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1 y hypersensitivity (also called sensory over-responsivity).
2 survival [DFS]) stratified by anti-HER2 Th1 responsivity.
3 ntegrate social information to modulate fear responsivity.
4 ce striatal, insular, and Rolandic operculum responsivity.
5 ic suppression of net motor excitability and responsivity.
6 ower function decrease following the peak of responsivity.
7 ssion could contribute to the reduced L-DOPA responsivity.
8 r plants sense temperature changes with high responsivity.
9 d is implicated in anxiety, pain, and stress responsivity.
10 n the visible light spectrum with high photo responsivity.
11 85~88% (VIS) and 26~40% (NIR) of theoretical responsivity.
12 35965, or CRF and were evaluated for stress responsivity.
13 tile stimulation and positively with tactile responsivity.
14 played significantly reduced HPA stress axis responsivity.
15 of HC function combined with a high frontal responsivity.
16 uring, but not after, the return of integrin responsivity.
17 ting palatable food contributes to increased responsivity.
18 r whether segmentation is an artifact of cue responsivity.
19 on nucleus accumbens medial shell and stress responsivity.
20 e used to endow insulin analogs with glucose responsivity.
21 ern is designed optimally for maximizing the responsivity.
22 ble to near-infrared photodetector with high responsivities.
23 logarithmic fit characterized by exceptional responsivity (20.89 Omega/pg mL(-1)), reproducibility (R
24 nm), an indirect bandgap, photoconductivity (responsivity = 4 +/- 1 mA/W), and stability for months i
25 h current gain (53.6), bandwidth (7 GHz) and responsivity (9.5 A/W) using a single crystalline indium
26 functional connectome in relation to reward responsivity across a population of adults with heteroge
27 creased baseline LC activity enhances neural responsivity across cortex and widening of attention to
30 showed blunted behavioral and cardiovascular responsivity after control infusions, which was normaliz
31 14-layer structures, MoS2 offers the highest responsivity among graphene, h-BN, and MoS2 devices and
33 e combination of ultra-broad bandwidth, high responsivities and fast operating speeds affords new opp
34 atter, however, exhibit significantly higher responsivities and quantum efficiencies, with similar da
37 tonergic changes in brain regions modulating responsivity and behavioral impairment were both prevent
39 ally driven by group differences in baseline responsivity and by opposite changes in neural activatio
41 e antennas have great promise for increasing responsivity and detection sensitivity of conventional p
42 sistors as a function of temperature and the responsivity and detectivity of the mid-IR photoconducto
44 baseline LC activity globally dampens neural responsivity and is associated with adaptive deployment
45 nsible for the temperature dependence of the responsivity and NEP of the GaN HEMT are also analyzed t
48 ir heightened hypothalamic-pituitary-adrenal responsivity and reduced stress-induced cognitive impair
49 reflected general antidepressant medication responsivity and related differentially to a repetitive
52 F]fallypride and d-amphetamine to measure DA responsivity and separately completed the effort expendi
53 ndous individual differences exist in stress responsivity and social defeat stress is a key approach
55 h the importance of SKA2 for cortisol stress responsivity and the development of PTSD and provide fur
56 the 2D MoS2 with metallic MoS2 showing high responsivity and the semiconducting phase exhibiting hig
57 postfertilization to alter offspring stress responsivity and, using zygote microinjection of the nin
58 MOR variants that may predict altered opioid responsivity and/or dependence in this subset of individ
59 selective detection ( approximately 5-8 V/W responsivity) and sensitivity performances (signal-to-no
60 estimation of insulin sensitivity, beta-cell responsivity, and hepatic insulin extraction from a mixe
62 d by increased stress-induced locomotion and responsivity, and reduced risk-aversion/fearfulness.
