ライフサイエンスコーパス: behavioral response

1 in regions significantly correlated with the behavioral response.

2 ard threat-associated stimuli is an adaptive behavioral response.

3 link the calls to a discriminative maternal behavioral response.

4 detects rewarding stimuli and coordinates a behavioral response.

5 intaining F-/G-actin equilibrium for optimal behavioral response.

6 plex, involving also a direct scaling of the behavioral response.

7 t induce a percept which, in turn, induces a behavioral response.

8 enzyme acts in these neurons to buffer this behavioral response.

9 nse, and remained localized to ALM until the behavioral response.

10 r, citalopram, revealed a genotype-dependent behavioral response.

11 phase coherence is associated with a faster behavioral response.

12 tches stimulus history to odor sensation and behavioral responses.

13 s motivational states to guide affective and behavioral responses.

14 inking auditory perception with sex-specific behavioral responses.

15 eural pathways link sound-related signals to behavioral responses.

16 ear filters that allow for the prediction of behavioral responses.

17 ain sensations to coordinate host-protective behavioral responses.

18 into mechanisms that can constrain adaptive behavioral responses.

19 r learning is essential to maintain accurate behavioral responses.

20 sequently, this directly influenced observed behavioral responses.

21 behaviorally relevant ensembles and correct behavioral responses.

22 BDNF release in driving scopolamine-induced behavioral responses.

23 ulation (TMS) with computational modeling of behavioral responses.

24 ulted in altered neurologic and/or locomotor behavioral responses.

25 the impact of these modulatory mechanisms on behavioral responses.

26 an be processed together to produce adaptive behavioral responses.

27 re derived from a Bayesian observer model of behavioral responses.

28 depletion of E2f3 isoforms in NAc on cocaine behavioral responses.

29 for T4 directional selectivity and ON motion behavioral responses.

30 onally selective and necessary for ON motion behavioral responses.

31 urogenesis, each blocks the ketamine-induced behavioral responses.

32 n important role in many brain functions and behavioral responses.

33 ion of 5-HT2B receptors to cocaine-dependent behavioral responses.

34 blocked chronic constriction injury-induced behavioral responses.

35 different contexts all gave rise to similar behavioral responses.

36 granule neurons play a crucial role in these behavioral responses.

37 otonergic neurons induce antidepressant-like behavioral responses.

38 us (DRN) serotonergic neurons induces robust behavioral responses.

39 odulation of amygdala-mediated emotional and behavioral responses.

40 or function and profoundly affect subsequent behavioral responses.

41 ial attention, multisensory integration, and behavioral responses.

42 ch signal aspects are necessary to reproduce behavioral responses.

43 better self-evaluation of the correctness of behavioral responses.

44 xetine actions on D1 receptor expression and behavioral responses.

45 l-to-trial correlations between neuronal and behavioral responses.

46 s opioids modulate many of our emotional and behavioral responses.

47 m mixing of biotic communities to individual behavioral responses.

48 ses sensory information to generate adaptive behavioral responses.

49 associations between sensory information and behavioral responses.

50 to reshape gene expression and control cell behavioral responses.

51 ed to inspect novel items and initiate rapid behavioral-responses.

52 t flexibility allows animals to modify their behavioral responses according to environmental cues, me

53 This behavioral response after tDCS coincided with an enhance

54 Behavioral response also affected the oviposition of T.

55 Here, we show that this behavioral response also requires Efa6, one of (at least

56 system mediates protective physiological and behavioral responses amid infection.

57 Antidepressant-relevant behavioral responses and (2R,6R)-HNK levels in the extra

58 with verapamil prevented scopolamine-induced behavioral responses and BDNF-tropomyosin receptor kinas

59 tral nervous system, and is involved in many behavioral responses and brain functions.

