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1  chronic social defeat stress-induced social avoidance behavior.
2 havior and it suppresses C. elegans pathogen avoidance behavior.
3 ve people less incentive to engage in public avoidance behavior.
4 ore odor indicate it to be required for full avoidance behavior.
5 he superior colliculus of rats during active avoidance behavior.
6 ted in activation of AVA neurons, evoking an avoidance behavior.
7 tor NSAID risk communication, and NSAID risk-avoidance behavior.
8 for larval nociception, is required for this avoidance behavior.
9 iatric disorders involving pathological harm avoidance behavior.
10  also reduced its ability to direct nematode avoidance behavior.
11 ound in the open field test, which maximizes avoidance behavior.
12 tive, thermoregulatory, social, and predator-avoidance behavior.
13 P-BM5 infection on learning and retention of avoidance behavior.
14 nuated nicotine-dependent changes in passive avoidance behavior.
15 lterations of neuronal structure and passive avoidance behavior.
16 ch as fear, aggression, and envy and lead to avoidance behavior.
17 nor did it prevent the persistence of social avoidance behavior.
18 , but had no effect on stress-induced social avoidance behavior.
19 sponses to cooling and are required for cool avoidance behavior.
20 t of the basal ganglia fully controls active avoidance behavior.
21 bens (NAcc) is necessary for signaled active avoidance behavior.
22 voidance conflict, regardless of approach or avoidance behavior.
23 but not in the adjacent NAcc core, disrupted avoidance behavior.
24 genetically activating these neurons induces avoidance behavior.
25 ver several seconds to reach a threshold for avoidance behavior.
26 rgence of cold hypersensitivity, and passive avoidance behavior.
27 lient mice, which was correlated with social avoidance behavior.
28 specific encounter rate to history-dependent avoidance behavior.
29  effects, reducing freezing and facilitating avoidance behavior.
30 imation of prospective risk and lead to risk avoidance behavior.
31  conditions that affect emotion and approach-avoidance behavior.
32 ropriate cues leads to a pernicious cycle of avoidance behaviors.
33 nserved innate immune responses and pathogen avoidance behaviors.
34 urons that are specialized for attractive or avoidance behaviors.
35 ngagement with rewarding stimuli and reduces avoidance behaviors.
36 ic substances and elicits food acceptance or avoidance behaviors.
37 ent in a subset of interneurons that control avoidance behaviors.
38  known about the genetics of social approach-avoidance behaviors.
39 netic excitation evokes rapid protective and avoidance behaviors.
40 gan, an olfactory structure mediating innate avoidance behaviors.
41 ically diverse kairomones can elicit similar avoidance behaviors.
42 engagement with rewarding stimuli and reduce avoidance behaviors.
43 retrospenial cortex likely to be involved in avoidance behaviors.
44 ive urges to perform irrational or excessive avoidance behaviors.
45 ns indicates that they are necessary for CO2-avoidance behavior [5].
46 nificantly negatively correlated with social avoidance behavior, a key behavioral abnormality induced
47 tible BM chimeras exhibited increased social avoidance behavior after exposure to either subthreshold
48                                              Avoidance behaviors after predator stress were highly de
49  analogous behavior by adapting both passive avoidance behavior and behavioral inhibition to threat l
50 use NCM lesions spared both successful noise-avoidance behavior and birds' auditory discrimination ab
51 nsory and central circuitry regulating light avoidance behavior and clock entrainment.
52       Behavioral results identified elevated avoidance behavior and decreased short-term memory at ei
53 BCs of the rd1 mouse reinstated innate light-avoidance behavior and enabled mice to distinguish betwe
54 id (50%), naked mole-rats showed significant avoidance behavior and increased Fos labeling in the nuc
55 campus with patients showing reduced passive avoidance behavior and inhibition across all threat leve
56 experiments, we showed that herbivores' risk-avoidance behavior and plants' antiherbivore defenses in
57      We found that IkappaKca enhanced social avoidance behavior and promoted thin spine formation.
58 fic place-cell pattern underlying inhibitory avoidance behavior and provides strong evidence for the
59 is expressed in neural circuits that mediate avoidance behaviors and is required for glutamate-gated
60 -to-PBL projection induced robust escape and avoidance behaviors and stress calls, whereas optogeneti
61 ga3, Gnao1) or by surgical axotomy abolished avoidance behaviors and/or cellular Ca(2+) responses to
62 tient concerns with amnesia, depressed mood, avoidance behaviors, and a prolonged recovery period.
