戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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.
14                                              Ultrasonic vocalizations (22-kHz) were positively correl
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
20 ated the expression of conditional freezing, ultrasonic vocalization, and defecation.
21 e behavior, altered social behavior, altered ultrasonic vocalization, and enhanced tone-cued and cont
22            Repetitive self-grooming, reduced ultrasonic vocalizations, and deficits in reversal of wa
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
25   The three "hits" had cumulative effects on ultrasonic vocalizations at postnatal day 3.
26 d robust deficits in social interactions and ultrasonic vocalizations, but displayed normal olfaction
27                            Nor did they show ultrasonic vocalizations during behavioral tests with re
28                                        While ultrasonic vocalizations elicited a rather weak populati
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
31 thalamus (VMN) depress lordosis but increase ultrasonic vocalization in female hamsters.
32  that SRPX2 reduction impairs development of ultrasonic vocalization in mice.
33 mental delay but a significant alteration in ultrasonic vocalization in response to such separation.
34 erience during development to produce normal ultrasonic vocalizations in adulthood.
35  interaction and maternal separation-induced ultrasonic vocalizations in pups.
36 notype differences were found on measures of ultrasonic vocalizations in social contexts, and no ster
37               Air puff stimuli that produced ultrasonic vocalizations induced Fos-LI to a more limite
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
40                     In the isolation-induced ultrasonic vocalization paradigm, 5HT1B knockout pups vo
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
44 withdrawal test and acoustic startle-induced ultrasonic vocalization test.
45  elevated plus maze, and an air puff-induced ultrasonic vocalization test.
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
52 pair pavlovian fear conditioning to a 22 kHz ultrasonic vocalization (USV) cue.
53 ion, and bout structure of isolation-induced ultrasonic vocalization (USV) of infant rats (Rattus nor
54                                          The ultrasonic vocalization (USV) response of the isolated i
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.
57 r changes in acoustic startle reactivity and ultrasonic vocalization (USV).
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
61                                 By recording ultrasonic vocalizations (USV) produced by adult male mi
62                   Throughout life, rats emit ultrasonic vocalizations (USV) when confronted with an a
63                      Rodents communicate via ultrasonic vocalizations (USVs) and newborn pups emit di
64                                       Rodent ultrasonic vocalizations (USVs) are a vital tool for lin
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
68                                Rat pups emit ultrasonic vocalizations (USVs) during cold challenge.
69 oximal orientation to a pup that is emitting ultrasonic vocalizations (USVs) far more than do virgin
70                It has been proposed that all ultrasonic vocalizations (USVs) in young rats are by-pro
71 ave hypothesized that, in adult rats, 50-kHz ultrasonic vocalizations (USVs) index a state characteri
72                                    Rats emit ultrasonic vocalizations (USVs) that are thought to serv
73                                Rat pups emit ultrasonic vocalizations (USVs) when isolated in a novel
74  (DA) systems modulate kappa opioid-mediated ultrasonic vocalizations (USVs), antinociception, and lo
75                                         Like ultrasonic vocalizations (USVs), DA signals were modulat
76                                              Ultrasonic vocalizations (USVs), freezing, and corticost
77 mber of spectro-temporal measures to compare ultrasonic vocalizations (USVs), which limits the abilit
78       Context- and cue-elicited freezing and ultrasonic vocalizations (USVs; 22 kHz) were measured af
79                          In addition, 22-kHz ultrasonic vocalizations were utilized to measure negati
80 ouch is associated with an increased rate of ultrasonic vocalizations, which are emitted at the whisk

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。