ライフサイエンスコーパス: sensory input

1 behavior serving as a scaffold to shape the sensory input.

2 for local search becomes less responsive to sensory input.

3 y enter neuronal nuclei from cytoplasm after sensory input.

4 ion of action potentials and transmission of sensory input.

5 is systematically modulated by variation in sensory input.

6 e spontaneous activity even without external sensory input.

7 C computationally processes motor output and sensory input.

8 physiological changes in response to altered sensory input.

9 ility, direction, and size of turns based on sensory input.

10 aimed at maximizing sampling of task-related sensory input.

11 with inference of the features that underlie sensory input.

12 although only when plasticity is induced by sensory input.

13 al to detect deviations from regularities of sensory input.

14 gic input with highly convergent feedforward sensory input.

15 udy of larval behaviour in response to local sensory input.

16 cal periods, when naive juveniles experience sensory input.

17 al activity, even in the absence of tasks or sensory input.

18 nable dendritic maturation in the absence of sensory input.

19 is robust to restraint-induced reduction in sensory input.

20 from the comparison of these beliefs against sensory input.

21 odels of the environment to predict upcoming sensory input.

22 cs of the recruitment of local inhibition by sensory input.

23 and manipulating information in phonological sensory input.

24 well top-down predictions fit with bottom-up sensory input.

25 rathreshold) stimuli: it filters and weights sensory input.

26 ter reliance on visual rather than olfactory sensory input.

27 l instruments, our actions generate auditory sensory input.

28 ability to reorganize to cope with changing sensory input.

29 e their code under noisy and/or inconsistent sensory input.

30 cesses that do not directly rely on auditory sensory input.

31 hat these behavioral adjustments improve the sensory input.

32 ral responses to the local statistics of the sensory input.

33 ng is directly driven by expectations of the sensory input.

34 st in cortical regions that are distant from sensory input.

35 ct sensory representations in the absence of sensory input.

36 sult of convergence, and not segregation, of sensory input.

37 the same neural representations as afferent sensory input.

38 cal periods and in response to alteration in sensory input.

39 basis of neuronal selectivity to features of sensory input.

40 environment requires integration of numerous sensory inputs.

41 the contents of working memory alongside new sensory inputs.

42 reflect recurrent connectivity or correlated sensory inputs.

43 chronized states and intermittently received sensory inputs.

44 transformed format, but not task-irrelevant sensory inputs.

45 xible and updatable representation of recent sensory inputs.

46 s of its behaviour that depend on multimodal sensory inputs.

47 f task features and selective integration of sensory inputs.

48 and disease is how cell populations adapt to sensory inputs.

49 information using a weighted average of the sensory inputs.

50 timize the transmission of information about sensory inputs.

51 dels of the world to minimize surprise about sensory inputs.

52 ierarchical model to infer the causes of its sensory inputs.

53 ative learning regions receive combinatorial sensory inputs.

54 vior thus enables animals to influence their sensory input, a concept referred to as active sensing.

55 n accuracy and generates robust detection of sensory inputs across various states of ongoing cortical

56 AIA responses require the coincidence of two sensory inputs: activation of AWA olfactory neurons that

57 rities in the sensory environment to predict sensory input, adjust behavior, and thereby maximize fit

58 s seem to bias the interpretation of current sensory input, akin to shifting endogenous attention tow

59 across comparatively drastic changes in the sensory input all the time.

60 f the ability to drive visual areas by their sensory inputs, allowing researchers to define visual ar

61 animals often do not discernibly respond to sensory input and are not overtly task-modulated.

62 ent a model of connections between olfactory sensory input and bees' mushroom bodies [6], incorporati

63 We found competing influences of immediate sensory input and choice memory on mouse choice.

64 humans can learn statistical regularities in sensory input and exploit this knowledge to improve perc

65 ations of object angles are constructed from sensory input and how they reorganize across learning.

66 fundamentally change how the neurons encode sensory input and motor output.

67 gic fibers, and are an integration center of sensory input and motor output.

68 for decoding reward category from olfactory sensory input and relaying this information to cognitive

69 a circuit that is right at the interface of sensory input and reward areas.

70 nmental exploration: preferential routing of sensory input and saccadic eye movements.

71 Because the TRN receives bottom-up sensory input and top-down cortical input, it could serv

72 stems vital for interpretation of sequential sensory inputs and consequent decision making.

73 her demonstrate that these interneurons gate sensory inputs and control pain through temporally coord

74 represents latent information independent of sensory inputs and future goals has not been determined.

