ライフサイエンスコーパス: tactile

1 euron pathophysiological mechanisms underlie tactile abnormalities in different ASD mouse models and

2 novel actuators, such as tunable lenses and tactile actuators.

3 However, tactile acuity did not explain the distortions observed

4 hannels to control neuronal excitability and tactile acuity through tonic inhibition of thalamic neur

5 ative to their length was predicted by their tactile acuity, supporting the influence of the cortical

6 ) between the felt and vicariously perceived tactile affectivity led to higher subjective embodiment

7 detection thresholds (p < 0.01), impaired C-tactile afferents (p < 0.05), and reduced amplitudes (p

8 Specific, peripheral C-tactile afferents contribute to the perception of tactil

9 C-tactile afferents form a distinct channel that encodes p

10 hy, quantitative sensory testing including C-tactile afferents, and pain-related evoked potentials.

11 ransduction properties of identified primary tactile afferents.

12 terestingly, peripheral nerve injury induces tactile allodynia and upregulates Ca(V)3.2 channels and

13 entration able to activate the HCAR2-reduced tactile allodynia in female WT mice, but not in the HCAR

14 males and females display a severe sustained tactile allodynia which is reduced by gabapentin but not

15 h dimethylfumarate (DMF) and BHB reduced the tactile allodynia.

16 proprioceptive deficits and fail to develop tactile allodynia.

17 n after SNL contributes nerve injury-induced tactile allodynia.SIGNIFICANCE STATEMENT Neuropathic pai

18 SnF(2) or hydroxyapatite were beneficial for tactile and air stimulus with high to moderate certainty

19 ept brain-to-spine interface (BTSI), whereby tactile and artificial sensory information are decoded f

20 ystems that provide not only visual but also tactile and audible three-dimensional (3D) content.

21 on operating principles that cannot produce tactile and auditive content as well.

22 -by-trial alertness and neuronal response to tactile and auditory stimulation.

23 sponses, here, we measured BOLD responses to tactile and auditory stimuli for both JMD patients and c

24 Also, potentials evoked by tactile and electrical stimuli showed different short-la

25 e pectoral filaments of threadfins have both tactile and gustatory functions.

26 derstanding the dissociable contributions of tactile and kinesthetic information to perception and ac

27 arly 50% between the no feedback and hybrid (tactile and kinesthetic) trials (p < 1.0E-16).

28 tribute to the processing and segregation of tactile and nociceptive information.

29 kground 5-HT3R mediated facilitation of both tactile and nociceptive spinal activity in the first thr

30 it modules that cooperate to convey thermal, tactile and noxious cutaneous signals from the spinal co

31 graphy of this facial and head motion during tactile and olfactory exploration.

32 tral to a wide range of functions, including tactile and pain perception, hearing, proprioception, an

33 m ABSTRACT: Numerous studies have documented tactile and proprioceptive deficits in children with cer

34 developed as a novel platform for delivering tactile and proprioceptive feedback in clinical applicat

35 t fibers, and pathways involved in conveying tactile and proprioceptive information to the DCN.

36 lassify, and discriminate various intermixed tactile and thermal stimuli using a machine-learning app

37 n nonhuman primates presented with auditory, tactile, and audio-tactile stimuli as they are progressi

38 The convergence of visual, tactile, and auditory signals at the level of individual

39 se components differentiated between visual, tactile, and auditory stimuli suggesting the presence of

40 keys (Macaca mulatta) in response to visual, tactile, and auditory stimuli.

41 statistically separable responses to visual, tactile, and auditory stimuli.

42 sian modeling with fMRI, we show that during tactile associative learning, prior expectations modulat

43 y the majority of the participants, with the tactile BCI being experienced as more intuitive.

44 ning either using an auditory BCI or using a tactile BCI.

45 In this study, we compared auditory and tactile BCIs, regarding training effects and cross-stimu

46 Studies of tactile behaviors in ant societies are now needed.

47 We first describe the multisensory (audio-tactile) characteristics of S1 and vPM neurons (mean and

48 ial scales and provide a limited window into tactile coding.

