ライフサイエンスコーパス: motor control

1 oscience are parallel advances in "synthetic motor control".

2 contribution of lower-level organization of motor control.

3 erms of the same computational principles as motor control.

4 inhibition (IHI) is essential for dexterous motor control.

5 the underlying articulatory nature of speech motor control.

6 treatment strategies targeted toward distal motor control.

7 ny of which are important models for sensory-motor control.

8 pre-motor cortex leads to early recovery of motor control.

9 specific roles of cholinergic modulation in motor control.

10 promote SNc DA neuron survival and/or proper motor control.

11 ch learns to generate predictive signals for motor control.

12 aviours such as reward-related learning, and motor control.

13 on the broader neurobiology of emotions and motor control.

14 r photo-activation, enabling light-dependent motor control.

15 ue and slowed movement initiation in healthy motor control.

16 ndamental limit to the maximum speed of fine motor control.

17 entire neuromechanical control loop of vocal motor control.

18 outgrowths to evolve a dorsal appendage with motor control.

19 ment in the cerebellum allowing for accurate motor control.

20 sky-compass information and/or higher sensor-motor control.

21 ement is critical for spatial perception and motor control.

22 MENT Gamma oscillations have a vital role in motor control.

23 tremor are an unavoidable component of human motor control.

24 ion, maintenance of balance and posture, and motor control.

25 e activation can be a descriptor of impaired motor control.

26 ts is a conserved mechanism of behaviour and motor control.

27 neuromechanical control loop of avian vocal motor control.

28 rsal striatum associated with motivation and motor control.

29 an vocalizations during vocal production and motor control.

30 e processes, including reward, attention and motor control.

31 ensation in insects and its role in adaptive motor control.

32 synchronized oscillation in primate sensory-motor control.

33 uggests a regulatory role of this region for motor control.

34 erse aspects of sensorimotor integration and motor control.

35 ing a causal role of these brain rhythms for motor control.

36 he study of the gene's role in general vocal motor control.

37 predicted sensory states to perform optimal motor control.

38 sor-motor mechanisms of vocal production and motor control.

39 s into how internal states affect biological motor control.

40 training promoted the appropriate inhibitory motor control.

41 bcortical nuclei implicated in cognitive and motor control.

42 ultimodal sensory integration, cognition and motor control.

43 tractable model for understanding descending motor control.

44 is expressed in brain areas associated with motor control.

45 ry literature in the broader field of speech motor control.

46 g conditions, sense organs are under active, motor control.

47 rmation may be used to influence vocal pitch motor control.

48 t influence perception, decision-making, and motor control.

49 goal-directed behaviors, habit learning, and motor control.

50 the dorsal striatum in cognitive as well as motor control.

51 eward sensitivity, independent of effects on motor control.

52 critical for informing any future models of motor control.

53 t these oscillations are not epiphenomena in motor control.

54 implements sensory processing, learning, and motor control.

55 The dorsal striatum is important for motor control.

56 bus pallidus (GPe) is critically involved in motor control.

57 ved to contribute to higher order aspects of motor control.

58 ease (PD) argue that the GPe is important in motor control.

59 ant for SNc DA neuron survival and/or proper motor control.

60 intelligence, such as vision, language, and motor control.

61 d, role in the reward-based imporvemenets in motor control.

62 on, in addition to their traditional role in motor control.

63 types in the pallidum have opposing roles in motor control.

64 ypal neurodevelopmental disorder of central, motor control.

65 for investigating neural mechanisms of limb motor control.

66 ring adolescence contributes to the improved motor control.

67 simulate key phenomena of working memory and motor control.

68 ut but was historically linked to high-level motor control.

69 motor cortical networks for speech and hand motor control.

70 anisms that cause both seizures and abnormal motor control.

71 for understanding the acquisition of speech motor control.

72 ic synapse function and modulates cerebellar motor control.

73 chanisms involved in body-ownership, such as motor control?

74 ies [1] where it functions in cognition [2], motor control [3], and sensory processing [4].

75 affect decision-making, they also influence motor control [6, 7].

76 onnectivity mainly in areas of sensorial and motor control, a result supported by the dFNC outcome an

77 the spinal cord and play important roles in motor control across different species.

78 odulate motor excitability, as it influences motor control across multiple pathways, one independent

79 ons highlight the critical role of PDE10A in motor control across species.