75 Animals use active sensing to respond to sensory inputs and guide future motor decisions.

76 on, the transformation of multiple competing sensory inputs and internal states into a unitary choice

77 Accurate integration of sensory inputs and motor commands is essential to achiev

78 removing their lungs to eliminate pulmonary sensory inputs and perfusing them with hyperoxic artific

79 e is less understood, as it is unclear which sensory inputs and physical processes matter a priori.

80 Therefore, cortical astrocytes respond to sensory inputs and regulate sensory-evoked neuronal netw

81 luence pain perception relative to bottom-up sensory inputs and the underlying neural underpinnings o

82 nt requires differentiating between external sensory inputs and those that are self-generated.

83 a remarkable capacity to adapt to changes in sensory inputs and to learn from experience.

84 process of inference, integrating bottom-up sensory inputs and top-down expectations.

85 he olfactory bulb, which integrate bottom-up sensory inputs and top-down inputs delivered by vast top

86 ay also be influenced by environmental cues, sensory inputs, and other behaviors, implying the involv

87 ible perceptual interpretations of ambiguous sensory inputs, and predicts forward in time.

88 t comparisons between anterior and posterior sensory inputs, and the changing ratios drive different

89 ctivity neurons respond to a narrow range of sensory inputs, and thus would be considered highly info

90 static but evolves dynamically with changing sensory inputs; another example is motor preparation and

91 that the behavior-driven improvements of the sensory input are highly suitable to overcome the sensor

92 chanisms for inferring and interpreting what sensory inputs are about.

93 sleep states in which spatially informative sensory inputs are absent.

94 g stability of LLAs, particularly when other sensory inputs are depleted or otherwise compromised.

95 In contrast, in the brain, sensory inputs are encoded through the activity of large

96 Contributions from altered peripheral sensory inputs are implicated in this process, but the u

97 to change stimulus representations even when sensory inputs are perceptually invisible.

98 or site of sensorimotor integration in which sensory inputs are processed to initiate appropriate mot

99 l predictive processing framework, bottom-up sensory inputs are still required to achieve early and r

100 sults and models lead to the hypothesis that sensory inputs are used in a recurrent manner to tune th

101 never a discrepancy between task context and sensory inputs arises, irrespective of the latter probab

102 How do neurons process such differential sensory inputs at the dendritic level?

103 ory modalities depends on the convergence of sensory inputs at the level of single neurons.

104 that propagating LFP patterns can represent sensory inputs at timescales relevant to visually guided

105 stsynaptic dynamics in response to increased sensory input, at a time when sensory information proces

106 cisions, organisms must appropriately filter sensory inputs, augmenting relevant signals and suppress

107 lays a central role in the prioritization of sensory input based on task relevance.

108 Blockade of sensory input before movement prevented BTP, whereas ner

109 xperiments: iterative spatial comparisons of sensory inputs between body parts is essential for organ

110 levels of consciousness, on past and ongoing sensory input, bodily information (e.g., interoception),

111 ptual choices depend not only on the current sensory input but also on the behavioral context, such a

112 o multiple task variables including not just sensory input but also the animal's action decision and

113 neralization across experiences of different sensory inputs but organized according to how that senso

114 he neurons that implement motor responses to sensory inputs but understanding how they evolved has be

115 tenance of task-relevant information without sensory input, but the underlying circuit mechanism rema

116 ed by the discriminability of the individual sensory inputs, but also by factors that increase the pe

117 Perception reflects not only sensory inputs, but also the endogenous state when these

118 orm a somatotopic map to integrate bilateral sensory inputs, but organizes the maps in a different wa

119 considering the integration of multimodal MF sensory input by individual CGCs.

120 for synaptic inhibition and potentiation of sensory input by opioids.

121 ion, we simultaneously manipulated bottom-up sensory inputs by varying stimulus contrast and top-down

122 This reveals a mechanism whereby parallel sensory inputs can be integrated and stored to elicit a

123 This capacity indicates that sensory inputs can rapidly and flexibly reconfigure the

124 n synaptic efficacy, combined with sustained sensory input, can result in profound and sustained effe

125 ce copy" of the motor command to inhibit the sensory input caused by active behavior [1].

126 In dust-covered flies, sensory inputs change as a result of successful cleaning

127 lectronically programmable communication and sensory input channel to the body, as demonstrated throu

128 f neuronal excitability at sites of neuronal sensory input (cilium) and neuronal output (synapse).

129 ir action potential discharge in response to sensory input, compared with naive littermate controls.

