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2 inding enhanced TRPA1 sensitivity and Ca(2+)-evoked potentiation of TRPA1 at low Ca(2+), but inhibite
4 ed responses did not affect any of the CCK-8-evoked responses, indicating that rather than acting on
6 Lastly, peptidergic corelease enhances ACh-evoked responses in MBONs, suggesting an interaction bet
7 eneral mucosal innervation by comparing acid-evoked c-Fos in wild-type and "taste blind" P2X2 /P2X3 d
10 to cause a significant reduction of activity-evoked release at two types of fast inhibitory synapses
13 ells, mitral cells have a prolonged afferent-evoked EPSC, which serves to amplify the synaptic input.
15 om epileptic mice displayed enhanced agonist-evoked P2X7 receptor currents, and synaptosomes from the
17 late Reader (FLIPR) assay to monitor agonist-evoked Ca(2+) signals in human primary skin fibroblasts.
22 phenotypes: (1) membrane excitability and AP-evoked Ca(2+) entry were impaired at synapses and (2) AP
23 (2) Na(+) channel beta2 subunits modulate AP-evoked Ca(2+)-influx, and (3) beta2 subunits maintain su
24 d macrophages and receptors that mediate ATP-evoked intracellular [Ca(2+)]i signals and cytokine prod
25 for P2X4 in determining the duration of ATP-evoked Ca(2+) responses and CXCL5 secretion in human pri
28 bit the potentiation without affecting basal-evoked NMDA currents, indicating that NMDAR-GluN2B recep
30 orward inhibition circuit, through which BLA-evoked activation of NAc shell (NAcSh) MSNs was fine-tun
32 It exists in distinct forms, including brush-evoked dynamic and filament-evoked punctate hypersensiti
33 bx1 (VT3(Lbx1) neurons): the mice lost brush-evoked nocifensive responses and conditional place avers
34 ise exposure, nor were click- or noise-burst-evoked auditory brainstem response thresholds different
35 erm dynamics and temporal summation of burst-evoked EPSPs were cell-type dependent: in principal cell
36 lated proton secretion, whereby the caffeine-evoked effect was (i) shown to depend on one of its cogn
38 thione levels are reduced, astrocyte calcium-evoked release of PgE2 is decreased and vasodilation tri
39 table asthma exhibited exaggerated capsaicin-evoked cough responses consistent with neuronal dysfunct
44 reatment that completely blocked all the Cch-evoked responses did not affect any of the CCK-8-evoked
45 ransfer and complete Freund's adjuvant (CFA)-evoked active immunization models compared to the refere
51 RTN-specific knockdown of Nalcn reduced CO2-evoked neuronal activation and breathing; hypoxic hyperv
53 ory cytokine interleukin (IL)-1beta with CO2-evoked responses was investigated using microglial block
55 s involved selectively in D1-MSNs in cocaine-evoked neuronal activity-mediated feedback regulation of
56 ecific effects of NMUR2 knockdown on cocaine-evoked locomotion were evaluated using viral-mediated RN
57 orexin receptor antagonist, reduced cocaine-evoked premature responses in 5-CSRTT when administered
59 ken together, these data reveal that cocaine-evoked synaptic plasticity in PL-mPFC is reversible in v
60 emory reactivation would reverse the cocaine-evoked plasticity and/or disrupt the cocaine-associated
61 emory reconsolidation), reverses the cocaine-evoked presynaptic and postsynaptic modifications in PL-
62 he rRPa of anaesthetized rats decreased cold-evoked BAT sympathetic nerve activity (SNA, nadirs: -72
64 e DLPFC measured as potentiation of cortical-evoked activity using paired associative stimulation (a
67 macological methods, we demonstrate that cue-evoked acetylcholine release, through distinct actions a
73 03V mutation nearly abolishes depolarization-evoked exocytosis (measured by membrane capacitance) and
76 nezumab on the cortical spreading depression-evoked activation of mechanosensitive primary afferent m
79 uits and design of protocols to reverse drug-evoked plasticity and to establish links of causality wi
82 concentration-dependently depressed C-fiber-evoked potentials in rats receiving spinal nerve ligatio
83 uced long-term potentiation (LTP) of C-fiber-evoked potentials, revealing a constituent role of both
87 d (74% of bladder capacity) above which flow-evoked bladder contractions were 252% larger and evoked
88 ered subunit stoichiometry or decreased GABA-evoked whole-cell current amplitudes, but with different
90 potentiates sub-maximal but not maximal GABA-evoked currents mediated by alpha1beta2gamma2 receptors,
91 nalysis revealed a reduction in maximal GABA-evoked Popen , suggesting impaired agonist efficacy.
