ライフサイエンスコーパス: vocalization

1 to produce the expiratory drive required for vocalization.

2 on driven by acoustic characteristics of the vocalization.

3 essential biomechanical parameters used for vocalization.

4 control of which is necessary for generating vocalization.

5 nal premotor interneuronal output system for vocalization.

6 to gain access to the motoneurons generating vocalization.

7 d/or during the monkeys' motor production of vocalization.

8 d confirmed that inactivating Kdm5a disrupts vocalization.

9 a time window of -700 ms to -500 ms prior to vocalization.

10 dation, decreased grip strength, and loss of vocalization.

11 t is selective for behaviorally relevant pup vocalizations.

12 size scales with the characteristics of its vocalizations.

13 called a syrinx, for the production of their vocalizations.

14 ted emission of isolation-induced ultrasonic vocalizations.

15 asured with both synthetic tones and macaque vocalizations.

16 novel (species-atypical) individual-specific vocalizations.

17 altering the number or pattern of ultrasonic vocalizations.

18 of an acoustic feature that is ubiquitous in vocalizations.

19 control of the spectro-temporal structure of vocalizations.

20 amental element of music, speech, and animal vocalizations.

21 te with changes in the acoustic structure of vocalizations.

22 arity of tone combinations to harmonic human vocalizations.

23 ated with reported population differences in vocalizations.

24 nalyzing real-time generated echoes of their vocalizations.

25 raining for singing and other highly-skilled vocalizations.

26 discriminating and learning species-specific vocalizations.

27 ,3], yet we know little about other types of vocalizations.

28 ere evident in footshock-elicited ultrasonic vocalizations.

29 malities similar to those found in the mouse vocalizations.

30 ct sound types- clicks, chirps, whistles and vocalizations.

31 w the consistent trajectories observed in WT vocalizations.

32 oral features in speech and species-specific vocalizations.

33 euronal responses of PyrNs to pup ultrasonic vocalizations.

34 r high-frequency stimuli, such as ultrasonic vocalizations.

35 including human speech and nonhuman primate vocalizations.

36 sensory perceptions and motor production of vocalizations.

37 a decade, based on daily detections of their vocalizations.

38 y when attending to salient infant and adult vocalizations.

39 ly relevant sounds, such as species-specific vocalizations.

40 nformation storage and processing of learned vocalizations.

41 edial frontal (DMF) cortex appear to control vocalizations.

42 e from, the cultural transmission of learned vocalizations.

43 to the learned relationships between natural vocalizations.

44 to learn meaningful representations of whale vocalizations.

45 that is contingent on their early, immature vocalizations.

46 ally encode individual identity in mammalian vocalizations [12], this is the first example of this ph

47 ability to produce learned, species-specific vocalizations - a rare trait in the animal kingdom - req

48 o assess the degree of N1 suppression during vocalization, a putative measure of auditory predictive

49 t these recording sites during times of high vocalization activity raises significant concerns that c

50 ars tuned to the dominant frequency of their vocalizations, allowing discrimination from background n

51 y is greater during active echolocation than vocalization alone.

52 been barriers for most laboratories to adopt vocalization analysis.

53 Neuronal circuits that control vocalization and breathing overlap and rely on motor neu

54 Ultrasonic vocalization and homing behavioral experiments were carr

55 the brain might support the coupling between vocalization and jaw oscillations to generate syllable s

56 striatal and global decrease of Mef2c rescue vocalization and striatal spinogenesis defects of Foxp2-

57 oire that consists of attraction, ultrasonic vocalization and urinary scent marking, and also serves

58 ection of 5-HT2CR shRNA AAV vector decreased vocalizations and anxiety- and depression-like behaviors

59 fants gradually improve coordination between vocalizations and body movement through a process that m

60 they sever the link between nonhuman primate vocalizations and cognition.

