ライフサイエンスコーパス: behavior

1 All measures were related to anxiety-like behavior.

2 ely universal science of human cognition and behavior.

3 renatal depressive symptoms as well as child behavior.

4 organizes these cues around the elements of behavior.

5 indfulness meditation might alter pro-social behavior.

6 ul modulator of anxiety- and depressive-like behavior.

7 cies and profoundly influence physiology and behavior.

8 in the association, from gene expression to behavior.

9 cuit mechanism by which octopamine modulates behavior.

10 l tools that can direct and control cellular behavior.

11 plex molecular networks that govern cellular behavior.

12 that potentiate anxiety- and depressive-like behavior.

13 bors they 'listen to' to determine their own behavior.

14 hts into the roles of Piezo in invasive cell behavior.

15 ining odorants to generate learned olfactory behavior.

16 te anchor cell specification and/or invasive behavior.

17 organization and the emergence of collective behavior.

18 onstrate a role of for in larval nociceptive behavior.

19 itochondrial hyperactivity and altered group behavior.

20 redicts the quality of ensuing memory-guided behavior.

21 between stimulus valence and stimulus-driven behavior.

22 d naloxone (NAL) to robustly modulate social behavior.

23 A) matrix, thereby altering the drug release behavior.

24 es, cerebrovascular structure, and cognition/behavior.

25 ressed individuals with and without suicidal behavior.

26 e neural mechanisms underlying cognition and behavior.

27 ciated with circadian outputs and sleep/wake behavior.

28 ack frequency, both with no effect on social behavior.

29 resholds or in capsaicin-induced nocifensive behavior.

30 regulator of cardiac PW1(+) cells fibrogenic behavior.

31 t, which significantly alters the transistor behavior.

32 rats increased nicotine self-administration behavior.

33 influences social preference and repetitive behavior.

34 sform ambiguous sensory data into successful behavior.

35 it facilitated extinction of cocaine-seeking behavior.

36 e the level of disorder show similar binding behavior.

37 e actomyosin cytoskeleton affects phagocytic behavior.

38 ongue cancer was associated with nociceptive behavior.

39 ordinated output of many individual cellular behaviors.

40 s involved in opioid-mediated physiology and behaviors.

41 finement of neuronal circuits and associated behaviors.

42 es through altering LN structures and T cell behaviors.

43 lated genes were associated with alcohol use behaviors.

44 h- but not pain-related scratching or wiping behaviors.

45 stingestive signals to modulate food-seeking behaviors.

46 atomical basis of the stress-related feeding behaviors.

47 in the brain to regulate depression-related behaviors.

48 ceptor, PAC1R, in alcohol withdrawal-induced behaviors.

49 and complex interactions underlying emergent behaviors.

50 bellar output for driving temporally precise behaviors.

51 y-, food reward- and nicotine reward-related behaviors.

52 irect pathways in the SNr and its associated behaviors.

53 terations in a constellation of ASD-relevant behaviors.

54 ions for grouped-ensemble coding of survival behaviors.

55 rd circuits, ultimately leading to addictive behaviors.

56 memories, as well as extinguish maladaptive behaviors.

57 een appetite neuron activity and consumption behaviors.

58 e to the transition from suicide thoughts to behaviors.

59 ptides have emerged to modulate such complex behaviors.

60 neural structure to support species-specific behaviors.

61 pable of continuously monitoring respiratory behaviors.

62 ses that may predispose to addiction-related behaviors.

63 community screenings, and healthcare seeking behaviors.

64 cuit and thereby regulate nicotine avoidance behaviors.

65 egulates various aspects of reward-motivated behaviors.

66 homeostatic contributor to complex bacterial behaviors.

67 e urban life and significantly modify travel behaviors.

68 roinflammatory cytokines and depression-like behaviors.

69 tant cold temperatures before adapting their behavior accordingly.

70 policy makers aiming to encourage prosocial behavior across all income groups.

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

72 Pain-induced defensive behaviors affecting fitness have also been reported in c

73 y, it intends to investigate the arrhythmias behavior after cardioneuroablation.

74 ng flexible memristors with stable switching behaviors after repeated mechanical bending as well as o

75 o loss in bioturbation ecosystem engineering behaviors after the mass extinction, and second, that th

76 developmental shift in microglial migratory behavior along vessels corresponded to when astrocyte en

77 evidence of the deep history of directional behavior among amniotes and may indicate an early origin

78 gnaling molecule in the coordination of cell behavior among prokaryotic species.

