ライフサイエンスコーパス: sensory

1 oanatomical features related to the enhanced sensory abilities of pterosaurs(9) are already present i

2 rders (ASD), but the neural basis underlying sensory abnormality is not completely understood.

3 heir responsivity, sensitivity, and roles in sensory acquisition and motor control in a light-weight

4 4 induced neuroplastic changes in trigeminal sensory afferents, increasing calcitonin gene-related pe

5 nol, providing spicy and fruity notes at the sensory analyses, and being appreciated for their body b

6 rovide a fast and reliable solution, whereas sensory analysis by trained panelists is expensive and t

7 Sensory analysis conducted by a trained panel showed tha

8 evaluate the homogeneity of several RMs for sensory analysis of virgin olive oil samples, using simi

9 Thermogravimetric analysis and quantitative sensory analysis.

10 RBITRAP, and 11 attributes were evaluated by sensory analysis.

11 No differences were observed in sensory analysis.

12 Cortical mechanisms of sensory and affective integration, however, remain poorl

13 e brain reward center that are implicated in sensory and affective manifestations of chronic pain.

14 l population code within regions involved in sensory and appetitive properties of taste.

15 gical role in regulating the function of the sensory and autonomic nervous system and endo- and exocr

16 examined mitochondrial motility in zebrafish sensory and motor axons.

17 of the peripheral nervous system for normal sensory and motor capabilities, analogous approaches to

18 stream effects of disrupting this process on sensory and motor circuits.SIGNIFICANCE STATEMENT Disrup

19 cell types that were defined based on their sensory and motor properties, providing insight into the

20 gh GSCORR was observed mainly in the primary sensory and motor regions, whereas low GSCORR was seen i

21 yer 5 corticopontine neurons strongly encode sensory and motor task information and are selectively n

22 , and hypothalamus, but was also observed in sensory and sensorimotor areas of the midbrain and hindb

23 exactly rules shape actions toward specific sensory and/or motor requirements remains unclear.

24 d, and reversible conduction block in motor, sensory, and autonomic nerves, but causes transient acti

25 lly exclusive feeding programs with distinct sensory appendages, meal sizes, digestive tract targets,

26 the presence of movement-related signals in sensory areas and discuss how their study, in the contex

27 ting the topographic organization of primary sensory areas in the neocortex are well studied, what ge

28 s, neural processing cascades from low-level sensory areas to increasingly abstract representations i

29 ression of predicted stimulus information in sensory areas, but how prior knowledge modulates process

30 Across sensory areas, neural microcircuits consolidate streams

31 ir biologically-active compounds, and to the sensory assessment.

32 However, systematic correlations between sensory attributes and native beer compounds have not be

33 at pancreatic islets are innervated by vagal sensory axons expressing Phox2b, substance P, calcitonin

34 rsal root crush injury, centrally-projecting sensory axons fail to regenerate across the dorsal root

35 regarding patterns of mate choice, including sensory biases, context dependence, and assortative mati

36 rregular 5-HT receptor density, or change in sensory bombardment may enhance internal broadcasts and

37 uced associative, but concurrently increased sensory, brain-wide connectivity.

38 A new study uses light to manipulate the sensory cells in our nose that respond to odors and reve

39 V7) could replace V1 without any discernible sensory change.

40 Overall, PLSR models that predicted wine sensory characteristics gave a poor to moderate R(2).

41 ere analysed for chemical, olfactometric and sensory characteristics.

42 o inform behavioral choice, but the relevant sensory comparisons and the underlying neural circuits a

43 onent regulatory system (BceRS) working in a sensory complex with an ABC-transporter (BceAB), togethe

44 eural signals that combine reward value with sensory confidence and guide subsequent learning.

45 The sensory consequences of our actions are thought to be pr

46 Researching the sensory corollaries of motor control thus can be crucial

47 te ICMS frequency up to ~200 Hz but that the sensory correlates of frequency were highly electrode de

48 les, we developed a reduced spiking model of sensory cortical circuits that incorporated the signatur

49 We observed a hierarchical gradient: sensory cortices aligned most quickly, followed by mid-l

50 ifferential effects on the primary motor and sensory cortices by using transcranial magnetic stimulat

51 rrangement highly reminiscent to that of the sensory cortices of mammals.

52 mus, operculum, frontoparietal cortices, and sensory cortices relative to the HCs.