61 ) target neurons activated by ultrasonic pup vocalizations and discover a functional synaptic network

62 The bat's adaptive control of sonar vocalizations and ear positioning occurs on a millisecon

63 produce highly specific effects in mouse pup vocalizations and establish the mouse as an attractive m

64 s, rivers, and oceans are filled with animal vocalizations and geological sounds.

65 s and compete with rivals by performing both vocalizations and hind limb gestural signals, called "fo

66 in infancy produced fewer isolation-induced vocalizations and in adulthood exhibited less anxiety-li

67 eceptor antagonist did not alter affiliative vocalizations and increased MDMA-induced social contact.

68 Perception of vocalizations and other behaviorally relevant sounds req

69 on Heschl's gyrus that process natural human vocalizations and pitch perturbations in the auditory fe

70 ngs overturn decades-old ideas about primate vocalizations and show that marmoset monkeys are a compe

71 per unit time and had longer pauses between vocalizations and that the entropy of the temporal seque

72 s shed new light on the diversity of primate vocalizations and vocal morphology, highlighting the imp

73 niaturized microphones to record spontaneous vocalizations and wireless autonomic monitors to record

74 discrepancies between the intended and heard vocalization, and contains information about the resulti

75 ve coordinated behaviors, such as breathing, vocalization, and locomotion.

76 x neurons when marmosets heard a conspecific vocalization, and that these changes corresponded to sub

77 uch sounds are normative events in mammalian vocalizations, and can be directly traceable to the nonl

78 riety of sound categories, including speech, vocalizations, and music, and we discuss how our underst

79 ocial signals carried by facial expressions, vocalizations, and social grooming.SIGNIFICANCE STATEMEN

80 combine to generate acoustic features of the vocalizations, and thus cannot meaningfully relate those

81 oral endoscopy, videofluoroscopy, ultrasonic vocalizations, and whole-body plethysmography were used

82 h showed social behavior impairment, altered vocalization, anxiety-like behavior, neuroanatomical abn

83 On encountering terrestrial predators, both vocalizations are combined into a "mobbing sequence," po

84 ficulties in identifying the extent to which vocalizations are constructed from shared, meaningless b

85 In adult animals, movement and vocalizations are coordinated, sometimes facilitating, a

86 Vocalizations are fundamental to mammalian communication

87 These vocalizations are generated by the emotional motor syste

88 Although mammalian vocalizations are predominantly harmonically structured,

89 In birds, the physical mechanisms by which vocalizations are produced and controlled remain unresol

90 produce elaborated and complex sequences of vocalizations, are of particular interest for this topic

91 We introduce methods for analyzing vocalizations as both discrete sequences and as continuo

92 n in the songbird forebrain by using natural vocalizations as stimuli and manipulating the category a

93 g forebrain leads to impairments in neonatal vocalizations as well as neocortical cytoarchitectonic a

94 "hits" had cumulative effects on ultrasonic vocalizations at postnatal day 3.

95 KCC2(E/+) mice also had abnormal ultrasonic vocalizations at postnatal days 10 to 12 and impaired so

96 ed in the perceptual processing of faces and vocalizations but also in their mnemonic processing.

97 cal for recognizing speech, music and animal vocalizations, but its neurobiological basis remains uns

98 rther increased emission of these ultrasonic vocalizations, but not milk ingestion.

99 not only modify distinct parameters of their vocalizations, but that these changes persist even after

100 They generate vocalization by activating the prefrontal-PAG-NRA-motone

101 Songbirds learn vocalizations by hearing and practicing songs.

102 By contrast, production of vocalizations by humans and animals involves complex and

103 otophone types emerge abundantly as early as vocalization can be observed in infancy, in preterm infa

104 tnut-crowned babbler (Pomatostomus ruficeps) vocalizations can be decomposed into perceptibly distinc

105 is plasticity in the degree to which learned vocalizations can change in both humans and songbirds is

106 Characterizing complex vocalizations can require considerable effort and a deep

107 esults refute the current theory for Xenopus vocalization, cavitation, and favor instead sound produc

108 The neural basis of how learned vocalizations change during development and in adulthood

109 Analysis of the EMGs demonstrated that these vocalizations consist of only small parts of the emotion

110 The results show that each type of vocalization consists of a specific, circumscribed motor

111 Numbers of adult words, child vocalizations, conversational turns, parent verbal respo

112 ity and standardize frequency measurement of vocalization data across species.

