ライフサイエンスコーパス: motive

1 ases it seems to offer no evident benefit or motive.

2 egion including a predicted helix-loop-helix motive.

3 y between financial incentives and intrinsic motives.

4 it mindset, further de-emphasizing intrinsic motives.

5 he happiness of a stranger, with no ulterior motives.

6 ory typically focuses on actions but ignores motives.

7 ioeconomic groups differ in these underlying motives.

8 ith psychiatric symptoms and drug use coping motives.

9 acteristics of caregivers and their possible motives.

10 served individual differences in reciprocity motives.

11 d by the highly conserved E(D)RY and Yx7K(R) motives.

12 rstand such behavior in terms of mutualistic motives.

13 ipate, which are based on strong reciprocity motives.

14 ignificantly in the total number of donation motives.

15 hen doing so also satisfied consequentialist motives.

16 out behavioral manifestations of egalitarian motives.

17 d esthetically appealing teeth as their main motives.

18 A classical question concerns the curiosity motives.

19 are hard to explain via evolutionary mating motives.

20 g them to underweight less salient intrinsic motives.

21 But what about his underlying motives?

22 behavior in economic games that pit honesty motives against self-interest, but did not affect decisi

23 fostered most when self- and other-oriented motives align.

24 The motives and decision making of potential living liver do

25 t Elsevier, the time has come to examine the motives and methods of those to whom we have entrusted t

26 pite persistent efforts in understanding the motives and patterns of human migration behaviors, littl

27 more compelling evidence in favor of mating motives and suggest the direction of future research for

28 Recognizing that there is a multiplicity of motives - and that the accessibility and strength of eac

29 hed when doing so satisfied only retributive motives, and punished considerably more when doing so al

30 ped by both instrumental and noninstrumental motives, and that this subjective value of information (

31 Therefore, although mutualistic motives are likely an important contributor to moral act

32 n content and volume regulation, such as ion-motive ATPase activity, are instrumental in chill-coma r

33 f SERCA and other evolutionarily related ion-motive ATPases.

34 nce of a fundamental bias, what we term the "motive attribution asymmetry," driving seemingly intract

35 ntroduce a model that takes into account the motive behind the action.

36 e aim was to investigate differences in food motives between socioeconomic groups by means of a DCE.

37 ove through interventions built around human motives, but these must be implemented more intensely.

38 ent either exclusively satisfied retributive motives by only inflicting harm on the transgressor, or

39 , or additionally satisfied consequentialist motives by teaching the transgressor a lesson.

40 and (3) an opioid cue engages the so-called 'motive circuit' only if it is imbued with incentive sali

41 d the associated neural activation of brain "motive circuits", while having no effect on conditioned

42 Finally, the motive classification assigned by our computational mode

43 In this commentary, we argue that a dual-motives conceptualization of self-control, together with

44 These results suggest that holding multiple motives damages persistence and performance in education

45 Cooperative motives do not explain how young children reject unfairn

46 lutionary psychology is laudable, but mating motives do not explain the beauty premium.

47 nce increases as the values of the competing motives draw closer together.

48 sk provides a paradigm where the exploratory motive drives learning and as such we view it as in the

49 endent conflict between selfish and generous motives during prosocial choice, consistent with ideas t

50 he only bioenergetic coupling site, a sodium-motive ferredoxin:NAD(+) oxidoreductase (Rnf) in the ace

51 UWO 241 exhibited increased thylakoid proton motive flux and an increased capacity for nonphotochemic

52 Plus, the motive for being fair originally was self-interest, not

53 y of anticipation, a form of noninstrumental motive for information seeking, in addition to instrumen

54 We argue that a strong but neglected motive for making collective decisions is minimizing the

55 We find an economic motive for PADDD events, given that the opportunity cost

56 ent evidence suggests that the psychological motives for choosing to reciprocate trust differ between

57 arose evolutionarily as a set of skills and motives for cooperating with others, and the ontogeny of

58 Motives for diving on artificial reefs were varied, but

59 Although people often assume that multiple motives for doing something will be more powerful and ef

60 ted information on donation decision making, motives for donation and anticipated social and physical

61 gain insight into the relative importance of motives for food choices.

62 DCE) is an innovative way to elicit implicit motives for food choices.

63 enience are typically indicated as important motives for food choices; however, it is largely unknown

64 ted whether retributive and consequentialist motives for punishment are present in children approxima

65 e, research suggests that different types of motives for the same action sometimes compete.

66 ential for therapeutic benefit were the main motives for trial participation, whereas the uncertainty

67 UCP1 dissipates the mitochondrial proton motive force (Deltap) generated by the respiratory chain

68 at these changes are coupled with the proton motive force (Deltap).