79 ical components inherently exhibit chromatic behavior and are typically optimized at discrete spectra

80 It has negative consequences on child behavior and brain development, yet the relationships am

81 stress exposure affect participants' choice behavior and decision speed in a two-stage sequential re

82 ocesses contribute to the control of feeding behavior and help organism's survival when they support

83 hese regulatory pathways to improve stomatal behavior and identify novel unexploited targets for alte

84 sional (3D) collective invasion to study the behavior and importance of protrusion-enriched RNAs.

85 shown great potential in predicting stomatal behavior and improving carbon cycle modeling.

86 el unexploited targets for altering stomatal behavior and improving crop plant productivity.

87 ning protocol increased conditioned freezing behavior and induced an IED; this effect was blocked wit

88 develops accurate spatiotemporal patterns in behavior and influences the perception of temporal inter

89 linked to mechanisms that govern appetitive behavior and its suppression.

90 eurons in Drosophila adults regulate feeding behavior and metabolism.

91 ta-unsaturated hydrazones is presented whose behavior and reactivity are governed by various types of

92 The Ash1l(+/-) mice manifested tic-like behaviors and compulsive behaviors that could be rescued

93 tion selection during challenging visuomotor behaviors and may possibly serve as a window into the su

94 ove cognitive deficits, revert autistic-like behaviors and protect against seizures.

95 Mosquitoes have daily rhythms in behaviors and show a wide range of activity patterns.

96 estigation of the neural basis of navigation behaviors and the evolution of these strategies in arthr

97 ium carrier gas to minimize nonideal mixture behavior, and (4) the direct measurement of pressure ins

98 ced anxiety-like behavior, fragmented social behavior, and altered ultrasonic vocalization patterns a

99 lationships among prenatal depression, child behavior, and children's brain structure remain unclear.

100 hed light on how mucus impacts P. aeruginosa behavior, and may inspire novel approaches for controlli

101 a comprehensive assessment of neuroanatomy, behavior, and neurophysiology.

102 orsolateral striatum (DLS) does for habitual behavior, and our research provides a key set of results

103 architecture underlies this special class of behavior, and review literature that suggests an affirma

104 cted by research comparing human and machine behavior, and that it should be essential to any such co

105 he fact that our methods for measuring human behavior are typically developed and validated for singl

106 vered that sleep-wake brain states and motor behaviors are coregulated by shared neurons in the subst

107 fferent temperature dependent band splitting behaviors are observed at the [Formula: see text] and M

108 an also promote dysfunctional reward-seeking behavior, as in overeating.

109 ous animals showed increased depression-like behaviors, as well as reduced expression of the mitochon

110 Pathological behaviors associated with various neuromuscular diseases

111 e approach, we investigated structural brain-behavior associations in an extensively phenotyped devel

112 ulates multiple phenotypes, including escape behavior, associative learning, immunity and longevity.

113 ments of these assemblies reveal Curie-Weiss behavior at high temperatures, without pairing of the 5f

114 Efforts to quantify behavior at scale are impeded by the fact that our metho

115 lar ROS increases or effects in MEA bursting behavior at sub-lethal dosages.

116 oddler gut microbiome and ASD-related social behaviors at age 3 years.

117 Our findings suggest that healthy behaviors at age 50, as well as improvements in behavior

118 ling approaches reveals the partly different behaviors at varying space velocities for the here prese

119 amyloid-beta and study the resulting coupled behavior between toxic protein clearance and proteopathi

120 ion is tracked and the similarity in general behavior between uniaxial and torsional loading, in spit

121 This behavior boosts Q beyond that of any multivalent scaffol

122 ostasis requires coordinating physiology and behavior both on an acute timescale to adapt to rapid fl

123 ovement in downstream areas that mediate the behavior, but does not drive it.

124 e to orchestrate this epithelial pathfinding behavior, but how this signal is received by epithelial

125 Such changes can lead to profound changes in behavior, but little is known about the precise molecula

126 ese data suggest a broad regulation of motor behavior by DA neurons within multiple hypothalamic nucl

127 ffects on the ACE-induced abnormal emotional behaviors by "calming down" the whole PrL.

128 lls were required to promote depressive-like behaviors by AI-2, as AI-2 administration did not promot

129 Such behavior can be isolated in the reinforcer devaluation t

130 These behaviors can largely be differentiated by the average d

131 , cAMP inhibition) and in vivo (anxiety-like behaviors, cannabimimetic effects, novel environment exp

132 as a predictor of infant scores on the Child Behavior Checklist.

133 uts, and the changing ratios drive different behavior choices.

