ライフサイエンスコーパス: aggressive behavior

1 l differences in compulsive "addiction-like" aggressive behavior.

2 ep and arousal, reward, fear, and social and aggressive behavior.

3 tor in the pathophysiology of antisocial and aggressive behavior.

4 s specific host, and is characterized by its aggressive behavior.

5 ilience to punishment-induced suppression of aggressive behavior.

6 to have the same deletion and presented with aggressive behavior.

7 sensory modality in the context of intermale aggressive behavior.

8 an be used clinically to predict the risk of aggressive behavior.

9 on of sex steroid-dependent reproductive and aggressive behavior.

10 ent studies analyzing isolated indicators of aggressive behavior.

11 ium rosenbergii to study the neural basis of aggressive behavior.

12 rse stressors and prevention of uncontrolled aggressive behavior.

13 the hope that this approach will reduce the aggressive behavior.

14 underlying manifestation of and variation in aggressive behavior.

15 lzheimer's disease and psychosis or agitated/aggressive behavior.

16 octopamine plays a role in the modulation of aggressive behavior.

17 te an indolent behavior and others show more aggressive behavior.

18 r than most existing methods used to measure aggressive behavior.

19 in the limbic circuitry mediating escalated aggressive behavior.

20 ative for both EGFRvIII and YKL-40 show less aggressive behavior.

21 In adults, fluoxetine treatment inhibited aggressive behavior.

22 d social sniffing and allogrooming, and less aggressive behavior.

23 is associated with the acquisition of a more aggressive behavior.

24 tral 5-HT may be especially prone to exhibit aggressive behavior.

25 reater efficacy than haloperidol in reducing aggressive behavior.

26 erized malignant neoplasms with particularly aggressive behavior.

27 ons by higher proliferative indices and more aggressive behavior.

28 l meningiomas (WHO grade II) with clinically aggressive behavior.

29 trition may help reduce later antisocial and aggressive behavior.

30 ave been correlated with heightened maternal aggressive behavior.

31 n the VNO and a specific defect in male-male aggressive behavior.

32 a quantitative trait locus (QTL) sting-2 for aggressive behavior.

33 be sufficient to selectively alter maternal aggressive behavior.

34 x and interconnected areas display impulsive aggressive behavior.

35 ital/medial prefrontal circuit and impulsive aggressive behavior.

36 ishment, but capital punishment is itself an aggressive behavior.

37 role of nitric oxide (NO) in male impulsive aggressive behavior.

38 powerful tool for analyzing the evolution of aggressive behavior.

39 erved in human prostate tumors and linked to aggressive behavior.

40 ce of interactions among these molecules and aggressive behavior.

41 be present in individuals with pathological aggressive behavior.

42 viduals respond to the eliciting of imagined aggressive behavior.

43 several biogenic amines and neuropeptides on aggressive behavior.

44 rders who exhibit relatively milder forms of aggressive behavior.

45 ian split on a six-item history of adulthood aggressive behavior.

46 s involving emotionally neutral behavior and aggressive behavior.

47 he orbitofrontal cortex in the expression of aggressive behavior.

48 f the frontal lobes often lead to abnormally aggressive behavior.

49 means of preventing and managing physically aggressive behavior.

50 aggressive tension during the imagination of aggressive behavior.

51 te their consequences for the development of aggressive behavior.

52 re crucially involved in the pathogenesis of aggressive behavior.

53 s consisting of autistic, hyperactive and/or aggressive behavior.

54 Exogenous T on its own did not modulate aggressive behavior.

55 which probably accounts for their clinically aggressive behavior.

56 are vascular tumor which has an intermediate aggressive behavior.

57 strate mesenchymal properties and coincident aggressive behavior.

58 duals with recurrent, problematic, impulsive aggressive behavior.

59 ing on female mate choice, pair-bonding, and aggressive behavior.

60 which ultimately could restart with similar aggressive behavior.

61 xia inducible factor-1alpha (HIF-1alpha) and aggressive behavior.

62 layed higher rates of proliferation and more aggressive behavior.