95 1,1-dioxide (BPAM344) potentiated glutamate-evoked currents of GluK2a 21-fold at the highest concent
96 uM, whereas no potentiation of the glutamate-evoked response was observed for 7-chloro-4-(2-fluoroeth
99 is continuum, we observed an increase in GVS-evoked hand force, with a simultaneous reduction in grou
100 ring LG, hand force was secondary to the GVS-evoked body sway response, indicating that the arm perfo
101 isotropy, FG skewed the direction of the GVS-evoked GRF vector towards the axis of baseline postural
102 gnetoencephalography, we show that heartbeat-evoked responses (HERs) in the DN covary with the self-r
103 he FGF13/Nav1.7 interaction reduced the heat-evoked action potential firing and nociceptive behavior.
104 leads to a reduction in ongoing hippocampal-evoked MSNs responses through the combined recruitment o
106 gative Rab35 mutant both inhibited histamine-evoked secretion of the WPB cargos von Willebrand factor
107 ating proteins (RabGAPs) inhibited histamine-evoked, Ca(2+)-dependent WPB exocytosis, presumably by i
108 w that cAMP mediates inhibition of histamine-evoked Ca(2+) signals by PGE2 Exchange proteins activate
109 We conclude that inhibition of histamine-evoked Ca(2+) signals by PGE2 occurs through "hyperactiv
111 , the small GTPase Arf6, supported histamine-evoked WPB exocytosis, as shown by knockdown and overexp
113 suggest that prolonged and aberrant hormone-evoked Ca(2+) increases may stimulate the production of
116 kout mice exhibited significantly fewer 5-HT-evoked scratching bouts compared with wild-type mice.
117 r the efficient generation of synaptic input-evoked nuclear calcium transients driving the expression
118 rief exposure to the neuropeptide kisspeptin-evoked long-lasting Ca(2+) plateaus that persisted for t
119 ferent regulatory mechanisms in the learning-evoked changes that occur in the VTA with repeated expos
123 potential (TRP) channels to integrate light-evoked signals with ambient mechanical, chemical and tem
125 short near-infrared pulses to modulate light-evoked ionic current from Channelrhodopsin-2 (ChR2) in b
128 sponsible for the direct inhibition of light-evoked spike responses, the slow inhibition of spiking a
129 To test this possibility, we recorded light-evoked Ca(2+) responses from dendrites of individual GAC
130 specific NAc core inputs, we recorded light-evoked excitatory postsynaptic currents following viral-
137 ion cells (RGCs) that controls mouse looming-evoked defensive responses through axonal collaterals to
141 cranial magnetic stimulation (TMS), 25 motor-evoked potentials (MEPs) were recorded before, and 10 ti
142 transcranial magnetic stimulation and motor-evoked potentials while healthy humans watched videos of
144 excitability and RT, such that larger motor-evoked potentials (MEPs) measured at rest were associate
146 e effect of ulnar nerve stimulation on motor-evoked potentials (MEPs) elicited by transcranial magnet
147 results show that the amplitude of the motor-evoked potentials recorded from the real hand is signifi
148 ospinal excitability was measured with motor-evoked potentials under transcranial magnetic stimulatio
149 strating cholinergic modulation of naturally-evoked and behaviorally-relevant dopamine signaling, the
150 iniature endplate currents (mEPCs) and nerve-evoked EPCs (eEPCs) under voltage-clamp, which, unlike c
151 s to have only subtle consequences for nerve-evoked excitatory postsynaptic currents: vesicle heterog