113 These data suggest that vocalization defects in mice carrying human stuttering m

114 ab Ser321Gly and Ala455Ser, produce the same vocalization deficit in 8-day-old pup isolation calls an

115 ic Gnptab-deficient mice displayed a similar vocalization deficit.

116 s between self-generated and passively heard vocalizations, detects discrepancies between the intende

117 edback refers to the monitoring of one's own vocalizations during call production and has been intens

118 Like humans, songbirds learn their vocalizations during development, and they provide an ex

119 involved in the production of self-initiated vocalizations during natural vocal communication.

120 gher detections of foraging and echolocation vocalizations during the night and of social signals dur

121 esponses for processing periodicity in human vocalizations during vocal production and motor control.

122 tions in emotional speech prosody, nonverbal vocalizations (e.g., crying), and (silent) facial expres

123 e causes of five distinct positive emotional vocalizations elicited by what adults would consider fun

124 signals, we showed that distinct patterns of vocalization emerge as male mice perform specific social

125 ult male MAR-ASD animals, as well as reduced vocalizations emitted in response to social cues with ro

126 ect and differentiate nuanced differences in vocalizations, even amid noisy environments.

127 Unlike the vocalizations exhibited by the majority of land vertebra

128 lfully produced "wookies" - an idiosyncratic vocalization exhibiting a unique spectral profile among

129 lly breeding teleost fish that (1) courtship vocalization exhibits an endogenous circadian rhythm und

130 ed on facilitating the detection of specific vocalization features, while the right ACx is a generali

131 xplain how ancient hominins began to produce vocalization flexibly, without binding to emotions or fu

132 pidly adapted sonar call design in the first vocalization following the jamming signal, revealing a r

133 ons further exhibit sharpened tuning for pup vocalizations following maternal experience.

134 r vocal organ transforms motor commands into vocalizations for social communication.

135 (GABARB1), breakdown of fats (cGMP-PK1), and vocalizations (FOXP2).

136 this issue here in a study of body size and vocalization frequencies conducted across 91 mammalian s

137 inverse relationships between body size and vocalization frequencies in primates and carnivores, fil

138 s inverse relationship between body size and vocalization frequencies is widely considered to be foun

139 : rigorous comparisons between body size and vocalization frequencies remain scarce, particularly amo

140 response to noise exposure were explained by vocalization frequency, nesting location and diet.

141 antaneously detect, localize and classify MM vocalizations from diverse species over an approximately

142 We compared vocalizations from mice engineered to carry a mutation i

143 st encode acoustic features that distinguish vocalizations from other sounds in the environment and g

144 eloped a microphone array system to localize vocalizations from socially interacting, individual adul

145 genetically triggered neonatal phenotype in vocalization generates a negative environmental loop in

146 eurochemical microstimulation also generated vocalizations (guttural sounds).

147 For over half a century now, primate vocalizations have been thought to undergo little or no

148 As Vldlr was previously implicated in avian vocalization, here we investigate vocalizations of neona

149 rlie the neural processing and perception of vocalizations.Here, we test the importance of vocalizati

150 nds with harmonic structures, such as animal vocalizations, human speech, and music.

151 direct access to the motoneurons involved in vocalization, i.e., the motoneuronal cell groups innerva

152 uses dysfunction in predictive coding during vocalization in a manner similar to the dysfunction obse

153 onist, ketamine, on predictive coding during vocalization in healthy volunteers and compared them wit

154 rd genetics approach selecting for defective vocalization in mice, we identified Kdm5a as a candidate

155 us tractus solitarius (NTS) is essential for vocalization in mice.