60 acteristics for species discrimination, with behavioral responses and computational results indicatin

61 Behavioral responses and GluA1 levels in the hippocampal

62 ure that modulates autonomic, endocrine, and behavioral responses and is a potential therapeutic targ

63 he target authors focus too much on adaptive behavioral responses and not enough on actual psychologi

64 HFD also increased behavioral responses and paw swelling to paw injection o

65 mechanosensitive information to drive rapid behavioral responses and protect teeth from damage.

66 d too late to account for spatially directed behavioral responses and, thus, only after remapping mus

67 st in deep layers of ALM, seconds before the behavioral response, and remained localized to ALM until

68 oendocrine cell coordinates an organism-wide behavioral response, and suggest that similar signaling

69 ls in response to acute stress is the normal behavioral response, and thus, MAGL inhibitors, which pr

70 s relationships among environmental stimuli, behavioral responses, and predicted outcomes.

71 Water consumption, thyroid hormone function, behavioral responses, and skull and jawbone measurements

72 has been previously associated with reward, behavioral responses are faster and more accurate compar

73 icin as a sensitizing stimulus, we show that behavioral responses are greater in the TG region and th

74 We show that these sustained behavioral responses are mediated by a long-lasting pote

75 Multiple neuroendocrine, autonomic and behavioral responses are regulated by the paraventricula

76 l moderated mediation analysis revealed that behavioral responses are significantly involved in the t

77 purely mechanical stimulus elicited the same behavioral response as a natural shaking signal, teasing

78 y signaled as a quantity and induced similar behavioral responses as learned threat probability.

79 riphery, allowing for more rapid and precise behavioral responses as required in the highly social gr

80 tion of both SPN populations on drug-induced behavioral responses, as these studies can contribute to

81 demonstrate that CGRP-induced headache-like behavioral responses at doses up to 3.8 mug are female-s

82 lay period, which is typically followed by a behavioral response based on the remembered information.

83 ionally, linear-nonlinear models can predict behavioral responses based only on sensory neuron activi

84 Visual stimuli can evoke complex behavioral responses, but the underlying streams of neur

85 The amygdala facilitates odor driven behavioral responses by enhancing the saliency of olfact

86 ation of CGRP to the cranial meninges causes behavioral responses consistent with headache in preclin

87 ecific optogenetic stimulation revealed that behavioral response depended on the activity of M2 neuro

88 These cellular and behavioral responses depended on the TRPA1 channel, whos

89 y stimuli, but whether they express atypical behavioral responses depends on top-down regulatory mech

90 nct or shared between patterns of aggressive behavioral responses directed at simulated conspecific v

91 we investigated an alternative view in which behavioral responses do not exclusively depend on but th

92 tic strength in the NAc shell and triggers a behavioral response driven by a drug-associated memory.

93 y animal's internal state, and determine the behavioral response during motivational conflict.

94 s projecting to PL more accurately predicted behavioral responses during competition than unidentifie

95 related to patients' retaliatory propensity (behavioral responses during the task) and parent-reporte

96 ricides with little or no information on the behavioral responses elicited after acaricide exposure.

97 Hunger shifts the behavioral response from aversion to attraction by enhan

98 ions that were too low to trigger observable behavioral responses from WT animals.

99 Valid cueing induced a behavioral response gain increase, higher asymptotic per

100 lliseconds, but the corresponding sub-second behavioral responses have not been adequately explored i

101 f mood.Rewards or punishments elicit diverse behavioral responses; however, the neural circuits under

102 Stressful events evoke long-term changes in behavioral responses; however, the underlying mechanisms

103 Participants' behavioral responses (i.e., satisfaction ratings) were m

104 neuronal connection, and reduced optokinetic behavioral response in zebrafish larvae.

105 or an animal's survival by ensuring adaptive behavioral responses in an ever-changing environment.

106 itored respiration to visualize anticipatory behavioral responses in an odor fear conditioning in rat

107 retards nerve conduction and impairs sensory behavioral responses in animals.

108 processing at the circuit level or abnormal behavioral responses in ASD mouse models, especially dur

109 generated, and how they modulate neural and behavioral responses in both mice and humans.