53 Together with findings from other sensory cortices, our results provide evidence of a comm

54 afferent and intrinsic activity to generate sensory cue and prediction error signals that are essent

55 ide a framework for understanding how innate sensory cues are processed to elicit adaptive behavioral

56 Therefore, by permitting unfiltered sensory cues to enter information processing and activat

57 emonstrated in a fully aquatic animal, where sensory cues used for orientation may differ dramaticall

58 e development inside the host in response to sensory cues, a process called activation.

59 All animals must transform ambiguous sensory data into successful behavior.

60 by integrating non-target metabolomics with sensory data.

61 these ion channel subunits partially rescue sensory defects in Caenorhabditis elegans osm-9 and tax-

62 evel of arbor growth: Under nutrient stress, sensory dendrites preferentially grow as compared to nei

63 gic population dynamics that disappears in a sensory-dependent process.

64 brain to rewire and recover from injury and sensory deprivation, it can lead to tinnitus as an unwan

65 Following chronic sensory deprivation, microglia undergo a morphological t

66 rovide anatomical and temporal signatures of sensory disconnection during sleep and pave the way to u

67 leus and medial thalamic nucleus, as well as sensory-discriminative pain, such as ventral posteromedi

68 activate sensory representations of trauma, sensory disinhibition can constitute a sensory mechanism

69 d for SGN peripheral axon extension into the sensory domain, we used a genetic sparse labeling approa

70 t may enhance internal broadcasts and reduce sensory drive and vice versa.

71 al circuits to recover from perturbations to sensory drive.

72 ay a key role in integrating spontaneous and sensory-driven activity.

73 We dissected the particular contributions of sensory-driven versus choice-correlated activity in the

74 Sensory dysfunction is a common consequence of many form

75 to evaluate the volatile composition and the sensory effect of the presence of Quaker beans in natura

76 These are gut sensory epithelial cells, and those that form synapses a

77 e geometry that links the environment to the sensory epithelium.

78 y, highly correlated with TVB-N, TVC, pH and sensory evaluation analysis.

79 properties of the jams were determined and a sensory evaluation made.

80 esponse elicited by an immediate, unexpected sensory event, which is potentiated when evoked during t

81 onset, or (2) an increase in the quality of sensory evidence.

82 ased learning with accumulation of uncertain sensory evidence.

83 second guess that is clearly informed by the sensory evidence.

84 I), resting-state functional MRI (fMRI), and sensory-evoked fMRI on 20 mice injected with alpha-syn f

85 cytes respond to sensory inputs and regulate sensory-evoked neuronal network activity maximizing its

86 For example, the magnitudes of sensory-evoked oscillations, as measured by auditory ste

87 During both spontaneous and sensory-evoked swimming, the total inhibitory current wa

88 emporoammonic input to differentiate between sensory experience and the stored representation of the

89 e that cross-modal temporal biases depend on sensory experience during an early sensitive period.

90 The earliest and most prevalent sensory experience includes tactile, thermal, and olfact

91 s to diversify circuit tuning in response to sensory experience.

92 ng pain intensity and possibly improving the sensory experience.

93 ation representation develops independent of sensory experience.

94 Our decisions often depend on multiple sensory experiences separated by time delays.

95 High levels of skeletal muscle sensory feedback related to peripheral fatigue developme

96 suffer from poor controllability and lack of sensory feedback.

97 bling intracortically controlled closed-loop sensory feedback.

98 aintaining normal dendritic arborization and sensory function to regulate escape and social behavior.

99 over 8 y in six domains-physical capability, sensory function, physiological function, cognitive perf

100 naptic plasticity and facilitate recovery of sensory function.

101 tment has been implicated in enhanced intact sensory function.

102 rive inhibited firing and suppressed overall sensory function.

103 The effects of these mutations on sensory functions have not been described so far.

104 rpes simplex virus 1 (HSV-1) from neurons in sensory ganglia such as the trigeminal ganglia (TG) is i

105 uma disrupts cochlear blood flow and damages sensory hair cells.

106 early visual cortex (V1-V3) predict stronger sensory imagery.

107 ng how neural networks process and represent sensory information and how these cellular signals instr

108 g natural behavior, animals actively acquire sensory information as they move through the environment

109 Within a predictive coding framework sensory information could be down-weighted in favour of

110 It also integrates sensory information from the periphery and sends ascendi

111 ing areas are involved in the maintenance of sensory information in working memory (WM).

112 h the continuous, high-dimensional stream of sensory information it receives.

