In this paper we study the mathematical model of the Goldbeter--Koshland switch, or futile cycle, which is a mechanism that describes several chemical reactions, in particular the so-called phosphorylation-dephosphorylation cycle. We determine the appropriate perturbation parameter epsilon (related to the kinetic constants and initial conditions of the model) for the application of singular perturbation techniques. We also determine the inner and outer solutions and the corresponding uniform expansions, up to the first order in epsilon , beyond the total quasi-steady state approximation (tQSSA). These expansions, in particular the inner ones, can be useful for the estimation of the kinetic parameters of the reaction by means of the ...
The quasi-steady-state approximation (QSSA) is a model reduction technique used to remove highly rea...
In this paper we find a new asymptotic expansion valid in enzymatic reactions where the total amount...
In this paper we expand the equations governing Michaelis-Menten kinetics in a total quasi-steady st...
In this paper we study the mathematical model of the Goldbeter-Koshland switch, or futile cycle, whi...
We show some recent results related to the application of singular perturbation techniques in the fr...
The complex intracellular signal transduction networks can be decomposed into simpler moduli, where ...
In this paper we study the model of the chemical reaction of fully competitive inhibition and determ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Deterministic models of enzymatic reactions based on the quasi-steady state assumption (QSSA) and to...
The Michaelis-Menten-Briggs-Haldane approximation and its extension, the total quasi-steady-state ap...
The transient kinetic behaviour of an open single enzyme, single substrate reaction is examined. The...
The paper outlines a general approach to deriving quasi-steady-state approximations (QSSAs) of the s...
AbstractWe study the two-dimensional reduction of the Michaelis–Menten reaction of enzyme kinetics. ...
The quasi-steady-state approximation (QSSA) is a model reduction technique used to remove highly rea...
In this paper we find a new asymptotic expansion valid in enzymatic reactions where the total amount...
In this paper we expand the equations governing Michaelis-Menten kinetics in a total quasi-steady st...
In this paper we study the mathematical model of the Goldbeter-Koshland switch, or futile cycle, whi...
We show some recent results related to the application of singular perturbation techniques in the fr...
The complex intracellular signal transduction networks can be decomposed into simpler moduli, where ...
In this paper we study the model of the chemical reaction of fully competitive inhibition and determ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Biochemistry in general and enzyme kinetics in particular have been heavily influenced by the model ...
Deterministic models of enzymatic reactions based on the quasi-steady state assumption (QSSA) and to...
The Michaelis-Menten-Briggs-Haldane approximation and its extension, the total quasi-steady-state ap...
The transient kinetic behaviour of an open single enzyme, single substrate reaction is examined. The...
The paper outlines a general approach to deriving quasi-steady-state approximations (QSSAs) of the s...
AbstractWe study the two-dimensional reduction of the Michaelis–Menten reaction of enzyme kinetics. ...
The quasi-steady-state approximation (QSSA) is a model reduction technique used to remove highly rea...
In this paper we find a new asymptotic expansion valid in enzymatic reactions where the total amount...
In this paper we expand the equations governing Michaelis-Menten kinetics in a total quasi-steady st...