134 een brain areas important for socioemotional behavior, cognitive, and motor function (e.g. amygdala,

135 These findings imply that the behavior concerning UV exposure is complicated by a gene

136 of secreted polysaccharides in the intricate behaviors coordinating bacterial multicellularity.

137 rt to determine the neural basis of adaptive behavior could benefit from renewed experimental and the

138 udy, in the context of natural freely moving behaviors, could advance models of sensory processing.

139 0.001) and actual consumption and purchasing behavior (d = -0.17; 95% CI: -0.30, -0.04; p = 0.012).

140 muscles, and this correlates with locomotor behavior deficit.

141 eceptor (OTR) plays critical roles in social behavior development.

142 nt learning mechanisms underpinning flexible behavior differed across developmental stages and reduce

143 Balfour and Shuker introduce animal sexual behaviors directed to members of the same sex.

144 We end with a special emphasis on social behavior, discuss whether unique GRN organization and ci

145 romal features (eg, rapid eye movement sleep behavior disorder, hyposmia, constipation), characterist

146 These findings suggest that migratory behavior does not require widespread modifications of br

147 reward, locomotor activity, and anxiety-like behavior], dopamine function [striatal expression of tyr

148 mechanism able to support linear transfer of behavior-driven/learned PC rates concurrently with backg

149 Near the critical drive, time crystal behavior emerges, in which the period of the limit cycle

150 Statistical analysis of the nonlinear behavior encoded in our record reveals the key role that

151 In addition to this behavior, equimolar mixtures of MG2a and PGLa formed sur

152 Aggression is a social behavior essential for securing resources and defending

153 This difference in structural behavior follows directly from hydrogen-bonding restrict

154 is and computer simulation reveal rich phase behavior for this simple model, featuring a broken-symme

155 spring characterized by reduced anxiety-like behavior, fragmented social behavior, and altered ultras

156 and line sensor, cannot capture the spectral behavior from noise to stable mode-locking.

157 intestinal physiology and stress-responsive behavior, functioning as a global regulator of organisma

158 This behavior has been reported across cancer types, both in

159 The importance of affect processing to human behavior has long driven researchers to pursue its measu

160 intensively, their green-state photophysical behavior has received less attention.

161 While these individual cell behaviors have been extensively studied, how cell shape

162 Selection behaviors have been studied under several intersecting u

163 cts of SSRIs on motor function and affective behavior, highlighting the potential benefits of 5-HT2C

164 nabling bacterial groups to coordinate their behavior in a density-dependent manner.

165 raining and acutely terminate learned search behavior in a subsequent recall test.

166 ss developmental stages and reduced flexible behavior in ASD was driven by less optimal learning on a

167 are altering wildlife habitats and wildlife behavior in complex ways.

168 ust framework to predict how complex network behavior in DCvNs emerges from the chemical landscape of

169 del accurately predicts participants' search behavior in different environments.

170 necessary for the expression of binge-eating behavior in female rats.

171 dual is going to retain from her cooperative behavior in future interactions.

172 that removing fruitless reveals this latent behavior in males.

173 these cells was correlated with anxiety-like behavior in mice and was partially dependent on T cell r

174 ow low-cost tools can automatically quantify behavior in naturalistic and social environments over lo

175 te the neural basis of reinforcement-related behavior in normal adolescent development and psychopath

176 of genetic mutations based-on proarrhythmic behavior in phenotypically variable populations.

177 provide novel insights into reduced flexible behavior in relation to clinical symptoms in ASD.

178 characterized limb coordination and walking behavior in response to transient activation of mechanos

179 nductive interfaces, which is an exploitable behavior in solar energy conversion and other applicatio

180 We explain this behavior in terms of how the concentration profile of th

181 Complex 2(+) presents a dynamic behavior in the solution that involves the synchronous c

182 of chemistry, pharmacology, physiology, and behavior in the study of opioids.

183 o synapses onto neurons implicated in social behavior in the ventral forebrain and show that Syt2a is

184 The ion transport behavior in these materials can be regulated through str

185 Discovery of such a feeding behavior in this ancient, terrestrial, and omnivorous an

186 allocation and acquisition, and the role of behavior in this process, will help to build more robust

187 A fundamental understanding of ion transport behavior in wood-based structures enhances the capabilit

188 Testosterone regulates dimorphic sexual behaviors in all vertebrates.

189 st intervention for reducing cocaine-seeking behaviors in animals when given during forced abstinence

190 tion is important for a range of ethological behaviors in mammals.

191 ring certain stereotypical dynamic community behaviors in noisy situations.

192 e withdrawal negatively impacts relapse-like behaviors in rats.

