ライフサイエンスコーパス: aggressive behavior

1 strate mesenchymal properties and coincident aggressive behavior.

2 duals with recurrent, problematic, impulsive aggressive behavior.

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

4 which ultimately could restart with similar aggressive behavior.

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

6 layed higher rates of proliferation and more aggressive behavior.

7 school performance, prosocial behavior, and aggressive behavior.

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

9 ting that it could contribute to synoviocyte aggressive behavior.

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

11 CL2 or BCL6 translocations conferring a very aggressive behavior.

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

13 tor in the pathophysiology of antisocial and aggressive behavior.

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

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

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

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

18 ent studies analyzing isolated indicators of aggressive behavior.

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

20 rse stressors and prevention of uncontrolled aggressive behavior.

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

22 underlying manifestation of and variation in aggressive behavior.

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

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

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

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

27 in the limbic circuitry mediating escalated aggressive behavior.

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

29 In adults, fluoxetine treatment inhibited aggressive behavior.

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

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

32 reater efficacy than haloperidol in reducing aggressive behavior.

33 erized malignant neoplasms with particularly aggressive behavior.

34 ons by higher proliferative indices and more aggressive behavior.

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

36 size >2 cm is independently associated with aggressive behavior.

37 trition may help reduce later antisocial and aggressive behavior.

38 ENs) and identify preoperative predictors of aggressive behavior.

39 e versus the consummatory (attack) phases of aggressive behavior.

40 dilation were independently associated with aggressive behavior.

41 61 asymptomatic cPanNENs <=2 cm displayed an aggressive behavior.

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

43 aggressive tension during the imagination of aggressive behavior.

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

45 are vascular tumor which has an intermediate aggressive behavior.

46 the neural circuit that generates male-type aggressive behavior.

47 ilience to punishment-induced suppression of aggressive behavior.

48 sensory modality in the context of intermale aggressive behavior.

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

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

51 several biogenic amines and neuropeptides on aggressive behavior.

52 te their consequences for the development of aggressive behavior.

53 re crucially involved in the pathogenesis of aggressive behavior.

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

55 which probably accounts for their clinically aggressive behavior.

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

57 ns to appetitive and consummatory sexual and aggressive behaviors.

58 specifics as well as simultaneously decrease aggressive behaviors.

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

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

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

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

63 understanding of the genetic architecture of aggressive behaviors.

64 ing domains show a division of labor on male aggressive behaviors.

65 at LS lesions lead to a dramatic increase in aggressive behaviors.

66 ogeneity resulting from a selection for more aggressive behaviors.

67 features of this malignancy account for such aggressive behavior?

68 (0.75 times as high; 95% CI: 0.57, 0.99) and Aggressive Behavior (0.82 times as high; 95% CI: 0.70, 0

69 decreased reproductive output, courtship and aggressive behaviors, 11-ketotestosterone (11KT), and sp

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

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

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

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

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

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

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

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

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

79 In honey bees, social cues broadly modulate aggressive behavior and brain gene expression.

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

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

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

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

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

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

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

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

88 cystamine-mediated TGase inhibition reduced aggressive behavior and movement in crayfish.

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

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

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

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

93 s important for the regulation of inter-male aggressive behavior and provide the first functional evi

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

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

96 phenotype of glioblastoma cells toward more aggressive behavior and therefore makes PGC-1alpha a pot

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

98 e suggesting shared genetic etiology between aggressive behavior and uncaring, and unemotional CU-tra

99 cea, Stomatopoda) are well studied for their aggressive behavior and unique visual system as well as

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

101 genome-wide association study of children's aggressive behavior and were used to calculate individua

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

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

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

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

106 Although aggressive behaviors and temperament are highly heritabl

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

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

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

110 For depression and anxiety, aggressive behavior, and attention-deficit/hyperactivity

111 Symptoms of depression and anxiety, aggressive behavior, and attention-deficit/hyperactivity

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

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

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

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

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

117 t LINC01268 influences emotional regulation, aggressive behavior, and suicide by violent means; the u

