ライフサイエンスコーパス: energetic

1 o the dissociation channels as well as their energetics.

2 which could strongly affect their curvature energetics.

3 olecular couplings that determine the system energetics.

4 e and thus essential for supporting cellular energetics.

5 via a secondary effect of improving cardiac energetics.

6 cardiac hypertrophy and improving myocardial energetics.

7 gnetic resonance spectroscopy for myocardial energetics.

8 ions of the central limit theorem to protein energetics.

9 e most spectroscopic measurements of protein energetics.

10 ularly fruitful in the context of ecological energetics.

11 metabolism, community dynamics and ecosystem energetics.

12 g by improving, preserving or rescuing brain energetics.

13 s have been undertaken to study its detailed energetics.

14 n and thrombosis by regulating mitochondrial energetics.

15 nance spectroscopy to demonstrate myocardial energetics.

16 systolic and diastolic function, myocardial energetics ((31)P-magnetic resonance spectroscopy), and

17 We show that male elephants increased their energetic allocation into reproduction with age as the p

18 nts alter their movement patterns, and hence energetic allocation, in relation to (a) reproductive st

19 lar dynamics simulations based on a detailed energetic analysis of the interactions involved in dimer

20 derstanding their specific roles requires an energetic analysis.

21 performed by these genes appear to alleviate energetic and biosynthetic bottlenecks to viral producti

22 r cells, glutamine is used for generation of energetic and biosynthetic requirements of the MDV infec

23 tinct metabolic programs that adjust to meet energetic and biosynthetic requirements to support effec

24 and practical NMR method for extracting both energetic and dynamic information on protein-cosolute in

25 Computed energetic and magnetic criteria of aromaticity reveal th

26 t an understanding of both DNA hybridization energetic and magnetic interactions is required to predi

27 Here, we present a unified energetic and mechanistic picture of metastable pore def

28 according to an optimisation of the relative energetic and reproductive gains each state offers.

29 f our computational modeling, including both energetic and structural analyses, are compared with nov

30 dynamics simulations are used to capture the energetics and atomic-level details of Mg(2+)-RNA intera

31 ielectrons, we obtain a clear picture of the energetics and density of states of the ammoniated elect

32 Whereas myocardial energetics and diastolic function are impaired in obesit

33 board the Thermosphere Ionosphere Mesosphere Energetics and Dynamics satellite from 2002 to 2007.

34 fferences influence chromatosome structures, energetics and dynamics.

35 teria can be used in the optimization of the energetics and efficiency of computations.

36 The corresponding energetics and feasibility that favor C-arylation versus

37 In nine humans, we recorded cardiac energetics and function before and after a single oral d

38 Precise quantification of the energetics and interactions that stabilize membrane prot

39 protein-protein interactions and clarify the energetics and kinetics of tubulin heterodimerisation.

40 atalytic interface, and thereby the reaction energetics and kinetics.

41 monstrate the correlation between myocardial energetics and measures of contractile function in the m

42 In evaluating cellular energetics and metabolism of t(11;14) and non-t(11;14) M

43 rial dysfunction and implicate mitochondrial energetics and redox signaling as therapeutic targets fo

44 a metabolic blockade hampering mitochondrial energetics and respiration.

45 ), spatially explicit assessments of species energetics and risk will be important to understanding t

46 ctility associated with a decline in cardiac energetics and show that the mechanism is likely a combi

47 focus has not been placed on the underlying energetics and specificity of the activation process.

48 mplexes of variable stoichiometries, binding energetics and WW domain occupancy.

49 The accessibility, relative energetics, and bonding nature of the states involved di

50 lular function, but their molecular details, energetics, and kinetics are still not fully understood.

51 Analysis of kinetics, energetics, and MD-predicted structures shows that the h

52 e preference, preserves cardiac function and energetics, and reduces cardiomyocyte hypertrophy during

53 Energetics are compared to the reaction of maleic anhydr

54 for organic solar cell design where material energetics are tuned through molecular electrostatic eng

55 The foundation for research into energetics arose from Meyerhof's experiments on oxidatio

56 e known to support this key process, but its energetic aspects remain unknown.

