ライフサイエンスコーパス: neural control

1 th data on muscle contractile physiology and neural control.

2 ion to pressure rise was due to an increased neural control.

3 dynamics are less stable and require greater neural control.

4 out obvious changes in vasomotor sympathetic neural control.

5 ), which may cause dysrhythmias and impaired neural control.

6 dressed in relation to heart development and neural control.

7 ed movement error into updates of predictive neural control.

8 ion of both genes in mature muscles is under neural control.

9 e enterocyte, independent of hormonal and/or neural control.

10 ination is achieved through emergent modular neural control.

11 to that of oscine vocal learning and complex neural control.

12 bouncing gaits does not require centralized neural control.

13 ation does not necessarily imply group-level neural control.

14 s to visually guided behavior and underlying neural control.

15 rapeutic potential of ultrasound for precise neural control.

16 regard for the underlying structure of their neural control.

17 and instead indicates saccade-type-specific neural control.

18 he evolution of behavioral diversity and its neural control.

19 is and directly within sperm, independent of neural control.

20 of secretary birds require fast yet accurate neural control.

21 change its stiffness and extensibility under neural control.

22 is essential for survival and under precise neural control.

23 avior emerged naturally, without closed-loop neural control.

24 a mechanical effect rather than a change in neural control.

25 bnormalities of ventilatory and upper airway neural control.

26 ity and maneuverability, thereby simplifying neural control.

27 apparent randomness, ocular drifts are under neural control.(6)(,)(7)(,)(8) However little is known a

28 resent evidence that, in addition to central neural control, a further level of temporal organization

29 By enabling precise, non-invasive neural control across timescales from milliseconds to mo

30 hanics resulting from dynamic interaction of neural control, active muscle, and system material/inert

31 ng and analysis revealed that the underlying neural control also switched between mutually incompatib

32 incontinence reflect the loss of coordinated neural control among the detrusor muscle, which increase

33 glia, has an important role in local enteric neural control and coordination of intestinal secretion

34 lvement of P2Y(1) receptors in local enteric neural control and coordination of intestinal secretion

35 Similarly, neural control and coordination of the DIAm in nonventil

36 e great advances in our understanding of the neural control and function of different brain states.

37 active and passive mechanisms, consisting of neural control and intrinsic mechanical stiffness of the

38 ive frontal plane motion requires additional neural control and is associated with falls, it would se

39 artery does not seem to be under sympathetic neural control and is refractory to modest alterations o

40 emptying is under complex neuroendocrine and neural control and may be influenced by multiple neurome

41 tational neuroethology, which jointly models neural control and periphery of animals, is a promising

42 xploring principles of circuit organization, neural control and resilience of locomotion, offering a

43 insights that can be derived from studies of neural control and sensing within a biomechanical contex

44 at the episcleral circulation is under tonic neural control and that either an upstream resistance si

45 (a robot load on locomotion without any BMI neural control), and (3) "BMI with elastic load" (in whi

46 c gastric muscle, disorders of the extrinsic neural control, and pyloric dysfunction that lead to gas

47 re creates constraints and opportunities for neural control; and continuous feedback between nervous

48 logical mechanism that may involve myogenic, neural control as well as metabolic regulations of cereb

49 spectral structure are indeed under central neural control at the level of RA, consistent with the i

50 developing the miniature coil technology for neural control by targeting ganglion cells.

51 By exploring identified neural control circuits in the appropriate functional an

52 which the robot loaded locomotion and a BMI neural control could counter this load).

53 e is to place increased reliance upon active neural control during times when increased sway renders

54 ing behavior called "optomotor response." As neural control elements, the large tangential horizontal

55 interactions between the active, passive and neural control elements.

56 of the electrophysiological experiments, the neural control engineering and brain-machine interface s

57 this periodic orbit is stable, i.e. how the neural control gain values have to be chosen for stable

58 we use this model to make predictions about neural control gains and compare these predictions with

59 minor evolutionary changes in morphology and neural control have transformed a muscle-powered system

60 lution of active vision and present testable neural control hypotheses for visually guided behavior a

61 primer for young researchers to learn about neural control in biological systems before applying the

62 tion, highlighting the importance of precise neural control in producing natural eyelid behavior.