110 red acyl-ghrelin induces antidepressant-like behavioral responses in mice, and mice with deleted ghre

111 mechanotransduction and mechanically-evoked behavioral responses in mice.

112 Here we encode multi-behavioral responses in microscopic self-propelled tori

113 hat the TRPA1 KO rat shows apparently normal behavioral responses in multiple models of pain and itch

114 rties, evaluated by electrophysiological and behavioral responses in Sprague-Dawley (SD) rats.

115 Orchestrating appropriate behavioral responses in the face of competing signals th

116 it is critical in governing the selection of behavioral responses in the face of competing signals.

117 ablish a critical role for prolactin-induced behavioral responses in the maternal brain, ensuring sur

118 erotonergic development, leading to impaired behavioral responses in zebrafish larvae.

119 e for eliciting much of the shaking signal's behavioral response, in one of the few examples of direc

120 nd the predictable pitfalls of its hardwired behavioral responses (including a maladaptive form of "i

121 Behavioral responses, including scototaxis, activity, ex

122 c feeding schedules (HFS) exhibit compulsive behavioral responses involving food anticipatory activit

123 alamic response and expression of compulsive behavioral responses involving meal anticipation and con

124 play any role in modulating the accuracy of behavioral responses is poorly understood.

125 Further evidence for DAMP signaling in behavioral responses is provided by evidence that HMGB1

126 Impaired inhibition of fear or behavioral responses is thought to be central to PTSD sy

127 ention deficits, but were normal in baseline behavioral responses, learning, memory, and sensorimotor

128 We find that behavioral responses made immediately after viewing a st

129 fferences in the 5-HT2 receptor synaptic and behavioral responses may be related to the lack of psych

130 ifficult to infer their collective effect on behavioral responses mediated by activity across populat

131 d gene clusters associated with the observed behavioral responses, mostly related to the stress axis.

132 athogen-induced ROS activate sod-1 dependent behavioral response non cell-autonomously.

133 open-access conditions that account for the behavioral response of fishers to the MPA; this approach

134 understanding of the detection threshold and behavioral response of fishes in response to crude oil i

135 resistance to these acaricides affected the behavioral response of T. urticae, especially in MET-I r

136 In this study, we evaluated behavioral responses of cabbage root flies [Delia radicu

137 -depth recorder to monitor physiological and behavioral responses of East Greenland narwhals after re

138 Here, we characterize behavioral responses of freely swimming larval zebrafish

139 We examined electrophysiological and behavioral responses of honey bees to microbial volatile

140 Interestingly, appetitive behavioral responses of wild type flies to hexanoic acid

141 These findings show that the influence of behavioral responses on perception is particularly stron

142 Behavioral response patterns suggest that OXT specifical

143 This behavioral response provides zooplankton with the capabi

144 integrate and translate these features into behavioral responses remains a major question.

145 impact of physiological resistance on these behavioral responses remains unknown in most pest specie

146 RN types were co-activated, the level of the behavioral response resembled the sum of the component r

147 Behavioral responses revealed that SZ patients exhibited

148 Behavioral responses showed a looming bias in that respo

149 the animal to select a socially appropriate behavioral response.SIGNIFICANCE STATEMENT Understanding

150 bitory balance in the PFC and its control of behavioral responses.SIGNIFICANCE STATEMENT A developmen

151 layed to VTA(GABA+) neurons mediating innate behavioral responses, suggesting a more general role of

152 cue-evoked dopamine response and changes in behavioral responses-supporting a role for dopamine in m

153 h necessary and sufficient for such forms of behavioral response suppression.

154 se stimuli reliably produce weaker circadian behavioral responses than those favoring L-opsin ("yello

155 hite noise elicits greater physiological and behavioral responses than tones even prior to conditioni

156 elicit different sensory, physiological, and behavioral responses that affect body weight.

