ライフサイエンスコーパス: energetic

1 All of the anions are highly energetic.

2 itylase UCH37 bind to RPN13 with independent energetics.

3 ritical for any general theory of organismal energetics.

4 surements of the VBM and electrode-dependent energetics.

5 On the basis of energetic analysis, the main transition was identified a

6 l responses during AD by sustaining cellular energetic and biosynthetic metabolism.

7 Models that best satisfy energetic and geometric constraints produce CMB spikes 8

8 onal theory investigations shed light on the energetic and geometric requirements of the different st

9 The computed energetic and kinetic features for the cavity wetting tr

10 optical flash that accompanied the extremely energetic and long-lived prompt gamma-ray emission from

11 ion of several developmentally stereotypical energetic and metabolic transitions, i.e., metabolic rep

12 olic PEP carboxylase or by limited supply of energetic and reductive equivalents.

13 or different cation types and the associated energetic and solvation contributions to ion selectivity

14 ially increase reliance on glutamate to fuel energetics and anaplerosis.

15 rane (MAM) plays a critical role in cellular energetics and calcium homeostasis; however, how MAM is

16 ully competent for maintaining mitochondrial energetics and cristae structure.

17 NRPSs exist, few studies have focused on the energetics and dynamics governing the interactions in th

18 as been achieved to understand the atomistic energetics and dynamics of ion-molecule reactions, such

19 our knowledge, the first predictions of the energetics and dynamics of the T4 injection machinery us

20 after the event, allowing us to diagnose the energetics and environment of the merger.

21 r, their performance is often limited by the energetics and geometry of the martensitic-austenitic ph

22 To test this hypothesis, interaction energetics and in vitro function of wild-type and D292V

23 Results showed that energetics and kinetics of NTD self-assembly are highly

24 , partly due to difficulties to quantify the energetics and kinetics of SNARE assembly.

25 s, here we describe the structure, dynamics, energetics and mechanism of assembly of multiple K-Ras d

26 The relationship between the adsorption energetics and OER kinetics, however, has not yet been e

27 tate transaminase (GOT) to maintain cellular energetics and protect the brain from ischemic stroke in

28 tional theory calculations that evaluate the energetics and reaction mechanisms for the dimerizations

29 ate that matrix architecture alters cellular energetics and that intracellular ATP:ADP ratio is relat

30 Here we present a detailed analysis of the energetics and thermodynamics of vesiculation by recours

31 -crystalline rubrene is selected because its energetics and transition dipole alignment uniquely allo

32 e given crucial insight into the mechanisms, energetics, and dynamics of O2 adsorption and dissociati

33 iency of oxygen utilization, improved muscle energetics, and protection against oxidative stress.

34 The central importance of oxygen, energetics, and redox homeostasis in immune cell metabol

35 ids have fundamental roles in the structure, energetics, and signaling of cells and organisms.

36 e hydrogen evolution reaction (HER), surface energetics, and stability.

37 of L- and S-OPA1 in mitochondrial fusion and energetics are ill-defined.

38 rmance of these models in predicting binding energetics as well as structural, electronic, and thermo

39 of the nucleotide substrate is controlled by energetics associated with nucleobase desolvation, where

40 We estimate the effects of changes in the energetics at the bilayer surfaces on the channel dwell

41 For instance, the energetic balances of larger animals are generally more

42 ecause of the reduced contact resistance and energetic barrier for electron transport.

43 by other viral proteins which help lower the energetic barrier to pore expansion.IMPORTANCE Influenza

44 nt with H-shift reactions over a substantial energetic barrier, we find that the rate coefficients of

45 Our work illustrates that large energetic barriers, prohibitive toward chemical reaction

46 ing a mutagenesis approach, we dissected the energetic basis for the TIGIT/nectin-2 interaction and r

47 In this work, we unearth the energetic basis of the observed dynamic allostery in a P

48 ibution of resources to the brain provide an energetic buffer during times of environmental stress.