69 Furthermore, the proton-motive force (PMF) across the inner-membrane acts at dis

70 the AgmU helix rotation is driven by proton motive force (PMF) and depends on actin-like MreB cytosk

71 ein export apparatus utilizes ATP and proton motive force (PMF) as the energy source to transport com

72 We present evidence that the proton motive force (pmf) drives T3SS secretion in Pseudomonas

73 The thylakoid proton motive force (pmf) generated during photosynthesis is th

74 p proteorhodopsin (pR) to control the proton-motive force (PMF) in vivo by illumination.

75 y ATP-powered transport, however, the proton motive force (PMF) is not required to keep P(i) in the p

76 The composition of the thylakoid proton motive force (pmf) is regulated by thylakoid ion transpo

77 Recent evidence suggests that the proton motive force (pmf) is the primary energy source for type

78 em of Gram-negative bacteria uses the proton motive force (PMF) of the cytoplasmic membrane to energi

79 B system couples cytoplasmic membrane proton motive force (pmf) to active transport of diverse nutrie

80 ns TonB, ExbB, and ExbD couple the CM proton motive force (PMF) to active transport of iron-sideropho

81 brane-bound molecular motor that uses proton-motive force (PMF) to drive the synthesis of ATP from AD

82 ane proteins harvest and transmit the proton motive force (PMF) to outer membrane transporters.

83 yoverdine (Fe-Pvd) by coupling to the proton motive force (PMF) via the inner membrane (IM) protein T

84 A-CT toxin translocation requires the proton-motive force (pmf) within target bacteria.

85 ltapsi), the major constituent of the proton motive force (pmf), is crucial for ATP synthesis, transp

86 Compounds that target the proton motive force (PMF), uncouplers, represent one possible c

87 ) and electrochemical gradient termed proton motive force (PMF), which provides the driving force for

88 tor-protein SecA, in concert with the proton motive force (PMF).

89 tonoplast and endomembranes to create proton motive force (pmf).

90 r levels of ATP and the disruption of proton motive force (PMF).

91 raising pH while maintaining a viable proton motive force (PMF).

92 strate receptor and the transmembrane proton motive force (PMF).

93 the cytoplasm by a pump powered by a proton motive force (PMF).

94 he cytosol of the host cell under the proton motive force (PMF).

95 nt to maintain a normal mitochondrial proton motive force (PMF).

96 tor enzyme FoF1-ATP synthase uses the proton-motive force across a membrane to synthesize ATP from AD

97 tential, and the determination of the proton motive force across its inner membrane under normal and

98 hanical coupling of the transmembrane proton motive force across mitochondrial membranes in the synth

99 1)F(o)-ATP synthase is powered by the proton motive force across the energy-transducing membrane.

100 ative phosphorylation by sustaining a proton-motive force across the inner membrane that is used to s

101 Pase upon addition of ATP generated a proton motive force across the membranes that powered antiporte

102 coupled to ubiquinone reduction, as a proton motive force across the mitochondrial inner membrane.

103 The pH component of the proton motive force across the thylakoid membrane was significa

104 smembrane electrical potential to the proton motive force across the thylakoid membrane.

105 reased contribution of DeltapH to the proton-motive force across thylakoids.

106 LAC1 transporters do not use proton or Na(+) motive force and are, thus, less energetically expensive

107 nthase complex that is coupled to the proton motive force and capable of making ATP.

108 at NorM simultaneously couples to the sodium-motive force and proton-motive force, and biochemically

109 membranes, which would dissipate the proton motive force and undoubtedly kill bacteria.

110 stems transport folded proteins using proton-motive force as sole energy source.

111 Metergoline disrupts the proton motive force at the bacterial cytoplasmic membrane and e

112 of TonB, ExbB, and ExbD, and uses the proton motive force at the inner membrane to transduce energy t

113 nse of TonB to presence or absence of proton motive force being modulated through ExbD.

114 discover that compounds disrupting proton motive force block natural competence (COM) and interrup

115 ke polyether drugs, TDA collapses the proton motive force by a proton antiport mechanism, in which ex

116 phenazines enable maintenance of the proton-motive force by promoting redox homeostasis and ATP synt

117 lated membranes with Delta5 generated proton-motive force by respiration as effectively as with wild-

118 ), conserves cellular energy when the proton-motive force collapses by inhibiting ATP hydrolysis.

119 r preparing the surface, but the directional motive force comes from Type IV pili.

