ライフサイエンスコーパス: preference

1 otpb affect both stress response and social preference.

2 ostnatal experience is not required for this preference.

3 a gene, and Ir68a mutation perturbs humidity preference.

4 y preference are also matched in orientation preference.

5 not randomised and was based on investigator preference.

6 s a quality attribute that leads to consumer preference.

7 r they preferred medication or CBT or had no preference.

8 NA can be directly detected without sequence-preference.

9 or GABA receptor antagonists alters kinship preference.

10 unaltered cocaine-induced conditioned place preference.

11 sensitisation and induced conditioned place preference.

12 derivatives were sufficient, for co-culture preference.

13 limits, aerobic metabolic scope and thermal preference.

14 s, which can differentially affect honey bee preference.

15 table (group number) influence the structure preference.

16 emories neutralizes previously learned odour preference.

17 ed in both ventricles with right ventricular preference.

18 hat KLK7 exerts a chymotryptic-like cleavage preference.

19 aminergic VTA-PFC projections elicited place preference.

20 the PFC inputs to the LHb suppresses social preference.

21 ative fates and ultimately determining color preference.

22 integration process and the leader-proximal preference.

23 lations of the Generalized Axiom of Revealed Preference.

24 for object motion in neurons with discrepant preferences.

25 as found to exert chymotryptic-like cleavage preferences.

26 termolecular interactions and conformational preferences.

27 is associated with more deontological moral preferences.

28 of other piscivores with contrasting thermal preferences.

29 activity into P450s with different substrate preferences.

30 y incorporates burden of disease and patient preferences.

31 ngth modifies nascent polybasic domain lipid preferences.

32 s of agents with similar and dissimilar food preferences.

33 als, experimental designs, and laboratories' preferences.

34 preferred food sources similar to their own preferences.

35 ive visual function and influence behavioral preferences.

36 g the chemical signatures that underlie host preferences.

37 n, thus modulating the GalNAc-Ts' long-range preferences.

38 on makers often rely on their own behavioral preferences.

39 as those between pairs with opposite context preferences.

40 id assist to understand the observed binding preferences.

41 rs explained all remaining variance in drink preferences.

42 , and other relevant variables on individual preferences.

43 gambling related cues that may moderate risk preferences.

44 cement of services to meet patient needs and preferences.

45 otential harms, benefits, costs, and patient preferences.

46 s three or more but has only modest sequence preferences.

47 he ItchyQuant than the NRS (23.6%) or had no preference (29.2%), P = 0.0015.

48 o use (45.8%) than the NRS (20.8%) or had no preference (33.3%), P = 0.008.

49 Strong frequency preferences across tonotopically mapped auditory cortex

50 Our personal preferences affect a broad array of social behaviors.

51 We propose that Tau's GDP preference allows the cell to independently regulate the

52 osterone failed to re-establish extinguished preference alone but produced a leftward shift in the do

53 wledge about critical residues and substrate preference among CCRs and provide, to our knowledge, the

54 sLac's substrate preference among monoaryls was also consistent with this

55 ural analysis revealed an array of different preferences among PLPs.

56 ons affects behavior using conditioned place preference and a task in which mice learn associations b

57 ally large parts like face outline and hair, preference and anti-preference of extreme facial feature

58 attenuated cocaine-induced conditioned place preference and blocked the cocaine-induced reduction of

59 d Cre lines during cocaine conditioned place preference and cocaine-induced locomotion.

60 nificantly reduced cocaine conditioned place preference and delayed learning of the drug-reinforced a

61 The theta-phase preference and excitatory strength of the afferent CA3 a

62 catalytic conditions with unusual heteroatom preference and high efficiency.

63 ymorphism (SNP), are associated with diurnal preference and higher Trait-Anxiety scores, supporting a

64 ivergence, gene loss, evolution of substrate preference and promiscuity.

65 variants/their combinations and both diurnal preference and the response to light.

66 However, the mechanism underlying this preference and the subsequent coordination between Mfd a

67 People consistently show preferences and behaviors that benefit others at a cost

68 rience of low social class may contribute to preferences and behaviors that risk excess energy intake

69 for sustaining CES should incorporate social preferences and consider multiple dimensions of biodiver

70 personally tailored to a resident' needs and preferences and directly offered to a resident contribut

71 rprisingly few correlations between resource preferences and maximal growth rate or biomass compositi

72 Wishing makes individual spiritual preferences and practices more accessible.

73 bit distinct peptide repertoires and binding preferences and present the alpha3135-145 epitope in dif

74 without distorting target-specific contrast preferences and spatial receptive fields.

