ライフサイエンスコーパス: social behaviour

1 netic and epigenetic underpinnings of animal social behaviour.

2 (Esr1), and investigated their role in male social behaviour.

3 ow for interventions promoting well-adjusted social behaviour.

4 recognition is a key component of successful social behaviour.

5 imaging and can give important insights into social behaviour.

6 of diversity that may apply to many forms of social behaviour.

7 Cooperation is central to human social behaviour.

8 , possibly conferring benefits to health and social behaviour.

9 example of an imprinted gene that regulates social behaviour.

10 RMG activity is essential for all aspects of social behaviour.

11 y transformed the ways that ecologists study social behaviour.

12 ent model for investigating the evolution of social behaviour.

13 st summarise the literature on their natural social behaviour.

14 mechanism for the rapid evolution of complex social behaviour.

15 sts; and the identification of violations of social behaviour.

16 ught to play a crucial role in emotional and social behaviour.

17 omising framework for understanding flexible social behaviour.

18 key life phase for developing well-adjusted social behaviour.

19 onable molecular participant in OT-dependent social behaviour.

20 a triad of behavioural impairments including social behaviour.

21 roviding broad implications for the study of social behaviour.

22 eedback loop between social standing and pro-social behaviour.

23 f cross-species data for research on macaque social behaviour.

24 nisms underlying pathogen-induced changes in social behaviour.

25 e experience has a long-lasting influence on social behaviour.

26 cation by chemical cues regulates C. elegans social behaviour.

27 nucleus accumbens (NAc), as well as altered social behaviour.

28 y transformed the ways that ecologists study social behaviour.

29 icroorganism-mediated metabolism that affect social behaviour.

30 nts with manifold facets of reproductive and social behaviour.

31 further understanding of mating systems and social behaviour.

32 de the brain contributes to the evolution of social behaviour.

33 social structure learning supports adaptive social behaviour.

34 racts important for emotional processing and social behaviour.

35 database on affiliative and agonistic animal social behaviour.

36 ample to understand the processes of complex social behaviour.

37 nvestigate the impact of genetic variants on social behaviour.

38 complex vocal sequences during goal-directed social behaviour.

39 social-semantic knowledge to guide and shape social behaviour.

40 ontainment, suggesting an important role for social behaviour.

41 worm to provide further insight into complex social behaviour.

42 al states are integrated to flexibly control social behaviour.

43 he flexibility and nuance needed for complex social behaviour.

44 (e.g., making norms salient) can promote pro-social behaviour.

45 w pronounced differences in their later-life social behaviour.

46 Conversation is an important and ubiquitous social behaviour.

47 Z scaffold protein Lnx1 required for initial social behaviour.

48 s regarding the impact of this technology on social behaviour.

49 ld hyperactivity, lower anxiety and impaired social behaviour.

50 frank neuronal loss and FTD-like changes in social behaviour.

51 granulin deficiency is sufficient to disrupt social behaviour.

52 low-level network in more complex high-level social behaviour.

53 ulate shoal cohesion, indicative of abnormal social behaviour.

54 ional asymmetry has evolved as an adjunct to social behaviour.

55 ve in mutants, but becomes hypoactive during social behaviour.

56 thesis linking directional lateralization to social behaviour.

57 ects of testosterone administration on human social behaviour.

58 ed in face expression processing involved in social behaviour.

59 minent, early and progressive impairments in social behaviour.

60 Animals display a repertoire of different social behaviours.

61 trate for competition between these opponent social behaviours.

62 e they have fundamentally important roles in social behaviours.

63 Cplx1(-/-) mice have pronounced deficits in social behaviours.

64 administration, with limited effects on non-social behaviours.

65 factors are known to shape the expression of social behaviours.

66 mine and serotonin are hypothesized to guide social behaviours.

67 ually dimorphic neural circuit that mediates social behaviours.

68 g(17,18) of male BNSTpr(Esr1) neurons during social behaviours.

69 e to regulate canonical stress responses and social behaviours.

70 n dysfunction in the expression of disrupted social behaviours.

71 atly increased zinc demand to display normal social behaviours.

72 all without observable changes in anxiety or social behaviours.

73 is often associated with distinctive or odd social behaviours.

74 changes in ecology, cognition, language and social behaviours.

75 halamic neural assemblies controlling innate social behaviours.

76 y in the VMHvl of male mice engaged in these social behaviours.

77 g normal and pathological sexually dimorphic social behaviours.