113 echanism leading to suppression of predicted sensory information remains unclear, and studies thus fa

114 Our data suggest that sensory information streams targeting the PPC may be imp

115 ain function that takes into account current sensory information that is weighted according to prior

116 To understand how the brain processes sensory information to guide behavior, we must know how

117 ssing synaptophysin and synaptotagmin 1, and sensory information transmitted from keratinocytes to se

118 Sensory systems constantly compare external sensory information with internally generated prediction

119 pect of fast activation is the processing of sensory information with limited delays.

120 Owing to the absence of tactile sensory information, prosthetic users must rely on incid

121 to make greater incorrect predictions about sensory information.

122 rons) connections, are crucial in processing sensory information.

123 ly interact with their environment to gather sensory information.

124 terized the anatomical pattern of pancreatic sensory innervation by combining viral tracing, immunohi

125 that the trigeminal ganglion, which provides sensory innervation to the face, is a rich source of Oxt

126 Major sensory innervation to the uterus is provided by spinal

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

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

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

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

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

132 is systematically modulated by variation in sensory input.

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

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

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

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

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

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

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

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

141 c, suggesting that suppression of PM altered sensory integration or the decision-making process rathe

142 ral nerves (sympathetic, parasympathetic and sensory) interact with tumour and stromal cells to promo

143 se regulates cytoskeletal dynamics, controls sensory ion channel localization, and is required to mai

144 of OSCs, activation and revival processes of sensory layers, small area analysis, and pattern recogni

145 er, there is conflicting evidence on whether sensory learning deficits align on the nonclinical end o

146 that motor control is an active component of sensory learning, demonstrating that a detailed understa

147 motor control can be an active component of sensory learning.

148 espread alterations in neural activity after sensory loss.

149 prove recovery in an animal model of chronic sensory loss.

150 id type 1 receptor (CB1) in the formation of sensory maps in the cerebral cortex, the topographic rep

151 auma, sensory disinhibition can constitute a sensory mechanism of intrusive re-experiencing in trauma

152 show the ability to discriminate between two sensory modalities (i.e. see vs smell) in an animal.

153 in social perception is evident for multiple sensory modalities and in many species.

154 Animals integrate information from different sensory modalities, body parts, and time points to infor

155 that similar processes are involved in other sensory modalities.

156 memory that are accessible to more than one sensory modality.

157 ans et al. reveals how a dedicated laryngeal sensory motor reflex circuit protects our airways from a

158 language requires exquisite coordination of sensory, motor, and cognitive processes.

159 es synaptic connectivity and function in the sensory-motor circuit to improve the SMA motor phenotype

160 ath, and reduced neuronal activity in spinal sensory-motor circuits.

161 rk (DMN), fronto-parietal network (FPN), and sensory-motor network (SMN)] function and operate.

162 th theta activity and could serve to enhance sensory-motor processing and memory consolidation during

163 might be related to learning or reinforcing sensory-motor relations in the sensory population.

164 Experiments aiming to understand sensory-motor systems, cognition and behavior necessitat

165 nnectivity within the sensory-motor, lateral sensory-motor, auditory, salience, and subcortical netwo

166 decreased functional connectivity within the sensory-motor, lateral sensory-motor, auditory, salience

167 The major sensory nerve pathway between the colon and central nerv

168 an interesting therapeutic target for human sensory nerve regeneration.

169 of the capsaicin receptor, TRPV1, outside of sensory nerves are unclear.

170 of these cation channels expressed in airway sensory nerves.

171 We propose that KIN-29/SIK acts in nuclei of sensory neuroendocrine cells to transduce low cellular e

172 starvation-dependent modulation of olfactory sensory neuron (OSN) function in the Drosophila larva.

173 The discovery of keratinocyte-sensory neuron synaptic-like contacts may call for a rea

174 The significance of sensory neuron targeting was pursued subsequently by tes

175 g the neuroendrocrine system and mediated by sensory neuronal prolactin receptor.

176 n hillock spiking mechanism of the olfactory sensory neurons (OSNs) have yet to be fully determined.

177 Primary olfactory sensory neurons (OSNs) project their axons directly to t

178 al regulation of molecular signaling between sensory neurons and non-target motor neurons.

