ライフサイエンスコーパス: social interaction

1 ces in D2- MSN activity were not specific to social interaction.

2 which emphasizes the critical importance of social interaction.

3 timulating mPFC D2R+ neurons disrupts normal social interaction.

4 ms and continued effects on parent and child social interaction.

5 ons and emotions is essential for successful social interaction.

6 d less anxiety-like behavior and deficits in social interaction.

7 associated with reduced intentions to pursue social interaction.

8 ives with merit include those that encourage social interaction.

9 ing behaviour, nest selection/maintenance or social interaction.

10 apparatus, muscles, the nervous system, and social interaction.

11 and increased calcium transients specific to social interaction.

12 al principles governing action choice during social interactions.

13 rs' preferences becomes vital for successful social interactions.

14 learning and memory, stress, addiction, and social interactions.

15 e hypothalamus and medial amygdala modulates social interactions.

16 t types of prosocial behaviors that exist in social interactions.

17 eutral hypothesis, without needing to invoke social interactions.

18 ocial information and potentially regulating social interactions.

19 that characterize most important real-world social interactions.

20 ) are believed to play an important role for social interactions.

21 sitive to costs, benefits, and errors during social interactions.

22 nary stasis may occur for traits involved in social interactions.

23 our emotional (limbic) brain and affect our social interactions.

24 enhanced visual awareness, attentiveness, or social interactions.

25 ion and have an important role in regulating social interactions.

26 er, this has not been investigated in direct social interactions.

27 the biological importance of eye contact for social interactions.

28 onverbal cue that plays an important role in social interactions.

29 ve important consequences for the outcome of social interactions.

30 the orbital cortex, a region associated with social interactions.

31 n exists between their mobility patterns and social interactions.

32 n and serve as chemical signals that mediate social interactions.

33 lay in a prisoner's dilemma game, a model of social interactions.

34 of motor behavior to enhance teacher/learner social interactions.

35 d by repetitive behaviors and impairments in social interactions.

36 to exploit them adequately during real-life social interactions.

37 ys display coherent motivations in different social interactions.

38 ies very rapidly, an ability that is key for social interactions.

39 ompete neighboring conspecific cells through social interactions.

40 n guide our decisions as we navigate complex social interactions.

41 to the influence of resource availability on social interactions.

42 tions have arisen about the impact of online social interactions.

43 riation in foraging patterns, refuge use and social interactions.

44 nerated "daisy-chain" vs. "star" networks of social interactions.

45 upport, face severe difficulties in everyday social interactions.

46 n the various social cues experienced during social interactions.

47 hood as deficits in communication skills and social interactions.

48 ors including learning, decision making, and social interactions.

49 from much greater exploration of sequential social interactions.

50 PVN OXT axon terminals in the VTA decreased social interactions.

51 nal signals, tune motivation, and coordinate social interactions.

52 bitat heterogeneity, novel disturbances, and social interactions.

53 many methods for inferring hierarchies from social interactions.

54 ments of the human species depend on complex social interactions.

55 be influenced by both habitat structure and social interactions.

56 el odors, reward expectation, and as part of social interactions [6-12].

57 ce core features of ASD, including decreased social interaction, aberrant communication, and increase

58 hat the DMPFC is finely tuned for processing social interaction above other categories and that this

59 During social interactions, activity in paraventricular nucleus

60 We then collected data on infants' social interactions (aggression, grooming, and play) and

61 minute rest, pinpointing neural synchrony to social interactions among affiliative partners.

62 Social interactions among animals can influence their re

63 Acoustic communication is fundamental to social interactions among animals, including humans.

64 Our results demonstrate that social interactions among consumers can have a dominant

65 erated games provide a framework to describe social interactions among groups of individuals.

66 In social interactions among mammals, individuals are recog

67 at selection to avoid non-cooperators limits social interactions among non-relatives, yet previous ev

68 thesis and suggest that large seed crops and social interactions among scatter-hoarders affect disper

69 xtent and location of a dedicated system for social interaction analysis suggest that this function i

70 rontal cortex that is exclusively engaged in social interaction analysis.

71 under conditions that model human drug use (social interaction and 29 degrees C ambient temperature)

72 induces a deficit in social recognition and social interaction and a reduced learning ability in adu

73 -sensing somatosensory neurons contribute to social interaction and anxiety phenotypes in mouse model

74 ms including repetitive behaviour, defective social interaction and audiogenic seizures.