75 sk of sudden cardiac death, as well as their preferences and values.

76 phylogenetic signals in environmental niche preferences and, especially, traits to help uncover the

77 develop social avoidance, decreased sucrose preference, and decreased time in the open arms of the e

78 s that are well matched in spatial frequency preference are also matched in orientation preference.

79 Projection and preference are taken as the two broadest criteria by whi

80 Beverage preferences are an important driver of consumption, and

81 , pheromone communication, and microclimatic preferences are aspects of its behaviour that depend on

82 decision making and challenge the idea that preferences are driven by an innate, universal, and stab

83 ognitive dissonance theory suggests that our preferences are modulated by the mere act of choosing.

84 oral studies repeatedly demonstrate that our preferences are modulated by the mere act of choosing.

85 ive coalitions form when politicians' policy preferences are private information, not known with cert

86 These preferences are shared with HLA-B*27 and Mamu-B*008, mol

87 Nettle's (P&N's) theory suggests that these preferences are unlikely to be appropriate when applied

88 Using health-care provider preference as an IV method, we propose a 2-step procedur

89 g information exchange; expressing treatment preferences; as well as agreement over the final treatme

90 bens (NAC) glutamate/Homer2 expression in MA preference/aversion.

91 Preference-based mitigation, such as reduced household w

92 ariable analysis that incorporated clinician preference-based, institutional variation in NSAID treat

93 By comparing the ant's landcover preferences before and after the invasion, we demonstrat

94 sh, Chromis viridis (Pomacentridae) - to use preference behaviour to regulate its body temperature.

95 The relative preference between the two factors can be tuned over a w

96 ronment play important roles in shaping food preferences; but the aetiology of variation in non-alcoh

97 Conversely, thermal preference can arise long before, and remain long after,

98 whose connectivity depends on their heading preferences, can sustain a bump-like activity pattern wh

99 tivity predicted the individual magnitude of preference change and the strength of cognitive dissonan

100 tan status to understand how wild pollinator preferences change across different continents.

101 Risk preferences changed substantially toward risk aversion a

102 crine strategy accordingly, based on patient preferences, comorbidities, and tolerability might be po

103 ucts show altered remote prior glycosylation preferences, confirming that the flexible linker dictate

104 ence on a critical involvement of the MTL in preference construction and value-based choices.

105 double-stranded DNA (dsDNA) without sequence-preference continues to be a major challenge.

106 Preference correlated with three emergent co-culture pro

107 nd burdens) consequences, patient values and preferences, cost, and feasibility.

108 apse maturation in cocaine-conditioned place preference (CPP).

109 H and blocked AMPH-induced conditioned place preference (CPP).

110 stribution of wait times to stabilize choice preferences despite trial-by-trial fluctuations in outco

111 e that simple rules regarding predicted risk preference do not hold across the complete range of each

112 eters of 20 healthy subjects with right-foot preference during treadmill walking at speeds of 1.1, 1.

113 nd that pairs of voxels with similar context preferences exhibited spontaneous correlations that were

114 Conditioned place preference, extinction and reinstatement of extinguished

115 These intermediates show an innate preference for a (Z)-configuration, although this can be

116 serine and phosphothreonine residues and the preference for a dianionic charge state of FHA-bound pTh

117 The WD40-containing KIF21B tail displays preference for a GTP-type over a GDP-type microtubule la

118 be the most effective hosts as a result of a preference for a ligand conformation where the aromatic

119 iption factor protein, has evolved a changed preference for a low-affinity, secondary binding motif.

120 ecifically, the ability of animals to show a preference for a novel face) robustly predicts cerebrosp

121 not the other subpopulations, decreased the preference for a social target.

122 in particular the Golgi apparatus, and has a preference for acetylating N termini of the transmembran

123 are activated by the metal systems, but the preference for activating these bonds depends on the nat

124 ltered glucose metabolism characterized by a preference for aerobic glycolysis.

125 for alternative hypotheses such as a female preference for aggressive males [8, 9].

126 tory looming bias, representing a perceptual preference for approaching auditory objects.

127 Here, we show that the H15 HA has a high preference for avian receptor analogs by glycan array an

128 ata show a pronounced nucleobase bias with a preference for binding poly (U) or d(T) while d(A) polym

129 rumental variable (IV) methods with operator preference for bivalirudin as the instrument were used.

130 its, the open complex only displays a slight preference for cations.

131 in HBV DNA and increased A3G's 5' nucleoside preference for deoxycytidine (5'-CC).