63 s remains a challenge, because access to the neural-control information for the arm is lost during am

64 Therefore, neural control is a general feature of the motor cortex,

65 trol over vocalization, indicating that some neural control is already shared with great apes.

66 relevance, and its relation to mechanisms of neural control is not well understood.

67 One possibility is that neural control is simplified by limiting the space of ha

68 ematics reflect a fundamental feature of the neural control mechanisms even in a highly repetitive mo

69 be crucial to advancing our understanding of neural control mechanisms for movement.

70 Both neural and non-neural control mechanisms may contribute to changes in h

71 with the idea that hierarchical, task-level neural control mechanisms previously associated with vol

72 or atropine (1 microM), suggesting that the neural control mechanisms responsible for MMCs in +/+ mi

73 ese results suggested that reduced-dimension neural control mechanisms such as muscle synergies can a

74 interactions between central and peripheral neural control mechanisms.

75 We propose a neural control model in which the spinal control generat

76 Circuit dissection approaches reveal the neural control network responsible, characterized by a m

77 Here we hypothesize that continuous neural control of a bionic limb can restore biomimetic g

78 irst application of the UCM framework to the neural control of a single muscle.

79 Indirect observations suggest that the neural control of accommodation may undergo adaptive rec

80 Neural control of adipose metabolism is mediated by symp

81 Dysfunctional neural control of airway smooth muscle (ASM) is involved

82 IAm only as an inspiratory pump, emphasizing neural control of airway, intercostal, and abdominal mus

83 entially, adding to our understanding of the neural control of alcoholism.

84 er, our experiments provide insight into the neural control of antennal movement and suggest that act

85 on in our understanding of the molecular and neural control of appetite and body weight, reviewed her

86 The neural control of appetite is important for understandin

87 The understanding of the neural control of appetite sheds light on the pathogenes

88 ction, it might be expected that sympathetic neural control of arteries and veins would differ.

89 ilization of standing, demanding more active neural control of balance.

90 riables or costs that may be relevant to the neural control of balance.

91 ll allow rapid advances in understanding the neural control of behavior and identifying pathologies o

92 Thus, delineating neural control of behavior requires a dissociation betwe

93 ant node in the orchestration of the complex neural control of behavior used in the courtship process

94 , we attempt to combine core ideas about the neural control of behavior with principles of display ev

95 e laboratory to understand evolution and the neural control of behavior.

96 iative learning frameworks to understand the neural control of behavior.

97 ata suggest that the PHA is important in the neural control of behavioral state, modulating aspects o

98 hese findings reveal a circuit logic for the neural control of behaviors that include both sexually m

99 vide exciting opportunities for studying the neural control of behaviour.

100 a critical role of the basal ganglia in the neural control of bimanual coordination.

101 An incomplete understanding of neural control of bladder function limits our ability to

102 re sex differences in arterial stiffness and neural control of blood pressure (BP) among older adults

103 he central nervous system, but their role in neural control of blood pressure during phosphate loadin

104 cific differences in obesity and sympathetic neural control of blood pressure is important in the pre

105 The reflex that provides rapid neural control of blood pressure is triggered by an unkn

106 oxia (CIH) elicits plasticity in the central neural control of breathing via serotonin-dependent effe

107 e investigate the role of V2a neurons in the neural control of breathing, an essential repetitive mot

108 In studies of the central neural control of breathing, little advantage has been t

109 l sex hormones play an important role in the neural control of breathing.

110 erotonin-dependent plasticity in the central neural control of breathing.

111 nce mechanism for neonatal sepsis preserving neural control of breathing.

112 f most clinical disorders that challenge the neural control of breathing.

113 erventions to treat various disorders of the neural control of breathing.

114 gest that Kv1.1 deficiency leads to impaired neural control of cardiac rhythmicity due in part to abe

115 ntral effect of this neurohormonal system in neural control of cardiovascular function remains poorly

116 in PRR is functional and plays a role in the neural control of cardiovascular functions.

