ライフサイエンスコーパス: behaviour

1 k for the evolution of indiscriminate sexual behaviour.

2 D) to determine their movements and swimming behaviour.

3 or the transgenerational inheritance of this behaviour.

4 sics responsible for their unusual nonlinear behaviour.

5 wo types of cities tend to display different behaviour.

6 netheless mediate different computations and behaviour.

7 ce of the experimental subject in studies of behaviour.

8 f the spatiotemporal neural codes underlying behaviour.

9 high socioeconomic status, and risky sexual behaviour.

10 he microbiome to alter reproduction and host behaviour.

11 r-loser experience did not influence contest behaviour.

12 al properties and high-fidelity shape memory behaviour.

13 dependent oscillations to a homogeneous bulk behaviour.

14 n the context of organ donation registration behaviour.

15 tering of species composition, abundance and behaviour.

16 aumatic stress disorder (PTSD), and suicidal behaviour.

17 text or intraspecific variation in dispersal behaviour.

18 e the proximate and ultimate drivers of this behaviour.

19 utcomes is a fundamental element of adaptive behaviour.

20 lineage-specific separation in cell-cycling behaviour.

21 host physiology, development, immunity, and behaviour.

22 e expression, concurrent with slowed cycling behaviour.

23 eness in determining initiation of agonistic behaviour.

24 grative area with distinct features of motor behaviour.

25 eriments as a manifestation of supercritical behaviour.

26 interventions promoting well-adjusted social behaviour.

27 providing unprecedented insight into animal behaviour.

28 corporates the multiple dimensions of choice behaviour.

29 est cells almost always only exhibit spiking behaviour.

30 he microenvironmental regulation of PCa cell behaviour.

31 ility of using the SBP to decode complicated behaviour.

32 hout perturbing their natural properties and behaviour.

33 s no association with cognition, language or behaviour.

34 poral organisation that promotes oscillatory behaviour.

35 table embedding that generalizes to external behaviour.

36 emporal pattern of resources in home ranging behaviour.

37 motor decision processes eliciting reactive behaviour.

38 as an individual's characteristic locomotor behaviour.

39 tic systems, leading to predictable eruptive behaviour.

40 ust, task-independent index of interpersonal behaviour.

41 st, muscimol, induced general disruptions to behaviour.

42 ts, with and without shade- or water-seeking behaviours.

43 expression to regulate impulsive-aggressive behaviours.

44 computations in various neural processes and behaviours.

45 weak, risk factors for suicidal thoughts and behaviours.

46 lationship between risk perceptions and risk behaviours.

47 te the cycle of impulsive and harm-avoidance behaviours.

48 night, to determine circadian adaptation and behaviours.

49 ield using telemetry to document risk-taking behaviours.

50 uronal density and decreased depressive-like behaviours.

51 antity of prey might influence their feeding behaviours.

52 estionnaire on COVID-19 related symptoms and behaviours.

53 udinal correlates) for suicidal thoughts and behaviours.

54 underlying changes in these mate preference behaviours.

55 ar effect of temperature was present in both behaviours.

56 earn online in the presence of goal-directed behaviours.

57 degree does urbanization affect antipredator behaviour?

58 -8) or semiconducting(9,10) to metallic-like behaviour(11).

59 n and motility(2,3), and brain-wired feeding behaviour(2).

60 due to their orientation-dependent transport behaviour(8-10) and lower defect concentrations(11,12).

61 assessing the local prevalence of migratory behaviour across large landscapes.

62 lso for the evolution of discriminate sexual behaviour across the animal kingdom.

63 proximately daily) rhythms of physiology and behaviour adapt organisms to the alternating environment

64 ion, violence experience and recent suicidal behaviour, alcohol use and recent suicidal behaviour, il

65 sh using simplified models that are based on behaviour alone.

66 hen the putative link between grid cells and behaviour along with their cognitive functions beyond na

67 are unlikely to have a sufficient effect on behaviour among female sex workers to change pregnancy i

68 limitations and to determine whether patient behaviour and anaphylaxis management improve with its us

69 erone is a key mediator of vertebrate social behaviour and can influence how individuals interact wit

70 experiment to investigate pangolin foraging behaviour and cognition, which may have implications for

71 ine how intraspecific variation in dispersal behaviour and community context influence dispersal dyna

72 distinctions between compulsive drug-seeking behaviour and compulsive drug-taking behaviour (that is,

73 f different baits on the attraction, surface behaviour and conditioning of white sharks Carcharodon c

74 al self-reported survey responses on health, behaviour and demographics.