132 the male-biased miR-2954-3p, shows conserved preference for dosage-sensitive genes on the Z Chromosom

133 Older age, female sex, preference for English, more education, health and visio

134 effect on WRN binding to DNA, decreasing the preference for G4 substrates by approximately 25%.

135 otonin 2C (5-HT2C)-selective agonists with a preference for Gq signaling.

136 terconversion from pH 0 to 9, with catalytic preference for H2 oxidation at all pH values.

137 iet intake, meal patterns, conditioned place preference for high-fat food, cue-induced reinstatement

138 Preference for higher over lower nicotine content cigare

139 IFNAR1) and IFNAR2, but, unusually, it had a preference for IFNAR1.

140 , we find that GEN1 exhibits a weak sequence preference for incision between two G residues that resi

141 We found that HsvA displays a preference for linear aliphatic polyamines as the amidin

142 It has been suggested that the preference for low WHRs evolved because low WHR provided

143 layers is presented, which reveals a marked preference for Mn to partition to the central layer.

144 human and rat monoamine oxidases with slight preference for monoamine oxidase B in both species.

145 rus, a nonpathogenic retrovirus, show higher preference for nongenic integrations than gammaretroviru

146 lely by foamy virus' modest insertional site preference for nongenic regions compared to gammaretrovi

147 actory conditioning experiments and that the preference for NPF neuron activation is dependent on NPF

148 react with many secondary metabolites with a preference for one among several pathways.

149 tive B- and E-pockets that coincide with the preference for P2 and P7 arginine anchors.

150 Their association with heterotrophs, preference for particles and resourceful metabolic trait

151 trated that EYA1 has a striking conformation preference for phospho-T58 of Myc.

152 howing a strong strand bias and a remarkable preference for polypurine/polypyrimidine sequences.

153 In keeping with increasing surgeon preference for porous implants, most studies identified

154 d MT piezosensors despite of the undoped-PPy preference for pure anion dynamics.

155 eased depression-like behavior and increased preference for rewarding stimuli.

156 urs in S/G2-phase cells, suggesting that the preference for S/G2 phase is independent of the nature o

157 allenges the MD view by demonstrating that a preference for sensory modality, vision or audition, def

158 th ASD were found to show a reduced relative preference for social rewards, indexed by a lower propor

159 There is a kinetic preference for substrates that have the transferring hyd

160 The high preference for the (S)-substrate is of synthetic value.

161 ficantly reduced DNA binding, but retained a preference for the 5caC modified E-box.

162 amic reaction pathway, with larger C(1)-C(6) preference for the angular quinoxalenediynes due to gain

163 The strong preference for the better matching lipid (dC16:1) near t

164 Na(+) and K(+) exhibit a significant preference for the centroid of the aromatic ring and dis

165 ed free energies of activation reproduce the preference for the experimentally observed major enantio

166 attributed to their differential phosphosite preference for the four PIN1 phosphosites.

167 We also demonstrate preference for the high-reward (3 pellet) lever was sele

168 The volunteers expressed a preference for the open MR system (p<0.01).

169 in heroin self-administration or the strong preference for the palatable food over heroin during the

170 found that the pyrrolic ring of Ryd displays preference for the R(4892)AGGG-F(4921) residues in the c

171 iruses was modified, there was a significant preference for the segment containing matched packaging

172 alamin riboswitches have a broad spectrum of preference for the two biological forms of cobalamin in

173 used for genomic analysis, there should be a preference for using lower gauge needles over higher gau

174 This rationalizes nature's preference for using O-rich ligand environments for the

175 anes and also observed that Ctn(15-34) has a preference for vesicles that mimic bacterial or tumor ce

176 strongly to voices and showed a significant preference for vocal compared with nonvocal sounds.

177 n responses to DMS across reef fish taxa - a preference for water with DMS and change in swimming beh

178 ed to both the increasing prevalence of, and preference for, foods high in calories, specifically fat

179 According to cognitive averaging theory, preferences for attractive faces result from their simil

180 es children's attention toward and affective preferences for attractive females.

181 for the migration, including the temperature preferences for each lipid, the favored curvature for ea

182 The importance of understanding patient preferences for life-sustaining treatment is well descri

183 y for these residues, but they retained high preferences for octane omega-hydroxylation.

184 ons between patient demographic factors with preferences for provider roles-oncology-directed care ve

185 re the chemical space that defines substrate preferences for the auxin uptake carrier AUX1.

186 ve interventions, they hold a broad range of preferences for treatment limitations that were not disc

187 or fracture based on a discussion of patient preferences, fracture risk profile, and benefits, harms,

188 Despite a wide range of feeding preferences from durophagy to piscivory, living otter sp

189 t increases, all of which lead to an evening preference (i.e., chronotype) during adolescence.

