ライフサイエンスコーパス: social behavior

1 circuit whose disrupted development affects social behavior.

2 in (5-HT) is critical for several aspects of social behavior.

3 al changes in social brain to development of social behavior.

4 pecific genes currently known to function in social behavior.

5 al ecology that negatively impacts offspring social behavior.

6 ship; hormones both influence and respond to social behavior.

7 nitive and motor dysfunction and deficits in social behavior.

8 f this peptide with various aspects of human social behavior.

9 ong basis in the fundamental neurobiology of social behavior.

10 lterations in circuit function and cognitive/social behavior.

11 ntial strategy for reversing depressive-like social behavior.

12 hers' pain is critical for understanding pro-social behavior.

13 is generally attributed to their remarkable social behavior.

14 from residual CCK-INTs and displayed altered social behavior.

15 systemic diazepam, which failed to increase social behavior.

16 abnormal measures of anxiety, depression and social behavior.

17 c conditions characterized by impairments in social behavior.

18 Oxytocin (OXT) modulates several aspects of social behavior.

19 limbic reward system known to be involved in social behavior.

20 Activation of the BLA but not CeA suppressed social behavior.

21 potential means of reversing depressive-like social behavior.

22 sought to understand how sex moderates human social behavior.

23 ns, Purkinje cells, and impairments in later social behavior.

24 s may be responsible for adaptive changes in social behavior.

25 in in conditions characterized with aberrant social behavior.

26 and correlations between brain responses and social behavior.

27 xiety, and are emerging as factors affecting social behavior.

28 ce after seizures displayed an impairment in social behavior.

29 rk that links changes in the CRF system with social behavior.

30 what contribution, if any, the ACC makes to social behavior.

31 mygdala are associated with perturbations in social behavior.

32 in the prefrontal cortex, thereby modulating social behavior.

33 ly prosocial effect of testosterone on human social behavior.

34 reviously reported autism model), influences social behavior.

35 ction, pain sensitivity, and, more recently, social behavior.

36 tests of discrimination learning, and infant social behavior.

37 mole-rat species with diametrically opposed social behavior.

38 ting a role for these neuropeptides in human social behavior.

39 enses for vertebrates regarding foraging and social behavior.

40 ies for treating patients with dysfunctional social behavior.

41 s into the mechanisms by which status guides social behavior.

42 of which are characterized by dysfunctional social behavior.

43 he left hemisphere control stress effects on social behavior.

44 ognition influence human decision making and social behavior.

45 ivity relates to a key real-world measure of social behavior.

46 ing strategies are crucial for understanding social behavior.

47 ffective interpretation of those actions for social behavior.

48 chanistic dissection of communication during social behavior.

49 l activity in limbic brain regions linked to social behavior.

50 2 levels, in association with alterations in social behavior.

51 he mPFC and CA3 hippocampus on cognitive and social behavior.

52 ntually higher-level cognitive processes and social behavior.

53 rates that questioning its existence impacts social behavior.

54 unctional consequences for the regulation of social behavior.

55 h brain and behavioral phenotypes, including social behavior.

56 ories, sensory and cognitive processing, and social behavior.

57 nxiety and social reward, two key aspects of social behavior.

58 ry olfactory system guides the expression of social behavior.

59 the prefrontal cortex can control and adapt social behavior.

60 three hits showed deficits in this aspect of social behavior.

61 texture novel object recognition and altered social behavior.

62 depression, cognition, stress response, and social behavior.

63 part of descending PFC pathways that control social behavior.

64 des implicated in motivational goal-directed social behavior.

65 t macronutrient compositions modulated human social behavior.

66 ze others' actions is an important aspect of social behavior.

67 s synaptic function, memory acquisition, and social behavior.

68 e female VMHvl that are involved in distinct social behaviors.

69 or profiles on brain areas involved in these social behaviors.

70 lved mechanisms dedicated to control complex social behaviors.

71 onverge and interact to coordinate divergent social behaviors.

72 tem as a potential cause of species-specific social behaviors.

73 sorimotor gating, discrimination memory, and social behaviors.

74 te causal factors of evolutionarily diverged social behaviors.

75 lved in the regulation of human and nonhuman social behaviors.

76 issociable modules to pattern and coordinate social behaviors.

77 algorithm to classify several well-described social behaviors.

78 tural investigation of odors associated with social behaviors.