193 regions that are important for memory-guided behaviors, in two tasks: one where attention was guided

194 xtinction, and second, that these persisting behaviors include deep tier, high-impact, complex ecosys

195 can infer asymmetry in predatory or foraging behavior, including predation scars on trilobites [7], d

196 The procedures were insensitive to other behaviors, including jumping and seizures.

197 p of CA1 neurons that robustly encode freeze behavior independently from spatial location.

198 C2I without C2II-CI did not reduce pain-like behavior indicating its intracellular delivery was requi

199 lts showing "when" it is important (i.e., at behavior initiation).

200 behaviors while controlling for pre-training behaviors, Injury Severity Score, postgraduate training

201 Research on migratory behavior is constrained by observational scale [2], limi

202 ent work, enhanced single-chain magnet (SCM) behavior is observed for a Mo(III) -Mn(II) chain that ex

203 However, that behavior is often characterized subjectively, creating o

204 However, such behavior is possible without storing images of shapes in

205 Behavior is readily classified into patterns of movement

206 olution to emerge, and whether the described behavior is robust to variations in the given setup.

207 A fundamental and defining feature of human behavior is the ability to generalize knowledge from the

208 integrated into the brain to drive migratory behavior is unknown.

209 The basis of diurnal versus nocturnal behaviors is driven by molecular clock timing, which cyc

210 We first characterized circadian rhythms of behavior, light responsiveness, and molecular timekeepin

211 Maintaining life-long health behaviors may be crucial to reduce late-life risk of dem

212 sight into the role that mutually beneficial behaviors might play in facilitating and stabilizing soc

213 rain nuclei can lead to pathological feeding behaviors, namely overconsumption of highly palatable fo

214 toms and prevention) and information-seeking behavior (number of web links demanded out of 10 propose

215 etition of information relating to different behavior occur largely outside of the BG.

216 round-level populations could be driving the behavior of An. cruzii, ultimately increasing its contac

217 nges in temperature could influence micellar behavior of bile salts, and in turn whether this affecte

218 s impossible to clinically separate observed behavior of cells from their environmental context, usin

219 In contrast to the behavior of crystalline materials, in the glass paddlewh

220 stal light sharing, which closely mimics the behavior of dual-ended readout, with the additional bene

221 rrent options to investigate the interfacial behavior of food proteins by determination of secondary

222 ding of the surface chemistry and nucleation behavior of iron(III) (hydr)oxides in subsurface and wat

223 ons of regulators and influence the emergent behavior of mitotic waves.

224 dy, we comprehensively assess the ionization behavior of nanoporous polyamide selective layers in sta

225 mical platform to characterize the catalytic behavior of NDH-2 from Caldalkalibacillus thermarum and

226 e switching because the statistical ensemble behavior of oxygen vacancy defects is deterministic even

227 olecular dynamics simulations to dissect the behavior of PRC2 on polynucleosome arrays.

228 gents has deep roots in the strategic social behavior of primates and that the anterior cingulate gyr

229 elevant to the synthesis and cotranslational behavior of some proteins.

230 theoretical framework to elucidate the phase behavior of the linker-mediated vitrimers, in which entr

231 ilize the lithium-metal anode, the solvation behavior of the solvent molecules must be understood bec

232 have resulted from altered distributions and behavior of their prey species, which are prone to respo

233 ions of 3D MEAs to monitor electromechanical behaviors of cardiomyocytes and neurons.

234 trafficking, analysis of specific migratory behaviors of lymphocytes within the tissue microenvironm

235 significantly influenced by the policies and behaviors of people in other, sometimes distant, regions

236 pothesized that the speciation and transport behaviors of phosphate ions are highly influenced by ele

237 In the end, all the 475 behaviors of supervisors to regulate autonomy in this st

238 ot promote susceptibility to depressive-like behaviors or SAA1 and SAA2 production in Th17-deficient

239 aviors at age 50, as well as improvements in behaviors over midlife, are associated with a lower risk

240 of time series that exhibit closely-related behaviors over time, even if the timing is not perfectly

241 1-methyl tryptophan reduced depressive-like behavior (P <= 0.001) compared to controls.

242 owed the highest benefit (>40%) for flossing behavior (P = 0.0005).

243 mediation models between the PRSBMI, eating behavior patterns, and obesity measures.

244 ncipal component analyses to identify eating behavior patterns, twin modeling to decompose correlatio

245 pic traits that have greatly impacted insect behavior, physiology, and evolution.

