戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 mory, and a progressive and dramatic loss of ultrasonic vocalizations.
5 social group that uses an array of sonic and ultrasonic vocalizations.
6 onal state by emitting two distinct types of ultrasonic vocalizations.
7 ressed blunted emission of isolation-induced ultrasonic vocalizations.
8 ts without altering the number or pattern of 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 eduction of Foxp1 correlates with defects in ultrasonic vocalizations.
13  littermates, produce an increased number of ultrasonic vocalizations.
14 responsiveness of auditory cortex neurons to ultrasonic vocalizations.
15 fferences were evident in footshock-elicited ultrasonic vocalizations.
16 ed excitatory and heterogeneous responses to ultrasonic vocalizations.
17 al separation-induced anxiety as measured by ultrasonic vocalizations.
18  rats, including affective responses such as ultrasonic vocalizations.
19 freezing which emerges at 2 weeks of age and ultrasonic vocalizations.
20                                              Ultrasonic vocalizations (22-kHz) were positively correl
21 ate exchanges.(2) Rodents frequently utilize ultrasonic vocalizations,(3)(,)(4)(,)(5) which, due to r
22 ure to bright light, they turn away and emit ultrasonic vocalizations, a cue to their parents to retu
23 degree of spontaneous locomotor activity and ultrasonic vocalizations, activity and ultrasounding in
24 ns blocked stress-induced freezing behavior, ultrasonic vocalizations, adrenocortical activation, and
25 al analysis, including home-cage monitoring, ultrasonic vocalization analysis, and precise gait asses
26                                              Ultrasonic vocalization and homing behavioral experiment
27 000 pmol), a mixed 5-HT(2) agonist, produced ultrasonic vocalization and reduced exploratory behavior
28 tformin rescued increased number of calls in ultrasonic vocalization and repetitive behavior in Fmr1(
29 ural repertoire that consists of attraction, ultrasonic vocalization and urinary scent marking, and a
30 D rat offspring displayed a reduction in pup ultrasonic vocalizations and a pronounced deficit in soc
31 rthritis pain-related behaviors (audible and ultrasonic vocalizations and hindlimb withdrawal reflexe
32 irments in testosterone's ability to restore ultrasonic vocalizations and scent marking, assessed wit
33 ated the expression of conditional freezing, ultrasonic vocalization, and defecation.
34 e behavior, altered social behavior, altered ultrasonic vocalization, and enhanced tone-cued and cont
35            Repetitive self-grooming, reduced ultrasonic vocalizations, and deficits in reversal of wa
36 unction and plasticity, learning and memory, ultrasonic vocalizations, and motor function; it also no
37       Transoral endoscopy, videofluoroscopy, ultrasonic vocalizations, and whole-body plethysmography
38 xhibiting resistance to change and decreased ultrasonic vocalization as well as abnormal levels of se
39 ped, repetitive behavior, and impairments in ultrasonic vocalization, as well as some associated feat
40   The three "hits" had cumulative effects on ultrasonic vocalizations at postnatal day 3.
41             KCC2(E/+) mice also had abnormal ultrasonic vocalizations at postnatal days 10 to 12 and
42 d robust deficits in social interactions and ultrasonic vocalizations, but displayed normal olfaction
43  neurons further increased emission of these ultrasonic vocalizations, but not milk ingestion.
44         Hence, we subjected rats to aversive ultrasonic vocalization calls emitted on one end of a li
45  a marked decrease in separation-induced pup ultrasonic vocalization calls, hyperactivity, repetitive
46 a finch, provides strong evidence that mouse ultrasonic vocalizations do not cluster as is commonly b
47                            Nor did they show ultrasonic vocalizations during behavioral tests with re
48 y receptive females and produced ~ 50% fewer ultrasonic vocalizations during mating.
49                                        While ultrasonic vocalizations elicited a rather weak populati
50 gh laboratory studies revealed that rodents' ultrasonic vocalizations encode rich information like em
51 ted submissive behavior (freezing and 22-kHz ultrasonic vocalizations) had higher levels of CCK in th
52 hat juvenile rats emit short, high-frequency ultrasonic vocalizations (high USVs, approximately 55 kH
53 thalamus (VMN) depress lordosis but increase ultrasonic vocalization in female hamsters.
