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1 ygdalar complex (BLA) evoked freezing and/or ultrasonic vocalization.
2 ivity bursts followed by freezing and 22-kHz ultrasonic vocalization.
3 ed for high, low, and random rates of infant ultrasonic vocalization.
4 littermates, produce an increased number of ultrasonic vocalizations.
5 responsiveness of auditory cortex neurons to ultrasonic vocalizations.
6 ed excitatory and heterogeneous responses to ultrasonic vocalizations.
7 al separation-induced anxiety as measured by ultrasonic vocalizations.
8 rats, including affective responses such as ultrasonic vocalizations.
9 increased neuronal responses of PyrNs to pup ultrasonic vocalizations.
10 ffective for high-frequency stimuli, such as ultrasonic vocalizations.
11 In mice, these displays include ultrasonic vocalizations.
12 freezing which emerges at 2 weeks of age and ultrasonic vocalizations.
13 eduction of Foxp1 correlates with defects in ultrasonic vocalizations.
15 degree of spontaneous locomotor activity and ultrasonic vocalizations, activity and ultrasounding in
16 ns blocked stress-induced freezing behavior, ultrasonic vocalizations, adrenocortical activation, and
17 000 pmol), a mixed 5-HT(2) agonist, produced ultrasonic vocalization and reduced exploratory behavior
18 rthritis pain-related behaviors (audible and ultrasonic vocalizations and hindlimb withdrawal reflexe
19 irments in testosterone's ability to restore ultrasonic vocalizations and scent marking, assessed wit
21 e behavior, altered social behavior, altered ultrasonic vocalization, and enhanced tone-cued and cont
23 xhibiting resistance to change and decreased ultrasonic vocalization as well as abnormal levels of se
24 ped, repetitive behavior, and impairments in ultrasonic vocalization, as well as some associated feat
26 d robust deficits in social interactions and ultrasonic vocalizations, but displayed normal olfaction
29 ted submissive behavior (freezing and 22-kHz ultrasonic vocalizations) had higher levels of CCK in th
30 hat juvenile rats emit short, high-frequency ultrasonic vocalizations (high USVs, approximately 55 kH
33 mental delay but a significant alteration in ultrasonic vocalization in response to such separation.
36 notype differences were found on measures of ultrasonic vocalizations in social contexts, and no ster
38 T) mice were impaired in social interaction, ultrasonic vocalization, memory-based behavioral alterna
39 seizure-like activity, but not the increased ultrasonic vocalizations or motor deficits, is rescued i
41 ings, MPO implants alone completely restored ultrasonic vocalizations, partially restored urine marki
42 s, including tests for social abnormalities, ultrasonic vocalizations, perseverative and stereotypic
43 ges in the social context for the display of ultrasonic vocalizations, scent marking, aggression, and
46 pairment, premature death, and an absence of ultrasonic vocalizations that are elicited when pups are
47 nt, Norway rat (Rattus norvegicus) pups emit ultrasonic vocalizations that can elicit maternal search
48 ctory investigation, and emission of complex ultrasonic vocalizations towards male and female conspec
49 eriorbital electromyography (EMG) and 22 kHz ultrasonic vocalization (USV) activities were measured c
50 y concurrently assessing freezing and 22 kHz ultrasonic vocalization (USV) as dependent measures of f
51 both 10 sec duration) and two different rat ultrasonic vocalization (USV) conditional stimuli (10 se
53 ion, and bout structure of isolation-induced ultrasonic vocalization (USV) of infant rats (Rattus nor
55 estigated the influence of social rearing on ultrasonic vocalization (USV) responses of 11- to 12-day
56 onditioned fear, including analgesia, 22 kHz ultrasonic vocalization (USV), defecation, and freezing.
58 two different behaviors [freezing and 22 kHz ultrasonic vocalization (USV)] elicited under three cond
59 ction in TSC2 heterozygous mice, we recorded ultrasonic vocalizations (USV) and found that although b
60 ere seen in the emission of prosocial 50-kHz ultrasonic vocalizations (USV) paralleled by a lack of s
65 ability to attenuate the increase in 22-kHz ultrasonic vocalizations (USVs) associated with alcohol
66 Adult rats emit increased rates of 50-kHz ultrasonic vocalizations (USVs) before receiving social
67 inal (PR) cortex impair fear conditioning to ultrasonic vocalizations (USVs) but have no effect on co
69 oximal orientation to a pup that is emitting ultrasonic vocalizations (USVs) far more than do virgin
71 ave hypothesized that, in adult rats, 50-kHz ultrasonic vocalizations (USVs) index a state characteri
74 (DA) systems modulate kappa opioid-mediated ultrasonic vocalizations (USVs), antinociception, and lo
77 mber of spectro-temporal measures to compare ultrasonic vocalizations (USVs), which limits the abilit
80 ouch is associated with an increased rate of ultrasonic vocalizations, which are emitted at the whisk
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