ライフサイエンスコーパス: sensorimotor

1 Our work informs how emerging sensorimotor ability comes to impact how and why animals

2 Although sensorimotor abnormalities are often present in these di

3 disorder characterized by multiple tics and sensorimotor abnormalities, the severity of which is typ

4 The aim of this study was to identify how sensorimotor adaptation of the upper limb, a cerebellar-

5 performance reaches asymptotic levels during sensorimotor adaptation.

6 sal frontoparietal circuit together with the sensorimotor and associative frontostriatal networks too

7 ng as well as to aftereffects on a number of sensorimotor and attention tasks, but whether these effe

8 ymptomatic period characterized by disrupted sensorimotor and attentional experience, leads to altere

9 The pons controls crucial sensorimotor and autonomic functions.

10 ral integrators are involved in a variety of sensorimotor and cognitive behaviors.

11 ism for conferring temporal flexibility upon sensorimotor and cognitive functions.

12 ion enhances consolidation, stabilizing both sensorimotor and cognitive prism after-effects.

13 was correlated with improved performance on sensorimotor and cognitive tests.

14 type of action requires an interface between sensorimotor and conceptual abilities.

15 Higher gamma connectivity between left sensorimotor and inferior parietal cortex was also found

16 a wide range of contralateral projections to sensorimotor and limbic structures.

17 so fine grained that the cortical sources in sensorimotor and medial prefrontal cortex even distingui

18 LD, which particularly affected the primary sensorimotor and parietal cortices and thalamus.

19 visual and parietal regions coordinated with sensorimotor and premotor areas.

20 ontrolled for attentional filtering ability, sensorimotor and temporal decay factors.

21 al and parietal lobe than primary regions of sensorimotor and visual function.

22 studied the effects of cognitive, emotional, sensorimotor, and mixed stressors on driver arousal and

23 l firing patterns within and across sensory, sensorimotor, and premotor layers.

24 Much as the sensorimotor apparatus shapes natural motor control, the

25 we recorded neural activity in a prefrontal sensorimotor area while monkeys naturally switched betwe

26 ly -400 ms before response, originating from sensorimotor areas including dmFC, precuneus, and poster

27 Instead, the neural plasticity in sensorimotor areas is sensitive to the temporal structur

28 itive, spatially selective activity found in sensorimotor areas of nonhuman primates.

29 anial direct current stimulation (tDCS) over sensorimotor areas to modulate neural lateralization pat

30 AG was functionally correlated with cortical sensorimotor areas, conducive to facilitating fight/flig

31 of connectivity between dorsal striatum and sensorimotor areas.

32 eocortical networks involved in mnemonic and sensorimotor aspects of navigation.

33 though the striatum is thought to consist of sensorimotor, associative and limbic domains, their prec

34 Here we show that sensorimotor attenuation occurs in 98% of adults in a po

35 This leads to sensorimotor attenuation-a reduction in the perceived in

36 Two patients subsequently were found to have sensorimotor autonomic neuropathy, whereas 2 others had

37 Active whisking is an important model sensorimotor behavior, but the function of the cerebellu

38 tical for learning the appropriate timing of sensorimotor behaviors, but whether and how appropriate

39 ransgenic mice are viable and display normal sensorimotor behaviors.

40 The findings suggest that sensorimotor beta-band rhythms disinhibit task-relevant

41 Auditory and sensorimotor brain areas interact during the action-perc

42 report the discovery in the forebrain HVC of sensorimotor 'bridge' neurons that simultaneously and se

43 bilateral corpus callosum was increased but sensorimotor CBF was decreased, particularly in the ipsi

44 ral executive, primary and secondary visual, sensorimotor, cerebellar, and auditory networks.

45 irst detailed characterization of rat spinal sensorimotor circuit development in the presence and abs

46 Adult rats can thus develop a novel cortical sensorimotor circuit that bypasses the lesion, probably

47 e lineage-related interneurons contribute to sensorimotor circuitry in the Drosophila larva.

48 ime courses in plasticity of associative and sensorimotor circuits across learning that involve chang

49 The sensorimotor circuits activated by twitching limbs, and

50 d, trigger abundant reafferent activation of sensorimotor circuits in the developing brain.

