ライフサイエンスコーパス: sensory feedback

1 ectively damaging a muscle without affecting sensory feedback.

2 hange, increasing the gains for the expected sensory feedback.

3 enerate behaviour and adapt it to changes in sensory feedback.

4 t also the gains associated with reaction to sensory feedback.

5 are difficult to control and do not provide sensory feedback.

6 modified after brief exposure to unexpected sensory feedback.

7 eural systems capable of anticipating actual sensory feedback.

8 with multiple forms of natural or surrogate sensory feedback.

9 nerve interfaces for prosthesis control and sensory feedback.

10 ng their target innervated muscle fibers and sensory feedback.

11 ern generating circuits can be overridden by sensory feedback.

12 nerate motor commands without the benefit of sensory feedback.

13 provides a potential pathway for meaningful sensory feedback.

14 entrally or whether it arises as a result of sensory feedback.

15 desired movement trajectories while ignoring sensory feedback.

16 r task and manipulate the uncertainty of the sensory feedback.

17 ribution and the level of uncertainty in the sensory feedback.

18 n of velocities-the prior-with evidence from sensory feedback.

19 d loop component, which is more dependent on sensory feedback.

20 grams operating independently from immediate sensory feedback.

21 its that drive rhythmic motor output without sensory feedback.

22 involve integration of intention, action and sensory feedback.

23 scles during cough, independent of laryngeal sensory feedback.

24 about the presence or role of other forms of sensory feedback.

25 absence of brain inputs and movement-related sensory feedback.

26 ts in which we controlled the reliability of sensory feedback.

27 es high levels of motor control and auditory sensory feedback.

28 nt the ongoing motor program or song-related sensory feedback.

29 nematics and body trajectories requires fast sensory feedback.

30 reotypical, but dynamically adapted based on sensory feedback.

31 correspondence between motor exploration and sensory feedback.

32 mpares expected with actual postarticulatory sensory feedback.

33 bsence of primary motor cortical activity or sensory feedback.

34 ng edge cells and thus the locomotor-related sensory feedback.

35 hythmogenesis, descending motor control, and sensory feedback.

36 to perform a grasp retrieval task requiring sensory feedback.

37 requires a complex neural network coupled to sensory feedback.

38 del that optimally integrates noisy, delayed sensory feedback about both motion and position to estim

39 on by integrating sensorimotor memories with sensory feedback about digit positions.

40 Thus, how sensory feedback affects both task-relevant and task-irr

41 ntal coordination can in fact be achieved by sensory feedback alone, without the intersegmental inter

42 lso consistent with a dynamic interaction of sensory feedback and central programming, presumably ada

43 Our data show that both sensory feedback and central systems of the spinal cord

44 on requires understanding the integration of sensory feedback and executive commands.

45 e rapid mechanical preflexes with multimodal sensory feedback and feedforward commands.

46 For optimal sensorimotor control, sensory feedback and feedforward estimation of a movemen

47 The precision of skilled movement depends on sensory feedback and its refinement by local inhibitory

48 emely fast decision processes in response to sensory feedback and modulation through attention in a n

49 otor patterns in the presence and absence of sensory feedback and related these motor program compone

50 t uses efferent copy of commands to the arm, sensory feedback, and an internal model of the dynamics

51 rain integrates feedforward control signals, sensory feedback, and predictions based on internal mode

52 tegration between feedforward estimation and sensory feedback, and therefore the putative motor and s

53 the integration of articulatory planning and sensory feedback, and via connections with primary motor

54 This provides insight into flies' multimodal sensory feedback architecture and constitutes a previous

55 ions with the mother and littermates and (2) sensory feedback arising from spontaneous infant movemen

56 e fictive locomotion-that is, without phasic sensory feedback as monitored by five muscle nerves in e

57 Rather, they favour sensory feedback as the source of the sense of movement.

58 fic modifications in the processing of local sensory feedback as well as modification of the activity

59 hich was recursively updated in light of new sensory feedback, as identified by a Bayesian learning m

60 re captured by modelling the consequences of sensory feedback at high gain.

61 adapt whenever its predictions fail to match sensory feedback at the end of the movement.

62 ythmic input from higher brain structures or sensory feedback because they contain an intrinsic sourc

63 ting oscillations to the environment through sensory feedback, but without guidance from the brain.

64 n primates have shown that motor control and sensory feedback can be achieved by connecting sensors i

65 nisms supporting initial motor output before sensory feedback can be processed are disrupted in ASD.

66 oprioceptor neurons, and for deciphering how sensory feedback can function within a defined neural ci

67 rve cords, refuting earlier conclusions that sensory feedback cannot coordinate swimming activity.