156 ubtype 1B (mel1b), shown to be important for vocalization in midshipman fish and songbirds.

157 synaptogenesis of corticostriatal inputs and vocalization in neonates.

158 It exerts opposing effects on vocalization in nocturnal versus diurnal species at the

159 y predicted whether subjects would produce a vocalization in response.

160 Vocalization in young mice is an innate response to isol

161 d microCT imaging, as well as measurement of vocalizations in a heliox atmosphere.

162 ulates selectivity for behaviorally relevant vocalizations in a specific part of the caudomedial nido

163 low frequency cries to tonal, higher pitched vocalizations in adults, are caused partially by larynge

164 Examination of rodent vocalizations in experimental conditions can yield valua

165 , and biomechanical modeling, we showed that vocalizations in infant marmoset monkeys undergo dramati

166 Deep, resonant vocalizations in particular may function in attracting m

167 action tests), and communication (ultrasonic vocalizations in pups).

168 ating bat controls the features of its sonar vocalizations in tandem with the positioning of the oute

169 crucial role of social feedback to immature vocalizations in the development of communication.

170 ties while they listened to infant and adult vocalizations in two conditions, together (in the same r

171 We recorded "fictive vocalizations" in the in vitro CPG from the laryngeal ne

172 ild dogs' (HWD) observed range and confirmed vocalizations indicate their potential to be a wild NGSD

173 al cues of density (frequency of territorial vocalizations) indicate that increases in social (acoust

174 e was evident even before subjects heard the vocalization, indicating that the probability of a conve

175 behavior; however, the extent to which mouse vocalizations influence social dynamics has remained elu

176 y, and, at the same time, they modulate this vocalization into words and sentences by activating the

177 atic motor system, they are able to modulate vocalization into words and sentences.

178 computational methods for projecting animal vocalizations into low dimensional latent representation

179 cts were successful by producing their novel vocalizations into the instrument, hence, confirming act

180 e demonstrated that predictive coding during vocalization is disrupted in schizophrenia.

181 information can be conveyed via gesture and vocalization is present in infancy.

182 A new study shows that nocturnal courtship vocalization is regulated by a circadian rhythm and pote

183 evant aspect of periodicity in natural human vocalizations, is encoded in Heschl's gyrus (HG), and ho

184 following muscles were recorded during these vocalizations: larynx (cricothyroid, thyroarytenoid, and

185 with the maternal mouse paradigm for natural vocalization learning.

186 e auditory system in response to conspecific vocalizations masked by noise.

187 We found that vocalizations matured sooner than postural and locomotor

188 parameters ex vivo, suggesting that in vivo vocalizations may also not be specified by unique motor

189 in the cat generates four different types of vocalization, mews, howls, cries, and hisses.

190 his implies that the frequency of blue whale vocalizations might be directly proportional to the size

191 rocesses that support auditory perception of vocalizations more generally.

192 Combining analyses of natural vocalizations, motorized excised larynx experiments, ten

193 king memory paradigm using naturalistic face-vocalization movies as memoranda.

194 he extraction of the semantic content of the vocalizations of African wild dogs, and the behaviors ge

195 We exploited the brief vocalizations of echolocating bats to trace the time cou

196 ariety of deep neural networks to detect the vocalizations of endangered North Atlantic right whales

197 The behavior and vocalizations of four group-housed squirrel monkeys were

198 e expectation that cries are the predominant vocalizations of infancy, our all-day recordings showed

199 re we show that state changes in the contact vocalizations of infant marmoset monkeys, which transiti

200 neuronal activity of male zebra finches and vocalizations of males and females that freely interact

201 d in avian vocalization, here we investigate vocalizations of neonatal mice with a reduction or absen

202 ot exclusive to human language: listening to vocalizations of nonhuman primates also supports infant

203 We found significant differences in the vocalizations of pups with the human Gnptab stuttering m

204 own for its importance in control of learned vocalizations of songbirds, displays predictive activity