63 school performance, prosocial behavior, and aggressive behavior.

64 nsporter, during P22-41 also increases adult aggressive behavior.

65 ting that it could contribute to synoviocyte aggressive behavior.

66 get for the prevention of alcohol-heightened aggressive behavior.

67 CL2 or BCL6 translocations conferring a very aggressive behavior.

68 specifics as well as simultaneously decrease aggressive behaviors.

69 onkeys) displaying affiliative, neutral, and aggressive behaviors.

70 in the dorsal raphe nucleus (DRN) escalated aggressive behaviors.

71 food, and demonstrated fewer species-typical aggressive behaviors.

72 ty, which in turn, is proposed to disinhibit aggressive behaviors.

73 dult behaviors develop, including sexual and aggressive behaviors.

74 pared with WT males in the rare instances of aggressive behaviors.

75 ogeneity resulting from a selection for more aggressive behaviors.

76 t alcohol's effects on mating, locomotor, or aggressive behaviors.

77 ns to appetitive and consummatory sexual and aggressive behaviors.

78 features of this malignancy account for such aggressive behavior?

79 (0.75 times as high; 95% CI: 0.57, 0.99) and Aggressive Behavior (0.82 times as high; 95% CI: 0.70, 0

80 t-intruder test they exhibited: 1) increased aggressive behavior; 2) potentiated corticosterone and t

81 ssion exhibited comorbid anxiety (76.7%) and aggressive behavior (56.7%).

82 adolescent expression of 5-HT1BRs influences aggressive behavior, a distinct set of 5-HT1B receptors

83 Male CFW mice that reliably exhibited aggressive behaviors after consuming 1 g/kg of alcohol r

84 In contrast, GABA agonists did not escalate aggressive behaviors after microinjection into the media

85 uate the efficacy of divalproex for reducing aggressive behavior among children 6 to 13 years old wit

86 hat elicit genetically programmed sexual and aggressive behaviors among conspecifics.

87 cinoma (CC) characteristics that have a more aggressive behavior and a poorer prognosis than classic

88 g adolescent development directly stimulates aggressive behavior and alters LAH 5HT and AVP developme

89 Administration During Adolescence Stimulates Aggressive Behavior and Alters Serotonin and Vasopressin

90 of many tissues and is responsible for their aggressive behavior and chemoresistance.

91 reeding stage, they display reproductive and aggressive behavior and have elevated circulating testos

92 ting behavior, they do not exhibit intermale aggressive behavior and have reduced body fat.

93 ut the influence of religious affiliation on aggressive behavior and how moral objections can reduce

94 stories of recurrent, problematic, impulsive aggressive behavior and in nonaggressive comparator subj

95 One goal is to delineate the type of aggressive behavior and its escalation with greater prec

96 al neoplasms associated with a small risk of aggressive behavior and metastasis.

97 r regulator of endocytosis, is predictive of aggressive behavior and metastatic ability in human brea

98 ssion was significantly associated with more aggressive behavior and more cancer deaths and supported

99 ent pattern and from passive to increasingly aggressive behavior and negative self-representation.

100 of ES cases and define a subset with highly aggressive behavior and poor chemoresponse.

101 CC may provide a partial explanation for the aggressive behavior and poor prognosis of these tumors i

102 They are associated with aggressive behavior and poor prognosis, and typically do

103 xpression of SHH, breast cancer cells showed aggressive behavior and rapid xenograft growth character

104 melanoma (CMM), already known for its highly aggressive behavior and resistance to conventional thera

105 eu gene in breast cancers is associated with aggressive behavior and resistance to therapeutic regime

106 There is an association between aggressive behavior and serotonergic dysfunction indepen

107 serotonin activity in setting thresholds for aggressive behavior and support a direct association bet

108 signaling may play a significant role in the aggressive behavior and treatment resistance of hypoxic

109 ers are associated with an increased risk of aggressive behavior and violent crime.

110 lymphoma (MCL) has been associated with more aggressive behavior and worse outcome.