57 suggest that VSG can improve alterations in energetics associated with p53 dysregulation.

58 rstood, and provides a means to evaluate the energetic balance of individuals under current environme

59 d a positively charged patch to decrease the energetic barrier for insertion into the bilayer.

60 in clusters at primed genomic loci lower the energetic barrier for nucleation of TAF15 condensates, w

61 reminiscent of the Gre-assisted reaction-the energetic barrier is similarly low, and the reaction inv

62 Grignard reagents allows us to overcome the energetic barrier of the dearomatization process and lea

63 coordination as responsible for lowering the energetic barrier to ring closure.

64 a critical role in synergistically reducing energetic barriers and accelerating reaction kinetics fo

65 in cytoskeleton can be harnessed to overcome energetic barriers to cell-cell fusion.

66 n the type of ATPase, but the structural and energetic basis of these mechanisms remains unclear.

67 Arctic sea ice will lead to an increasingly energetic Beaufort Gyre with eddies playing a greater ro

68 rediction (CSP) to understand the underlying energetics behind the structural transformation and disc

69 ariants enthalpically favor on-dyad binding, energetic benefits are significantly higher for GH1.0, s

70 semiconductors and the ill-defined relative energetics between semiconductors and molecules used in

71 ffinity sites, which bind NC with exothermic energetics, binding to these sites occurs endothermicall

72 ithin the interfacial region and reduces the energetic burden of calcium stress in mitochondria.

73 allenged early pterosaurs by imposing a high energetic burden, thus requiring flight to provide some

74 patiotemporal gait parameters in relation to energetics, but it remains unclear why people reduce asy

75 Both reversibility and energetic calculations suggest these fibrils are less st

76 ll populations of geometries with favourable energetics can play outsized roles in singlet fission pr

77 morphologies of the active layer lead to an energetic cascade for charge carriers, suppressing pathw

78 , thereby further depleting NAD+ to cause an energetic catastrophe and cell death.

79 How GCBCs meet the energetic challenge of rapid proliferation is poorly und

80 heir annual cycles, animals face a series of energetic challenges as they prioritise different life h

81 ht) was associated with improvement of these energetic changes such that there was no significant dif

82 lueprint to objectively study functional and energetic changes through geological time at a more nuan

83 Weight loss reverses these energetic changes.

84 The energetic chemical reaction between Zn(NO(3) )(2) and Li

85 Energetic collisions with background gas can cause struc

86 ve as nodal nucleotide-dependent sensory and energetic components regulating a diversity of effectors

87 ment of the thermal hazards of a potentially energetic compound.

88 A model that can predict energetic conditions that provide significant tumor grow

89 initio calculations but also to evaluate the energetic connectivities among the minima.

90 n grana diameter and stacking, a decrease in energetic connectivity between photosystem II (PSII) rea

91 However, due to energetic considerations, small rings are often difficul

92 ected residues with alanine to determine the energetic contribution of each side chain to forming an

93 the hexameric channel provide a substantial energetic contribution to Orai1 activation.

94 considers atomic interaction types and their energetic contributions as input features applied to the

95 es the side chain identity by optimizing the energetic contributions of that side chain in each of th

96 Analysis of energetic contributions reveals a dominance of nonpolar

97 terizing spatial, temporal, vibrational, and energetic correlations with Lithium motion.

98 Owing to the energetic cost associated with CO(2) release in carbon c

99 y protein binding-thus prepaying some of the energetic cost incurred from deforming the DNA.

100 s sinusoidally with a period of 10.65 bp and energetic cost of 1.37 KBT for sites that are positioned

101 Extensive remodeling, achieved at the energetic cost of a G-C base pair, explains how a single

102 ts of vertebrate muscle performance, and the energetic cost of breaching is high enough that repeated

103 ealed that following rules (1) decreased the energetic cost of decision-making; and (2) expanded rule

104 ymmetry plays a dominant role in shaping the energetic cost of gait asymmetry.