179 d a co-culture system of trigeminal ganglion sensory neurons and vascular endothelial cells (VEC) and

180 Ringer is expressed in sensory neurons before and after injury, and is cell-aut

181 erative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury

182 human intrafusal muscle fibers, DRG organoid sensory neurons contact their peripheral targets and rec

183 Diverse sensory neurons exhibit distinct neuronal morphologies w

184 Sex peptide is detected by sensory neurons in the uterus(2-4), and silences these n

185 Deletion of LXR alpha/beta from sensory neurons lead to pain-like behaviors.

186 background potassium current in the primary sensory neurons of the dorsal root and trigeminal gangli

187 Peripheral sensory neurons regenerate their axon after nerve injury

188 We found that conditional knockout of Grp in sensory neurons results in attenuated non-histaminergic

189 s are heavily innervated by nociceptors, the sensory neurons that detect noxious stimuli, leading to

190 nformation transmitted from keratinocytes to sensory neurons through SNARE-mediated (syntaxin1) vesic

191 that processes information perceived by two sensory neurons to control the induction of hydrogen per

192 The molecular mechanisms that enable sensory neurons to remain flexible and adapt to a partic

193 Photoreceptors are highly specialized sensory neurons with unique metabolic and physiological

194 in by the collective population responses of sensory neurons, and an object presented under varying c

195 We identified a subpopulation of olfactory sensory neurons, defined by receptor expression, whose a

196 onditions induce physiological regulation of sensory neurons, which is critical for the maintenance o

197 light of population-wide correlations among sensory neurons.

198 as a regulator of dendritic arborization in sensory neurons.

199 involved in nociceptive pathways, including sensory neurons.

200 ea, diarrhea, anorexia, vomiting, peripheral sensory neuropathy, and keratitis/keratopathy.

201 ormance were plausibly explained by elevated sensory noise.

202 es a bony system supporting soft tissues and sensory organs implicated in either olfactory or thermor

203 While animals track or search for targets, sensory organs make small unexplained movements on top o

204 Free-sorting paired odour testing using sensory panellists identified similarities and clear dif

205 Nonetheless, mechanistic details of these sensory pathways are still sparse and represent a challe

206 A new study has revealed that sensory pathways represent category information, but tha

207 determinants of tip-link-mediated inner-ear sensory perception and elucidate protocadherin-15's stru

208 brain regions, serving an essential role in sensory perception and motor execution.

209 ipheral nerve injuries significantly affects sensory perception and quality of life.

210 assessment of basic assumptions in cutaneous sensory perception and sheds new light on the pathophysi

211 The efficiency of drug delivery and sensory perception is intertwined with mucoadhesive syst

212 how this approach can be used to improve the sensory perception of reduced sucrose sponge cakes.

213 pact of sugar reduction reformulation on the sensory perception of sponge cakes and demonstrates how

214 s, which could significantly influence their sensory perception.

215 Over up to 29 days, stimulation evoked sensory percepts in consistent locations in the missing

216 ry neurons and excitatory neurons track with sensory perturbation.

217 tely regulates both spectral sensitivity and sensory plasticity.

218 fitness, and underscore the need to consider sensory pollutants alongside traditional dimensions of t

219 electrophysiological findings of peripheral sensory polyneuropathy.

220 tor adaptations are accompanied by increased sensory pooling onto interneurons as well as species-spe

221 r reinforcing sensory-motor relations in the sensory population.

222 of mechanosensing in a biopolymer network, a sensory process involved in cellular behavior, medical d

223 ons in cognition [2], motor control [3], and sensory processing [4].

224 revious experience is critical for efficient sensory processing and improved behavioral outcomes.

225 It is unclear to what extent sensory processing areas are involved in the maintenance

226 Norepinephrine adjusts sensory processing in cortical networks and gates plasti

227 the course of learning plays a role in early sensory processing in olfaction.

228 ight into the mechanisms underlying enhanced sensory processing prior to target selection.

229 uces loss of consciousness (LOC) and affects sensory processing remains poorly understood.

230 (FHM2) mutation have slower clearance during sensory processing, as well as previously undescribed sp

231 in future studies of upstream and downstream sensory processing.

232 widely assumed to enhance the sensitivity of sensory processing.

233 ly moving behaviors, could advance models of sensory processing.

234 ng the main contributors to the chemical and sensory profile of aged beer.

235 oft drink formulation and presented suitable sensory profiles as well as high colour stability during

236 Functional and sensory properties of phenol-enriched foods varied as a

237 ings on the textural, handling, cooking, and sensory properties of YAN.

238 Apart from their sensory properties, we will also discuss how electrochem

239 volatiles, were associated with appreciated sensory properties, with alpha-pinene as the main volati

240 ity, peroxide value, volatile compounds, and sensory properties.

241 ing (RL) problems differing in structural or sensory properties.