80 of premotor activity to temporal profiles of motor control activity and manipulate (e.g., time warp)

81 nd emotion in the same way that it modulates motor control advances the understanding of the mechanis

82 severed axons is fundamental to reestablish motor control after spinal-cord injury (SCI).

83 onto-central sites typically associated with motor control, after which sensorimotor beta-bursting re

84 ple neuronal cell types that are critical to motor control and arise from distinct progenitor domains

85 quency relationships requires high levels of motor control and auditory sensory feedback.

86 ns (seizure, cognitive failure, muscular and motor control and brain-malformation) to comprehensively

87 he dynamical neural processes that underline motor control and can inform the design of BMIs.

88 rojection systems, such as those for vision, motor control and cognition.

89 ht presynaptic mechanisms that mediate human motor control and cognitive development.

90 ron level, the important subthalamic role in motor control and coordination and indicate the effect o

91 oth upper and lower extremities, its role in motor control and coordination and its changes in Parkin

92 Silencing BmAce1 impacted motor control and development to a greater extent than s

93 e limbic system, have key roles in learning, motor control and emotion, but also contribute to higher

94 understanding of the fundamental concepts of motor control and enable more selective targeting of bra

95 ntribute to sustained attention and top-down motor control and have never before been the subject of

96 including sensation from diverse modalities, motor control and higher cognitive processes.

97 ent initiation and execution; and the other, motor control and inhibition.

98 lls and participates in synaptic plasticity, motor control and learning that are impaired in CB(1) re

99 l to theories of cerebellar contributions to motor control and learning.

100 trols, was noted in brain regions related to motor control and motivation to act, including the suppl

101 y, and transcriptomics in nuclei relevant to motor control and motivation.

102 mly link sleepwalking to the neuroscience of motor control and motor awareness and may complement for

103 existing literature on CNS contributions to motor control and motor learning in healthy individuals

104 It plays key roles in motor control and motor learning, memory formation, and

105 STATEMENT The cerebellum plays a key role in motor control and motor learning.

106 osed following a standardized examination of motor control and often presents with cognitive decline

107 Glycinergic synapses play a central role in motor control and pain processing in the central nervous

108 nic, debilitating problems including loss of motor control and paresthesia, and generates maladaptive

109 cerebellar circuits involved in feedforward motor control and posterior cerebellar circuits involved

110 Here we ask whether and how motor control and redirected somatosensory stimulation p

111 ial striatum (DMS) is critically involved in motor control and reward processing, but the specific ne

112 ological processes like learning and memory, motor control and reward, and pathological conditions su

113 studies in nonhuman primates have shown that motor control and sensory feedback can be achieved by co

114 passage of time in healthy and pathological motor control and shed new light on the processes underl

115 hese results suggest a role of the dmPFC for motor control and show that tACS-induced behavioral chan

116 epresented in cortical areas devoted to hand motor control and successfully discriminated individual

117 , the role of corticocortical connections in motor control and the principles whereby selected cortic

118 r goal-directed behaviour, social cognition, motor control and vegetative functions, including fronto

119 The neurobehavioral mechanisms of human motor-control and learning evolved in free behaving, rea

120 ance for coordinate alignment during ongoing motor control, and for map calibration in future biomime

121 bcortical structures, critically involved in motor control, and makes synaptic contacts with dopamine

122 for many individuals with diseases affecting motor control, and recently it has shown promise for imp

123 phenotype in areas important for cognition, motor control, and respiration.

124 sses such as learning and memory, attention, motor control, and sensory processing.

125 ve to the contributions of sensory feedback, motor control, and task performance strategy, and will l

126 work emergence during sensory processing and motor control are greatly facilitated by technologies th

127 dopaminergic medication, deficits in higher motor control are less responsive.

128 channels that function specifically in fine motor control are unknown.

129 present a compensatory mechanism for loss of motor control as a consequence of dopamine depletion.

