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1 S2, and studying dynamic regulation of Gq/11-evoked Ca(2+) signaling and vascular contraction.
2 inding enhanced TRPA1 sensitivity and Ca(2+)-evoked potentiation of TRPA1 at low Ca(2+), but inhibite
3 d primes secretory granules (SGs) for Ca(2+)-evoked secretion in various secretory cells.
4 ed responses did not affect any of the CCK-8-evoked responses, indicating that rather than acting on
5 , and beta3 nAChR subunit expression and ACh-evoked currents.
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
8                                     Activity-evoked responses appear normal while both excitatory and
9 taining both resting blood flow and activity-evoked changes therein.
10 to cause a significant reduction of activity-evoked release at two types of fast inhibitory synapses
11 otion component, is the predominant activity-evoked change across the entire bouton population.
12 to measure the synaptic dynamics of afferent-evoked input at physiological stimulus frequencies.
13 ells, mitral cells have a prolonged afferent-evoked EPSC, which serves to amplify the synaptic input.
14                                      Agonist-evoked effects on barrier permeability and cytoskeletal
15 om epileptic mice displayed enhanced agonist-evoked P2X7 receptor currents, and synaptosomes from the
16 indicating that the mutation impairs agonist-evoked gating.
17 late Reader (FLIPR) assay to monitor agonist-evoked Ca(2+) signals in human primary skin fibroblasts.
18          In addition to potentiating agonist-evoked responses, all three compounds reduce receptor de
19 in levels and showed less pronounced agonist-evoked calcium signals compared to MVECs.
20                    Specifically, the agonist-evoked temporal Ca(2+) release profile and protein kinas
21                    It is unclear how alcohol-evoked plasticity in the DMS contributes to alcohol cons
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
26            Moreover, no significant auditory-evoked responses accompanied this prethreshold entrainme
27                               These auditory-evoked responses, distinguished by robust, broad-band in
28 bit the potentiation without affecting basal-evoked NMDA currents, indicating that NMDAR-GluN2B recep
29 n of MSNs, timing-contingently dictating BLA-evoked activation of MSNs.
30 orward inhibition circuit, through which BLA-evoked activation of NAc shell (NAcSh) MSNs was fine-tun
31              Whereas the status of brainstem-evoked potentials did not predict the recovery of sensor
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
37        We demonstrate that astrocyte calcium-evoked production of the vasodilator PgE2 is critically
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
40 ients, despite small reductions in capsaicin-evoked cough.
41           We sought to investigate capsaicin-evoked cough responses in a group of patients with well-
42 cough frequency (primary outcome), capsaicin-evoked cough, and patient-reported outcomes.
43 ensors and their responsiveness to carbachol-evoked store release ( 400 nM).
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
46  fast and slow components of the cholinergic-evoked inhibition, and a delay in IPSC latency.
47 hannels/receptors involved in acidic citrate-evoked itch.
48     TDAG8(-/-) mice displayed attenuated CO2-evoked freezing and sympathetic responses.
49                                 Finally, CO2-evoked neuronal firing in patch-clamped subfornical orga
50 role for astrocytes in the regulation of CO2-evoked CBF responses.
51  RTN-specific knockdown of Nalcn reduced CO2-evoked neuronal activation and breathing; hypoxic hyperv
52                                      The CO2-evoked activity of these interneurons is subject to extr
53 ory cytokine interleukin (IL)-1beta with CO2-evoked responses was investigated using microglial block
54 f OXR antagonists to attenuate acute cocaine-evoked impulsivity.
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
58           Thus, we hypothesized that cocaine-evoked plasticity in PL-mPFC may underlie cocaine-associ
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
63         The influence of the STN on continue-evoked activity in the pre-SMA was predicted by interind
64 e DLPFC measured as potentiation of cortical-evoked activity using paired associative stimulation (a
65  and down-regulation of individual cells' CS-evoked responses.
66 ue significantly and selectively inhibits CS-evoked activity.
67 macological methods, we demonstrate that cue-evoked acetylcholine release, through distinct actions a
68                            We found that cue-evoked neural firing in the ventral pallidum (VP) reflec
69 ntiated synaptic efficacy as well as current-evoked postsynaptic spiking.
70       All three monoamines decreased current-evoked spike firing of lOFC neurons and this action requ
71  factor of lysosomal biogenesis, for decorin-evoked endothelial cell autophagy.
72 ated energy sensor kinase, prevented decorin-evoked TFEB induction and nuclear localization.
73 03V mutation nearly abolishes depolarization-evoked exocytosis (measured by membrane capacitance) and
74 cellular Ca(2+) signaling and depolarization-evoked exocytosis.
75  secretion, including reduced depolarization-evoked Ca(2+)-influx and beta-cell exocytosis.
76 nezumab on the cortical spreading depression-evoked activation of mechanosensitive primary afferent m
77 nhibins can be proposed to mitigate diabetes-evoked BRB breakdown.
78                                         Drug-evoked plasticity at excitatory synapses on medium spiny
79 uits and design of protocols to reverse drug-evoked plasticity and to establish links of causality wi
80 m in the context of previously reported face-evoked FPs in macaque auditory cortex.