111 irst evidence that phytoestrogens can affect aggressive behavior and, concurrently, alter hormonal st

112 y for adolescents experiencing problems with aggressive behavior and/or impulse control associated wi

113 weaned at young ages show more abnormal and aggressive behaviors and cognitive deficits compared to

114 detect male-specific pheromones that elicit aggressive behaviors and dictate the choice of sexual pa

115 Although aggressive behaviors and temperament are highly heritabl

116 sleep, school performance, and prosocial and aggressive behaviors and that these effects are mediated

117 , but not P2-21 or P182-201, increases adult aggressive behavior, and 5-HTT blockade from P22-P41 red

118 n therapy, greater genomic instability, more aggressive behavior, and a poor clinical prognosis.

119 ent video games, leading to desensitization, aggressive behavior, and gender inequity in opportunitie

120 How brains are hardwired to produce aggressive behavior, and how aggression circuits are rel

121 rates of depressive symptoms, substance use, aggressive behavior, and internalizing problems but fast

122 ong with depressive symptoms, substance use, aggressive behavior, and internalizing problems.

123 age regression, hyperactivity, impulsive and aggressive behavior, and mental retardation developed in

124 of patients with dementia exhibit physically aggressive behavior, and this aggression is strongly lin

125 gous null mice showed deficits in mating and aggressive behaviors, and the deficiencies in Sk3(-/-) m

126 Impulsive and aggressive behaviors are both modulated by serotonergic

127 ed functional impairment, alcohol misuse, or aggressive behavior as comorbid factors occurring with P

128 enes that have been previously implicated in aggressive behavior as well as many novel loci, includin

129 ant determinant of tumor differentiation and aggressive behavior, as well as a potential therapeutic

130 in a clinical research program in impulsive aggressive behavior at an academic medical center.

131 d not appear to require the overt display of aggressive behavior because it was present in both the d

132 group sizes that they preferred and in their aggressive behavior; both of these behaviors influenced

133 ow concentration of CSF 5-HIAA is related to aggressive behavior but does not show the same relations

134 In summary, androgens induced aggressive behavior but they did not regulate serotonin.

135 in have been implicated in the regulation of aggressive behavior, but it has remained challenging to

136 Specifically, T caused an increase in aggressive behavior, but only among men scoring relative

137 T can rapidly (within 60 minutes) potentiate aggressive behavior, but only among men with dominant or

138 he alpha7 nAChR as an important regulator of aggressive behavior, but the underlying neurobiological

139 and cortisol have been proposed to influence aggressive behavior by altering the neural processing of

140 nt feedback loop, whereby it promotes a more aggressive behavior by human prostate cancer cells.

141 he present report, a detailed examination of aggressive behavior by using mutant strains and other te

142 The molecular mechanisms accounting for the aggressive behavior caused by the lack of neuronally der

143 Epistasis for aggressive behavior causes cryptic genetic variation in

144 ociation remained significant after previous aggressive behavior, childhood neglect, family income, n

145 Alcohol misuse or aggressive behavior comorbidity was present in approxima

146 siRNA in CSLCs resulted in the inhibition of aggressive behavior, consistent with the inhibition of E

147 baseline levels of testosterone (T) promote aggressive behavior, decades of research have produced f

148 The frequency of aggressive behavior declined significantly during the fi

149 data suggest that the specific type of overt aggressive behavior demonstrated by these models may be

150 Aggressive behaviors directed toward adult males, by con

151 dels, indicate that the distinctive types of aggressive behaviors displayed by these two murine model

152 Traditional measurements of aggressive behavior have relied on a territorial context

153 Within aggressive behavior, IA and callous unemotional (CU) tra

154 Alcohol can escalate aggressive behavior in a significant subgroup of rodents

155 Loss of p27 is associated with aggressive behavior in a variety of tumors, including Ba

156 implicated in the control of male sexual and aggressive behavior in a variety of vertebrates.

157 m is followed by heightened anxiety-like and aggressive behavior in adults.

158 gnature for metabolic uptake and patterns of aggressive behavior in advanced breast cancer.