105 ymmetry plays a dominant role in shaping the energetic cost of gait asymmetry.

106 Given the energetic cost of generating and propagating action pote

107 teps in hominins may be linked to minimizing energetic cost of locomotion, the origin of the human-li

108 l data on bacteria allows us to evaluate the energetic cost of supercoiling during transcription.

109 the EMP can be reproduced by considering the energetic cost of surviving in harsh environments and HM

110 e favorable binding energy competes with the energetic cost of the growing edge and the elastic stres

111 4) was found to result in a 10-x increase in energetic cost over typical shark head morphologies.

112 ge, and suggest that benefits may come at an energetic cost that animals are unwilling or unable to p

113 However, how the energetic cost that is associated with distorting the DN

114 mmodated in membrane proteins without severe energetic cost, which, in turn, serve as a platform to f

115 h cellular process(es) drive this increasing energetic cost.

116 be balanced against the movement's predicted energetic cost.

117 ng reconstructions enable the computation of energetic costs and machinery demands of each secreted p

118 However, the mechanics and energetic costs associated with the breaching behaviors

119 g and expanding cells were analysed, and the energetic costs for metabolite biosynthesis and accumula

120 ion, selection, and drift and evaluating the energetic costs of cellular structures and functions.

121 In addition to the energetic costs of neural computation and transmission,

122 More generally, our results suggest the energetic costs of synthesizing nutrients may provide a

123 adaptation events provides evidence of tight energetic coupling between metabolism and regulatory reo

124 ed by uncertainty, steady-state models using energetic data along with plastic concentration in prey

125 By correlating energetics data with the molecular rearrangements measur

126 An energetic decomposition reveals, for slowly ejecting pro

127 This pattern appears to be driven by energetic deficiencies caused by responses to environmen

128 multiple signaling cascades to overcome the energetic deficiency.

129 in the understanding of the nature of these energetic deficits and to develop therapies directed at

130 l perturbations can be employed to break the energetic degeneracy and provide selective transformatio

131 e suPAR-treated HK-2 cells showed heightened energetic demand and mitochondrial superoxide generation

132 y vulnerable to O(2) deprivation due to high energetic demand.

133 to be completely elucidated how the altered energetic demands associated with lactation in dairy cow

134 The reduction of energetic demands imposed by overload relief allowed the

135 r, as the disease progresses, the myocardial energetic demands increase and the myocardium becomes en

136 The energetic demands of a cell are believed to increase dur

137 nt rule, which could reduce the metabolic or energetic demands of decision-making.

138 oxic limits are substantially reduced by the energetic demands of ecological activity, a trait that v

139 essary to maintain pregnancy and/or meet the energetic demands of lactation in years of poorer prey a

140 First, because of the energetic demands of larger brains and their influence o

141 Our results suggest that increases in the energetic demands of pinto abalone caused by ocean acidi

142 that change morphology to adapt to cellular energetic demands under both physiological and stress co

143 wers ATP synthesis and adjusts metabolism to energetic demands via cellular signaling.

144 and reflects the balance between growth and energetic demands.

145 loid co-assembly as well as insight into the energetic determinants involved in templating amyloid as

146 terparts, allowing investigators to identify energetic differences and providing insight into sources

147 ntioselective binding of chiral guests, with energetic differences DeltaDeltaG(293 K) up to 0.7 kcal

148 Energetic dissection revealed the contributions of the a

149 We report the profiling of spatial and energetic distributions of trap states in metal halide p

150 with the C2B domain functioning as the main energetic driver, and the C2A domain acting as a facilit

151 n of light by a chemical species provides an energetic driving force for an electron-transfer reactio

152 analysis to determine temporal coupling and energetics during activation.