75 However, tools to track the systemic behaviour and dynamics of leukocytes non-invasively in v

76 s for future research linking humans, animal behaviour and ecology.

77 Investigating behaviour and energy use across these periods is fundame

78 e know less about their effects on herbivore behaviour and especially on spatial patterns of damage.

79 networks and the causal modulation of human behaviour and experience with iES.

80 odel repositions semantics, language, social behaviour and face recognition into a continuous frontot

81 mes softened with a "liquid-like" mechanical behaviour and gains superior malleability and deformabil

82 Patients showed reduced habitual behaviour and increased responses in the hippocampus tha

83 inks between the individual ecophysiological behaviour and its evolutionary gain would increase our u

84 namics of multicomponent intracellular phase behaviour and its interplay with the nonequilibrium acti

85 new links between avian physiology, ecology, behaviour and life history, while demonstrating the impo

86 In summary, aggressive cancer cell behaviour and reduced drug responsiveness was observed w

87 vulnerability factors for specific types of behaviour and the optimal management strategies.

88 We reproduce both the re-entrant melting behaviour and the polymorphism of the solid phase.

89 Mating behaviour and the timing of reproduction can inhibit gen

90 s to investigate changes in gene expression, behaviour and welfare after fin clipping and swabbing.

91 the importance of studying both group-level behaviours and individual relationships to more fully un

92 utative roles governing certain evolutionary behaviours and mood modulation.

93 nternal state to elicit both variable innate behaviours and reinforced behaviours that may promote ma

94 ment of the superior colliculus in defensive behaviours and visual threat detection.

95 ndard deviation increase in lifetime smoking behaviour) and an independent causal effect of alcohol c

96 ompound classes and their mass spectrometric behaviour, and poses the risk of missing unknown, potent

97 rs were compared to 26 patients without such behaviours, and 31 elderly healthy controls.

98 ce as a phase of rapid change in cooperative behaviours, and highlight this as a key developmental wi

99 ences with asthma, symptoms, self-management behaviours, and relationship to asthma control and quali

100 tention for changing drug use patterns, risk behaviours, and susceptible subgroups (eg, PWID experien

101 focusing on among-individual differences in behaviour ('animal personality') has been blooming for o

102 -level resilience were identified in nurses' behaviour: anticipatory resilience, responsive resilienc

103 Dam building and food caching behaviours appear to be specializations for cold winter

104 Oculomotor behaviours are commonly used to evaluate sensorimotor di

105 ther the intent and neural encoding of these behaviours are similar or different.

106 eotypies-repetitive, unvarying, functionless behaviours -are common abnormal behaviours that often ar

107 appreciate the distinctive character of this behaviour as a display of fairness put into practice.

108 share the same basic influences on avoidance behaviour as more primary aversive stimuli such as physi

109 Apart from a few studies on their ensemble behaviour (as monolayers or thin films), this potential

110 ing state with antiferromagnetic Curie-Weiss behaviour, as expected for a Hubbard model in the strong

111 unexplored approach to realize protein-like behaviour at the single-polymer-chain level in a predict

112 ontinue to influence these habitat selection behaviours at increasing distances from outside of their

113 We investigated variation in two behaviours at three different temperatures and in a temp

114 to gather information about a trustee's past behaviour before deciding whether or not to trust them.

115 Differences were elicited in cognition and behaviour between bvFTD and FTD-ALS, and patients carryi

116 all, our results suggest that differences in behaviour between native and introduced species are one

117 are phenotypic differences in cognition and behaviour between patients with FTD-ALS and bvFTD alone.

118 l networks we observed that there is scaling behaviour between the information required to describe a

119 timing of gene expression, and variation in behaviour between them.

120 Across different behaviours, both in water and on land, dynamic body acce

121 en states' that are not reflected in ongoing behaviour but rather carry information about prior actio

122 Therefore, collective behaviour can be an emergent selective driver for undiff

123 Cooperative behaviour can have profound effects on demography.

124 e of the impairment in oculomotor and ocular behaviours caused by EtOH administration across a range

125 t of a tailored, evidence-based brief health behaviour change intervention (leaflet) on self-reported

126 ted and the need for PrEP fluctuates as risk behaviours change.

127 ing common individual socioeconomic and risk behaviour correlates.

128 The study of animal behaviour could benefit greatly from generally expanding

129 Theoretical studies suggest that dispersal behaviour could either cause or prevent the propagation

130 Understanding participant behaviour could support better use of the data, by accou

131 We establish that the social behaviour deficits in offspring exposed to MIA can be te

132 op on chickadee mobbing calls and vary their behaviour depending on the threat encoded in those calls

133 Mutant zebrafish exhibit different behaviours depending on the genetic background of the fi

134 lf-reported weight status, and other dietary behaviours, derived from GB Kantar FMCG.

