ライフサイエンスコーパス: aggression

1 en enrichment of room air can overcome this 'aggression'.

2 re-escalation phase but not during escalated aggression.

3 it from a broader conceptualization of human aggression.

4 social behavior and the neural circuitry of aggression.

5 g NMDARs in the PLmPFC in alcohol-heightened aggression.

6 are essential for male but not female mouse aggression.

7 gnaling is necessary and sufficient to limit aggression.

8 apply to forms of aggression beyond reactive aggression.

9 eventing the development of chronic physical aggression.

10 wired hypothalamus-mediated male territorial aggression.

11 factor facilitate, while serotonin inhibits, aggression.

12 frequent sleep disturbances and episodes of aggression.

13 henotype that frequently includes persistent aggression.

14 erstanding the nature and evolution of human aggression.

15 uring the task) and parent-reported reactive aggression.

16 es in the neural regulation of dominance and aggression.

17 about implicit attitudes toward violence and aggression.

18 y serve as an important biomarker of disease aggression.

19 ve an elevated risk for maladaptive reactive aggression.

20 mus (VMHvl)-a region required for male mouse aggression.

21 and BLA reactivity was positively related to aggression.

22 al properties through reduction in impulsive aggression.

23 gorical expression of pathological impulsive aggression.

24 ating implicit attitudes toward violence and aggression.

25 have critical influence on behavior, such as aggression.

26 e behaviour but had no impact on mobility or aggression.

27 uli displaying an expression associated with aggression.

28 ition (e.g., freeloading, displacements) and aggression.

29 atively correlated with rates of territorial aggression.

30 ts an effective pathway for suppressing male aggression.

31 n observed in humans-by signs of distress or aggression.

32 re environmental anxiety, training, and fear/aggression.

33 and Self-control in Humans (CLASH) model of aggression.

34 environments to rigid routine behaviors and aggression.

35 tions from the range cause impulsiveness and aggression.

36 male prairie voles displaying affiliation or aggression.

37 any tumors and their correlation with cancer aggression.

38 vl(Esr1+) cells are indispensable for female aggression.

39 at tempers rather than fuels poverty-induced aggression.

40 l pathways that bias Drosophila males toward aggression.

41 p or aggression song has opposite effects on aggression.

42 of NE, is known to promote both arousal and aggression.

43 gins and underemphasizes economic origins of aggression.

44 orrectly notes the low frequency of reactive aggression.

45 circuits to impede processing and to promote aggression.

46 ect behaviours such as olfactory learning or aggression.

47 (VMH) that are critical for male territorial aggression.

48 esting an evolutionary origin for compulsive aggression.

49 to dysregulate threat reactivity and promote aggression.

50 in the fly's auditory organ elicit abnormal aggression.

51 o developmental challenges and environmental aggressions.

52 of the sexual coercion hypothesis [7]: male aggression (1) is greatest against cycling females, (2)

53 nding in promoting social order and reducing aggression [4, 5].

54 humans that also engages in male intergroup aggression [7].

55 staff intervention in response to escalated aggression, a continuum between support and control.

56 humans have a high propensity for proactive aggression, a trait shared with chimpanzees but not bono

57 e1 and -e2 mutant males displayed heightened aggression accompanied by convergent expression changes

58 In explaining variation in violent aggression across populations, the age structures of tho

59 sive behaviors, leading to paradoxical tumor aggression after therapy.

60 group discrimination and sometimes defensive aggression against threatening (members of) out-groups.

61 e which aims to extinguish or reduce patient aggression/agitation irrespective of its cause, and impr

62 und a more positive implicit attitude toward aggression among individuals with lesions to the dlPFC a

63 eptides and their interactions in modulating aggression and affiliation.

64 terone's influence on males often centers on aggression and antisocial behavior, contemporary theoris

65 at scan-time was negatively related to both aggression and basolateral amygdala (BLA) reactivity to

66 Impulsive aggression and borderline personality disorder, but not

67 ckdown of Chrna7 in the DG enhanced baseline aggression and eliminated the serenic effects of both ni

68 and can induce antisocial effects including aggression and envy.

69 involves circuits that link innate feeding, aggression and fear.

70 project axons to brain regions implicated in aggression and fear.

71 were examined in the context of measures of aggression and impulsivity in physically healthy subject

72 role of serotonin 1B receptors (5-HT1BRs) in aggression and impulsivity, but this has never been eval

73 m harassment and punishment, by showing that aggression and matings are temporally decoupled.

