inactive

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

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

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

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

216 mprised up to 2% of the total Rca protein in unstressed leaves but increased three-fold in leaves exp

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

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

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

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

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

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

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

224 First, we show that in unstressed male and female California mice, inhibition o

225 icle emitted more conditioned responses than unstressed males.

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

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

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

229 Unstressed mice demonstrated recognition of the novel ob

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

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

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

233 In unstressed mice, forced expression of hMCIP1 resulted in

234 alone is insufficient to induce vigilance in unstressed mice, suggesting that mechanisms modulating s

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

236 but neither process affected fear memory in unstressed mice.

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

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

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

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

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

242 Unstressed mutant larvae show similar defects in transcr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 enhanced TNT formation between stressed and unstressed PCa cells as well as from stressed PCa to ost

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

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

261 peptides of increased abundance in hai1-2 in unstressed plants and in plants exposed to low-water pot

262 trons, ectopic HIN1 expression (35S:HIN1) in unstressed plants mimicked the increased splicing effici

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

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

265 prevent activation of the stress response in unstressed plants.

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

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

268 e solute proline without negative effects on unstressed plants.

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

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

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

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

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

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

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

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

277 reduce tissue breakdown resulting from PD in unstressed rats.

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

279 al neurons were observed compared to control unstressed rats.

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

281 The unstressed refolding rate of MSD is ~17 s(-1) and slows

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

283 In unstressed rodents, endogenous peripheral acyl-ghrelin r

284 and anxiety-like behaviors were assessed in unstressed, RSD, and RSD + human MSC groups.

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

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

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

288 owing mCPP administration when compared with unstressed sedentary controls.

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

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

291 imilar type will tend to self-organize in an unstressed system to a positively skewed frequency distr

292 2ird1) that is expressed in the cytoplasm of unstressed tenocytes translocated into the nucleus upon

293 10 mm in length, donating resources from the unstressed to the stressed projection in response to int

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

295 sed emitted fewer conditioned responses than unstressed vehicle controls.

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

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

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

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

300 1-3, more H1-3 is bound to chromatin than in unstressed wild-type plants.