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The fluxes through glycolytic enzymes in Saccharomyces cerevisiae are predominantly regulated at posttranscriptional levels

, , , , , , , , , , , and . Proc. Natl. Acad. Sci. U. S. A., (2007)

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The fluxes through glycolytic enzymes in Saccharomyces cerevisiae are predominantly regulated at posttranscriptional levels, , , , , , , , , and 2 other author(s). Proc. Natl. Acad. Sci. U. S. A., (2007)Similar temperature dependencies of glycolytic enzymes: an evolutionary adaptation to temperature dynamics?, , , , , , , and . BMC Syst. Biol., (2012)An in vivo data-driven framework for classification and quantification of enzyme kinetics and determination of apparent thermodynamic data, , , , and . Metab. Eng., (2011)Formate as an auxiliary substrate for glucose-limited cultivation of Penicillium chrysogenum: impact on penicillin G production and biomass yield, , , , and . Appl. Environ. Microbiol., (2007)A method for estimation of elasticities in metabolic networks using steady state and dynamic metabolomics data and linlog kinetics., , , and . BMC Bioinform., (2006)A new framework for the estimation of control parameters in metabolic pathways using lin-log kinetics, , , , and . Eur. J. Biochem., (2004)Escherichia coli responds with a rapid and large change in growth rate upon a shift from glucose-limited to glucose-excess conditions, , and . Metab. Eng., (2011)Degeneration of penicillin production in ethanol-limited chemostat cultivations of Penicillium chrysogenum: A systems biology approach., , , , , , , , , and 2 other author(s). BMC Syst. Biol., (2011)Glucose-methanol co-utilization in Pichia pastoris studied by metabolomics and instationary 13C flux analysis., , , , , , , , and . BMC Syst. Biol., (2013)