51 nectivity related to movement exploration in sensorimotor circuits involved in somatic memory and dec

52 ime, reorganization and refinement of spinal sensorimotor circuits occurs as supraspinal projections

53 l parallel processing within associative and sensorimotor circuits that challenges and refines existi

54 The delineation of sensorimotor circuits that guide exploration begins with

55 Detailed descriptions of brain-scale sensorimotor circuits underlying vertebrate behavior rem

56 Excitation of left sensorimotor circuits, during an adaptive cognitive stat

57 gions.Active locomotion requires closed-loop sensorimotor co ordination between perception and action

58 information, provided we adopt the view that sensorimotor computation manipulates desired movement tr

59 ide insight into brain areas responsible for sensorimotor computation, we used complex categorization

60 ions of MT and LIP and motivate inquiry into sensorimotor computations that may intervene between MT

61 ceptual suppression may arise from efficient sensorimotor computations, assuming that perception and

62 cerebellar atrophy and decreased cerebellar-sensorimotor connectivity.

63 These results highlight the importance of sensorimotor constraints in abstract rule formation and

64 n rules are also an opportunity to establish sensorimotor constraints that influence how the behavior

65 llows for highly detailed representations of sensorimotor context, enabling downstream Purkinje cells

66 like embodied cognition, common coding, and sensorimotor contingency that do not sequentially separa

67 rocesses account for module selection during sensorimotor control and learning.

68 related to sudden disruptions in prefrontal sensorimotor control and rapid, reward-dependent reorgan

69 Computational models of sensorimotor control have emphasized the importance of t

70 gh there has been considerable research into sensorimotor control in humans, the steps between sensor

71 of beta oscillations have been implicated in sensorimotor control in the basal ganglia of task-perfor

72 ankle muscle control is adjusted rapidly in sensorimotor control loops as opposed to longer-term err

73 action options, computes multiple competing sensorimotor control policies in parallel before impleme

74 irection; it requires the specification of a sensorimotor control policy that sets feedback gains sha

75 Current models of sensorimotor control posit that motor commands are gener

76 rity within tracts known to connect cortical sensorimotor control regions dictates the functional inf

77 ding of the function of beta oscillations in sensorimotor control, and provides further insight into

78 llar involvement in cognition, as well as in sensorimotor control, is increasingly recognized and is

79 e therefore critical to our understanding of sensorimotor control.

80 d for more complex synchrony of higher-order sensorimotor coordination, proprioceptive and tactile fe

81 representation of learning models and their sensorimotor copies.

82 ctivated by designer drug) receptor hM4Di in sensorimotor cortex and AAV-expressing Cre in C7/C8 dors

83 nderwent photothrombotic stroke of the right sensorimotor cortex and chronic implantation of a stimul

84 tionship between focal reorganization in the sensorimotor cortex and everyday behavior.

85 nalyses revealed a negative correlation over sensorimotor cortex between gamma-oscillatory activity a

86 at either 10 or 20 Hz and was imposed on the sensorimotor cortex contralaterally or ipsilaterally to

87 Microbeam irradiation of sensorimotor cortex did not affect weight gain and motor

88 post-movement beta activity (13-30 Hz) over sensorimotor cortex in young healthy subjects indexes th

89 d by cortical evoked potentials (EPs) in the sensorimotor cortex of awake, behaving monkeys.

90 iMSNs) and optically stimulated inputs from sensorimotor cortex or intralaminar thalamus in brain sl

91 he result of the characterization of the rat sensorimotor cortex tolerance to microradiosurgical para

92 Finally, specific subregions of sensorimotor cortex were identified in which deep brain

93 eural oscillations originating from the left sensorimotor cortex, and directed toward auditory region

94 aining induces significant plasticity in the sensorimotor cortex, manifested as improved discriminabi

95 sults from maladaptive reorganization of the sensorimotor cortex, suggesting that experimental induct

96 ts with stronger alpha suppression over left sensorimotor cortex, whereas the Taylor illusion correla

97 performance and less EEG mu suppression over sensorimotor cortex.

