ライフサイエンスコーパス: social behavior

1 ate attack frequency, both with no effect on social behavior.

2 to modulate the mesolimbic reward system and social behavior.

3 coccus xanthus is a model bacterium to study social behavior.

4 echanism and demonstrate its contribution to social behavior.

5 led aberrant regulation of genes involved in social behavior.

6 des a useful and generative account of human social behavior.

7 d memory, anxiety and stress regulation, and social behavior.

8 Stress changes our social behavior.

9 not address the neural mediation of complex social behavior.

10 llum in controlling the reward circuitry and social behavior.

11 rontal cortex (PFC), a structure involved in social behavior.

12 is influenced by numerous factors, including social behavior.

13 cal circuit modulating aversion, reward, and social behavior.

14 anism that contributes to motor function and social behavior.

15 an important transitional period in hominin social behavior.

16 and sensory function to regulate escape and social behavior.

17 uster important in governing male and female social behavior.

18 USV production without disrupting non-vocal social behavior.

19 h brain and behavioral phenotypes, including social behavior.

20 ry olfactory system guides the expression of social behavior.

21 nderlie seasonal variation in human mood and social behavior.

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

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

24 g motor patterning, homeostatic control, and social behavior.

25 ntually higher-level cognitive processes and social behavior.

26 rates that questioning its existence impacts social behavior.

27 unctional consequences for the regulation of social behavior.

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

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

30 the prefrontal cortex can control and adapt social behavior.

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

32 texture novel object recognition and altered social behavior.

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

34 part of descending PFC pathways that control social behavior.

35 des implicated in motivational goal-directed social behavior.

36 t macronutrient compositions modulated human social behavior.

37 ether mindfulness meditation might alter pro-social behavior.

38 pyramidal neurons (PNs) in male mice during social behavior.

39 e a tipping point in the evolution of larval social behavior.

40 cial effects of total P2X7R depletion on the social behavior.

41 l individual (G(i)) in the regulation of its social behavior.

42 dmPFC-PVI is linked to long-term impacts on social behavior.

43 f OT and naloxone (NAL) to robustly modulate social behavior.

44 forebrain, coinciding with the emergence of social behavior.

45 roves the animals' neurological function and social behavior.

46 estion whether they actually differ in their social behavior.

47 ashort-range communication that shapes mouse social behavior.

48 es in maintaining homeostasis and regulating social behavior.

49 es in regulation of reproductive cycling and social behaviors.

50 ly encodes spatial and sensory cues to drive social behaviors.

51 ese circuits and their downstream effects on social behaviors.

52 d foraging, predator avoidance, and numerous social behaviors.

53 ined the role of LPS O-antigen in M. xanthus social behaviors.

54 ble social environment and engage in complex social behaviors.

55 iety- and depression-like, sensorimotor, and social behaviors.

56 undation for studying its functional role in social behaviors.

57 actions may have influenced the evolution of social behaviors.

58 personal preferences affect a broad array of social behaviors.

59 lved mechanisms dedicated to control complex social behaviors.

60 onverge and interact to coordinate divergent social behaviors.

61 issected brain nuclei that are important for social behaviors.

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

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

64 tion of this circuit reversed these impaired social behaviors.

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

66 ale reproductive state or its role in female social behaviors.

67 (PFC) and establishment of appropriate adult social behaviors.

68 is key to understanding the neurobiology of social behaviors.

69 pituitary and forebrain regions involved in social behaviors.

70 s between early-childhood gut microbiome and social behaviors.

71 o the mechanisms and evolution of vertebrate social behaviors.

72 viors in the domains of 1) communication and social behavior, 2) music consumption, 3) app usage, 4)

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

74 ce pheromone sensitivity, thereby modulating social behavior according to animals' life-history stage

75 tocin (OT) is critical for the expression of social behavior across a wide array of species; however,

76 increasingly implicated in the regulation of social behavior across model organisms.

77 e vomeronasal organ (VNO) mediates important social behaviors across different species, including agg

78 nfluence neurodevelopment and programming of social behaviors across diverse animal species.

79 licated in the regulation of a wide range of social behaviors across taxa.