159 , with measures reflecting history of actual aggressive behavior in all participants.

160 with measures reflecting a history of actual aggressive behavior in all subjects.

161 receptors and play a key role in modulating aggressive behavior in animal models.

162 edly that B cell depletion induced transient aggressive behavior in BDC2.5 diabetogenic T cells and r

163 t hypersensitivity and thus reduce anger and aggressive behavior in borderline personality disorder o

164 deficiency in monoamine oxidase A results in aggressive behavior in both humans and mice.

165 t addresses the prevention and management of aggressive behavior in children and adolescents.

166 Assays to quantify aggressive behavior in Drosophila melanogaster have been

167 ent in the evolution of different degrees of aggressive behavior in honey bees involved changes in re

168 d the oncogene Neu, which is associated with aggressive behavior in human breast cancers, in MCF-7 ce

169 cation of the N-myc proto-oncogene signifies aggressive behavior in human neuroblastoma.

170 plays a key role in shaping competitive and aggressive behavior in humans, possibly by modulating th

171 ral circuits in which alpha7 nAChRs regulate aggressive behavior in male mice.

172 immunization and the importance of avoiding aggressive behavior in males.

173 ing whether acutely increasing T potentiates aggressive behavior in men.

174 ral circuits mediating threat processing and aggressive behavior in men.

175 een associated with enhanced cell growth and aggressive behavior in other tumors.

176 d functionally relevant biomarker to predict aggressive behavior in patients with meningioma.

177 the genetic architecture that predisposes to aggressive behavior in people is challenging because of

178 validated decision-making game that measures aggressive behavior in response to social provocation.

179 own about the molecular mechanisms mediating aggressive behavior in swine.

180 lopride showed dose-dependent suppression of aggressive behavior in the absence of changes in mobilit

181 least moderately agitated, and 28% reported aggressive behavior in the previous week.

182 We measured changes in aggressive behavior in the selected subpopulations with

183 Consistent with their aggressive behavior in the wild, male chimpanzees were r

184 l in its natural habitat and that we can use aggressive behavior in this species as an index of cross

185 the lungs of CTL-treated mice exhibited more aggressive behavior in vivo.

186 rcuit may be beneficial for the treatment of aggressive behaviors in childhood ADHD.

187 r agonist that enhances growth but increases aggressive behaviors in female pigs.

188 PD, a region associated with both sexual and aggressive behaviors in rats, hamsters, and mice, showed

189 cute sleep deprivation profoundly suppresses aggressive behaviors in the fruit fly, while other socia

190 ship may relate to the motivation to produce aggressive behaviors in the immediate future.

191 nsummatory sexual behaviors and consummatory aggressive behaviors in this species.

192 However, most aggressive behavior, including invasion and purported ca

193 EMT is associated with aggressive behavior, increased stem-like characteristics

194 blast-like synoviocytes (FLS) display unique aggressive behavior, invading the articular cartilage an

195 Aggressive behavior is a complex social behavior that is

196 mic changes in these neurotransmitters while aggressive behavior is in progress.

197 Aggressive behavior is observed across animal taxa and i

198 Aggressive behavior is pervasive throughout the animal k

199 Among children with ADHD whose chronic aggressive behavior is refractory to optimized stimulant

200 Our results support the view that TP-induced aggressive behavior is the result of a TP-mediated neuro

201 n effect of violent video game play on later aggressive behavior, little is known about the psycholog

202 Youths with aggressive behavior, male gender, severe emotional illne

203 a mirror, in which case, despite expressing aggressive behavior, males did not experience either a v

204 sets of patients have short attention spans, aggressive behaviors, mood disorders, or schizophrenia.

205 ent development to brain areas implicated in aggressive behavior, most notably the latero-anterior hy

206 aging implicate altered reward processing in aggressive behaviors, no previous studies have documente

207 Neither aggressive behavior nor yawning (indicators of androgen

208 However, the genes responsible for the aggressive behavior observed in this group are largely u

209 ine/paracrine factor that contributes to the aggressive behavior of aRMS cells, perhaps through a pos

210 nase-2 (COX-2) expression contributes to the aggressive behavior of breast and other malignancies.