75 nd cognitive symptoms, including deficits in social interaction and cognitive inflexibility.

76 ectrum disorder (ASD) is defined by impaired social interaction and communication accompanied by ster

77 ntal abnormalities characterized by impaired social interaction and communication, stereotypic behavi

78 g infants with a strong foundation for later social interaction and learning.

79 uction of depressive-like states measured in social interaction and light/dark tests.

80 dging that decisions are constructed through social interaction and organizational context.

81 ojections modulates other behaviors, such as social interaction and perseverant investigation of a no

82 the effects of CRS, as shown by an increased social interaction and reduced passive behavior in a for

83 l disability characterized by impairments in social interaction and repetitive behavior, and is also

84 station of symptoms that include deficits in social interaction and repetitive or stereotyped interes

85 istered to naive and stressed mice tested in social interaction and resident-intruder tests (n = 8-14

86 xhibit neurocognitive behavioral deficits in social interaction and sensorimotor gating tasks.

87 Crmp4-KO mice showed decreased social interaction and several alterations of sensory re

88 d by impairments in social communication and social interaction and the presence of repetitive behavi

89 ent theories capitalizes on the link between social interaction and visual perception: effective inte

90 potentiation of MDMA-induced hyperthermia by social interaction and warm ambient temperature, such po

91 core behavioral criteria, unusual reciprocal social interactions and communication, and stereotyped,

92 IBD) report impairments in daily activities, social interactions and coping.

93 may hinder emotional recovery from negative social interactions and decrease pleasure derived from p

94 ignificantly impaired object recognition and social interactions and elevated repetitive behaviors, w

95 Oxytocin is important for social interactions and maternal behaviour.

96 tworks to identify the existence of negative social interactions and other social processes.

97 de is sensitive to changes in stress levels, social interactions and pharmacological manipulations, a

98 Oxytocin promotes social interactions and recognition of conspecifics that

99 This impairment negatively impacts social interactions and relationships.

100 unctions beyond mere reproduction to mediate social interactions and relationships.

101 s toward understanding mechanisms underlying social interactions and their disorders such as autism.

102 PFC pyramidal neurons as well as cognition, social interaction, and anxiety.

103 Dose-dependent disruptions in motivation, social interaction, and attention were produced by PACAP

104 s of mood and anxiety disorders (motivation, social interaction, and attention).

105 valuated the impact of antipsychotic review, social interaction, and exercise, in conjunction with pe

106 0 for 14 days reduced hyperarousal, improved social interaction, and improved natural behaviors such

107 ffect prefrontal D3 receptors alter anxiety, social interaction, and reversal learning.

108 rate non-toxic dose of MDMA (9 mg/kg) during social interaction, and we administered potential treatm

109 ulse inhibition, increased anxiety, impaired social interaction, and working memory deficit.

110 , impaired fine motor skills, subtly altered social interactions, and decreased dendritic spine densi

111 ance individuals maintain from others during social interactions, and into which intrusion by others

112 of household and individual characteristics, social interactions, and maternal capabilities for child

113 ement, executive function, memory, language, social interactions, and quality of life.

114 genic mice displayed normal social approach, social interactions, and repetitive motor stereotypies t

115 quently changing the evolutionary outcome of social interactions; and by modifying the evolutionarily

116 Existing assays of social interaction are suboptimal, and none measures pro

117 emory deficits, anxiolytic-like effects, and social interaction are under the control of 5-HT2AR, but

118 Yet, mammalian social interactions are extremely complex, involving bot

119 Social interactions are important in everyday life for p

120 Sustained cooperative social interactions are key to successful outcomes in ma

121 Social interactions are often powerful drivers of learni

122 in verbal and non-verbal communication, and social interactions, as well as the presence of repetiti

123 cient to express the rewarding properties of social interactions, assessed using a socially condition

124 2b) Social interaction at mealtimes should be encouraged.

125 ace interactions with mothers have increased social interactions at 2 and 5 months.

126 ch is central in building the foundations of social interaction, attachment, and cognition, and early

127 Perceptual and social interaction atypicalities could reflect co-expres

128 ngbirds and humans is strongly influenced by social interactions based on sensory inputs from several

129 resilience to social stress as quantified by social interaction behavior and sucrose preference.