79 personal preferences affect a broad array of social behaviors.

80 ehaviors, including anxiety, repetitive, and social behaviors.

81 as well as for correct sensory learning and social behaviors.

82 tion of this circuit reversed these impaired social behaviors.

83 de oxytocin has been linked to a plethora of social behaviors.

84 t effect does activation of amygdala have on social behavior?

85 and basolateral amygdala (BLA) in regulating social behavior?

86 hat differ in pigmentation and components of social behavior [3-5].

87 facilitate motor readiness to join in during social behavior [9-11].

88 emonstrate cognitive deficits, autistic-like social behavior, aberrations in synaptic plasticity, an

89 uropsychiatric disorders that have prominent social behavior abnormalities are autism spectrum disord

90 exploration to enhance our understanding of social behavior abnormalities.

91 environments, and integrate observations of social behavior across ecological contexts.

92 h allows for rapid, automated measurement of social behaviors across diverse experimental designs and

93 ifferences, with either brash or circumspect social behavior advantageous to secure mating opportunit

94 ysiology may contribute to the disruption of social behavior after developmental social deprivation,

95 this review summarizes evidence showing that social behavior also regulates aspects of inflammatory a

96 Inhibition of either structure increased social behavior, although the effect was greater followi

97 links between ASDs and typical variation in social behavior and adaptive functioning.

98 conditional Pten mouse models have impaired social behavior and brain development.

99 n conventional testing paradigms, marmosets' social behavior and cognition are more similar to that o

100 p CB1R transmission strongly disrupts normal social behavior and cognition.

101 , we describe key facets of marmoset natural social behavior and demonstrate that emerging behavioral

102 The human frontal lobe is important for social behavior and executive function; it has increased

103 orco mutants exhibit severe deficiencies in social behavior and fitness, suggesting they are unable

104 mammalian species, including humans, exhibit social behavior and form complex social groups.

105 is the extent to which associations between social behavior and gene expression are conserved among

106 sociogenomics explores the relations between social behavior and genome structure and function.

107 ectionally modulate PFC activity and measure social behavior and global functional magnetic resonance

108 arding IN-OT effects on typical and atypical social behavior and guide future experiments (e.g., rega

109 activity contributes to a predisposition for social behavior and how this is modulated by narcissisti

110 The amygdala is a critical mediator of social behavior and is implicated in social symptoms of

111 l week was sufficient to prevent deficits in social behavior and learning abilities in adult mutant m

112 PFC activation suppressed social behavior and modulated activity in a number of re

113 he complexities of life histories, including social behavior and multicellularity, can only be unders

114 d atypicalities in brain regions involved in social behavior and other core ASD-related behavioral de

115 ht a key role for brain energy metabolism in social behavior and point to mitochondrial function in t

116 emale mice exposed to ES displayed decreased social behavior and preference for sucrose, along with i

117 ulation dynamics to model the coevolution of social behavior and recognition.

118 central role in the regulation of mammalian social behavior and relationships.

119 ionship between intrinsic brain activity and social behavior and show how personality could contribut

120 ights open new vistas on the neural basis of social behavior and social impairment.

121 ates executive function, sensory gating, and social behavior and that attention deficit hyperactivity

122 tures of this framework using the example of social behavior and the neural circuitry of aggression.

123 ala (MeA) is a key region for performance of social behaviors and still undergoes maturation during t

124 MA and its enantiomers increased affiliative social behaviors and vocalizations, whereas methamphetam

125 re -1.7 SD for cognitive ability, 2.2 SD for social behavior, and -1.3 SD for neuromotor performance

126 and to have differential effects on anxiety, social behavior, and depressive-like signs.

127 complex behaviors ranging from food intake, social behavior, and even pathological conditions, such

128 om defeated donors showed less anxiety, more social behavior, and increased hippocampal cell prolifer

129 in mice causes impaired cognition, abnormal social behavior, and microcephaly in accordance with the

130 mine-disrupted prepulse inhibition, improved social behavior, and novel object recognition memory in

131 ut seizures, gait abnormalities, problems of social behavior, and other variable features.

132 eference in infancy, forced swim test (FST), social behavior, and sexual motivation in adulthood-in t

133 essential neurologic processes such as mood, social behavior, and sleep.

