ライフサイエンスコーパス: behaviour

1 ward systems to drive changes in affiliative behaviour.

2 altered or inappropriate neural function and behaviour.

3 visual experience during natural exploratory behaviour.

4 able but flexible neural activity and animal behaviour.

5 uding hierarchical organisation and emergent behaviour.

6 nt role in homeostasis and guiding motivated behaviour.

7 orphological development, ageing, cancer and behaviour.

8 de-differentiation and aggressive biological behaviour.

9 that intervention strategies have on system behaviour.

10 neuronal loss and FTD-like changes in social behaviour.

11 ty did, however, not lead to more altruistic behaviour.

12 IV despite significantly lower rates of risk behaviour.

13 ked fiber lasers are known for their complex behaviour.

14 by tailored advice would modify help-seeking behaviour.

15 erns, group association events, and foraging behaviour.

16 amines, which suggest it is not an aversive behaviour.

17 ly thought to be incompatible with inherited behaviour.

18 l circuits put information at the service of behaviour.

19 temporal structure that exhibits oscillatory behaviour.

20 nificantly with processing loss and textural behaviour.

21 n deficiency is sufficient to disrupt social behaviour.

22 tions for in-silico experiments of zebrafish behaviour.

23 of the mechanisms by which SES may influence behaviour.

24 n networks, and that this in turn can modify behaviour.

25 forming voltages and more reliable switching behaviour.

26 cytoplasmic protein domain on the clustering behaviour.

27 -related compounds directly influence insect behaviour.

28 ls of the complex show identical vapochromic behaviour.

29 ole of IL-17 modulating circuit function and behaviour.

30 theory to study an emergent adaptive animal behaviour.

31 state model as the best descriptor of diving behaviour.

32 ay a central role in controlling growth cone behaviour.

33 -gap and thus non-metallic or molecular-like behaviour.

34 eir function impacts learning, cognition and behaviour.

35 ns conformed strongly to predicted power-law behaviour.

36 ing the GABAergic network restored gathering behaviour.

37 ity of learned information to optimize their behaviour.

38 o investigate how well they can support such behaviours.

39 the control of alcohol addiction-associated behaviours.

40 differ in their mating systems and parental behaviours.

41 ement of each C. elegans neuron in locomotor behaviours.

42 relations between prosocial traits and game behaviours.

43 molecules as a method to control collective behaviours.

44 ks can autonomously generate irregular motor behaviours.

45 tive conditions through their physiology and behaviours.

46 osocial motivations underlying economic game behaviours.

47 order (MDD) as well as suicidal thoughts and behaviours.

48 mical access to redox-based cell signals and behaviours.

49 ient and chronic reductions of goal-directed behaviours.

50 ransducing mechanical forces into joint cell behaviours.

51 enia (20 [8%]), coughing (16 [7%]), abnormal behaviour (13 [5%]), and diarrhoea (12 [5%]).

52 time top: -43%; time bottom: +93%; abnormal behaviours: +138%; inability to ascend: +280%) over a lo

53 In order to demonstrate EDL behaviour, a sputtered 200 nm-thick SiO2 electrolyte was

54 es groups of samples that share their global behaviour across heterogeneous datasets.

55 ained significantly associated with relevant behaviours after controlling for the family structure.

56 , and beyond the microbial realm.Cooperative behaviour among individuals provides a collective benefi

57 We explored the factors motivating such behaviour among leopards in the Sabi Sand Game Reserve,

58 Divergent migration behaviours among individuals or among populations are an

59 al role of Phf8 in mammalian development and behaviour and establish a direct link between Phf8 expre

60 ally extremely challenging to predict cyclic behaviour and fatigue life under a realistic load spectr

61 homozygous mutant for disc1, we investigated behaviour and functioning of the hypothalamic-pituitary-

62 thyroid cancer-despite its unique biological behaviour and less favourable outcomes.