211 l cells; the degree of oxidation varied with aggressive behavior of each cell line.

212 The aggressive behavior of glioblastomas, including resistan

213 PTBN1 may influence the stem cell traits and aggressive behavior of HCC cell lines.

214 ed as promoting invasion and correlates with aggressive behavior of human cancers and thus agents tha

215 he molecular pathways that contribute to the aggressive behavior of human cancers is a critical resea

216 identify metabolic features that support the aggressive behavior of human neuroendocrine (NE) cancers

217 plications of other CAs points to a uniquely aggressive behavior of hypo-13 CA (present in 16% of pat

218 mechanism by which IRS-2 contributes to the aggressive behavior of hypoxic tumor cells.

219 carcinomas and suggest an intrinsically more aggressive behavior of IBD-associated colon carcinomas c

220 )-c-Src signaling module may account for the aggressive behavior of integrin alpha(v)beta(3)-expressi

221 cancers and may account in part for the more aggressive behavior of interval-detected cases.

222 ted by heparanase, an enzyme associated with aggressive behavior of many cancers.

223 A role for Aurora kinases in the aggressive behavior of mesotheliomas is of potential cli

224 hat are known to play important roles in the aggressive behavior of myeloma tumors.

225 lish that EGFR-MET signaling is critical for aggressive behavior of NSCLCs and rationalize its contin

226 e of the genetic and molecular bases for the aggressive behavior of pancreatic cancer have been uncov

227 ling the molecular mechanisms underlying the aggressive behavior of pancreatic cancer is a necessary

228 of these fusion transcripts may underlie the aggressive behavior of PCa.

229 The mechanisms underlying the potential for aggressive behavior of prostate cancer (PCa) remain elus

230 ion is an important mechanism underlying the aggressive behavior of prostate cancer cells and their r

231 Stat5 was associated with more biologically aggressive behavior of prostate cancer.

232 t that MUC1 dysregulation is associated with aggressive behavior of PTC and may serve as a prognostic

233 The aggressive behavior of RDEB-associated SCCs remains unex

234 ee of Aurora A expression may play a role in aggressive behavior of RTs and that targeting expression

235 prostatic biopsy to predict indolent versus aggressive behavior of the cancer after surgery.

236 stions on the neuromodulators that influence aggressive behavior of the fruit fly Drosophila melanoga

237 berrant epigenetic changes results in a more aggressive behavior of the tumor.

238 However, our understanding of the potential aggressive behavior of these cancers has been largely ba

239 ma has previously been shown to regulate the aggressive behavior of these tumor cells.

240 d whether DLX4 overexpression contributes to aggressive behavior of this disease.

241 ion of Prox1 was sufficient to induce a more aggressive behavior of tumors growing in syngenic mice,

242 ne expression traits might contribute to the aggressive behavior of tumors with TP53 mutation.

243 hymal transition (EMT), which contributes to aggressive behavior of tumors.

244 losses at chromosome 2q are associated with aggressive behavior of various forms of human neoplasia.

245 eviously unanticipated role in mediating the aggressive behavior of vascular neoplasms such as KS.

246 ion paradox is solved to the extent that the aggressive behavior of which victims were accused was fr

247 On the other hand, reduced aggressive behaviors of alphabetaERKO mice mimicked thos

248 increased alpha-tubulin acetylation and the aggressive behaviors of basal-like breast cancers, with

249 agulation, coagulation factor FVIIa enhances aggressive behaviors of breast cancer cells, but the und

250 argeting of FAK was sufficient to revert the aggressive behaviors of these structures.

251 umor progression, but the dependence of this aggressive behavior on tumor-stromal interaction is poor

252 g, we were able to experimentally evoke this aggressive behavior only when an auditory cue (advertise

253 easures were also separately associated with aggressive behavior (OR = 1.09, 95% CI: 1.04-1.14 and OR

254 Children whose aggressive behavior persisted at the conclusion of the l

255 bute to their effects on specific sexual and aggressive behaviors pose significant challenges for mou

256 ent of developmentally limited impulsive and aggressive behaviors rather than psychotic symptoms.