157 In fishes, olfactory cues evoke behavioral responses that are crucial to survival; howev

158 amina terminalis in regulating endocrine and behavioral responses that are involved in maintaining ca

159 Many chemosensory stimuli evoke innate behavioral responses that can be either appetitive or av

160 lis AT1aR neurons induces neuroendocrine and behavioral responses that increase blood pressure.SIGNIF

161 ionship between colonic tissue integrity and behavioral responses that is not often assessed in studi

162 e is controlled by endocrine, autonomic, and behavioral responses that maintain blood volume and perf

163 emia alters the cascade of physiological and behavioral responses that maintain euglycemia.

164 tress elicits neuroendocrine, autonomic, and behavioral responses that mitigate homeostatic imbalance

165 gnitive control is the ability to modify the behavioral response to a stimulus based on internal repr

166 vivo LTH manifests as a persistently reduced behavioral response to an odorant encountered for 4 cont

167 One mutant gave a greater physiological and behavioral response to an odorant that affects ovipositi

168 The behavioral response to antidepressants is closely associ

169 ressive disorder or in mediating the delayed behavioral response to antidepressants.

170 of NPAS2 in the NAc reduces the conditioned behavioral response to cocaine in mice.

171 G-CSF) as a neuroactive cytokine that alters behavioral response to cocaine, increases synaptic dopam

172 content of VWM has been shown to affect the behavioral response to concurrent visual input, suggesti

173 have reported that food odors enhance flies' behavioral response to cVA, specifically in virgin femal

174 Nocturnal mosquitoes exhibit a behavioral response to divert away from surfaces when vi

175 tidepressant-like activity and enhancing the behavioral response to fluoxetine.

176 establish p75NTR as a novel regulator gating behavioral response to food scarcity and time-of-day dep

177 tate of redox homeostasis could underlie the behavioral response to harmful microbial species.

178 of GABAergic IP/MnR interconnections in the behavioral response to nicotine.

179 pha'3 compartment plays a causal role in the behavioral response to novel and familiar stimuli as a c

180 Animals exhibit a behavioral response to novel sensory stimuli about which

181 ate gyrus PV cells plays a major role in the behavioral response to novelty and stress.

182 Social decision-making underlies an animal's behavioral response to others in a range of social conte

183 r's disease (AD) with an abnormally enhanced behavioral response to pitch perturbation.

184 tion session suggested a correlation between behavioral response to right temporal lobe tACS and func

185 al circuitry mediating the physiological and behavioral response to satiation and noxious/stressful s

186 hestrating the neuroendocrine, autonomic and behavioral response to stressful situations.

187 We characterized the behavioral response to subthreshold stress in mice with

188 l adulthood was not alone sufficient for the behavioral response to the pheromone.

189 owing in part to an initial overgeneralized behavioral response to the safe category.

190 virtue of a hunger-dependent switch in their behavioral response to this stimulus.

191 processing of sensory stimuli, not just the behavioral response to those stimuli.

192 Here, we evaluated the behavioral response to whisker stimulation in mice lacki

193 pening the acquisition of cardiovascular and behavioral responses to a Pavlovian threat cue.

194 eta-arrestin as a potential player mediating behavioral responses to acute alcohol exposure.

195 ordination of neuroendocrine, autonomic, and behavioral responses to acute and chronic stress.

196 ally long delays between tactile stimuli and behavioral responses to aid relating oscillatory activit

197 (fruit fly), demonstrating that PLD mediates behavioral responses to alcohol in vivo.

198 rs (GPCRs) that are associated with aberrant behavioral responses to alcohol.

199 Physiological and behavioral responses to ammonia depend at least in part

200 quirement for PV+ interneurons of the NAc in behavioral responses to AMPH, and they raise the possibi

201 sed within the alBST contributes to multiple behavioral responses to anxiogenic threats, yet also ser

202 responses in auditory cortex and recovery of behavioral responses to auditory and vestibular stimulat

203 sugar-sweetened beverage intake on brain and behavioral responses to beverage stimuli.We performed an

204 r leads to the loss of the physiological and behavioral responses to chronic antidepressants.

