ライフサイエンスコーパス: behavior

1 ory detection) and approach (to obtain food) behavior.

2 lopmental, and contextual factors in shaping behavior.

3 A) transmission mediates numerous aspects of behavior.

4 netic marks interact to shape differences in behavior.

5 ing the genetics of animal (including human) behavior.

6 es in compulsive "addiction-like" aggressive behavior.

7 ion in space, as manifestation of collective behavior.

8 tension during the imagination of aggressive behavior.

9 ors (AABCS) on weight, body composition, and behavior.

10 ce in the higher-order regulation of feeding behavior.

11 s associated with compulsive alcohol-seeking behavior.

12 r switching produces up or down reversals of behavior.

13 seful for predicting future risk of suicidal behavior.

14 ironment-which function in the modulation of behavior.

15 age) prediction of patients' future suicidal behavior.

16 de object information relevant to memory and behavior.

17 hotomy between top-down and bottom-up driven behavior.

18 ence suggests that it modulates drug-related behavior.

19 oxyglucose uptake and aggressive oncological behavior.

20 ine-induced locomotor and place conditioning behavior.

21 during behavior and in the sleep state after behavior.

22 g information, or surprise is fundamental to behavior.

23 and behavioral phenotypes, including social behavior.

24 notonically with force, indicating slip-bond behavior.

25 n discrimination was evident in the animals' behavior.

26 e discrimination was evident in the animals' behavior.

27 3 and 60-64 years were influenced by smoking behavior.

28 ctory system guides the expression of social behavior.

29 gical relevance of the observed thermotactic behavior.

30 rameter space that corresponds to a specific behavior.

31 or as two core exemplars of early disruptive behavior.

32 en to their heart' to guide their altruistic behavior.

33 omic characteristics and aggressive clinical behavior.

34 l, and may exhibit a distinctive immunologic behavior.

35 cannot be explained by changes in appetitive behavior.

36 nto a categorical format underlying flexible behavior.

37 e of spatial information during navigational behavior.

38 dergic signaling to influence physiology and behavior.

39 sensory responsiveness and controlling motor behavior.

40 o, and in Drosophila, a few showed anomalous behavior.

41 ctrophysiology to computational modeling and behavior.

42 s how simple networks of neurons can control behavior.

43 A nutrient signals to modulate food-directed behavior.

44 al cells precisely to drive olfactory-guided behavior.

45 tory markers can directly modulate affective behavior.

46 ccount for attention-related improvements in behavior.

47 al cells to ensure coordinated multicellular behavior.

48 bout and less able to control fear or safety behaviors.

49 on affect patient's actual medication-taking behaviors.

50 ion that bacteria use to regulate collective behaviors.

51 diminished depression-like and anxiety-like behaviors.

52 enables bacteria to use it to direct future behaviors.

53 manipulate beneficial and harmful bacterial behaviors.

54 l preferences affect a broad array of social behaviors.

55 ct subsets are thought to regulate different behaviors.

56 ampal neurogenesis and hippocampus-dependent behaviors.

57 of further consummatory, social, and sexual behaviors.

58 ffectiveness for treating schizophrenia-like behaviors.

59 ynamic systems that demonstrate nonintuitive behaviors.

60 rstanding of the physics underlying material behaviors.

61 ion of dopamine release and dopamine-related behaviors.

62 NAc may promote abstinence from drug-taking behaviors.

63 in cervical cancer screening and sexual risk behaviors.

64 itters and neurocircuits as well as specific behaviors.

65 n systems are shown to have highly nonlinear behavior across force conditions that may be exploited a

66 able to studies of dynamic mechanics on cell behavior across many cell types and contexts.

67 tes the possibility of predicting individual behaviors across tasks with patterns of brain activity.

68 s drastically changed the membranes' dynamic behavior, almost completely negating the previously obse

69 ortance of continuing surveillance of sexual behaviors, alongside vaccine status, to predict future d

70 tribution of Mrgprs to SP-induced scratching behavior and activation of cultured dorsal root ganglion

71 impulsivity and their relation to antisocial behavior and adversity are poorly understood.

72 ection to higher brain that influence innate behavior and are essential for learned responses to tast

73 markedly and persistently elevate ingestive behavior and body weight and ultimately resulted in a do

74 The strain-hardening behavior and chain alignment are found to depend on the

75 rience during development alters nociceptive behavior and circuit physiology in Drosophila larvae.

76 factors that shape their differentiation and behavior and describe how macrophages change during prot

77 Our data suggests that mouse behavior and EEG recordings are not sensitive to decreas

78 x transformations can occur, causing altered behavior and effects compared to the pristine NPs.