49 Thus, the energetic burden of pH regulation is offloaded from hypo

50 ter plays a vital role in electron transport energetics by electrowetting the cofactors in the chain

51 termined structures, as well as offering (i) energetic calculations to minimize loops, (ii) docking m

52 ial membranes and the resultant boost to the energetic capacity of eukaryotic cells.

53 hosphoinositol tetrakisphosphate) are highly energetic cellular signals interconverted by the diphosp

54 te the phase-change mechanism, including the energetic changes involved.

55 is strongly biased towards the excitation of energetic charge carriers in the Pt shell.

56 usion injury and were similarly analyzed for energetic cofactors.

57 l for maintaining cristae tightness and thus energetic competency.

58 y designing high-performance and insensitive energetic compounds for practical applications is throug

59 for the first time that the frontier orbital energetics (conduction band minimum (CBM) and valence ba

60 rom electrostatics theory and to measure the energetic consequences of the nucleic acid electrostatic

61 however, insight into the stoichiometric and energetic constraints of cyanobacterial diurnal growth i

62 , because they exhibit a side chain-specific energetic contribution determined by the change in nonpo

63 This potentially high energetic contribution from jelly-falls highlights a pos

64 tact partners, and DeltaGtert, the favorable energetic contribution from the formation of tertiary co

65 les have been explicitly represented and the energetic contribution of the solvent during ligand bind

66 registration of smaller domains; whereas the energetic contribution of undulations increases with mem

67 erface are presumably stabilizing, but their energetic contribution to dimerization has yet to be det

68 .C wobble system further allowed us to parse energetic contributions and extract estimates for the el

69 The approach assuming independent energetic contributions from GABAergic drugs enables, at

70 However, relative energetic contributions of the individual contacts in th

71 igand binding sites, allowing us to rank the energetic contributions of these individual interactions

72 of denaturant urea to reveal the individual energetic contributions of various ligand-functional gro

73 unctional binding sites for propofol and the energetic contributions stemming from propofol binding t

74 ing the central contact deliver the decisive energetic contributions to enable this remarkable bondin

75 In addition to energetics, controlled electrochemical charge injection

76 Herein, we present direct measurements of energetic cooperativity in an experimental system in whi

77 lic, mechanical, and perceptual estimates of energetic cost associated with a range of asymmetries to

78 C18:1+dC22:1 mixture can be explained by the energetic cost associated with compressing the lipids to

79 Lunge feeding entails a high energetic cost due to the drag created by an open mouth

80 heory that the sensorimotor system minimizes energetic cost during locomotion has long been supported

81 A movement model predicted a higher energetic cost for PAH-resistant subpopulations when see

82 tical high temperatures should incur greater energetic cost in NAL than SAL via an elevated metabolic

83 in respiration rate, potentially due to the energetic cost of mucus production.

84 Additional constraints due to the energetic cost of proofreading also play a role in the e

85 d regulation of the thick filament makes the energetic cost of the systole rapidly tuned to the mecha

86 ch may potentially increase the duration and energetic cost of their journeys.

87 Remarkably, despite the low energetic cost of this transition, quantities such as th

88 ces of the host, a detailed estimate for the energetic cost of viral synthesis is largely lacking.

89 To quantify the energetic cost of viruses to their hosts, we enumerated

90 Last, using our predictions for the energetic cost of viruses, we provide estimates for the

91 ne or two sites often comes at a significant energetic cost to fold stability.

92 interpretation on hominin territoriality and energetic costs invested by hominin groups.

93 These findings are relevant to understanding energetic costs of evolutionary elaboration and reductio

94 Hydrodynamic theory predicts that the energetic costs required for fishes to swim should vary

95 (stroke frequency >25 strokes per minute and energetic costs three to six times the resting rate of e

96 To minimize energetic costs, trans-Gulf migrants should stop over wh

97 For one model system, energetic coupling between domains has been shown to be

98 opose a metric for quantifying the degree of energetic coupling between experimentally measured degre

99 complemented by modular cycles that measure energetic coupling between separable domains.