205 simulated predator presence by broadcasting vocalizations of their main predators, leopards or eagle

206 sed by the bat for spatial orientation-sonar vocalizations-offering support for the hypothesis that s

207 Natural sounds such as vocalizations often have covarying acoustic attributes,

208 evolution of speech required the addition of vocalization onto this scaffold in order to turn such ja

209 tral species, but added voluntary control of vocalization onto this via the evolution of a new brain

210 athway neural responses become selective for vocalizations or how the underlying encoding mechanisms

211 propagate direct (high and low threat raptor vocalizations) or indirect (high and low threat chickade

212 mals are intrinsically sensitive to neonatal vocalizations, or instead learn about vocal cues for par

213 ing that is not explained by their courtship vocalizations, parental care of eggs, or nest defense ag

214 nted social behavior, and altered ultrasonic vocalization patterns at 6-12 weeks of age.

215 vioral phenotypes including altered neonatal vocalization patterns.

216 nd that mice with the mutation emitted fewer vocalizations per unit time and had longer pauses betwee

217 Vocalizations play a significant role in social communic

218 exhibit multisensory responses to faces and vocalizations presented simultaneously.

219 itional detection algorithms for the primary vocalization produced by this species, the upcall.

220 t], [Formula: see text]) were presented with vocalizations produced in either a happy, angry or neutr

221 mance were related to the type and number of vocalizations produced.

222 lize across the high variability inherent in vocalization production and classify them into behaviora

223 ias test [8], to show that 50 kHz ultrasonic vocalizations provide a quantifiable and graded measure

224 pressure levels and the estimated effective vocalization radii, estimated through spherical spreadin

225 correlated with the loudness (amplitude) of vocalization, ranging from approximately 1 to 50 particl

226 e region: fin, humpback, blue and minke have vocalization rate trends that are highly correlated to t

227 The recorded vocalization rates are diel (24 h)-dependent for all MM

228 Males and females jointly increased their vocalization rates during chases.

229 cation deficits, as assessed with ultrasound vocalization recordings.

230 s simply responded to a particular face or a vocalization regardless of the task period, others exhib

231 avioral responses to natural and synthesized vocalizations rely on the presence of discrete frequency

232 which forebrain neurons trigger or suppress vocalization remain unknown.

233 inputs to the PAG that trigger and suppress vocalization, respectively, while also establishing the

234 ion between communication sounds masked by a vocalization-shaped stationary noise from multiunit resp

235 Event-related band power responses to vocalizations showed sustained frequency following respo

236 Mice, for instance, emit ultrasonic vocalizations, signals above the range of human hearing,

237 sulted in deficits in the flow of ultrasonic vocalizations similar to speech deficits of humans who s

238 hus have been copious, functionally flexible vocalization, starting in infancy and continuing through

239 formation flow enclosed in fast time-varying vocalization streams emitted by conspecifics.

240 an brain copes with information from natural vocalization streams remain poorly understood.

241 o speak but has no apparent effect on innate vocalizations such as human laughing and crying or monke

242 Vocalizations such as mews and cries in cats or crying a

243 d potential elicited by speech sounds during vocalization (talk) and passive playback (listen) were c

244 fundamental frequency (f(o)) as well as two vocalization tasks in which their perceived f(o) was mod

245 cortical neurons better discriminated target vocalizations than cortical ones and in each structure,

246 first year of life produced more speech-like vocalizations than girls and that the effect size was mo

247 aughter is a stereotyped, innate, human play vocalization that provides an ideal simple system for ne

248 ed before marmosets even heard a conspecific vocalization that, as a population, almost perfectly pre

249 The typical durations of marine mammal vocalizations that carry over great distances are found

250 espiratory amplitude result in the different vocalizations that comprise infant vocal sequences.

