ライフサイエンスコーパス: rate equation

1 uter simulation of the complete steady state rate equation.

2 ate curves could be fitted to a second order rate equation.

3 responses are determined by a dynamic firing-rate equation.

4 the integrated form of the Michaelis-Menten rate equation.

5 sis sample using a zero-intercept, K/V-based rate equation.

6 tinine based estimated glomerular filtration rate equations.

7 is evaluated by a numerical solution of the rate equations.

8 tants, and (2) on the classical steady state rate equations.

9 r regression with numeric integration of the rate equations.

10 tected using estimated glomerular filtration rate equations.

11 that combines material balances and kinetic rate equations.

12 he excitonic reservoir described by a set of rate equations.

13 ons which is not captured by standard firing rate equations.

14 rk of the Deltag-based excitonic model using rate equations.

15 he pseudo-first-order or pseudo-second-order rate equations.

16 ically alter the reaction's Michaelis-Menten rate equations.

17 data were analyzed using the complete set of rate equations.

18 phase-phase (log-log) representations of the rate equations.

19 required to achieve analytical solutions of rate equations.

20 is method can also be used with steady-state rate equations.

21 eterminant of the Jacobian of the underlying rate equations, (2) minimization of the objective functi

22 which can be described by single-exponential rate equations, A(t) = A(o)(1- e (-kt)) and A(t) = A(o)e

23 for experimental verification and for use in rate equations accounting for nucleation-mediated fibril

24 servations with existing established kinetic rate equations allows the prediction of nanoparticle dis

25 synthesis are determined, and the resulting rate equation, along with a stereochemical analysis of t

26 elaxation dynamics to the underlying coupled rate equation and revealing that trap-state Auger recomb

27 nts (SmI2, amine, water) are involved in the rate equation and that the rate of electron transfer is

28 regression of the analytic integrals of the rate equations and by nonlinear regression with numeric

29 Fe, and Ru catalysts, which show similar FTS rate equations and cluster size effects.

30 Rate equations and elementary steps were similar for deh

31 The retrieved rate equations and parameters can be used for scanning p

32 ted by numerically integrating the nonlinear rate equations and performing linear stability analysis,

33 rate behavior, from those mechanisms derived rate equations, and then tested the mechanisms against o

34 t, and thermal effects using a comprehensive rate equation approach and a temperature-dependent pulse

35 The rate equation approach and temperature-dependent pulsed-

36 ay/atom interactions using a straightforward rate equation approach augurs favourably for extension t

37 erforms both a classical Kalman filter and a rate equation approach when applied to patch-clamp data

38 found that our approach, in contrast to the rate equation approach, yields a realistic uncertainty q

39 time resolution of fluorescence data than a rate equation approach.

40 sets, it identifies more parameters than the rate equation approach.

41 Kinetic glomerular filtration rate equations are not accurate enough for glomerular fi

42 -state model reveals that the classic Huxley rate equation, as modified for thermodynamic self-consis

43 hereas the joint-space method used metabolic rate equations based on joint parameters.

44 article is concerned with rapid-equilibrium rate equations, but this method can also be used with st

45 Then, combining hybridization rate equations, calculated free energies of hybridizatio

46 d from the polyamine spermine, whose complex rate equation can include terms for a variety of medium

47 Our rate equation combines Butler-Volmer (BV) electrode kine

48 kinetic problem and its reduction to simple rate equations; computation of binding rate constants; q

49 ound state is best described by second-order rate equations, consistent with the expectation for comp

50 n and mRNA translation, based on first-order rate equations, coupled with a set of nonlinear equation

51 furcation analysis of deterministic reaction rate equations derived from the model, and find that the

52 homogeneous reconstructing surfaces leads to rate equations described by our nonlinear scaling law.

53 A rate equation describing the cellular starch degradation

54 ity (e.g. a protein or drug) to retrieve the rate equations describing it; the associated parameter v

55 model based on numerical integration of the rate equations describing the reaction mechanism.

56 i levels) by invoking a full solution to the rate equations describing transitions across the band ga

57 All known estimated glomerular filtration rate equations displayed high biases and unacceptable er

58 ce long term rhythms that are independent of rate equations (e.g. Arrhenius).

59 eaction sequence, the numerator terms of the rate equation exert an effect in the paired flux control

60 con will be the most intense: one based on a rate equation for calculating ion flux using values from

61 ailed comparison with the traditionally used rate equation for covalent inhibition is presented.

62 before P(i) and validate utilization of the rate equation for ordered binding to interpret differenc

63 lowing a tractable algebraic solution to the rate equation for substrate hydrolysis.

64 , the corresponding Wilson-Cowan type firing rate equation for such an inhibitory population does not

65 This article describes an integrated rate equation for the time course of covalent enzyme inh

66 tal data, we derive a chemical mechanism and rate equations for a kinetic multilayer model of surface

67 We have derived the rate equations for all likely sequential bireactant mech

68 ped, which enables the generation of generic rate equations for all reactions in a model.