135 ieties and (3) societally variable prosocial behaviour develops concurrently with the responsiveness

136 Differences in reproductive behaviours did affect survival such that warming tempera

137 nner-loser effect on initiation of agonistic behaviour (display, non-damaging aggression, biting and

138 unlikely that they actually made use of this behaviour due to a lack of predation pressure and no rec

139 while the plates show distinct ferromagnetic behaviour due to the strong competition between the inte

140 nhances the desire to engage in cool-seeking behaviour during passive heat stress.

141 ed particles with a range of active swimming behaviours embedded within the currents of a high-resolu

142 tration and scan rate dependant irreversible behaviour evident at glassy carbon and gold transducers

143 euronal cell types were identified for risky behaviour (excitatory), major depression (inhibitory), s

144 demonstrates that individual differences in behaviour explain important differences in survival but

145 of convection cells are responsible for this behaviour for [Formula: see text], which also increases

146 he importance of individual thermoregulatory behaviours for understanding species' vulnerability to c

147 heir structures to transform their regulated behaviour from the molecular to the supramolecular level

148 articularly challenging to study dynamic HSC behaviour, given that the visualization of HSCs in the n

149 o and used spliffs, the following spliff use behaviour groups were less likely to have their first jo

150 Unlike behaviour, happiness is not sensitive to learning-irrele

151 Likewise, both obesity and addictive behaviours have similar correlations with broad personal

152 on lifetime self-harm ideation and self-harm behaviour (i.e. any lifetime self-harm act regardless of

153 Impulse control behaviours (ICBs) are a range of behaviours linked by th

154 l behaviour, alcohol use and recent suicidal behaviour, illicit drug use and depression, depression a

155 Some behaviours improved, notably hand hygiene and keeping th

156 ery and a virtual casino to assess impulsive behaviour in a naturalistic fashion, 55 patients with Pa

157 te hidden Markov model (HMM) to detect musth behaviour in a subset of sequential tracking data.

158 on morphology, bang sensitivity and climbing behaviour in comparison between single and pairwise dosa

159 the importance of natural patterns of facial behaviour in emotional expressions, and demonstrate the

160 is one of the first to quantify antipredator behaviour in endemic species after the eradication of in

161 ted provides a new avenue to study materials behaviour in extreme environments.

162 Behaviour in FTD-ALS was dominated by apathy.

163 al diversity of monomers, to achieve uniform behaviour in heterogeneous systems.

164 l cross-breeding incident to study migratory behaviour in naturally occurring hybrids as well as in t

165 rogramme could effectively improve self-care behaviour in patients with heart failure.

166 form current predictive models of mechanical behaviour in polymer-composite materials, particularly a

167 ear, and wolf habitat selection and movement behaviour in response to anthropogenic habitat modificat

168 different expression dynamics leads to rich behaviour in response to cold and a wide range of vernal

169 ments, which facilitates the study of larval behaviour in response to local sensory input.

170 glutamate and GABA correlate with impulsive behaviour in several neuropsychiatric diseases and there

171 hrough active inference can support adaptive behaviour in spite of, and indeed because of, their depa

172 externalist account that understands social behaviour in terms of its environment-involving dynamics

173 analysed locomotor activity and anxiety-like behaviour in the offspring.

174 l skills, little is known about their social behaviour in the wild.

175 sia negated the reduction in anxiety-related behaviour in tunnel compared with tail handled BALB/c mi

176 o predict behaviours on land versus foraging behaviour in water (R(2) = 0.75).

177 males, but not males, modified their jumping behaviour in weight-dependent manner, but only when they

178 combined with selection for novel mammalian behaviours in Late Triassic cynodonts, drove the functio

179 Post-inflammatory behaviours in rodents are widely used to model human dep

180 Dynamic triplet-exciton behaviours including thermally activated delayed fluores

181 ng treatment, and then measured reproductive behaviours, including the number, size and burial depth

182 ized mechanisms that drive predator and prey behaviour, incorporating environmental realism not possi

183 dence that colony-wide escape (i.e., flight) behaviour increased during drone flights, at any altitud

184 demonstrate that learning via goal-directed behaviour indeed constrains models to behaviorally relev

185 he ASI neuron are all required for avoidance behaviour induced by bacterial small RNAs, and for the t

186 Although friendship as a social behaviour is an evolved trait that shares many similarit

187 This critical behaviour is confined to a small area in the density-ele

188 at a daily scale, and the clear signal that behaviour is environmentally forced through optimisation

189 Quantification of behaviour is essential for biology.

190 s (such as teaching transgressors that their behaviour is inappropriate).