54  that SRPX2 reduction impairs development of ultrasonic vocalization in mice.
55 mental delay but a significant alteration in ultrasonic vocalization in response to such separation.
56 erience during development to produce normal ultrasonic vocalizations in adulthood.
57 ocial interaction tests), and communication (ultrasonic vocalizations in pups).
58  interaction and maternal separation-induced ultrasonic vocalizations in pups.
59 notype differences were found on measures of ultrasonic vocalizations in social contexts, and no ster
60               Air puff stimuli that produced ultrasonic vocalizations induced Fos-LI to a more limite
61 T) mice were impaired in social interaction, ultrasonic vocalization, memory-based behavioral alterna
62  interaction and acoustic characteristics of ultrasonic vocalizations of C9BAC mice subjected to repe
63         An alternative mechanism is found in ultrasonic vocalizations of rodents, which are establish
64 seizure-like activity, but not the increased ultrasonic vocalizations or motor deficits, is rescued i
65                     In the isolation-induced ultrasonic vocalization paradigm, 5HT1B knockout pups vo
66 ings, MPO implants alone completely restored ultrasonic vocalizations, partially restored urine marki
67 ior, fragmented social behavior, and altered ultrasonic vocalization patterns at 6-12 weeks of age.
68 ulating IL-6 two-fold, alters post-pubescent ultrasonic vocalization patterns, reduces sociability, a
69 s, including tests for social abnormalities, ultrasonic vocalizations, perseverative and stereotypic
70 MeO-DMT also substantially suppresses social ultrasonic vocalizations produced during mating behavior
71 affective bias test [8], to show that 50 kHz ultrasonic vocalizations provide a quantifiable and grad
72                                  Analysis of ultrasonic vocalizations revealed distress calls from Ta
73 ges in the social context for the display of ultrasonic vocalizations, scent marking, aggression, and
74                     Mice, for instance, emit ultrasonic vocalizations, signals above the range of hum
75 tab gene resulted in deficits in the flow of ultrasonic vocalizations similar to speech deficits of h
76  elevated plus maze, and an air puff-induced ultrasonic vocalization test.
77 withdrawal test and acoustic startle-induced ultrasonic vocalization test.
78 pairment, premature death, and an absence of ultrasonic vocalizations that are elicited when pups are
79 nt, Norway rat (Rattus norvegicus) pups emit ultrasonic vocalizations that can elicit maternal search
80 ctory investigation, and emission of complex ultrasonic vocalizations towards male and female conspec
81 eriorbital electromyography (EMG) and 22 kHz ultrasonic vocalization (USV) activities were measured c
82 y concurrently assessing freezing and 22 kHz ultrasonic vocalization (USV) as dependent measures of f
83  both 10 sec duration) and two different rat ultrasonic vocalization (USV) conditional stimuli (10 se
84 pair pavlovian fear conditioning to a 22 kHz ultrasonic vocalization (USV) cue.
85          Furthermore, we identified impaired ultrasonic vocalization (USV) in a severe SMA mouse mode
86 ion, and bout structure of isolation-induced ultrasonic vocalization (USV) of infant rats (Rattus nor
87                                          The ultrasonic vocalization (USV) response of the isolated i
88 estigated the influence of social rearing on ultrasonic vocalization (USV) responses of 11- to 12-day
89 onditioned fear, including analgesia, 22 kHz ultrasonic vocalization (USV), defecation, and freezing.
90 r changes in acoustic startle reactivity and ultrasonic vocalization (USV).
