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2 the numbers and suppressive capacity of IL-2-deprived Tregs with striking increases in CD25, CTLA-4,
4 in Matrigel(R) culture, whereas miR-199a-5p-deprived cells exhibited enhanced angiogenesis in vitro.
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
12 mTOR activation, by refeeding of amino acid-deprived cells or by TSC2 shRNA, activated SGK1 and p27
18 prostate cancer progression and in androgen-deprived CRPC cells, suggesting that CRPC possesses an e
20 a population of enhancer modules in androgen-deprived cultures showed nucleosome-depleted regions (ND
22 me activities also were observed in androgen-deprived tumors, consistent with pAKT-dependent HK2 prot
24 ssion was undetectable in localized androgen-deprived tumors and in metastases without prior androgen
27 mphocytes recruited into regressing androgen-deprived tumors by C-X-C motif chemokine 13 (CXCL13), a
29 in maintaining the AR pathway under androgen-deprived conditions in castration-resistant prostate can
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
37 concentrations were lower during the calorie-deprived diet (P < 0.001) than during the fully fed diet
39 o the inactivating interaction of the copper-deprived N-metal binding extension with the headpiece do
44 ransfusion into recipient animals, these dox-deprived mature megakaryocytes generated functional plat
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
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
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
62 sed higher levels of BIM under growth factor-deprived conditions and reduced Mcl-1 on stimulation.
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
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
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
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
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
96 in previous studies from 18 monocularly form-deprived and 32 normal monkeys reared under ordinary lab
98 refractive errors in the two groups of form-deprived monkeys, either with or without foveal ablation
100 tropias, and in 6 of these monkeys, the form-deprived eyes were more hyperopic than their fellow eyes
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.
107 apoptosis by promoting autophagy in glucose-deprived cardiomyocytes in vitro and in post-myocardial
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
117 embly after readdition of glucose to glucose-deprived cells are controlled by the glycolysis flow.
121 Beginning 12 h after treatment, glucose-deprived human hepatocellular carcinoma (HepG2) cells de
123 al transcription, was decreased in glutamine-deprived cells, which corresponded with a dramatic reduc
125 paragine further proved crucial in glutamine-deprived ECs to restore protein synthesis, suppress ER s
127 cally integrated analyses showed how hormone-deprived LNCaP cells could transdifferentiate to a nonma
130 eless maintained surface Glut1 levels in IL3-deprived cells, possibly via enhanced recycling of inter
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
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
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
148 It has been demonstrated in mice that LC-deprived epithelia are rapidly replenished by short half
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
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
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
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
169 were either nicotine deprived (n = 12), non-deprived (n = 12) or deprived but were allowed to smoke
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
179 ved-eye response without a change in the non-deprived eye response, NR2A-knockout mice fail to exhibi
185 lmonary leukocyte cultures from T cell Notch-deprived mice produced less IFN-gamma, IL-5, and IL-13 t
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
191 icroenvironment is characterized by nutrient-deprived conditions in which the cancer cells have to ad
194 by its association with Beclin1 in nutrient-deprived cells, our studies revealed that HCV-mediated a
196 at could restore blood perfusion in nutrient-deprived regions where angiogenic resources are most nee
198 exploration-exploitation trade-off: nutrient-deprived flies focus on specific patches while satiated
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.
207 s miRNA mediates immunosuppression in oxygen-deprived regions of tumors where cancer stem-like cells
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
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
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
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
233 ession in CD230/PrP(C) was observed in serum-deprived cells in association with increased generation
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
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
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
257 cantly depolarized in Hcrt neurones in sleep-deprived mice as compared with controls (P < 0.01, t tes
261 significantly improved performance in sleep-deprived monkeys; however, the nasal delivery method was
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
269 ivation, and reduced aggression places sleep-deprived flies at a competitive disadvantage for obtaini
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.
276 retin-1 (orexin-A) was administered to sleep-deprived (30-36 h) rhesus monkeys immediately preceding
287 d in the draining lymph nodes (dLNs) in Treg-deprived mice, it was profoundly reduced at the infectio
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
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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