ライフサイエンスコーパス: -deprived

1 These IL-15-deprived CD8(+) T cells did not acquire the phenotype of

2 the numbers and suppressive capacity of IL-2-deprived Tregs with striking increases in CD25, CTLA-4,

3 ells made anergic, TGF-beta-treated, or IL-2-deprived; all possible modes of Treg action.

4 in Matrigel(R) culture, whereas miR-199a-5p-deprived cells exhibited enhanced angiogenesis in vitro.

5 sponse and induction of MMP-1 in miR-199a-5p-deprived HMECs.

6 Surprisingly, IL-7-deprived diabetogenic T(E/M) cells remained present in t

7 The VAD mice were fed with a vitamin A-deprived diet after birth.

8 The vitamin A-deprived rod outer segments were 60% to 70% the length a

9 Unlike bleaching adaptation, the vitamin A-deprived rods maintained near normal saturating (dark) c

10 Contrasting phototransduction in vitamin A-deprived Xenopus rods with phototransduction in constitu

11 89) when expressed transiently in amino acid-deprived 293T cells.

12 mTOR activation, by refeeding of amino acid-deprived cells or by TSC2 shRNA, activated SGK1 and p27

13 Connectivity was decreased in activity-deprived circuits by functional silencing of synapses, w

14 xposed clusters by 17% relative to the agrin-deprived clusters on the same myotube.

15 lls will resume proliferation in an androgen-deprived environment.

16 nsitive LNCaP cells under basal and androgen-deprived conditions.

17 Eligible androgen-deprived men were randomly assigned to one of four daily

18 prostate cancer progression and in androgen-deprived CRPC cells, suggesting that CRPC possesses an e

19 (ROS), p53 levels and cell death in androgen-deprived CRPC cells.

20 a population of enhancer modules in androgen-deprived cultures showed nucleosome-depleted regions (ND

21 In androgen-deprived men, neither venlafaxine nor soy proved effecti

22 me activities also were observed in androgen-deprived tumors, consistent with pAKT-dependent HK2 prot

23 ways, pAKT levels were increased in androgen-deprived tumors.

24 ssion was undetectable in localized androgen-deprived tumors and in metastases without prior androgen

25 ashes occur in approximately 80% of androgen-deprived men.

26 ferent metastases in the context of androgen-deprived metastatic prostate cancer.

27 mphocytes recruited into regressing androgen-deprived tumors by C-X-C motif chemokine 13 (CXCL13), a

28 dy we explore AR function under the androgen-deprived conditions characteristic of CRPC.

29 in maintaining the AR pathway under androgen-deprived conditions in castration-resistant prostate can

30 Under androgen-deprived conditions, NDRs at the TMPRSS2 enhancer were m

31 d for CRPC cell proliferation under androgen-deprived conditions.

32 te epithelial (LHSR-AR) cells under androgen-deprived conditions.

33 L-arginine-deprived T cells upregulated system L amino acid transpo

34 ASNS by small-interfering RNAs in asparagine-deprived media led to growth inhibition in both androgen

35 n kinase A activity is abnormal in astrocyte-deprived neurons but restored by TSP1, so protein kinase

36 By investigating BBS12-deprived retinal explants and the Bbs12(-/-) murine mode

37 concentrations were lower during the calorie-deprived diet (P < 0.001) than during the fully fed diet

38 Here, colostrum-deprived calves persistently infected with HoBi-like pes

39 o the inactivating interaction of the copper-deprived N-metal binding extension with the headpiece do

40 )-MLKL necrosis pathways potentiated cystine-deprived necrosis.

41 alpha and MEKK4 dramatically reduces cystine-deprived death.

42 In cytokine-deprived cells, PPARgamma attenuates the decline in ATP

43 r than mock vector control BMMCs in cytokine-deprived conditions.

44 ransfusion into recipient animals, these dox-deprived mature megakaryocytes generated functional plat

45 tes stresses generated by E2 in long-term E2-deprived cells that trigger apoptosis.

46 MCF10A AR cells were overlaid on top of EGF-deprived MCF10A cells showed that the AR membrane precur

47 on of EGFR upon Src overexpression under EGF-deprived conditions, further supporting this model-gener

48 h's largest ecosystem, are especially energy-deprived systems.