190 ndividuals adjusting their behaviour), niche preference (i.e., individuals dispersing to particular s

191 The aerobic glycolytic preference in NLRX1(-/-) effector T cells is combined wi

192 osterior brain that are sufficient to elicit preference in our assay.

193 extinction and reinstatement of extinguished preference in response to low-dose cocaine administratio

194 scular influenza vaccination should be given preference in these patients.

195 dopamine signaling in tuning spatial pattern preferences in a simple nervous system.

196 ural differences in grooming-handclasp style preferences in captive chimpanzees [2], we tested the al

197 blishment of binocularly matched orientation preferences in cortical neurons.

198 same principles can also explain amino acid preferences in immunogenic epitopes and highlight opport

199 anism across species, leading to averageness preferences in primates.

200 Model preference is assessed and correlation coefficients acro

201 Understanding how selection acts on risk preference is crucial to interpreting and predicting beh

202 but the mechanism explaining this intriguing preference is unclear.

203 e importance accorded attractiveness in mate preferences is culturally shaped and likely evolutionari

204 This bias is large where the expression of preferences is unconstrained by residential and lineage

205 ology of variation in non-alcoholic beverage preferences is unknown.

206 g a predictive model (AUC = 0.77), physician preference largely determined which medication a patient

207 omain to circumvent its native extender unit preference leads concurrently to a change of mechanism i

208 This paradoxical preference may account for the frequency with which thes

209 We conclude that self-rated preferences may not provide a straightforward and direct

210 d that ignoring patients' personal goals and preferences may result in reduced rates of adherence.

211 tion and provide care congruent with patient preferences might target individuals at higher risk.

212 minal prior glycosylation (GalNAc-O-Ser/Thr) preferences modulated by the lectin domain.

213 t pairing of activation caused neither place preference nor aversion.

214 he proposed sex difference in attractiveness preferences, nor the fitness-related outcomes of attract

215 ge has functionally conserved local sequence preferences, occurs in cleavage cluster regions (CCRs),

216 ice-chamber (shuttle box) was used to assess preference of 28 pre-settlement stage larvae from reef f

217 Collectively, our data implicate intrinsic preference of AID for structured substrates and uncover

218 that can overcome the inherent thermodynamic preference of an olefin, providing synthetically useful

219 c and FGGY proteins showed a clear substrate preference of both kinases for d-ribulose over a range o

220 ermination in prediction (R(2)) and ratio of preference of determination (RPD).

221 e face outline and hair, preference and anti-preference of extreme facial features (e.g., very large/

222 photoreceptor fates shifts the innate color preference of flies from green to blue.

223 These changes result in a mating preference of genetically modified males for wild-type f

224 Here we show that the typical preference of male mice for females is eliminated in mut

225 ticipants (66.7%) had a calculated treatment preference of mastectomy only; 39 of these women (47.6%)

226 level, surround input organizes the spatial preference of neurons into a continuous map of the space

227 We show that the localization preference of the GrabFP traps can impose a novel locali

228 ecular helicity is biased toward the helical preference of the sergeant.

229 The molecular structure and conformational preferences of 1-phenyl-1-X-1-silacyclohexanes C5H10Si(P

230 Quantitative comparisons of the binding preferences of 400 peptides allowed us to construct a po

231 used to model changes in the conformational preferences of a model peptide during the transition fro

232 e the "common knowledge" assumption that the preferences of all politicians are public information.

233 ly, does not accurately reflect the encoding preferences of cells in those areas.SIGNIFICANCE STATEME

234 urate prediction of the sugar conformational preferences of chemically modified nucleosides in soluti

235 cular cargos through the NPC, the processing preferences of individual 2A(pro) predict RV genotype-sp

236 The cleavage preferences of Kallikrein-related peptidase 7 (KLK7) hav

237 To determine the subsite preferences of KLK7 in a global setting, we used a mass

238 ress this issue, we investigated the folding preferences of oligonucleotides from a chromosomal break

239 for the different remote prior glycosylation preferences of the GalNAc-Ts.

240 we biochemically characterize the substrate preferences of the helix-hairpin-helix (HhH) domains of

241 n together, these results reveal the binding preferences of the Itch PRR toward its most common SH3 d

242 f metazoan miRNAs, focusing on the targeting preferences of the let-7 and miR-10 families.

243 tive site; however, intrinsic conformational preferences of the substrate resulted in predominately u

244 e effect of unmeasured patient resuscitation preferences on issues critical for researchers and resea

245 Interestingly, orientation preference (OP) maps in the visual cortex are found in c

246 on produced significant increases in alcohol preference, operant self-administration, and relapse.

