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1 ion of IFN-gamma by differentiated Th1 cells is more sensitive to 3-BrPa than is the production of IL
3 t predicted slopes of community size spectra are more sensitive to a given change or error in realize
4 t here that DCD-deficient mutants of E. coli are more sensitive to a series of different antibiotics,
5 , the timing of leaf emergence and flowering was more sensitive to a given increase in summer tempera
7 rate of self-renewal and proliferation, and were more sensitive to a panel of cancer drugs compared
9 nterestingly, STI1-haploinsufficient neurons were more sensitive to AbetaO-induced cell death and cou
13 a indicate that the stomata of Juniperus may be more sensitive to acid deposition than to increasing
14 ltahycB or DeltahycC single-deletion strains were more sensitive to acid than the wild-type strain, b
19 iminary evidence that LV twist mechanics may be more sensitive to adrenergic control in males than in
20 yte-specific PPAR-gamma knockout mice, which were more sensitive to adriamycin and not protected by s
22 our results show that IRF8-deficient B cells were more sensitive to Ag stimulation and were resistant
26 findings suggest that LV twist mechanics may be more sensitive to alterations in adrenergic stimulati
28 at animals exposed to alcohol in adolescence are more sensitive to an unexpected variation in reward
30 ccus aureus Further, a mutant S. aureus that is more sensitive to antimicrobial peptides was killed m
31 at paroxysmal nocturnal hemoglobinuria cells are more sensitive to APC-activated serum due to deficie
33 m PBMCs and pretreated with both HIV and LPS were more sensitive to apoptosis when cocultured with HI
37 s thaliana Pht1;5, cells expressing PvPht1;3 were more sensitive to arsenate, and accumulated more ar
38 ntly affected Rsoil , but Rsoil under shrubs was more sensitive to Asat than that under bunchgrasses.
39 that B. cinerea-infected Slshn3-RNAi plants are more sensitive to B. cinerea and produce more hydrog
40 bserved that a prpC mutant and a yvcK mutant were more sensitive to bacitracin compared with the WT s
43 ed that the aminopropyl moiety of spermidine is more sensitive to C-methylation, which it is essentia
44 capacity of Spop-null murine prostate cells was more sensitive to c-MYC inhibition than that of Spop
46 diac skinned fibres reconstituted with D145E are more sensitive to Ca(2+) than fibres reconstituted w
47 under low intensity UV, cells turned out to be more sensitive to cadmium, a priority pollutant widel
48 ed a new reversible near-infrared probe that is more sensitive to calcium as compared to other biolog
49 yomavirus middle T antigen in JNK2(-/-) mice were more sensitive to CDDP compared with those in JNK2(
51 assemblages from more constant environments were more sensitive to change leading to poorer function
52 e contacts tend to be cell-type specific and are more sensitive to changes in genome ploidy than the
53 measure rates of decline in mortality, which are more sensitive to changes in health policy than are
54 URM1 pathway proteins are unstable and hence are more sensitive to changes in the translational capac
55 has agonist binding, which has been shown to be more sensitive to changes in OR occupation than is an
56 provides complementary information that can be more sensitive to changes in the local chemical envir
57 lts suggest that territorial morphotypes may be more sensitive to changes in the spatial environment,
58 observation by showing that ExsA expression is more sensitive to changes in free RsmA than other mem
59 e strength of the monsoon in a climate model is more sensitive to changes in surface heat fluxes from
60 ority effects; and species whose growth rate is more sensitive to changes in the environment experien
63 parasites with an indirect life cycle would be more sensitive to changing environmental conditions t
64 iments revealed that the assembly of Abeta42 was more sensitive to chiral substitutions than was Abet
65 ed in vivo by proteases; the C5 V802 variant was more sensitive to cleavage with elastase and the "C5
