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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

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