130 ary, STN gamma activity may support flexible motor control as it did not only increase during movemen

131 Brain dopamine is critical for normal motor control, as evidenced by its importance in Parkins

132 n red nucleus (RN), a brain region linked to motor control, as male and female rats performed a novel

133 ith inputs required for accurate posture and motor control, as well as perceptual stability, during e

134 enetic tools offers the possibility to study motor control at single-neuron resolution, and soon thro

135 uence on neurocircuits involved in voluntary motor control, awareness and emotional regulation (eg, s

136 frontal areas lies at the core of cognitive-motor control because the outflow of parietofrontal sign

137 is missing is how these different domains of motor control become coordinated over the course of deve

138 In analyzing the decision-making and motor-control behaviors of various animals, we considere

139 eta bursts in sensorimotor cortex in healthy motor control better than sham feedback.

140 ation is broadly divided into gross and fine motor control, both of which depend on proprioceptive or

141 O) sensory end organs is critical for normal motor control, but how distinct MS and GTO afferent sens

142 basal ganglia (BG) are critical for adaptive motor control, but the circuit principles underlying the

143 activity in several brain areas involved in motor control, but the mechanisms promoting this activit

144 me is a fundamental characteristic of neural motor control, but the principles underlying its formati

145 is accepted as being critical for voluntary motor control, but what functions depend on cortex is st

146 rent hypotheses are that dopamine influences motor control by 'invigorating' movements and regulating

147 ement in the central complex participates in motor control by a distributed, flexible code targeting

148 cific CST stimulation, we show a direct limb motor control by sprouting CST axons, providing direct e

149 osition is automatically set using a stepper motor controlled by a microcontroller.

150 Our results show that motor control can be an active component of sensory lear

151 , where they provide rhythmic input to major motor control centers.

152 nformation forwarded to a major supsraspinal motor control centre, the cerebellum.

153 bly, the region of the brain responsible for motor control (cerebellum) is small and lacking foliatio

154 role in addiction, nAChRs also contribute to motor control circuitry.

155 tion between the sleep and autonomic/somatic motor control circuits suggests that a primary function

156 nking genetic pathways to vocal learning and motor control circuits, as well as for novel insights in

157 t roles in the development and modulation of motor control circuits.

158 and innervate multiple arousal-promoting and motor-control circuits through extensive collateral proj

159 anticipatory and reactive aspects of speech motor control, comparing the performance of patients wit

160 The neural mechanisms of executive and motor control concern both basic researchers and clinici

161 nia can be viewed as a corruption or loss of motor control confined to a single motor skill.

162 Adaptive motor control critically depends on the interconnected n

163 ontrast, medication did not improve internal motor control deficits concurrent to missing effects at

164 Adaptive motor control depends critically on an animal's ability

165 wn about how topographic representations for motor control develop and interface with sensory maps.

166 "higher" areas may be related to the loss of motor control due to the 6-OHDA lesion.

167 To investigate sensory-motor control during the buzz of the insectivorous bat M

168 Current theories of motor control emphasize how the brain may use internal m

169 ssociated with nonvisual sensory perception, motor control, endocrine release, and attention.

170 (moderate-quality evidence), tai chi, yoga, motor control exercise, progressive relaxation, electrom

171 The IM-AA mice also had impaired motor control, exercise capacity, and grip strength.

172 coordinates.SIGNIFICANCE STATEMENT Cortical motor control exhibits clear lateralization: each hemisp

173 Present studies are confounded by motor control facilitating movements that are integrated

174 or the deficits that occur in skilled distal motor control following dopamine depletion, and highligh

175 or learning affects the whole body, changing motor-control from head to toe.

176 e IN + FUS treated mice, indicating improved motor control function in the treated hemisphere.

177 tion, emotion, somato-sensory, cognitive and motor-control functions, particularly in the memory area

178 The role of cortical oscillations in motor control has been a long-standing question, one vie

179 red neuronal circuits, but their function in motor control has not been established.

180 erebellar vermis, long associated with axial motor control, has been implicated in a surprising range

181 towards a comprehensive study of descending motor control, here we estimate the number and distribut

182 ith an empirically based model of descending motor control how neural circuits could interact with ch

183 performance, i.e. finger tapping, and higher motor control, i.e. internally and externally cued movem

184 tivity, and roles in sensory acquisition and motor control in a light-weight model organism.

185 development of brain regions associated with motor control in a manner that is detectable with fetal

186 nderstanding neural activity dynamics during motor control in both intact and dysfunctional nervous s

187 ted disease that leads to occasional loss of motor control in combination with variable other symptom

188 tation (Trp-gamma (1) ) known to affect fine motor control in Drosophila Moreover, we identify aberra

189 of the mechanisms contributing to disordered motor control in HD.

