ライフサイエンスコーパス: sensorimotor

1 imals exhibit neurophysiological defects and sensorimotor abnormalities paralleled by defective perip

2 ine-scale dynamics of complex and meaningful sensorimotor actions.

3 t lesion studies examining a causal role for sensorimotor activation in conceptual task performance h

4 rimotor inhibition in females and predictive sensorimotor activation in males.

5 Traditional views of sensorimotor adaptation (i.e., adaptation of movements t

6 Here we tested whether implicit sensorimotor adaptation and strategic re-aiming used to

7 TATEMENT Latent motor memories formed during sensorimotor adaptation manifest as improved adaptation

8 success signals can modulate learning during sensorimotor adaptation tasks, primarily through engagin

9 However, latent memories formed during sensorimotor adaptation, manifest as improved relearning

10 trol, or sustained, providing information on sensorimotor adaptation.

11 icant gain in information results from these sensorimotor adjustments.

12 y different neurophysiological properties of sensorimotor alpha- and beta-band rhythms.

13 The cerebellum plays a crucial role in sensorimotor and associative learning.

14 n into overlapping clusters, with regions in sensorimotor and attentional networks exhibiting the gre

15 mia, tPA knockout mice developed more severe sensorimotor and cognitive deficits and greater axonal a

16 ironmental) and neurobiological factors (eg, sensorimotor and cognitive functions) in contemporary mo

17 ction and atrophy and improves the long-term sensorimotor and cognitive recovery against ischemic str

18 signature of the motor system, used by both sensorimotor and frontal areas involved in the trial-by-

19 egates in multiple brain regions and exhibit sensorimotor and motor learning deficiencies.

20 the amplitude and the rate of long bursts of sensorimotor and prefrontal beta oscillations (13-30 Hz)

21 of stimulus-locked speech representations in sensorimotor and premotor cortex, combined with diffuse

22 In sensorimotor and premotor cortex, we observed reliable a

23 rently noisy, e.g. due to the variability of sensorimotor and visceral responses to physical exertion

24 ntrolateral prefrontal) areas, as well as in sensorimotor and visual cortices.

25 tion loci (e.g., subregions of the salience, sensorimotor, and default networks) that were significan

26 ain nucleus HVC (proper name), a cortex-like sensorimotor area of songbirds, otherwise known for bein

27 nd local correlations is stronger in primary sensorimotor areas and weaker in association areas such

28 We also highlight how neural dynamics in sensorimotor areas are involved in beat-based timing.

29 y index the downstream modulation of primary sensorimotor areas by engaging mirror neuron activity.

30 wed a significant MPH-induced FC increase in sensorimotor areas in the functional circuit associated

31 alamus, but was also observed in sensory and sensorimotor areas of the midbrain and hindbrain.

32 road-band neural signals from three cortical sensorimotor areas simultaneously.

33 ompanied by beta-band desynchronization over sensorimotor areas, whereas movement cancellation is acc

34 activity, reflecting an experience-dependent sensorimotor association.

35 Sound-evoked neuronal responses changed with sensorimotor associations shortly after sound onset, and

36 ly dystonia, early tonic motor features, and sensorimotor aura.

37 on (transmural potential difference), rectal sensorimotor (barostat; sensory thresholds, tone respons

38 ns in the brain; however, relationships with sensorimotor behavior are rarely considered.

39 Validated measures of sensorimotor behavior in awake, behaving animals reveale

40 r their specialization and ultimately adjust sensorimotor behavior to fit the environment.

41 complementary but distinct aspects of visual sensorimotor behavior.

42 t learns a perceptual task, restructures its sensorimotor behavior.

43 Sensorimotor behaviors require processing of behaviorall

44 pivotal roles in generating a wide range of sensorimotor behaviors, including protective and correct

45 differential computational roles in distinct sensorimotor behaviors.

46 opportunity for comprehensive 3D analysis of sensorimotor behaviour and its neural basis.

47 asks, but no overt differences in many other sensorimotor behaviours.

48 de further evidence of a causal link between sensorimotor beta bursts and movement initiation and sug

49 owed by short-latency increases of bilateral sensorimotor beta-burst rates, suggesting that motor inh

50 y associated with motor control, after which sensorimotor beta-bursting re-initiates.