100 MPAB, but with negative rather than positive energetic coupling to GABA binding.

101 fusion, selective transport, osmotic forces, energetic couplings) could have been crucial for the coh

102 The subsequent energetic crisis induced two cellular responses involvin

103 sevengill shark Notorynchus cepedianus, with energetics data from the literature, to construct a bioe

104 a border between mechanisms where the usual energetic definition of intermediates is not meaningful.

105 In situations of higher energetic demand decreased mitochondrial calcium uptake

106 est night-time lighting likely increased the energetic demand of dogwhelks through stress, encouragin

107 fission as a normal adaptation to increased energetic demand.

108 l role in the heart, responsible for meeting energetic demands and regulating cell death.

109 itions and cellular dysfunction, but how the energetic demands are monitored and met in response to p

110 oduce a sodium gradient that may sustain the energetic demands required for its rapid multiplication.

111 nine nucleotide pool in response to cellular energetic demands.

112 unsustainable ATP concentrations for various energetic demands.

113 ce spectroscopy experiments that explore the energetic details of donor-acceptor oligorotaxane foldam

114 Thus, ENPP1 deficiency confers an energetic disadvantage to PCs for long-term survival and

115 ng polymers is known to be enhanced when the energetic disorder of the polymer is minimized.

116 e of recombination of charge carriers, their energetic distribution and the mode of transport are mad

117 relaxation of photo-generated charges and in energetic distribution, is similar to the anatase phase

118 In order to probe the energetics, dynamics, and molecular mechanism for the pr

119 When combined, the favorable energetic effects in the WG translated into a 92-kcal/d

120 Predicting the energetic effects of protein mutations can improve our f

121 lows us to disentangle diffusivity from free-energetic effects.

122 d increased it in distal segments with lower energetic efficiency.

123 grees hollow cone, which is filled with more energetic electrons determined by the injection dynamics

124 nthermal electron components.The creation of energetic electrons through plasmon excitation has impli

125 The creation of energetic electrons through plasmon excitation of nanost

126 titative insights into the interplay between energetic, entropic, and nuclear quantum effects on the

127 ng these two pathways in response to complex energetic, enzymatic, and metabolic cues.

128 Here, we report the identification of an energetic epitope by determining the interfacial hot-spo

129 Damuth's 'energetic equivalence rule' supported Van Valen s conjec

130 cyclic, bradycardic state that reduces daily energetic expenditure by 10% and counteracts heart rates

131 both the conformational flexibility and the energetic factor of binding, we successfully identified

132 ity functional theoretical studies show that energetics favor CO oxidation on single Pd atoms support

133 To assess the energetic favorability of nonnative versus native intera

134 Energetic flexibly in U. bilobatum highlights the fundam

135 he accumulation of lipids represents a large energetic flux for many species, so figuring out how thi

136 regulated by a series of metabolites in the energetic flux within the cell.

137 yses showed that the TCRs shared a conserved energetic footprint on the HLA-E molecule, focused aroun

138 ltimately becomes an order of magnitude more energetic for periods of weeks in response to the passag

139 tal edges also display favourable adsorption energetics for water oxidation under electrochemical con

140 ts are once again exploring the chemical and energetic forces that shape growth, development and matu

141 the driving mechanism for the generation of energetic free electrons.

142 the ribosome, and that a sufficient level of energetic frustration is needed for fast-translating cod

143 el strategy that relies on the principle of 'energetic frustration'.

144 The resulting energetics-function model reveals the rate-limiting proc

145 -offs between kleptoparasitic losses and the energetic gains derived from killing larger prey.

146 resulting rainbow photocathodes with forward energetic gradient for charge separation and subsequent

147 etabolite exchange that are structured along energetic gradients.

148 mplexes, including structural heterogeneity, energetic heterogeneity, and functional heterogeneity.

149 coupling that greatly reduces the molecular energetic heterogeneity.