68 lternatively, an M. tuberculosis ctpJ mutant is more sensitive to Co(2+) than Fe(2+), whereas mutatio
76 ade experiments demonstrated that Th17 cells are more sensitive to CTLA-4 coinhibition and therefore
78 In contrast, cell lines with low REST score were more sensitive to cytotoxic drugs including Mitomyc
79 ction mutants, as well as the d-LDH mutants, were more sensitive to d-lactate and MGO, indicating tha
80 Our results indicate that soil respiration was more sensitive to decreased than increased precipita
81 tory cytokines and matrix metalloproteinases were more sensitive to DEN induction in the absence of T
83 The modified Rankin Scale and Barthel Index were more sensitive to detecting changes in outcome than
85 derived from MR metrics that are thought to be more sensitive to differences in myelination (putativ
86 mulation scenarios showed that CSIA profiles are more sensitive to different degradation conditions c
87 amma is provided in trans, but these strains are more sensitive to DNA damage compared with strains t
89 rmore, R137Q mouse embryo fibroblasts (MEFs) were more sensitive to DNA-damaging reagents, such as me
90 d to be superior to antagonists because they are more sensitive to dopamine concentrations and may se
91 s it is possible that sign tracking behavior is more sensitive to dopamine modulation, we evaluated t
92 ng the unphosphorylated form of Numb by Plk1 are more sensitive to doxorubicin, a classical chemother
94 simulations show that maize yield reduction was more sensitive to drought stress than to heat stress
95 sis that autonomic cardiovascular regulation is more sensitive to E2 exposure in women with low ortho
96 Contrary to our hypothesis, the moth fauna was more sensitive to elevational differences within the
97 ponses in the gamma lobe, suggesting that it is more sensitive to elevations of cAMP and that it is r
100 4a), suggesting that DPCs from balding scalp are more sensitive to environmental stress than nonbaldi
102 ion and reduced both Tg and RH0, thus blends were more sensitive to environmental moisture than the i
111 tral Africa, and Oceania; these regions will be more sensitive to future climate change impacts.
112 important copepod species, Oithona spp., may be more sensitive to future high pCO2 conditions compare
113 of synaptic transmission by GABAB receptors is more sensitive to GABA than enhancement by GABAA rece
115 -scale climate oscillations) or whether they are more sensitive to global change effects that are loc
116 ents suggested that the intermingling degree was more sensitive to global changes in transcription th
119 under the control of their native promoters are more sensitive to heat stress (as indicated by incre
121 ralia (Faviidae, Poritidae, and Acroporidae) are more sensitive to heat stress than their hosts, exhi
122 ving in moderate cold and moderate hot areas are more sensitive to heat waves than those living in co
124 arlier flowering taxa, such as P. spachiana, were more sensitive to heat than later flowering taxa, s
127 uals with increased oxidative metabolism are be more sensitive to hepatotoxicity following PERC expos
130 ciferase gene in response to heat stress and was more sensitive to high temperature than the wild typ
131 ype, germination and establishment of ice1-2 were more sensitive to high glucose concentrations than
132 dence that stem cetaceans, the archaeocetes, were more sensitive to high-frequency sound than their t
134 osarcoma cells with elevated levels of hTdp1 were more sensitive to histone deacetylase inhibitors va
135 are unable to control the fungal burden and are more sensitive to Histoplasma infection than wild-ty
136 in neural crest cell development, some genes are more sensitive to hypoxia than others, demonstrating
137 cells overexpressing mitochondrial Omi/HtrA2 were more sensitive to hypoxia and reoxygenation (H/R) i
139 ed at hippocampal glutamatergic synapses and are more sensitive to ifenprodil, indicating an increase
140 nes with enhanced REST activity was found to be more sensitive to IGF1R, VEGFR and ABL inhibitors.
142 alence and prevalence stratified by subgroup were more sensitive to imputation method and settings.
