ライフサイエンスコーパス: behavioral task

1 DA antagonists on new learning (of a similar behavioral task).

2 gnetic resonance spectroscopy, and RT with a behavioral task.

3 1 mainly regulates baseline learning in this behavioral task.

4 mportance of different visual cues used in a behavioral task.

5 ocessing elements involved in conducting any behavioral task.

6 lated to sensory and motor events during the behavioral task.

7 n a hippocampus-dependent object recognition behavioral task.

8 ulations of activity performed better on the behavioral task.

9 stimuli even when they are unrelated to the behavioral task.

10 cessing efficiencies recorded in an auditory behavioral task.

11 entification than to other components of the behavioral task.

12 the number of trials needed to complete the behavioral task.

13 ary considerably during repeated trials of a behavioral task.

14 after the monkeys had used the stimuli in a behavioral task.

15 eived face-identity similarity obtained in a behavioral task.

16 1 improves deficits in the Morris water-maze behavioral task.

17 on-human primates (NHP) while they perform a behavioral task.

18 diated controls in the hippocampal-dependent behavioral task.

19 (V1) during acquisition of a visually guided behavioral task.

20 th performance on a concurrent pitch-related behavioral task.

21 depending on the role of the neurons in the behavioral task.

22 city at the two recording sites in a trained behavioral task.

23 mpaired performance in a macrovibrissa-based behavioral task.

24 l platforms, and are thus independent of the behavioral task.

25 y may reflect the engagement of neurons in a behavioral task.

26 g, but this has mostly been tested in simple behavioral tasks.

27 habenula, while animals anticipated upcoming behavioral tasks.

28 state of neurons and their participation in behavioral tasks.

29 e in autism- and mental retardation-relevant behavioral tasks.

30 ations between brain size and ecological and behavioral tasks.

31 showed prominent deficits in effort-related behavioral tasks.

32 beta plaque pathology and memory deficits in behavioral tasks.

33 and scopolamine into the OB during olfactory behavioral tasks.

34 w striatal FSIs change their activity during behavioral tasks.

35 e evolves that is tailored to the demands of behavioral tasks.

36 within intact animals as they freely perform behavioral tasks.

37 e in controlling motor responses during most behavioral tasks.

38 ediate neurotransmission interrogated by our behavioral tasks.

39 tation of results obtained in other kinds of behavioral tasks.

40 athway during performance of a wide range of behavioral tasks.

41 analog bromodeoxyuridine following specific behavioral tasks.

42 currents and improve performance on several behavioral tasks.

43 ding in vivo multielectrode recording during behavioral tasks.

44 perficial brain structures during head-fixed behavioral tasks.

45 iological state and other aspects of complex behavioral tasks.

46 by the disruption of neuronal integrity and behavioral tasks.

47 d serotonergic neurons in animals engaged in behavioral tasks.

48 ore the importance of such regulation during behavioral tasks.

49 rate of extinction learning across different behavioral tasks.

50 romotes further improvement in CST-dependent behavioral tasks.

51 pulation of cells in mice performing complex behavioral tasks.

52 cells and dentate gyrus-dependent cognitive behavioral tasks.

53 provide efficient training on sophisticated behavioral tasks.

54 h short- and long-term memory in a number of behavioral tasks.

55 ore and after monkeys learned to perform two behavioral tasks.

56 lowing of gamma also slows reaction times on behavioral tasks.

57 GluN2D-deficient mice were used in a set of behavioral tasks.

58 rred resilience to SD as measured in several behavioral tasks.

59 ures of animals, neuroscientists use several behavioral tasks.

60 at distinct neural pathways mediate distinct behavioral tasks [1, 2].

61 zed for cognitive changes using a battery of behavioral tasks 4-6 weeks later.

62 intensively studied law governing almost all behavioral tasks across species.

63 performance decrements using six independent behavioral tasks administered between separate cohorts 1

64 However, how the nature of a behavioral task affects the neural mechanisms of reinfor

65 To understand how learning new behavioral tasks affects neuronal representations, we re

66 During moving and flickering periods, the behavioral task alternated between sustained attention a

67 both when medicated and unmedicated, in two behavioral tasks: an incentive motivation task that invo

68 en sounds were presented in the absence of a behavioral task and reward.

69 Thus, the use of parallel behavioral tasks and analyses in monkeys and humans reve

70 I-779 improved performance on four different behavioral tasks and decreased aggregate formation in a

71 ocampal CA1 neurons in rats during different behavioral tasks and determining axonal projections with

72 ce of perirhinal cortex (PR) in a variety of behavioral tasks and disease processes.

73 ced age, rats show deficits on PER-dependent behavioral tasks and fewer PER principal neurons are act

74 ced were on the order of those seen in other behavioral tasks and imaging studies of awake animals.