63 psychological distress, IBS-related fear and avoidance behaviors, and IBS-related disability were inv
64 psychological distress, IBS-related fear and avoidance behaviors, and IBS-related disability, with th
65 t between neural pathways for preference and avoidance behaviors, and it suggests that hybrids might
66 ult eclosion, host fruit odor preference and avoidance behaviors, and mating site fidelity) cascade t
67                                        Thus, avoidance behavior appears hardwired into the olfactory
68 and long-term habituation (LTH) of olfactory avoidance behavior are believed to arise from the select
69 esses that support free-operant instrumental avoidance behavior are still unknown.
70 chain dynamics will depend on which predator-avoidance behaviors are allowed to occur and measured.
71 e NAccSh was just as effective at disrupting avoidance behavior as bilateral NAccSh inactivations, su
72 m, SHR again displayed significantly reduced avoidance behavior as compared with both WKY and Wistar
73                                              Avoidance behavior-avoiding social situations for fear o
74 tically to detect low salient stimuli during avoidance behavior, but are redundant during detection o
75 ual access to neural networks of feeding and avoidance behavior, but their final effects are regulate
76       Odor hedonic valence controls approach-avoidance behaviors, but also modulates ongoing behavior
77       Further, collagen IX elicits a similar avoidance behavior by neural crest cells in vitro.
78                           Nonetheless, light avoidance behavior can be mediated in the absence of bra
79               PQ-treated worms have enhanced avoidance behavior compared to untreated ones, suggestin
80 strate that mechanisms underlying joining or avoidance behavior differ among species, as do types of
81 s) have been shown to reinforce instrumental avoidance behavior due to their ability to signal the ab
82 says, we show that AWC(OFF) is essential for avoidance behavior following noxious heat stimulation by
83                 By contrast, overtraining of avoidance behavior had no effect on patient performance.
84                                         Self-avoidance behavior has been shown to depend on cell-spec
85 ation of natural polymorphisms that modulate avoidance behavior has enabled an improved understanding
86                   Our finding of spontaneous avoidance behavior has striking similarities to the enha
87  of pain, which is hypothesized to result in avoidance behavior, has been described as an obstacle to
88                             The magnitude of avoidance behavior, however, was mediated by winter seve
89 ilitating trauma-related intrusive thoughts, avoidance behaviors, hyperarousal, as well as depressed
90 dual function of affecting both approach and avoidance behavior in a predator-prey predicted manner.
91 Aergic projections from mPFC to NAcc induces avoidance behavior in a real-time place preference task,
92  ascr#3 (asc-DeltaC9; C9) pheromone triggers avoidance behavior in adult hermaphrodites [3-7].
93 ing conditions, successfully reversed social avoidance behavior in adult socially isolated mice.
94 ay of deterrent natural products that induce avoidance behavior in biological adversaries.
95 activity leads to reduced SDS-induced social avoidance behavior in both WT and Tph2KI mice.
96 ptor (GR) homolog, mediates UV-light-induced avoidance behavior in C. elegans.
97 cies that result in a higher level of public avoidance behavior in equilibrium does not necessarily l
98 emands, both important issues given approach-avoidance behavior in humans is less tied to predation a
99      DMXB (0.5 mg/kg, i.p.) improved passive avoidance behavior in lesioned animals in a mecamylamine
100  pupillary light reflex and locomotory light avoidance behavior in mice lacking retinal photoreceptor
101      Clemastine successfully reversed social avoidance behavior in mice undergoing prolonged social i
102 ect effects; DMIEs) and by inducing predator-avoidance behavior in prey (trait-mediated indirect effe
103  a well learned, hippocampus-dependent place avoidance behavior in rats that requires cognitive contr
104 increased firing rates, bursting events, and avoidance behavior in susceptible mice were completely r
105 effects of electrolytic MT lesions on escape/avoidance behavior in the place escape avoidance paradig
106 uroendocrine signaling pathway that promotes avoidance behavior in the simple animal host Caenorhabdi
107 measure used to examine sensory approach and avoidance behavior in worms.
108 oned place aversion, whereas cocaine-induced avoidance behaviors in a runway operant paradigm were ab
109 al defeat, a model that induces long-lasting avoidance behaviors in a subset of mice responsive to se
110  in the ink secretion of sea hares and cause avoidance behaviors in neighboring conspecifics.