74 analysis of chronological sequences between aggression and matings ruled out other coercive mechanis

75 aring in the control of Drosophila intermale aggression and open perspectives to decipher how hearing

76 o nerves is associated with increased cancer aggression and poor patient outcome.

77 simple relationship between testosterone and aggression and provide causal evidence for a more comple

78 ria terminalis, which suppresses territorial aggression and reduces contextual fear.

79 n variable of interest for predicting cancer aggression and response to therapy.

80 Aggression and responsiveness to noxious stimuli are ada

81 al role of the VMHvl in both male and female aggression and reveal the existence of two previously un

82 re less understood and often associated with aggression and social unrest.

83 pport of CLASH, and other possible causes of aggression and violence (e.g., wealth, income inequality

84 Maladaptive aggression and violence are associated with dysfunction

85 evolutionarily explains the biogeography of aggression and violence as strategic adaptation.

86 Maladaptive aggression and violence can lead to interpersonal confli

87 differences within and between countries in aggression and violence in terms of differences in clima

88 e various exceptions, a general rule is that aggression and violence increase as one moves closer to

89 erent predictions about the distributions of aggression and violence within and between societies.

90 explanations for these large differences in aggression and violence within countries and around the

91 rol are important determinants of inhibiting aggression and violence.

92 aping individual and societal differences in aggression and violence.

93 ltimately explain the poleward declension of aggression and violence.

94 mpletely through the causal chain underlying aggression and violence.

95 differences within and between countries in aggression and violence.

96 exhibited consistent individual variation in aggression and web weight only.

97 volution of traits that favour between-group aggression and within-group cooperation (e.g. parochial

98 critical for regulating retaliation/reactive aggression and, when dysfunctional, contributes to react

99 ypes characterized by dominance, competitive aggression, and active coping strategies appear to be mo

100 ronger and better coordinated than out-group aggression, and defender groups survived roughly 70% of

101 her implicate alpha7 nAChRs in regulation of aggression, and demonstrate that hippocampal alpha7 nACh

102 c subnucleus previously known as a locus for aggression, and discovered that social-fear and aggressi

103 hich involve negative emotions such as fear, aggression, and envy and lead to avoidance behavior.

104 s support previous neurobiological models of aggression, and extend them by demonstrating that fast a

105 as diverse as body temperature, respiration, aggression, and mood.

106 ion recapitulates learning impairment, hyper-aggression, and motor defects, all of which are insensit

107 nctionally link mucinous proteins with tumor aggression, and offer a new view of the cancer glycocaly

108 with a special focus on feeding, courtship, aggression, and postmating behaviors.

109 Mental health nurses are exposed to patient aggression, and required to manage and de-escalate aggre

110 ry serves as the foundation for the CLimate, Aggression, and Self-control in Humans (CLASH) model of

111 We propose a new model, CLimate, Aggression, and Self-control in Humans (CLASH), that hel

112 mmented on the theoretical model of CLimate, Aggression, and Self-control in Humans (CLASH).

113 ry processing, locomotor control, courtship, aggression, and sleep.

114 aring of a limited water resource, decreased aggression, and strongly defined dominance ranks (an ind

115 unctions, such as circadian rhythms, reward, aggression, anxiety, and fear.

116 14 techniques used in response to escalated aggression applied on a continuum between support and co

117 We show that although levels of aggression are driven, in part, by between-group selecti

118 olved in the development of chronic physical aggression are generally the product of an intergenerati

119 tus), in which both exploratory tendency and aggression are heritable.

120 es of white matter connectivity in impulsive aggression are warranted.

121 f the central amygdala and the hypothalamic 'aggression area', suggest that the ACo can initiate defe

122 be a promising therapeutic intervention for aggression arising in certain forms of neuropsychiatric

123 the concept of de-escalation of violence and aggression as described within the healthcare literature

124 each neuromodulatory molecule on Drosophila aggression, as well as effects of receptor proteins wher

125 mptoms of ADHD, sleep disruption, hypotonia, aggression, ASD, and ID.

126 amus and then the lateral septum to modulate aggression associated with mate guarding.

127 nstruction-carried over to affect focal male aggression at a later time and with a new opponent.

128 tanding of links between nurses' exposure to aggression, attitudes to, and actual involvement in, coe

129 ediating antidepressant responses and normal aggression behavior.