130 ional whisker tracking demonstrated that the sensory input components that best discriminate angles (

131 It is not clear whether these two sensory inputs convey redundant or complementary informa

132 portantly, this activation is evident before sensory input corresponding to the stimulus position is

133 e resulting mixture of crossed and uncrossed sensory inputs creates bilateral whisker maps in the tha

134 hose studies tend to focus on the effects of sensory input deprivation, a process that rarely occurs

135 Sensory inputs did not interrupt this ongoing signal but

136 C. flexa thus rapidly converts sensory inputs directly into multicellular contractions.

137 VIP neurons are activated by non-sensory inputs, disinhibiting E and FS neurons.

138 Here, we show that the membrane-associated sensory input domain of PA1396 has five transmembrane he

139 atory pattern after ALI result not only from sensory input due to pulmonary damage and dysfunction bu

140 mplications for patients who lack peripheral sensory input due to spinal cord or nerve lesions.

141 t enable GCs to spike rapidly in response to sensory input during each sniff cycle.

142 r's perspective can "stand in" for one's own sensory input during perceptual decision making.

143 ceptual form, and can stand in for one's own sensory input during perceptual decision making.

144 tions in the fruit fly, which act to inhibit sensory input during sleep.

145 tions in how circuits are shaped by incoming sensory inputs during critical periods of development.

146 h on somatotopic remapping following loss of sensory input (e.g., arm amputation).

147 , the theory combines prior expectation with sensory input, explores different possible perceptual in

148 Does sensory input flow into the brain as a stream, or does i

149 The loss of sensory input following a spinal deafferentation injury

150 f the Zpld1 mutant mice is caused by loss of sensory input for rotary head movements (detected by cri

151 e canonical broadcast neurons that integrate sensory inputs for transmission to distributed downstrea

152 or unimodal noise by relying on simultaneous sensory input from another modality.

153 The basolateral amygdala (BLA) integrates sensory input from cortical and subcortical regions, a f

154 results suggest that Zic2 neurons integrate sensory input from cutaneous afferents with descending s

155 The thalamus receives sensory input from different circuits in the periphery.

156 rates of neural spiking can be modulated by sensory input from experimental haltere movements (drive

157 oot/dorsal column) in male monkeys to remove sensory input from just the opposing digits (digits 1-3)

158 tical diagnostic prediction: a non-preferred sensory input from one modality, which activates the neu

159 ntral vestibular neurons also receive direct sensory input from peripheral afferents.

160 ory input from the nodose ganglia and spinal sensory input from the dorsal horn.

161 s in face muscles raises the question of how sensory input from the face is used to control muscle ac

162 ally, PPG neurons receive monosynaptic vagal sensory input from the nodose ganglia and spinal sensory

163 l system is composed of circuitry connecting sensory input from the retina to the processing core of

164 Preventing sensory input from TRPV1-expressing fibers failed to alt

165 y influenced by social interactions based on sensory inputs from several modalities.

166 campus are considered key for disambiguating sensory inputs from similar experiences in memory, a pro

167 en known that the somatosensory cortex gates sensory inputs from the contralateral side of the body.

168 e show that both the piriform cortex and its sensory inputs from the olfactory bulb represent chemica

169 uestion by dissociating the effect of coital sensory inputs from those of male ejaculate.

170 tions, humans can distinguish self-generated sensory inputs from those that are elicited externally.

171 sults suggest that AVA are hub neurons where sensory inputs from threat and reward sensory modalities

172 These discoveries suggest that sensory input guides action selection by modulating inte

173 These results indicate that ascending sensory input guides the compensatory plasticity that no

174 on of neural responses due to the history of sensory input has been observed across all sensory modal

175 the role of glial cells in the processing of sensory input has gained increasing interest.

176 of dopamine in cognitive control: (i) gating sensory input, (ii) maintaining and manipulating working

177 tivity that compensates for "task positive", sensory input in another region) balancing neural activi

178 using genetic and surgical manipulations of sensory input in mouse somatosensory thalamocortical neu

179 ms develop in tandem and that alterations in sensory input in one system can affect the connections a

180 results advance our knowledge on the role of sensory input in the generation of the neural drive to m

181 es an optimal balance between prediction and sensory input in the interpretation of spoken language.

182 hasic mechanism that regulates processing of sensory inputs in the cerebellum.

183 near GC proximal dendrites and by activating sensory inputs in the glomerular layer in truncated GCs

184 (overnight) exposure to dramatically enhance sensory inputs in the second postnatal week led to a sig

185 ons, and reduced their firing in response to sensory input, in both males and females.

186 We find unexpected structure in sensory inputs, in the transfer of information about dif

187 uration-dependent structure, suggesting that sensory input-independent mechanisms guide grooming beha

188 understanding the neural mechanisms by which sensory input influences aging may uncover novel therape

189 l cortical areas is crucial for transforming sensory input into behavioral actions.