153 hic mismatches caused by changes in consumer energetics during periods of low resource availability h

154 Therefore, we aim to clarify the myocardial energetic dysregulation in (reverse) remodeling, mainly

155 ng enables humpback whales to achieve 7x the energetic efficiency (per lunge) of krill foraging, allo

156 in translocases and function with double the energetic efficiency of ClpAP variants with completely a

157 re primarily responsible for bifurcating the energetic electron belt, which typically exhibits a sing

158 at surface plasmon resonance (SPR)-generated energetic electrons play an essential role in this photo

159 We concentrate on the dynamics of energetic electrons propagating along a radially divergi

160 e study show that the R163C mutations alters energetics even at temperatures that do not typically in

161 e strong suction flows comes at considerable energetic expense.

162 ir lobular appendages, which may indicate an energetic failure; and (2) a loss of connexin 36, sugges

163 herself have sufficient energy during this 'energetic fast'?

164 HLA using a comparatively broad and balanced energetic footprint, with interactions distributed over

165 d sulfurization is verified by thermodynamic energetics for most of low-valence metal compounds.

166 This provides a structural and energetic framework for interpreting current experiments

167 her case, due to the high penetration of the energetic gamma rays emitted by (137)Cs, the individual

168 ivator that controls expression of metabolic/energetic genes, programming cellular responses to nutri

169 itters will require a greater control of the energetics governing these chirality amplification effec

170 To date, most cardiac energetics have been performed using (31)P-NMR, which re

171 The sensitivity of heterogeneous energetic (HE) materials (propellants, explosives, and p

172 e-1 diabetes, accompanied by altered cardiac energetics, impaired mitochondrial function, and oxidati

173 These findings show that significant energetic impairment is already established in moderate

174 mon adaptive metabolic alterations preceding energetic impairment: a switch from fatty acid to carboh

175 p therapies directed at improving myocardial energetics in failing hearts.

176 we present a method of assessing myocardial energetics in the isolated mouse heart using (1)H-NMR sp

177 The current understanding of glucose-based energetics in vivo is based on the quantification of glu

178 y of combining evolutionary, topological and energetic information for scoring docked conformations.

179 The geometric and energetic insights between nanocarrier and their small m

180 s progress, females often shift from greater energetic investment in many small offspring towards inv

181 strates that high vacuum is not required for energetic ion acceleration, which relaxes target debris

182 formed through irradiation of the sulfide by energetic ions of the solar wind.

183 en spatiotemporal gait asymmetry and walking energetics is currently under debate.

184 ained non-oxidative contribution to exercise energetics is the critical power, which occurs at a meta

185 separated states, providing insight into the energetic landscape of a heterogeneous polymer-electroly

186 r results unravel a comprehensive map of the energetic landscape of nuclease-dead Cas12a (dCas12a) fr

187 ophy and oxidative stress allowed myocardial energetics, left ventricle hypertrophy, and diastolic dy

188 rmediary between environmental variation and energetic, life-history and ecological outcomes.

189 be a new catalytic strategy to transcend the energetic limitations of visible light by electrochemica

190 o spawn ensembles of synthetic heterogeneous energetic material microstructures.

191 bjects, methods, and metrics relevant to the energetic materials community and provides an overview o

192 terrorism, the effective detection of highly energetic materials is one of the critical procedures ne

193 s to the practical application of real-world energetic materials.

194 te to signal transduction for the sensing of energetic materials.

195 Understanding the principles of VILI energetics may provide valuable insights and guidance to

196 g in-depth 3D structural analysis, revealing energetic mechanisms for the sequence- and salt-dependen

197 Oxygen plays a crucial role in energetic metabolism of most eukaryotes.

198 that neuron or glial density, mitochondrial energetic metabolism, and/or inflammation contribute to

199 sect AnxA6(-/-) mice liver proliferation and energetic metabolism.

200 lations using a simplified "structure-based" energetic model.

201 ure of the gas-phase molecule, dosed with an energetic molecular beam, was into a metastable chemisor

202 foraging patch use in response to increased energetic need, highlight the degree to which animal pop

203 onse to changes in resource availability and energetic need.