130 alue by reducing the potential for escalated aggression, benefiting both senders and receivers by fac

131 that shrub landcover significantly moderates aggression between nests, suggesting nests are more rela

132 t that the CLASH model may apply to forms of aggression beyond reactive aggression.

133 ychopathy) scores, and with higher levels of aggression (but not rule-breaking).

134 gher levels of externalizing symptoms (e.g., aggression) but not internalizing symptoms (e.g., depres

135 has highlighted monoaminergic influences on aggression, but a mechanistic account of how monoamines

136 Aggression by dominant individuals within groups was the

137 Bullying data support the CLASH model of aggression by suggesting that climate may moderate the f

138 Monge referred to 'climatic aggression', by which he meant the negative consequences

139 d cellular mechanisms controlling Drosophila aggression can shed light on neural principles governing

140 This modulation of aggression cannot be accounted for by linear integration

141 such as pair bonding, social recognition and aggression causally increases humans' willingness to eng

142 ing evidence on the neural basis of explicit aggression centered on the ventromedial prefrontal corte

143 t, humans have a low propensity for reactive aggression compared with chimpanzees, and in this respec

144 Aggression directed by male baboons at females during th

145 evolved in bonobos as the risk of intergroup aggression dissipated and the benefits of bonding betwee

146 rdination of collective action for out-group aggression, doubling the aggressor's success rate (Exp.

147 ation promoted wing extension and suppressed aggression during photostimulation, whereas aggression r

148 nd have a greater prevalence of violence and aggression (e.g., higher homicide rates).

149 P < .001); 5 of 7 syndrome scales, including aggression (effect size, 0.36; P < .001), sleep (effect

150 underlie synaptic plasticity associated with aggression escalation.

151 structure is a key predictor of coalitionary aggression even in the absence of meaningful resource st

152 individuals will seek out opportunities for aggression, even in the absence of threat-provoking cues

153 latitudinal gradients of heat, poverty, and aggression finds that heat-induced aggression is mediate

154 om ANAs, we tested additional mice for their aggression following preferential antagonism of GluN2D-c

155 , animals often experience elevated rates of aggression from conspecifics, and they may also be threa

156 aimed at subordinating out-groups (out-group aggression) from those aimed at defending the in-group a

157 lected data on infants' social interactions (aggression, grooming, and play) and self-scratching (a p

158 The debate on the developmental origins of aggression has historically opposed genetic and environm

159 The involvement of serotonin in aggression has traditionally been attributed to impaired

160 Psychosis (hazard ratio=2.007), agitation/aggression (hazard ratio=2.946), and any one clinically

161 ood to select an alternative reinforcer over aggression, heightened relapse vulnerability and progres

162 The bimodal classification of human aggression helps solve two important puzzles.

163 c circuits are known to encode initiation of aggression; however, little is known about the neural me

164 ed social interaction, compulsive behaviors, aggression, hyperactivity, anxiety, depression, and soma

165 tures underpinning implicit attitudes toward aggression in a unique sample of combat veterans with tr

166 ypothesis that lithium use reduces impulsive aggression in addition to stabilizing mood.

167 mantine, or intra-PLmPFC memantine increased aggression in AHAs, but only in the absence of alcohol.

168 ohol produced a pathological-like pattern of aggression in AHAs; these mice shifted their bites to mo

169 , are used to treat psychosis, agitation and aggression in Alzheimer's disease.

170 racted with prior alcohol intake to escalate aggression in ANAs.

171 Aggression in borderline personality disorder (BPD) is t

172 ikely to be effective in treating pathologic aggression in both female and male subjects.

173 be sensitive to "addiction-like" features of aggression in CD-1 mice.

174 Aggression in Drosophila is context-dependent and can th

175 ptor-expressing neurons (OARNs) that control aggression in Drosophila.

176 Intra-ILmPFC memantine had no effect on aggression in either AHAs or ANAs.

177 e disproportionately responsible for violent aggression in every society, and increases in violence t

178 Until now, data comparing anger and aggression in female and male patients with BPD have bee

179 mic injection of a 5-HT1a agonist stimulated aggression in female hamsters and inhibited aggression i

180 Experience-dependent escalation of aggression in female hamsters depends on activation of m

181 n the hypothalamus to regulate dominance and aggression in females and males.

182 in males, whereas injection of AVP inhibited aggression in females and stimulated aggression in males

183 stemically administered fluoxetine increased aggression in females and substantially reduced aggressi

184 irst-line response to potential violence and aggression in healthcare settings.

