ライフサイエンスコーパス: thermodynamics

1 This is a consequence of statistical thermodynamics.

2 teaus due to finite size effects on reaction thermodynamics.

3 owing the independent tuning of kinetics and thermodynamics.

4 mplications for the calculation of solvation thermodynamics.

5 ipid model, with minimal perturbation to the thermodynamics.

6 oretical techniques for estimating solvation thermodynamics.

7 is one of the oldest and venerable rules of thermodynamics.

8 r provide a complete picture of the solution thermodynamics.

9 state has are questions about truly quantum thermodynamics.

10 copy, and computational analyses of reaction thermodynamics.

11 sembly; (4) speculative links to equilibrium thermodynamics.

12 ramatically alter nucleic acid structure and thermodynamics.

13 l postulation arising from the second law of thermodynamics.

14 on and O2 release steps rather than only the thermodynamics.

15 of the entropy state function in macroscopic thermodynamics.

16 LC using the basic principles of statistical thermodynamics.

17 odeling approach to capture its pH-dependent thermodynamics.

18 for reactivity, rather than the equilibrium thermodynamics.

19 cted to deviate substantially from classical thermodynamics.

20 tbed to explore its molecular structures and thermodynamics.

21 ransport modeling which is based on chemical thermodynamics.

22 relationship exists between information and thermodynamics.

23 ns is introduced to clarify how kinetics and thermodynamics affect evaporation/condensation process a

24 nd are rationalized through first-principles thermodynamics and ab initio molecular dynamics.

25 ity can be used to investigate hybridization thermodynamics and binding interactions.

26 indow carries important consequences for the thermodynamics and biogeochemistry of ecosystems, both d

27 horoughly reviewed, with special emphasis on thermodynamics and catalyst design considerations.

28 theory calculations provide insight into the thermodynamics and catalytic cycle of the amide-to-ester

29 haracterizing DNA hybridization kinetics and thermodynamics and enabling emerging applications in gen

30 of known base modifications on RNA pairing, thermodynamics and folding are being determined in relat

31 bioactive compounds showing specific binding thermodynamics and following similar pharmacokinetic mec

32 the-art understanding of hydrate interfacial thermodynamics and growth kinetics, and the physiochemic

33 As dictated by the Second Law of Thermodynamics and its fluctuation theorem corollaries,

34 ty at physiological K(+) concentrations, its thermodynamics and kinetic properties have not been char

35 The force-dependent thermodynamics and kinetic properties of the major speci

36 itation based upon fundamental principles of thermodynamics and kinetics are not available, despite t

37 This allows a more accurate estimate of the thermodynamics and kinetics associated with drug-target

38 inspired by this modularity-that RNA folding thermodynamics and kinetics can be quantitatively predic

39 Finally, the results reveal that the thermodynamics and kinetics of Amt (un)binding is very s

40 We study the thermodynamics and kinetics of an RNA toehold-mediated s

41 irpins that can detect sequence selectivity, thermodynamics and kinetics of binding for small drugs a

42 he sequence selectivity and characterize the thermodynamics and kinetics of binding in a single assay

43 A novel approach to the study of binding thermodynamics and kinetics of carbohydrate-protein inte

44 ents without compromising precise control of thermodynamics and kinetics of chaperone-client interact

45 The thermodynamics and kinetics of DNA oligonucleotide hybri

46 To gain insight into the contrasting thermodynamics and kinetics of DNA recognition by these

47 target engagement is a function of both the thermodynamics and kinetics of drug-target interactions,

48 We characterized equilibrium thermodynamics and kinetics of folding and self-associat

49 Thermodynamics and kinetics of H2O splitting are largely

50 ed by macromolecules, which affects both the thermodynamics and kinetics of in vivo processes.

