ライフサイエンスコーパス: exploratory behavior

1 swimming behavior - reflecting a switch to "exploratory behavior".

2 ty to engage in weak regulatory linkage, and exploratory behavior.

3 and were crucial for generating appropriate exploratory behavior.

4 units that were coactive during a particular exploratory behavior.

5 (-/-) females display an increased olfaction-exploratory behavior.

6 oming and eating and maximal activity during exploratory behavior.

7 avior control column concerned with foraging/exploratory behavior.

8 chanism, possibly IR-mediated, to elicit pro-exploratory behavior.

9 production in the nucleus accumbens restores exploratory behavior.

10 disrupts somatosensory electrophysiology and exploratory behavior.

11 ced anxiety-related responses with increased exploratory behavior.

12 avoidance and immobility, while showing less exploratory behavior.

13 e mutant SCA1 mice have an increased initial exploratory behavior.

14 theta phase, but exacerbated hypoactivity in exploratory behavior.

15 S1) of freely moving mice engaged in tactile exploratory behavior.

16 cing signals and network dynamics underlying exploratory behavior.

17 iven by non-specific baseline differences in exploratory behavior.

18 activation of a subset of the neurons during exploratory behavior.

19 ng environments, was associated with reduced exploratory behavior.

20 e-evaluated this constraint as a function of exploratory behavior.

21 ation of a subset of the same neurons during exploratory behavior.

22 l-scales - follows later around the onset of exploratory behavior.

23 their sensitivity to pheromones that inhibit exploratory behavior.

24 terns, reduces anxiety levels, and increases exploratory behavior.

25 cy restricted to aged animals with preserved exploratory behavior.

26 uitry in parallel with the emergence of this exploratory behavior.

27 period increased sitter but not rover adult exploratory behavior.

28 hageal ganglia (SOG) of larvae during active exploratory behavior.

29 ns to produce a male-specific, goal-oriented exploratory behavior.

30 enough to keep up with the eye during normal exploratory behavior.

31 ty, suppressed feeding, and depressed social exploratory behavior.

32 irregular intervals, producing probabilistic exploratory behaviors.

33 ble neural networks activated during spatial exploratory behaviors.

34 n and the regulation of goal-directed versus exploratory behaviors.

35 nd CA1-CA3 regions of the hippocampus during exploratory behaviors.

36 odalities is an active process that involves exploratory behaviors.

37 al theta and nasal respiratory rhythm during exploratory behaviors.

38 ing to a role in balancing goal-directed and exploratory behaviors.

39 ents, animals perform complex yet structured exploratory behaviors.

40 c variants of foraging (for) to affect adult exploratory behavior, a phenotype that is critical for f

41 In this paper, we report exploratory behavior abnormalities that appear well befo

42 Participants with AUD showed reduced exploratory behavior across gain and loss environments,

43 cies that are likely to occur during natural exploratory behavior, activation of fast-spiking interne

44 Distinctive tip cell exploratory behavior, adhesion, and basement membrane cl

45 al and organizational functions to stimulate exploratory behavior and acts downstream of the gonadal

46 x modulate sensory responses based on global exploratory behavior and arousal state, but their functi

47 rleukin (IL)-2 is a cytokine that influences exploratory behavior and central dopamine activity in ro

48 ish become immobile ('freeze'), show reduced exploratory behavior and do not habituate to this stress

49 ostnatal ablation of these neurons increased exploratory behavior and enhanced responses to cocaine.

50 Female presence during the PEI delayed exploratory behavior and facilitated vocalization and er

51 he NAcSh directly influences novelty-seeking exploratory behavior and facilitates self-administration

52 e improved Abeta-associated hyperactivity in exploratory behavior and hypoactivity in QW and expanded

53 of the zebrafish epithalamus causes reduced exploratory behavior and increased cortisol levels, indi

54 es correlated with pain-related decreases in exploratory behavior and increased expression of nocicep

55 ving premotor signals that are important for exploratory behavior and learning.

56 mTORC2-AKT assembly occurs within minutes of exploratory behavior and localizes to sparse synapses th

57 n addition, we noted sex-specific effects on exploratory behavior and long-term hippocampal memory in

58 elop a discrete choice model that allows for exploratory behavior and multiple stages of decision mak

59 hree reinstatement modalities, while sparing exploratory behavior and natural reward seeking, making

60 uency and the occurrence of both stereotyped exploratory behavior and novelty-related memory deficits

61 rning and memory functions that occur during exploratory behavior and rapid eye movement sleep.