98 eta desynchronization is a shared feature of sensorimotor cortical activity in Parkinson's disease an

99 A key role for DLS is to transform sensorimotor cortical input into firing of output neuron

100 These observations suggest that sensorimotor cortical neurons corepresent rewards and mo

101 thout a movement disorder by reducing excess sensorimotor cortical phase-amplitude coupling that is c

102 well as theta coherence between auditory and sensorimotor cortices, was stronger in the second listen

103 ) to entrain brain rhythms in left and right sensorimotor cortices.

104 d enhanced connectivity between auditory and sensorimotor cortices.

105 istic mechanisms were related to activity in sensorimotor corticostriatal circuitry.

106 the neurophysiological underpinnings of this sensorimotor coupling in humans.

107 Our findings show that testing sensorimotor de-adaptation could provide a potential pre

108 though behavioral effects of value biases in sensorimotor decision making have been widely studied, l

109 esses, aperiodic sampling is associated with sensorimotor decision making within specific frontal, st

110 sms that contribute to the Drosophila larval sensorimotor decision to startle, explore, or perform a

111 Here we developed an adaptive sensorimotor decision-making task for head-fixed mice, r

112 biased state of preparation for an impending sensorimotor decision.

113 During sensorimotor decisions, competitive interactions among n

114 rmobaric oxygen therapy completely prevented sensorimotor deficit (P < 0.02) and near-completely Day

115 on of theta could underlie the cognitive and sensorimotor deficits associated with neurodevelopmental

116 py prevents both selective neuronal loss and sensorimotor deficits in a rodent model mimicking true t

117 28 post-mortem) and marked and long-lasting sensorimotor deficits, normobaric oxygen therapy complet

118 raining resulted in moderate improvements of sensorimotor deficits.

119 as a result of signal dependent noise and of sensorimotor delays.

120 neonatal imitation based on the analysis of sensorimotor development.

121 tate predictor can mimic certain outcomes of sensorimotor diseases.

122 The discovery of predictive, non-sensorimotor encoding in granule cells is a major depart

123 and influenced functional connectivity among sensorimotor, executive, and limbic networks.

124 a significant feature of the infant's early sensorimotor experience, and therefore may play a key ro

125 connectivity constraints that do not require sensorimotor experience.

126 others which, by uncoupling the dynamics of sensorimotor facilitation, could ultimately perturbe mot

127 Rapid limb-specific sensorimotor feedback adaptation may be advantageous for

128 Our work investigated mechanisms of dynamic sensorimotor feedback control by analyzing patterns of n

129 sent serial motor decision making within the sensorimotor feedback loop intrinsic to tracking?

130 The resulting sensorimotor-focused approach offers an account of LIP a

131 atase-expressing neurons in the auditory and sensorimotor forebrain of zebra finches.

132 mans makes it worth pursuing for recovery of sensorimotor function after injury to the central nervou

133 lators and their effects on gastrointestinal sensorimotor function and conducted an evidence-based re

134 d estrogens has been shown to rapidly affect sensorimotor function and sexual motivation in birds.

135 Dose-dependent improvement in sensorimotor function in rats implanted with CTX-DP 4 we

136 volume as measured by 9.4T MRI and improved sensorimotor function-this protection was lost with GOT

137 ed neurodegeneration and improved poststroke sensorimotor function.

138 chanisms themselves impact processes such as sensorimotor function.

139 ue to emotional problems, was independent of sensorimotor functional neurological symptom severity an

140 anually parcellated into its associative and sensorimotor functional subregions.

141 Finally, the integration of sensorimotor functions by the PAG is considered, as part

142 cts neural circuits performing cognitive and sensorimotor functions driving performance enhancement.

143 st that BACE1's role in myelination and some sensorimotor functions is consistent between mice and ra

144 eased, and this was associated with improved sensorimotor functions.

145 e, worsened neurological scores, and reduced sensorimotor functions.

146 Specifically, higher concentrations of sensorimotor GABA are associated with more selective cor

147 the majority of RTT-associated behavioural, sensorimotor, gait and autonomic (respiratory and cardia

148 fects on preconscious, automatic measures of sensorimotor gating and auditory sensory processing that

149 macological inhibition of p110delta reversed sensorimotor gating and cognitive deficits.