68 hort period of rapid finger-tapping (without sensory feedback) caused subjects to underestimate the n

69 Sensory feedback, central pattern generators, and supras

70 rate rhythmic motor output in the absence of sensory feedback, commonly called central pattern genera

71 ides a mechanism for temporal integration of sensory feedback consistent with PI control.

72 uggesting that O-mannosylation regulates the sensory feedback controlling muscle contractions.

73 (3) Removal of sensory feedback did not affect step coordination or tim

74 However, the quality of the sensory feedback during a movement can depend substantia

75 ircuits may participate in the evaluation of sensory feedback during calibration of motor performance

76 In contrast, sensory feedback during locust flight or to multiple cor

77 ry information at night and by evaluation of sensory feedback during the day interact to produce the

78 with a strengthening of the motor effects of sensory feedback during tonic contraction and with reduc

79 To distinguish these hypotheses, we examined sensory feedback effects during targeted wiping organize

80 However, because sensory feedback entrains the stepping rhythm, it is dif

81 d many models of learning assume that larger sensory feedback errors drive larger motor changes.

82 Without sensory feedback, flies cannot fly.

83 g so, the nervous system strongly suppresses sensory feedback for extended periods of time in compari

84 mportant implications in providing realistic sensory feedback for prosthetic-hand users.

85 ssed by swimming leeches may be regulated by sensory feedback from both ventral and dorsal longitudin

86 ot, providing it with dynamic coloration and sensory feedback from external and internal stimuli.

87 pares timing on the order of microseconds of sensory feedback from from its high-frequency (approxima

88 rated to switch reflex responses to urethral sensory feedback from maintaining continence to producin

89 tion of coordinated body movements relies on sensory feedback from mechanosensitive proprioceptors.

90 Animals depend on sensory feedback from mechanosensory afferents for the d

91 Group Ia/II sensory feedback from muscle spindles has a predominant

92 somatosensory neocortex occur in response to sensory feedback from myoclonic twitching, we hypothesiz

93 of reinnervated chest skin may allow useful sensory feedback from prosthetic devices and provides in

94 Sensory feedback from sleep-related myoclonic twitches i

95 of normal motor cortex maps in M1 depends on sensory feedback from somatosensory maps.

96 Sensory feedback from stretch receptors, neurons that de

97 ducing a method for providing the brain with sensory feedback from the actuators, and designing and b

98 sults demonstrate the complementary roles of sensory feedback from the bladder and urethra in regulat

99 We used a novel preparation to manipulate sensory feedback from the bladder and urethra independen

100 Previous studies showed that sensory feedback from the body wall is important and som

101 eral M1 in Kallmann's subjects may be due to sensory feedback from the involuntarily mirroring hand.

102 persisted in the proximal stumps deprived of sensory feedback from the periphery.

103 usands of skeletal muscle twitches each day; sensory feedback from the resulting limb movements is a

104 udy shows that their preservation depends on sensory feedback from the spinal cord to the brain: if f

105 nds of limb twitches are produced daily, and sensory feedback from these movements is a substantial d

106 motor activity of the animal and the ensuing sensory feedback from this activity could directly influ

107 , which is a prerequisite to the notion that sensory feedback from twitches not only activates sensor

108 oduce twitching as well as those that convey sensory feedback from twitching limbs to the spinal cord

109 ms that produce twitching, and the role that sensory feedback from twitching plays in sensorimotor sy

110 patterns reflected an optimal reweighting of sensory feedback gains to minimize postural instability.

111 which learn their vocal motor behavior using sensory feedback, have specialized a portion of their co

112 additional influences present in vivo (e.g., sensory feedback, hormonal modulation) could alter the m

113 In this paper, we evaluate the role of sensory feedback in intersegmental coordination using bo

114 nervous system processes multiple sources of sensory feedback in such short time intervals, given tha

115 The role of sensory feedback in the activation and organization of s

116 s into the interplay of central networks and sensory feedback in this model organism.

117 moved through a virtual environment without sensory feedback, indicating that theta oscillations hav

118 The central nervous system uses sensory feedback information during movement to detect a

119 Sensory feedback is a ubiquitous feature of guidance sys

120 Sensory feedback is crucial for learning and performing

121 comparison between the predicted and actual sensory feedback is made, and information about unpredic

122 ntegrator hypothesis, except that additional sensory feedback is needed, from proprioceptors in the n

123 The first problem is that sensory feedback is noisy and delayed, which can make mo

124 lay an important role in extinction, corneal sensory feedback is not necessary.

125 Sensory feedback is not required for the CPGs to generat

126 w each of these topics and suggest that when sensory feedback is reliable, it is used to adapt the mo

127 When sensory feedback is unreliable, subjects adapt the stiff

128 eep) of rehearsed motor output and predicted sensory feedback is used to adaptively shape motor outpu

129 Sensory feedback is, however, required to modify or coor

130 parately through processes involving ongoing sensory feedback loops.