120 the electron transport chain and the proton motive force consisting of a membrane potential (DeltaPs

121 mechanism, the ATPase activity and/or proton motive force could be used to energize the protein trans

122 e potential or the pH gradient of the proton motive force did not prevent As(III) uptake, whereas dis

123 al bc(1) complex are dependent on the proton-motive force due to the energy transduction.

124 ve bacteria, the cytoplasmic membrane proton-motive force energizes the active transport of TonB-depe

125 l periphery and proteins that use the proton-motive force for ATP production in the cell interior nea

126 charide facilitates but does not provide the motive force for gliding.

127 periplasmic loops require SecA or the proton motive force for membrane translocation.

128 Both species utilize proton-motive force for movement.

129 h in complex with ExbB-ExbD links the proton motive force generated across the inner membrane with en

130 designing pumps for the generation of proton-motive force in artificial and reengineered photosynthes

131 e employ a new method to quantify the proton motive force in living cells from the redox poise of the

132 so be targets because 1 collapsed the proton motive force in membrane vesicles.

133 Protein translocation under a proton motive force is catalyzed by a series of nonspecific pol

134 t regulation of electron transfer and proton motive force is crucial for protection of PSI against ph

135 y studies have demonstrated that this proton-motive force not only drives the secondary transporters

136 061 pH units per min, equivalent to a proton motive force of 3.6 mVmin(-1) Remarkably, the facile rec

137 and reduces efflux by dissipating the proton motive force of the cytoplasmic membrane in P. aeruginos

138 TonB systems transduce the proton motive force of the cytoplasmic membrane to energize sub

139 tions, accounts for the effect of the proton-motive force of the reaction rate, and simulates superox

140 active auxin transport relies on the proton motive force over the cellular membrane, allocation of a

141 roteins associated with mitochondrial proton-motive force production preferentially in the cell perip

142 motor, including torque-speed and speed-ion motive force relationships, backstepping, variation in s

143 spiratory complexes that generate the proton-motive force required for the synthesis of ATP in mitoch

144 rons, but in doing so, it generates a proton motive force that controls the rate of photosynthesis.

145 id oxidation (FAO) contributes to the proton motive force that drives ATP synthesis in many mammalian

146 y-transducing membrane to support the proton-motive force that drives ATP synthesis.

147 ls rely on the nuclear ruler to modulate the motive force that enables their passage through restrict

148 e membrane potential component of the proton-motive force throughout the cell in response to spatiall

149 ane proteins ExbB and ExbD couple the proton-motive force to conformational changes in TonB, which ar

150 ces the ubiquinone pool and generates proton motive force to power ATP synthesis in mitochondria.

151 ross the membrane responsible for the proton motive force to produce ATP.

152 mechanism by which it may harness the proton motive force to produce energy.

153 acteria and mitochondria, couples the proton motive force to the generation of NADPH.

154 B system couples cytoplasmic membrane proton motive force to TonB-gated outer membrane transporters f

155 ansmit its conformational response to proton motive force to TonB.

156 pe maintenance and homeostasis of the proton motive force under a variety of growth conditions.

157 ase in nonphotochemical quenching and proton motive force under conditions where metabolism was limit

158 The proton motive force unfolds and translocates LF and OF through

159 plasts also rapidly build up a strong proton-motive force upon a dark-to-light transition, which help

160 hydrolysis is required to generate a proton-motive force using the ATP synthase complex during ferme

161 mobile in the membrane (even when the proton motive force was depleted), more than one-half of the S(

162 elationship between ATP synthesis and proton motive force was highly regulated by the concentrations

163 Components of proton-motive force which could impair protein insertion into a

164 It proceeds by the generation of a proton-motive force which facilitates aminoglycoside uptake.

165 ndria, it is difficult to measure the proton motive force while simultaneously measuring the redox po

166 esulted in a buildup of the thylakoid proton motive force with subsequent activation of non-photochem

167 tron transfer chain and the decreased proton motive force within the lumenal space partially explain

168 membrane potential, pH gradient, and proton-motive force without the need for genetic manipulation o

169 electrochemical potential difference (proton motive force) across the illuminated thylakoid membrane

170 proton ionophores (CCCP, inhibitor of proton motive force), we found that intracellular NPs in nalB1

171 ouples to the sodium-motive force and proton-motive force, and biochemically identify protein regions

172 an inward flow of H(+) driven by the proton motive force, and conformational changes in FliG2 driven

173 the dependence of respiration on the proton motive force, and the expected flux-force relationships

174 about the regulation of the thylakoid proton motive force, ATP/NADPH balancing mechanisms (cyclic and

175 tation is driven by the transmembrane proton-motive force, by a mechanism where protons pass through

176 Translocation is driven by the proton motive force, composed of the chemical potential, the pr

177 Its product, the proton-motive force, is composed of an electrical potential and

178 n by inhibition of the inner membrane proton motive force, significantly advancing our understanding

179 und, collapsed both components of the proton motive force, similar to other cationic amphiphiles.