75 the tonic activity level of a neuron during behavioral tasks and its encoding of reward-related cues

76 impaired cognition in hippocampally mediated behavioral tasks and reduced synaptic plasticity of hipp

77 in sensory perception.SIGNIFICANCE STATEMENT Behavioral tasks and training and testing history affect

78 sing of speech sounds even in the absence of behavioral tasks and when the sounds are not in the focu

79 We show that, for almost all behavioral tasks, and for a wide range of limitations on

80 t young neurons contribute to performance in behavioral tasks, and there is no clear relationship bet

81 nd to successfully explain the full range of behavioral task- and response-switch costs across first

82 well established, quantitative, reproducible behavioral tasks, appropriate Ns, correct statistical me

83 n changes in neuronal activity when specific behavioral tasks are being learned.

84 antially sharpened spatial tuning during the behavioral tasks as compared with idle conditions, with

85 , we reversibly decreased MD activity during behavioral tasks assessing elementary cognitive processe

86 In the behavioral task, BD showed a higher number of risky choi

87 scillations often are triggered by events or behavioral tasks but rarely outlast the event that trigg

88 has been observed not only following complex behavioral tasks, but also after random foraging in fami

89 ributed neural circuits is required for many behavioral tasks, but the mechanisms that coordinate the

90 On the behavioral task, children (7- to 11-year-olds) had high

91 f the CREBalphaDelta- mice in three distinct behavioral tasks: contextual fear conditioning, spatial

92 s, Arc was most responsive to differences in behavioral task demands.

93 al and neurochemical studies during specific behavioral tasks demonstrate a more restricted spectrum

94 display striking differences in a number of behavioral tasks depending on hippocampal function, such

95 Macaque monkeys were trained for a behavioral task designed to determine the trial-by-trial

96 significant performance-based decrements on behavioral tasks designed to interrogate hippocampal and

97 d performance on a range of fluid processing behavioral tasks (dot-comparison, digit-symbol, Trails-A

98 findings demonstrate that the nature of the behavioral task dynamically shifts the locus of integrat

99 Furthermore, different behavioral tasks evoke distinct patterns of theta/high g

100 rotocol can be performed in conjunction with behavioral tasks for studying a variety of cognitive fun

101 Because the two behavioral tasks have different motivational, perceptual

102 Experiments using a number of behavioral tasks have shown that rats with lesions of Ce

103 Specifically, we used a novel behavioral task in combination with computational modeli

104 By using a novel behavioral task in combination with functional magnetic

105 Spatial navigation is often used as a behavioral task in studies of the neuronal circuits that

106 sal raphe nucleus encodes participation in a behavioral task in terms of its future motivational outc

107 ted with improvements in a passive avoidance behavioral task in Tg2576 mice.

108 Finally, we designed a behavioral task in which human observers judged the shap

109 s to cingulate-hippocampus coordination in a behavioral task in which rats choose from four possible

110 this pattern by recording single units in a behavioral task in which rewards were unexpectedly deliv

111 Monkeys performed a behavioral task in which they attended to a visual stimu

112 that a group of dorsal raphe neurons encode behavioral tasks in a systematic manner, tracking progre

113 opportunity to image brain activation during behavioral tasks in animal models of human conditions.

114 A battery of behavioral tasks in C57BL/6J mice was used to assess cha

115 e at eye opening, and performance in several behavioral tasks in male and female SHR, Wistar-Kyoto (W

116 each domain of the RDoC and propose a set of behavioral tasks in model systems that reflect aspects o

117 Animals then received a battery of behavioral tasks in order to evaluate activity levels, a

118 Functional imaging and behavioral tasks included face-emotion processing paradi

119 rmalities in multiple schizophrenia-relevant behavioral tasks including prepulse inhibition, response

120 11Fip5 KO mice performed normally in several behavioral tasks, including fear conditioning, but showe

121 d demonstrate superior memory in a number of behavioral tasks, including object recognition.

122 mporal associations typically encountered in behavioral tasks involve times on the order of seconds.

123 ning; acquisition and retention of a Rotarod behavioral task is significantly better in K(b)D(b-/-) m

124 Our ability to learn a wide range of behavioral tasks is essential for responding appropriate

125 temporal information in cerebellum-dependent behavioral tasks is in part computed locally in the cere

126 We addressed this using behavioral tasks isolating distinct aspects of fear lear

127 We used behavioral tasks isolating distinct aspects of learning

128 Even in the context of simple behavioral tasks, it is unclear how well each of these m

129 eral reversible inactivation of LIP on three behavioral tasks known to evoke nonspatial responses.