134 behavioral testing, including assessment of social behaviors, and corticostriatal functional connect

135 increases in reward thresholds, decreases in social behaviors, and decreases in correct responses and

136 rs, ground neural synchrony in key nonverbal social behaviors, and highlight the role of human attach

137 s, and produced elevated anxiety, attenuated social behaviors, and impaired hippocampus-dependent lea

138 ytocin (OT) is associated with a plethora of social behaviors, and is a key topic at the intersection

139 5 and Oxtr in the the regulation of discrete social behaviors, and suggest that deficits in social in

140 VPA-treated rats exhibited impairments in social behaviors, and this difference was more pronounce

141 texts, including our tendencies for mindless social behaviors, anthropomorphism, uncanny feelings tow

142 ce now shows that inflammatory processes and social behavior are actually powerful regulators of one

143 ons of the co-regulation of inflammation and social behavior are discussed.

144 Various aspects of social behavior are influenced by the highly conserved c

145 and suggest that the molecular hallmarks of social behavior are likely to differ with the level of s

146 immune system and the processes that govern social behavior are separate, non-communicating entities

147 MDMA-induced increases in social behaviors are 5-HT2A, but not 5-HT1A, receptor de

148 Social behaviors are crucial to all mammals.

149 sive behaviors in the fruit fly, while other social behaviors are unaffected.

150 rimination, broadly defined as alteration of social behavior as a function of genetic relatedness amo

151 erpinnings of this developmentally important social behavior, as well as the mechanism of action of t

152 ehaviors established linkage to two loci for social behaviors (at 14q and 15q) and one locus for repe

153 exaggerated protein synthesis, inappropriate social behavior, behavioral inflexibility, altered dendr

154 lead to irreproducible assessment of murine social behavior between laboratories.

155 e models produced FST deficits and decreased social behavior, but did not change sexual motivation.

156 ated the prefrontal cortex in the control of social behavior, but the neural circuits that mediate th

157 Marijuana exerts profound effects on human social behavior, but the neural substrates underlying su

158 with changes in circadian, reproductive, and social behavior, but whether these animals also suffer f

159 Thus caspase-3 is essential for a subset of social behaviors, but despite similar hyper-locomotion i

160 romodulators and genetic factors involved in social behaviors, but mechanistic understanding of gende

161 to have an important role in the increase in social behaviors, but the mechanisms underlying these ef

162 er systems are involved in the expression of social behaviors, but their individual roles in specific

163 demonstrates significant modulation of adult social behavior by both of these neuropeptides and their

164 ormation within the PL-NAc may contribute to social behavior by supporting social-spatial learning.

165 with ASD made from thin slices of real-world social behavior by typically-developing observers are no

166 ommunication networks and demonstrating that social behavior can be predicted with high precision.

167 Kin selection theory, as an explanation for social behavior, can benefit from much greater explorati

168 more attention to the dynamics of human and social behavior change.

169 ndogenous peptide well known for its role in social behaviors, childbirth, and lactation, is a promis

170 preoptic area (mPOA), an essential node for social behaviors, comprises molecularly diverse neurons

171 This kind-selective social behavior could provide immediate fitness benefits

172 ject recognition memory, partially normalize social behavior, decrease conditioned avoidance respondi

173 tation of the maternal odors rescued FST and social behavior deficits induced by early-life abuse and

174 een shown to differentially regulate diverse social behaviors, depending on the age and/or sex of the

175 in Awash, Ethiopia, which differ markedly in social behavior despite evolutionary propinquity.

176 concerning various features of ant and human social behavior do not adequately reflect present knowle

177 concerning various features of ant and human social behavior do not reflect adequately the present kn

178 eals that OT plays a crucial role in setting social behaviors during a period just after birth.

179 tic function and plasticity, energy balance, social behaviors, emotions, and cognition.

180 g to potentially include spatial navigation, social behavior, feeding and reward.

181 number of physiological functions as well as social behavior following the binding of its agonist, va

182 show MDMA-specific increases in affiliative social behaviors following MDMA administration, in conco

183 map the neural substrates of locomotion and social behaviors for Drosophila melanogaster using autom

184 he contribution of a specific OXT cluster to social behavior from the general otpa(-/-) deficits.

185 The study of insect social behavior has offered tremendous insight into the

186 Deciphering the neural mechanisms of social behavior has propelled the growth of social neuro

187 rated Arid1b heterozygous mice, which showed social behavior impairment, altered vocalization, anxiet

188 Aggression is a universal social behavior important for the acquisition of food, m

189 l stimuli that contributes to development of social behavior in adulthood.