51 sent in trial-average data), suggesting that sensorimotor beta-bursting signifies an inhibited motor

52 Finally, we identify sensorimotor brain regions that project on to Chx10 reti

53 e the function of the superior colliculus, a sensorimotor brainstem structure, in de novo PD patients

54 Indeed, during movement initiation, sensorimotor burst-rates steadily decreased, lateralizin

55 ronger effects the more strongly they engage sensorimotor capacities.

56 Neuroimaging evidence for disrupted central sensorimotor circuitry suggests that there may be unreco

57 uracy under naturalistic conditions, but the sensorimotor circuits extracting these cues and implemen

58 Therefore, our results show that spinal sensorimotor circuits generate backward locomotion but r

59 Here, we tested the hypothesis that sensorimotor circuits within the spinal cord generate ba

60 consistent with locomotion reorganize spinal sensorimotor circuits.

61 We have shown that sensorimotor conflicts illuminate otherwise-hidden balan

62 as a joint dynamic system both in classical sensorimotor contexts and reward-related, cognitive proc

63 primates, suggesting a pivotal link between sensorimotor control and temporal processing, as well as

64 Sensorimotor control during overt movements is character

65 g.SIGNIFICANCE STATEMENT Current theories of sensorimotor control suggest that, rather than selecting

66 light on this relationship in the context of sensorimotor control, we assessed prediction-related mea

67 the sensory and motor response components of sensorimotor control.

68 able forces acting on glabrous skin and fine sensorimotor control.

69 ant accuracy and discrimination processes of sensorimotor control.

70 flexibility required to perform appropriate sensorimotor control.

71 bination of passive body dynamics and active sensorimotor control.

72 Historically viewed as a simple sensorimotor controller with homogeneous architecture, t

73 cognition, affect, and behavior regulation, sensorimotor coordination, and executive function.

74 anied by an increase in ipsilesional primary sensorimotor cortex activity following the intervention.

75 for changes in structural morphometry of the sensorimotor cortex and found that individuals with stro

76 LS) is the orofacial projection field of the sensorimotor cortex and is involved in the development o

77 edback from movements in driving activity in sensorimotor cortex and underscore the necessity of moni

78 between the occurrence of beta bursts in the sensorimotor cortex before the go-cue and slowed movemen

79 been reported, such as the activation of the sensorimotor cortex during dreamed hand clenching.

80 on in activity in the contralesional primary sensorimotor cortex during motor execution.

81 ta-band rhythms modulate excitability of the sensorimotor cortex during psychophysically-controlled m

82 on cause of disability, which often leads to sensorimotor cortex dysfunction above the spinal injury

83 ving distal upper limbs, linked to increased sensorimotor cortex excitability, as seen in cortical my

84 senting an animal's position and movement in sensorimotor cortex has been found to continually reconf

85 rocorticography signals from the ipsilateral sensorimotor cortex in 10 patients undergoing deep brain

86 Beta oscillations decreased in the sensorimotor cortex in adolescents after practice, but i

87 aimed to investigate the causal role of the sensorimotor cortex in generating movement and bodily se

88 ate volitional suppression of beta bursts in sensorimotor cortex in healthy motor control better than

89 tDCS over the sensorimotor cortex interferes with dream movement durin

90 ndergoing awake craniotomy has revealed that sensorimotor cortex is functionally organized for signin

91 ed electrocorticographic recordings from the sensorimotor cortex of people with refractory epilepsy a

92 eflecting the occurrence of beta bursts over sensorimotor cortex quantified in real time.

93 VTS) alters afferent proprioceptive input to sensorimotor cortex that controls speech.

94 During self-touch, the sensorimotor cortex was functionally connected to the in

95 s, was observed concomitantly, involving the sensorimotor cortex, associative areas, and limbic struc

96 less of the effector used in the association sensorimotor cortex, in the left intraparietal sulcus an

97 While neural activity was recorded from sensorimotor cortex, the participant produced a large va

98 to volitionally suppress beta bursts in the sensorimotor cortex, with training being accompanied by

99 4 Hz), and beta (15-25 Hz) oscillations over sensorimotor cortex.