150 Prepulse inhibition (PPI) is an example of sensorimotor gating and deficits in PPI have been demons

151 t in prepulse inhibition (PPI), a measure of sensorimotor gating commonly deficient in individuals wi

152 me degradation pathway may contribute to the sensorimotor gating deficiency and cognitive disorders i

153 Finally, mice lacking IgSF21 show a sensorimotor gating deficit.

154 eases tic-like responses and elicits TS-like sensorimotor gating deficits in the D1CT-7 mouse, one of

155 ehavioral deficits in social interaction and sensorimotor gating tasks.

156 y on stress sensitivity, cognitive function, sensorimotor gating, and prefrontal cortical transcripti

157 3 m of age, mutant mice displayed increased sensorimotor gating, anxiety, hypoactivity, and decrease

158 elevant to schizophrenia, including impaired sensorimotor gating, discrimination memory, and social b

159 ry-adrenal axis stress response and impaired sensorimotor gating, phenotypic effects that were associ

160 behavioral responses, learning, memory, and sensorimotor gating.

161 alysis providing new molecular insights into sensorimotor gating.

162 rning and memory, anxiety-like behaviour and sensorimotor gating.

163 construct the neonate mind, going far beyond sensorimotor imitation.

164 form of neonatal imitation that goes beyond sensorimotor imitation.

165 e neuronal loss associated with long-lasting sensorimotor impairment but normal magnetic resonance im

166 neuronal death, microglial inflammation and sensorimotor impairment that characterize this rodent tr

167 troke could improve recovery from persistent sensorimotor impairment.

168 The neural correlates of spaceflight-induced sensorimotor impairments are unknown.

169 tial functional recovery from stroke induced sensorimotor impairments.

170 le cells may play a role in the filtering of sensorimotor information in the cerebellum.

171 f a perturbation rather than to the specific sensorimotor information reflecting the evolving instabi

172 m similar functions in processing limbic and sensorimotor information, respectively.

173 h and matrix neurons receive both limbic and sensorimotor information.

174 teral striatum, we show that associative and sensorimotor inputs co-engage early in action learning a

175 refrontal cortex to dorsomedial striatum and sensorimotor inputs from motor cortex to dorsolateral st

176 Disengagement of associative, but not sensorimotor, inputs predicts individual differences in

177 ical networks involved in diverse aspects of sensorimotor integration and motor control.

178 So far, most of our knowledge about sensorimotor integration comes from visually guided reac

179 nformation in the mammalian brain, regulates sensorimotor integration during goal-directed locomotion

180 Prior research on sensorimotor integration has emphasized visuomotor proce

181 The vast majority of research on sensorimotor integration has used artificial stimuli and

182 We study the signaling mechanisms underlying sensorimotor integration in C. elegans during olfactory

183 Sensorimotor integration regulates goal-directed movemen

184 about a wide range of brain functions, from sensorimotor integration to cognition; hence, the measur

185 Experience alters the sensorimotor integration to generate specific behavioral

186 For efficient sensorimotor integration, the brain has therefore to com

187 ry neuron firing under natural conditions of sensorimotor integration, we recorded from primary mecha

188 internal feedforward estimation in Bayesian sensorimotor integration.

189 le within laminae of the SC to support rapid sensorimotor integration.

190 Our investigation of the sensorimotor interactions in pulsatile electrolocation s

191 s an exception, training on closed-loop (CL) sensorimotor interfaces, such as action video games and

192 w and existing reconstructions of Drosophila sensorimotor (larva) and visual (adult) systems.

193 Here, we propose a sensorimotor learning and control model that can be used

194 However, the neural basis of sensorimotor learning is poorly understood.

195 ructive signals to the cerebellum that drive sensorimotor learning.

196 l ganglia (BG) integrate inputs from diverse sensorimotor, limbic, and associative regions to guide a

197 served pull-push circuit at the lowest-level sensorimotor loop provides a mechanism for the rapid mod

198 tracing allowed us to identify second-order sensorimotor loops that control vibrissa movements by ro

199 (PPC), and frontal motor (fMC) cortices for sensorimotor mapping in mice during performance of a mem

200 d activity underlying successful guidance of sensorimotor mapping is unknown.

201 leep, is today well-documented, the detailed sensorimotor mechanisms permitting locomotion and furthe

202 atures such as sensory trick, which suggests sensorimotor mismatch as the basis.