49 terest was painful response measured through tactile, cold, and air stimuli.

50 uation occurs because the brain predicts the tactile consequences of our self-generated movements.

51 ng who received either high (HC) or low (LC) tactile contact from their parents have differences in t

52 simultaneously deliver visual, auditory and tactile content, using acoustophoresis as the single ope

53 the MATD delivers simultaneous auditive and tactile content.

54 posterior and anterior insula lesions reduce tactile, contralateral and ipsilateral pleasantness sens

55 A tactile cue to uncrossed or crossed hands was either inf

56 al abilities, which rely on chemosensory and tactile cues and, to a lesser degree, on vision.

57 recognition occurs via visual, chemical, or tactile cues that dictate cooperative versus competitive

58 oral predictability of tactile targets using tactile cues, which preceded the target by either consta

59 f mice running on a treadmill populated with tactile cues.

60 glove sensor array, we record a large-scale tactile dataset with 135,000 frames, each covering the f

61 tudy shows that animal choices during active tactile decision making can be predicted from mechanosen

62 tes in the motor cortex of mice performing a tactile decision task.

63 lation and in vivo calcium imaging to assess tactile defensiveness and barrel cortex activity in youn

64 cal sensory circuits is a potential cause of tactile defensiveness in autism.SIGNIFICANCE STATEMENT W

65 h can lead to maladaptive behaviors, such as tactile defensiveness.

66 le X syndrome (FXS), and frequently leads to tactile defensiveness.

67 We found that deviant stimuli enhanced tactile detection and were encoded in L2/3 neural tuning

68 o attend to one hand in order to detect rare tactile deviant stimuli at this hand while ignoring tact

69 deviant stimuli at this hand while ignoring tactile deviants at the other hand and tactile standard

70 llations, replicating previous findings, and tactile DFI to occipital beta oscillations, a rhythm typ

71 lts show that V5/hMT+ plays a causal role in tactile direction processing, and strengthen the case fo

72 Overall, these findings indicate that active tactile discrimination by rats is characterized by much

73 while freely moving rats performed an active tactile discrimination task.

74 perceptual performance of animals performing tactile discrimination tasks through LC-norepinephrine o

75 ving rodents can make simultaneous bilateral tactile discrimination without whisking.SIGNIFICANCE STA

76 vibrissal somatosensory cortex during active tactile discrimination.

77 made forced-choice judgments of which of two tactile distances felt bigger, one oriented with the pro

78 resent peripherally available drugs to treat tactile-driven pain following neuropathy.

79 tterns, suggesting a somatotopically precise tactile encoding capability of the mechanosensory dorsal

80 tosensory (S1) cortex in normally housed vs. tactile-enriched mice, using GCaMP6s imaging.

81 aracterize the effect of the prior belief of tactile events on connections mediating the outcome of p

82 isual and auditory events but not visual and tactile events.

83 analogous preparatory response for unrelated tactile events.

84 of natural textures-which span the range of tactile experience and engage all the known mechanisms o

85 Motion is an essential component of everyday tactile experience: most manual interactions involve rel

86 ns of touch, such as those that occur during tactile exploration, is poorly understood.

87 During active tactile exploration, the dynamic patterns of touch are t

88 virtual gratings through a process of active tactile exploration.

89 1) and tactile (Expt.

90 to rapidly and efficiently use the tool as a tactile extension of the body.

91 system that has yet to be properly examined: tactile facial bristles in birds.

92 le embedded sensors to provide comprehensive tactile feedback of a human hand when touching or holdin

93 Due to loss of tactile feedback the assessment of tumor margins during

94 Subjects received tactile feedback using three biologically inspired stimu

95 sFES) of the lower-limbs, proprioceptive and tactile feedback, balance control through overground wal

96 ped a model to simulate the responses of all tactile fibers innervating the glabrous skin of the hand

97 re also sensitive to abrupt perturbations of tactile flow during running.