78 ex and anterior temporal lobes in supporting social behaviour?

79 skills (3.86, 1.41 to 6.31), and 0.2 for pro-social behaviours (0.07, 0.02 to 0.12).

80 skills (7.53, 5.14 to 9.92) and 0.2 for pro-social behaviours (0.08, 0.03 to 0.13).

81 viours (1.77 (1.48 to 2.12); n=47 280), anti-social behaviour (1.73 (1.44 to 2.06); n=54 993), multip

82 -known actions in parturition, lactation and social behaviour(1), and has become an intriguing therap

83 t gesture use (3.22, -0.60 to 7.04) and VABS social behaviour (3.28, -1.43 to 7.99).

84 ster males during a complex, visually guided social behaviour(8-11).

85 ominance specifically among other aspects of social behaviour, a finding supported by the observed in

86 xually immature mice that controls an innate social behaviour, a response pathway through the accesso

87 Maladaptive social behaviour accordingly was a major force that cont

88 Maladaptive social behaviour accordingly was a major force that cont

89 de important new insights into the nature of social behaviour across species, facilitate greater inte

90 n reported to modulate amygdala activity and social behaviour across species.

91 imental work that addresses how kin-selected social behaviours affect virulence.

92 ess), imprinted genes may evolve to modulate social behaviour, although so far no such instance is kn

93 een strongly implicated in the regulation of social behaviour and anxiety, potentially contributing t

94 Testosterone is a key mediator of vertebrate social behaviour and can influence how individuals inter

95 riven model repositions semantics, language, social behaviour and face recognition into a continuous

96 n identification, but significant changes in social behaviour and in subjective emotional state are r

97 ted with social interaction help to motivate social behaviour and influence preferences for different

98 marizes recent studies in the epigenetics of social behaviour and offers perspectives on emerging tre

99 le is known of the link between personality, social behaviour and population structure.

100 scourse comprehension is a hallmark of human social behaviour and refers to the act of interpreting a

101 fied neuroligin as an important regulator of social behaviour and segregate the importance of this ge

102 tification, and the group had impairments in social behaviour and significant changes in their subjec

103 in humans including emotion identification, social behaviour and subjective emotional state, and tha

104 e consistent with a role of JH in modulating social behaviour and suggest that eusocial evolution was

105 e importance of between-group variability in social behaviour and the impact of replication on hypoth

106 that PX-RICS-deficient mice exhibit ASD-like social behaviours and ASD-related comorbidities.

107 es, including virulence, stress tolerance or social behaviours and biofilm development.

108 educed the empathy perception gap, increased social behaviours and expanded social networks months la

109 eurons controlling homeostatic functions and social behaviours and lay ground for examining the dynam

110 aride (LPS) injections affects two different social behaviours and three alternate measures of social

111 ng videos and distinguish both positive (pro-social behaviour) and negative (anxiety, depression, pee

112 ant role in the evolution and maintenance of social behaviour, and 'helpers' can maximize indirect fi

113 pression identification, had some changes in social behaviour, and had significant changes in their s

114 xpression identification, had some change in social behaviour, and had significant changes in their s

115 nd face emotional expression identification, social behaviour, and the subjective experience of emoti

116 language development, positive and negative social behaviours, and independence; parenting risk; hom

117 ity to explore whether widespread changes in social behaviour are associated with changes in automati

118 emical changes underlying human emotions and social behaviour are largely unknown.

119 In particular, while changes in social behaviour are prominent in bvFTD alone, there may

120 Inappropriate social behaviours are early and distinctive symptoms of

121 he responding neurons that regulate specific social behaviours are largely unknown.

122 Social behaviours are not localized to subdivisions of t

123 dified landscapes is especially important as social behaviours are simultaneously threatened by human

124 ssible role in processing whether particular social behaviours are, or are not, appropriate.

125 the mouse hypothalamus, that underlie innate social behaviours, are shaped by social experience.

126 n shown to affect social group structure and social behaviour as well as individual fitness of the pr

127 avioural classification system, LABORAS) and social behaviour (as a measure of anxiety) in rats follo

128 reproductive physiology and numerous related social behaviours, as do oxytocin (mammals) and its homo

129 neurodevelopmental condition affecting early social behaviour, but links to underlying social brain f

130 re key determinants of individuals' observed social behaviour, but quantifying these spatial componen

131 vered do not include frequency dependence or social behaviour, but the approach is capable of extensi

132 populations, with potential implications for social behaviour by increasing the number of potential i

133 The coordination of social behaviours by RMG suggests an anatomical hub-and-

134 om appetitive to consummatory phases of male social behaviours by shaping sex- and behaviour-specific

135 rithmic level, and that changing the goal of social behaviour can also change social specificity.