191 Adaptive behaviour is necessary to cope with the complexity of pr

192 equently used to guide such campaigns, human behaviour is often ill-represented, if at all.

193 idence that individual variation in foraging behaviour is shaped by animal personality traits, such a

194 e network activity is transformed into human behaviours, it is necessary to identify task-specific ne

195 lse control behaviours (ICBs) are a range of behaviours linked by their reward-based, repetitive natu

196 and acidification (OA) affect key ecological behaviours (locomotion speed and foraging success) and m

197 s suggests that individuals expressing risky behaviours might be of overall higher quality but the la

198 k preferences, and indeed the motivations of behaviour, not so simple or straightforward to interpret

199 point is approached in a way reminiscent to behaviour observed in magnetic counterparts.

200 striking switch from in-phase to anti-phase behaviour occurs, signalling a reorganization of the cli

201 , we provide evidence that (1) the prosocial behaviour of adults is predicted by what other members o

202 that the stereotyped group diving and vocal behaviour of beaked whales has benefits for abatement of

203 hoton polymerisation and explore the dynamic behaviour of defects when confined by polymer structures

204 This work captures the dynamic behaviour of E2 and has direct relevance to the interact

205 An electrochemical behaviour of FNX was studied on a glassy carbon electrod

206 ow bulk properties arise from the collective behaviour of individual structures.

207 The behaviour of lithium metal within the MIEC channels sugg

208 The behaviour of males, which have higher wing loading requi

209 does not accurately capture the biology and behaviour of many mosquito vectors that refeed frequentl

210 on has been shown to improve the rehydration behaviour of milk protein isolate (MPI).

211 vel, observing changes in the conformational behaviour of monomers, with a possible link to aggregati

212 metrics to describe the temporal and spatial behaviour of participants, as well as variation in the d

213 irected towards influencing the prescription behaviour of practitioners through 'key opinion leaders'

214 ged particles, for instance: to evaluate the behaviour of proposed designs, to determine the effects

215 bit are known(5), each reflecting a distinct behaviour of quantum fluctuations in a Cooper pair conde

216 due to a general trend of the bulk or to the behaviour of single genotypes.

217 Further, we uncover an inverse power law behaviour of spectral measures with the power correspond

218 is sufficient to predict the complex genomic behaviour of STRs, including abundance and mutational co

219 re provides limited insights to the emerging behaviour of the described biological system under diffe

220 , we observe prominent and robust hysteretic behaviour of the graphene resistance with an externally

221 f recording the early stage of uniaxial flow behaviour of the irradiated material with sufficient acc

222 Inferring the locomotor behaviour of the last common ancestor (LCA) of humans an

223 East Atlantic pattern) on the non-stationary behaviour of the NAO throughout the Common Era, likely v

224 ric and pulse techniques confirmed the redox behaviour of the new compound with concentration and sca

225 ted with abnormalities in brain function and behaviour of the offspring(4).

226 cell and tissue types of the composition and behaviour of the oscillator.

227 out-group negativity towards the collective behaviour of their in-group.

228 Contrarily, by investigating the behaviour of two types of lead-iodide based single cryst

229 that may provide insight into the biological behaviour of various bone tumours is highlighted.

230 dy temporal variations in the occurrence and behaviour of vocalizing cetacean species.

231 ability of our automated methods to identify behaviours of individual animals with a mean average pre

232 to a smaller change in cortisol release and behaviour on the first day of analysis compared to fin c

233 bration coefficients are required to predict behaviours on land versus foraging behaviour in water (R

234 rences in building characteristics, occupant behaviour or household factors.

235 reality (VR/AR) environments to investigate behaviour or train motor skills, we expect that the insi

236 neural processes are specialised for social behaviour, or are shared with other 'non-social' cogniti

237 st in our study resulted in context-specific behaviours, or that behavioural responses to a novel foo

238 o progressively acquire adult-like migratory behaviours, or which aspects take longer to refine durin

239 vector host choice over 3 years and resting behaviour over 4 years following a mass long-lasting ins

240 Together, findings identify brain-behaviour pathways for maladaptive habitual learning and

241 nts of flight muscle physiology, morphology, behaviour, phenology and environmental data, analysing t

242 s (PRS) for self-harm ideation and self-harm behaviour predict suicide attempt, suicide thoughts and

243 ide thoughts and NSSH, and PRS for self-harm behaviour predicted suicide thoughts and suicide attempt

244 xes that describe variation in participants' behaviour: recording intensity, spatial extent, recordin

245 These behaviours reflect risk-taking and allow individuals to

246 ase, complicating our understanding of brain-behaviour relationships and making it challenging to dev

247 brain networks, providing insight into brain-behaviour relationships in patients with dementia.

