ライフサイエンスコーパス: exploratory behavior

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

2 production in the nucleus accumbens restores exploratory behavior.

3 disrupts somatosensory electrophysiology and exploratory behavior.

4 ced anxiety-related responses with increased exploratory behavior.

5 avoidance and immobility, while showing less exploratory behavior.

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

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

8 cy restricted to aged animals with preserved exploratory behavior.

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

10 period increased sitter but not rover adult exploratory behavior.

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

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

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

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

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

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

17 and were crucial for generating appropriate exploratory behavior.

18 units that were coactive during a particular exploratory behavior.

19 oming and eating and maximal activity during exploratory behavior.

20 their sensitivity to pheromones that inhibit exploratory behavior.

21 avior control column concerned with foraging/exploratory behavior.

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

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

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

25 ents, animals perform complex yet structured exploratory behaviors.

26 irregular intervals, producing probabilistic exploratory behaviors.

27 ble neural networks activated during spatial exploratory behaviors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 The exploratory behavior, chelatable Zn content, activities

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

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

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

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

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

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

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

70 Exploratory behaviors during learning determine what is

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

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

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

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

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

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

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

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

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

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

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

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

83 Although exploratory behavior in rodents has been widely studied,

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

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

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

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

88 We modulated exploratory behavior in this task by optically stimulati

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

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

91 Effective exploratory behaviors involve continuous updating of sen

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

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

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

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

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

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

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

99 Sniffing and whisking typify the exploratory behavior of rodents.

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

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

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

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

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

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

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

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

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

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

110 During exploratory behavior, rats brush and tap their whiskers

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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