136 Likewise, variation in social behaviour can dictate climate responses.

137 In the nests of these societies, collective social behaviours can modify the patterns of individual

138 This demonstrates that simple social behaviours can result in the repression of consis

139 r emotion prediction errors potently guiding social behaviours challenge standard decision-making mod

140 d executed commands(1,2) and is critical for social behaviours, cognition and emotion(3-6).

141 iverse range of functions including anxiety, social behaviour, cognitive activities and nociception.

142 ver, show that emotion expressions shape pro-social behaviour, communicate one's intentions to others

143 s of human conditions comorbid with impaired social behaviour, could offer new and natural avenues fo

144 Human social behaviour crucially depends on our ability to rea

145 nflammation can ameliorate the expression of social behaviour deficits by directly affecting neuronal

146 ie the beneficial effects of inflammation on social behaviour deficits in mice.

147 We establish that the social behaviour deficits in offspring exposed to MIA ca

148 These mice show ASD-resembling social behaviour deficits.

149 has established that effects of hormones on social behaviour depend on characteristics of both indiv

150 lations regulating homeostatic functions and social behaviours develop during these transitions remai

151 When we tested social behaviour directly, Cplx1(-/-) mice failed to dem

152 files, showed higher levels of inappropriate social behaviours ('disinhibition') and demonstrated mor

153 This is partly because social behaviours do not fossilize, making it difficult

154 ion neurons, including those involved in non-social behaviours, drive male interactions with the fema

155 ffect of non-pharmaceutical interventions on social behaviour during disease outbreaks, epidemics, an

156 alized in the cellular level for the initial social behaviour during postnatal developmental stage.

157 ions), false beliefs (delusions) and deviant social behaviour (e.g. loss of interest in others, bizar

158 'social concepts' (i.e. concepts describing social behaviour: e.g. 'polite', 'stingy') as compared w

159 Innate social behaviours emerge from neuronal circuits that int

160 agents has a positive or negative impact on social behaviour, equality and cooperation in such a dil

161 Evidence of a snapshot of social behaviour, especially parental care, can be deter

162 ave implicated the amygdala in emotional and social behaviours, especially those related to fear and

163 ility of detecting treatment differences for social behaviours even if the total number of animals wa

164 How social behaviours evolve remains one of the most debated

165 al of sociobiology is to explain how complex social behaviour evolves, especially in social insects,

166 in hunger or inebriation state affected the social behaviours exhibited by two closely-related nestm

167 r associated with genetic variation in a non-social behaviour: explorative genotypes elicited most ag

168 During social behaviours, flies need to focus on nearby flies(9

169 asopressin (AVP) seem to modulate a range of social behaviour from parental care to mate guarding.

170 tional facial expressions, its role in human social behaviour has remained unclear.

171 ficance of non-social selection pressures on social behaviours has received little attention.

172 thways that underlie microbial influences on social behaviour have implicated brain regions and circu

173 volved in higher-order cognition and complex social behaviours, have identified true and potential hu

174 an Syndrome (AS) to identify Ube3a-dependent social behaviours, highlighting potential cross-species

175 anthropopressure (fishing activity), risking social behaviour impairment in exposed dolphins.

176 Across 36 datasets of spatial and social behaviour in >58,000 individual animals, spanning

177 behaviour, representing the first example of social behaviour in a Mesozoic mammal.

178 he evolution of communication, cognition and social behaviour in apes at the University of St Andrews

179 al circuit that regulates parental-offspring social behaviour in C. elegans and that this provides ev

180 ngs provide the earliest evidence of complex social behaviour in Dinosauria, predating previous recor

181 The impairment of social behaviour in FTD has typically been attributed to

182 ly insults could result in severely impaired social behaviour in later childhood and adolescence.

183 can be an important mediator of variation in social behaviour in lizards, even overriding the influen

184 Understanding the neurobiology of social behaviour in mammals has been considerably advanc

185 vasopressin(4-6), which regulate aspects of social behaviour in mammals(7).

186 Infections can change social behaviour in multiple ways, with profound impacts

187 model for understanding memory, learning and social behaviour in neonate animals.