100 teral geniculate nucleus of the thalamus and sensorimotor cortex.

101 asal ganglia, thalami, and orbitofrontal and sensorimotor cortex.

102 postmovement clear-out of the motor plan in sensorimotor cortex.

103 seven tasks, with mainly decreased GSCORR in sensorimotor cortex.

104 y of anterior prefrontal inhibition over the sensorimotor cortex.

105 tion in the mouse visual thalamus as well as sensorimotor cortex.

106 a rhythm (15-30 Hz) is a prominent signal of sensorimotor cortical activity.

107 tablishing task-relevant neural manifolds in sensorimotor cortical areas and how the geometry and dyn

108 uced frequency of transient beta-bursts over sensorimotor cortical areas before movement initiation a

109 us to myoclonic epilepsy, caused by abnormal sensorimotor cortical discharges.

110 tant for interoception, including insula and sensorimotor cortical regions.

111 ion stages was reduced after practice in the sensorimotor cortices of the adolescents, but was strong

112 increases in beta (12-30 Hz) suppression in sensorimotor cortices related to performance during spee

113 Primary sensorimotor cortices showed selectivity for the hand in

114 based source contributions from auditory and sensorimotor cortices were apparent after isochronous be

115 At sensorimotor cortices, there was a broadband power incre

116 s being largely diffuse and extensive beyond sensorimotor cortices.

117 ehavior in a homeostatic attempt to preserve sensorimotor coverage under changing environmental condi

118 o record granule neuron responses to diverse sensorimotor cues targeting visual, auditory, somatosens

119 ited the technical advantages of the Aplysia sensorimotor culture system to examine the role of RSK i

120 show that the stroke-induced asymmetry in a sensorimotor (cylinder) test is reversed by transplantat

121 iffuse axonal hypomyelination, and permanent sensorimotor deficit.

122 2.51-17.28, p = 0.009), a presentation with sensorimotor deficits (OR = 13.71, 95% CI = 2.68-24.73,

123 l MRI findings, a clinical presentation with sensorimotor deficits, and a treatment delay > 4 weeks a

124 tor behaviours are commonly used to evaluate sensorimotor disruption due to ethanol (EtOH).

125 otor behaviours are often used as metrics of sensorimotor disruption due to ethanol (EtOH); however,

126 ted movements underlie adaptation to radical sensorimotor distortions.

127 Colonic sensorimotor disturbances and pelvic floor dysfunction (

128 ific computations, abstracted from low-level sensorimotor elements.

129 ixation exposed a backward redistribution of sensorimotor exploratory resources.

130 ganization and representational structure of sensorimotor features underlying sign language phonology

131 Thus, this sensorimotor flexibility arises from distinct mechanisms

132 eneralized improvements in other measures of sensorimotor forepaw function.

133 ayed, peripheral infusion of NT3 can improve sensorimotor function after ischemic stroke.

134 We evaluated sensorimotor function and activities of daily life pre-

135 We examined the sensorimotor function of anatomically distinct outputs f

136 res (diagnosis), pathophysiology (intestinal sensorimotor function, microbiota, immune dysregulation,

137 d connect to generate a system that performs sensorimotor functions critical for survival.

138 (~13-30 Hz), which have long been linked to sensorimotor functions, at the time when these adaptive

139 ty of the DCN implicate them in a variety of sensorimotor functions, beyond their commonly accepted r

140 To consolidate insights into their sensorimotor functions, this review examines the morphol

141 ect touch and significantly improved several sensorimotor functions.

142 of ectopic dendrites in neurons and enhanced sensorimotor gating behavior in mice.

143 SA-born WT mice exhibited sensorimotor gating deficits (males), increased reward p

144 .2(dp/+) mice did not exhibit the SZ-related sensorimotor gating deficits, psychostimulant-induced hy

145 g that pathologies associated with disrupted sensorimotor gating, such as with schizophrenia, could b

146 impairments in social approach behavior and sensorimotor gating, whereas MIA offspring with a low in

147 nstrating the importance of these neurons in sensorimotor gating.