247 tle consensus among researchers as to either preference or psychometric adequacy.

248 ncial and prosocial biases are the result of preferences or prejudices similar to those displayed tow

249 ences in treatment decisions reflect patient preferences or treatment biases requires further study.

250 sual critical period causes shifts in ocular preference, or dominance, toward the open eye in primary

251 nM IC50 values for HDAC6 with up to 15-fold preference over HDAC1, >3500-fold selectivity over HDAC4

252 Most participants displayed moral preferences, placing a higher cost on harming others tha

253 Here, we used a conditioned place-preference procedure to investigate the effects of optog

254 long-term outcomes and patient and societal preferences regarding risk of SSI versus risk of AKI is

255 Patient preferences regarding which provider handles the followi

256 he present study, we use a conditioned place preference/reinstatement paradigm in mice to directly te

257 ligands to YKL-40, addressing thermodynamic preference relative to chito-oligosaccharides.

258 that these three models adopt conformational preferences, relying on eight-, six- or five-membered H-

259 e acyltransferases alter their acyl acceptor preferences, resulting in reversal of their order of rea

260 The preference shift was associated with cortical thinning o

261 e structure and dynamics, and thus substrate preference, simultaneously and sequentially.

262 aly donated buccal DNA and completed diurnal preference, sleep quality/timing and sleepiness/mood que

263 During social transmission of food preference (STFP), mice form long-term memory of food od

264 hin the NAC shell of mice and we reversed MA preference/taking by lowering endogenous glutamate and/o

265 ogenic C57BL/6J mice that varied in their MA preference/taking, to examine the glutamate underpinning

266 Further, the left cortex showed a stronger preference than the right cortex for stimuli leading fro

267 gation challenges, and they may have diverse preferences that influence end-of-life care.

268 compass energy expenditure and macronutrient preference, the luminal composition of the gut (i.e., th

269 In a design using basic features of revealed preference theory, we measured in rhesus monkeys the fre

270 of individual cortical neurons' orientation preferences through the two eyes, likely a key step in t

271 in the design of novel therapeutic agents in preference to compounds targeting a single receptor or e

272 The endogenous agonist dopamine binds with preference to D2/3 HIGH receptors relative to D2/3 LOW r

273 alyst can override its innate stereochemical preference to dictate the preferred enantiomer of the re

274 Srs2, Srs2 displays a slight but significant preference to disrupt extending D-loops over unextended

275 e do know that human infants at birth show a preference to engage with a top-heavy, face-like stimulu

276 cylation has favored five-membered rings, in preference to four membered rings.

277 Place preference to heroin was not modified, but remarkably, m

278 he specificity nor does it change the length preference to match that of STAT6.

279 There is a binding preference to negatively charged sites on the protein, c

280 cuss that sanctioning is likely to evolve in preference to partner choice in any symbiosis where part

281 This preference to sample inlying items was linked to decisio

282 al titration calorimetry (ITC), with binding preference to telomere RNA (TERRA) sequences.

283 om inverse resolution limit; it has a strong preference to triangles.

284 at recombinant BAR and PAT exhibit substrate preference toward phosphinothricin over the 20 proteinog

285 a social context without mating biases later preference towards a partner, indicating that this circu

286 roteins, clathrin and dynamin, show a strong preference towards positive membrane curvatures with a r

287 The constructed-preference tradition within behavioral decision research

288 I, A, S7 and T1, characterized their cutting preferences, trinucleotide periodicity patterns and cove

289 e analyzed Prp enzyme kinetics and substrate preference using a fluorogenic peptide cleavage assay.

290 phically organized according to the modality preference (visual, auditory, and bimodal) of its neuron

291 ographically organized according to modality preference (visual, auditory, and bimodal) when analyzed

292 Cathepsin G's P2' preference was determined by screening against a P2' div

293 A much larger preference was observed for thiols, sulfides, and alkene

294 herbivory and lead to the shift in the host preference, we analyzed whole genome sequences from labo

295 Aesthetic preferences were consistent across psychographic groups

296 with congruent visual and vestibular heading preferences, whereas they stabilize tuning for object mo

297 hibited both social and physical interaction preference, which, in the temporal lobe, mapped onto a f

298 d an increase in biological motion orienting preference with RG7713 (ES=0.8, p=0.047) and a non-signi

299 and IGKV/IGLV gene usage, as well as pairing preferences with a particular presence of the IGHV5-51:I

300 health information or shared decision-making preferences would be met.