79 pathogens can influence or manipulate insect behavior and fitness by altering plant quality and defen

80 as the consequences of these changes for the behavior and fitness of insect herbivores.

81 (SWRs) occur both in the awake state during behavior and in the sleep state after behavior.

82 drug-related cues reinstated cocaine-seeking behavior and increased AMPK and p70s6k phosphorylation i

83 ety-like behavior, decreased depression-like behavior and increased preference for rewarding stimuli.

84 Parental behavior and knowledge were assessed through immediate (

85 implicated in diverse domains of sex-biased behavior and pathology, but we lack a basic understandin

86 m seizures and better scores with respect to behavior and quality of life than did those who continue

87 eason in wild Arctic foxes may affect mating behavior and reproductive success.

88 Task behavior and self-reported self-reliance for decision-ma

89 pen new vistas on the neural basis of social behavior and social impairment.

90 de gliomas (LGGs) are heterogeneous in their behavior and the strategies used for clinical management

91 due to diabetes contribute to different VSMC behavior and thus vascular disease.

92 We compared the biomechanical behavior and vascular healing profile of a novel thin-wa

93 d by both a high occurrence of perseverative behaviors and a lack of deliberation during the SWM test

94 riefly describe some successes in predicting behaviors and describe the challenges over the next few

95 Mechanistically linking movement behaviors and ecology is key to understanding the adapti

96 mands for movement associated with different behaviors and environments.

97 cells were dispensable for acute nociceptive behaviors and for aversion induced by thermal pain or a

98 rger for reports of internal states than for behaviors and for negative mental states and physical sy

99 ogram holds the potential to improve patient behaviors and outcomes, current research on the program

100 g approximations by restricting the range of behaviors and states considered.

101 of stock-outs, in-country purchasing, usage behavior, and breadth of available purchasing options to

102 Foraging is a fundamental behavior, and many types of animals appear to have solve

103 verbearing in their narrative, aggressive in behavior, and often exhibit questionable moral character

104 ures, gait abnormalities, problems of social behavior, and other variable features.

105 und neural synchrony in key nonverbal social behaviors, and highlight the role of human attachment in

106 system has key roles in sexual and emotional behaviors, and is a likely candidate system for the inte

107 hich parallel biogenic amine signaling tunes behavior appropriately to nutrient conditions.SIGNIFICAN

108 atomic chains and the resulting anisotropic behavior are clearly revealed.

109 How these different aspects of cell behavior are coordinated through a single receptor is no

110 owever, their spatiotemporal dynamics during behavior are poorly understood.

111 that neural circuits supporting model-based behavior are structurally homologous to and overlapping

112 A statistical study of the cracking behavior as a function of crystal orientation in a laser

113 RBS) was employed to understand this unusual behavior as to whether it is a mixture of two phases, la

114 e authors highlight irritability and callous behavior as two core exemplars of early disruptive behav

115 ain the counterintuitive pseudocontact shift behavior, as well as a striking solvent dependence.

116 s reveal roles of gap junctions in a complex behavior at cellular resolution and provide a tool for s

117 play a more heterogeneous range of migratory behaviors at later stages of development, with the acqui

118 This prey switching behavior attenuated an iconic predator-prey interaction

119 lities, i.e. learning impairment and nesting behaviors based on passive avoidance, T-Maze, and nestin

120 we have simultaneously measured nociceptive behavior, brain activity, and levels of physiological st

121 These dynamic changes influence multiple behaviors but are particularly important for reproductio

122 convergence in circuits underlying motivated behavior, but it remains unclear how its inputs from dif

123 ifically, T caused an increase in aggressive behavior, but only among men scoring relatively high in

124 to pain control, drug reward, and addictive behaviors, but underlying circuit mechanisms have been p

125 he brain processes information and generates behavior by employing a wide array of different cell typ

126 Memory can inform goal-directed behavior by linking current opportunities to past outcom

127 ism fosters tolerance of diverse beliefs and behaviors by forbidding judgment on foreign societal cod

128 In these mixtures, the phase behavior can be tuned from a mixed state to a coexistenc

129 re to persuasive messages can predict health behavior change.