98 d vision, we discuss the first evidence of a tactile "fovea" in birds and how this led to detailed st

99 rding microsaccades while people performed a tactile, frequency discrimination task enabled us to tes

100 e for investigating both normal and abnormal tactile function in healthy and clinical populations.

101 e use of psychophysical experiments to probe tactile function.

102 Here we use a scalable tactile glove and deep convolutional neural networks to

103 Using a low-cost (about US$10) scalable tactile glove sensor array, we record a large-scale tact

104 d the relationships between touch threshold, tactile gnosis, and mechanoreceptor and sensory fiber fu

105 surgical procedures to complement visual and tactile guidance.

106 ptors (NMDARs) in primary afferents leads to tactile hypersensitivity across skin types, and loss of

107 involved in CD155 binding to poliovirus and Tactile in human.

108 tantly, they provide novel evidence that the tactile-induced DFI is instead mediated by the speed of

109 oscillatory correlates of the auditory- and tactile-induced double flash illusion (DFI), a phenomeno

110 ory-to-visual areas leading to the same (but tactile-induced) DFI share similar properties with the a

111 ic devices are needed to efficiently process tactile information in a parallel and low power manner.

112 New research shows that tactile information in the cortex rises and falls in pha

113 ntly limits our understanding of the role of tactile information in the human grasp itself-for exampl

114 Tactile information is detected by thermoreceptors and m

115 to functional changes in these major hubs of tactile information processing, whisker stimulation duri

116 erneuron populations have been implicated in tactile information processing.

117 datasets with which to probe the use of the tactile information that humans rely on when grasping ob

118 The automatic remapping between skin-based tactile information to a location in external space has

119 manipulating objects, we use kinesthetic and tactile information to form an internal representation o

120 ic dorsal column (PSDC) pathway transmitting tactile information to the brain are poorly characterize

121 ubcortical pathway allows fast re-routing of tactile information to the occipital cortex, but this ha

122 the integration of exteroceptive visual and tactile information.

123 sed on asymmetry, (2) even in the absence of tactile input, whisker positioning and asymmetry neverth

124 eceptors and we rely on integrating cold and tactile inputs from A-type skin nerve fibres to sense we

125 The integration of visual, auditory, and tactile inputs in the amygdala may serve social communic

126 of the network in a way that converts analog tactile 'inputs' into digital colorimetric 'outputs'.

127 evolutionarily conserved mediator of thermal-tactile integration in cutaneous mechanoreceptors.

128 We used an audio-tactile integration task to measure the PPS boundary at

129 improve owner's well-being, (e.g. human-dog tactile interaction increases owner's self-esteem), and

130 indicating an added benefit of close contact tactile interaction.

131 Research has suggested that tactile judgment of speed is influenced by physical prop

132 ic feedback system was designed to allow for tactile, kinesthetic, and vibrotactile feedback, with th

133 These findings preclude privileged C-tactile-lamina I-spinothalamic projections and imply int

134 precision of prediction during probabilistic tactile learning.SIGNIFICANCE STATEMENT In a probabilist

135 aps in somatosensory cortex, suggesting that tactile localisation involves coding of abstract feature

136 w research demonstrates systematic errors of tactile localisation, involving confusions of body parts

137 riments demonstrating that the perception of tactile localization on a static body part is strongly a

138 Sighted humans concurrently encode tactile location in skin-based and, after integration wi

139 n in the human grasp itself-for example, how tactile maps are used to identify objects and infer thei

140 Conventional visual and tactile methods for assessing lesion activity are not re

141 Tactile mislocalizations can depend on the timing of suc

142 cts of sensory congruency between visual and tactile modalities in the sense of body ownership.

143 timing of successive stimulations [2, 4, 5], tactile motion mechanisms [6], or processes that "remap"

144 Much of the research on the neural basis of tactile motion perception has focused on how direction i

145 es have reported activations associated with tactile motion perception in visual motion area V5/hMT+,

146 whether these areas are causally involved in tactile motion perception.

147 ce directions and strain profiles in various tactile motions (shear, pinch, spread, torsion, and so o

148 Here, auditory-tactile multisensory neurons were predominant and consti

149 multiple cortical areas that are involved in tactile, multisensory, and spatial processing.