51 roxide core and the resulting effects on the thermodynamics and kinetics of its hydrogen-atom abstrac

52 g of the protein can significantly alter the thermodynamics and kinetics of local conformational exch

53 ons and show that crystal packing alters the thermodynamics and kinetics of local conformational exch

54 m of this mutual regulation, we measured the thermodynamics and kinetics of PLC-beta3 binding to Galp

55 ioned to answer open questions regarding the thermodynamics and kinetics of polyQ folding and aggrega

56 rotein surfaces by measuring the equilibrium thermodynamics and kinetics of protein folding in the co

57 Thermodynamics and kinetics of reactive solutions used i

58 The thermodynamics and kinetics of ring-opening polymerizati

59 the structural underpinnings of the observed thermodynamics and kinetics of the conformational change

60 Both the thermodynamics and kinetics of the pertinent reactions w

61 giving controlled gel times dictated by the thermodynamics and kinetics of the system.

62 ccurately modeled by taking into account the thermodynamics and kinetics of tile attachment and detac

63 We combine statistical thermodynamics and kinetics to model Cas9:crRNA complex

64 Screening of the binding thermodynamics and kinetics with a wide range of aptamer

65 The controlling physical properties (thermodynamics and kinetics) are described first, follow

66 catalysts, explanations of their stability (thermodynamics and kinetics) are discussed, challenges f

67 tate explosive reactions are built upon both thermodynamics and kinetics, and then successfully used

68 that will allow manipulation of RNA folding thermodynamics and kinetics.

69 m, C-methylation is the preferred pathway of thermodynamics and kinetics.

70 ssible in this hemilabile system and map the thermodynamics and mechanism of the transition.

71 Determining the structures, kinetics, thermodynamics and mechanisms that underlie conformation

72 plays a great role in redefining the plasma thermodynamics and molecular formation.

73 we systematically compare the hybridization thermodynamics and protein accessibility of several DNA

74 er estimators break down, including the full thermodynamics and rare-event kinetics from high-dimensi

75 The thermodynamics and reaction pathway of sulfur cathode in

76 The Li-binding thermodynamics and redox potentials of seven different q

77 st, at small to moderate surface areas, bulk thermodynamics and the energetics of the aqueous phase d

78 hysicochemical mechanics reduces to standard thermodynamics and the Gibbs-Duhem relation, and we show

79 band structure, electronic nature of charge, thermodynamics and the limit of phonon scattering throug

80 veal additional structural parallels between thermodynamics and the theory of entanglement.

81 s a pivotal role in determining the reaction thermodynamics and thereby catalytic mechanism and activ

82 e dye molecular structure on the interaction thermodynamics and therefore on the nanoparticle structu

83 d mechano-enyzmatic couplings, but interface thermodynamics and thermodynamic transitions are the ori

84 discussion on the fundamental assumptions in thermodynamics and to engage in research activities earl

85 bents and their use as separating agents via thermodynamics and/or kinetics and molecular sieving.

86 , terahertz spectroscopy, mass spectroscopy, thermodynamics, and computer simulations to reveal how w

87 Therefore, the structures, thermodynamics, and kinetics of dienamine intermediates

88 a direct connection between protein cost and thermodynamics, and provides a physically plausible and

89 complicated physics, unintuitive stochastic thermodynamics, and the existence of alternative theorie

90 al metamaterials, designed by transformation thermodynamics are artificial structures that can active

91 of RSSH to peroxyl radicals, where favorable thermodynamics are bolstered by a secondary orbital inte

92 gned thermal metamaterials by transformation thermodynamics are disassembled as unit-cells thermal sh

93 gs, and developments in the field of quantum thermodynamics are making measurements of transport stat

94 utational tools for evaluating water-centric thermodynamics are reviewed.

95 nd we show that the First and Second Laws of thermodynamics are satisfied for our system plus bath mo

96 efinition of thermal operations, the laws of thermodynamics are unified in this framework, with the f

97 Basic principles of kinetics and thermodynamics are used to address problems of initiatio

98 vior is in apparent contradiction with basic thermodynamics, as usually the higher the pH the more ca

99 rmation about their structure, kinetics, and thermodynamics at atomic resolution.

100 istic assessment of the complex kinetics and thermodynamics at play.

101 ows the study of redox reaction kinetics and thermodynamics at single molecular level using DNA as a

102 provide a route to studying non-equilibrium thermodynamics at the atomic level.

103 ping to drive the development of theories of thermodynamics at the microscopic scale.