188 on interactions in humans, and mechanisms of social behaviour in non-human primates, and may have imp

189 al reproductive traits gives rise to complex social behaviour in non-reproductive helpers.

190 Acute intranasal OT at 0.3 IU improved social behaviour in Oprm1(-/-) mice 5 min after administ

191 and virulence is crucially dependent on the social behaviour in question.

192 ver was used to investigate the evolution of social behaviour in repeated Prisoner's Dilemma, Chicken

193 siological state influences food sharing and social behaviour in social insects is poorly understood.

194 with an externalist account that understands social behaviour in terms of its environment-involving d

195 full-length mutant protein display abnormal social behaviour in the absence of acute neurodegenerati

196 x social skills, little is known about their social behaviour in the wild.

197 ction, and initiating a surprising degree of social behaviour in these mostly solitary animals.

198 ffers new perspectives on the key drivers of social behaviour in wild populations.

199 the spread of disease and the prevalence of social behaviour in wildlife.

200 individuals may benefit from altering their social behaviours in a context-dependent manner.

201 apted ecotypes and cryptic morphs, divergent social behaviours in birds and insects, as well as alter

202 on of oxytocin temporally mitigates autistic social behaviours in experimental settings, it remains i

203 pamine availability has been shown to change social behaviours in experimental tasks, and dopamine de

204 not only explains the observed impairment of social behaviours in FTD, but also assimilates both cons

205 functionally associated with species-typical social behaviours in male vertebrates.

206 essures and host-pathogen interactions alter social behaviours in many animals(1-4).

207 vasopressin influences male reproductive and social behaviours in several vertebrate taxa through its

208 Social behaviours in species as diverse as honey bees an

209 Social behaviours in termites are regulated by sophistic

210 on and exposure on a range of individual and social behaviours in young adult bees.

211 in has a conserved role in regulating animal social behaviour including parental-offspring interactio

212 acterium Myxococcus xanthus exhibits several social behaviours, including aggregation of cells into s

213 mental disorder characterised by deficits in social behaviour, increased repetitive behaviour, anxiet

214 -wide circuits that coordinate affective and social behaviours intersect in the amygdala.

215 developments for collecting data remotely on social behaviour involve indirect inference of associati

216 daptive caloric intake, and those regulating social behaviours, involve related circuitry(4-7), but t

217 Although friendship as a social behaviour is an evolved trait that shares many si

218 The conflict between pro-self and pro-social behaviour is at the core of many key problems of

219 and psychiatric disorders in which disturbed social behaviour is commonplace.

220 Human social behaviour is complex, and the biological and neur

221 Social behaviour is coordinated by a network of brain re

222 In mice, social behaviour is driven by pheromones, chemical signa

223 Knowledge of social behaviour is essential for appropriate social con

224 auma impairs brain reward function such that social behaviour is no longer rewarding, leading to seve

225 Social behaviour is substantially shaped by internal phy

226 An essential component of well-adjusted social behaviour is the ability to update our beliefs ab

227 the causes of individual-level variation in social behaviours is crucial for understanding the evolu

228 n for its role in lactation, parturition and social behaviours--is required for proper muscle tissue

229 ice exhibit enlarged ventricles and impaired social behaviour, locomotor activity, and learning and m

230 ma, a species with marked sex differences in social behaviour, mating strategies and foraging.

231 These sex differences in social behaviour may underpin male-biased acquisition of

232 se in the non-SSLP areas, with more positive social behaviour (mean difference 0.45, 95% CI 0.09 to 0

233 Empathy is a complex social behaviour mediated by a network of brain structur

234 o norm violations are two important forms of social behaviour modelled in economic games.

235 cific mirroring responses to specific infant social behaviours (modified mirroring to communicative s

236 Moreover, selection on social behaviours occurred at a local scale ('soft selec

237 The social behaviour of F. primaevus suggests that the capac

238 teractions that are an important part of the social behaviour of M. xanthus.

239 Finally, improvements in the social behaviour of Oprm1(-/-) mice were greater and lon

240 Learning social behaviour of others strongly influences one's own

241 have profound effects on the demography and social behaviour of tetrapods.

242 ged individuals were recorded along with the social behaviour of their groups.