131 nly gated in conditions where proprioceptive sensory feedback matched the motor-based expectation.

132 Sensory feedback may also increase task-irrelevant varia

133 of urinary retention and incontinence where sensory feedback may engage these reflexes inappropriate

134 We speculate that sensory feedback might adapt recruitment of muscle syner

135 ossibilities include prosthetic control with sensory feedback, monitors, and stimulation signals rela

136 This sensory feedback needs to be selectively modulated in a

137 t is neither directly available from passive sensory feedback nor compatible with outgoing motor comm

138 ration of sympathetic responses and afferent sensory feedback of visceral state via the spinal cord.

139 ol is studied in populations, the effects of sensory feedback on variability must also be understood

140 commands, known as corollary discharge (CD), sensory feedback, or some combination of both.

141 central motor command by opening or closing sensory feedback pathways.

142 Despite the key role urethral sensory feedback plays in regulation of the lower urinar

143 dual differences in motor neuronal activity, sensory feedback provides each subject access to a commo

144 ach can be used to provide a rich artificial sensory feedback signal, suggesting a new strategy for r

145 Sensory feedback signals recorded from peripheral nerves

146 expenditure are privy to continuous visceral sensory feedback signals that presumably modulate appeti

147 ained by a postural system that is driven by sensory feedback signals.

148 based on the integration of feedforward and sensory feedback signals.SIGNIFICANCE STATEMENT The defe

149 Furthermore, the systematic removal of three sensory feedback streams (auditory, proprioceptive, and

150 Animals use a form of sensory feedback termed proprioception to monitor their

151 first stage of vibrissa scanning control via sensory feedback that provides reflexive protraction in

152 ivity of the newborn hippocampus arises from sensory feedback that sequentially activates the neocort

153 nexpected, adjustment of lick position or to sensory feedback that varied with task condition.

154 s because of the complex flight dynamics and sensory feedback that would be required to perform such

155 Is sensory feedback the mechanism for reducing individualit

156 ing motor commands and associated vestibular sensory feedback, the direction of vestibular-evoked ank

157 w that by incorporating such state-dependent sensory feedback, the optimal solution incorporates acti

158 Sensory feedback through spinal circuitries is integrate

159 hese movements are completed too quickly for sensory feedback to be useful.

160 otein O-mannosylation is required for normal sensory feedback to control coordinated muscle contracti

161 The brain uses sensory feedback to correct behavioral errors.

162 ircuitries effectively integrating immediate sensory feedback to efferent pathways controlling muscle

163 ain's ability to use pre-motor variation and sensory feedback to guide behavior toward a specific tar

164 ontrols, suggesting an increased reliance on sensory feedback to guide speech articulation in this po

165 During skill learning, the brain relies on sensory feedback to improve motor performance.

166 depends upon stabilization reflexes that use sensory feedback to maintain trajectories and orientatio

167 el of identified motor neurons, we show that sensory feedback to motor program components highly corr

168 o establish the contribution of hip-mediated sensory feedback to spinal interneuronal circuits during

169 rd-sized robot with an active tail that used sensory feedback to stabilize pitch as it drove off a ra

170 when a new behavior changes the spinal cord, sensory feedback to the brain guides further change that

171 erators." The contribution of proprioceptive sensory feedback to the coordination of locomotor activi

172 gesting that the twitches themselves provide sensory feedback to the infant hippocampus, as occurs in

173 on, and peristaltic contraction by providing sensory feedback to the locomotor CPG circuit in larvae.

174 the chordotonal organs (chos), in providing sensory feedback to the locomotor CPG circuit with dias

175 to skin, to provide a pathway for cutaneous sensory feedback to the missing hand.

176 ing the RORbeta orphan nuclear receptor gate sensory feedback to the spinal motor system during walki

177 er limb prostheses is limited by the lack of sensory feedback to the user.

178 dly depressing reflex that provides positive sensory feedback to the vibrissa musculature during simu

179 ajority, with abnormal postural control when sensory feedback was limited (SOTABN).

180 e take into account such state-dependency in sensory feedback we asked people to make movements in wh

181 we show that a simple form of proprioceptive sensory feedback, wherein local muscle activation is fun

182 tor aspects of postural control, with normal sensory feedback, while the SOT equilibrium scores measu

183 Although integration of sensory feedback with internal motor programs is importa

184 ough Av may function to integrate multimodal sensory feedback with vocal-learning circuitry and coord

185 e manipulation of neural circuits processing sensory feedback within the mammalian CNS.