91 two different behaviors [freezing and 22 kHz ultrasonic vocalization (USV)] elicited under three cond
92 ction in TSC2 heterozygous mice, we recorded ultrasonic vocalizations (USV) and found that although b
93                                        These ultrasonic vocalizations (USV) are typically described a
94 ere seen in the emission of prosocial 50-kHz ultrasonic vocalizations (USV) paralleled by a lack of s
95                                 By recording ultrasonic vocalizations (USV) produced by adult male mi
96                                              Ultrasonic vocalizations (USV) were measured at PND12 du
97                   Throughout life, rats emit ultrasonic vocalizations (USV) when confronted with an a
98 ed two distinct vocal modes: soft, variable, ultrasonic vocalizations (USVs) ancestral to rodents, us
99                      Rodents communicate via ultrasonic vocalizations (USVs) and newborn pups emit di
100                                       Rodent ultrasonic vocalizations (USVs) are a vital tool for lin
101                           Here, we study how ultrasonic vocalizations (USVs) are represented in the b
102 acterized their receptive fields using mouse ultrasonic vocalizations (USVs) as a natural and etholog
103  ability to attenuate the increase in 22-kHz ultrasonic vocalizations (USVs) associated with alcohol
104    Adult rats emit increased rates of 50-kHz ultrasonic vocalizations (USVs) before receiving social
105 inal (PR) cortex impair fear conditioning to ultrasonic vocalizations (USVs) but have no effect on co
106                                        Mouse ultrasonic vocalizations (USVs) contain predictable sequ
107                                Rat pups emit ultrasonic vocalizations (USVs) during cold challenge.
108        Adult male mice produce high rates of ultrasonic vocalizations (USVs) during courtship interac
109                            Male mice produce ultrasonic vocalizations (USVs) during courtship to faci
110 oximal orientation to a pup that is emitting ultrasonic vocalizations (USVs) far more than do virgin
111                                              Ultrasonic vocalizations (USVs) fulfill an important rol
112 uctal gray (PAG) that gate the production of ultrasonic vocalizations (USVs) in mice (i.e. PAG-USV ne
113 rain neurons important for the production of ultrasonic vocalizations (USVs) in mice.
114                It has been proposed that all ultrasonic vocalizations (USVs) in young rats are by-pro
115 ave hypothesized that, in adult rats, 50-kHz ultrasonic vocalizations (USVs) index a state characteri
116                                    Rats emit ultrasonic vocalizations (USVs) that are thought to serv
117                                    Mice emit ultrasonic vocalizations (USVs) that communicate sociall
118                                              Ultrasonic vocalizations (USVs) were altered in both sex
119                                Rat pups emit ultrasonic vocalizations (USVs) when isolated in a novel
120 istinguishable by the presence or absence of ultrasonic vocalizations (USVs)(2-4), respectively.
121  triggers male mice to emit innate courtship ultrasonic vocalizations (USVs)(4,5).
122 reased rates of social investigation, social ultrasonic vocalizations (USVs), and mounting during sam
123  (DA) systems modulate kappa opioid-mediated ultrasonic vocalizations (USVs), antinociception, and lo
124                                         Like ultrasonic vocalizations (USVs), DA signals were modulat
125                                              Ultrasonic vocalizations (USVs), freezing, and corticost
126 Whereas both Peromyscus and Mus pups produce ultrasonic vocalizations (USVs), Peromyscus pups also pr
127 mber of spectro-temporal measures to compare ultrasonic vocalizations (USVs), which limits the abilit
128 iving vocal cord closure and eliciting mouse ultrasonic vocalizations (USVs).
129 l communication through a rich repertoire of ultrasonic vocalizations (USVs).
130       Context- and cue-elicited freezing and ultrasonic vocalizations (USVs; 22 kHz) were measured af
131                          In addition, 22-kHz ultrasonic vocalizations were utilized to measure negati
132  and social behavior (social interaction and ultrasonic vocalizations) were examined in adult male Li
133 owed alterations in acoustical parameters of ultrasonic vocalizations, which also differed in functio
134 ouch is associated with an increased rate of ultrasonic vocalizations, which are emitted at the whisk
135                      We found an increase in ultrasonic vocalizations with simpler morphologies produ
136 bumetanide and accompanied by alterations in ultrasonic vocalization without changes in homing behavi

 
Page Top