148 1 hours after the last blast) also prevented sensorimotor impairment on a rotarod task 30 days later,

149 the nature and developmental organization of sensorimotor information in vermal granule neurons of th

150 termined by specific semantic features (e.g. sensorimotor information), or may abstract away from spe

151 complex integration and distribution hub for sensorimotor information.

152 speech discrimination were characterized by sensorimotor inhibition in females and predictive sensor

153 ltering cerebellar learning by modifying how sensorimotor input is represented at the input layer of

154 ell established, but less is known about how sensorimotor integration affects auditory perception.

155 h locomotion, suiting them to participate in sensorimotor integration associated with cerebellum-depe

156 The vermal cerebellum is a hub of sensorimotor integration critical for postural control a

157 The sensorimotor integration during unconstrained reaching m

158 halamus is considered an important aspect of sensorimotor integration for active touch in the somatos

159 n a previous study, we demonstrated abnormal sensorimotor integration in patients with Alzheimer's di

160 Sensorimotor integration in the cerebellum is essential

161 We hypothesize that a key function of sensorimotor integration is the facilitated processing o

162 he first evidence for evolutionary change in sensorimotor integration related to diversification of c

163 cerebellum, which is known to regulate rapid sensorimotor integration, raising the question of cerebe

164 alamic brain regions play important roles in sensorimotor integration, very little is known about the

165 For sensorimotor integration, we identified a key forebrain

166 our actions are thought to be predicted via sensorimotor integration, which involves anatomical and

167 icospinal and sensory cortex excitability or sensorimotor integration.

168 ever, little is known about the evolution of sensorimotor integration.

169 nge motor cortex intracortical inhibition or sensorimotor integration.

170 e premotor circuits involved in swimming and sensorimotor integration.

171 us of the basal ganglia and is a key site of sensorimotor integration.

172 ut and which may be involved in higher order sensorimotor integration.

173 short-interval intracortical inhibition, and sensorimotor interaction, i.e. short-latency afferent in

174 In 16 healthy volunteers, we probed sensorimotor interactions in face motor cortex (fM1) usi

175 Humans typically make near-optimal sensorimotor judgements but show systematic biases when

176 mework, we explore the principles that guide sensorimotor learning across these scales, and set the s

177 and implicit motor adaptation by designing a sensorimotor learning paradigm that drives adaptive chan

178 This memory is the foundation for later sensorimotor learning, resulting in the production of a

179 f spindles and slow oscillations may support sensorimotor learning.

180 onvergent operation of multiple processes in sensorimotor learning.

181 ATEMENT The corticostriatal pathway controls sensorimotor, learning, and action control behaviors and

182 tive action models were used comparably at a sensorimotor level in both autistic and neurotypical ind

183 r a novel role for the cerebellum in dynamic sensorimotor map calibration, of potential importance fo

184 tly triggered when an adaptive change in the sensorimotor mapping is required, whereas the reduction

185 delling revealed that reward information and sensorimotor markers of exertion were combined in a Baye

186 ue that such predictive capacity relies on a sensorimotor mechanism responsible for simulating others

187 Finally, we show that latent sensorimotor memories driven by task errors comprise at

188 rors and sensory prediction errors to latent sensorimotor memories, we perturbed target locations to

189 LP via task-concurrent NIBS over the primary sensorimotor missing hand cortex (S1/M1).

190 We have previously shown in the Aplysia sensorimotor model that distinct isoforms of persistentl

191 m accurately discriminated trials identified sensorimotor mu components with characteristic alpha and

192 modulated by both amplitude and phase of the sensorimotor mu-alpha rhythm.

193 cillations, it is less clear for the central sensorimotor mu-alpha rhythm.

194 of rhythmic MNS, delivered at 12 Hz, entrain sensorimotor mu-band oscillations, whereas pulse trains

195 zed in resting-state networks (RSNs) such as sensorimotor network (SMN), salience network (SN), and d

196 amine with aberrant iFC between the auditory-sensorimotor network and thalamus.

197 essive theta-band synchronisation across the sensorimotor network and widespread engagement of cortic

198 Restless legs syndrome is a sensorimotor network disorder.

199 re more densely connected, in particular the sensorimotor network, also tend to be affected early dur

200 semblance to voxel activity in a distributed sensorimotor network, extending throughout the dorsal vi

201 In the auditory-sensorimotor network-centred system, patients had reduce

202 orrelated positively with increased auditory-sensorimotor network-ventrolateral-thalamus iFC.