203 in ChIs reduces akinesia, bradykinesia, and sensorimotor neglect.

204 rk (TLN), and subcortical network (SCN), and sensorimotor network (SMN) were selected as representati

205 In the patient group, these sensorimotor network abnormalities were coupled with red

206 negatively with the integrity of the primary sensorimotor network and corticospinal tract.

207 th reduced resting-state cohesiveness of the sensorimotor network in patients with bipolar disorder.

208 ctional magnetic resonance imaging to assess sensorimotor network strength and interhemispheric conne

209 While FC in the resting-state sensorimotor network was similar in psALS and controls,

210 showed reductions in the cohesiveness of the sensorimotor network.

211 reflecting a larger debate over the role of sensorimotor networks in specifying behavior.

212 tial cognition and navigation (the "map") to sensorimotor networks involved the control of movement (

213 y and motor processing (auditory, visual and sensorimotor networks).

214 s a non-linear remnant resulting from random sensorimotor noise from multiple sources, and non-linear

215 re-examination of the extent to which random sensorimotor noise is required to explain the non-linear

216 linearly related to the input, attributed to sensorimotor noise.

217 onnectivity degree and comparatively shorter sensorimotor path length implicated by the AF entail eme

218 ctivity degree of relevant areas and shorter sensorimotor path length, is crucial.

219 he contribution of different elements in the sensorimotor pathway, providing a unique tool for studyi

220 Brain-machine interfaces (BMI) create novel sensorimotor pathways for action.

221 ry building blocks under-represented in core sensorimotor pathways, thereby enabling the construction

222 known proprioceptive dysfunction to enhance sensorimotor performance.

223 have implications for the study of detailed sensorimotor plasticity in the context of both learning

224 The selective (dis)inhibition of cortical sensorimotor populations is governed by rhythmic neural

225 tinct functions, including top-down control, sensorimotor prediction, and integration.

226 o the same postsynaptic neuron in an Aplysia sensorimotor preparation, we found that each form of LTF

227 play a versatile and active role in adaptive sensorimotor prioritization.SIGNIFICANCE STATEMENT In ma

228 ze during adolescence, while those affecting sensorimotor processes do not.

229 sts an enhanced involvement of attention and sensorimotor processes, selectively when speech was pote

230 s our observations and demonstrates how this sensorimotor processing eventually biases the animal tra

231 ngs reveal EEG correlates of tightly coupled sensorimotor processing in the human brain, and support

232 inal injury reduce mobility and often impair sensorimotor processing in the spinal cord leading to sp

233 Sensorimotor processing is a critical function of the hu

234 heir generation and how they are affected by sensorimotor processing remains unclear.

235 hanged by this manipulation, indicating that sensorimotor processing was not required to elicit them

236 ectivity and nonimaging measures relating to sensorimotor processing, affective and nonaffective cogn

237 ccadic suppression originates from efficient sensorimotor processing, indicating that the brain share

238 e a general role in spatial cognition beyond sensorimotor processing.

239 iotypes, consistent with their cognitive and sensorimotor profiles, and provided stronger discriminat

240 y of the supplementary motor cortex with the sensorimotor putamen predicted more severe tics.

241 m delayed sensory information; (2) learn new sensorimotor realities; and (3) control a motor system i

242 nal cord makes a significant contribution to sensorimotor recovery, but this structural plasticity is

243 bilitative training to significantly promote sensorimotor recovery.

244 es a gap between our understanding of simple sensorimotor reflexes and our understanding of truly com

245 (ctDCS), and sham tDCS (stDCS) over the left sensorimotor region.

246 ue salience by decreasing the involvement of sensorimotor regions and by engaging greater frontal reg

247 g and precuneus functional connectivity with sensorimotor regions and strengthened the associations b

248 nterhemispheric coordination among bilateral sensorimotor regions coupled with the left frontoparieta

249 ms after stimulus onset, localized to dorsal sensorimotor regions including middle cingulate, somatos

250 ese results suggest that rapid activation of sensorimotor regions interacts with cognitive valuation

251 sound sequences, whereas neurons in ventral sensorimotor regions showed broad response profiles to n

252 Upon exposure to a new sensorimotor relationship, motor behaviors iteratively c

253 dy structural description, are distinct from sensorimotor representations, such as the body schema.