190 aberrant basal ganglia output and disordered motor control in HD.

191 lation, opening new avenues for the study of motor control in health and disease.

192 acterizing the impact of sensory feedback on motor control in healthy and sensory-impaired population

193 vestigated pathways, which are important for motor control in healthy individuals.

194 n of mammalian CS systems that improved fine motor control in higher primates.

195 portant for the development of proper speech motor control in humans.

196 pparent uniqueness of the corticalization of motor control in humans.

197 Patients also regained voluntary motor control in key muscles below the SCI level, as mea

198 onal activity in restoring communication and motor control in patients suffering from devastating neu

199 dulating cortical mechanisms for fine distal motor control in patients.SIGNIFICANCE STATEMENT We show

200 tract (RST) provides a parallel pathway for motor control in primates, alongside the more sophistica

201 The reason for this sudden amelioration of motor control in REM sleep is unknown, however.

202 ning normal thalamocortical oscillations and motor control in the adult brain, and suggest that the d

203 ing and has repeatedly been shown to reflect motor control in the primary motor cortex.

204 In the future, human studies of spinal motor control, in close collaboration with animal studie

205 ssociated with reorganization of regions for motor control, including orofacial movements, in the pri

206 edback control.SIGNIFICANCE STATEMENT Speech motor control is a complex activity that is thought to r

207 y in order to ensure accurate perception and motor control is a fundamental neuroscientific question.

208 Our results show that motor control is an active component of sensory learning

209 e of the corticospinal/pyramidal system over motor control is an expected consequence of increasing b

210 ollectively, the postnatal emergence of fine motor control is associated with a relative broadening o

211 Tongue motor control is critical to the pathogenesis of obstruc

212 Trunk motor control is crucial for postural stability and prop

213 al maximum (CTmax), the temperature at which motor control is lost in animals, has the potential to d

214 The sensory modality most tightly linked to motor control is mechanosensation.

215 Accurate motor control is mediated by internal models of how neur

216 The neurophysiological basis of motor control is of substantial interest to basic resear

217 Furthermore, since motor control is studied in populations, the effects of

218 A remarkable feature of motor control is the ability to coordinate movements acr

219 A critical component of motor control is the integration of sensory information

220 Predictive motor control is ubiquitously employed in animal kingdom

221 s that the pallidum plays a critical role in motor control, it has been difficult to establish the ca

222 is essential for sports performance and fine motor control, it has been repeatedly confirmed that hum

223 This not only affects our understanding of motor control, it may serve in the development of brain

224 prioceptive feedback is crucial for accurate motor control, little is known about how downstream circ

225 uggests that cortical engagement in hindlimb motor control may depend on the behavioral context.

226 also suggest that a modular organization of motor control may mediate not only coordination of multi

227 ur findings suggest feature integration, and motor control may occur as simultaneous operations withi

228 ggest that some forms of decision-making and motor control may share a common utility in which the br

229 tal area and retrorubal field, that regulate motor control, motivated and addictive behaviours.

230 ontributed to the development of finer vocal motor control necessary for speech production.

231 ions between the principal nodes of the fine motor control network in patients with writer's cramp an

232 an aberrant downstream influence on the fine motor control network in writer's cramp, which could be

233 llum has been shown to be part of the speech motor control network, its functional contribution to fe

234 hesized to form a crucial part of the speech motor control network.

235 hat impaired prefrontal modulation of speech-motor-control network and additional recruitment of righ

236 ns with the dorsal attention network and the motor-control network and negative correlations with the

237 thin the default mode, frontal-parietal, and motor control networks.

238 We apply our technique to an in silico motor control neuroscience experiment, using the algorit

239 n primates and humans have revealed that the motor control of facial expressions has a distributed ne

240 The present Review deals with the motor control of facial expressions in humans.

241 nterpreting the devastating consequences for motor control of lesions at different nodes of this inte

242 for enabling enhanced and more natural fine motor control of paralyzed limbs by BCI-FES neuroprosthe

243 el by which these triggers may impact on the motor control of skilled movement.

244 led to enhanced LMC functionality for finer motor control of speech production.