117 These findings suggest that a decline in the neural control of ChBF and vessel diameter may explain t

118 TPR will shed new light on the function and neural control of circadian rhythms.

119 red for a better understanding of integrated neural control of circulatory function and arterial bloo

120 ide a paradigm shift in our understanding of neural control of complex behaviors.

121 Neural control of coordinated movements is widely though

122 rgent themes such as the modular genetic and neural control of dimorphic behavior are broadly applica

123 The neural control of disjunctive saccades is still poorly u

124 The present work reveals a novel neural control of dynamic body patterning for communicat

125 study was to determine the role of autonomic neural control of dynamic cerebral autoregulation in hum

126 cAMP in these areas may be important in the neural control of eating.

127 l cluster in the dorsal thalamus involved in neural control of electric behaviors.

128 The EOM pulleys may simplify neural control of eye movements by implementing a commut

129 s that Purkinje cell activity influences the neural control of eye movements in several distinct ways

130 Continuing advances have rendered the neural control of eye movements one of the best understo

131 Insight into the neural control of feeding has previously focused mainly

132 ic blockades have now shown that sympathetic neural control of FHRV was potently suppressed between p

133 Therefore, we investigated the neural control of finger musculature when the index fing

134 Understanding the neural control of functional reflexes and how they are m

135 ides a molecular framework for understanding neural control of gastrointestinal physiology.

136 utput and has important implications for the neural control of grooming.

137 hanges indicate alterations to the intrinsic neural control of gut functions mediated by the enteric

138 The neural control of hand movement involves coordination of

139 itric oxide synthase (nNOS) would impair the neural control of heart rate following physical training

140 etic cardiac vagal neurons that dominate the neural control of heart rate.

141 is on the translation of basic principles of neural control of heart rhythm that have emerged from ex

142 o autonomic dysfunction and dysregulation of neural control of hepatic functions including glucose me

143 sought to re-evaluate the model of autonomic neural control of HR in humans during progressive increa

144 The dominant neural control of human airway mucus secretion is cholin

145 nward currents play an important role in the neural control of human movement and are influenced by n

146 Cerebral lateralization may be important in neural control of immune function.

147 rather than silencing, this circuit affords neural control of immune responses.

148 netics has improved our understanding of the neural control of immunity.

149 The striatum has an essential role in neural control of instrumental behaviors by reinforcemen

150 , experimental data on the hydrodynamics and neural control of interactions between fish and vortices

151 ever, despite considerable research into the neural control of lactation, an understanding of the sig

152 movements are fast and difficult to resolve, neural control of lingual kinematics remains poorly unde

153 They are discussed in the context of neural control of locomotion in crustacea and insects.

154 r a comprehensive understanding of jellyfish neural control of locomotion.

155 em, one of the main sense organs involved in neural control of locomotion.

156 into the organization of spinal circuits and neural control of locomotion.

157 ves developmental phenotypes associated with neural control of lung breathing.

158 g time-resolved activation, we show that the neural control of male courtship song can be separated i

159 lt Drosophila involved in the triggering and neural control of male- and female-like elements of cour

160 t highlights the challenges in understanding neural control of mammalian behaviors, many (considerabl

161 t highlights the challenges in understanding neural control of mammalian behaviours, many (considerab

162 procal release is a central mechanism in the neural control of many physiological processes including

163 rine effects in the testis and ovary and the neural control of maternal and sexual behaviors.

164 ion during fixation, previous studies of the neural control of microsaccades measured the movement of

165 a structural foundation for analysis of the neural control of movement and serve as a guide for stud

166 nd have provided a comprehensive view of the neural control of movement at the motor unit level.

167 l dynamics and physiological noise may alter neural control of movement in both healthy and pathologi

168 Investigating the neural control of movement in general, and the cortical

169 , the "neural modes." We discuss a model for neural control of movement in which the time-dependent a

170 Understanding flexibility in the neural control of movement requires identifying the dist

171 Our findings reveal a novel pathway for neural control of movement whereby the somatosensory cor

172 alysis, which is widely used in the study of neural control of movement, predicts commensurately low-

173 become a powerful tool for investigating the neural control of movement, providing insights into moto

174 However, for neural control of movement, they currently must be integ

175 we propose a new conceptual framework of the neural control of movement, which merges the concept of

176 The neural control of movements in vertebrates is based on a

177 While investigating the neural control of movements, we recently discovered a to

178 Neural control of muscle function is fundamental to anim

179 ates a role for oestrogen in the sympathetic neural control of muscle haemodynamics during exercise.