185 ChR signaling have also been shown to reduce aggression in human 15q13.3DS.

186 ng-standing debate about the significance of aggression in human nature is misconceived, because both

187 cture of the central neuromodulatory role of aggression in human subjects.

188 tween plasma markers of oxidative stress and aggression in human subjects.

189 kers of oxidative stress would be related to aggression in human subjects.

190 he neural basis of implicit attitudes toward aggression in humans using a modified version of the Imp

191 favored increased in-group prosociality over aggression in late human evolution.

192 d inflammation is associated with behavioral aggression in lower mammals and humans, we hypothesized

193 ression in females and substantially reduced aggression in males, there may be substantial gender dif

194 aggression in female hamsters and inhibited aggression in males, whereas injection of AVP inhibited

195 hibited aggression in females and stimulated aggression in males.

196 iques are recommended to manage violence and aggression in mental health settings yet restrictive pra

197 In contrast, GTS-21, which reduces aggression in mice, reduced DG granule cell activity dur

198 haviour: explorative genotypes elicited most aggression in opponents.

199 ss variable than participation in intergroup aggression in other primate species; (ii) males often pa

200 Pharmacological treatments for agitation and aggression in patients with Alzheimer's disease have sho

201 Recent work argued that the levels of aggression in social spider colonies are explained by gr

202 By contrast, these neurons cannot elicit aggression in socially housed males that intrude in anot

203 the neurocognitive processes associated with aggression in such individuals, but we know remarkably l

204 ity to anger expressions on women's reactive aggression in the Social Threat Aggression Paradigm (STA

205 erlying neurobiology of maladaptive reactive aggression in youths with DBD who have relatively low le

206 ding the in-group against possible out-group aggression (in-group defense).

207 ation, in addition to efficacy for agitation/aggression, included reductions in the frequency of irri

208 s that mediate a specific influence of OA on aggression, independent of any effect on arousal.

209 when dysfunctional, contributes to reactive aggression, independent of level of callous-unemotional

210 Escalated aggression is a behavioral sign of numerous psychiatric

211 Aggression is a prevalent behavior in the animal kingdom

212 as an instance of interspecific combat; such aggression is a social feature of modern ants.

213 Aggression is a universal social behavior important for

214 Increased aggression is common after traumatic brain injuries and

215 In such contexts, aggression is commonly used to obtain desired resources.

216 s an essential means of resolving conflicts, aggression is expressed by both sexes but often at a hig

217 Instead, our analyses suggest that aggression is favoured primarily as a selfish strategy t

218 The biology of proactive aggression is less well known and merits increased atten

219 ituations (Routine Activity Theory) in which aggression is likely to unfold.

220 erty, and aggression finds that heat-induced aggression is mediated by poverty and that heat tempers

221 hat D1-like receptor regulation of selective aggression is mediated through downstream activation of

222 rence between these two species is that male aggression is more frequent and intense in male-dominate

223 social interactions such as male territorial aggression is poorly understood.

224 reased between dMBD-R2-deficient males while aggression is reduced.

225 The neurobiology underlying escalated aggression is unknown and is particularly understudied i

226 studied using anxiety (light/dark test) and aggression (mirror test) paradigms.

227 factor that triggers aggression (The General Aggression Model), or the notion that warm temperature a

228 whereas peer punishment increased out-group aggression more than in-group defense without affecting

229 rkers correlated with a composite measure of aggression; more specifically, 8-hydroxy-2'-deoxyguanosi

230 ression, and discovered that social-fear and aggression neurons are intermixed but largely distinct.

231 and its expression correlates with increased aggression of human gliomas.

232 rocesses within each stage, including venom, aggression, olfactory recognition as well as growth and

233 se intergenerational mechanisms and physical aggression onset in infancy, it appears clear that preve

234 n can bias the output of P1 neurons to favor aggression over inter-male courtship.

235 n's reactive aggression in the Social Threat Aggression Paradigm (STAP).

236 es have shown that the frequency of physical aggression peaks in early childhood and then decreases u

237 In the aggression phase, men with BPD exhibited higher activity

238 Two major types of aggression, proactive and reactive, are associated with

239 more aggression than controls and receiving aggression reduces juvenile hormone (JH) titers.

240 d that dogs were more likely to develop fear/aggression related issues early on, whilst issues relate

241 oss of antidepressant efficacy and increased aggression-related behavior.

242 In experiment 3, cluster analysis of the aggression-related measures identified a subset of "addi

243 l neural basis for this type of pathological aggression remains elusive.