190 how a brainwide dynamical system transforms sensory input into behavioral output.

191 To investigate how the brain translates sensory input into decisions during active sensation, we

192 itatory spinal interneurons are recruited by sensory input into functional circuits to generate persi

193 the body, putatively by engendering noisier sensory input into motor decision processes eliciting re

194 sual cortical areas and then transform these sensory inputs into a final conscious percept.

195 Bacteria convert changes in sensory inputs into alterations in gene expression, beha

196 Neurons convert synaptic or sensory inputs into cellular outputs.

197 tegration of light and temperature and gates sensory inputs into circadian clock neuron networks.

198 Hyper-reactivity to sensory input is a common and debilitating symptom in in

199 Filtering relevant signals from noisy sensory input is a crucial challenge for animals [1, 2].

200 Incoming sensory input is condensed by our perceptual system to o

201 Olfactory sensory input is detected by receptor neurons in the nos

202 However, optimizing sensory input is difficult due to the predominantly nonl

203 ocess of inferring physical reality from the sensory input is highly influenced by previous knowledge

204 the problem of extracting elevation from the sensory input is ill-posed, since the spectrum results f

205 IGNIFICANCE STATEMENT The continuous flow of sensory input is not processed in an analog fashion, but

206 s challenging, in part because the timing of sensory inputs is affected by the animal's behavior.

207 al-to-trial variability impacts detection of sensory inputs is not fully understood.

208 tivity carry more information about external sensory inputs is widely accepted in neuroscience.

209 om thousands of cortical neurons with shared sensory inputs, it is unknown whether correlated noise l

210 s with superficial axonal projections to the sensory input layer of the MOB.

211 s enable persistent firing in the absence of sensory input, maintaining information through recurrent

212 servations indicate that blocking peripheral sensory input may prevent BTP and targeting central site

213 nce; however, it remains unclear exactly how sensory input modifies brain circuits.

214 Based on their sensory input, motor output, and involvement in dopamine

215 e conditions (race car driving) to study the sensory inputs, motor outputs, and brain states which ch

216 abundance, intrinsic physiology, feedforward sensory input, neuromodulation, synaptic output, and fun

217 conscious states that are neither shaped by sensory input nor able to be expressed by motor output.

218 rtex, but recent work has suggested that new sensory inputs obligatorily wipe out this information.

219 Our results provide a quantification of the sensory input of echolocating bats in collective group f

220 ntribution of visual input to the multimodal sensory input of the EC is significantly larger than in

221 We found that the sensory inputs of copulation cause a reduction of post-c

222 monstrate that Hip14 regulates depression of sensory inputs onto an identified hindbrain neuron and p

223 different operating modes that favor either sensory input or recurrent processing in the prefrontal

224 namically infer hierarchical structures from sensory input (or to hierarchically structure output), b

225 Moreover, we provide evidence that sensory inputs other than visual inputs can support grid

226 Combining sensory inputs over space and time is fundamental to vis

227 isual world.SIGNIFICANCE STATEMENT Combining sensory inputs over time is fundamental to seeing.

228 n in a protocol that requires integration of sensory input (PAS) and not when plasticity was induced

229 rons to assay divergent versions of the same sensory input pattern.

230 ole in converting broad, highly overlapping, sensory input patterns into odor-selective population re

231 plays a critical role in transforming broad sensory input patterns into odor-selective population re

232 on across glomeruli when driven by realistic sensory input patterns, but that global inhibitory netwo

233 t layer 6 (L6) CTs may be activated by extra-sensory inputs prior to anticipated sounds, we performed

234 interglomerular connectivities were tuned by sensory input profile decorrelated odor representations

235 The spatiotemporal structure of the sensory input provides information for the computation o

236 at is modulated by the predictability of the sensory input, providing evidence for predictive coding

237 bacteria to integrate at least two different sensory inputs, quorum sensing (via RhlR-driven activati

238 hart between the insula cortex (IC), a major sensory input region of the lateral and capsular part of

239 e of hundreds of milliseconds even while the sensory input remained, on average, stationary.

240 respond to the same incrementally delivered sensory input, revealed a significant correspondence bet

241 of neurons in the barrel cortex to incoming sensory input signals.

