Thermodynamic constraints for biochemical networks
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Publication:2187646
Recommendations
- Stoichiometric and constraint-based analysis of biochemical reaction networks
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- Flux balance analysis: a geometric perspective
- A new constraint-based description of the steady-state flux cone of metabolic networks
- Generic flux coupling analysis
Cites work
Cited in
(21)- Some consequences of thermodynamic feasibility for chemical reaction networks. Considering thermodynamic feasibility in current CRN research
- Integrated stoichiometric, thermodynamic and kinetic modelling of steady state metabolism
- Quantitative flux coupling analysis
- A Graphic Formulation of Nonisothermal Chemical Reaction Systems and the Analysis of Detailed Balanced Networks
- Determination of flux directions by thermodynamic network analysis: Computing informative metabolite pools
- Conditions for duality between fluxes and concentrations in biochemical networks
- Generic flux coupling analysis
- Precision and sensitivity in detailed-balance reaction networks
- Metabolic pathway analysis using a Nash equilibrium approach
- Energy-based analysis of biomolecular pathways
- Metabolic impact assessment for heterologous protein production in \textit{Streptomyces lividans} based on genome-scale metabolic network modeling
- Flux balance analysis: a geometric perspective
- Bond graph modelling of the cardiac action potential: implications for drift and non-unique steady states
- Flux modules in metabolic networks
- Optimizing enzymatic catalysts for rapid turnover of substrates with low enzyme sequestration
- Programming substrate-independent kinetic barriers with thermodynamic binding networks
- Capturing the essence of a metabolic network: a flux balance analysis approach
- Stoichiometric and constraint-based analysis of biochemical reaction networks
- Enzyme allocation problems in kinetic metabolic networks: optimal solutions are elementary flux modes
- Network thermodynamics of biological systems: a bond graph approach
- A variational principle for computing nonequilibrium fluxes and potentials in genome-scale biochemical networks
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