143 er levels of labile iron in blood stages and are more sensitive to increased iron levels in liver sta
144 s suggests that soil moisture and Rs tend to be more sensitive to increased precipitation in more ari
145 he number of cancer stem cells (CSCs), which are more sensitive to induction of DICE than non-CSC, wh
146 ase-dependent apoptosis in HeLa cells, which are more sensitive to inhibition by 1 in the presence of
148 rowth of Arabidopsis thaliana seedling roots is more sensitive to inhibition by A2C than is cotyledon
150 euroblastoma and monocyte cell lines; and 4) was more sensitive to inhibition by N-butyldeoxynojirimy
151 c mutations in the autoinhibitory domain and was more sensitive to inhibition of the kinase as compar
152 ells, a number of resistant cell populations were more sensitive to inhibition by the MEK inhibitor s
153 operated only in this axon population, which was more sensitive to injury than neighboring myelinated
154 suggesting that the RRV-T48-nsP1(6M) mutant is more sensitive to innate antiviral effectors than RRV
157 cantly reduced levels of iron and copper and was more sensitive to iron and copper toxicity than its
158 confirmed by observing that the luxS mutant was more sensitive to killing by hydrogen peroxide, sugg
159 hat transformed proliferating cells from HCC are more sensitive to knockdown of integrins than normal
160 uced, suggesting that primary body formation is more sensitive to Lfng dosage than is secondary body
161 n-2 is less processive, and its processivity is more sensitive to load, suggesting that processivity
168 , adolescent rats took cocaine more readily, were more sensitive to lower doses, showed greater escal
169 with increased KRAS mutant allele frequency were more sensitive to MAP kinase inhibition, and CRISPR
173 ocytes, Caucasian skin-derived keratinocytes were more sensitive to melanosome treatment as shown by
177 rast to DMC1, joint molecules formed by HOP2 are more sensitive to mismatches and are efficiently dis
179 increased expression of Mn transporters and were more sensitive to Mn toxicity than null plants.
181 results suggest that anxiety-like behaviour is more sensitive to modulation of serotonin than is agg
182 f tonic inhibition in the dentate gyrus that was more sensitive to modulation by the anesthetic etomi
183 positions suggests that tropical rainforests are more sensitive to moisture deficits than high temper
184 The probe hybridization signal was found to be more sensitive to molecular crowding, whereas the apt
185 rial energetics and BSEP functional activity are more sensitive to more severe manifestations of DILI
186 predominantly mitochondrion-targeted CYP2D6 were more sensitive to MPTP-mediated mitochondrial respi
187 This suggests that the benthic community was more sensitive to MWCNTs than to the bulk carbon mat
189 nally, aqueous drainage from Cav-1(-/-) eyes was more sensitive to nitric oxide (NO) synthase inhibit
190 us species and those with animal-based diets were more sensitive to noise than birds with plant-based
192 timulated regions have much longer cilia and are more sensitive to odorants than those in weakly stim
194 A and the double DeltampkC DeltasakA mutants were more sensitive to osmotic and oxidative stresses, a
195 hA DeltasakA and DeltaschA DeltampkC mutants were more sensitive to osmotic stress than the correspon
196 yofibrillar proteins from alpha-white fibres were more sensitive to oxidation and thermal denaturatio
197 oncogenic effect, cells with TSC deficiency were more sensitive to oxidative stress and dependent on
200 ontrary, we found that bok-deficient neurons were more sensitive to oxygen/glucose deprivation-induce
206 ion of microsatellite repeat-containing RNAs is more sensitive to perturbation than transcription of
207 predicts that early-successional ecosystems are more sensitive to perturbations than mature systems,
208 r, TCS new (TCSn), which, compared with TCS, is more sensitive to phosphorelay signaling in Arabidops
209 els of Hypoxia Inducible Factor (HIF)-2alpha are more sensitive to physapubescin-mediated apoptosis a
210 tem we examined if green (grazing) food webs are more sensitive to plant invasions compared to brown
211 least in the present cohort, this technique was more sensitive to PRD changes than was quantitative
212 ipitation additions and reductions, but ANPP was more sensitive to precipitation additions than reduc
213 Across functional groups, radial growth was more sensitive to precipitation distribution, such a
214 expressed in cls leaves, and cls protoplasts are more sensitive to programmed cell death effectors, U
215 ., [1-3]), whereas the right hemisphere (RH) is more sensitive to prosodic (suprasegmental) cues.
216 ed to the B2.3/4 particles, the B1 particles were more sensitive to protease digestion and had greate
217 that AML samples bearing FLT3-ITD mutations are more sensitive to proteasome inhibitors than wild-ty
218 1) morphometric analyses of cardiac function are more sensitive to proximal effects of crude oil-deri
219 e symptoms implies that the human genome may be more sensitive to qualitative variations in well-bein
220 hat PANC1 xenografts treated with clofibrate are more sensitive to radiation than untreated xenograft
221 s argue that 0.5 mL subvolumes of tumors may be more sensitive to radiation and may need less radiati
222 glioblastoma cells, but p53 wild-type cells were more sensitive to radiation and photofrin doses tha
223 n contrast, induction of NF-kappaB signaling was more sensitive to reduced affinity between TRIM21 an
224 rized monolayers, Myo1c-knockdown (KD) cells were more sensitive to reduced calcium concentration.