49 Specifically, energy-deprived anaerobes overwhelmingly rely upon the higher A

50 ytic activator PFKFB3, rendering them energy-deprived, ROS- and autophagy-deficient, apoptosis-sensit

51 t of BKM120 and fulvestrant against estrogen-deprived ER(+) xenografts but not LYN(D189Y)-expressing

52 d IGF-1 promotes wound repair in an estrogen-deprived animal model, the ovariectomized (Ovx) mouse, p

53 ressed in non-oviduct tissue and in estrogen-deprived oviduct by a strong repressor site located from

54 sions were also seen in a long-term estrogen-deprived breast model, where significant downregulation

55 Long-term estrogen-deprived MCF-7:5C cells were used to model the postmenop

56 -induced apoptosis in the long-term estrogen-deprived MCF7:5C cells.

57 However, in experience-deprived cortex, a much greater proportion of spines lac

58 r to the emergence of face domains, but face-deprived monkeys did not, indicating that face looking i

59 tivation by ligand exposure in growth factor-deprived cells induces Akt activation in the FET, CBS, a

60 catastrophe and rapid death of growth factor-deprived cells.

61 t inhibited apoptotic death of growth factor-deprived cells.

62 sed higher levels of BIM under growth factor-deprived conditions and reduced Mcl-1 on stimulation.

63 Growth factor-deprived hematopoietic cells do not engage in glucose-de

64 Elafin is induced in growth factor-deprived HMECs as they enter a quiescent (G0) state, sug

65 nd initiate apoptosis in nerve growth factor-deprived sympathetic neurons and axotomized RGCs.

66 cts as a central regulator of trophic factor-deprived motor neuron survival by suppressing nitric oxi

67 haperone was nitrated in both trophic factor-deprived motor neurons and PC12 cells incubated with per

68 a caspase-dependent manner in trophic factor-deprived sensory axons and was required for this in vitr

69 male-male mounting (MMM) behaviour in female-deprived desert locust males infected with the entomopat

70 ary fiber deprivation, together with a fiber-deprived, mucus-eroding microbiota, promotes greater epi

71 ation of endothelial alk1 expression to flow-deprived arteries fails to rescue Alk1 activity or norma

72 Fluid-deprived Sprague-Dawley rats acquired a strong CTA [via

73 Food-deprived flies reduce the gain of a visual-motion-sensit

74 en it encounters food, and animals in a food-deprived state slow even more than animals in a well-fed

75 n the ASH chemosensory neurons to allow food-deprived animals to delay response to the aversive stimu

76 The slowing responses of well-fed and food-deprived animals in the presence of food represent disti

77 ehension was only evoked in trained and food-deprived animals, suggesting that a motivation-gated mot

78 files of AGRP neurons from well-fed and food-deprived young adult mice.

79 that signal food delivery when rats are food-deprived can substantially potentiate feeding later when

80 ured under two motivational conditions: food-deprived rats given standard chow or ad libitum-fed rats

81 y different in the fed vs. fasted (>8 h food-deprived) state.

82 cial for marine bacteria, especially in food-deprived environments of the deep sea.

83 visual wide-field motion was reduced in food-deprived flies.

84 drives a distinct foraging strategy in food-deprived larvae.

85 , feed efficiency, and weight regain in food-deprived male and female C57BL/6J mice.

86 tion nearly eliminates acute feeding in food-deprived mice.

87 ad libitum-maintained rats, and chow in food-deprived rats, but only at the 30-ng dose.

88 oinjected into the ACC, OFC, and DMS of food-deprived rats just prior to operant learning sessions.

89 EXPERIMENT 1: Five groups of overnight food-deprived male Sprague Dawley rats were injected with exe

90 (1) Overnight food-deprived rats were presented with a 10% sucrose solution

91 In this setting, food-deprived rats suppress eating when presented with a tone

92 cular [4V] application of leptin to the food-deprived animal, before TRH injection, yields a substant

93 pid metabolism were up-regulated in the food-deprived animals, with a novel class of taurine-containi

94 ulating peptide hormone secreted by the food-deprived stomach.

95 ed in differentially expressed genes in form-deprived eyes.

96 in previous studies from 18 monocularly form-deprived and 32 normal monkeys reared under ordinary lab

97 ively analyzed in visual area 2 (V2) of form-deprived macaque monkeys.

98 refractive errors in the two groups of form-deprived monkeys, either with or without foveal ablation

99 ed monkeys were more hyperopic than the form-deprived eyes of the normal-light-reared monkeys.