180 e also find that at low values of the proton motive force, the transport by Lyp1 is comparatively slo

181 addition to their contribution to the proton motive force, they mediate viability under oxygen-relate

182 ergy distribution, in the form of the proton-motive force, throughout the mouse skeletal muscle cell.

183 ry antiporters, powered by an imposed proton motive force, we established a method for purification a

184 correlates with the depletion of the proton motive force, which is indicated by the potential-sensit

185 The CpxRA regulon did not affect proton motive force-dependent antimicrobial peptide resistance;

186 We found a proton motive force-dependent effect on H. ducreyi's resistance

187 iphilic substrates from the cell in a proton-motive force-dependent fashion.

188 om proton motive force-independent to proton motive force-dependent interactions with TonB, catalyzin

189 is study, we examined the role of the proton motive force-dependent multiple transferable resistance

190 stance; however, 35000HPmtrC had lost proton motive force-dependent peptide resistance, suggesting th

191 ing that the MTR transporter promotes proton motive force-dependent resistance to LL-37 and human bet

192 is typical for FNTs, and, strikingly, proton motive force-dependent transport as observed for PfFNT h

193 in of ExbD appears to transition from proton motive force-independent to proton motive force-dependen

194 y vancomycin, rhamnolipids facilitate proton-motive force-independent tobramycin uptake, and 2-heptyl

195 E. coli relied on neither of the two proton motive force-linked systems, Ton and Tol-Pal, for transp

196 p A colicins typically parasitize the proton-motive force-linked Tol system in the inner membrane via

197 conformational change resulting from proton motive force-mimicking pH conditions.

198 The torque is provided by stator units, ion motive force-powered ion channels known to assemble and

199 on the inner membrane, disrupting the proton motive force.

200 termembrane space contributing to the proton motive force.

201 -dinitrophenol as an inhibitor of the proton motive force.

202 ctor, into the host cytosol under the proton motive force.

203 y 2-3 components of machinery and the proton motive force.

204 e into the flagellum is driven by the proton motive force.

205 r is generated from the transmembrane proton-motive force.

206 ated to eliminate competition for the proton motive force.

207 at move in helical trajectories using proton motive force.

208 on, the SecA ATPase motor, and the TM proton motive force.

209 TP becomes much more dependent on the proton-motive force.

210 mutant that we assign to a decreased proton motive force.

211 e to the pumping of protons against a proton motive force.

212 ump in the cell membrane powered by a proton-motive force.

213 termembrane space contributing to the proton motive force.

214 human cells at high and physiological proton motive force.

215 e inner membrane, contributing to the proton-motive force.

216 ococcus aureus, rapidly collapses the proton motive force.

217 related stress responses, and loss of proton motive force.

218 instead of c(11), is functional at lower ion motive force.

219 he conformational response of ExbD to proton motive force.

220 e inner membrane, contributing to the proton-motive force.

221 derived from the cytoplasmic membrane proton motive force.

222 tion of the electric component of the proton motive force.

223 genes encoding proteins that generate proton motive force.

224 d from oxygen reduction to generate a proton motive force.

225 power and substantially dissipate the proton motive force.

226 e inner membrane without altering the proton motive force.

227 l change and how it is coupled to the proton motive force.

228 usceptibility in MRSP by compromising proton-motive-force-dependent TetK-mediated efflux of the antib

229 Egalitarian motives form a powerful force in promoting prosocial beh

230 he benefits of organ donation and altruistic motives had the greatest impact on the support for organ

231 a supramodal association with understanding motive; however, connectivity among the MZS and MNS duri

232 ucture of social influence) and human social motives (i.e., the process of social influence wherein o

233 theoretical relevance) of strong reciprocity motives, I argue in this response that their efficacy (a

234 Thus, the strength of short-run coordination motives in social dilemmas determines the prospects for

235 ation and oil/water separation are principal motives in the surge to develop novel means for sustaina

236 nce of both retributive and consequentialist motives in young children.

237 image, but also by instrumental or strategic motives, in anticipation of future misbehavior.

238 ve enabled unscrupulous actors with ulterior motives increasingly to circulate fake news, misinformat

239 tegration as the gradual mapping of implicit motives into a coherently organized self-system.

240 relative prevalence of different reciprocity motives is highly stable across participant samples.