104 Here, we extend a thermodynamics-based model of gene expression, called GE

105 While in line with previous thermodynamics-based models of a general RNA folding mec

106 ng approach to this problem is that taken by thermodynamics-based models that interpret an enhancer s

107 rticles, signals a breakdown of conventional thermodynamics because MBL systems do not thermalize and

108 To investigate the underlying thermodynamics, binding constants were determined at 25.

109 Our results demonstrate how information thermodynamics can be used to improve functionality of m

110 of phase-separation effects into activation thermodynamics can lead to a CCN number concentration th

111 results indicate that kinetics, and not just thermodynamics, can significantly alter the efficiency o

112 quantifying the relative importance of ocean thermodynamics, circulation and biogeochemistry in a glo

113 The equilibrium constant of a reaction with thermodynamics closely approximating that of a desired m

114 e surprising that the laws of nonequilibrium thermodynamics, combined with Maxwell's equations, sugge

115 ss can be understood in terms of equilibrium thermodynamics considerations.

116 Simultaneously, thermodynamics control the formation of either a keto or

117 These correlations imply that thermodynamics controlled goethite and hematite reductio

118 Nonequilibrium thermodynamics describes the rates of transport phenomen

119 gical review and perspective, we discuss how thermodynamics determines both the overall potential of

120 Variance in tissue thermodynamics during cryothermal ablation depends on th

121 article, we have also analyzed kinetics and thermodynamics during dual exchange process, showing our

122 mperature dependence of binding kinetics and thermodynamics (e.g., melt/denaturation profile) in a si

123 nding the entanglement evolution unveils how thermodynamics emerges in isolated systems.

124 re and interfacial interactions to petroleum thermodynamics, enabling a first-principles approach to

125 es can be determined by stoichiometry and/or thermodynamics, especially in the presence of a base.

126 A wide variety of kinetic and thermodynamics experiments, ranging from single-molecule

127 Stochastic thermodynamics extends classical thermodynamics to small

128 environments it has been shown that classic thermodynamics favour the production of CO2 from CH4, wh

129 The thermodynamics for adding and removing HCN from pI under

130 m and the Demon, including the second law of thermodynamics for bare and coarse grained entropy produ

131 Calorimetric assessment of binding thermodynamics for hemagglutinin 306-319 peptide variant

132 the mechanism for catalysis by altering the thermodynamics for hydride transfer to CO2 from a key di

133 This equality expresses the second law of thermodynamics for isothermal processes arbitrarily far

134 plify the prediction of folding kinetics and thermodynamics for structured RNAs from their parts.

135 However, the thermodynamics governing the molecular recognition and i

136 fully reversible and strictly adheres to the thermodynamics governing the reactions.

137 The laws of thermodynamics governing the trickle-charge and rapid di

138 Computational analysis of H2 activation thermodynamics guided rational catalyst development.

139 Thermodynamics-guided probe design and empirical optimiz

140 The use of ligand binding thermodynamics has been proposed as a potential success

141 nger on what is genuinely quantum in quantum thermodynamics has remained a challenge.

142 erefore rarely applied, because kinetics and thermodynamics hinder the process.

143 ally advanced our understanding of nanoscale thermodynamics, however putting a finger on what is genu

144 its that change capsid assembly kinetics and thermodynamics in a predictable manner.

145 scuss the manifestation of the second law of thermodynamics in quantum physics and uncover special si

146 -well system, thus exploring its finite-time thermodynamics in relation to the settlement of nonclass

147 Kinetics and thermodynamics in supramolecular systems are intimately

148 exchange mechanism is believed to affect the thermodynamics in the formation of binary systems compos

149 Thermodynamics in the left atrium-pulmonary vein (PV) ju

150 Is there a second law of thermodynamics in this regime?

151 veloped fundamental limitations on nanoscale thermodynamics, in terms of a set of independent free en