245 us arm and provide a basis for investigating motor control of the entire arm, which may aid the futur

246 uggesting separate (but coordinated) central motor control of the two behaviors based on multimodal i

247 nd-effectors in patients with some voluntary motor control of wrist and finger extensors after stroke

248 g impulsive behavior derived from inhibitory motor control or planning capacity deficits in healthy a

249 oss acquired amputees, individuals' reported motor control over their phantom hand positively correla

250 lum in a broad range of functions, including motor control, perception, language, working memory, cog

251 Applying a noise-reduction cost to optimal motor control predicted that reward can increase both ve

252 membrane assembly platform and a cytoplasmic motor controls pseudopilus assembly.

253 lia have been widely explored in relation to motor control, recent evidence suggests that their mecha

254 of changing material properties can simplify motor control, reducing the computational load on the de

255 sorimotor systems, top-down modulation helps motor-control regions "select" movement patterns.

256 tive early postnatally, a functional sensory-motor control relies on a delayed maturation and network

257 We suggest that a functional sensory-motor control relies on a delayed maturation and network

258 w active head movements influence downstream motor control remains elusive.

259 the precise role of the cerebellum in speech motor control remains unclear, as it has been implicated

260 Successful motor control requires accurate estimation of our body i

261 Understanding the basis of such motor control requires understanding how the firing of d

262 ome of major experimental advances in speech motor control research and discuss the emerging findings

263 es at which individuals grew torpid and lost motor control, respectively) of 88 ant species from this

264 ortex, potentially diversifying its roles in motor control.SIGNIFICANCE STATEMENT The common assumpti

265 rtle hindlimb scratching as a model for fine motor control, since this behavior involves precise limb

266 y of the other) may attest to well-developed motor control, so long as this limb independence does no

267 y integrated the sensory feedback into their motor control strategies while performing experimental t

268 ons that affect their gait by changing their motor control strategy.

269 sed previously about the status of PPTg as a motor control structure.

270 procedure to engage the motor cortex during motor control studies, gait rehabilitation, and locomoto

271 he importance of goal-directed behaviors for motor control studies, rehabilitation, and neuroprosthet

272 ications for our understanding of the speech motor control system in humans.

273 Cd CSP being a major component of the medial motor control system.

274 pertaining to early maldevelopment of ocular motor control systems.

275 underlying dimension shared by several visuo-motor control tests of the Nike battery.

276 umans have a distinguishing ability for fine motor control that is subserved by a highly evolved cort

277 arose in tandem with mechanisms of adaptive motor control that rely on basal ganglia circuitry.

278 as the sensorimotor apparatus shapes natural motor control, the BMI pathway characteristics may also

279 w a brain region classically associated with motor control, the cerebellum, may influence hippocampal

280 t advances in decoding cortical activity for motor control, the development of hand prosthetics remai

281 In computational modelling of sensory-motor control, the dynamics of muscle contraction is an

282 (1968-2018) of behavioral neurophysiology of motor control, the neural mechanisms that allow such coo

283 ol over audio-vocal interaction during vocal motor control, the PFC needs to be involved.

284 present a new computational model of speech motor control: the Feedback-Aware Control of Tasks in Sp

285 Early computational motor control theories have proposed that the cerebellum

286 Computational motor control theories have suggested that cerebellar in

287 The cerebellum influences motor control through Purkinje target neurons, which tra

288 ially due to abnormalities in how they learn motor control throughout development.

289 Researching the sensory corollaries of motor control thus can be crucial to understand sensory

290 We focus on studies spanning motor control, timing, decision-making, and working memo

291 velop a computational model that articulates motor control to economic decision theory, to dissect th

292 ain computations ranging from perception and motor control to memory and cognition.

293 model that ultimately links descending vocal motor control to tissue vibration and sound requires emb

294 Perception and motor control traditionally are studied separately.

295 siders the disorder a modifiable disorder of motor control, we are optimistic that research will yiel

296 ite widespread diversity in behavior and its motor control, we know little about the evolution of cor

297 el in situ perfused preparation for studying motor control, we show that malformation of these spinal

298 ctional assessments of strength, balance and motor control were performed in 30 masters athletes (16

299 adult Foxa1/2 mutant mice, independently of motor control, which could be rescued by L-DOPA treatmen

300 Monitoring our performance is fundamental to motor control while monitoring other's performance is fu