180 xes and can only arise from the anticipatory neural control of muscle length that is necessary for ba

181 y that opens new avenues in the study of the neural control of muscles in humans.

182 al motor cortical state dynamics reflect the neural control of naturalistic reach-and-grasp behaviors

183 rphic behavior are broadly applicable to the neural control of other behaviors.

184 circuits can be readily used to interrogate neural control of other visceral organs.

185 ons are the final common pathway for central neural control of ovulation.

186 However, neural control of palatable food intake is poorly unders

187 at at 85% of gestation the potential for VIP neural control of paracrine (e.g., glucocorticoid/catech

188 Improved understanding of the neural control of parental interactions in animals shoul

189 The neural control of reaching entails the specification of

190 The neural control of renal function is exerted by the centr

191 ypothalamic pathways that participate in the neural control of reproduction and summarizes what is kn

192 ivity was an existing data set examining the neural control of respiration and cough.

193 ion has been found to play a key role in the neural control of rhythmic swimming behaviour in Xenopus

194 rapezius and for the first time explores the neural control of SA.

195 To understand the neural control of saccade sequences, we recorded from th

196 covert processes examined using data on the neural control of saccadic eye movements.

197 Our data provide evidence for neural control of salivary gland by MIP and SIFamide fro

198 may involve mast cell-mediated protection of neural control of secretory function.

199 as an open-source platform for studying the neural control of sensorimotor behaviour in an embodied

200 Accurately modelling the neural control of sensorimotor behaviour requires an ana

201 have uncovered new mechanisms underlying the neural control of sex-specific behaviors.

202 We conclude that in humans sympathetic neural control of skeletal muscle oxygenation is sensiti

203 eline sleep, further differentiating between neural control of sleep homeostasis and daily fluctuatio

204 Rapid advances in the neural control of social behavior highlight the role of

205 The neural control of social behaviors in rodents requires t

206 central molecular mechanisms regulating the neural control of sodium excretion remain unclear.

207 ically relevant models of phonation with the neural control of speech has not been developed.

208 hting the therapeutic potential of targeting neural control of SSCs.

209 nt afferent information to contribute to the neural control of stepping.

210 The neural control of sugar consumption is critical for norm

211 t exposure to microgravity impairs autonomic neural control of sympathetic outflow in response to per

212 Neural control of synergist muscles is not well understo

213 Dysregulated neural control of systemic inflammation postinjury is li

214 The neural control of tasks such as rapid acquisition of pre

215 ork under three themes: (a) biomechanics and neural control of the accommodative apparatus, (b) its b

216 l role of monoamines and histamine may be in neural control of the adult human heart.

217 Changes in the neural control of the airways contribute to bronchoconst

218 usly, we have shown that TNX is required for neural control of the bowel by a specific subtype of mai

219 ic nucleus (PVN) have been implicated in the neural control of the cardiovascular response to stress.

220 f medical devices for counteracting impaired neural control of the cardiovascular system.

221 We speculate that autonomic neural control of the cerebral circulation is tonically

222 is known about the effects of sildenafil on neural control of the circulation or about the effects o

223 he detailed mechanistic underpinnings of the neural control of the DIAm and the symphonic coordinatio

224 SIGNIFICANCE STATEMENT: Neural control of the dynamic body patterning of cephalo

225 Neural control of the function of visceral organs is ess

226 nervous system (ENS) provides the intrinsic neural control of the gastrointestinal tract (GIT) and r

227 finger muscles, and in part from distributed neural control of the hand.