257 hA5 receptor may be involved in mediation of aggressive behavior regulated, in part, by hypothalamic

258 ith pancreatic cancer, yet the basis for its aggressive behavior remains elusive.

259 ever, a clear effect of sleep deprivation on aggressive behaviors remains unclear.

260 measure was the proportion of children whose aggressive behavior remitted, defined by post-trial rati

261 spectrum (n = 82; 30.1%), and disruptive or aggressive behavior spectrum (n = 60; 22.1%) disorders.

262 lap during calling bouts consistently evoked aggressive behavior; stimuli lacking bimodal temporal ov

263 The most intense positivity correlated with aggressive behavior such as intraocular tissue invasion

264 These CSLCs exhibit aggressive behavior, such as increased cell growth, migr

265 terone selectively increases status-relevant aggressive behaviors, such as responses to provocation,

266 nergic turnover were coincident with altered aggressive behavior, suggesting a relationship between t

267 on of CD-1 mice demonstrate "addiction-like" aggressive behavior, suggesting an evolutionary origin f

268 ns important in the regulation of sexual and aggressive behavior suggests that local estrogen synthes

269 5% confidence interval (CI): 1.13, 2.32] and Aggressive Behavior syndromes (1.29 times greater; 95% C

270 on appears to be more effective for reducing aggressive behavior than medication alone.

271 As these tumors exhibited highly aggressive behavior, the possibility of exploiting the i

272 ough the PE group exhibited higher levels of aggressive behavior, there were no statistically signifi

273 ely, while injection of SCH-23390 suppressed aggressive behavior, these reductions were met with alte

274 displayed heightened avoidant, anxious, and aggressive behaviors, those with hippocampal lesions als

275 ssion leads to a proliferative advantage and aggressive behavior through largely unknown mechanisms.

276 breast cancer therefore conspires to promote aggressive behavior through pleiotropic effects.

277 chorea, pyramidal signs and a compulsive and aggressive behavior to self injure.

278 outbred lines of rats selected for tame and aggressive behavior toward humans for >64 generations.

279 dicate that the serotonergic system inhibits aggressive behavior toward same-sex conspecifics, while

280 Melanoma exhibits increased incidence and aggressive behavior under transplant-related immunosuppr

281 e knock-out mice that exhibit alterations in aggressive behavior, very little progress has been made

282 Aggressive behavior was closely associated with moderate

283 ne levels and the expression of intraspecies aggressive behavior was evaluated in two murine models.

284 The puzzle is that the propensity for aggressive behavior was supposedly reduced as a result o

285 dorants to females to increase resident male aggressive behavior, we find that female mice undergo re

286 Television viewing and aggressive behavior were assessed over a 17-year interva

287 l scenario, the imagined scenarios involving aggressive behavior were associated with significant emo

288 Multiple genes associated with aggressive behavior were increased in the androgen-indep

289 Children with preexisting aggressive behavior were more likely to be victims of ph

290 lon should have a positive relationship with aggressive behavior, whereas AVT-ir neuronal features in

291 ltaNp63 expression characterized tumors with aggressive behavior, whereas tumors with high TAp63 expr

292 n understanding the etiology of disorders of aggressive behavior, whether genetic or environmental in

293 Rats continued to display aggressive behavior while being sampled, and they perfor

294 lzheimer's disease and psychosis or agitated/aggressive behavior who were randomly assigned to receiv

295 s cell carcinoma (HNSCC) is characterized by aggressive behavior with a propensity for metastasis and

296 e genome contributes to the manifestation of aggressive behavior with widespread epistatic interactio

297 The final outcome measure was aggressive behavior, with aggressive cognitions (normati

298 ceptible to predators and will also modulate aggressive behavior within a territory of limited or dep

299 the imaginal evoking of scenarios involving aggressive behavior would be associated with a modulatio

300 assessed the extent to which T's effects on aggressive behavior would depend on variability in trait