80 Here, we consider research that examines how social behaviors affect not one, but both partners in a

81 of the most frequently reported and studied social behaviors affected by autism spectrum disorder (A

82 rgeted MR knockout was sufficient to disrupt social behavior and alter behavioral responses to novelt

83 Social behavior and amygdala deficits (volume, neurogene

84 red oxytocin reaches the brain and modulates social behavior and cognition.

85 on neural pathways that are associated with social behavior and connect the prefrontal cortex (PFC)

86 egree of importance of social media in their social behavior and daily routines.

87 We also show that a lack of CD38 alters social behavior and emotional responses.

88 ), in addition to significant alterations in social behavior and executive functions.

89 ToM is engaged ubiquitously in our everyday social behavior and features a specific developmental tr

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

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

92 e we explore the bidirectional links between social behavior and genome architecture by considering v

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

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

95 ating the bidirectional relationship between social behavior and immune signaling and highlight recen

96 Thus, unraveling the link between social behavior and immune signaling is a fundamental ch

97 EIA produced disruptions in social behavior and increases in repetitive behaviors th

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

99 Adaptive social behavior and mental well-being depend on not only

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

101 for native representations of sex in shaping social behavior and reveal a neural mechanism underlying

102 es C), salinity (45ppt), and pH (7.65 pH) on social behavior and sheltering preference in P. argus.

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

104 velopment of forebrain neurons implicated in social behavior and stress.

105 ion of the OT system is necessary to promote social behavior and that mice with abnormal social behav

106 ractions are essential for the expression of social behavior and the development of adaptive social r

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

108 ) has been functionally associated with both social behavior and with domain-general information proc

109 notypes, impaired fear conditioned learning, social behaviors and discrimination memory.

110 tially negatively impact anxiety-related and social behaviors and may do so via different mechanisms

111 experience-dependent plasticity in an innate social behavior, and a potential hormone-dependent basis

112 by reduced anxiety-like behavior, fragmented social behavior, and altered ultrasonic vocalization pat

113 istent with diurnal activity, well-developed social behavior, and cursorial hunting [5].

114 thecoids are highly variable in habitat use, social behavior, and diet, a signature dental feature un

115 elationship between our bodily responses and social behavior, and emphasize the importance of studyin

116 level, we consider how viruses might affect social behavior, and how quarantine, ironically, could m

117 The pituitary neuropeptide oxytocin promotes social behavior, and is a potential adjunct therapy for

118 ase, particularly in regions associated with social behavior, and most intriguingly, around the time

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

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

121 vestibularis, appear to induces deficits in social behaviors, and alters neurotransmitter levels in

122 bilities in functions linked to personality, social behaviors, and cognitive functions.

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

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

125 leus accumbens (NAc) play important roles in social behaviors, and human neuroimaging implicates both

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

127 te that TRPM8 regulates dimorphic sexual and social behaviors, and potentially constitutes a signalos

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

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

130 The mechanisms underlying social behavior are complex, but we now know that immune

131 Interestingly, the effects of L. reuteri on social behavior are not mediated by restoring the compos

132 experience-dependent maturation to regulate social behavior are poorly understood.

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

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

135 Social behaviors are crucial to all mammals.

136 and suggest that tradeoffs between opposing social behaviors are managed at the gene regulatory leve

137 Social behaviors are ubiquitous and crucial to an animal

138 ells was sufficient to reconstruct microbial social behavior, as witnessed by expression of the NO-in

139 gdala and hippocampal deficits and decreased social behavior at PN13.

140 ions at postnatal days 10 to 12 and impaired social behavior at postnatal day 60.

141 nfant/toddler gut microbiome and ASD-related social behaviors at age 3 years.

142 chanistic understanding of the substrates of social behaviors at multiple levels of neurobiology, ran

143 vior, and most intriguingly, around the time social behavior becomes apparent.

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

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

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

147 neurons receive particular inputs to control social behavior by coordinating the responses of the muc

148 ty by postnatal day 15 but failed to restore social behavior by postnatal day 60.

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

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

151 al to evolutionary fitness, animals regulate social behaviors by integrating signals from both their

152 rrect microbial tissue growth and associated social behavior can be reconstructed in culture.