251 cs are involuntary, repetitive movements and vocalizations that occur in bouts, typically many times

252 Animals produce vocalizations that range in complexity from a single rep

253 ditions, a change in the auditory component (vocalization), the visual component (face), or both comp

254 When this response followed the onset of vocalization, the magnitude of the response was the same

255 Nesting males produce nocturnal vocalizations to attract females [13].

256 The use of vocalizations to communicate information and elaborate s

257 Humans and vocal animals use vocalizations to communicate with members of their speci

258 species use pitch trajectories in their own vocalizations to distinguish sound categories, such as i

259 oothed whales) rely upon echoes of their own vocalizations to navigate and find prey underwater [1].

260 large carnivore, presenting playbacks of dog vocalizations to pumas in central California.

261 y of howler monkeys shows that males who use vocalizations to ward off rivals invest less in producin

262 ocalizations.Here, we test the importance of vocalization-typical spectral features in behavioral rec

263 Vocalizations typically have spectral structure; power r

264 Songbirds communicate through learned vocalizations, using a forebrain circuit with convergent

265 These ultrasonic vocalizations (USV) are typically described and evaluate

266 the emission of prosocial 50-kHz ultrasonic vocalizations (USV) paralleled by a lack of social appro

267 Ultrasonic vocalizations (USV) were measured at PND12 during two, 3

268 Throughout life, rats emit ultrasonic vocalizations (USV) when confronted with an aversive sit

269 Rodent ultrasonic vocalizations (USVs) are a vital tool for linking gene m

270 Here, we study how ultrasonic vocalizations (USVs) are represented in the brain of mot

271 (PAG) that gate the production of ultrasonic vocalizations (USVs) in mice (i.e. PAG-USV neurons).

272 Ultrasonic vocalizations (USVs) were altered in both sexes.

273 ble by the presence or absence of ultrasonic vocalizations (USVs)(2-4), respectively.

274 ctro-temporal measures to compare ultrasonic vocalizations (USVs), which limits the ability to addres

275 tion through a rich repertoire of ultrasonic vocalizations (USVs).

276 mice when they produce ultrasonic courtship vocalizations (USVs).

277 Songbirds, like humans, learn vocalizations via tutor imitation and possess a speciali

278 he state of the frontal cortex at the time a vocalization was heard, and not by a decision driven by

279 N1 suppression to self-produced vocalizations was significantly and similarly diminished

280 rforming playbacks with natural and modified vocalizations, we show that males are sensitive to call

281 s of the electromyograms (EMGs) during these vocalizations were analyzed.

282 Mouse vocalizations were recorded throughout the experiment, a

283 f the infants' home language environment and vocalizations were recorded when the infants were 6, 10,

284 ons was slightly decreased when tone-vocoded vocalizations were tested.

285 behavior (social interaction and ultrasonic vocalizations) were examined in adult male Lister-hooded

286 ession both before and during self-initiated vocalizations when marmosets, a highly vocal New World p

287 manner that resembled how humans alter their vocalizations when speaking to infants, that was distinc

288 s increased affiliative social behaviors and vocalizations, whereas methamphetamine had only modest e

289 ected in the fundamental frequency (f(o)) of vocalizations, whereby lower f(o) indicates larger body

290 control circadian rhythms, reproduction, and vocalization, which may be selected upon over evolutiona

291 tions in acoustical parameters of ultrasonic vocalizations, which also differed in function of the so

292 gs (NGSD) are identifiable by their namesake vocalizations, which are unlike any other canid populati

293 , but not with self-initiated or spontaneous vocalizations, which casts doubt on the role of the fron

294 pecially for learned natural categories like vocalizations, which often share overlapping acoustic fe

295 dy, human vocalizers produced a steady-state vocalization while rhythmically moving the wrist or the

296 er activation in the left ACx in response to vocalizations, while the right ACx responded more to fre

297 to apical vocal membranes, producing louder vocalizations with higher efficiency.

298 ustics is that large animals tend to produce vocalizations with lower frequencies than small animals.

299 neurons show a high degree of invariance for vocalizations within a call-type.

300 and accompanied by alterations in ultrasonic vocalization without changes in homing behavior.