69 r precursor conversion to monomers, discrete rate equations for formation of small-sized clusters, an

70 Using numerical solutions to the rate equations for nucleated polymerization and analytic

71 rations have been used in the formulation of rate equations for simple bimolecular and monomolecular

72 for the giant squid axon, we have determined rate equations for the activation and inactivation prope

73 Complete axial rate equations for the alkenes and alkynes were derived,

74 We solved the rate equations for the cascade numerically and found tha

75 ar strain, and use that in a coarse-graining rate equation formulation for constructing a mechanism m

76 Mechanism-based FTS rate equations give activation energies that reflect the

77 numerical integration of mechanism-specific rate equations has been used to test specific kinetic mo

78 We now integrate the tQSSA rate equation in closed form, without resorting to furth

79 kinetic parameters in the full-ordered bi bi rate equation in the absence of products, with both NADH

80 ow fitting based on numerical integration of rate equations, in the dynamic simulation rate constants

81 e of race in estimated glomerular filtration rate equations, including its relationship with structur

82 rell-Chance" mechanism yields a steady-state rate equation indistinguishable in form from the observe

83 The overall form of the rate equation is unchanged: final rate = k(1f)[Hg][C-H(1

84 An order-of-magnitude fusion rate equation is used to estimate whether the predicted

85 tegration concentrations versus time of such rate equations led to a realistic description of the sys

86 e ring-expansion pathway is described by the rate equation, log(k/s-1) = (12.5 +/- 0.1) - (4.9 +/- 0.

87 An Eley-Rideal mechanism and rate equation may be used to describe the epoxidation ki

88 A three-level rate equation model is proposed to describe the photogen

89 ctivity and excitation measurements, using a rate equation model.

90 Using a rate-equation model for the time-dependent absorbance ch

91 These features can be reproduced by a rate-equation model only if it accounts for both the vib

92 energy was extracted by the phenomenological rate-equation model we developed.

93 LIAD by fitting the experimental data with a rate-equation model, from which we extract a correct pre

94 vant for lasing, we observe breakdown of the rate-equation model, indicating a buildup of a highly co

95 stributions of excited-state carriers with a rate-equation model, we distinguish these two types of i

96 We present a simple rate-equations model, which well reproduces the observed

97 Rate equation modeling confirms that a continuous distri

98 g of Ln(3+) ion combinations by differential rate equation modeling identifies Ho(3+)/Tm(3+) or Tm(3+

99 xperimental and computational analysis shows rate equation models are able to predict compositions fo

100 ferent from the predictions of deterministic rate equation models.

101 Here we investigate the rate equation of redox reactions involving reduction by

102 nological rate constants that enter into the rate equations of conventional chemical kinetics.

103 n approximation scheme for deriving reaction rate equations of genetic regulatory networks.

104 nd sizes of each molecular species, into the rate equations of the model.

105 The theory leads to a generalized Huxley rate equation on the bond-distribution function, n(zeta,

106 Rate equations on fibril disappearance are deduced from

107 Instead of using chemical reaction rate equations or rules-based fragmentation libraries, t

108 chastic differential equation), and reaction rate equation (ordinary differential equation) represent

109 cal kinetic model conformed to the following rate equation over a one hundred-fold range of acrylamid

110 We analyze the rate equation predictions using simple scaling estimates

111 Mathematical modeling, based on biochemical rate equations, provides a rigorous and reliable tool fo

112 bromo-4-fluorobenzene displays the following rate equation: rate = k(obs)[R(3)SiOK](0)[ArylBr](0), wi

113 and a macroscopic description using reaction rate equations (RREs) is no longer accurate.

114 Mathematical properties of the new rate equation show that, for such contaminated materials

115 curately prescribed by the mechanism-derived rate equations, similar in functional form on Ru, Co, an

116 Rate equation slope coefficients for K/V of 0.39 (AV acc

117 ermined by numerical solution of the coupled rate equations that describe this competition to the exp

118 In this study, rate equations that predict the regulatory kinetic behav

119 engineering approach to simplify the overall rate equation, thus allowing the accurate and quantitati

120 A novel rate equation to characterize the dose-response behavior

121 We develop a rate equation to describe the population dynamics within

122 In the absence of a rate equation to explain the allosteric effects in a tet

123 In contrast, fitting the newly derived rate equation to inhibitor dose- response curves can, in

124 the photo-excited carrier dynamics and use a rate equation to relate radiative and non-radiative reco

125 ng with numerical integration of appropriate rate equations to analyze the progress curves, while the

126 py results are combined with mechanism-based rate equations to assess the structure and thermodynamic

127 a mathematical model using force balance and rate equations to describe how motors sliding the highly

128 should not use kinetic glomerular filtration rate equations to estimate glomerular filtration rate in

129 By generalizing nucleation rate equations to include dissolution, we arrive at a mo

130 ach proceeds via numerical solution of model rate equations to yield the time dependence of each micr

131 ent overall diffusion tensors, and a master (rate) equation to describe the transitions between these

132 ns and particle-morphology-dependent kinetic rate equations under full consideration of the aqueous p

133 n be applied to biological networks based on rate equations using a fitness function that quantifies

134 tion model behavior with that predicted by a rate equation version of the same system.

135 The rate equation was nu(N)=k(obs)[Tau](o)[nitrite](o)(2), t

136 Using mean-field rate equations, we show that (i) when [HSPG] is much hig

137 The exchange curve is fit to a rate equation, where the rate constants are proportional

138 s is analyzed by solving a system of coupled rate equations, where exciton recycling mechanisms are i

139 ctromyography data and used muscle metabolic rate equations, whereas the joint-space method used meta

140 nd solving a general linear mixed inhibition rate equation with a global curve fitting program.