190 Here we review the unique properties of social behavior in ASD and WS, and discuss the major the

191 onally, brain responses were associated with social behavior in boys but not in girls.

192 ption are tightly associated with changes in social behavior in halictid bees.

193 dy of literature has examined its effects on social behavior in humans.

194 T consistently influences a wide spectrum of social behavior in humans.

195 Analysis of social behavior in juvenile animals indicated that there

196 an OT receptor (OTR) antagonist L-368,899 on social behavior in male and female California mice expos

197 hat climate is likely to affect individuals' social behavior in many ways.

198 ult in long-term alterations in activity and social behavior in mice.

199 Compensatory social behavior in nonhuman animals following maternal l

200 e separate roles of the amygdaloid nuclei in social behavior in primates.

201 SD and WS, and discuss the major theories in social behavior in the context of these disorders.

202 lution to this tension-and the adaptation of social behavior in this game-hinges on the game's learni

203 Conversely, inhibiting these cells enhances social behavior in VPA-exposed mice.

204 are capable of acoustic duetting, a complex social behavior in which males and females tightly contr

205 inputs to the vHPC are capable of modulating social behaviors in a bidirectional manner.

206 , and controls the overt expression of these social behaviors in a threshold-dependent, inverse manne

207 een implicated in the regulation of numerous social behaviors in adult and juvenile animals.

208 Further, the rescue of social behaviors in an ASD mouse model suggests that inv

209 ements of spontaneous, ecologically relevant social behaviors in group-housed animals.

210 g direct evidence consistent with human-like social behaviors in H. erectus.

211 Game theory describes social behaviors in humans and other biological organism

212 tosis and neural plasticity, alters specific social behaviors in male mice, while leaving females una

213 n regions that might mediate visually guided social behaviors in males.

214 ed, quantitative, and accurate assessment of social behaviors in mammalian animal models has limited

215 lacking oxytocin, a neuropeptide modulating social behaviors in many species.

216 st evidence that oxytocin increases positive social behaviors in newborns.

217 social and emotional content elicit natural social behaviors in primates.

218 d the hormonally modulated timely display of social behaviors in rats.

219 The neural control of social behaviors in rodents requires the encoding of phe

220 Exogenous oxytocin promotes social behaviors in several species, including human and

221 Myxobacteria are known for complex social behaviors including outer membrane exchange (OME)

222 e neural and molecular mechanisms underlying social behavior - including their functional significanc

223 sets will become an essential model of human social behavior, including its dysfunction in neuropsych

224 hy may be key for understanding disorders of social behavior, including psychopathy and autism.

225 ome segregation, sporulation, aerotaxis, and social behaviors, including luminescence as well as biof

226 whereas physical EE has negative effects on social behavior indicates that preclinical studies focus

227 or automatic detection and quantification of social behaviors involving close and dynamic interaction

228 Social behavior is a basic behavior mediated by multiple

229 psychiatric disorders.SIGNIFICANCE STATEMENT Social behavior is largely controlled by brain neuromodu

230 Social behavior is often shaped by the rich storehouse o

231 The shift from solitary to social behavior is one of the major evolutionary transit

232 , indicating that the genomic basis for this social behavior is relatively specific to honey bees.

233 , the impact of this variability on specific social behaviors is unknown.

234 hether such a capacity can coevolve with the social behavior it supports.

235 al prefrontal cortex) has been implicated in social behavior, it is not clear which neurons are relev

236 individual, sex, and species differences in social behavior later in life.

237 vidence that inflammatory processes regulate social behavior, leading to characteristic changes that

238 s, anxiety, repetitive-stereotyped behavior, social behavior, learning and memory.

239 Complex social behaviors lie at the heart of many of the challen

240 els have shown that amygdala is critical for social behavior, many of these studies contradict one an

241 3Dq was used to induce PFC activation during social behavior measured in the three-chamber sociabilit

242 as arousal, but whether they control complex social behaviors more specifically is not clear.

243 tic tectum, as well as in a few nodes in the social behavior network, including cell populations that

244 ical node in the highly conserved vertebrate social behavior network.

245 ted brain regions known collectively as the "social behavior neural network" (SBNN).

246 ss may adversely impact cognition and future social behavior of adolescents.