248 ular incitants of these complex reproductive behaviours remain unknown.

249 vection represents a new class of collective behaviour resulting only from the balance between hydrod

250 This behaviour results from total-flux feedback mediated by c

251 tivates future research moving beyond solely behaviour scores to explain stroke recovery and establis

252 Both behaviours showed significant changes as the temperature

253 alysis characterises oscillatory time series behaviours such as cycles, but accurate estimation requi

254 terventions in children can improve specific behaviours, such as joint attention, language and social

255 Risk-averse behaviours, such as standing on 'safe' blocks and testin

256 ed for predicting clinically relevant tumour behaviours, such as treatment response and emergence of

257 caques' facial morphology and their observed behaviour supporting a shared facial signalling system i

258 This transformed behaviour suppresses shear-banding in bulk samples in no

259 he sign and magnitude of selection on social behaviour than that experienced by static characters lik

260 ngitudinal shifts in host-choice and resting behaviour that are consistent with adaptation to evade L

261 ith autism exhibit early differences in gaze behaviour that may be associated with subsequent cogniti

262 ntrol of clinicians but not for more complex behaviours that also required patient engagement.

263 Animal behaviours that are superficially similar can express di

264 fects of sickness should be lower for social behaviours that bestow greater benefits to inclusive fit

265 Thus, similar behaviours that express different internal states are en

266 ctive interventions to increase adherence to behaviours that individuals in communities can enact to

267 th variable innate behaviours and reinforced behaviours that may promote mate encounters and mate sel

268 functionless behaviours -are common abnormal behaviours that often arise in suboptimal conditions.

269 seeking behaviour and compulsive drug-taking behaviour (that is, use).

270 those seen during the corresponding wakeful behaviour, the causal mechanisms underlying specific dre

271 oupled receptors that control physiology and behaviour, the Robo-Slit midline repulsion system, and t

272 ssential for adequate expression of maternal behaviour, thereby ensuring proper development of the of

273 The spread of behaviours through animal social networks have often bee

274 of invasive predators, reducing antipredator behaviour to levels lower than found on pristine islands

275 ing animals are predicted to adjust foraging behaviour to variable wind conditions to minimize moveme

276 on of specific dietary and physical activity behaviours to greater adiposity among urban migrants cou

277 ing that individuals can adjust their social behaviours to match experienced conditions.

278 king-off, their most energetically expensive behaviour, to favourable wind conditions.

279 trials, lizards performed more chemosensory behaviour (tongue flicks, lip smacks and substrate licki

280 , males of many species can exhibit mounting behaviour towards same- or opposite-sex conspecifics(1),

281 ces, but leave key elements of cognition and behaviour unexplained.

282 Agonistic behaviour, up to reciprocal fighting, in contest 2 was c

283 F1 offspring, screening for anxiety-related behaviours using the elevated-plus maze, light-dark box,

284 Cool-seeking behaviour was determined from total time receiving cooli

285 This behaviour was modulated at the individual level, where r

286 aloperidol became cataleptic, whereas normal behaviour was observed in rats that received the PEG-hal

287 Such behaviour was validated with fresh apple juice in which

288 l of decision uncertainty and change-of-mind behaviour, we demonstrate that this phenomenon is associ

289 ng the validity of using GPS to infer at-sea behaviour when answering behavioural or ecological quest

290 ding scheme simplifies readout for WM-guided behaviour, whereas the low-dimensional dynamic component

291 theoretical insight into the origins of this behaviour, which is inconsistent with electron heating,

292 xperience should engage in more antipredator behaviour, which leads to a larger change in travel spee

293 This structure stems from female philopatric behaviours, which could further be detected by weak but

294 , brain imaging phenotypes and externalizing behaviours with genome-wide data for EDU/SES.

295 uple QTL for divergence in visual preference behaviours with population genomic and gene expression a

296 cies also differed in their thermoregulatory behaviours, with some - such as the Ringlet Aphantopus h

297 ld displays a remarkable variety of temporal behaviours, with some fields of physics showing to be mo

298 nking sexual dimorphism, ontogeny and social behaviour within this taxon, and clarifies hypotheses co

299 and cost-effective for targeting prescribing behaviours within the control of clinicians but not for

300 edented insight into chemical and structural behaviour, yielding not just an average outcome but repo