62 Maternal B-GOS supplementation increased exploratory behavior and reduced expression of hippocamp

63 Dynamic calcium activity was greater in exploratory behavior and REM sleep than in quiet wakeful

64 In exploratory behavior and REM sleep, Abeta impaired hippo

65 s in the freely behaving animal, we examined exploratory behavior and short-term memory in control an

66 t fashion, driving neuronal hyperactivity in exploratory behavior and slow wave sleep (SWS), yet supp

67 memory deficits and sex-specific effects in exploratory behavior and spatial hippocampal memory, whi

68 use it is sensitive to various parameters of exploratory behavior and spatial memory performance.

69 potential roles of resonance during natural exploratory behavior and specifically suggest that reson

70 dividuals with the highest travel frequency, exploratory behavior and structural centrality.

71 of neural circuits involved specifically in exploratory behavior and suggest that some of the psycho

72 Behavioral tests identified changes in exploratory behavior and turning bias (lateralization),

73 a few hours of treatment, the larvae ceased exploratory behavior and were unresponsive to external s

74 ared to chow on anxiety, novelty-seeking and exploratory behaviors and also on acetylcholine (ACh) ne

75 ction in the frontal cortex regulates innate exploratory behaviors and causally promotes exploratory

76 rs of medial entorhinal cortex during active exploratory behaviors and overnight sleep.

77 battery of diverse learning tasks as well as exploratory behaviors and stress reactivity.

78 imals with rmTBI 3 days apart showed reduced exploratory behaviors and subtle spatial learning memory

79 xploration, the interaction between discrete exploratory behaviors and the specific, immediate and pe

80 ing changes in stress-related behavior (i.e. exploratory behavior) and whole-brain GABA(A) receptor s

81 the degree to which they elicit approach, or exploratory behavior, and avoidance, or anxiety-related

82 e life span, enhances locomotor activity and exploratory behavior, and diminishes breathing variabili

83 These effects on light/dark box exploratory behaviors are associated with reduced anxiet

84 expression both when evaluated shortly after exploratory behavior as well as after longer time interv

85 Poly I:C-exposed dams favor non-pup-directed exploratory behavior at the expense of pup retrieval.

86 ng for extended periods and increasing their exploratory behavior at the midline, suggesting that Sem

87 first showed sexual dimorphism in social and exploratory behaviors between the mouse strains.

88 POR and PER is necessary for context-guided exploratory behavior but not for associating fear with c

89 ect on rat spatial maze learning, memory, or exploratory behavior, but eliminated both early- and lat

90 oustic exploration was correlated with other exploratory behaviors, but not with emergence latency.

91 gests that it plays a role in the control of exploratory behaviors by coordinating the activities of

92 nce that long-range temporal correlations in exploratory behavior can predict perceptual performance,

93 oint to this problem is the observation that exploratory behaviors can rapidly cause selective hippoc

94 witch of migration mode that promotes T-cell exploratory behavior, characterized by partial decelerat

95 The exploratory behavior, chelatable Zn content, activities

96 ificial intelligence (AI)-driven decoding of exploratory behaviors, CLOSER proposes the standardizati

97 nce probability, Px = .92) and had increased exploratory behavior compared with healthy controls (mea

98 The results suggest that, unlike self-exploratory behavior, contingent facial and body movemen

99 provide delayed dendritic inhibition during exploratory behavior, contributing to the maintenance of

100 nucleus of the solitary tract), locomotor or exploratory behavior control and reward prediction (nucl

101 ncluding novelty-induced hyperlocomotion and exploratory behavior, defective motor control, and motor

102 However, active palpation and exploratory behaviors did result in the largest and most

103 ished the power of theta oscillations during exploratory behavior, disrupted spatial coding by place

104 Exploratory behaviors during learning determine what is

105 in long-lived species, resulting in greater exploratory behavior early in life followed by more rapi

106 Young animals engage in variable exploratory behaviors essential for the development of n

107 of spinal nociceptive neurons and changes in exploratory behavior evoked by capsaicin injection.