247 geometries on the subcellular structure and social behavior of bacteria.

248 f plants and freshwater shapes the diets and social behavior of chimpanzees, our closest living relat

249 - and 40-fold gain in potency in vivo in the social behavior of mice and zebrafish.

250 We focused on the social behavior of outer membrane exchange (OME), in whi

251 review emphasizes recent discoveries in the social behavior of outer membrane exchange, wherein kin

252 es of microhabitat and functional niche, the social behavior of termites reduces the stochastic eleme

253 the physical characteristics, movement, and social behaviors of dozens of interacting free-moving ne

254 t is exceedingly difficult to understand the social behaviors of fossil hominins directly from fossil

255 ecause these two molecules are important for social behavior, our study sheds light on the specific n

256 o be implicated in the regulation of complex social behavior, particularly empathy and parenting.

257 als use acoustic signals across a variety of social behaviors, particularly courtship.

258 ant perception, reproductive physiology, and social behavior plasticity.

259 ytocin, a neuropeptide implicated in various social behaviors, plays a crucial role in the formation

260 d domains of psychopathology (indiscriminate social behavior, posttraumatic stress disorder, attentio

261 al. (2016) find that stress-induced abnormal social behavior reflects aberrant prefrontal regulation

262 re hindering progress in the study of insect social behavior remain.

263 ween genetic variation, neurophysiology, and social behavior remains a challenge.

264 Understanding the complexity of social behavior requires integration across levels of an

265 Adaptive social behavior requires transmission and reception of s

266 nipulate the primate amygdala for effects on social behavior, revealed that (1) the amygdala, as a cr

267 s, trade-offs in the fitness consequences of social behaviors seem to promote neuronal and molecular

268 Individual variation in social behavior seems ubiquitous, but we know little abo

269 anasal OT influences a large number of human social behaviors should be viewed with healthy skepticis

270 genic GFAP-thymidine kinase rats resulted in social behavior similar to disrupted rats.

271 elationships among many brain regions during social behavior, simultaneously recording activity along

272 domains: cognitive ability (Full-Scale IQ), social behavior (Social Responsiveness Scale), and neuro

273 nergy balance, as well as neuromodulation of social behavior, stress regulation, and associative lear

274 w that oxytocin modulates various aspects of social behaviors such as empathy, trust, in-group prefer

275 Oxytocin is a neuropeptide important for social behaviors such as maternal care and parent-infant

276 neuropeptide that mediates complex mammalian social behaviors such as pair bonding, social recognitio

277 his happens in several key brain regions for social behavior, such as the amygdala and insula.

278 n important role in both normal and abnormal social behavior, such that targeting these cells can eli

279 owed the emergence of taxon-specific complex social behaviors, such as intense parental care in the C

280 Similarly, patterns of social behavior that distinguish modern humans from othe

281 ences of ultrasociality, an advanced form of social behavior that evolved independently in both socia

282 xperimental work in an invertebrate model of social behavior, the honey bee, revealed distinct brain

283 nstream regions that have been implicated in social behavior: the nucleus accumbens (NAc), amygdala,

284 al predictions is essential for constructive social behavior, their single neuronal basis and causal

285 thology and individual differences in insect social behavior, thus providing an example of how compar

286 and theory on climate-related variables and social behavior to allow for both positive and negative

287 Natural selection designs some social behaviors to depend on flexible learning processe

288 ased on time spent by adult mice engaging in social behaviors toward a juvenile mouse, compared with

289 ross time, and, crucially, they rarely study social behavior under naturalistic circumstances.

290 rences in Oxtr expression in the brain drive social behavior variation.

291 Social behavior was assessed 2 weeks later using a three

292 Social behavior was assessed using Crowleys sociability

293 tential habituation to broadcasted calls and social behavior, we developed a hierarchical observation

294 mechanisms by which chemoreceptors regulate social behaviors, we investigated the roles of a critica

295 Deficits in social behavior were observed in both sexes.

296 and also for understanding the evolution of social behaviors, which has been challenging for evoluti

297 zygous mice exhibited abnormal cognitive and social behaviors, which were rescued by treatment with a

298 nist attenuated the MDMA-induced increase in social behaviors, while a 5-HT1A receptor antagonist did

299 mislocalization of Pten causes inappropriate social behavior with intact learning and memory, a profi

300 neural basis of healthy and disturbed human social behavior with minimal a priori assumptions.