150 asp and manipulate an object, populations of tactile nerve fibers become activated and convey informa

151 Other types of bodily experiences, such as tactile or vestibular sensations, were not affected by t

152 ve finger displacements biased participants' tactile orientation judgements (experiment 1).

153 g peripheral mechanosensory neurons to treat tactile over-reactivity and select ASD-related behaviors

154 s directly on mechanosensory neurons reduced tactile over-reactivity in six distinct ASD models.

155 stimate their weight and explore the typical tactile patterns that emerge while grasping objects.

156 r freely behaving rats can discriminate fine tactile patterns while running, in particular when stimu

157 and revealing a crossmodal coupling between tactile perception and oculomotor action.

158 ensory perturbations in visual, auditory and tactile perception are core problems in fragile X syndro

159 Active tactile perception combines directed motion with sensory

160 ssential for real-time health monitoring and tactile perception in robots.

161 In the somatosensory nerves, the tactile perception of texture is driven by spatial and t

162 udy, we investigated the effect of providing tactile perception on motor coordination during routine

163 h touch signals to enable spatially accurate tactile perception, but other functions of phase coding

164 ors are involved in modulating gustatory and tactile perception.

165 in designing suitable sensors and restoring tactile perceptions, pain perception dynamics and its de

166 ial representations can account for atypical tactile percepts in some neurological patients and amput

167 le afferents contribute to the perception of tactile pleasure, but the brain areas involved in their

168 etic stimulation (TMS) while moving a single tactile point across the fingertip, and used signal dete

169 To produce attenuation, the tactile predictions need to be time-locked to the moveme

170 rames encoded by oscillatory activity during tactile processing were probed by adopting either an unc

171 y plays a similar role in spatial coding for tactile processing, that is, after the stimulus has been

172 neural coding of spatial information during tactile processing.

173 m of rodents is a widely used model to study tactile processing.

174 abnormalities in sensory functions, such as tactile, proprioceptive and nociceptive processing, have

175 life of chocolate and affects its visual and tactile quality, all of which are serious concerns for c

176 Human skin has different types of tactile receptors that can distinguish various mechanica

177 lementation of closed-loop VNS paired with a tactile rehabilitation regimen could improve recovery of

178 VNS paired with tactile rehabilitation resulted in a significant and nea

179 Moreover, VNS paired with tactile rehabilitation resulted in significant generaliz

180 op vagus nerve stimulation (VNS) paired with tactile rehabilitation to enhance synaptic plasticity an

181 usly evaluate the ability of VNS paired with tactile rehabilitation to improve recovery in an animal

182 Equivalent tactile rehabilitation without VNS failed to improve sen

183 that alpha-band directly reflects automatic tactile remapping processes.

184 n but challenge the role of external-spatial tactile representations when attributing touch to a limb

185 Here, we introduce the Tactile Resistive Annularly Cracked E-Skin (TRACE) senso

186 e; p75(fx/fx) mice had normal taste and oral tactile responses.

187 onto-parieto-occipital cortical areas during tactile sampling.

188 studied for decades in the context of direct tactile sensation, but recent work has indicated that ra

189 the mechanoreceptor responses that underlie tactile sensation.

190 MS) of the somatosensory cortex evokes vivid tactile sensations and can be used to convey sensory fee

191 Second, tactile sensing capability such as the detection of pres

192 s deployed to detect moving orientation in a tactile sensing system.

193 hat probably functioned in thermoregulation, tactile sensing, signalling and aerodynamics.

194 es of layer 5b basal dendrites during active tactile sensing.

195 tackle the grand challenges in pressure- and tactile-sensing applications, in particular, with recent

196 r the past decade, a brand-new pressure- and tactile-sensing modality, known as iontronic sensing has

197 he High ED group, physiological arousal, and tactile sensitivity (d') were increased when self-focuse

198 ve body parts affording different degrees of tactile sensitivity and visual accessibility.