204 reduce GABAergic tone, which in turn reduces energetic needs in a hypoxic habitat.

205 ve cells of the renal tubule also pair their energetic needs to the regulation of diverse cellular pr

206 r level, we examined the effects of the most energetic North Atlantic hurricane season in 50 years on

207 ts of future climate change on the wintering energetics of a freeze-tolerant amphibian, the Wood Frog

208 rganization to the binding specificities and energetics of adhesion receptors.

209 thin hydrophobic reaction pockets alters the energetics of adsorption and catalysis, but a mechanisti

210 F-actin where the corresponding interaction energetics of billions of conformational poses were rank

211 The energetics of binding and the rate constants suggest tha

212 Moreover, we find similar energetics of binding regardless of the presence of the

213 y functional theory is used to determine the energetics of charge accumulation and O-O bond formation

214 We also show that the energetics of cross-beta stacking by polyglutamine would

215 ction-activation strain model to explain the energetics of different pathways.

216 Next the structure and relative energetics of dioxacarbeniun ions are covered with empha

217 t repercussions on understanding the overall energetics of excitation energy transfer and charge sepa

218 ration experiments may precisely dissect the energetics of hybrid formation on the ribosome.

219 In this work, we probe the competing energetics of inserting a solute in different membrane e

220 del that correlates the import flux with the energetics of large cargo transport through the NPC.

221 Herein, we measure the prevalence and energetics of multiplex H-bonds that are formed between

222 We unveil the mechanism and free energetics of nucleotidyl transfer reaction in an SNT ca

223 dominance of the clusters in determining the energetics of POM crystals.

224 ffective tool for rapidly characterizing the energetics of protein interactions.

225 description of the nucleation mechanism and energetics of small metastable pores and illustrates a s

226 iving zebra-fish embryos and to estimate the energetics of specific developmental events.

227 e interaction and fully map the site-binding energetics of Syt1 both in the absence and presence of C

228 lved information on structure, dynamics, and energetics of the Hsp104 molecular machinery, even durin

229 etermination of the structure, dynamics, and energetics of these engineered structures in bilayer mem

230 Organic semiconductors require an energetic offset in order to photogenerate free charge c

231 e establish the influence of the interfacial energetics on the electron and hole transfer rates separ

232 n of Ph(2)P(O)H and PhX revealed a favorable energetics only for the loss of iodide following the oxi

233 g a nonconsumptive effect (NCE) with unknown energetic or fitness costs.

234 ormal neuron or glial density, mitochondrial energetics, or neuroinflammation in ASD, alongside wides

235 -corrected SCAN not only retains the correct energetic ordering for water hexamers but also reduces t

236 ng self-interaction error does not alter the energetic ordering of the different water isomers with r

237 he CofActor, we accomplished both light- and energetic/oxidative stress-gated control of this interac

238 of the substituents onto the structural and energetics parameters of these processes.

239 Energetic particle generation is an important component

240 rmative to our understanding of how the most energetic particles in the universe are generated.

241 equent thermal energy dissipation induced by energetic particles, a fundamentally new phenomenon is r

242 an affect the natural environment of charged energetic particles, for decades there remained little d

243 conclusion is additionally supported by the energetic pathways and NBO charges calculated at UCCSD a

244 and metabolome showed the used of alternate energetic pathways, metabolite sinks and bottlenecks, an

245 o be extensively compared to CDI in terms of energetic performance.

246 erobic naphthalene oxidation pathway from an energetic perspective.

247 Although altered energetics play a central role in MH, MH-susceptible hum

248 n action is preserved to protect fundamental energetic processes in the muscle.

249 ogenation of carbon monoxide-rich ice and/or energetic processing of methane condensed on water ice g

250 anelles best known for their central role in energetics, producing adenosine triphosphate to power mo

251 sent how chamber background pressure affects energetic proton acceleration from an ultra-intense lase

252 ll allow a broader examination of myocardial energetics providing a valuable tool to aid in the under

253 ) on board the Fermi spacecraft provided the energetic radiation measurements.