242 otypes with unknown chemical composition and sensory quality is extremely important since these data

243 -butyrolactone also contributed to score and sensory quality of coffee beverage.

244 However, phenols may negative affect sensory quality of food.

245 associations between metabolite profile and sensory quality, by integrating non-target metabolomics

246 vars and likely contribute to differences in sensory quality.

247 -harvest treatments, oxidative stability and sensory quality.

248 plitude-seemingly giving rise to a change in sensory quality; on others, they were not.

249 lear inner hair cells (IHCs) are specialized sensory receptors able to provide dynamic coding of soun

250 Injury to the sensory receptors shortly after birth leads to predictab

251 in the alpha to beta range in task-relevant sensory regions have been suggested to play an important

252 amodal patterns included activity in primary sensory regions not directly relevant to the task (e.g.,

253 riments in pea protein samples confirmed the sensory relevance of the identified compounds and indica

254 to enter information processing and activate sensory representations of trauma, sensory disinhibition

255 ns the gap junctions and induces a repulsive sensory response to the training odorants, which togethe

256 with which convergence enables stereotypy in sensory responses despite random connectivity.

257 prominent in layer 1 of cortex as opposed to sensory responses that activate layer 4 first and sequen

258 DTA showed no accumulation in the muscle and sensory results demonstrated that the lowest concentrati

259 ast side-chain dynamics of the alpha-helical sensory rhodopsin II and the beta-barrel outer membrane

260 streams segregate many diverse features of a sensory scene.

261 memories to detect relevant cues in complex sensory scenes.

262 or further revealing the neural mechanism of sensory selection and distractor suppression.

263 or control thus can be crucial to understand sensory sensation and perception under naturalistic cond

264 easures of autistic traits, systemizing, and sensory sensitivity, and, on average, lower on self-repo

265 These results show how local sensory signals can be transformed into a global, multim

266 vide the foundation for the gut to transduce sensory signals from the intestinal milieu to the brain

267 ia in barrel cortex by chronically depriving sensory signals via whisker trimming for the animals' fi

268 ation by impairing the central processing of sensory signals.

269 , including the inhibition of self-generated sensory signals.

270 combining past experiences with new incoming sensory signals.

271 s that will process information from similar sensory space exhibit highly correlated electrical activ

272 In sensory-specific Piezo2-deficient mice, the distribution

273 sis may emerge because of a failure to learn sensory statistics, resulting in an impaired representat

274 m of how memory consolidation is affected by sensory stimulation during sleep.

275 Empirical studies found that sensory stimulation during SWS can selectively enhance m

276 activity in the somatosensory cortex during sensory stimulation.

277 wo to five times larger than those evoked by sensory stimulation.

278 tigated the cortical activity in response to sensory stimuli in these conditions.

279 t the primate amygdala acts, in part, like a sensory structure for the affective import of stimuli an

280 the peripheral nerves, causing weakness and sensory symptoms.

281 There is an ever-rising interest in this sensory system as a neurobiological model to study devel

282 ccording to the efficient coding hypothesis, sensory systems are adapted to maximize their ability to

283 l changes in key regions of the learning and sensory systems associated with anesthesia-induced learn

284 Sensory systems constantly compare external sensory info

285 f sound.SIGNIFICANCE STATEMENT In developing sensory systems, groups of neurons that will process inf

286 Three sensory systems, the olfactory, gustatory, and solitary

287 sing and thus enhances performance on intact sensory systems.

288 , and investigated their modulation during a sensory-task, whisker stimulation.

289 mulus, using mechanical/thermal quantitative sensory testing (MQST or TQST), were performed at the me

290 Quantitative sensory testing showed abnormal findings.

291 As in sensory thalamic systems, large amygdalar terminals inne

292 This VNS-dependent restoration of sensory thresholds was maintained for several months aft

293 to invoke mechanical specializations of the sensory tissue.

294 ited a variety of amplitude modulations from sensory to cognitive, notably by choice and accumulated

295 lux, particularly in neurons associated with sensory transduction.

296 dynamics of the external world and estimates sensory uncertainty by combining past experiences with n

297 We manipulate sensory uncertainty by varying retinal eccentricity.

298 Crucially, trial-by-trial manipulation of sensory uncertainty is a key test to whether humans perf

299 on" in the sense that they take into account sensory uncertainty via a heuristic rule.

300 anisms represent uncertainty associated with sensory variables.

301 ide critical insight to preserve the natural sensory world.