108 tion in the fly brain, changed the amount of exploratory behavior exhibited by sitter adults when the

109 variant developed obesity and reduced social exploratory behavior; female mice heterozygous for the s

110 imary focal site, and impaired locomotor and exploratory behavior for up to 1 month post-exposure.

111 To maximize lifetime fitness, the exploratory behavior has to be flexible, but which behav

112 , but the quiescent periods between bouts of exploratory behaviors have not been well studied.

113 ulthood did not affect rover or sitter adult exploratory behavior; however, early nutritional adversi

114 sed hyperactivity, anxiety, novelty-seeking, exploratory behavior, impulsivity, and alcohol-seeking,

115 We investigate the factors guiding exploratory behavior in a dataset consisting of 195,333

116 this work shows that rats adapt their active exploratory behavior in a homeostatic attempt to preserv

117 more, we show that M5 receptors can modulate exploratory behavior in a sex-specific manner, without a

118 recent article, Sommer-Trembo et al. linked exploratory behavior in African cichlids to a SNP in the

119 g in miscoordination of swimming and reduced exploratory behavior in aged adults.

120 ve habituation (OSH) can be observed both in exploratory behavior in an open arena and in a stereotyp

121 d dopamine activity, that dopamine modulates exploratory behavior in animals, and that Parkinson's di

122 Moreover, these mice are deficient in exploratory behavior in both open-field and novel-object

123 CRFR1 knockout mice displayed an increased exploratory behavior in both the Elevated Plus-maze (EPM

124 While computational models can explain exploratory behavior in constrained laboratory tasks, it

125 We also observed signatures of exploratory behavior in eye movements, such as quicker,

126 Hypoxic exposure rapidly induced exploratory behavior in larvae and arrested the cell cyc

127 ilone D also partially reversed the impaired exploratory behavior in Mecp2(308/y) male mice.

128 namics across the striatum during self-paced exploratory behavior in mice.

129 t the model captures the major components of exploratory behavior in multiple timescales: single excu

130 ion of D(3)R from dopamine neurons increased exploratory behavior in novel environments and enhanced

131 ent modification of these connections during exploratory behavior in rats by optogenetically inhibiti

132 To modify exploratory behavior in response to male pheromone, adul

133 Although exploratory behavior in rodents has been widely studied,

134 ed sugar preference and intake and decreased exploratory behavior in subordinate, but not intermitten

135 been previously implicated in regulation of exploratory behavior in the absence of male-produced sig

136 levels of anxiety-like behaviors and reduced exploratory behavior in the elevated plus maze and light

137 eptors in the BNSTAL had opposing effects on exploratory behavior in the elevated plus-maze, somatic

138 dopaminergic circuitry to mediate changes in exploratory behavior in the hungry state.

139 mice also fail to develop adult patterns of exploratory behavior in the open field and show deficits

140 We modulated exploratory behavior in this task by optically stimulati

141 back loop underlies previously characterized exploratory behaviors in C. elegans.

142 d behavioral sequences and notably decreased exploratory behaviors in DN mice.

143 on in the nucleus accumbens and accompanying exploratory behaviors in male and female mice.

144 lin acetylation in brain and stimulate mouse exploratory behaviors in novel, but not familiar environ

145 (HSD), and specifically evaluated social and exploratory behaviors in their control-fed offspring.

146 fundamental and widespread behavioral trait, exploratory behavior, in one of the largest adaptive rad

147 sults show that the non-specific increase in exploratory behavior induced by replacing corticosteroid

148 Effective exploratory behaviors involve continuous updating of sen

149 ogical and genomic information, we show that exploratory behavior is linked to macrohabitat niche ada

150 However, when mates and food coincide, male exploratory behavior is suppressed and males are retaine

151 essed, but odr-10 expression remains low and exploratory behavior is suppressed less than in starved

152 Octopuses show exploratory behavior, learning, and retention of spatial

153 Postweaning isolation reduced exploratory behavior, maternal LG, and oxytocin receptor

154 ize that the cognitive mechanisms underlying exploratory behavior may differ across individuals depen

155 se findings reveal how variability caused by exploratory behavior might help to mitigate other undesi

156 ctory fear conditioning causes a decrease in exploratory behavior, mimicking odor-evoked fear memory

157 -specific alterations in olfactory function, exploratory behavior, motor movement or anxiety-related

158 throughout platform capable of measuring the exploratory behavior of hundreds of individual flies sim

159 of behavior in the open field; however, the exploratory behavior of males is significantly more vari

160 m plays a quintessentially important role in exploratory behavior of mice and other nocturnal rodents

161 tigated this phenomenon in rats during their exploratory behavior of rearing.