100 tropias, and in 6 of these monkeys, the form-deprived eyes were more hyperopic than their fellow eyes

101 In eight of these form-deprived monkeys, the fovea and most of the perifovea of

102 Infecting glucocorticoid-deprived cells with influenza A virus disrupted the norm

103 Glucose-deprived melanoma cells depend on both oxidative phospho

104 ollected from cells under normal and glucose-deprived conditions, estimating the relative flux change

105 p27 levels and suppressed basal and glucose-deprived levels of autophagy in cardiomyocytes in vitro.

106 hosphorylation were observed between glucose-deprived and normal glucose-treated cells.

107 apoptosis by promoting autophagy in glucose-deprived cardiomyocytes in vitro and in post-myocardial

108 o be three times as rapid as that in glucose-deprived cells.

109 iratory chain have altered levels in glucose-deprived lymphocytes from patients with BPD.

110 However, treatment of glucose-deprived cells with a small dose (1 mm) of glucosamine b

111 Consistent with this, treatment of glucose-deprived cells with an inhibitor of O-GlcNAcase (O-(2-ac

112 oss of cell viability in a subset of glucose-deprived melanoma cells, but synergizes with acetate to

113 was prebound with Sirt2 in serum or glucose-deprived cells, and the complex dissociated following in

114 rgin exacerbated apoptosis in oxygen-glucose-deprived cells during reoxygenation.

115 e effects were evaluated with oxygen/glucose-deprived and control neuronal cells in vitro.

116 Xe-ELIP delivery to oxygen/glucose-deprived neuronal cells improved cell viability in vitro

117 embly after readdition of glucose to glucose-deprived cells are controlled by the glycolysis flow.

118 After readdition of glucose to glucose-deprived cells, glucose-dependent V1Vo reassembly was pr

119 e and after readdition of glucose to glucose-deprived cells.

120 Transiently glucose-deprived wild-type cells respond to glucose addition wit

121 Beginning 12 h after treatment, glucose-deprived human hepatocellular carcinoma (HepG2) cells de

122 Viral yield in glutamine-deprived cells or in cells treated with an inhibitor of

123 al transcription, was decreased in glutamine-deprived cells, which corresponded with a dramatic reduc

124 kinase allowed LC3-II induction in glutamine-deprived cells.

125 paragine further proved crucial in glutamine-deprived ECs to restore protein synthesis, suppress ER s

126 sole eIF2alpha kinase of yeast, in histidine-deprived cells.

127 cally integrated analyses showed how hormone-deprived LNCaP cells could transdifferentiate to a nonma

128 P cells cultured for long periods in hormone-deprived conditions.

129 R transcriptional program even under hormone-deprived conditions.

130 eless maintained surface Glut1 levels in IL3-deprived cells, possibly via enhanced recycling of inter

131 me efficiently reactivated within the immune-deprived nervous tissue.

132 of Neutravidin in undiluted, immunoglobulin-deprived human serum samples.

133 educed V-ATPase proton transport in inositol-deprived wild-type cells.

134 l imaging were significantly larger in input-deprived than normal input single-digit regions and were

135 ting protein that binds to mTORC1 in insulin-deprived cells and whose in vitro interaction with mTORC

136 nd, ferritin2 abundance is decreased in iron-deprived cells, indicative of the operation of iron-nutr

137 itro and reversed anemia progression in iron-deprived mice.

138 PB(nu)) also mediate iron delivery into iron-deprived cells.

139 At birth, the newborns of monkeys iron-deprived during pregnancy had significantly lower hemogl

140 overexpression impaired the survival of iron-deprived flies.

141 id not differ significantly between the iron-deprived and control dams, and the fetuses and newborns

142 By the third trimester, 79% of the iron-deprived dams and 29% of the control monkeys had a hemog

143 ms, and the fetuses and newborns of the iron-deprived dams were not growth retarded relative to the c

144 the growth of plants maintained in the iron-deprived medium.

145 sis of mutant and parental strain under iron-deprived conditions indicated a role of ALL1 in iron hom

146 ucella abortus 2308 during growth under iron-deprived conditions, and mutational studies indicate tha

147 rn blot analysis following growth under iron-deprived conditions.

148 It has been demonstrated in mice that LC-deprived epithelia are rapidly replenished by short half

149 The least-deprived patients are almost twice as likely to be refer

150 d the depressive behavioral profile of light-deprived rats.