246 metic effects, novel environment exploratory behavior, pre-pulse inhibition, conditioned avoidance re

247 a mechanistic understanding for the observed behaviors, predominantly focusing on the cell-nanostruct

248 o characteristic mitotic somal translocation behavior previously only observed in human development,

249 Self-reported knowledge, attitudes, and behaviors related to COVID-19.

250 Insights into the characteristics and behaviors related to late eating may be useful in the de

251 oes not harmonize with the notion that brain-behavior relationships are flexible and may involve inte

252 Thus, delineating neural control of behavior requires a dissociation between stimulus valenc

253 Goal-directed behavior requires the interaction of multiple brain regi

254 ss them.SIGNIFICANCE STATEMENT Healthy human behavior requires the suppression or inhibition of erran

255 erence impairments and repetitive/inflexible behaviors, respectively, in male PC-Tsc1 mutant mice.

256 unbiased screen for increased female chasing behavior revealed the involvement of another sexually di

257 salt selection process, the salt dissolution behavior should be well understood.

258 s were likely capable of forays onto land, a behavior similar to that of extant horseshoe crabs.

259 exhibits fast velocity and superprocessivity behavior similar to WT KIF1A.

260 itive neural marker of suicidal thoughts and behaviors (STBs) or nonsuicidal self-injury (NSSI), and

261 The 3-factor model of sexual behavior stigma cut across social contexts among MSM in

262 ex-specific effects on social- and affective behavior, stress regulation, and neural activity.

263 system function, and fundamental changes in behaviors such as learning, memory, and social interacti

264 n model may be useful in promoting healthier behaviors such as smoking cessation or in aiding persons

265 ent on circadian clocks to regulate critical behaviors, such as foraging orientation and navigation,

266 ng and then apparently reversing, a peculiar behavior that can be modeled by accounting for different

267 d persistent changes in DHPG-induced LTD and behavior that were not present under basal conditions.

268 in strong attraction to a live human host, a behavior that wild-type males never display, suggesting

269 manifested tic-like behaviors and compulsive behaviors that could be rescued by the tic-relieving dru

270 on, geologists have documented fault valving behavior, that is, cyclic changes in pressure and unstea

271 entives are often effective at inducing good behavior, they've been shown to have self-image costs: T

272 Lgmn evokes pain-like behavior through PAR(2) Exposure of pain-sensing neurons

273 ed the effects of charge patterning on phase behavior through sequence shuffling.

274 neurons may help shape threat-reward choice behaviors through interacting with other neurons.

275 e, decreased motivation, and compulsive-like behavior to acquire cocaine, and it facilitated extincti

276 rared radiation, responding with specialized behaviors to prevent overheating of their wings.

277 armacological inhibition, we define the cell behaviors underlying each stage of vascular remodeling a

278 Achieving this behavior using conventional approaches is challenging be

279 Higher MLVI indicates worse adherence behavior; values >=2.5 are predictive of late allograft

280 and Rho-kinase in mediating depression-like behaviors via dendritic remodeling of NAc D1-MSNs and ma

281 hich memories predicted drinking, real-world behavior was assessed in patients with AUD at baseline a

282 y Psi, the temporal variability of hydraulic behavior was explored in relation to soil water supply,

283 cal neurons and synapses underlying rhythmic behavior, we analyzed the circuits' response to modifica

284 Energy balance and eating behavior were also normal, even after exposure to high-f

285 in mood or self-reports of suicidal ideation/behavior were observed.

286 Data on social and reproductive behaviors were collected from six tapirs (three males, t

287 a diverse set of contexts influences citizen behavior when formal democratic institutions erode or di

288 rcuit induced social deficits and repetitive behaviors, whereas activation of Purkinje cells (PCs) in

289 Epithelial remodeling involves ratcheting behavior whereby periodic contractility produces transie

290 he first time, to our knowledge, the dynamic behavior whereby Tfh cells migrate in human GC and highl

291 timates from the literature for other animal behaviors, which suggests that problem-solving is a stab

292 ost-training group differences in leadership behaviors while controlling for pre-training behaviors,

293 are necessary and sufficient for male sexual behaviors, while VMHvl-projecting PA(Esr1+) cells are ex

294 l defeat stress (CSDS) in mice and evaluated behavior with PsychoGenics' SmartCube, a high-throughput

295 s, which exhibit stable Li stripping/plating behaviors with low overpotential of ~6 mV at 200 degrees

296 ltiple brain regions in control of multistep behavior, with MD regions particularly involved in proce

297 0% of the fish displayed extensive fathering behavior within 90 min.

298 ought to study how YAP influences tumor cell behavior within the circulatory system.

299 the effects of the compound in dysregulated behaviors within the transgenic models.

300 An attract-and-kill trap based on psyllid behavior would fill a niche for monitoring and control.