130 social withdrawal in female mice and reduced social interaction behavior in female mice naive to defe

131 e appearance of depression-like and abnormal social interaction behaviors reminiscent of depressive d

132 asp3(-/-) males showed significantly reduced social interaction behaviors when exposed to a freely mo

133 Laboratory experiments show that social interactions between bacterial cells can drive ev

134 ominated by the presence of scenes involving social interactions between characters.

135 tics are signals that coordinate cooperative social interactions between coexisting bacteria.

136 ly-grounded, socially-neutral model (i.e. no social interactions between genotypes) for the life cycl

137 cteristics of individual agents, but also to social interactions between multiple agents.

138 temporal sulcus (pSTS) to stimuli depicting social interactions between two agents, compared with (i

139 havioral diversity, varying their input to a social interaction both qualitatively and quantitatively

140 ned vocal communication, the neurobiology of social interactions, brain development, and ecology.

141 ctions, both features that often covary with social interaction but may be difficult to disentangle u

142 on, or joint action, is a crucial element of social interaction, but the dynamics of nonverbal inform

143 Autism is characterized by impairments of social interaction, but the underlying subpersonal proce

144 on-human primate calls often mediate complex social interactions, but are generally regarded as acous

145 contribute to these social impairments, but social interaction by definition involves more than one

146 er positive or negative emotional states, as social interaction can be rewarding and social isolation

147 we test the hypothesis that the topology of social interaction can causally explain some of the cros

148 egy in choosing ties where to allocate their social interactions can be quantitatively described and

149 thus providing mechanistic insight into how social interactions can generate rewarding experiences.

150 re more cohesive, and personality traits, as social interactions can have functional consequences for

151 ctivity during bond formation, revealing how social interactions can recruit brain reward systems to

152 In addition, during iterative social interactions, choices might change dynamically as

153 II treatments reverse the typical defects in social interaction, cognitive/executive functions, and r

154 cts before weaning age and impaired juvenile social interaction, coinciding with the early onset of A

155 ion-level lateralization is present only for social interactions common and frequent in the species'

156 ristic behavioral traits, including impaired social interaction, communication difficulties and repet

157 lopmental syndrome characterized by impaired social interaction, communication, and repetitive behavi

158 rs (ASD) are characterized by impairments in social interaction, communication, and repetitive or res

159 d perceptual processing, executive function, social interaction, communication, and/or intellectual a

160 104 adults during a male-female naturalistic social interaction, comparing romantic couples and stran

161 Examined phenotypes included social interaction, compulsive behaviors, aggression, hy

162 eason why individuals with FXS tend to avoid social interactions, contributing to their isolation.

163 certain behavioural abnormalities including social interaction deficit and repetitive grooming behav

164 ing development, but not in adulthood, cause social interaction deficits and anxiety-like behavior.

165 ects contribute to anxiety-like behavior and social interaction deficits in ASD mouse models.

166 wer doses of CBD also improved autistic-like social interaction deficits in DS mice.

167 Likewise, social interaction deficits were not corrected by STN-HF

168 avioral phenotypes, including hyperactivity, social interaction deficits, and increased repetitive be

169 autistic-like behaviours including anxiety, social interaction deficits, and repetitive behaviour.

170 tile sensitivity, anxiety-like behavior, and social interaction deficits, but not lethality, memory,

171 splenomegaly, enlarged lymph nodes, and mild social interaction deficits, but not motor dysfunction.

172 h sexes, only male Casp3(-/-) mice exhibited social interaction deficits, which is interesting given

173 nk3 mutant mice show repetitive grooming and social interaction deficits.

174 further introduction of confirmation bias in social interactions, defined as the tendency of an indiv

175 Perception, cognition, and social interaction depend upon coordinated neural activi

176 Successful social interactions depend on people's ability to predic

177 nts is the scaffolding upon which speech and social interactions develop.

178 Face perception, which is critical for daily social interactions, develops from childhood to adulthoo

179 Positive social interactions during the juvenile and adolescent p

180 The family meal and social interactions during the meal are important events

181 the extraction of important information for social interaction (e.g., person identity).

182 Face-to-face social interactions enhance well-being.

183 nable sophisticated sensory tasks, including social interaction, environmental exploration, and tacti

184 ial expressions is an essential component of social interaction, especially for preverbal infants.