153 Although social behavior can have a strong genetic component, it

154 We propose that social behavior can influence genome architecture via as

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

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

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

158 The African wild dog is known for its highly social behavior, co-ordinated pack predation, and striki

159 ted impairment in selected communicative and social behaviors combined with superior executive functi

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

161 may vary in their genotypes, also influences social behavior, creating the possibility for indirect g

162 Pten mutant mice exhibit social behavior deficits, elevated synaptic inhibition i

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

164 ntal cortex of neonatal Pten mutants rescued social behavior despite exacerbating excessive levels of

165 tocin receptor (OTR) plays critical roles in social behavior development.

166 We end with a special emphasis on social behavior, discuss whether unique GRN organization

167 Aggression is a social behavior essential for securing resources and def

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

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

170 nvestigating the biological basis of primate social behavior from an evolutionary perspective.

171 e Ontology (GO) categories mainly related to social behavior, functional and metabolic adaptive proce

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

173 ies of neuropeptide regulation of vertebrate social behavior have mainly focused on the vasopressin-o

174 social behavior and that mice with abnormal social behavior have reduced numbers of PVH-OT neurons.

175 Mice are used to study the neurobiology of social behavior; however, the extent to which mouse voca

176 signaling and highlight recent work linking social behavior, immune function, and dopaminergic signa

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

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

179 o explore influence of acute oil exposure on social behavior in a gregarious fish native to the Gulf

180 compound was found to improve surrogates of social behavior in adults with autism spectrum disorder

181 ut shoals and tested different components of social behavior in adults.

182 MDMA increases social behavior in animal models and has shown promise i

183 anxiety-like behaviors in males and reduced social behavior in females.

184 n be one of the most important indicators of social behavior in fossil species, but the effects of ti

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

186 dely used to explore mechanisms of mammalian social behavior in health and disease, raising the quest

187 ant methamphetamine (MA), on two measures of social behavior in healthy young adults: (i) responses t

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

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

190 that the ACC has a role in the regulation of social behavior in mice and indicate that ACC dysfunctio

191 er brain development, cognitive ability, and social behavior in mice require the ubiquitin ligase TRI

192 ukin-17 (IL-17) during inflammation promotes social behavior in mouse models of neurodevelopmental di

193 Compensatory social behavior in nonhuman animals following maternal l

194 ersive system in the brain and implicated in social behavior in preclinical models.

195 ic acid receptor-positive modulator improved social behavior in Shank3 mutant mice.

196 lizes to synapses onto neurons implicated in social behavior in the ventral forebrain and show that S

197 Finally, aberrant social behavior in these mice was rescued by administrat

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

199 ven microdroplets that regenerates microbial social behavior in tissues.

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

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

202 olysis of polysaccharides, which can trigger social behaviors in bacteria resulting from the producti

203 different AVT cell types in reproduction and social behaviors in both sexes.

204 dysfunctions and fully corrected deficits in social behaviors in developing mice with lengthy Sevo ex

205 This suggests that group-level social behaviors in drosophilid species are shaped by di

206 ct as a mediator for the negative effects of social behaviors in humans.

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

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

209 in 8 (TRPM8), regulates dimorphic sexual and social behaviors in mice.

210 e that cortical Foxp2 is required for normal social behaviors in mice.

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

212 humans and unspecific paradigms for modeling social behaviors in rodents, our understanding of the mo

213 vel and cell-type-specific instantiations of social behaviors in rodents.

214 ce multiple barriers, including cultural and social behaviors in settings such as academic conference

215 sent sex of other animals and govern ensuing social behaviors in sexually naive males.

216 ing effects of UNC0642 on NMDAR function and social behaviors in Shank3-deficient mice.

217 mplicated in neural mechanisms of vertebrate social behavior including morph-specific actions on voca

218 oject to multiple targets and control innate social behaviors including aggression and mounting.

219 communication is essential for coordinating social behaviors including courtship, mating, parenting,

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

221 (Esr1)) play a causal role in the control of social behaviors, including aggression.

222 Social behaviors, including behaviors directed toward yo

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

224 epertoire of intercellular communication and social behaviors, including quorum sensing (QS).

225 Yet, most real-world social behaviors involve dynamic, coevolving decisions b

226 ve patterns, physical activity, and emerging social behaviors involving interpersonal violence.