152 Thermodynamics is a highly successful macroscopic theory

153 The gate structure and thermodynamics is a result of the self-assembly of the s

154 Since relativistic thermodynamics is a topic that can be treated as part of

155 DNA hybridization thermodynamics is critical for accurate design of oligon

156 Thermodynamics is the phenomenological theory of heat an

157 The second law of thermodynamics is well known for determining the directi

158 n PTP, and given the basis of this method in thermodynamics, it is expected to be generally useful in

159 new insights into the statistical nature of thermodynamics, kinetics and function from different lig

160 Markov state models (MSMs) to report on the thermodynamics, kinetics, and accessible states of BTK's

161 Similarly, in thermodynamics Kirchhoff's law dictates that the absorpt

162 In apparent contradiction to the laws of thermodynamics, Maxwell's demon is able to cyclically ex

163 Here, we propose a statistical thermodynamics model of gene expression using DNA shape

164 s calculations combined with the statistical thermodynamics modelling predict that the adsorption den

165 tailed account of the steady-state kinetics, thermodynamics, molecular modeling, and cell biology stu

166 We then used a thermodynamics-motivated analysis of secreted protein le

167 e colloids is a signature of the first-order thermodynamics nature of this phase transition.

168 yet been quantified, in terms of kinetics or thermodynamics, nor has the underlying molecular mechani

169 This value is compared to the thermodynamics of a hydrogen bond determined by similar

170 e energy landscape and the folding/unfolding thermodynamics of a hyperstable RNA tetraloop obtained t

171 relationships, enzyme kinetics, and binding thermodynamics of a novel series of 2-thiohydantoin and

172 We carry out a detailed investigation of the thermodynamics of a series of isochoric, diffusionless s

173 ntific studies on artwork, we study here the thermodynamics of a thermometer made of zisha ceramic, r

174 Regression analysis indicates that the thermodynamics of addition of methane to trans-(PH3)2IrX

175 e accurate determination of the kinetics and thermodynamics of adsorption.

176 y has the potential to directly quantify the thermodynamics of allosteric interactions, but usually f

177 for the majority of the inherent unfavorable thermodynamics of aoQM formation.

178 Here, we investigate in detail the thermodynamics of assembly of diphenylalanine (FF).

179 the finding that through tuning of both the thermodynamics of binding/activation and the degree of p

180 that allows us to quantitatively assess the thermodynamics of biomolecular recognition between a hum

181 Even less is known about the thermodynamics of biomolecule-solvent interactions and h

182 This study reports the thermodynamics of bound species derived from ethene, pro

183 A study of electronic factors governing the thermodynamics of C-H and N-H bond addition to Ir(I) com

184 probe is an effective tool for exploring the thermodynamics of cancer cell migration and invasion.

185 determining the intrinsic directionality and thermodynamics of chemo-mechanical coupling than are the

186 re of a minor conformation, the kinetics and thermodynamics of conformational exchange, and the effec

187 The kinetics and thermodynamics of copper binding to SliLPMO10E-Ext are i

188 The binding kinetics and thermodynamics of dipeptidyl peptidase (DPP)-4 inhibitor

189 facilitated by computationally encoding the thermodynamics of DNA hybridization for automated design

190 We investigate the kinetics and thermodynamics of DNA origami dimerization using flat re

191 We experimentally assessed the kinetics and thermodynamics of electron transfer (ET) from the donor

192 n exceptionally large effect on the rate and thermodynamics of electron transfer.

193 We find that the thermodynamics of FF assembly displays the typical chara

194 Exploiting the favorable thermodynamics of gammaPNA-gammaPNA interactions, the an

195 perimental model system, we investigated the thermodynamics of genome release associated with destabi

196 Thermodynamics of H2 O2 binding and decay kinetics of th

197 iterature, and quantum chemically calculated thermodynamics of hard-hard, hard-soft, and soft-soft ad

198 velop a FRET-based methodology to assess the thermodynamics of hetero-interactions in the plasma memb

199 This result contrasts the partitioning thermodynamics of highly and moderately hydrophobic chem

200 Benefiting from the more favorable thermodynamics of HMF oxidation than that of OER, the ce

201 This is achieved by evaluating the thermodynamics of hybridization for full-length oligonuc

202 y of our approach by examining the hydration thermodynamics of hydrophobic and ionic solutes and the