130 FORCE trained networks reproduce behaviors comparable in complexity to their inspired cir

131 CMT2D mice display changes in sensory behavior concordant with the afferent imbalance, which i

132 Several of these risk-taking behaviors constituted a behavioral syndrome that signifi

133 Olfactory perception and behaviors critically depend on the ability to identify a

134 zed by hyperactivity, decreased anxiety-like behavior, decreased depression-like behavior and increas

135 ogical models which exhibit such paradoxical behavior depend on the presence of exogenous environment

136 identify idiopathic rapid eye movement sleep behavior disorder (IRBD) patients at risk for short-term

137 t, and fundamental understanding of cellular behavior during hypoxia.

138 IR40a-dependent pathways drive hygrosensory behavior: each is important for dry-seeking by hydrated

139 Analysis of temperature-directed behaviors elicited by persistent PKC-2 activation or inh

140 sources of ALAN can broadly effect migratory behavior, emphasizing the need to better understand the

141 olymerize and depolymerize stochastically, a behavior essential for cell division, motility, and diff

142 populations effectively normalizing all the behaviors examined.

143 Human behaviors exhibit ubiquitous correlations in many aspect

144 Excited state behavior follows predicable patterns.

145 opores alone, it is possible to change their behavior from dampers to molecular springs.

146 canteen infrastructure to improve purchasing behavior from primary school canteens.

147 in social groups, stress-induced changes in behavior have the potential to act as a source of inform

148 eal-world stimuli that are most relevant for behavior (i.e., speech, voice).

149 Aggression is a universal social behavior important for the acquisition of food, mates, t

150 nt, together with heightened anxiety-related behavior in a stressful environment.

151 easurements to explore their bioaccumulation behavior in a subarctic lake.

152 are machines for high-throughput analysis of behavior in Drosophila and other animals.

153 ects of miRNA regulation on a complex innate behavior in Drosophila and suggests that miRNAs may be c

154 etails governing OM-induced modulation of XB behavior in failing human myocardium are unclear.

155 Here we explore the X chromosome behavior in female and hermaphrodite meioses.

156 Although claudin strand behavior in fibroblasts may not fully recapitulate that

157 drial metabolism and further affecting motor behavior in HD mice, thus constituting a promising agent

158 Sickness behavior in humans is characterized by low mood and fati

159 the CNS, we used CGRP-induced light-aversive behavior in mice as a measure of migraine-associated pho

160 n-outcome memory, resulting in goal-directed behavior in mice that would otherwise express stimulus-r

161 uitry involved in the two types of orienting behavior in mice, we injected retrograde tracer into the

162 actic against stress-induced depressive-like behavior in mice.

163 uggested that core deficits in goal-directed behavior in obsessive-compulsive disorder (OCD) are caus

164 R) antagonists on measures of impulsive-like behavior in rats were evaluated using the five-choice se

165 s that robustly exhibit the desired abstract behavior in realistic physical models and in experimenta

166 species complex towards increased zoophilic behavior in recent years.

167 How PFC ensembles represent shifts in behavior in response to changes in these contingencies r

168 itions.SIGNIFICANCE STATEMENT Animals adjust behavior in response to environmental changes, such as f

169 nations also account for increased prosocial behavior in situations in which attractive individuals a

170 strongly required in order to explain their behavior in solution and in biological environment.

171 of strained cycloalkynes can influence their behavior in subsequent reactions, providing opportunitie

172 between different types of observed crawling behavior in the dynamical phase diagram, such as self-tr

173 ant animals displayed increased anxiety-like behavior in the elevated plus maze and in a light/dark b

174 to this tension-and the adaptation of social behavior in this game-hinges on the game's learning dyna

175 y information and facilitate decision-making behaviors in C. elegans.

176 he extracellular loops of OprH show distinct behaviors in different LPS environments.

177 ved collaborative and undermining coparental behaviors in infancy and preschool, assayed oxytocin (OT

178 sophila; while most mutations showed similar behaviors in yeast, in vitro, and in Drosophila, a few s

179 offers an avenue to understand dynamic cell behavior, including processes such as induced pluripoten

180 ct to brain structures that govern motivated behavior, including the ventral tegmental area (VTA).

181 tic transmission controls brain activity and behaviors, including food intake.

182 ersible and enhanced at higher temperatures, behaviors indicative of active recruitment to the nucleo

183 e supporting the effectiveness of a consumer-behavior intervention using an existing online canteen i

184 A physical model for this behavior involving a combination of tranverse diffusion

185 king difference in compulsive-like locomotor behavior is also based on differential VTA innervation.

186 In addition, analogous photochemical behavior is also demonstrated on other MV(2+)/BU6 crysta

187 this study suggest that synchronous maternal behavior is associated with increased dopamine responses

188 We conclude that this behavior is best explained by a form of path integration

189 in female presence is attenuated and mating behavior is impaired.