162 Sniffing and whisking typify the exploratory behavior of rodents.

163 is process impacts the development of normal exploratory behaviors of adult mice.

164 d flavored solutions, metabolic indices, and exploratory behavior on the elevated plus maze in male C

165 ptors are extremely hypoactive in a test for exploratory behavior (open-field test), showing markedly

166 benula inhibited social play, but not social exploratory behavior or locomotor activity.

167 ubsets of aged animals displayed stereotyped exploratory behavior or memory deficits.

168 There were no differences in exploratory behavior or motor function, fasting lipid le

169 (+/R455H) mice were not impaired in tasks of exploratory behavior or procedural motor learning.

170 cocaine SA were not caused by differences in exploratory behavior or sampling because these behaviors

171 al choline supplementation causes changes in exploratory behaviors over the lifespan and preserves so

172 creased maternal clinging (P =.02), enhanced exploratory behavior (P =.005), and increased food consu

173 h other or to AUD subjects, BED had enhanced exploratory behaviors particularly in the loss domain.

174 alter the excitatory/inhibitory balance and exploratory behaviors, possibly as a result of the incre

175 s, cannabimimetic effects, novel environment exploratory behavior, pre-pulse inhibition, conditioned

176 s, cannabimimetic effects, novel environment exploratory behavior, pre-pulse inhibition, conditioned

177 owever, Sca1 null mice demonstrate decreased exploratory behavior, pronounced deficits in the spatial

178 During exploratory behavior, rats brush and tap their whiskers

179 k linkage, compartmentation, redundancy, and exploratory behavior reduce the interdependence of compo

180 C. elegans mate searching is a male-specific exploratory behavior regulated by two competing needs: f

181 y to stand up on their hind limbs: a typical exploratory behavior seen in healthy mice.

182 Neural circuits mediating exploratory behavior should therefore integrate experien

183 A detailed analysis of exploratory behavior showed that both the ALDO- and RU36

184 ads to abnormality in locomotor activity and exploratory behavior, signs of anxiety and hypomyelinati

185 neonatal lesion and investigated effects on exploratory behavior, spatial learning and anxiety in mi

186 at degrades performance and reward-dependent exploratory behavior that improves performance.

187 n learning a water maze task and in vertical exploratory behavior that increased with age and were se

188 contrast, during whisker movements and other exploratory behaviors, the system is primed to detect th

189 amic grayscale objects that relies on innate exploratory behavior to assess color and contrast vision

190 its caudal segment helps control foraging or exploratory behavior to obtain or avoid specific goal ob

191 Rodents whisk and sniff during exploratory behavior to sample odorants and surfaces.

192 and in what ways children with ASD generate exploratory behaviors to toys in natural, unconstrained

193 neurons, interneurons, and motor neurons in exploratory behaviors under different conditions.

194 On P28, marked reduction in exploratory behavior was noted after seizures only in th

195 to investigate the cortical contributions to exploratory behavior, we analyzed single-neuron activity

196 ate the cognitive and neural determinants of exploratory behaviors, we manipulated the control that h

197 Working memory and exploratory behavior were higher for SHR at both testing

198 The first differences in exploratory behaviors were evident by 4 weeks of age, wh

199 osterone, but spatial learning abilities and exploratory behaviors were severely compromised compared

200 early life displayed increasing boldness and exploratory behavior when foraging outdoors, demonstrati

201 by-trial basis, lower firing rates predicted exploratory behavior, whereas higher rates predicted an

202 produced ultrasonic vocalization and reduced exploratory behavior while increasing the latency to inv

203 ion of the DRN(DAT)-BNST projection promoted exploratory behavior, while the DRN(DAT)-BLP projection

204 n the cerebral cortex in males to coordinate exploratory behaviors with whole-body metabolic state.

205 rats exhibited deficits in adaptability and exploratory behavior, with aberrant outcome-driven value

206 oraging functions such as working memory and exploratory behaviors, with increased pain sensitivity,

207 bited varying syndromes in defensiveness and exploratory behaviors, yet further research is necessary