63 schematic summary showing the links between behaviour and life-history observed by Nakayama, Rapp &

64 textual nature of incentive value and choice behaviour and may offer insights into psychopathologies

65 These results indicate that the behaviour and properties of the same MUs can be monitore

66 re related to decreases in voluntary running behaviour and provide guidance for understanding the neu

67 Individual animals vary in their behaviour and reactions to novel situations.

68 ences were corrected for health-care-seeking behaviour and recruitment.

69 isms selecting for consistent differences in behaviour and social plasticity.

70 BABR activity causing increased anxiety-like behaviour and susceptibility to seizures.

71 An individual's foraging behaviour and time allocated to feeding have direct cons

72 imperative to understand its damage-tolerant behaviour and to discern the mechanisms of damage evolut

73 informing future research into the medicinal behaviours and dosing of this living antibacterial.

74 rried is associated with healthier lifestyle behaviours and lower mortality and may reduce risk for d

75 of their environment, creating selection on behaviours and other traits.

76 try containing VLS D2-MSNs control motivated behaviours and that VLS D2-MSN loss-of-function is a pos

77 s a causal relationship between their health behaviours and the patient response and adoption of publ

78 ication of key parameters controlling system behaviour, and facilitates predictive-design of motility

79 spite its prevalence, the drivers of caching behaviour, and its impacts on individuals, remain poorly

80 erted changes in the morphology, physiology, behaviour, and life history of lizards.

81 ends on whether treated patients change risk behaviour, and on treatment coverage: higher coverage re

82 ding response to oxidative stress, addictive behaviour, and regulatory functions emphasizing the impo

83 n a cohort study compares demographics, risk behaviour, and sexually transmitted infections (STI) in

84 ions addressing the domains of mental state, behaviour, and substance use are likely to be most succe

85 status, depressive symptoms, health-related behaviours, and chronic conditions showed that work stre

86 ff1b+ neurons, implicated in anxiety-related behaviours, and corticotrophin releasing hormone (crh) n

87 chological processes that predict aggressive behaviour are also typically associated with violent sel

88 biological problem, and what differences in behaviour are due to different model assumptions and abs

89 Socioeconomic differences in behaviour are pervasive and well documented, but their c

90 he consequences of loss of Lpd in the CNS on behaviour are unknown.

91 Specifically, present-oriented behaviours are adaptive for young people (e.g., in terms

92 nvironmental contexts in which phenotypes or behaviours are described.

93 ies the neural pathways involved in survival behaviours are highly conserved and there is a consensus

94 se hypothalamus, that underlie innate social behaviours, are shaped by social experience.

95 The optical behaviour as a function of its hydrogen content makes ha

96 diving states, and labelling all subsurface behaviour as deep dives or shallow dives discounts a sig

97 ent in chemical signalling, and not foraging behaviour, as a leading factor driving the diversity in

98 nce appeared to have little effect on client behaviour, as evidenced by consistency of visit rates, c

99 of their digits provide evidence of roosting behaviour, as in dermopterans and bats, and their feet h

100 various surfaces can give clues as to gecko behaviour, as well as towards designing synthetic adhesi

101 The strongest brain-behaviour associations (the 'peak clusters') were in the

102 hat nurses should be role models for healthy behaviours assumes a causal relationship between their h

103 tion, and ultimately probing and controlling behaviour at the quantum level.

104 can be tuned in order to exhibit the desired behaviour at the selected wavelength region.

105 ire might have been driven by the observer's behaviour at the time of caching.

106 ve regulation, and anorexia nervosa-specific behaviours at 12 months after surgery, as well as change

107 dolescent risky substance use and antisocial behaviour attenuated the remaining associations, with th

108 transiting and area-restricted search (ARS) behaviours, believed to indicate foraging activities.

109 ined qualitative features, such as switching behaviour, bistability or oscillations.