63 , stress-induced potentiation of amphetamine responsivity, and the increase in DA associated with str
64 ypically due to early absorption cutoff, low responsivity, and/or large dark/noise current under bias
66 adolescents who show elevated reward region responsivity are at increased risk for initial onset of
68 y, risk-taking behavior, and elevated stress responsivity are prominent symptoms of mania, a behavior
72 nput optical power as low as 6.2 pW with the responsivity as high as 2.4 x 10(7) A/W when operating a
74 ugh photoconductive gain mechanisms, achieve responsivity as large as 10(7) A W(-1) and a detectivity
75 tate EEG signature indexed prefrontal neural responsivity, as measured by concurrent transcranial mag
76 llel charge-voltage conversion and different responsivity at each pixel induces extra readout and pat
78 eshold voltage, the device showed fairly low responsivities but fast response times, as well as a con
79 tation produced indistinguishable effects on responsivity but caused opposite shifts in tuning prefer
83 ths, with three orders of magnitude enhanced responsivity compared to pristine graphene photodetector
84 hat heightened dopaminergic prediction error responsivity contributes to adolescent reward seeking.
86 over 1-year follow-up, but reward circuitry responsivity did not predict future overweight/obesity o
88 ship between insulin secretion and beta-cell responsivity differed significantly between genotypes.
91 nal surfaces that exhibit complex multimodal responsivity, e.g., to light, heat, pH, etc., although h
92 tional care in infancy show reduced HPA axis responsivity, even years after they are placed in suppor
93 o those without demonstrated heightened fear responsivity, exaggerated and prolonged corticosterone r
95 has been achieved and shows an extraordinary responsivity exceeding 2600 A W(-1) with fast photorespo
96 in damage, are unable to show any behavioral responsivity, expose the limits of the neuromuscular sys
97 sic emotional operations (e.g., recognition, responsivity, expression), through to high-order, comple
98 ry was associated with reduced reward region responsivity, extending results from studies that compar
101 inear regression was used to estimate neural responsivity for each individual, namely the capacity to
102 This is accompanied by a shift in cortical responsivity from sensory (posterior) regions to executi
103 to the mid-infrared range, with mid-infrared responsivity higher than 1 A W(-1), as required by most
104 t a systematic study of the intrinsic motion responsivity in 2D nanomechanical systems using a Fresne
106 ss dark current density while retaining high responsivity in an ultrasensitive nonfullerene OPD.
108 oattractant protein-1, together with reduced responsivity in diastolic BP, heart rate, and cortisol,
109 ate at signal modulation surpassing -100 dB, responsivity in excess of -600 dB.V(-1) and switching ra
110 k for obesity show elevated reward circuitry responsivity in general, coupled with elevated somatosen
111 , is related to a reduction in reward-region responsivity in humans, paralleling the tolerance observ
113 histone acetylation of Cdk5 regulates stress responsivity in male mice, we hypothesized that such a m
114 ng that PDE11A4 negatively regulates lithium responsivity in mice suggests that the PDE11A SNPs ident
116 2 calcium imaging was used to assess glucose responsivity in neurons isolated from the MAN and single
121 hese findings suggest that heightened reward responsivity in the brain to food and sexual cues is ass
123 ci of dysconnectivity associated with reward responsivity in the nucleus accumbens, the default mode
125 and consistent with altered offspring stress responsivity, including increased expression of glucocor
126 little dopamine signaling and reward region responsivity increases risk for overeating, suggesting q
136 ngs show that a relative reduction in neural responsivity is correlated to the behavioural effect.
139 hermally responsive nanoparticles, where the responsivity is endowed by a responsive polymeric corona
140 Based on clinical observations, sensory over-responsivity is hypothesized to reflect atypical neural
141 charge/discharge, and reliable environmental responsivity is made by using multi-scale conjugated blo
145 disrupted within the IT cortex, whereas face responsivity (neutral faces > scrambled faces) and face
146 than 430 MOmega K(-1) below 6 K), leading to responsivities of 1 x 10(10) V W(-1), a figure that is f
147 ntact disorder to modulate the light and gas responsivities of the device; unexpectedly, it multiplie
149 , 25% quantum efficiency (corresponding to a responsivity of 0.31 A/W), 3 GHz bandwidth, and 30 nA da
150 tectors exhibit room-temperature (300K) peak responsivity of 0.6 A/W at ~1.7 mum, corresponding to a
151 a cut-off wavelength at ~1.7 mum and gives a responsivity of 1.5 AW(-1) and implied detectivity of 6.