130 Memory, behavioral tasks, locomotor activity, presence of human

131 t also substantially improves performance on behavioral tasks of spatial learning and memory that are

132 To enable the effects of behavioral tasks on functional connectivity to be measur

133 Behavioral task performance that requires processing fin

134 100s of neurons can code sensory inputs and behavioral task performance within psychophysical limits

135 te hippocampal regions and layers to support behavioral task performance.

136 ed low spatial selectivity, but rather coded behavioral task phases toward reaching goal sites.

137 ts for information processing during certain behavioral tasks, raising the possibility of modulation

138 By training monkeys on various behavioral tasks, recent studies have begun to character

139 RG2 KOs performed abnormally in a battery of behavioral tasks relevant to psychiatric disorders.

140 works that were either modulated or not by a behavioral task remained segregated during quiet wakeful

141 To assess this hypothesis, we conducted a behavioral task requiring immediate free recall of word-

142 berrant neuroanatomy, perform poorly on many behavioral tasks, resulting in potential interpretationa

143 ed and spared performance across these seven behavioral tasks reveals that the FPC mediates explorati

144 Utilizing a behavioral task shown to be sensitive to disruptions in

145 urons could be activated in any epoch of the behavioral task (stimulus presentation, delay, response)

146 about different aspects associated with the behavioral task that are subserved by multiple brain-mem

147 sensory-discrimination learning ability in a behavioral task that depends heavily on the barrel corte

148 temporal co-occurrence of reward, even in a behavioral task that does not require the subject to eng

149 Using a behavioral task that induces high levels of intermanual

150 ion are impaired in object-place learning, a behavioral task that induces hippocampal mGluR-LTD in vi

151 ral correlates at the single-unit level in a behavioral task that probes response inhibition without

152 DA release in subregions of the NAc during a behavioral task that spatiotemporally separated sequenti

153 Using a behavioral task that specifically measures the condition

154 le neurons in ACC as rats performed the same behavioral task that we have used to dissociate signed f

155 functional magnetic resonance imaging, and a behavioral task that yields successful recognition with

156 is CGG KI mouse model of FXTAS was tested on behavioral tasks that emphasize spatial information proc

157 , heterozygotes performed more accurately in behavioral tasks that primarily depend on sustained aler

158 same time point, animals were also tested in behavioral tasks that probe the functional integrity of

159 te, primates [1, 2] have performed poorly in behavioral tasks that require ToM abilities, despite the

160 However, these conclusions are based on behavioral tasks that themselves promote a serial arrang

161 On each trial of their behavioral task, the monkeys responded to a foveal visua

162 nformation was made irrelevant to observers' behavioral task, the MVPA analysis of LOC and the other

163 econd phase, after completion of the initial behavioral tasks, the same rats were treated once daily

164 otor activity was a component of many of the behavioral tasks, this was measured at various stages of

165 is no difference between the two groups on a behavioral task thought to index compulsivity (marble bu

166 analysis of fMRI data collected for the same behavioral task to ascertain the cortical origins of eac

167 g anatomical difference between species, the behavioral tasks used to probe decision-making and the m

168 olfactory bulb are dependent on the specific behavioral tasks used.

169 ile they were engaged in one of two distinct behavioral tasks: virtual target amplitude discriminatio

170 the trigeminal somatosensory system, a novel behavioral task was developed that required rats to disc

171 , odor sampling from the two nostrils in the behavioral task was highly lateralized.

172 Striatal dopamine efflux during behavioral tasks was determined by brain microdialysis c

173 formance of TG2(Tg)/Syn(Tg) animals on motor behavioral tasks was worse relative to Syn(Tg) mice.

174 Using a novel behavioral task, we demonstrate that head-fixed mice can

175 I in human subjects and a specially designed behavioral task, we examined the effect of the subjects'

176 t of electrical interference relative to the behavioral task, we found that completion of processing

177 In a behavioral task, we found that performance was superior

178 ted data and human fMRI data obtained during behavioral tasks were used to validate this method.

179 For instance, during learning of a behavioral task, when an animal is very alert and expect

180 onsistent with previous reports, using other behavioral tasks, which show decreased behavioral effici

181 PKR enhances learning and memory in several behavioral tasks while increasing network excitability.

182 animals, novelty recognition and exploratory behavioral tasks with assessment of structural and funct

183 o reconcile the form of separation tested in behavioral tasks with how it is conceptualized according

184 ats were tested in a novel hierarchy of four behavioral tasks with increasing cognitive demand.

185 theta cell activity have typically involved behavioral tasks with modest cognitive demands.

186 gions crucial for performance on clusters of behavioral tasks without a priori separation into task t

187 role of brain regions involved in different behavioral tasks without differential alterations in the