150 We find that the energetic HOMO-LUMO gap, a correlate of chemical reactiv

151 ical excitation of surface plasmons produces energetic hot electrons that can be collected to facilit

152 the plasmon resonance of aluminum to supply energetic hot-carriers and increases optical absorption

153 gical cardiolipin stabilization reverted the energetic impairment, confirming the initial mitochondri

154 showed the plankton community appeared more energetic in May, and relatively healthy in Gonghu Bay w

155 tatively, membrane tension will alter gating energetics in proportion to the change in projected area

156 antigen structures reveal stereochemical and energetic influences on MAIT cell activation, enabling d

157 The exposure of the Earth's surface to the energetic input of rainfall is one of the key factors co

158 ecules that do not dissociate appreciably on energetic ion bombardment.

159 clic aromatic hydrocarbon (PAH) molecule and energetic ion is a subject of interest in different area

160 Energetic ions traveling in solids deposit energy in a v

161 By manipulating a tightly focussed beam of energetic ions, often gallium (Ga(+)), FIB can sculpt na

162 ical time-resolved method to probe the local energetic landscape and electronic dynamics at such inte

163 mutual orientations, thus tuning the overall energetic landscape and ensuring highly efficient light-

164 with which we can now describe the complete energetic landscape of the Cdc42-binding site on ACK.

165 s shown to vary depending on the spatial and energetic landscape, which dictates the relative couplin

166 ength N is extended up to 10.5 modifying the energetic levels.

167 plantar flexion exercise occurs at a common energetic limit in all subjects.

168 is an essential ecosystem process and a key energetic link between higher trophic levels, decomposer

169 ritin proteins to create a stable and highly energetic liquid composed of aluminium nanoparticles and

170 nted in four conditions that created similar energetic masking but either high or low informational m

171 rs' ability to overcome informational versus energetic masking of speech.

172 zed production and applications as a "green" energetic material and a potential catalyst for differen

173 ow a superior hydrogen-free 5/6/5 fused ring energetic material, 1,2,9,10-tetranitrodipyrazolo[1,5-d:

174 uld lead to future practical applications as energetic materials.

175 display promising performance properties as energetic materials.

176 h other and to machineries with functions in energetics, membrane organization, and quality control.

177 s the possible effects on cuticle integrity, energetic metabolism and immune response.

178 Complex alterations in cerebral energetic metabolism arise after traumatic brain injury

179 function in the skin and suggests a role for energetic metabolism in epidermal biology.

180 UCP2 can regulate oxidative stress and/or energetic metabolism.

181 In addition to its activity as an energetic metabolite, BHB is increasingly understood to

182 ording to a U-shaped curve, with an expected energetic minimum at intermediate cruising speeds and in

183 th oxygen, safely holds electrons at a local energetic minimum during the oxidation of plastohydroqui

184 , to date no complete datasets have shown an energetic minimum for swimming fish at intermediate spee

185 ppenheimer molecular dynamics of VUV-excited energetic molecules have been conclusively observed dire

186 e profile of NAL shifted with changes in key energetic molecules, whereas these were unaffected in SA

187 ppenheimer molecular dynamics of VUV-excited energetic molecules.

188 y described how metabolic flux adapts to the energetic needs of a developing organism, but also empha

189 supply of glucose is too low for the body's energetic needs, such as during periods of prolonged exe

190 role of ecological pressures on integrative energetic networks and the still poorly understood energ

191 ore than 80% of the fast ions are reduced to energetic neutral atoms and demonstrate the feasibility

192 o Marinimicrobia clades, occupying different energetic niches, express nitrous oxide reductase, poten

193 We found that a 1-h deprivation of the main energetic nutrients is an appropriate strategy to abolis

194 o) is an independent property describing the energetics of an isolated side chain in the bilayer.