151 oma slowed down tumor growth in a lymphocyte-deprived environment but promoted immune escape in a lym

152 their ability to proliferate under magnesium-deprived situations and under anchorage-independent grow

153 by evidence of an increase in ROS in matrix-deprived cells in the luminal space of mammary acini, an

154 rvival when apoptosis is inhibited in matrix-deprived cells.

155 cer-spheroids leads to death of inner matrix-deprived cells, whereas matrix-attached cells are resist

156 riate behavioral training enables monaurally-deprived adult humans to exploit both of these adaptive

157 This may be because more-deprived patients are less suitable for a trial-as a res

158 ral was less likely for patients in the more-deprived quintiles compared with the least deprived (IMD

159 a large scale within 30 min to a switch to N-deprived conditions turning on a largely gluconeogenic m

160 In contrast with N-deprived cells, the TAGs in hypoxic cells were enriched

161 Performance losses when nap-deprived are not recovered during subsequent overnight s

162 2O2 block cytochrome c redistribution in NGF-deprived neurons.

163 which paralleled increased cell death in NGF-deprived PC-12 cells.

164 n these ROS of adding NGF to cultures of NGF-deprived neurons.

165 for some small negative effects in nicotine-deprived participants.

166 is suppressed when pt4 mutants are nitrogen-deprived, possibly the result of compensation by PT8, a

167 es taking place in the membranes of nitrogen-deprived E. oleoabundans, including lipid metabolism, pr

168 ressure (20% (deprived) compared to 11% (non-deprived), difference: 9.0% (95%CI: 4.7%-13.4%)).

169 were either nicotine deprived (n = 12), non-deprived (n = 12) or deprived but were allowed to smoke

170 mRNA up-regulation in both deprived and non-deprived groups following acute restraint.

171 mapping and compared BEN between chronic non-deprived smokers and non-smoking controls.

172 We compared non-deprived animals to animals subjected to 24 h of DEP at

173 nist muscimol could alter food intake in non-deprived rats.

174 ndomised evidence exists among adults in non-deprived settings.

175 ive for the compensatory potentiation of non-deprived inputs.

176 erse occlusion, inactivation of only the non-deprived (fellow) eye for 10 days produced a complete re

177 al-cortex-dependent behavior through the non-deprived eye (NDE) during deprivation, and enabled enhan

178 d exhibit precocious potentiation of the non-deprived eye inputs.

179 ved-eye response without a change in the non-deprived eye response, NR2A-knockout mice fail to exhibi

180 delayed strengthening of inputs from the non-deprived eye.

181 Notch-deprived myelin-reactive T cells had preserved activatio

182 Notch-deprived T cells showed markedly decreased production of

183 Although Notch-deprived T cells proliferated and expanded in response t

184 Both CD4(+) and CD8(+) Notch-deprived T cells had preserved expansion in lymphoid org

185 lmonary leukocyte cultures from T cell Notch-deprived mice produced less IFN-gamma, IL-5, and IL-13 t

186 However, Notch-deprived alloreactive CD4(+) T cells retained significan

187 However, Notch-deprived T cells failed to accumulate in the CNS after i

188 row chimeras increased accumulation of Notch-deprived T cells in the CNS after immunization but did n

189 Additionally, two fasted groups were nurse-deprived for two cycles before being euthanized at postn

190 cts in insulin receptor mutants and nutrient-deprived animals.

191 icroenvironment is characterized by nutrient-deprived conditions in which the cancer cells have to ad

192 es from lipid-induced damage during nutrient-deprived or replete states.

193 m the selective pressure of a harsh nutrient-deprived microenvironment.

194 by its association with Beclin1 in nutrient-deprived cells, our studies revealed that HCV-mediated a

195 hat UCP2 expression is increased in nutrient-deprived murine and human islets.

196 at could restore blood perfusion in nutrient-deprived regions where angiogenic resources are most nee

197 Importantly, DCAP kills nutrient-deprived microbes and sterilizes bacterial biofilms.

198 exploration-exploitation trade-off: nutrient-deprived flies focus on specific patches while satiated

199 ents, display phenotypes similar to nutrient-deprived and Tor mutant larvae.