111 rences in these structures may contribute to avoidance behaviors in PG.
112 n Caenorhabditis elegans for a wide range of avoidance behaviors in response to chemical repellents,
113 annel mutation alters temporal filtering and avoidance behaviors initiated by ASH on similar timescal
114 g reconsolidation of fear memory transformed avoidance behavior into approach behavior in a virtual b
115 evious studies have demonstrated that escape/avoidance behavior is dependent on activity in the anter
116 erefore, a robust neural correlate of active avoidance behavior is found in the superior colliculus,
117                                    Engrained avoidance behavior is highly adaptive when it keeps away
118 n vivo and found that recovery of the visual avoidance behavior is inhibited by drugs that block cell
119                                         This avoidance behavior is stimulated by chemical cues from i
120 ination of social stimuli and affiliation or avoidance behavior is thought to guide social recognitio
121 he most part by innate traits rather than by avoidance behavior learned through disagreeable experien
122                                  Thus, while avoidance behaviors may prevent acute lethality, slow re
123 o disperse, or focusing on only one predator-avoidance behavior, may be underestimating TMIEs.
124 oustically cued, discriminative instrumental avoidance behavior of rabbits.
125      Here, we show robust olfactory-mediated avoidance behavior of zebrafish to cadaverine and relate
126 he lesions did not affect the acquisition of avoidance behavior or prevent the reduction of CRs in re
127 y control both reward-seeking and punishment-avoidance behaviors, presumably through its projections
128 a, a gustatory receptor normally involved in avoidance behaviors, receive input for both attractive a
129 ral NAccSh inactivations, suggesting learned avoidance behavior requires an intact BA-NAccSh circuit.
130 fear conditioning, representing approach and avoidance behaviors, respectively.
131 epressible motor effects (i.e., approach and avoidance behaviors) seen within the first hour after in
132  toward future disasters to more maladaptive avoidance behaviors, somatic symptoms, or medical proble
133          Prey often employ multiple predator-avoidance behaviors, such as dispersal or reduced foragi
134 ial therapeutic targets for the treatment of avoidance behavior symptomatic of anxiety disorders.
135           In mice, CO2 produces freezing and avoidance behavior that has been suggested to depend on
136            Xenopus tadpoles exhibit a visual avoidance behavior that improves with visual conditionin
137 onobese diabetic (NOD) mice induced a social avoidance behavior that was not observed in C57BL/6 mice
138                      OCD is characterized by avoidance behaviors that fail to extinguish, and DBS cou
139 y the PAG, such as the dorsal PAG generating avoidance behavior, the lateral PAG generating fight and
140 taxis, aggregation, locomotion, and pathogen avoidance behaviors through the activity of the NPR-1 ne
141 ose of V-PN and DC4-PN, which mediate innate avoidance behavior to carbon dioxide and acidity, respec
142   We then assayed a tectally-mediated visual avoidance behavior to evaluate behavioral impairment and
143 mission in which people can engage in public avoidance behavior to minimize the likelihood of acquiri
144 tremely complex, involving both approach and avoidance behaviors toward specific individuals.
145 sociation, modulate prosocial and inbreeding-avoidance behaviors toward specific potential siblings.
146 pes of two LC types closely resemble natural avoidance behaviors triggered by a visual loom.
147 t (normally attractive to flies) elicits the avoidance behavior typical of CO2.
148  of revaluation of an aversive reinforcer on avoidance behavior using pharmacological agents, thereby
149 re diminished and glr-1-dependent nose-touch avoidance behavior was defective in grld-1 mutants.
150 tput" centromedial amygdala nuclei mediating avoidance behavior was negatively correlated with moneta
151  during the extinction test, suggesting that avoidance behavior was sensitive to the current incentiv
152 ical paw withdrawal thresholds and in escape/avoidance behavior were detected as compared to the sham
153 of avoidance-directing MBONs and odor-driven avoidance behavior, whereas their inhibition enhances od
154  nematode Caenorhabditis elegans shows CO(2) avoidance behavior, which requires a pair of ciliated se
155 ays contribute critically to cocaine-induced avoidance behaviors, while also participating in recipro
156  However, food stimuli also tended to elicit avoidance behavior (withdrawal and avoidance turns) at c
157 . elegans--TOL-1--is required for a pathogen-avoidance behavior, yet how it promotes this behavior is

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