195 ated pairs has been extensively studied, the energetics of cation-pi-driven self-assembly in molecula

196 rfacial confinement fundamentally alters the energetics of cation-pi-mediated assembly: an insight th

197 However, the energetics of cooperativity are complicated by solvent e

198 Surface energetics of demineralised whey (DMW), skimmed milk (SM

199 nctional theory to characterize the relative energetics of each intermediate, including the importanc

200 ions associated with the origin of life, the energetics of early metabolisms, and climate through the

201 prospect of resolving the conformations and energetics of elementary steps in the activation process

202 ontaining subunits is varied, we address the energetics of gating and establish whether gating is a c

203 Combined with the energetics of glutamate binding to the LBD and the energ

204 Little is known about the energetics of growing hair follicles, particularly in th

205 esonance energy transfer to characterize the energetics of homo- and heterooligomer interactions betw

206 anostructured solutes and calculate the free energetics of interfacial water density fluctuations, wh

207 methods require a precise description of the energetics of intermolecular interactions.

208 Here, we quantitatively examine the energetics of intrinsic affinities, characterize the sto

209 pmin - is critical for estimating the total energetics of non-thermal electrons produced by cluster

210 Structures and energetics of o-, m-, and p-quinonimide anions (OC6H4N(-

211 ured in 13 different solvents to examine the energetics of O...S, O...Se, S...S, O...HC, and S...HC c

212 ycle analysis, an approach for exploring the energetics of protein-protein or protein-ligand interact

213 -to-open TM domain transition in the overall energetics of receptor activation, we designed point-mut

214 crunching and anti-scrunching, and we define energetics of scrunching and anti-scrunching.

215 e surface areas, bulk thermodynamics and the energetics of the aqueous phase drive cryptomelane forma

216 l a reactivity model that reaches beyond the energetics of the cascade itself, incorporating an ensem

217 powerstroke mechanism) is the result of the energetics of the complete myosin-V cycle and is not the

218 mers and have characterized the kinetics and energetics of the conformational switch.

219 e constants >/= 4000 s(-1)) and quantify the energetics of the cysteine disulfide redox-reaction (rev

220 Reaction energetics of the double (2H(+)/2e(-)), i.e., the first

221 an active site water network can have on the energetics of the forward reaction and how metals or enz

222 l ligand cooperative reactions, changing the energetics of the process when different dearomatized pi

223 Evaluation of bonding and energetics of the remarkable product was accomplished co

224 In this work we study the structure and energetics of triple junctions in graphene using a multi

225 be exploited if it is associated with either energetic or survival costs.

226 Juno's energetic particle and plasma detectors measured electro

227 h is ascribed to an accretion disk corona of energetic particles akin to those seen in the solar coro

228 Such an energetic pathway between jelly-falls and N. norvegicus

229 ide empirical evidence of the presence of an energetic pathway between jellyfish and a commercially i

230 high density of corner sites and lower-lying energetic pathway.

231 Combining sequence and energetic patterns using machine-learning algorithms fur

232 nsitivity, were investigated, as well as the energetic performance (e.g., detonation velocities and d

233 were investigated to evaluate the integrated energetic performance.

234 environment (DeltaG+/-) will not affect the energetic perturbation from a mutation in a tertiary con

235 The ligand creates a local energetic perturbation that propagates in the form of do

236 y accretes matter, it gives rise to a highly energetic phenomenon: an active galactic nucleus.

237 rial shows excellent photo sensitivity under energetic photons.

238 design of transmitters in terms of molecular energetics, photophysics, binding affinity, stability, a

239 orbital energies, can help shed light on the energetic, physical, and spectroscopic properties of sem

240 Multiple energetic pre-supernova eruptions are expected to occur

241 Computational analysis describes the energetic profile for the stepwise removal of three H at

242 ispensable in this regard for recording full energetic profiles of protein unfolding and permitting d

243 ings are consistent with modular but complex energetic properties of RNA structural motifs and will a

244 The energetic properties of the new materials are competitiv

245 were synthesized and the physicochemical and energetic properties, including density, thermal stabili

246 ce probes are subject to damage arising from energetic proton (H(+)) irradiation.