152 cident NMDAR activation and can augment NMDA-evoked currents with high intracellular Ca(2+) buffering
153 mulation requires IP3Rs and can depress NMDA-evoked currents with modest intracellular Ca(2+) bufferi
155 spine density, concomitant with reduced NMDA-evoked currents and impaired NMDAR-dependent insertion o
160 Our results show that, by allowing odor-evoked suppression as well as excitation, the responsive
163 ted that a bidirectional code with both odor-evoked inhibition and excitation in single olfactory sen
164 th olfactory and orbitofrontal cortical odor-evoked activity, which is expressed in a performance- an
165 show that D. sechellia exhibits derived odor-evoked attraction and physiological sensitivity to the a
167 tral and tufted cells display different odor-evoked responses and are thought to form parallel channe
170 the patterning of plCoA and PCx inputs, odor-evoked neural ensembles in both areas are equally capabl
171 hip, we used optical imaging to observe odor-evoked activity in populations of olfactory bulb inhibit
173 ities and distinct temporal patterns of odor-evoked responses in MCs and TCs emerge in part due to di
174 ation revealed that exhalation preceded odor-evoked activity and reversible inactivation of olfactory
175 activity upon familiarization requires odor-evoked activity in the dopaminergic neuron innervating t
176 mygdala nonetheless strongly suppressed odor-evoked activity in GABAergic inhibitory interneuron popu
177 VP2 neurons preferentially inhibits the odor-evoked activity of avoidance-directing MBONs and odor-dr
178 ivation preferentially strengthened the odor-evoked synaptic output of weakly activated populations o
181 erall modest increase in resting and odorant-evoked responses during serotonergic afferent stimulatio
182 zed and awake mice to visualize both odorant-evoked excitation and suppression in OB output neurons (
183 optical neurophysiology to visualize odorant-evoked OSN synaptic output into olfactory bub glomeruli
186 inoadamantane-2-carboxylic acid derived P2X7-evoked glutamate release inhibitor and 4-amino-tetrahydr
187 aptic receptors, and that of globus pallidus-evoked inputs is mediated by presynaptic receptors.
190 nistration of VU6001221 attenuated potassium-evoked ACh levels in prefrontal cortex measured with in
191 n of synaptic efficacy, and action potential-evoked and spontaneous neurotransmission can be segregat
192 evel.SIGNIFICANCE STATEMENT Action potential-evoked and spontaneous neurotransmission have been obser
194 neurotransmission, whereas action potential-evoked neurotransmission remained relatively normal.
195 vous system (CNS) synapses, action potential-evoked neurotransmitter release is principally mediated
201 slices, we determined whether flow/pressure-evoked increases or decreases in parenchymal arteriole v
206 is effect was present in ongoing and sensory-evoked activity and was not replicated by acute ketamine
207 stematically tracked spontaneous and sensory-evoked activity with extracellular recordings of primary
211 requisite for the full expression of sensory-evoked NVC responses, indicating that ACh may alter the
214 ins of an interneuron RIA, where the sensory-evoked signal suppresses the motor-encoding signal to tr
215 resynaptic inhibition and changes to sensory-evoked reflexes, arguing that the RORbeta inhibitory INs
218 electroencephalography, absent somatosensory-evoked potential, absent pupillary or corneal reflexes,
219 er clinical, neurophysiologic (somatosensory-evoked potential), and biochemical prognosticators.