110 ubjects did not remain at one level of MB/MF behaviour but rather displayed a shift towards more MB b

111 Little is known about its ecology and behaviour, but unusual specialisations of visual pigment

112 dressing health knowledge and health seeking behaviour, buttressing existing health services, and con

113 ulsed nuclear magnetic resonance and thermal behaviour by differential scanning calorimetry.

114 lts demonstrate that this new and unexpected behaviour can be ascribed to an interplay between time-d

115 roof of concept that cancer cells' malignant behaviour can be dominated by their microenvironment.

116 To explore if this behaviour can be extended to saprophytic mycobacteria, w

117 ls explaining between-species differences in behaviour can be used to understand that corresponding i

118 Cooperative behaviours can be damaged by the emergence of 'cheating'

119 nerships using data from survey of injecting behaviour carried out in London, UK.

120 To determine whether behaviour change was related to group attendance, we use

121 cy makers, particularly those interested in "behaviour change" policy.

122 undamental role in determining the network's behaviour, characterising the influence of each of the s

123 ombined gene expression studies with protein behaviour characterization in Welwitschia mirabilis to t

124 dependent markers and predictors of suicidal behaviours converging to this increased risk.

125 that the emergence of cannibalism-avoidance behaviour depends strongly on assumptions about parasite

126 genetic diversity after evolution of gentle behaviour, despite selection on standing variation.

127 The distribution of migration behaviours did not vary between populations, sexes, body

128 Rapid eye movement (REM) sleep behaviour disorder (RBD) is characterised by complex mot

129 ysfunction, depression, anxiety and probable behaviour disorder, but not cognitive dysfunction or mot

130 ygoscelis papua) and recorded their foraging behaviour during chick guarding.

131 can display both wave-like and particle-like behaviour during thermal transport.

132 ts, and combining computational modelling of behaviour, fMRI and PET measurements of DA D1 availabili

133 We studied sentinel behaviour following immigration in a habituated populati

134 om each other is fundamental to a variety of behaviours from grasping objects to navigating.

135 n rhythms are 24-h rhythms in physiology and behaviour generated by molecular clocks, which serve to

136 opy, spin-orbit-torque-induced magnetization behaviour has attracted attention because of its intrigu

137 xhibiting nontrivial electronic and magnetic behaviours, have been proven to play a crucial role in p

138 tween melt structure, viscosity and eruptive behaviour holds despite the variable water content and o

139 erns ensures proper gene regulation and cell behaviour, impacting normal development and fertility.

140 demonstrate an artificial form of predatory behaviour in a community of protease-containing coacerva

141 on, convey messages relevant to coordinating behaviour in a foraging ecology, such as cooperation, se

142 The appearance of nematic behaviour in a prototypical heavy-fermion superconductor

143 ed rewards, leading to more present-oriented behaviour in a range of domains.

144 otentials while mice engaged in unrestricted behaviour in a variety of environments and while perform

145 Competition also influenced behaviour in an Ultimatum Game, such that winners were m

146 es to snake toxins, has the ability to alter behaviour in animals through inhibition of nicotinic ace

147 icantly altered a nicotinic receptor induced behaviour in C. elegans and increased locomotor activity

148 ach study area to investigate health-seeking behaviour in cases of self-reported fever lasting less t

149 The unusual auxetic behaviour in combination with other remarkable propertie

150 step towards rudimentary forms of collective behaviour in communities of artificial cell-like entitie

151 ibutions in on- and off-times as well as 1/f behaviour in corresponding emission power spectral densi

152 inary labelling and classification of sexual behaviour in dementia as appropriate or inappropriate of

153 Here we investigate male-male mounting (MMM) behaviour in female-deprived desert locust males infecte

154 r, the mechanisms responsible for collective behaviour in mosquitoes are not well understood.

155 al and provide a route to controlling the DW behaviour in nanoscale device structures.

156 has previously been used to image plasmonic behaviour in nanostructures in an electron microscope, b

157 rse pseudo Hall-Petch to a pseudo Hall-Petch behaviour in nc-silicene at a critical grain size of 17.