247 The highly energetic proton generates a time-varying field that is

248 A reduced charge state on the energetic proton in the condensed phase of water results

249 yet remains a lack of systematic studies of energetic proton induced changes in the photoelastic pro

250 Water molecules along the path of the energetic proton undergo ionization at individual molecu

251 Around Earth, trapped energetic protons, electrons and other particles circula

252 imprint of longitudinal range straggling for energetic protons.

253 their trans-interactions only within a small energetic range, suggesting that cell adhesion is an ela

254 ectrophiles that are needed for these highly energetic reactions by using O2, electrons, and metals o

255 ential, which may in particular allow highly energetic reactions in fuel cells.

256 energy dissipation has been used to give an energetic reasoning as to the behaviour seen with respec

257 For energetic reasons, macroscopic drops of liquid form near

258 effects, and how this affects mitochondrial energetics, redox balance and the emission of reactive o

259 ly reducing nature of photosystem I, and the energetic requirements placed on the pigments to operate

260 Understanding the structural and energetic requisites of ligand binding toward its molecu

261 ially lethal consequences of depleting their energetic reserves over water.

262 owed aging shows that, compared to controls, energetic resources are directed more toward somatic mai

263 Energetic resources in hypoxic tumor regions are constra

264 and mobilisation aids understanding of their energetic responses to rapid environmental change.

265 To clarify and contextualize the energetic results, natural bond orbitals were used to ev

266 Strong fidelity facilitated stable energetic rewards and low risk, while weak fidelity faci

267 of ammonia oxide adducts in hydroxylammonium energetic salts could lead to future practical applicati

268 of the corresponding mono/dihydroxylammonium energetic salts.

269 s has the potential of deprotonation to form energetic salts.

270 inues to develop, debate still surrounds the energetic significance and physicochemical origins of th

271 gamma-turns is also identified, with similar energetic stability.

272 uggest that cycloarenes gain little, if any, energetic stabilization from global delocalization, obvi

273 Energetic stabilization of one of the CDN constituents l

274 mong individuals and was unrelated to age or energetic state.

275 on of metabolic homeostasis depending on the energetic state.

276 tly impacts systemic metabolism in different energetic states.

277 1184+/-10 ms, P<0.001), and impaired cardiac energetic status (phosphocreatine/gamma-adenosine tripho

278 hondrial fusion, thus coupling mitochondrial energetic status and morphology.

279 for NPY, AGRP, POMC, and CART in regulating energetic status in A. burtoni females during varying me

280 ght that the benefit of therapies to improve energetic status of the heart may vary depending on the

281 e dwarf, and which often generate bright and energetic stellar outbursts.

282 tic networks and the still poorly understood energetic strategies of animals in the tropics.

283 n the allosteric mechanism; we show that the energetic strength of coupling of the gates is strongly

284 known to play an important role in cellular energetics, stress defense, and neoplastic transformatio

285 in neuronal circuits, and from environmental energetic stressors such as food deprivation and physica

286 ate single layer systems and calculate their energetics, structural, electronic, and elastic properti

287 e use calculations to unravel differences in energetics, structures and reactivities of relevant Mg2+

288 ed in protein-protein docking, as well as an energetic term considering the contribution made by the

289 The mechanisms and the energetics that drive the folding of these proteins are

290 rs (glutamate receptors), and to change cell energetics through mitochondrial biogenesis.

291 will allow local electrostatic potential and energetics to be measured within nucleic acids and their

292 nnels are metabolic sensors that couple cell energetics to membrane excitability.

293 e an entatic state for modest yet accessible energetics to modulate chemical function.

294 hermodynamic remodeling of the mutant gating energetics toward its wild-type counterpart.

295 and thermodynamic remodelling of the gating energetics towards that of wild-type CTFR.

296 There is an energetic trade-off between producing workers, which con

297 timing is therefore not solely determined by energetic trade-offs but by the game theoretic problem o

298 fferent people, from my encouraging mentors, energetic trainees, and inspiring colleagues.

299 als the smallest macrocycle to have the most energetic VHF-VHF state and hence highest energy density

300 direct O2 formation in single collisions of energetic water ions with oxidized cometary surface anal