152 strate a high open-circuit voltage of 1.3 V, responsivity of 10.1 A W(-1) , specific detectivity of 9
155 tion of 12.43 fm Hz(-1/2) and an outstanding responsivity of 170 nV fm(-1), which is comparable to th
157 room temperature that exhibits a remarkable responsivity of 2900 VW(-1), detectivity of 1.1 x 10(9)
158 ate interfacial design, a record high device responsivity of 4.5 x 10(3) A/W at 7 V is achieved, indi
159 hotodetector exhibits a peak extrinsic photo-responsivity of 518, 30, and 2.2 mA W(-1) at 3.4, 5, and
160 frared photo-transistor is fabricated with a responsivity of 97.5 A W(-1) and detectivity of 1.17 x 1
162 ow dark current of a photodiode and the high responsivity of a photoconductor ( approximately 721-1,0
165 re, we compared the influence of 5-HT on the responsivity of brain dynamics during facial-emotion pro
166 n the light absorption layer can improve the responsivity of graphene photodetectors to approximately
169 neurochemically mediated differences in the responsivity of key 'limbic' regions (including amygdala
170 a 'junk-food' diet, consistent with greater responsivity of mesolimbic circuits in obesity-susceptib
173 weight gain is associated with a decrease in responsivity of regions associated with taste and reward
174 3 year follow-up period show an increase in responsivity of reward and attention regions to a cue si
175 l that obese versus lean humans show greater responsivity of reward and attention regions to palatabl
176 d that this overeating may further attenuate responsivity of reward circuitry in a feedforward proces
178 otypes per a multilocus composite, show less responsivity of reward regions that primarily rely on DA
179 gained body fat did not show a reduction in responsivity of reward regions to milkshake receipt or c
180 shake receipt and a simultaneous decrease in responsivity of reward regions to milkshake receipt vers
181 on regions to palatable food cues, but lower responsivity of reward regions to palatable food receipt
185 ualification, such as linearity and spectral responsivity of the detection system, spectral irradianc
187 ith subjective ratings of itchiness, and the responsivity of the left BA44 reflected individual diffe
191 model-based fMRI analysis revealed a reduced responsivity of the ventral striatum to reward predictio
192 No differences were found regarding the responsivity of the ventral striatum to the receipt of a
194 on-graphene conductive photodetector shows a responsivity of up to 10(5 )A/W at room temperature (27
195 ngth-specific detection, with an input power responsivity of up to 38 V W(-1), referenced to incident
197 -4Cl, are presented, showcasing a remarkable responsivity over 0.5 A W(-1) in the NIR spectral region
198 o induced a pronounced increase in beta-cell responsivity (PHItotal) that was largely due to an enhan
199 Owing to their tunable bandgaps, the peak responsivity position and photoresponse edge of Se(x) Te
200 emerged, with delta and beta band (3/15 Hz) responsivity prevailing in the right hemisphere and thet
202 recise fashion that early childhood parental responsivity prospectively and independently predicts st
205 d hypothalamic-pituitary-adrenal stress axis responsivity, recapitulating phenotypes previously repor
206 b and chemotherapy), depressed anti-HER2 Th1 responsivity (recurrence, 2 of 25 [8%], vs nonrecurrence
207 um chow for 3+ weeks exhibit greater lithium responsivity relative to wild-type (WT) littermates in t
209 r controlling for confounding, anti-HER2 Th1 responsivity remained independently associated with recu
210 elper type 1 response metrics were anti-HER2 responsivity, repertoire (number of reactive peptides),
212 ons, combined with excess subcortical limbic responsivity, resulting in the selection of foods most c
214 e for experimental investigations into their responsivity, sensitivity, and roles in sensory acquisit
215 nse food results in attenuated reward-region responsivity specifically to that food, which suggests t
216 gest that distributed, multi-component brain responsivity supports cognition across the adult lifespa
217 ab plus chemotherapy-treated patients by Th1 responsivity, Th1-nonresponsive patients demonstrated a
219 evice with significantly larger photocurrent responsivity than previously reported antenna-based geom
220 ship between a dimensional measure of reward responsivity (the reward sensitivity subscale of the Beh
221 ) (pTEGMA) that exhibits significant thermal responsivity; the resulting hydrogels collapsed by up to
222 advantages of the exceptional-point-enhanced responsivity, they do show that the fundamental sensitiv
223 lectronic nose system, which showed improved responsivities to low molecular weight alcohols compared
224 ession in 16 SLC6A4 genotyped marmosets with responsivity to 5HT(2A) antagonism during the human intr
227 hertz sensors are typically limited in their responsivity to a narrow slice of the incident field pro
228 with decreased cardiovascular and behavioral responsivity to acute stressors in humans that may incre
230 unctional MRI tasks, which measured amygdala responsivity to angry facial expressions and ventral str
232 es of the high trait anxious phenotype: high responsivity to anxiety-provoking stimuli and an exagger
233 the high trait-like anxiety phenotype: high responsivity to anxiety-provoking uncertain threat and r
234 c field significantly reduces the biological responsivity to blue light of the cryptochrome receptor
236 lly indicative of altered norepinephrinergic responsivity to changes in this aspect of environmental
237 nty-one days after FLX treatment, behavioral responsivity to cocaine (0, 2.5, 5, 10, or 20 mg/kg) con
238 s, and propelled by both impulsivity and the responsivity to cocaine-linked cues ('cue reactivity').