158 e predicted growth regime and emulsification behaviour in relation to interfacial tension as modelled

159 Our results indicate that subsurface behaviour in short-finned pilot whales is more complex t

160 pression and phosphorylation and contractile behaviour in single membrane-permeabilized cardiomyocyte

161 We interpret this behaviour in terms of the properties of our model in the

162 onitor-Parent Form to report on adolescent's behaviour in the previous 4 weeks.

163 hic lithic technologies as well as the human behaviour in the region.

164 acted by the particle-specific agglomeration behaviour in this study.

165 or the first time, to dynamically track cell behaviours in intact moving joints.

166 benzocaine also appears to induce avoidance behaviours in medaka (Oryzias latipes); but etomidate co

167 , that generalizes to a wide range of animal behaviours in moving fluids.

168 mals was also enough to suppress exploratory behaviours in recipient naive animals.

169 factor for mental illness, display abnormal behaviours in response to stress, but the mechanisms thr

170 ncountering lions was high and changed their behaviours in risky areas to minimise predation threat.

171 two sexes that links individual-level mating behaviour (in an individual-based model) to population-l

172 Specific behaviours included year-round river residency and multi

173 ial spin ice can lead to specific collective behaviour, including emergent magnetic monopoles, charge

174 e the extent to which variation in migratory behaviour influences individual fitness across a populat

175 that might lead to enhanced multi-component behaviour integration.

176 Endogenous testosterone promotes behaviours intended to enhance social dominance.

177 This knowledge allows developing new behaviour interfering strategies, increasing the options

178 hat intrapopulation variability in migratory behaviour is a general feature of the spatial ecology of

179 Moreover, the food-leaving behaviour is conspecific and pheromone dependent: C. ele

180 messes", and no predictive model for relaxor behaviour is currently available.

181 We demonstrate that this unusual cyclic behaviour is governed by a type of correlated 'necklace'

182 evice orientation and doping shows that this behaviour is intrinsic, substantial, robust and present

183 Generous behaviour is known to increase happiness, which could th

184 This behaviour is likely to be common in a wider family of co

185 This peculiar behaviour is lost when external perturbations overcome a

186 Such behaviour is mostly attributed to some special re-entran

187 y is inversely associated with and sedentary behaviour is positively (and independently) associated w

188 role of extrinsic mortality risk in driving behaviour is probably important, but strong evidence is

189 ials presented herein its liquid-crystalline behaviour is rather different, indicating an unexpected

190 nce of mechanical forces in influencing cell behaviour is widely recognized, whereas the importance o

191 Here, we make the case that a cluster of behaviours is associated with lower socioeconomic status

192 metalloprotease, MT1-MMP to promote invasive behaviour leading to basement membrane disruption.

193 1) with nearly massless relativistic fermion behaviour (m( *) = 0.04 - 0.05m0, where m0 is the free-e

194 facilitators and designed to promote healthy behaviours mainly related to water, sanitation, and hygi

195 These sex differences in social behaviour may underpin male-biased acquisition of infect

196 Although these behaviours may have an aerodigestive function, such an a

197 Point prevalence of ICD behaviours (mMIDI; primary analysis) was stable across v

198 violations are two important forms of social behaviour modelled in economic games.

199 Rabies virus induces drastic behaviour modifications in infected hosts.

200 sual properties such as strongly directional behaviour, negative refractive indexes and topologically

201 lasticity (i.e., individuals adjusting their behaviour), niche preference (i.e., individuals dispersi

202 e find no evidence for dissipation-dependent behaviour, nor for any CC in the strict one-photon limit

203 ll be simultaneously satisfied, display rich behaviours not found elsewhere in nature.