228 P2Y1 receptors (P2Y1R), mediates inhibitory neural control of the intestines.

229 Although peripheral neural control of the lacrimal gland is well established

230 a relation is critical to understanding the neural control of the lower urinary tract and how dysfun

231 We examined the neural control of the respiratory system of littermate w

232 ilitation but its therapeutic effects on the neural control of the trunk after spinal cord injury (SC

233 es several clues to the understanding of the neural control of the unusual sleep phenomenology presen

234 gonist, to examine the role of mGluR5 in the neural control of the urinary bladder and in the inhibit

235 unctional organization of the optic lobe and neural control of the various body patterns by the optic

236 rminals and adjacent ganglion cells suggests neural control of these contractile cells.

237 premotor neurons potentially involved in the neural control of these eye movements.

238 The level of flexibility in the neural control of these motor units remains a topic of d

239 ulate torpor in mouse, little is known about neural control of torpor in other endothermic animals, i

240 entative inertial parameters using real-time neural control of torques in non-human primates (M. radi

241 We found that neural control of torques leads to ballistic, possibly m

242 nds and consolidates knowledge regarding the neural control of trapezius and for the first time explo

243 Neural control of upright stability, on the other hand,

244 ew the current state of our knowledge of the neural control of vergence and ocular accommodation in p

245 the animal literature and sheds light on the neural control of vigor.

246 In songbirds, much is known about the neural control of vocal behavior; however, little is kno

247 Despite a large body of work on the neural control of walking in invertebrates and vertebrat

248 ltiplicity associated with the nature of the neural controls of these components in the cephalopod br

249 We hypothesize that the peripheral neural control on cardiovascular activity prompts and su

250 Brain-machine interfaces can allow neural control over assistive devices.

251 ts in our understanding of the mechanisms of neural control over organ function and (2) advances in t

252 From a neural control perspective, these findings indicate how

253 mportantly, this abrupt switch in underlying neural control polluted fingertip force vector direction

254 ed experimental programs for delineating the neural control principles that have evolved to coordinat

255 tiple forms of attention, but the underlying neural control process remains obscure.

256 therapeutics via cell-type-specific optical neural control prosthetics.

257 e 5-HT abnormalities in distinct respiratory neural control regions can be initiated by prolonged hyp

258 and cephalopods to snakes and birds, combine neural control, sensory feedback and compliant mechanics

259 the single physiological assumption that the neural control signals are corrupted by noise whose vari

260 ry feature-based attention involves top-down neural control signals from the frontoparietal network t

261 gress has been made, including evaluation of neural control signals, sensor testing in humans, signal

262 ively switches between mutually incompatible neural control strategies to bridge the abrupt transitio

263 ovides a simple, but plausible, account of a neural control strategy that has been the center of deba

264 ng the simplest mechanical configuration and neural control strategy.

265 of development during which the respiratory neural control system exhibits a heightened vulnerabilit

266 ent simplicity of breathing belies a complex neural control system, the breathing central pattern gen

267 tial to elucidate behavioral fingerprints of neural control systems involved in emotional signaling.

268 dely used kinematic analyses in the study of neural control systems.

269 Given the complexity of the neural control task, invertebrates, with their numerical

270 eature of human life, comprises an intricate neural control task.

271 ral arm (Manual Control, MC) or under direct neural control through a brain-machine interface (Brain

272 or program was learned when the animals used neural control to achieve water reward (e.g. more inform

273 Furthermore, MN used neural control to open and close a prosthetic hand, and

274 d stepping movements to serve as a source of neural control to undertake these tasks.

275 nctions that originate from abnormalities in neural control, underscoring the need to understand how

276 walking accounting for both biomechanics and neural control, using a modeling approach.

277 the well known inverted pendulum model, and neural control, using a proportional-derivative controll

278 ere obtained when the vector of experimental neural controls was representative of the discharge acti

279 a powerful alternative to current methods of neural control, which rely predominantly on electrical a

280 are more stable and less dependent on active neural control, while the frontal plane dynamics are les

281 Enhanced neural control with age, however, did not contribute the

282 gs point to an unanticipated new modality of neural control with broad implications for nervous syste

283 s from serous cells and is principally under neural control with muscarinic agonists, substance P, an

284 This device offers reversible neural control, with potential applications in both rese