203 general framework to relate the equilibrium thermodynamics of ice binding to a surface and the noneq

204 native mass spectrometry (MS), to determine thermodynamics of individual ligand binding events to pr

205 We also determined for the first time the thermodynamics of individual lipid binding to the ammoni

206 In this letter we study thermodynamics of information using an experimentally fe

207 employ a theoretical model for the shape and thermodynamics of intrinsically helical filaments bound

208 termolecular forces, and consequently on the thermodynamics of materials defined by this elusive bond

209 n-alpha3 alters the interaction kinetics and thermodynamics of mDiaN with RhoA.GTP and DAD.

210 Thermodynamics of milk components (milk fat, xanthine ox

211 progress has been a solid foundation in the thermodynamics of molecular systems.

212 It has long been recognized that the thermodynamics of mRNA-tRNA base pairing is insufficient

213 Here, we characterized the kinetics and thermodynamics of mtSSB binding to ssDNA by equilibrium

214 ensitive technique for probing structure and thermodynamics of multivalent protein-ligand interaction

215 elucidate the electronic structure and redox thermodynamics of Ni-only and mixed NiFe oxyhydroxide th

216 expected to contribute significantly to the thermodynamics of protein dissociation.

217 energy perturbation methodology to model the thermodynamics of protein mutation for two specific prob

218 water within a binding pocket can alter the thermodynamics of protein-ligand association.

219 rface of a protein is thought to mediate the thermodynamics of protein-ligand interactions.

220 The thermodynamics of QD/SMM interaction and antigen/QDSM in

221 has been much progress in understanding the thermodynamics of quantum systems, even for small indivi

222 ned alpha3FnY DeltaE degrees 's to model the thermodynamics of radical-transfer reactions in FnY-RNRs

223 n make use of well-established models of the thermodynamics of RNA structures formation, RNA-RNA inte

224 with design approaches based on equilibrium thermodynamics of RNA structures.

225 ch range from the fundamental aspects of the thermodynamics of self-assembly through to the developme

226 Here, we determined the kinetics and thermodynamics of single-stranded break ligation by LIG3

227 Here, we scrutinized the kinetics and thermodynamics of small homomeric Lewis X-Lewis X ensemb

228 ing a sound and general understanding of the thermodynamics of such non-equilibrium scenarios could u

229 The thermodynamics of switching and performance of the devic

230 However, the kinetics and thermodynamics of the binding to many sensor surfaces ha

231 sothermal titration calorimetry provided the thermodynamics of the binding.

232 l speciation depends only on the equilibrium thermodynamics of the chemical system.

233 The kinetics and thermodynamics of the encapsulation of benzene, cyclohex

234 tron transfer from CdSe-->CaI and activation thermodynamics of the initial step of proton reduction i

235 Here, we show how the thermodynamics of the interaction control the shape of t

236 The thermodynamics of the interaction of the food colourant

237 d average local ionization energies (ALIEs), thermodynamics of the products, and the transition-state

238 trostatics was used to calculate the coupled thermodynamics of the protonation of the extracellular-f

239 The cation effect on the thermodynamics of the reaction is more complex and is co

240 he anion seems to play a primary role in the thermodynamics of the reaction that is endothermic and e

241 d the Al(OtBu)3 additive on the kinetics and thermodynamics of the reaction.

242 The bonding in 25 and the mechanism and thermodynamics of the reactions have been studied using

243 chemistry allows for delicate control of the thermodynamics of the self-assembly process, which enabl

244 ssed offering insights into the kinetics and thermodynamics of the switching process.