203 reveal a unified functional organisation of sensorimotor networks in the entire central nervous syst

204 ork with the superior frontal, auditory, and sensorimotor networks, and the salience network with the

205 For centromedial thalamus, connectivity to sensorimotor networks, parietal-temporal-occipital netwo

206 ork integration between the default mode and sensorimotor networks.

207 The Reach Cage allows systems-level sensorimotor neuroscience studies with full-body movemen

208 es neuroimaging evidence through the lens of sensorimotor neuroscience.

209 ternal perturbations, intrinsic sources like sensorimotor noise perturb the running motion incessantl

210 sed as the result of nuisance processes like sensorimotor noise, fatigue, or disengagement.

211 al division (vLGN) projects subcortically to sensorimotor nuclei, including the superior colliculus (

212 models that can quantitatively capture basic sensorimotor operations.

213 drites as output apparatus to drive distinct sensorimotor outcomes.

214 us/superior parietal lobule (consistent with sensorimotor output).

215 ecision without concomitant changes in other sensorimotor parameters such as hand movement, licking,

216 act action functions independent of specific sensorimotor parameters, paralleling sensory feature-ind

217 rcellation includes 234 priors from frontal, sensorimotor, parietal, temporal, occipital, cingular an

218 on the relationship between these events and sensorimotor performance suggests that they are the biol

219 ptation manifest as improved adaptation when sensorimotor perturbations are reencountered.

220 Our central hypothesis was that provocative sensorimotor perturbations, delivered in a highly instru

221 plications of diabetes, in particular distal sensorimotor polyneuropathy (DSPN), is unclear.

222 corneal nerve measures are lower in diabetic sensorimotor polyneuropathy (DSPN).

223 We developed a comprehensive sensorimotor predator-prey simulation, modeling numerous

224 pecific brain pathway found to transmit such sensorimotor prediction signals in nonhuman primates.

225 ), memory (i.e., hippocampus, r = 0.32), and sensorimotor processes (i.e., anterior cerebellum, r = 0

226 t subjective decisions apart from many other sensorimotor processes and are of wide sociological impa

227 anterior portion of the IPS and involved in sensorimotor processing, and an 'intermediate' cluster o

228 emispheric information transfer, heteromodal sensorimotor processing, and executive control of motor

229 ay in modulating spider vision, higher order sensorimotor processing, and motor patterning.

230 and cerebellum both play important roles in sensorimotor processing, however, precise connections be

231 ural systems, particularly those involved in sensorimotor processing, sociality or cognition, may rev

232 lum, as well as the contribution of abnormal sensorimotor processing.

233 sleep SW in cortical circuit plasticity and sensorimotor recovery after stroke and provide a clinica

234 whether CMR affects OP1/OP4 connectivity and sensorimotor recovery after stroke.

235 ns to enhance central plasticity can improve sensorimotor recovery and define CL-VNS as a readily tra

236 These results suggest enhanced sensorimotor recovery post-stroke after CMR.

237 accelerates nerve regeneration and promotes sensorimotor recovery.

238 hat promotes neuroplasticity and facilitates sensorimotor recovery.

239 4 h of acute SCI is associated with improved sensorimotor recovery.

240 aneous nerves (DCNs) activates a nociceptive sensorimotor reflex and the same afferent stimulation al

241 ght classes of dorsal excitatory INs make to sensorimotor reflex responses.

242 in spinal somatosensory processing, namely, sensorimotor reflexes are driven by the differential spa

243 g and the tutor song in NCM and a downstream sensorimotor region, HVC, respectively.

244 creases with age, with higher involvement of sensorimotor regions and medial brain structures.