200 that exosomes supply amino acids to nutrient-deprived cancer cells in a mechanism similar to macropin

201 ve mTORC1 signalling in cells under nutrient-deprived conditions and neonatal lethality in mice, whic

202 Ras-transformed cells to grow under nutrient-deprived conditions in vitro and in a mouse xenograft sy

203 tion of lipids, or lipophagy, under nutrient-deprived conditions, and FXR inhibited this response.

204 phagous fungi and occurs only under nutrient-deprived conditions.

205 ular survival and homeostasis under nutrient-deprived conditions.

206 ung by diverting blood flow away from oxygen-deprived areas towards regions rich in O2.

207 s miRNA mediates immunosuppression in oxygen-deprived regions of tumors where cancer stem-like cells

208 y to selectively induce cell death in oxygen-deprived tissue such as tumors.

209 sed levels of alginate in response to oxygen-deprived conditions.

210 When seedlings were oxygen-deprived, the frequency of ribosomes at the start codon

211 We found that P-deprived pnp mutants develop aborted clusters of lateral

212 These new observations for pattern-deprived animals provide an anatomical basis for the wel

213 o the nucleus and induced specifically in Pi-deprived roots and shoots.

214 terning, and for stem-cell maintenance in Pi-deprived roots.

215 induction, respectively, in the roots of Pi-deprived seedlings, whereas Pi deficiency-mediated induc

216 e genes in both the genotypes grown under Pi-deprived condition, the abundance of LmPAP1 transcripts

217 in autophagosomes in IMCD cells of potassium-deprived rats by immunogold electron microscopy.

218 ll antigen receptor repertoire in progenitor-deprived thymus grafts implied that many thymocytes were

219 lementation suppressed miR395 induction in S-deprived plants (ii) miR395 is induced in Arabidopsis se

220 al role in the transport of SO(4)(2-) into S-deprived cells.

221 lcisome formation compared with wild-type, S-deprived cells and dies more rapidly than wild-type cell

222 trout, Salmo trutta , from Lake Mjosa (a Se-deprived lake) and Lake Losna (a reference lake), Norway

223 reminiscent of sperm isolated from selenium-deprived rodents or from mice specifically lacking mitoc

224 in two distinct cortical regions: a sensory-deprived region characterized by a decrease in inhibitor

225 of layer IV in "sensory-spared" and "sensory-deprived" cortices of glutamate acid decarboxylase 67 (G

226 required for plastic adjustments in sensory-deprived cortex.

227 rgely to layer I of barrel cortex in sensory-deprived rats.

228 1 significantly elevated proteins in sensory-deprived synapses, 22 of which were validated by immunob

229 reveal that in the visual cortex of sensory-deprived mice, dendritic spine enlargement correlates wi

230 from a sensory modality can recruit sensory-deprived cortical areas to process information from the

231 r is suppressed in growth-arrested and serum-deprived cells, suggesting that end-joining activity in

232 Furthermore, serum-deprived cells in culture show an upregulated EGFR/JAK3/

233 ession in CD230/PrP(C) was observed in serum-deprived cells in association with increased generation

234 In serum-deprived cells, PPARgamma attenuated the decline in ATP,

235 in and decreased PC3 cell viability in serum-deprived conditions.

236 duction of Prx III mRNA and protein in serum-deprived human cardiac fibroblasts.

237 presses rapamycin-induced apoptosis in serum-deprived MDA-MB-231 cells in a protein kinase Cdelta (PK

238 the liver of fasted rats as well as in serum-deprived mouse embryo fibroblasts lacking both 4E-BP1 an

239 tenance of Mcl-1 protein expression in serum-deprived Tsc2(-/)(-) cells are dependent largely on the

240 Exposure of serum-deprived RGC-5 cells to PI 3-kinase or Akt inhibitors in

241 ributes to the apoptotic resistance of serum-deprived Tsc1/2-deficient cells in part by increasing th

242 proximately 8 h and include plating of serum-deprived VSM or ASM cell suspension on membrane precoate

243 t anti-apoptotic effects of PDGF-BB on serum-deprived ST88-14 cells can be inhibited by W7, implicati

244 70% of maximal in amino acid replete, serum-deprived 293E cells.

245 ation and enhanced cell survival under serum-deprived conditions.