245 The locations and thermodynamics of the waters are derived from a WaterMap

246 lations and free energy methods to study the thermodynamics of their interaction with membranes in th

247 ifying mutations in NTIMP1 and NTIMP2 on the thermodynamics of their interactions with MMP1, MMP3, an

248 this model by investigating the dynamics and thermodynamics of this membrane anchor on a POPC bilayer

249 Structural effects on the thermodynamics of this reaction are assessed.

250 sent a detailed analysis of the kinetics and thermodynamics of this reaction, also known as the "rege

251 Simultaneous control of the kinetics and thermodynamics of two different types of covalent chemis

252 and periodic DFT calculations to analyze the thermodynamics of two families of topologically distinct

253 hniques to investigate the folding/unfolding thermodynamics of two three-way junctions with a closed

254 nt a detailed analysis of the energetics and thermodynamics of vesiculation by recourse to nonlinear

255 d using a combination of circular dichroism, thermodynamics, optical tweezers and calorimetry techniq

256 part of an undergraduate course of classical thermodynamics or modern physics, the review and our own

257 nt methods might not adequately estimate the thermodynamics, or that other cellular processes (e.g.,

258 ing the Lewis acid-base reaction concept and thermodynamics perspective and highlight the relevant ch

259 Here we design new fluxing agents, from a thermodynamics perspective that takes into account combi

260 The second law of thermodynamics places constraints on state transformatio

261 Thermodynamics plays an important role in governing thes

262 With thermodynamics predating quantum theory, research now ai

263 =Cl and I showed that in the case of iodide, thermodynamics prevents the production of benzene and fa

264 Here, using heat transfer and thermodynamics principles, we show how Bui et al's concl

265 studies linking oxide reduction kinetics to thermodynamics remain scarce.

266 Medicinal targeting of heterodimer thermodynamics represents a plausible strategy for prolo

267 Probing their thermodynamics represents challenge because of lack of a

268 The change in clamp thermodynamics requires distant alpha-clamp and varphi-c

269 Thermodynamics reveals that the low temperature of the s

270 The value of thoroughly understanding the thermodynamics specific to a drug discovery/design study

271 further exploited for analytical purposes or thermodynamics studies.

272 demonstrated by fluorescence, absorption and thermodynamics study.

273 eta homology model using prediction of water thermodynamics suggested an optimization strategy for th

274 mation of Z-dienamines and their unfavorable thermodynamics support high ee values.

275 sopentenyl pyrophosphate with more favorable thermodynamics than the native pathway.

276 Passivity is a fundamental concept in thermodynamics that demands a quantum system's energy ca

277 Within the framework of linear irreversible thermodynamics, the maximum-power efficiency is obtained

278 he most accepted version of the third law of thermodynamics, the unattainability principle, states th

279 The construction of a relativistic thermodynamics theory is still controversial after more

280 that we have derived by assuming the laws of Thermodynamics to be covariant.

281 spectroscopy, site-directed mutagenesis, and thermodynamics to elucidate the mechanisms of eIF2B acti

282 Stochastic thermodynamics extends classical thermodynamics to small systems in contact with one or m

283 ene Expression Modeling Based on Statistical Thermodynamics), to incorporate chromatin accessibility

284 conformational fluctuations and equilibrium thermodynamics underlying these processes.

285 Far-from-equilibrium thermodynamics underpins the emergence of life, but how

286 ate and a thermally excited state with their thermodynamics using the variant 118R1 of T4 lysozyme as

287 Using first-principles thermodynamics we examined the theoretical stability of

288 antagonists in terms of binding affinity and thermodynamics, we demonstrate that depending on the Fim

289 blems, and using the formalism of stochastic thermodynamics, we derive a set of design principles for

290 elations extend to nucleic acid kinetics and thermodynamics, we followed the folding of P4-P6, a doma

291 of enzymes and the backward flux dictated by thermodynamics, we further refine the correspondence bet

292 Guided by thermodynamics, we have synthesized two mixed-linker zir

293 the theoretical framework of nonequilibrium thermodynamics, we present a widely applicable mechanism

294 In the framework of quantum thermodynamics, we propose a method to quantitatively de

295 we are seeing that one can formulate laws of thermodynamics when only a small number of particles are

296 ides an integral framework for linking ocean thermodynamics with biogeochemistry.

297 lution of the Maxwell's demon paradox linked thermodynamics with information theory through informati

298 nlightening illustration of the interplay of thermodynamics with quantum information.

299 review of the main theories of relativistic thermodynamics, with an special emphasis on the physical

300 In the standard framework of thermodynamics, work is a random variable whose average