190 that the study of the link between brain and behavior is impossible without a guiding vision.

191 , the authors conclude that early disruptive behavior is neurodevelopmental in nature and should be r

192 Antisocial behavior is often assumed to reflect aberrant risk proce

193 Addressing how neural circuits underlie behavior is routinely done by measuring electrical activ

194 ght or circular trajectories, and the motile behavior is sensitive to conditions at the cell boundary

195 Interestingly, this elastic behavior is transferable to small networks, where we fou

196 Animal behavior is ultimately the product of gene regulatory ne

197 ocess is found to follow a diffusion-limited behavior leading to core-shell morphologies.

198 ke timing drive differences in perception or behavior, leaving it unclear whether the information in

199 n has used artificial stimuli and simplified behaviors, leaving open questions about nervous system f

200 ting treatment of epilepsy and autistic-like behaviors linked to DS with CBD.

201 ide new insights into their electrocatalytic behavior, mass transport, and interactions with surfaces

202 w predictions of the sensory consequences of behavior may be generated in other sensory structures an

203 Consequently, newborn behaviors may serve both biological and social-cognitive

204 ty behavior, which would make sun protective behavior more likely, could be promoted and supported by

205 derstanding dopamine processing of motivated behavior; most critically, it indicates that dopamine ne

206 Fundamentally, collective behavior must arise from the actions of individual cells

207 ems chemistry aims to emulate the functional behavior observed in living systems by constructing chem

208 , retinal, and scleral cells, similar to the behavior observed in macrophages.

209 Sex-specific mating behaviors occur in a variety of mammals, with the medial

210 radionuclide tracer test, the environmental behavior of (233)U, (237)Np, (242)Pu, and (243)Am was in

211 of the interface on the electrical transport behavior of a small-resistance GaSb sample and explained

212 We find that the behavior of brookite, both in the dynamics of relaxation

213 The behavior of C, H, and S in the solid Earth depends on th

214 cross-linking on the anisotropic mechanical behavior of C-(A-)S-H.

215 ed that AqJAG disproportionally controls the behavior of cells with adaxial identity in vegetative ti

216 e increased our understanding of the dynamic behavior of complex multiprotein systems.

217 ntitative understanding of the intracellular behavior of drug-loaded nanoparticles, and provides insi

218 es in understanding the adsorption and phase behavior of fluids confined in ordered nanoporous materi

219 notubes (LGC), are fabricated to emulate the behavior of Li metal and Li-free Li metal anodes, respec

220 Results indicate that antioxidant behavior of limonene, linalool and citral occurs by co-o

221 rmation mechanisms underlying the mechanical behavior of materials is the key to fundamental and engi

222 We study the phase behavior of microspheres in the presence of poly(N-isopr

223 This results in the net behavior of nodes composing resting-state networks ident

224 factor, which determines sequence-dependent behavior of peptides in HILIC.

225 n regarding the ionization and fragmentation behavior of peroxy acids in mass spectrometers.

226 could be confirmed by differential migration behavior of protein fragments in gel electrophoresis.

227 e polymorphisms, considering depth-dependent behavior of similarity metrics for identical and unrelat

228 Prediction of thermal behavior of SOA can be achieved by a concise number of d

229 The behavior of SoPIN1 and PIN1b in Arabidopsis illustrates

230 contribute critically to the mechanochemical behavior of stress fibers, actin arcs, and cortical acti

231 amics (BOMD) simulations examine the dynamic behavior of syn- and anti-CH3 CHOO at the air-water inte

232 in nature when one considers the collective behavior of the double-twist cylinders.

233 The dynamic collision behavior of the electro-oxidation of single Ag nanoparti

234 the previously baffling substrate-inhibition behavior of the enzyme.

235 roach was developed to better understand the behavior of the flatulence-causing oligosaccharides in c

236 ng (5, 10, and 100 nm), due to the transient behavior of the metal interface layer.

237 f the spatial game can be predicted from the behavior of the replicator equation for the modified gam

238 he payoff matrix, and once this is done, the behavior of the spatial game can be predicted from the b

239 say predicted here because in some cases the behavior of the spatial game is different from that of t

240 (CNT) for extrusion-because of the peculiar behavior of water in extreme confinement.