81             These results indicate that face-evoked FP responses in auditory cortex are not generated
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
84 ptic long-term potentiation (LTP) of C-fiber-evoked potentials.
85  including brush-evoked dynamic and filament-evoked punctate hypersensitivities.
86 orphine-resistant forms of von Frey filament-evoked punctate mechanical hypersensitivity.
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
89            Propofol potentiated maximal GABA-evoked currents mediated by alpha1(D43C)beta2gamma2 and
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.
92                       The amplitudes of GABA-evoked currents from the mutant alpha1beta2gamma2(R136*)
93              Recently, a counterpart of gaze-evoked eye nystagmus was identified for head movements;
94 ine-based modulators to potentiate glutamate-evoked currents at recombinantly expressed KARs.
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
97 MDA receptors and potentiate their glutamate-evoked currents.
98                   Interestingly, the glycine-evoked currents in dissociated DRD1-positive MSNs were p
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
105 ected by PGE2, but PGE2 attenuated histamine-evoked IP3 accumulation.
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
110                  Munc13-4 promotes histamine-evoked WPB exocytosis and is present on WPBs, and secret
111 , the small GTPase Arf6, supported histamine-evoked WPB exocytosis, as shown by knockdown and overexp
112 eceptors, through cAMP and PKA, to histamine-evoked Ca(2+) signals.
113  suggest that prolonged and aberrant hormone-evoked Ca(2+) increases may stimulate the production of
114 ivation leading to a reduction in ongoing HP-evoked MSN responses.
115                          In comparison, 5-HT-evoked inhibitory responses in the AOB arose due to a po
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
120                                        Light-evoked vasopressin release contributes to the responses
121 nges in synaptic cleft pH accompanying light-evoked changes in HC membrane potential.
122 r the T cell receptor complex inhibits light-evoked Ca(2+) transients.
123  potential (TRP) channels to integrate light-evoked signals with ambient mechanical, chemical and tem
124 ices from postnatal day (P)12-14 mice, light-evoked EPSCs were large (> 1 nA at -70 mV).
125 short near-infrared pulses to modulate light-evoked ionic current from Channelrhodopsin-2 (ChR2) in b
126 xpand in graded fashion independent of light-evoked input.
127                        Measurements of light-evoked responses from individual BC synaptic terminals s
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-
131         Lesioning the habenula reduces light-evoked climbing.
132                                    The light-evoked excitatory postsynaptic potentials in some types
133                     Examination of the light-evoked postsynaptic currents in these ON-type orientatio
134                                    The light-evoked synchronous activity caused robust excitation of
135 photoreceptor systems cooperate for UV light-evoked acute responses.
136                             In mice, looming-evoked defensive responses are triggered by the superior
137 ion cells (RGCs) that controls mouse looming-evoked defensive responses through axonal collaterals to
138 f DRN serotoninergic neurons reduces looming-evoked defensive behaviours.
139 ted currents during episodes of mechanically-evoked SD.
140                                Moreover, MNT-evoked EEG activity showed physiologically plausible res
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
143 threshold test stimulus (TS) to elicit motor-evoked potentials (MEPs) in the right hand.
144  excitability and RT, such that larger motor-evoked potentials (MEPs) measured at rest were associate
145                               The mean motor-evoked potential amplitude increase was 31% of the basel
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
154 ty associated with a strong decrease of NMDA-evoked currents.
155 spine density, concomitant with reduced NMDA-evoked currents and impaired NMDAR-dependent insertion o
156            However, whether an altered NMDAR-evoked changes in Ca(2+) (NMDAR-DeltaCa(2+) ) signalling
157 s concomitant with the refinement of noxious-evoked limb reflexes.
158                                         Odor-evoked Ca(2+) responses showed net facilitation across a
159 P generated during conditioning affects odor-evoked responses in the MB.
160      Our results show that, by allowing odor-evoked suppression as well as excitation, the responsive
161 to the OB modulate both spontaneous and odor-evoked neural responses.
162 nt alterations in their spontaneous and odor-evoked spiking properties.
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
166 rs from attraction to avoidance, as did odor-evoked olfactory sensory neuron excitation.
167 tral and tufted cells display different odor-evoked responses and are thought to form parallel channe
168 identity can be made solely using early odor-evoked neural activity.
169                           Functionally, odor-evoked responses of mitral cells, which are normally inh
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
172 cular mechanism and functional roles of odor-evoked inhibition remain largely unknown.
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
179                        Remarkably, this odor-evoked inhibition of olfactory sensory neurons elicited
180                                   While odor-evoked excitation in peripheral olfactory cells is known
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
184 erved under both natural and optogenetically-evoked conditions.
185 ed fibroblasts exacerbates pressure overload-evoked fibrosis.
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.
188 , and gallein all inhibited recovery of PAR2-evoked Ca(2+) signaling.
189              This revealed that perturbation-evoked responses were initially restricted to output-nul
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
193 um buffering, or decreasing action potential-evoked calcium influx.
194  neurotransmission, whereas action potential-evoked neurotransmission remained relatively normal.