243 estigate this, we examined the cognitive and social behaviours of complexin 1 knockout mice (Cplx1(-/

244 asuring the locomotion, feeding, arousal and social behaviours of groups of mice or rats, we show tha

245 R pathway and rescues neuronal responses and social behaviours of male Cttnbp2 mutant mice.

246 fects of prenatal glucocorticoid exposure on social behaviour: offspring from glucocorticoid-treated

247 19 data as well as external factors (such as social behaviour or climate variables), to develop predi

248 he group did not have significant changes in social behaviour or in their subjective emotional state.

249 ive and neural processes are specialised for social behaviour, or are shared with other 'non-social'

250 stering of organisms can be a consequence of social behaviour, or of the response of individuals to c

251 tes are inherently associated with a complex social behaviour, parenting.

252 ant implications for the evolution of animal social behaviour, particularly complex interactions such

253 over a causal mechanism for pathogen-induced social behaviour plasticity, which can promote genetic d

254 tic and neural circuits can profoundly alter social behaviour, providing a potential molecular mechan

255 uggests that testosterone enhances strategic social behaviour rather than dominance seeking behaviour

256 Across species, a major axis of variation in social behaviour relates to how offspring are reared.

257 ional modelling suggests that these adaptive social behaviours rely on mental representations of info

258 consolidation and learning; and (iv) mediate social behaviours, reproduction and embryonic developmen

259 Differentiated social behaviours should be favoured for fast life histo

260 However, primate social behaviour shows strong evidence for phylogenetic

261 of neural activity in brain areas linked to social behaviour, social cue processing, and anxiety/str

262 ., changes in activity, foraging, vigilance, social behaviour, space use, and reproductive behaviour)

263 ers of the same species, as cues to regulate social behaviours such as pup suckling, aggression and m

264 emotion-like states, which may be linked to social behaviours such as rescuing others from danger.

265 individuals is essential to many aspects of social behaviour, such as the maintenance of stable soci

266 es are shaped by valuation of other people's social behaviour, such that they empathize with fair opp

267 Social behaviours, such as aggression or mating, proceed

268 ons as components of pheromones that mediate social behaviours, such as caste and nestmate recognitio

269 Microorganisms are capable of remarkable social behaviours, such as forming transient multicellul

270 Infants adaptively modulate their social behaviours, such as gaze-following, to social con

271 Innate social behaviours, such as mating and fighting, are fund

272 Elephant social behaviour suggests that individuals use odour to

273 The ease of finding anti-social behaviours suggests that cheaters may be common i

274 on in the sign and magnitude of selection on social behaviour than that experienced by static charact

275 a crucial determining effect on the type of social behaviour that evolves.

276 Biofilm formation is a social behaviour that generates favourable conditions fo

277 a gustatory-olfactory aspect of early infant social behaviour that is, in part, reliant on pre-natal

278 a unified neurocognitive model of controlled social behaviour that not only explains the observed imp

279 Mating and aggression are innate social behaviours that are controlled by subcortical cir

280 Social behaviours that benefit survival can promote slow

281 Effects of sickness should be lower for social behaviours that bestow greater benefits to inclus

282 ttle is known about its consequences for the social behaviours that hold society and democracy togeth

283 ore rigidly determined altricial patterns of social behaviour, the roles of post-reproductive group m

284 By linking landscape genetics and social behaviour, the social resistance hypothesis gener

285 language can reveal clues to their emotions, social behaviours, thinking styles, cultures and the wor

286 sian comparative methods to infer changes in social behaviour through time, thereby allowing us to ev

287 xis, and show that the microbiome can affect social behaviours through discrete neuronal circuits tha

288 f three interventions: a theory of normative social behaviour (TNSB) intervention, including provisio

289 for localized strategies based on feral pig social behaviour to enhance global control efforts.

290 onstrating that individuals can adjust their social behaviours to match experienced conditions.

291 However, although mice show different social behaviours towards adults, juveniles and neonates

292 Consider the range of social behaviours we engage in every day.

293 for measuring individual motor behaviour and social behaviour, we found that behaviours such as anten

294 pecialized circuits may grant specificity to social behaviours, whereas multidimensional processing f

295 changes in home cage behaviour and decreased social behaviour which, in contrast to motor function, a

296 ticularly dramatic when negatively affecting social behaviour, which fundamentally determines individ

297 s vary in home range-associated foraging and social behaviours, which may increase the spread and int

298 ccur because of within-individual changes in social behaviour, with correlated changes in spatial beh

299 haviours, deficits in cognition and atypical social behaviours, with the greatest impact on male offs

300 eses linking sexual dimorphism, ontogeny and social behaviour within this taxon, and clarifies hypoth