254 ing conditions relevant to the detection and sensorimotor response to mechanical perturbations to the

255 We propose that lPAG is involved with sensorimotor responses to breathlessness, while the vlPA

256 cortex (PFC) is thought to flexibly regulate sensorimotor responses, perhaps through modulating activ

257 ructure according to the approximately 20 Hz sensorimotor rhythm, and that it dynamically adapts thes

258 eoff, perched dragonflies employ a series of sensorimotor rules that determine the time of takeoff an

259 Evidence of an internal sensorimotor scaling system allowing individuals to achi

260 irements change, individuals use an internal sensorimotor scaling system to adapt movements to mainta

261 The integration of sensorimotor signals to internally estimate self-movemen

262 terplay between MEG signals from the primary sensorimotor (SM1) cortex and the contraction force of 1

263 lie orofacial tactile sensitivity issues and sensorimotor stereotypies characteristic of RTT.

264 However "light touch", a sensorimotor strategy based on light fingertip support,

265 the associative striatum (P=0.003, ES=1.39), sensorimotor striatum (P=0.003, ES=1.41) and the pallidu

266 tum and left ventrolateral prefrontal cortex-sensorimotor striatum and fewer normalized streamlines i

267 in the right dorsolateral prefrontal cortex-sensorimotor striatum and in the left and right ventrola

268 ft and right ventrolateral prefrontal cortex-sensorimotor striatum in chronic schizophrenia patients.

269 Aberrant reinforcement signals to the sensorimotor striatum may be fundamental for the formati

270 in the right dorsolateral prefrontal cortex-sensorimotor striatum negatively correlated with Trail-M

271 ht-hemisphere dorsolateral prefrontal cortex-sensorimotor striatum predicted worse cognitive control

272 atum), 1.0344 (limbic striatum), and 1.0189 (sensorimotor striatum) in line with the hypothesis that

273 triatum, and ventrolateral prefrontal cortex-sensorimotor striatum).

274 ive striatum, dorsolateral prefrontal cortex-sensorimotor striatum, ventrolateral prefrontal cortex-a

275 the infant rat red nucleus (RN)-a brainstem sensorimotor structure-exhibits theta (4-7 Hz) oscillati

276 A goal of many sensorimotor studies is to quantify the stimulus-behavio

277 The sensorimotor synapse of Aplysia expresses different form

278 Circuits in the sensorimotor system (e.g., spinal cord) are thought to b

279 ge affects how we perceive the world and the sensorimotor system actively guides our perception.

280 tail communicative knowledge penetrating the sensorimotor system and directly affecting pointing traj

281 us work on perceptual decision making in the sensorimotor system has shown population dynamics in the

282 The presumed role of the primate sensorimotor system is to transform reach targets from r

283 The theory that the sensorimotor system minimizes energetic cost during loco

284 rmation by using some unique features of the sensorimotor system of the weakly electric fish.

285 nstrate how the proposed model can explain a sensorimotor system's ability to compensate for delays d

286 s an important step toward understanding the sensorimotor system's algorithms for updating its intern

287 a oscillations are a dominant feature of the sensorimotor system.

288 t principles, or is it fully embodied in the sensorimotor system?

289 Rather, inflexible sensorimotor systems and/or atypical transition between

290 tor variability may also be a feature of how sensorimotor systems operate and learn.

291 op, yet the neural substrate underlying this sensorimotor task in the vertebrate brain remains elusiv

292 iature brain can achieve in highly demanding sensorimotor tasks and suggests the presence of equivale

293 lateral whisker maps perform well in general sensorimotor tasks but show poor performance in specific

294 ination including cycloplegic refraction and sensorimotor testing within 6 months of the testing date

295 were comparable with the control animals in sensorimotor tests.

296 This demonstrates that a short sensorimotor training challenging proprioception can a)

297 e propose that these cells are involved in a sensorimotor transformation whereby information on the l

298 Although we know a great deal about where sensorimotor transformations leading to saccadic eye mov

299 models, can uncover the circuit structure of sensorimotor transformations.

300 d and enhanced through exposure to increased sensorimotor variability.