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

119 Neural circuits that underlie aggressive behavior are therefore likely under the contr

120 Impulsive and aggressive behaviors are both modulated by serotonergic

121 Sexual and aggressive behaviors are fundamental to animal survival

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

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

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

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

126 size >2 cm was independently associated with aggressive behavior both in the whole cohort and in the

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

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

129 rs of the effects of stress on prosocial and aggressive behavior, but call for refinement in future r

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

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

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

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

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

135 16B function promotes lengthened displays of aggressive behaviors by male mice during the resident in

136 Epistasis for aggressive behavior causes cryptic genetic variation in

137 Alcohol misuse or aggressive behavior comorbidity was present in approxima

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

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

140 The frequency of aggressive behavior declined significantly during the fi

141 Aggressive behaviors directed toward adult males, by con

142 CU traits, (b) explain the severe pattern of aggressive behavior displayed by children with elevated

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

144 s underlie the divergence of male and female aggressive behaviors, from their monomorphic appetitive/

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

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

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

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

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

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

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

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

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

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

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

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

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

158 lation in the hemolymph and strongly reduces aggressive behavior in crayfish.

159 Assays to quantify aggressive behavior in Drosophila melanogaster have been

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

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

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

163 lateral habenula neurons, thereby governing aggressive behavior in male mice.

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

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

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

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

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

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

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

171 ow altered cellular behaviors and diminished aggressive behavior in response to MEK inhibition.

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

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

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

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

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

177 y expressed in specific brain nuclei causing aggressive behavior in the white-throated sparrow.

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

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

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

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

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

183 f TMEM16B function lengthens the displays of aggressive behaviors in male mice.

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

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

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

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

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

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

190 This neuronal class can promote aggressive behavior independent of another sex determini

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

192 Aggressive behavior is a complex social behavior that is

193 Inter-male aggressive behavior is a prominent sexually dimorphic be

194 Aggressive behavior is observed across animal taxa and i

195 ), although dsx is involved in ensuring that aggressive behavior is performed only toward males.

196 Aggressive behavior is pervasive throughout the animal k

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

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

199 attack experience leading to an increase in aggressive behavior, known as aggression priming, activa

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

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

202 inant role of fru in specifying sex-specific aggressive behavior may underscore a genetic mechanism t

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

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

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

206 Neither aggressive behavior nor yawning (indicators of androgen

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

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

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

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

211 The aggressive behavior of glioblastomas, including resistan

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

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

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

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

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

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

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

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

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

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

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

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

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

225 ion factor, in defining the stemness and the aggressive behavior of pancreatic cancer.

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

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

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

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

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

231 These results provide the evidence that aggressive behavior of radioresistant BC is caused by CD

232 The aggressive behavior of RDEB-associated SCCs remains unex

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

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

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

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

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

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

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

240 TAK1 is implicated in aggressive behavior of TNBC, while means are not fully u

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

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

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

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

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

249 iotropic effects of TNFalpha playing role in aggressive behaviors of TNBC subtype while its deficienc

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

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

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

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

254 d this up-regulation is associated with more aggressive behavior, radioresistance, and recurrence of

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

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

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

258 enetic mechanism that generates sex-specific aggressive behavior remains largely unknown.

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 l) are essential regions for male sexual and aggressive behaviors, respectively.

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

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

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

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

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

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 wer risk of depressive and anxiety symptoms, aggressive behavior symptoms, and attention-deficit/hype

270 5% confidence interval (CI): 1.13, 2.32] and Aggressive Behavior syndromes (1.29 times greater; 95% C

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

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

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

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

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

276 as not found to have a significant effect on aggressive behavior, though dominant females had elongat

277 ests that the cerebellar vermis may regulate aggressive behavior, though the cerebellar circuits and

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

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

280 re a genetic mechanism that allows male-type aggressive behavior to evolve at least partially indepen

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

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

283 these neuronal populations can also promote aggressive behavior toward male flies, this capacity req

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

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

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

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

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

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

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 er attainment: They engaged in more dominant-aggressive behavior, which positively predicted attainin

294 uantify their importance as risk factors for aggressive behavior, which resulted in 40 top-ranked and

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

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

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

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

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

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