227 However, whether the effect of L. reuteri on social behavior is generalizable to other ASD models and

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

229 Social behavior is often shaped by the rich storehouse o

230 A long-standing assumption in social behavior is that leadership incurs costs as well

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

232 nin has received attention as a regulator of social behavior largely because of studies demonstrating

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

234 ys an important role in regulating mammalian social behaviors, linking it to social affiliation in pa

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

236 be critical to understanding collective and social behaviors, multicellular development, and ecologi

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

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

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

240 or (PAM) VU0155041 (2.5 and 5 mg/kg) rescued social behavior, normalized stereotypies and anxiety and

241 expression of Hmp, allowing regeneration of social behavior observed in tissues.

242 el of insight into the kinship structure and social behavior of a Late Neolithic community.

243 To further dissect social behavior of Galphai2(-/-) mice, we performed a 3-

244 et these results in terms of observations on social behavior of humans.

245 decision making to quantify and predict the social behavior of other drivers and to behave in a soci

246 other agents has deep roots in the strategic social behavior of primates and that the anterior cingul

247 In Experiment 2, social behavior of STs and GTs was compared using social

248 At the cellular level, the different social behaviors of M. xanthus involve extensive cell-ce

249 model using swine, which results in altered social behaviors of piglet offspring.

250 Prolonged or exaggerated alterations in social behavior often accompany altered immune signaling

251 biological and paleoecological aspects (e.g. social behavior, ontogenetic changes, sexual dimorphism,

252 response to the species' past climate, other social behaviors, or a combination of these factors.

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

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

255 or patterns are ubiquitous in nature, impact social behavior, predator avoidance, and protection from

256 Social behaviors recruit multiple cognitive operations t

257 vity, gene expression, in vivo responses and social behavior relevance.

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

259 hypothalamic excitatory inputs essential for social behaviors remain elusive.

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

261 ropeptide-containing neurons to variation in social behavior remains critically important.

262 s role in specific brain areas for mammalian social behaviors remains largely unknown.

263 e molecular and circuit mechanisms mediating social behaviors remains relatively limited.

264 on of the PVH-OT neurons to promote adaptive social behavior responses.SIGNIFICANCE STATEMENT Althoug

265 nderlie seasonal variation in human mood and social behavior.SIGNIFICANCE STATEMENT Seasonal rhythms

266 actions, brain dimorphisms, reproductive and social behaviors, sleep function, and adult neurogenesis

267 comotor activity, core body temperature, and social behavior (social interaction and ultrasonic vocal

268 ng-tailed, and bonnet macaques, we collected social behavior, spatial data, and human-interaction dat

269 Extreme social behaviors such as extraordinary acts of altruism

270 ng hunger intensity would curb expression of social behaviors such as mating or territorial aggressio

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

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

273 and leads to deficits in juvenile and adult social behavior, suggesting that altered C4 expression c

274 ent and suppressing amygdala activity during social behavior testing.

275 ntestinal barrier dysfunction and changes in social behavior that correlates with compositional chang

276 tive tactics exhibit stereotyped patterns of social behavior that diverge widely between individuals

277 is well known to regulate a diverse array of social behaviors, the mechanism in which OT acts to prom

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

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

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

281 a and Yersinia, consistent with selection of social behavior to retain genes associated with pathogen

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

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

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

285 tochondria modulate neuronal homeostasis and social behavior under physiopathological conditions.

286 ocin (OXT) is an important neuromodulator of social behaviors via activation of both oxytocin recepto

287 ine, regulates goal- and reward-directed and social behaviors, wakefulness, and sleep.

288 ASD-related social behavior was assessed at age 3 years using Social

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

290 To quantify social behaviors, we need to measure both the stochastic

291 here a new, environment-mediated taxonomy of social behaviors where organisms are categorized by thei

292 ough the lateral septum (LS), contributes to social behavior, which is disrupted in ASD.

293 Thus, these two strains differ in their social behavior, which should be taken into consideratio

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

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

296 : ventrally targeted constructs rescued only social behavior, while those expressed dorsally selectiv

297 POA galanin neurons in reproductive-related social behaviors with implications for the evolution of

298 via CoREST as central to programming of ant social behavior, with potential far-reaching implication

299 dine-induced hyperactivity and increased pro-social behavior without decreasing core body temperature

300 that oxytocin, a neuropeptide implicated in social behavior, would normalize neural abnormalities in