195 vous system (CNS) synapses, action potential-evoked neurotransmitter release is principally mediated
196 te Ca(2+) influx to trigger action potential-evoked neurotransmitter release.
197 Cs) is the major trigger of action potential-evoked synaptic release.
198                             Action potential-evoked vesicle fusion comprises the majority of neurotra
199                                    Thus, PPN-evoked burst spiking of SNc dopaminergic neurons in vivo
200 duction reduced the magnitude of lever press-evoked inhibition.
201  slices, we determined whether flow/pressure-evoked increases or decreases in parenchymal arteriole v
202                                     Propofol-evoked currents mediated by alpha1(T47R)beta2gamma2 and
203                    GABA-, THIP- and propofol-evoked currents mediated by alpha1(T47R)beta2gamma2 rece
204  naturally express PAR2 and mediate protease-evoked inflammation and nociception.
205                                      Sensory-evoked activity is potently suppressed by anaesthesia.
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
208 eriods for the development of normal sensory-evoked responses in the visual cortex.
209  causes GABAB-mediated inhibition of sensory-evoked dendritic Ca(2+) activity.
210 quirement for the full expression of sensory-evoked neurovascular coupling responses.
211 requisite for the full expression of sensory-evoked NVC responses, indicating that ACh may alter the
212  demand may allow dynamic control of sensory-evoked signal flow in the neocortex.
213 ramatic impairments in both types of sensory-evoked signals.
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
216 motor frequency, but did not disrupt the SNc-evoked graded control of locomotion.
217                                          SNL-evoked mechanical hypersensitivity was attenuated, accom
218 electroencephalography, absent somatosensory-evoked potential, absent pupillary or corneal reflexes,
219 er clinical, neurophysiologic (somatosensory-evoked potential), and biochemical prognosticators.
220                               Although sound-evoked responses are normal at 1 month, by 4 months, mut
221 le SGNs showed reduced spontaneous and sound-evoked firing rates.
222 ure thalamocortical input layer 4, and sound-evoked spike latencies were longer in layer 4 than in su
223                                     As sound-evoked responses from the auditory nerve grew progressiv
224 essively weaker following denervation, sound-evoked activity in the cortex-and, to a lesser extent, t
225               A vigorous, long-lasting sound-evoked afterdischarge (LSA) is seen in a subpopulation o
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
228         Together our results show that sound-evoked activity and topographic organization of the cort
229 educed suprathreshold amplitude of the sound-evoked auditory nerve compound action potential.
230 oduce force that greatly increases the sound-evoked vibrations of the basilar membrane.
231                 PIP2 depletion reduced spike-evoked Ca(2+) entry and voltage-gated Ca(2+) currents.
232 sias, the most common deep brain stimulation-evoked adverse effect.
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
236 arrel cortex during spontaneous and stimulus-evoked conditions.
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
247 n led to an increase in the gain of stimulus-evoked visual responses.
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
250         Recent studies suggest that stimulus-evoked and spontaneous neurotransmitter release processe
251         The present data shows that stimulus-evoked neural responses, known to be modulated by attent
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
257 anges in whole-brain activity using stimulus-evoked functional magnetic resonance imaging.
258 ur results support a model in which stimulus-evoked exocytosis in retinal ribbon synapses is SNARE-de
259                                       Stress-evoked cytokine/chemokine responses, or sterile inflamma
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
262                                         Task-evoked regional brain activations during the early and l
263 onal correlation (RSFC) subnetworks and task-evoked activity, it is unclear whether individual variat
264                We found that estimating task-evoked activity flow (the spread of activation amplitude
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
267 PSCs without altering spontaneous or thermal-evoked transmission.
268                                          TMS-evoked responses related to phosphene perception were si
269                                 However, TMS-evoked activity of individual neurons has remained large
270 essed this issue through the analyses of TMS-evoked responses recorded over a 29 h sleep deprivation
271 f the N45, a GABAAergic component of the TMS-evoked EEG response.
272 t in vivo electrophysiological access to TMS-evoked neuronal activity 0.8-1 ms after TMS onset.
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.
275 emichannels as downstream mediators of toxin-evoked ATP release.
276 key populations in the generation of vaccine-evoked antibody responses.
277 le to mimic, albeit partially, the vanilloid-evoked activation pattern of the wt receptor.
278 the body along the direction of a vestibular-evoked disturbance.
279 pper limb plays an active role in vestibular-evoked balance responses.
280 confirms the functional nature of vestibular-evoked arm movement.
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
283        Furthermore, modulation of vestibular-evoked muscle responses occurred rapidly ( approximately
284  and somatosensory physiology with vibration-evoked electroencephalographic potentials.
285 elay on full-field, pattern-reversal, visual-evoked potentials.
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
291 etic silencing of these TRCs abolished water-evoked responses in taste nerves.
292 , indicating that the hedonic value of water-evoked responses is highly internal-state dependent.
293       Cerebrovascular reactivity and whisker-evoked neurovascular coupling responses were measured at
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
296 ce) allows for convenient imaging of whisker-evoked neural activity in vivo.
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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