241 Furthermore, the distribution of motives is relatively unaffected by changes to the salie

242 implementation and the MZS in understanding motive, it remains unknown to what extent these systems

243 Mating motives lead decision makers to favor attractive people,

244 de evidence that such an information-seeking motive may also underpin infants' demonstrated preferenc

245 ate that these psychological group-dominance motives mediate the effects of macrolevel functioning on

246 mptoms confer risk of dependence, and coping motives mediate this risk.

247 outcomes in a field context in which various motives occur naturally and long-term educational and ca

248 in the context of the debate surrounding the motive of the wall-builders.

249 A primary motive of this Perspective is to work out how to think a

250 The chief motive of this review is to cover the recent advances on

251 We assessed the impact of the motives of over 10,000 West Point cadets over the period

252 lete academic freedom and without commercial motives on over 3,500 projects, publishing more than 3,2

253 When social dilemmas exhibit a coordination motive (or strategic complementarity), tolerant trigger

254 nts were asked to attribute emotions, social motives, or both to a set of facial displays.

255 n agar surfaces in groups, using flagella as motive organelles.

256 ltiple lines of evidence suggest that mating motives play a more important role in driving financial

257 roborates the notion that fundamental social motives play an important role in biases that favor attr

258 rch team and consent process, and altruistic motives play significant roles in the decision-making pr

259 The current net efficiency to produce motive power from silicon photovoltaic modules is estima

260 ause intergroup interactions often are mixed-motive rather than strictly zero-sum, groups often negot

261 ccount of how monoamines regulate antisocial motives remains elusive.

262 the VHS in those who self-harm for different motives requires further exploration.

263 be more powerful and effective than a single motive, research suggests that different types of motive

264 improve CRAd's efficacy, we cloned into F512 motives responsive to hypoxia (hypoxia-responsive elemen

265 ATP synthesis, the ferredoxin-fueled, sodium-motive Rnf complex.

266 s are over-determined, and a multiplicity of motives should be considered in explaining them.

267 Fear is a graded central motive state ranging from mild to intense.

268 vidence suggests the importance of intrinsic motives such as curiosity or need for novelty, mediated

269 cepts "reuse" and are built upon fundamental motives such as survival, safety, and consumption.

270 psychology, which explores how human social motives such as the need for accuracy or the need for af

271 e their 'just deserts') and consequentialist motives (such as teaching transgressors that their behav

272 l transgressions to satisfy both retributive motives (such as wanting antisocial others to receive th

273 does not support this notion of conflicting motives, suggesting instead that thinking about self and

274 of Nup214 in detail and identify several FG motives that are required for this interaction.

275 racy in collective decisions and less on the motives that drive individuals to make these decisions.

276 n-seeking that aims to integrate the diverse motives that drive information-seeking and its avoidance

277 is reflected in people's minds as dominance motives that underpin ideologies and actions that ultima

278 ding to nucleotide changes in conserved 5.8S motives, the significantly lower GC contents in at least

279 We also explore how a speaker's motive to form a shared reality with listeners can moder

280 Although distrust is low, the apparent motive to gain research money is distrusted.

281 a modified symmetric PDG, also allows these motives to be disentangled.

282 ma game in which they could reveal prosocial motives towards an ingroup (ingroup-love) and hostility

283 -containing dipeptides having the structural motives typical of turn inducers.

284 tive oxidase (AOX) in plants is a non-proton-motive ubiquinol oxidase that is activated by redox mech

285 -trade markets scope is given to speculative motives unavailable where goods perish on purchase.

286 s argue that only asymmetric games allow the motives underlying defense and attack to be disentangled

287 others, and the ontogeny of these skills and motives unfolds in part naturally and in part as a resul

288 mong the MZS and MNS during the inference of motive was modality specific, being significantly strong

289 specific, being significantly stronger when motive was understood from actions in videos compared to

290 at was negatively affected when instrumental motives were also in evidence.

291 Economic motives were the major cause for discontinuation of mark

292 fically, research suggests that instrumental motives, which are extrinsic to the activities at hand,

293 the activities at hand, can weaken internal motives, which are intrinsic to the activities at hand.

294 ther sequence contexts including CHG and CHH motives, which cannot be evaluated by these pyrosequenci

295 a flat denial of the existence of pro-social motives--which it was not intended to be.

296 rences across several alternative pro-social motives, whose distribution in a population is stable.

297 implementation ("How is she doing it?") and motive ("Why is she doing it?") for actions presented in

298 understanding the implementation ("how") or motive ("why") of an action.

299 is best characterized as strategic or mixed-motive, with cooperative and competitive elements influe

300 ether holding both instrumental and internal motives yields negative outcomes in a field context in w