242 the benefit of counteracting self-generated sensory input.SIGNIFICANCE STATEMENT Neuronal circuits t

243 les relevant information to be selected from sensory inputs so it can be processed in the support of

244 expressing IGCs are more strongly excited by sensory input stimulation and MC activation is suppresse

245 creased inhibition by IGCs, MCs responded to sensory input stimulation with decreased depolarization

246 Computational modeling predicts that higher sensory input strength to the head will cause anterior g

247 standing involves an integration of multiple sensory inputs such as vision, vestibular and somatosens

248 formed glomerular patterns of odorant-evoked sensory input (taken from previously-published datasets)

249 The sensory input that an animal receives is directly linked

250 In V1, sensory inputs that do not match the predictions lead to

251 brought about by the absence of uncorrelated sensory input, the connectivity structure of the network

252 Downstream of the nociceptive sensory input, the neural signals trigger protective (no

253 tes thought to receive segregated streams of sensory input: the lateral dendrite receives mechanosens

254 factory bulb, are known to broadly integrate sensory input through specialized synapses on their dist

255 ally relevant information from the stream of sensory inputs through the hierarchy of cortical areas.

256 illations driven by contextual (but missing) sensory input, thus entirely reflecting endogenous neura

257 vely, flies may track the temporal change in sensory input to a given body part to measure cleaning e

258 system in Gnathonemus petersii allow for the sensory input to be computationally reconstructed, enabl

259 n the middle, where the algorithms that link sensory input to behavioral output can provide a solid f

260 c) plasticity, where changing the mapping of sensory input to behavioral output requires a strong rei

261 lationship strongly depends on the nature of sensory input to cortex: stimuli that increase the numbe

262 matrices that encompass all connections from sensory input to end-organ output across the entire anim

263 inguish external stimuli from self-generated sensory input to guide appropriate behaviors.

264 inergic input with broadly tuned feedforward sensory input to modulate principal cell activity select

265 d through simple, repeatable rules that link sensory input to motor output: we refer to these rules a

266 EMENT Due to the difficulty of measuring the sensory input to moving sense organs, active perceptual

267 ght to merge information on motor output and sensory input to orchestrate interaction with the enviro

268 hibitory interneurons are driven by visceral sensory input to play a major role in gating viscerosens

269 cclusion allows us to experimentally control sensory input to subregions of visual cortex while inter

270 rning, valence coding, and stress, can shape sensory input to the brain and early sensory processing

271 olfactory processing as early as the primary sensory input to the brain by modulating norepinephrine

272 olecules in the nose and provide the initial sensory input to the brain's olfactory bulb.

273 ABSTRACT: Sensory input to the master mammalian circadian clock, t

274 oming movement is determined by the ratio of sensory inputs to different body parts.

275 rtices provide noisy but otherwise veridical sensory inputs to downstream processes that accumulate a

276 the frontal cortex, allowing the mapping of sensory inputs to motor outputs to incorporate prior sta

277 tered by, grid cell input; (3) plasticity in sensory inputs to place cells is key for pattern complet

278 contribute to the enhanced ability of these sensory inputs to sensitize central nociceptive networks

279 te the highly structured organization of the sensory inputs to the OB, even simple monomolecular odor

280 ce that repeated stress specifically damages sensory inputs to this region.

281 itries that specialize in processing certain sensory inputs to trigger stereotyped motor outputs.

282 tory bulb plays a central role in processing sensory input transduced by receptor neurons.

283 cessing based on the behavioral relevance of sensory input ultimately enhances and stabilizes the rep

284 Cortical responses to sensory inputs vary across repeated presentations of ide

285 By varying the time when sensory input was removed, we determined that the critic

286 is dependent on internal models, but not on sensory input, we have the opportunity to map visual fea

287 izations and computational reconstruction of sensory input, we show how electrosensory flow is active

288 duced inhibition and potentiation of primary sensory input were abrogated in Oprm1-cKO mice.

289 e, spontaneous CBV changes in the absence of sensory input were driven by volitional whisker and body

290 ecting target stimuli by comparing bottom-up sensory inputs (what the monkeys were looking at) and to

291 ical proposal that associative plasticity of sensory inputs, when combined with attractor dynamics, c

292 sult shows promising results that vestibular sensory input while walking could be affected through ma

293 Layer four receives the densest bottom up sensory inputs, while layers 2/3 and 5 receive top down

294 ence (STFP), the combination of an olfactory sensory input with a social cue induces long-term memory

295 peech perception involves the integration of sensory input with expectations based on the context of

296 through which the brain integrates external sensory inputs with internal expectation signals remains

297 encountered, requires complex integration of sensory inputs with previous experience.

298 ential process in which our brains integrate sensory inputs with prior expectations to make sense of

299 ption is a process of inference, integrating sensory inputs with prior expectations.

300 y areas of the cerebral cortex integrate the sensory inputs with the ongoing activity.