246 Sleep-deprived (Sleep-Dep) rats were compared with yoked force

247 Sleep-deprived and fatigued doctors pose a safety risk to them

248 We used our in vitro model and sleep-deprived animals to map the metabolic pathways activated

249 f the deterioration of signals made by sleep-deprived honey bees and humans is generalizable, then im

250 sulin insensitivity, while chronically sleep-deprived individuals are more likely to develop obesity,

251 hus, eveningness in obese, chronically sleep-deprived individuals compounds the cardiovascular risk a

252 ns predict the success of encoding for sleep-deprived individuals relative to those who have slept no

253 Accordingly, HSCs from sleep-deprived mice have higher levels of SOCS genes expressio

254 The improved performance in sleep-deprived animals was accompanied by orexin-A related alt

255 ediately normalize pain sensitivity in sleep-deprived animals, without affecting sleep debt.

256 dFB neurons in sleep-deprived flies tend to be electrically active, with high

257 cantly depolarized in Hcrt neurones in sleep-deprived mice as compared with controls (P < 0.01, t tes

258 nhances neurogenesis in hippocampus in sleep-deprived mice.

259 ficantly enhances NPC proliferation in sleep-deprived mice.

260 storation normalizes reward seeking in sleep-deprived mice.

261 significantly improved performance in sleep-deprived monkeys; however, the nasal delivery method was

262 mance-restoring effects of caffeine in sleep-deprived subjects.

263 on challenge the claim of increasingly sleep-deprived societies.

264 affected task performance in alert non-sleep-deprived animals.

265 esembles the cortical transcriptome of sleep-deprived mice, and plastic changes as reflected by AMPA

266 of caffeine on the PVT performance of sleep-deprived subjects and, therefore, can be used for determ

267 or vigilance task (PVT) performance of sleep-deprived subjects.

268 ndependent dataset involving partially sleep-deprived participants.

269 ivation, and reduced aggression places sleep-deprived flies at a competitive disadvantage for obtaini

270 These changes may render sleep-deprived individuals less able to anticipate the locatio

271 Here we show that sleep-deprived honey bees (Apis mellifera) exhibit reduced pre

272 onal stimuli judged as pleasant in the sleep-deprived group, the extent of which exclusively correlat

273 signing were 4.5 times higher for the sleep-deprived participants than for the rested participants.

274 Neurocognitive tasks may tax the sleep-deprived resident more than well-learned technical skill

275 minergic signaling associated with the sleep-deprived state.

276 retin-1 (orexin-A) was administered to sleep-deprived (30-36 h) rhesus monkeys immediately preceding

277 When rested, but not when sleep-deprived, subjects responded more quickly to targets tha

278 Then, 1-2 hours after sodium-deprived rats ingested salt (a hypertonic 3% solution of

279 P1) resulted in stunted seedlings in sucrose-deprived medium.

280 Sulfur-deprived cells of Chlamydomonas reinhardtii have been sh

281 d to sustained hydrogen production in sulfur-deprived Chlamydomonas reinhardtii cultures.

282 Moreover, the data suggest that sulfur-deprived cells accumulate proteins with fewer sulfur-con

283 scule degeneration does not occur in sulphur-deprived mtpt4 plants.

284 f reactive oxygen/nitrogen species in target-deprived neurons.

285 ammation in the long-term survival of target-deprived afferent neurons.

286 We revealed that TE-deprived ICMs derived from 32-cell blastocysts are still

287 d in the draining lymph nodes (dLNs) in Treg-deprived mice, it was profoundly reduced at the infectio

288 In trophic-deprived cortical neurons, knockdown of endogenous PDK1

289 rhizi uredospores, detached leaves of urease-deprived plants developed a significantly higher number

290 the protein extracts from transgenic urease-deprived plants than in extracts from non-transgenic con

291 Water-deprived animals had to learn to localize an object with

292 Water-deprived rats initially received a single odor-toxicosis

293 Water-deprived rats were either conditioned to attend to a con

294 In Experiment 1, water-deprived rats had 5-min access to saccharin followed by

295 s for reward valuation we had food and water-deprived subjects make risky choices for money, food, an

296 firing in the LHb of freely behaving, water-deprived rats before and after an ethanol-induced (1.5 g

297 lectron micrographs revealed that both water-deprived and NaCl-treated plants had elevated osmium acc

298 or was only observed when animals were water-deprived but not under food- or salt-depleted conditions

299 ay kinetics and larger amplitudes in whisker-deprived barrels than those in nondeprived barrels in ag

300 somatosensory cortex of unilaterally whisker-deprived adult mice, the current study demonstrates that