199 hether they differ from shoes in maintaining tactile sensitivity during walking, especially at initia

200 egnancy yielded adult offspring with altered tactile sensitivity in two aversive somatosensory behavi

201 phenotypes spanning morphology, locomotion, tactile sensitivity, and habituation learning in 135 str

202 viding protection and comfort at the cost of tactile sensitivity, cushioned footwear also lowers rate

203 m with a passive piezoelectric device as the tactile sensor.

204 Soft tactile sensors employing such network electrodes exhibi

205 Although sensitive and accurate tactile sensors have been produced on optical and electr

206 Thus, the position of these mobile tactile sensors reflects a behavioral and movement-prepa

207 rinting approach is employed to fabricate 3D tactile sensors under ambient conditions conformally ont

208 how that, in mice, the movement of whiskers (tactile sensors used to extract information about textur

209 Moreover, we show that these tactile sensors when arrayed enabled fast reliable one-t

210 de-off between sensitivity and hysteresis in tactile sensors when using soft materials.

211 he sensitivity and pressure-sensing range of tactile sensors, the intrinsic viscoelasticity of soft p

212 active touch to optimize the acuity of their tactile sensors.

213 Processing of tactile sensory information in rodents is critically dep

214 Owing to the absence of tactile sensory information, prosthetic users must rely

215 t is unclear how this contributes to altered tactile sensory processing in the mature CNS.

216 tterns presented on the tongue using electro-tactile sensory substitution devices (SSDs) have been su

217 Tactile shape recognition requires the perception of obj

218 n-noise performance in CI users using: (1) a tactile signal derived using an algorithm that could be

219 iate for a real-world application, and (3) a tactile signal that could readily be produced by a compa

220 rtantly, the inability to record and analyse tactile signals currently limits our understanding of th

221 Insights from the tactile signatures of the human grasp-through the lens o

222 In their natural habitat, a buried tactile sound transducer was used to emit simulated traf

223 e before, plays a strong role in structuring tactile spatial perception.

224 alpha-band activity is directly involved in tactile-spatial transformation and suggest instead that

225 ctivity relative to behavioral indicators of tactile-spatial transformations.

226 all types of mechanoreceptors from mice and tactile-specialist birds.

227 rphic cortical computations in large-brained tactile specialists.

228 irds and how this led to detailed studies of tactile specializations in waterfowl and sensorimotor sy

229 oring tactile deviants at the other hand and tactile standard stimuli at both hands.

230 ebellar vermis has a crucial role in a delay tactile startle learning paradigm in mice.

231 Vibro-tactile stimulation (VTS) alters afferent proprioceptive

232 Each keypress triggered synchronous tactile stimulation at a randomized location on the immo

233 However, the perceived location of a tactile stimulation can differ from its physical locatio

234 and electrophysiological signals elicited by tactile stimulation co-localized to the ipsilateral dors

235 so exhibit natural variation in the level of tactile stimulation delivered by the parents to the offs

236 mice were more sensitive to relatively weak tactile stimulation in a vibrissa motion detection task.

237 n studies by near-nerve technique, including tactile stimulation of mechanoreceptors, were followed f

238 in multi-talker noise with and without vibro-tactile stimulation of the wrist in CI users, before and

239 echanisms modifiable by effects of postnatal tactile stimulation on glucocorticoid receptor gene expr

240 show using magnetoencephalography (MEG) that tactile stimulation produces occipital cortex activation

241 uring attentional orienting in expectance of tactile stimulation reflected external spatial coding in

242 icipants reported the location of the second tactile stimulation relative to the first.

243 the hand that moved was placed far from the tactile stimulation site (experiments 4 and 5).

244 alpha-Band suppression following tactile stimulation was lateralized relative to the stim

245 r) system in the context of direct touch and tactile stimulation, but recent work has shown that rats

246 g global activation to visual, olfactory and tactile stimulation, particularly in the brainstem/cereb

247 urons in primary somatosensory cortex during tactile stimulation, we found that stimulus onset and of

248 orm a distinct channel that encodes pleasant tactile stimulation.

249 er, the production of the saccades guided by tactile stimulation.

