ライフサイエンスコーパス: neural control

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

2 dynamics are less stable and require greater neural control.

3 out obvious changes in vasomotor sympathetic neural control.

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

5 dressed in relation to heart development and neural control.

6 ed movement error into updates of predictive neural control.

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

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

9 of secretary birds require fast yet accurate neural control.

10 change its stiffness and extensibility under neural control.

11 is essential for survival and under precise neural control.

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

13 bnormalities of ventilatory and upper airway neural control.

14 ity and maneuverability, thereby simplifying neural control.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 interactions between central and peripheral neural control mechanisms.

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

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

50 Neural control of adipose metabolism is mediated by symp

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

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

53 The neural control of appetite is important for understandin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

85 The neural control of hand movement involves coordination of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 The neural control of reaching entails the specification of

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

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

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

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

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

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

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

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

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

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

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

133 The neural control of social behaviors in rodents requires t

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

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

136 The neural control of sugar consumption is critical for norm

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

138 Neural control of synergist muscles is not well understo

139 Dysregulated neural control of systemic inflammation postinjury is li

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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