222 ure thalamocortical input layer 4, and sound-evoked spike latencies were longer in layer 4 than in su
224 essively weaker following denervation, sound-evoked activity in the cortex-and, to a lesser extent, t
226 brain, and in-vivo optical imaging of sound-evoked activity was achieved through the electrophoretic
227 brainstem of cats, spatial patterns of sound-evoked Ve can resemble, strikingly, Ve generated by curr
233 indings indicate that deep brain stimulation-evoked functional activation maps obtained intraoperativ
234 c activation of D1R-SPNs reduces stimulation-evoked dopamine release and that bath application of a K
235 tion is how STRF maturation affects stimulus-evoked correlated activity between pairs of LGN neurons
237 nd that fluctuations in ongoing and stimulus-evoked population activity in primate visual cortex modu
238 mportant question to answer because stimulus-evoked correlated activity likely plays a role in establ
239 , the spatial relationships between stimulus-evoked BOLD activations and local correlations of BOLD s
240 The modeled neurons showed both stimulus-evoked activity and spontaneous activity under physiolog
241 o-photon microscopy to record light stimulus-evoked Ca(2+) signals in cone axon terminals and horizon
242 troencephalography (EEG) to measure stimulus-evoked visual responses from human subjects while they p
243 urves and bidirectionally modulates stimulus-evoked activity patterns and improves auditory detection
244 he reproducibility and stability of stimulus-evoked activation locations within and across both modal
245 on-chip monitoring and analysis of stimulus-evoked calcium responses of intact C. elegans at various
246 ansmission signals independently of stimulus-evoked release and highlight its role as a key regulator
248 ines norepinephrine and dopamine on stimulus-evoked cortical responses suggest that the catecholamine
249 ould be used for monitoring sensory stimulus-evoked responses in behaving rats by measuring hemodynam
252 ssing at short RSIs, indexed by the stimulus-evoked P1 component, was predicted by an ERP measure of
253 to account for the link between the stimulus-evoked visual responses and attentional modulations of b
254 cant change in oxCCO in response to stimulus-evoked activation in human infants and open new vistas f
255 quency connectivity) and transient, stimulus-evoked activity predictive of trial-by-trial memory form
256 imary function of the unconditioned stimulus-evoked activity of BLA neurons is to maintain the salien
258 ur results support a model in which stimulus-evoked exocytosis in retinal ribbon synapses is SNARE-de
260 supports the hypothesis that systemic stress-evoked sterile inflammation is initiated by the sympathe
261 oparietal cortex consisted of greater target-evoked activations for distracter-absent trials (central
263 onal correlation (RSFC) subnetworks and task-evoked activity, it is unclear whether individual variat
265 that depressed adolescents show limited task-evoked vs resting-state connectivity (termed 'inflexibil
266 ed calcium indicators to measure temperature-evoked responses in hundreds of neurons across the trige
270 essed this issue through the analyses of TMS-evoked responses recorded over a 29 h sleep deprivation
273 en the animal is inactive, the apparent tone-evoked responses reflect an arousal-mediated resumption
274 sorganized lens, microcephaly, reduced touch-evoked motility, and highly disorganized myofibers.
281 ults suggest that the function of vestibular-evoked arm movements is to maintain the accuracy of the
282 velocity-dependent modulation of vestibular-evoked muscle activity was retained during split-belt wa
286 detection of multifocal steady state visual-evoked potentials associated with visual field stimulati
287 and sectoral multifocal steady state visual-evoked potentials metrics to discriminate glaucomatous f
288 he global BCI multifocal steady state visual-evoked potentials parameter was 0.92 (95% CI, 0.86-0.96)
289 neurons, ensembles of neurons, and visually-evoked potentials (VEPs) in response to task light cues,
290 These included an increase in the visually-evoked firing of regular spiking, presumptive excitatory
292 , indicating that the hedonic value of water-evoked responses is highly internal-state dependent.
294 st, chronic ACh deprivation hindered whisker-evoked CBF responses and the amplitude and power in most
295 w that in Mecp2-deficient male mice, whisker-evoked activity is roughly topographic but weak in the b
297 t new cortical regions downstream of whisker-evoked sensory processing during active exploration.
298 d the effects of varying ACh tone on whisker-evoked NVC responses in rat barrel cortex, measured by c
299 ild-type and Fmr1 KO mice in overall whisker-evoked activity, though 45% fewer neurons in young Fmr1
300 d ACh tone significantly potentiated whisker-evoked CBF responses through muscarinic ACh receptors an
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