241 Tm(3+) or Ho(3+) ion on optical temperature behavior of Y2O3:Er(3+) microtubes is investigated by an

242 ntifying molecular signatures of coordinated behaviors of cancer cells as a population - in turn may

243 Understanding phase behaviors of nanoconfined water has driven notable resea

244 Characterizing the binding behaviors of RNA-binding proteins (RBPs) is important fo

245 Here, we investigate the dynamic behaviors of the entropic uncertainty relation of an ato

246 We also monitored the behaviors of X-linked non-coding transcripts before and

247 ing synaptic integrity and performing animal behavior on T1R3KO mice.

248 hydrophobicity, spreading patterns, and flow behavior on various sized fluidic patterns.

249 tion density and collectively initiate a new behavior once a critical density is reached.

250 mouse, compared with time spent in nonsocial behavior or remaining immobile.

251 ted action selection, countering habit-based behavior otherwise facilitated by developmental stress h

252 in (AVP), and measured coparenting and child behavior problems at 6 years.

253 Cooperative behaviors provide a collective benefit, but are consider

254 the mesolimbic nuclei as the core of reward behavior regulation.

255 ion, the potentially different ADAR1 binding behaviors related to its editing activity, as well as th

256 tion patterns that reflect the causal neuron-behavior relationship.

257 n of neuroscience when it comes to the brain-behavior relationship: behavioral work provides understa

258 egulation on the genetic programs underlying behavior remain largely unexplored.

259 Mapping whole-brain activity during behavior represents one of the biggest and most exciting

260 mediating control of male and female sexual behavior, respectively.

261 CS was unrelated to behavior, self-esteem and depressive symptoms adjusted f

262 New work on innate escape behavior shows that mice spontaneously form a spatially

263 e long-lasting extinction of alcohol-seeking behavior.SIGNIFICANCE STATEMENT Alcohol use disorder is

264 as signaling molecules to regulate stem cell behaviors such as migration.

265 ved social interaction, and improved natural behaviors such as nesting and marble burying as well as

266 y anchovies, demonstrated a range of feeding behaviors such as oblique, vertical, and lateral lunging

267 e accounting for known phenomenological cell behaviors, such as contact inhibition of locomotion and

268 This suggests that behaviors, such as overeating or drug taking, might be e

269 estibular recovery to support normal balance behaviors, suggesting a therapeutic benefit to balance w

270 This behavior supports social cohesion by providing a key mec

271 This study used state-level Youth Risk Behavior Surveillance System (YRBSS) data from January 1

272 ed on passive avoidance, T-Maze, and nesting behavior tests.

273 , which substantially restricts the range of behaviors that can be studied.

274 mygdala (BLA) contributes to emotion-related behaviors that differ between males and females and acro

275 es reducing infection, animals can engage in behaviors that lower the impact of the infection.

276 hin biofilm communities can coordinate their behavior through cell-to-cell signaling.

277 foraging payoff, 49% of birds switched their behavior to a higher-payoff foraging technique after onl

278 s in the anastasis genes, pathways, and cell behaviors to those activated in wound healing and identi

279 time spent by adult mice engaging in social behaviors toward a juvenile mouse, compared with time sp

280 ere characterized, and their electrochemical behavior towards SY was investigated.

281 tic stimulation of these projections affects behavior using conditioned place preference and a task i

282 r psychosis for violent ideation and violent behavior using the Structured Interview for Psychosis-Ri

283 The approach integrates cellular behaviors via agent-based modeling (ABM) and hemodynamic

284 tation while suppressing inertial cavitation behavior was designed and validated using a dual-transdu

285 administration and cue-induced reinstatement behavior was measured after intracerebroventricular inje

286 This behavior was only observed when animals were water-depri

287 The behavior we report appears to be general, implying that

288 ly driven, but not self-directed, repetitive behaviors were exacerbated in lesioned mice.

289 Sickness behaviors were quantified based on time spent by adult m

290 e cortical activity), and facial expression (behavior) were acquired in individual infants following

291 s of biological networks and cause alternate behaviors when they occur across many genes.

292 rt accurate memory storage and memory-guided behavior, whereas sleep SWR reactivation is better suite

293 itive attitudes and beliefs about sun safety behavior, which would make sun protective behavior more

294 ntentional imitation, the dyad shows mimicry behaviors, which are automatic, but do not fade through

295 -184 showed a linear sorption and outgassing behavior with no-hysteresis over the entire temperature

296 owing defined primary study outcomes: coping behavior with respect to itching (P < .001), quality of

297 kely candidate system for the integration of behavior with the hormonal reproductive axis.

298 NG2/CSPG4 may have different effects on cell behavior with tumor progression.

299 transplants produced differential effects on behavior, with PV-enriched populations effectively norma

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