241 p period experienced an increase in striatal responsivity to cues for palatable foods compared to tho
242 rovide evidence that differential behavioral responsivity to E2-WD in PMD reflects intrinsic differen
243 Single neurons exhibited diverse mixtures of responsivity to each of the three actions and these mixt
244 Weight gain leads to reduced reward-region responsivity to energy-dense food receipt, and consumpti
246 er attention-, gustatory-, and reward-region responsivity to food cues but reduced reward-region resp
247 d period of overeating may increase striatal responsivity to food cues, and that maintaining a balanc
248 ce striatal, insular, and Rolandic operculum responsivity to food cues, which might decrease risk for
251 , coupled with elevated somatosensory region responsivity to food, which may lead to overeating that
252 an alternate context after conditioning and responsivity to foot shock were unaffected by optogeneti
254 data demonstrate that by diversifying their responsivity to growth cues, distinct coronary progenito
257 ow NPY expression, thereby increasing neural responsivity to negative stimuli within key affective ci
258 muscle is necessary for normal postsynaptic responsivity to neurotransmitter release and for normal
259 ; no interactions were apparent for amygdala responsivity to neutral faces, or striatal responsivity
265 logy in depotentiating neural and behavioral responsivity to prior emotional events remains unknown.
266 d regions to milkshake receipt or changes in responsivity to receipt and anticipated receipt of monet
268 eceptor BP(ND), including study of DA system responsivity to rewarding stimuli, and increasing power
269 terized by greater motor activity, increased responsivity to sensory stimuli, and greater emotional l
272 D70; adulthood) we examined their behavioral responsivity to sucrose (1%) on a two-bottle choice desi
273 difference in within-network connectivity or responsivity to syntactic processing demands despite gra
274 d to relate to dopamine D2 receptor density (responsivity to tactile stimuli, performance on a learni
275 of cell firing; (8) ketamine reduces network responsivity to the environment; (9) ketamine effect cou
276 e, OCD patients reported increased emotional responsivity to the outcomes of their choices and to the
279 zation, which may contribute to the enhanced responsivity to uncertain rewards or the reinforcing eff
280 veractivation was found to induce heightened responsivity to uncertain, low-imminence threat while bl
282 ty of nil or negative effect in language and responsivity to vowel change (P1: ES-0.62, CI -2.42 to 0
283 ometry because of, in most cases, their poor responsivities toward nuclear magnetic resonance, ultrav
285 ualize the dependence of motion transduction responsivity upon 2D material type and number of layers,
288 mp recordings revealed that EGC subthreshold responsivity was far broader than indicated by GCaMP6f C
290 children living in poverty, amygdala threat responsivity was positively associated with inflammation
293 ces where the adult showed greater autonomic responsivity were associated with faster infant quieting
295 hene conductive photodetector has ultra-high responsivity when operating at low temperature, which pr
296 he threshold voltage, the device showed high responsivities with additional gain, but slow rise and r
299 We show that sleep deprivation enhances pain responsivity within the primary sensing regions of the b