254 ngerprints of a civilian Russian water-water energetic reactor (VVER) fuel at the end of its lifetime

255 molecular stages coordinated by the cellular energetics regulator mTORC1.

256 ive cooperativity in ATP hydrolysis, and the energetic requirement for at least 12 ATP molecules to b

257 electron flow through the membrane, meeting energetic requirements and anaplerotically generating tr

258 In this study, we analyzed the bacterial energetic requirements associated with these cellular al

259 phy of diverse marine species to fundamental energetic requirements that are shared across the animal

260 ts association with life-history plasticity, energetics research in red squirrels has overturned seve

261 How much and when a consumer adds to its energetic reserves or invests in reproduction are key be

262 tic fluctuations of an individual consumer's energetic reserves while foraging and reproducing on a l

263 ection between (spatial) delocalization and (energetic) resonance stabilization embedded in VB theory

264 Although we have not yet investigated the energetic response of squirrels to elevated density or i

265 ) might enhance neuronal and oligodendrocyte energetics, resulting in improved cell function, repair,

266 region, we identified an area of heightened energetic risk in the northwestern part of the Great Lak

267 , acting via hormones that modulate cerebral energetics, RNA therapeutics and complementary multimoda

268 terials as well as foundational knowledge of energetic science new to most chemists.

269 ve continental ice sheets predicts a tidally energetic Snowball ocean due to the reduced ocean depth,

270 The energetic span analysis reveals the reductive eliminatio

271 span for methylene fluorination and a higher energetic span for methyl fluorination, which is consist

272 licit participation of Ag results in a lower energetic span for methylene fluorination and a higher e

273 the pH is accompanied by both a significant energetic stabilization and decreased nuclease sensitivi

274 The energetic stabilization, however, is not strong enough t

275 Understanding the energetic state of the heart is essential for unraveling

276 Our understanding of the energetic state of water in relevant processes is limite

277 d by thermodynamic variables which track the energetic state of water such as water activity and wate

278 alters the fibril structure to a more stable energetic state.

279 Recognising activity as a determinant of energetic status, the predictability of activity variati

280 uced ejection fraction display reductions in energetic status.

281 During Caenorhabditis elegans sleep, energetic stores are allocated to nonneural tasks with a

282 IPK1-deficient cells are unable to cope with energetic stress and are vulnerable to low glucose level

283 s the lysosomal defects and vulnerability to energetic stress and prolongs the survival of RIPK1-defi

284 hed light on the regulation of mTORC1 during energetic stress and unveil a point of crosstalk between

285 lin ratio), sensitize AMPK activation to the energetic stress induced by the dietary transition durin

286 Aging did not increase sensitivity to energetic stress or social status.

287 Here we investigate whether acute changes in energetic stress signal in the spatially isolated axon w

288 voked hypertrophic remodeling with increased energetic stress.

289 that RIPK1 promotes mTORC1 inhibition during energetic stress.

290 onal mitochondrial mobility during localized energetic stress.SIGNIFICANCE STATEMENT As the main prov

291 al cellular response that depends on tissue, energetic, stress and signaling contexts.

292 y, through the inclusion of evolutionary and energetic terms.

293 FRB 200428 is just 30 times less energetic than the weakest extragalactic FRB observed so

294 DFT studies with relative energetics that support the kinetically controlled react

295 strated that S-OPA1 can maintain cristae and energetics through its GTPase activity, despite lacking

296 ing (WMS) method is used to provide accurate energetics to benchmark a density functional for direct

297 amics of the trophic network using ecosystem energetics to data from a large grassland biodiversity e

298 in immune function is largely attributed to energetic trade-offs rather than specific nutrient const

299 s), which are critically sensitive to spatio-energetic variations of the molecular structure.

300 These energetics were readily reproduced by density functional