245 , they do not support the embodied view that sensorimotor regions are necessary to tasks of action ve

246 rophy connected to a network of higher-order sensorimotor regions beyond perirolandic cortex, matchin

247 ntly report a negative impact of diabetes on sensorimotor regions in the brain; however, relationship

248 t is still not clear whether spatial maps in sensorimotor regions known to guide overt and covert spa

249 such motor memory components outside primary sensorimotor regions likely underlies a parsimonious neu

250 re is ongoing debate regarding the role that sensorimotor regions play in conceptual processing, with

251 hypothesized that beta-band activity within sensorimotor regions relates to implicit adaptive proces

252 striatum, and hyper-excitability of cortical sensorimotor regions that might contribute to the occurr

253 tion network involving superior temporal and sensorimotor regions; and a network between posterior in

254 riments set up a paradigm for studying rapid sensorimotor reinforcement in a circuit that is right at

255 accessed about food dishes, domain-selective sensorimotor-related cortical representations continue t

256 at they can (and should) be used to describe sensorimotor relationships relevant for behaviour rather

257 hange in visual conditions required implicit sensorimotor remapping, which may reflect enhanced senso

258 d learning through synchronous activation of sensorimotor representational cortices.

259 ct from the primary and secondary cerebellar sensorimotor representations linked with the spinal cord

260 Lesions of the anterior lobe primary sensorimotor representations produce dysmetria of moveme

261 proprioceptor subtypes to construct complex sensorimotor representations that mediate diverse behavi

262 owed less anxiety-like behavior and improved sensorimotor responses to a noxious cold stimulus.

263 onally linked to consistently reported brain sensorimotor RSNs.

264 rol, awareness and emotional regulation (eg, sensorimotor, salience, central executive networks).

265 tivity that allows participants to learn new sensorimotor schemes.

266 were summarised by mean difference (MD) for sensorimotor scores and common odds ratio (cOR) for AIS

267 on, beta-bursting was prominent at bilateral sensorimotor sites.

268 y reductions of beta-bursting over bilateral sensorimotor sites.

269 gait adaptability in response to discordant sensorimotor stimulations.

270 ly test long-held theories about encoding of sensorimotor stimuli in the cerebellum and compare the i

271 network-centred system, patients had reduced sensorimotor striatum dopamine synthesis capacity, which

272 salience network and thalamus, and aberrant sensorimotor striatum dopamine with aberrant iFC between

273 urs earliest and most severely in the caudal sensorimotor striatum, a subdivision of the striatum imp

274 r movements of the limb corresponding to the sensorimotor stroke lesion site compared with spontaneou

275 Despite evidence from sensorimotor stroke showing that early injury responses

276 ortically, sending inhibitory projections to sensorimotor structures, including the superior collicul

277 (P = 0.004) and associative (P = 0.002) and sensorimotor subdivisions (P = 0.007).

278 region of the subthalamic nucleus and in its sensorimotor subregion and for attention/memory in the a

279 c condition whereby individuals present with sensorimotor symptoms incompatible with other neurologic

280 -term facilitation (LTF) in cultured Aplysia sensorimotor synapses rely on the activities of differen

281 Using the sensorimotor system as a model of cortical processing, w

282 Taken together, our work suggests that the sensorimotor system relies on temporally recent and spat

283 y may embed complex relationships within the sensorimotor system.

284 ngertips to address this issue in the intact sensorimotor system.

285 Findings further suggest involvement of the sensorimotor systems in language lateralization and its

286 of tactile specializations in waterfowl and sensorimotor systems in parrots.

287 concepts are represented in the same neural sensorimotor systems that were involved in their acquisi

288 ynapses and mediate behavioral recovery in a sensorimotor task.

289 time course that resembles both traditional sensorimotor tasks and conversational speech.

290 However, research on sensorimotor timing has rarely considered the tight inte

291 Timescales increase along the principal sensorimotor-to-association axis across the entire human

292 anging limb biomechanics and influences from sensorimotor training (Nurture).

293 OXT population activity reflects the sensorimotor transformation of the noxious stimulus, wit

294 e we investigate such strategies in a common sensorimotor transformation task.

295 This general principle could organize sensorimotor transformations across animal species.

296 network correlates with a global retuning of sensorimotor transformations during foraging that leads

297 Finally, we found that the sensorimotor transformations in the zebrafish auditory s

298 of these goal-directed actions relies on 3D sensorimotor transformations that are experience-depende

299 ystems-level framework for understanding the sensorimotor transformations that underlie natural socia

300 We found that rapid sensorimotor twitches, called pumps, occurring during fr