225 le measurements within continental interiors are more sensitive to regional flux deeper into the cold
228 Compared to highway vehicles, VSP for OSVs is more sensitive to rolling resistance and less sensiti
230 y) with salinity, suggesting rare taxa might be more sensitive to salinity than their abundant counte
231 In agreement, plants deficient for SERF1 are more sensitive to salt stress compared with the wild
236 , since nonacclimated pdat1 mutant seedlings were more sensitive to severe heat stress, as indicated
239 t daily timescales, rates of carbon exchange were more sensitive to soil moisture variation in grassl
240 Adsorption equilibrium on the strong sites was more sensitive to solution conditions than overall r
243 cell lines harboring high levels of pY128Cas are more sensitive to SRC family kinase inhibitor Dasati
244 hibitory neurons, whereas excitatory neurons are more sensitive to stimulus specific bottom-up inputs
245 hermore, it better models MAO inhibition and is more sensitive to stress-induced reinstatement than n
246 Across a wide range of estimates, models were more sensitive to structural assumptions about link
247 ned spatiotemporal structure of networks may be more sensitive to subtle network changes that accompa
248 that B6 terminals, relative to D2 terminals, were more sensitive to synaptic fatigue principally beca
249 and found that hourly precipitation extreme was more sensitive to temperature than other categories
250 d at higher temperatures because respiration was more sensitive to temperature than photosynthesis me
254 hat EpCAM(+) HCC cells cultured as spheroids are more sensitive to TGF/beta-induced epithelial-mesenc
256 schizophrenia and suggest that these animals are more sensitive to the effects of stress in youth.
258 ble strategy-emerge later in development and are more sensitive to the influence of social norms.
259 ls from CIE mice, suggesting that DR neurons are more sensitive to the inhibitory effects of acute et
260 yrotropin in samples collected from the cord are more sensitive to the iodine status of mothers; howe
261 ttings: First, we show that triallelic sites are more sensitive to the parameters of a population tha
262 f parental divorce or high genetic liability are more sensitive to the pathogenic effects of PD.
263 ese data could indicate that individuals who are more sensitive to the sensory properties of food hav
264 Conversely, MetS subjects without IR may be more sensitive to the detrimental effects of HSFA int
265 and indicates that marine top predators may be more sensitive to the rate of ocean warming rather th
268 o viral infections and that the Th1 response is more sensitive to the level of miR-17-92 expression.
271 ailed to inhibit DTMUV in avian cells, DTMUV was more sensitive to the antiviral effects of type I in
272 les were less numerous and their trafficking was more sensitive to the inhibitory effects of Vps4A-EQ
273 However, remarkably, children with autism were more sensitive to the average direction in the pres
276 st 2,5-dimethoxy-4-iodoamphetamine (DOI) and were more sensitive to the effects of the selective 5-HT
277 cells grown out of the blood of PAH patients were more sensitive to the effects of type I IFN than ce
278 studies demonstrated that these two mutants were more sensitive to the expression of the interferon-
279 Further studies showed that these mutants were more sensitive to the expression of the interferon-
281 ndance, transgenic plants overexpressing KEG were more sensitive to the inhibitory effects of formate
283 ted with increased mitochondrial density and were more sensitive to the mitochondrial Ca(2)(+) unipor
286 vation in response to O3 Further, aging glia were more sensitive to the proinflammatory effects of O3
287 ing endogenous and engineered DDR2 mutations were more sensitive to the SFK inhibitor dasatinib than
289 ceptibility, and that central Red Sea corals are more sensitive to thermal anomalies as compared to t
291 K-Ras dependency, as K-Ras-independent cells are more sensitive to topoisomerase inhibitors, and depl
294 ity profiles, we predicted BUB1B(S) cells to be more sensitive to type I and II topoisomerase inhibit
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