185 le for what they do, as happens in countless social interactions every day?

186 from direct-pathway MSNs caused deficits in social interaction, excessive grooming, and decreased ex

187 ced social interaction, while a reduction in social interaction following CSDS was not observed when

188 Many previous studies reported loss of social interactions following permanent damage to the am

189 riterion in evaluating candidate partners in social interaction generally.

190 increased repetitive behavior, and decreased social interaction, hallmarks of ASDs.

191 ential neurocognitive evaluation of observed social interactions has remained an open question.

192 Here, we show that social interactions have a major effect on fish grazing

193 ve datasets that capture human movements and social interactions have catalyzed rapid advances in our

194 Cells without significant multi-cellular social interactions have surprisingly complex behaviors:

195 r, Tshz1 cKOs display significantly impaired social interaction (i.e., increased passivity) regardles

196 ced cold and mechanical allodynia as well as social interaction impairment.

197 nction and learning abilities, alteration of social interaction, impairment of normal housetraining,

198 We tested the hypothesis that social interaction impairments in people with schizophre

199 tween brains of human dyads during real-time social interaction in a joint attention paradigm.

200 is elicited various responses on the role of social interaction in infancy, the methodological issues

201 Our results reveal an alteration in social interaction in patients with schizophrenia that i

202 In contrast, intranasal OT increased social interaction in stressed male mice and reduced fre

203 s well as deficits in cognitive function and social interaction in these mice.

204 al amygdala triggered a profound increase in social interactions in dyads of monkeys highly familiar

205 ations for our understanding of economic and social interactions in our society.

206 While the implications of social interactions in phenotypically mixed populations

207 ming can have a pervasive effect on abnormal social interactions in schizophrenia patients.

208 a neural correlate of the representation of social interactions in the human brain.

209 t rely on chemo- and acoustic signalling for social interactions in their dispersed social systems.

210 Social interactions in vertebrates are complex phenomena

211 tensive SCIN ablation results in exacerbated social interactions, in which normal social contacts wer

212 (anhedonia, depression, anxiety, and altered social interaction), including some humans with GRIK4 du

213 on of turn-taking which underlies a range of social interactions, including communication and languag

214 Social interactions increasingly take place online.

215 In addition, social interaction induces synaptic potentiation (LTP) i

216 Social interaction inherently involves the subjective ev

217 pmental disability characterized by atypical social interaction, interests or body movements, and com

218 Antipsychotic review plus the social interaction intervention significantly reduced mo

219 domly assigned to antipsychotic review, to a social interaction intervention, and to an exercise inte

220 ts (pharmacological manipulations, ontogeny, social interactions) involving transitions in-and-out of

221 Impaired social interaction is a defining feature of autism spect

222 Observed impairment in reciprocal social interaction is a diagnostic hallmark of autism sp

223 Social interaction is a fundamental behavior in all anim

224 The reward generated by social interactions is critical for promoting prosocial

225 The emerging pattern of social interactions is highly predictable and invariant

226 is sensitivity to the presence and nature of social interactions is not easily explainable in terms o

227 This sensitivity to social interactions is strongest in a specific subregion

228 When the temporal ordering of social interactions is taken into account, active forage

229 cial networks in an era of ever-diversifying social interaction layers.

230 rony is a possible neural marker for dynamic social interactions, likely driven by shared attention m

231 uish between statistical effects and genuine social interaction may lead to unwarranted conclusions a

232 Meaningful social interactions modify behavioral responses to senso

233 social influences, little is known about how social interactions modulate vocal learning.

234 eotypes, but in the complexity of real world social interactions, most of our individuating informati

235 Auditory communication is central to the social interactions of many animals.

236 Human choice behaviors during social interactions often deviate from the predictions o

237 , anxiety-related behavior, innate fear, and social interactions, often only when food is accessible.

238 processes such as the powerful influence of social interaction on beliefs and preferences.

239 eotyped/repetitive behaviors and deficits in social interaction or communication), but neither result

240 ess nonpharmacological interventions such as social interaction or exercise are provided in parallel.

241 For domains as complex as social interaction or natural movement, however, the rel

242 osed by rival groups, intragroup affiliative social interactions, or coordinated behavior alone.

243 al reverts might not necessarily be negative social interactions, our analysis points to the existenc

244 ls interacting with an unfamiliar mouse in a social interaction paradigm.