205 modulation, enabling them to drive opposite behavioral responses to CO2.

206 potential target genes that may underlie the behavioral responses to cocaine in Npas2 mutant females.

207 A-independent, mechanisms that contribute to behavioral responses to cocaine, including psychomotor s

208 expression of PGC-1alpha in D1-MSNs enhanced behavioral responses to cocaine, while expression in D2-

209 major homeostatic modulator of molecular and behavioral responses to cocaine.

210 s to dopamine neurons fundamentally regulate behavioral responses to cocaine.

211 tion of ATP-P2X4 signaling reduced reflexive behavioral responses to cold and heat stimuli.

212 Here, we review the plasticity of behavioral responses to different odor types according t

213 Diurnal rhythms are commonly found in behavioral responses to drugs of abuse with drug sensiti

214 e been widely implicated in the cellular and behavioral responses to drugs of abuse.

215 tes activity within the nucleus accumbens or behavioral responses to drugs of abuse.

216 substance, is involved in many cellular and behavioral responses to ethanol.

217 which a PNN protein facilitates appropriate behavioral responses to experience by dynamically gating

218 Inhibitory engrams can reduce behavioral responses to familiar stimuli, thereby result

219 ctopamine neurons are required for sustained behavioral responses to fast-moving, but not slow-moving

220 Importantly, loss of appetitive behavioral responses to fatty acids in IR25a and IR76b m

221 rojections dissociate the cardiovascular and behavioral responses to fluid imbalance.

222 ls, and going without other basic needs) and behavioral responses to hardship (pawning items and seek

223 There was no association between behavioral responses to hardship and cognitive performan

224 Benefits previously observed in behavioral responses to iDC steps delivered after sustai

225 Irs play critical roles in the detection and behavioral responses to important classes of host odors

226 uitoes' innate temporal attraction/avoidance behavioral responses to light and their regulation by ci

227 l electrophysiological phototransduction and behavioral responses to light.

228 hub that is able to coordinate autonomic and behavioral responses to many types of stimuli.

229 A dissociation between the absence of behavioral responses to motor commands and the evidence

230 We show that behavioral responses to natural and synthesized vocaliza

231 ns humans perform are near optimal, and that behavioral responses to natural stimuli can be studied w

232 Gpr151- knockout (KO) mice show diminished behavioral responses to nicotine and self-administer gre

233 iors, including models of mood disorders and behavioral responses to nicotine.

234 inoids have similar bidirectional effects on behavioral responses to nociceptive vs. non-nociceptive

235 ypothalamic activity establishes appropriate behavioral responses to novel and familiar objects.

236 emotionality, we use rats bred for distinct behavioral responses to novelty.

237 ficient to disrupt social behavior and alter behavioral responses to novelty.

238 its identity, can lead to striking shifts in behavioral responses to objects.

239 tic resonance imaging; and investigated main behavioral responses to opiates, including motivation to

240 ns controls aggregation behavior and related behavioral responses to oxygen, pheromones, and food in

241 they navigate heterogeneous landscapes, and behavioral responses to perceived risk can structure eco

242 ly obtainable with other techniques, such as behavioral responses to pharmacological manipulations an

243 ticolimbic drive may promote abnormal stress behavioral responses to predator odor during protracted

244 tive network.SIGNIFICANCE STATEMENT Although behavioral responses to predatory threat are essential f

245 hich likely reflects the utmost relevance of behavioral responses to protect the body.