250 tion, could hear, see, smell, and respond to tactile stimulation.

251 not they spike repetitively during sustained tactile stimulation; the former are subclassified as Typ

252 hrony within 600 ms between the movement and tactile stimulations was necessary for the effect (exper

253 s have used artificially long delays between tactile stimuli and behavioral responses to aid relating

254 Differentiation between self-produced tactile stimuli and touch by others is necessary for soc

255 ivity and defensive behaviors in response to tactile stimuli are common symptoms in autism spectrum d

256 Tactile stimuli are integrated and processed by neuronal

257 presented with auditory, tactile, and audio-tactile stimuli as they are progressively anesthetized w

258 s and stiffness, for the ability to perceive tactile stimuli at frequencies experienced during walkin

259 The effect generalized to tactile stimuli delivered to other body sites (experimen

260 d to reflect the automatic transformation of tactile stimuli from a skin-based, somatotopic reference

261 avior of revealing warning colors only after tactile stimuli from predator attack.

262 sets of similar mildly aversive auditory and tactile stimuli in 42 high-functioning children and adol

263 nes.SIGNIFICANCE STATEMENT Overreactivity to tactile stimuli is a common symptom in autism spectrum d

264 ection Task (SSDT), which involved detecting tactile stimuli on the cheek in the presence or absence

265 In contrast, when judging visual or tactile stimuli presented on their own body surface, or

266 ons and L2/3 neurons continually integrating tactile stimuli with running.

267 ce learned to discriminate 'go' from 'no-go' tactile stimuli(10,11) and adapt their behaviour upon re

268 Participants received two tactile stimuli, each to a different limb-hand or foot-a

269 ot replicate the afferent signals of natural tactile stimuli.

270 subtypes that exhibit distinct responses to tactile stimuli.

271 significantly stronger for noxious than for tactile stimuli.

272 profound deficits in responses to taste and tactile stimuli.

273 attention on the ability to correctly detect tactile stimuli.

274 Animals adaptively respond to a tactile stimulus by choosing an ethologically relevant b

275 When humans indicate on which hand a tactile stimulus occurred, they often err when their han

276 Locating a tactile stimulus on the body seems effortless and straig

277 that newborns' saccadic reaction times to a tactile stimulus simultaneous to sounds with different i

278 the threshold for detection of an additional tactile stimulus was elevated.

279 For tactile stimulus, the following active ingredients showe

280 strontium and potassium were beneficial for tactile stimulus, with moderate certainty.

281 monkeys judged the presence or absence of a tactile stimulus.

282 Two haptic interfaces-a tactile surface and a kinesthetic glove-are demonstrated

283 essential for the perception of fine-grained tactile surfaces.

284 regarding the cortical organization of this tactile system.

285 Moreover, microsaccades occurring around the tactile target presentation are associated with reduced

286 nd that microsaccades are inhibited prior to tactile targets and more so for constant than variable i

287 e manipulated the temporal predictability of tactile targets using tactile cues, which preceded the t

288 s, revealing a tight crossmodal link between tactile temporal expectation and oculomotor action.

289 dorsal premotor cortex during comparison of tactile temporal patterns can be understood in terms of

290 d most prevalent sensory experience includes tactile, thermal, and olfactory stimulation delivered to

291 st human lesion study on the perception of C-tactile touch in right hemisphere stroke patients (N = 5

292 defensive and emotional responses, and light tactile touch may induce unpleasant itch sensations (mec

293 band lateralization does not index automatic tactile transformation.

294 A tactile, UV- and solar-light multi-sensing smart recharg

295 auditory training group that switched to the tactile version but not vice versa.

296 x using calcium imaging in mice running in a tactile virtual reality.

297 nitive efficiency correlated among auditory, tactile, visual, and audiovisual tasks.

298 eshold tasks involving subjective reports of tactile, visual, or auditory stimuli during the same mag

299 s, has sustained effects on audio-visual and tactile-visual temporal biases and resolution.

300 d a task in which mice distinguished between tactile "word" sequences constructed from distinct vibra