204 Our measurements show that the elastic behaviour of (Al,Fe)-bearing bridgmanite is markedly dif

205 Examination of the sintering behaviour of 45 European examples reveals that it is the

206 Here we explore the deformation and failure behaviour of a representative folded gneiss, by combinin

207 oncentration and advance affect the foraging behaviour of a top Antarctic predator, the southern elep

208 theoretical analyses, we interpret the phase behaviour of archetypal IDP sequences and demonstrate th

209 d as a case study to demonstrate the dynamic behaviour of bimetallic systems during activation to pro

210 pressure, density, temperature, composition) behaviour of binary (CH4 + C3H8) and (Ar + CO2) mixtures

211 The 3D model demonstrates reasonable behaviour of control as well as mutant phenotypes.

212 read in orogenic settings, on the mechanical behaviour of crustal rocks are largely unknown.

213 quence of differences in the crystallisation behaviour of different TAGs.

214 Secreted CLIC3 promotes invasive behaviour of endothelial cells to drive angiogenesis and

215 aneous tendency to breathe air influence the behaviour of entire groups, and whether such influences

216 Understanding the behaviour of flexible metal-organic frameworks (MOFs)-po

217 This study investigated the behaviour of key aroma compounds in the presence of huma

218 mental evidence for the suggested absorption behaviour of low and highly permeable compounds.

219 iments can provide insights into the dynamic behaviour of materials, but have only recently been appl

220 e present the first description of the vocal behaviour of penguins in the open ocean and discuss the

221 he effect of such substances on the foraging behaviour of pollinators is poorly understood.

222 s of DNA labelling that also distinguish the behaviour of recently divided and quiescent cells.

223 Diving behaviour of short-finned pilot whales is often describe

224 sms are often studied as populations but the behaviour of single, individual cells can have important

225 stigate these questions, we have studied the behaviour of single-crystal La2-xSrxCuO4 films through w

226 has been growing interest in the mechanical behaviour of skin due to the rapid development of micron

227 can be extended to investigate the kinematic behaviour of somatic cells emerging from hESC differenti

228 loped a mathematical model that captures the behaviour of the cells, enables identification of key pa

229 M) stray fields, in both the superconducting behaviour of the film and the three-dimensional (3D) mag

230 The low-temperature behaviour of the heat capacity, including a high value o

231 g bridgmanite is markedly different from the behaviour of the MgSiO3 endmember.

232 ion, and how this depends on the density and behaviour of the remaining cancer cells.

233 sis confirms the predicted chaotic dynamical behaviour of the Solar System, and provides a constraint

234 nd developmental stage largely determine the behaviour of the system.

235 Following cold treatment, the ripening behaviour of the three groups of fruits was analysed (3

236 e BDI symmetry class stems from the distinct behaviour of the translational and rotational degrees of

237 important implications to understanding the behaviour of these cells in vivo.

238 Indirect effects of LMH on the behaviour of these consumers, however, have received com

239 Thereafter, allergic behaviour of this glycated protein was compared with its

240 This work aimed at investigating the behaviour of Trolox, vitamin E analogue, in presence of

241 ral changes in contact structure and ranging behaviour of wildlife may impact disease dynamics.

242 work, we further systematically revealed the behaviours of a toggle switch across scales from single-

243 ols that accurately describe and predict the behaviours of engineered gene circuits.

244 ms are critical to understanding the unusual behaviours of heterochromatin, and how chromatin domains

245 e-induced unusual melting and solidification behaviours of metals are reported that effectively solve

246 will be useful for studying fundamental spin behaviours, opening the door to exploring new applicatio

247 n oral health checklist improves oral health behaviour or oral health state in those thought to be at

248 Goal-directed behaviour outside of spatial navigation similarly requir

249 To assess the presence of ICD behaviours over a 2-year period, and evaluate patients'

250 degree of heterogeneity for effects on most behaviours, possibly due to the limited number of trials

251 These behaviours reflect the interactions of the dopaminergic

252 rain regions conforming to established brain-behaviour relationships (i.e. episodic memory: medial te

253 This migratory behaviour relaxes the boundaries between the fluid dynam

254 gin in the retina and mediate this important behaviour remain unclear.