246 Individuals can show several behavioral responses to reduce competition for habitat,

247 lies abuse vulnerability by facilitating the behavioral responses to repeated cocaine, such as locomo

248 ine their role in mediating inflammatory and behavioral responses to repeated social defeat stress (R

249 Stress is widely known to alter behavioral responses to rewards and punishments.

250 Together, these results suggest that the behavioral responses to rosiglitazone are mediated throu

251 1 mice also had more robust dopaminergic and behavioral responses to salient visual stimuli, which we

252 tween SCN states is critical for maintaining behavioral responses to seasonal change, but the mechani

253 inactivation attenuating both unconditioned behavioral responses to somatic pain and fear-memory for

254 Behavioral responses to some noxious thermal and mechani

255 tmc triple mutants lacked behavioral responses to sound and head movements, while

256 Learned behavioral responses to sounds depend largely on the exp

257 space and use post hoc analysis to determine behavioral responses to specific activations.

258 how neuromodulatory states like stress alter behavioral responses to stimuli.

259 the limbic-hypothalamic system important for behavioral responses to stress and alcohol, and glutamat

260 ng of these circuits in early life modulates behavioral responses to stress in adulthood.

261 ng the neurobiological mechanisms underlying behavioral responses to stress is necessary to improve t

262 the dentate gyrus, but its role in mediating behavioral responses to stress is unknown.

263 the limbic-hypothalamic system important for behavioral responses to stress, and glutamate transmissi

264 om brain regions implicated in autonomic and behavioral responses to stress, as well as direct input

265 cleus accumbens (NAc) regulates mood-related behavioral responses to stress.

266 hestrates neurophysiological, autonomic, and behavioral responses to stress.

267 decreased their neuronal as well as animals' behavioral responses to sucrose and AA.

268 their neuronal responses as well as animals' behavioral responses to sucrose and AA.

269 First, IR76b mutants exhibited clear behavioral responses to sucrose and acetic acid (AA) at

270 arious studies have shown blunted neural and behavioral responses to the experience of reward in depr

271 rea 14, to a group of unoperated controls on behavioral responses to the presentation of a fake rubbe

272 imuli are encountered can engender different behavioral responses to the same stimulus.

273 The augmented behavioral responses to the selective serotonin reuptake

274 How behavioral responses to these different modalities are p

275 ensory cues are processed to elicit adaptive behavioral responses to threat and will help to identify

276 Behavioral responses to threat are critical to survival.

277 f lower-order subcortical representations to behavioral responses to threat in adult humans.

278 ate defensive responses toward more adaptive behavioral responses to threatening stimuli.

279 XT neurons or loss of the peptide attenuates behavioral responses to TRPA1 activation.

280 ts are revealing how the fly brain generates behavioral responses to visual stimuli.

281 n 3 (EB3) and SRC kinase in the neuronal and behavioral responses to volitionally administered cocain

282 for both positive and negative emotional and behavioral responses to warmer temperatures.

283 e role of these OFC subregions in regulating behavioral responses under threat.

284 They lack acoustic-evoked behavioral responses, vestibular-induced eye movements,

285 A similar behavioral response was observed with another MGL inhibi

286 This tuning of behavioral responses was specific to cues associated wit

287 detecting spinally versus centrally mediated behavioral responses, we chemogenetically activated noci

288 These plant behavioral responses were initially investigated more th

289 Behavioral responses were more similar to the identity-b

290 s were provided from 3 months of age, but no behavioral responses were noted when these were worn.

291 Behavioral responses were subsequently replicated in 2 p

292 Intraoperative behavioral responses were used as a secondary verificati

293 (categorized according to their hormonal and behavioral responses) were assessed by multimodal neuroi

294 This was corroborated in behavioral responses, where IRD patients showed slower a

295 the auditory cortex predicted the timing of behavioral responses, whereas tone-evoked cortical coupl

296 adult male Long Evans rats and aligned this behavioral response with APA events using a Whole Transc

297 r 28 days with paroxetine and assessed their behavioral response with the forced swim test (FST).

298 his framework can be used to quantify animal behavioral responses with implications for ecology and c

299 The ability to coordinate behavioral responses with metabolic status is fundamenta

300 "Tribute in Light" in New York, quantifying behavioral responses with radar and acoustic sensors and