245 e and phenotypic composition appear to alter social interaction patterns, which leads to differential

246 n signaling in adults is sufficient to alter social interaction preferences in males as well as respo

247 be relevant to the normalization of negative social interaction processing in psychiatric disorders c

248 ing--is plastic, and can be improved through social interactions, providing infants with a strong fou

249 velopmental consequences, impacting infants' social interaction quality and opportunities for learnin

250 g or aversive emotional memory formation and social interaction/recognition behaviors via intra-NASh

251 hough many species' signal transmissions and social interactions rely on extended bouts of coordinate

252 oordinate their brain response online during social interactions remain unclear.

253 ulation modulates the processing of negative social interactions remains unclear.

254 Such models typically assume simple social interactions restricted to pairs of individuals;

255 In contrast, after the disaster, frequent social interactions reverted back to predicting improved

256 sense of purpose, motivation, emotional and social interactions, role functioning, and engagement in

257 us was on inferring single, mode-independent social interaction rules that reproduced macroscopic and

258 itive function score (P=0.04) and quality of social interaction score (P=0.01) in the kidney disease

259 e and increased motivation for nonaggressive social interactions, similar to what is reported in huma

260 notion that warm temperature allows for more social interaction situations (Routine Activity Theory)

261 moral commitments generates features of our social interaction so familiar that they rarely strike u

262 contains information about the nature of the social interaction-specifically, whether one agent is he

263 rcuits underlying developmentally programmed social interactions such as male territorial aggression

264 ess exposure, female mice were tested in the social interaction, sucrose preference, tail suspension,

265 task tests but remained dysregulated in the social interaction test.

266 lters interactions with a conspecific in the social interaction test.

267 donic behavior in the sucrose preference and social interaction tests produced by two different chron

268 response and what are the specific cues in a social interaction that signal a change in social status

269 as well as the different temporal scales of social interactions that are at play.

270 Furthermore, social interactions that rapidly enhanced learning incre

271 n comedy (sitcom) depicting seminaturalistic social interactions ("The Office", NBC Universal) in the

272 n the biological basis of nonhuman primates' social interactions, their underlying motivations remain

273 viduals' breeding locations, including other social interactions themselves.

274 ments in the investigation of 2-person human social interaction to investigate interaction difficulti

275 wever, empirical evidence linking microlevel social interactions to large-scale environmental outcome

276 ivo Selective SCIN ablation leads to altered social interactions together with exacerbated spontaneou

277 Individual computations and social interactions underlying collective behavior in gr

278 Despite the complexity of social interactions, we show that networks of coupled he

279 P2X7 receptor deficient mice (P2rx7-/-), the social interactions were increased, whereas the PCP indu

280 After the disaster, social interactions were linked to improved survival.

281 Social interactions were observed in pairs of highly fam

282 ) when individuals were tested alone affects social interactions when fish were retested in groups of

283 enarios rather than participation in genuine social interactions where genuine resources are at stake

284 rm "socialtaxis," that unifies infotaxis and social interactions, where each individual in the group

285 rom the dorsal striatum produced deficits in social interaction, whereas deletion from the ventral st

286 keys were more likely to invent new forms of social interaction, whereas younger monkeys were more li

287 les plasticity in vocal timing to facilitate social interactions, whereas in the case of songs, plast

288 in many decision-making scenarios, including social interactions wherein the identities and strategie

289 can strongly influence adult phenotypes and social interactions, which in turn affect key evolutiona

290 weak selection on a game-theoretic model of social interactions, which we also validate using indivi

291 defeat stress (SSDS) as observed by reduced social interaction, while a reduction in social interact

292 measure the valence of aggressive inter-male social interaction with a smaller subordinate intruder a

293 onarily conserved manner, by the stress of a social interaction with an unfamiliar conspecific and ca

294 ed experimental designs, we demonstrate that social interactions with adult tutors for as little as 1

295 Chd8(+/del5) mice displayed normal social interactions with no repetitive behaviors but exh

296 Adolescents' hostile social interactions with outgroup members and uncompromi

297 rtical top-down network that is required for social interactions with potential implications for sens

298 logy combines quantitative genetic models of social interactions with stochastic processes to model t

299 ore, experimental results regarding apparent social interactions within chimeric mixes can be qualita

300 atus in virtually all human groups and shape social interactions within them.