255 Valley-spin locking behaviour results in selective net spin flow inside bulk

256 Furthermore, this phonon-assisted dynamical behaviour shows great sensitivity to the vibrational tem

257 s likely to favour individual differences in behaviour, social plasticity (i.e., individuals adjustin

258 s (95% CI: 1.02, 1.48) independent of health behaviours, socio-demographic and diet-related factors,

259 ce modulated the influence of predictions on behaviour: spatial/temporal predictability improved spat

260 derstanding the relationship between patient behaviour, staff response and environmental influences o

261 compacta and ventral tegmental area regulate behaviours such as reward-related learning, and motor co

262 lts suggest that DN participate in voluntary behaviour, such as the execution of antisaccades, and mo

263 care broadly, whereas others affect specific behaviours, such as nest building.

264 roviding a pathway by which group-beneficial behaviours, such as storytelling, can evolve via individ

265 structures that contribute to reward-seeking behaviours, such as the ventral striatum and midline tha

266 producing the effects of splicing on channel behaviour suggests that the voltage sensor in the first

267 ntial means to tune the exploitable electric behaviour that arises from motion of the imidazolium gue

268 microclimatic preferences are aspects of its behaviour that depend on multimodal sensory inputs.

269 developmentally regulated changes in mitotic behaviour that may relate to the role of RG cells to pro

270 Stimulation also produced drinking behaviour that was inhibited as water was ingested, sugg

271 nd river residency and multiple lake-migrant behaviours that involved movements between lakes and riv

272 trating its value in accessing the microbial behaviours that shape marine ecosystems.

273 bient flow or execute preprogrammed vertical behaviours, the simultaneous measurements at multiple, k

274 m amorphous to crystalline thermal transport behaviour through manipulation of the vibrational landsc

275 een implicated in regulation of drug-seeking behaviours through aversion-mediated learning.

276 Taking inspiration from this behaviour to realize high-density, low-power neuromorphi

277 viridis (Pomacentridae) - to use preference behaviour to regulate its body temperature.

278 m microbial competitors are likely to evolve behaviours to control or manipulate the animal's associa

279 ilizing both endogenous and ectopic cellular behaviours to dismantle the aberrant structures.

280 losely related to zebrafish showed avoidance behaviours to etomidate, but not benzocaine or MS-222; a

281 ly modulated to enhance females' affiliative behaviour towards a partner.

282 agers' knowledge, attitudes, confidence, and behaviour towards employees with mental health problems,

283 ously demonstrating the hallmark of rational behaviour, transitivity.

284 citly linking predation events to individual behaviour under natural conditions is challenging and th

285 elusive, but we can clarify aspects of their behaviour using dental microwear texture analysis.

286 genes linked to differences in nest-building behaviour, vasopressin is differentially expressed in th

287 a model of cell mechanics revealed that this behaviour was accompanied by a modulation of the cells'

288 Surprisingly, the qualitative behaviour was conserved among different cell-lines: all

289 Similar behaviour was observed for (E)-2-hexenal.

290 Prevalence of ICD behaviours was relatively stable across the 2-year obser

291 e coincident simple spikes during cerebellar behaviours, we varied the proportion (0-20 of 40) and pr

292 niques to provide new insights into movement behaviour when applied to large datasets of animal track

293 onse to darkness but exhibits wild-type (WT) behaviour when exposed to abscisic acid (ABA) or CaCl2 .

294 acting dynamical systems can have unexpected behaviours when the signal between the vertices are time

295 throughout the Cretaceous also altered fire behaviour, which should link more strongly to mortality

296 gate the brain mechanisms that link generous behaviour with increases in happiness.

297 f the same underlying trait, or are distinct behaviours with different aetiologies.

298 in nucleus postulated to influence rewarding behaviour) with respect to wheel running and sedentary f

299 ON and OFF responses exhibited antagonistic behaviour, with the strongest ON responses shortly after

300 rpin their stability, reactivity and dynamic behaviour within a common theme related to (changes in)