244 s depression, childhood abuse, and impulsive aggression, report inconsistent results.

245 d that an ecological account of violence and aggression requires consideration of societal and cultur

246 aggression during photostimulation, whereas aggression resumed and wing extension was inhibited foll

247 insight into the neural circuits modulating aggression reward processing.

248 weakened by their state of stress (rendering aggression risky and/or unnecessary).

249 current smokers showed significantly higher aggression scores compared with both nonsmokers and ex-s

250 In stage 2, NPI Agitation/Aggression scores were reduced from 5.8 to 3.8 with dext

251 We then tested them for relapse to aggression seeking after forced abstinence or punishment

252 uppression of aggression seeking, relapse to aggression seeking, progressive ratio responding, and pu

253 em for choice-based voluntary suppression of aggression seeking, relapse to aggression seeking, progr

254 on of the VMHvl accelerated moment-to-moment aggression-seeking and intensified future attack.

255 ound that VMHvl neurons became active during aggression-seeking and that their activity tracked chang

256 Inactivation of the VMHvl reduced aggression-seeking behavior, whereas optogenetic stimula

257 To explore this directly, we utilized an aggression-seeking task in which male mice self-initiate

258 s that promote self-initiated or 'voluntary' aggression-seeking when no threat is present.

259 th a known role in attack, was essential for aggression-seeking.

260 R availability and from increased behavioral aggression seen in active smokers.

261 nding, and punishment-induced suppression of aggression self-administration.

262 tinence or punishment-induced suppression of aggression self-administration.

263 , the occurrence of two major types of human aggression solves the execution paradox, concerned with

264 rther, we show that exposure to courtship or aggression song has opposite effects on aggression.

265 ing rates, however, were not associated with aggression, suggesting that reduced dispersal rates were

266 Following aggression testing, messenger RNA expression and protein

267 Female hamsters were given five daily aggression tests with or without prior treatment with th

268 ccurately high fighting ability receive more aggression than controls and receiving aggression reduce

269 anxiety-like behaviour and altered levels of aggression that are modulated by the neurotransmitter se

270 ullying was defined as repeated, intentional aggression that is targeted at a person who cannot easil

271 verage temperature as a factor that triggers aggression (The General Aggression Model), or the notion

272 en by traits reflecting good manners and non-aggression (the politeness aspect of Big Five agreeablen

273 asures of their exposure to various types of aggression, their attitudes towards seclusion and restra

274 en mental health nurses' exposure to patient aggression, their emotions, their attitudes towards coer

275 functioning and support the use of physical aggression to solve problems.

276 Fluoro-Gold, and tested for affiliation and aggression toward a female partner or novel female subje

277 on in animals [4, 5], in which repeated male aggression toward a female provides the aggressor with d

278 Here, we test whether male aggression toward females functions as sexual coercion i

279 female mouse model of RSDS by inducing male aggression toward females through chemogenetic activatio

280 y toward closer genetic relatives and direct aggression toward less closely related individuals.

281 intained through the expression of selective aggression toward novel conspecifics.

282 who self-harm may have an increased risk of aggression toward others, but this association has been

283 terpersonal rejection and directing physical aggression toward others.

284 ral judgements regarding the function of the aggression; trial-and-error; ingrained local custom (esp

285 eking task in which male mice self-initiated aggression trials to gain brief and repeated access to a

286 idence of a link between these and increased aggression/use of restrictive practices.

287 Since the aggression used by executioners is proactive, the execut

288 sence of wing extension triggered persistent aggression via an internal state that could endure for m

289 ) Why is there so much variation in reactive aggression/violence between people living in the same en

290 Trait aggression was found to positively modulate connectivity

291 Aggression was significantly higher in dyads using only

292 Exposure to mild and severe physical aggression was unrelated to nurses' emotions.

293 rcuit mechanism of LS-mediated modulation of aggression, we examined the influence of LS input on the

294 ntrol study, markers of oxidative stress and aggression were assessed in human subjects with historie

295 However, T's effects on aggression were strongly influenced by variation in trai

296 ncreased, while ad lib spiders reduced their aggression when their adult condition increased.

297 Inactivation of these cells reduced female aggression whereas their activation elicited attack.

298 Verbal aggression which appears targeted, demeaning or humiliat

299 inical studies of the treatment of escalated aggression, with the added benefit that emerging therape

300 d OA neuronal genome exhibited a decrease in aggression without altering male-male courtship.