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Results: 6,071
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  • van Deun, K., Smilde, A. K., Thorrez, L., Kiers, H. A. L., & van Mechelen, I. (2013). Identifying common and distinctive processes underlying multiset data. Chemometrics and Intelligent Laboratory Systems, 129, 40-51. https://doi.org/10.1016/j.chemolab.2013.07.005
  • Kouril, T., Esser, D., Kort, J., Westerhoff, H. V., Siebers, B., & Snoep, J. L. (2013). Intermediate instability at high temperature leads to low pathway efficiency for an in vitro reconstituted system of gluconeogenesis in Sulfolobus solfataricus. The FEBS Journal, 280(18), 4666-4680. https://doi.org/10.1111/febs.12438
  • Mensonides, F. I., Bakker, B. M., Cremazy, F., Messiha, H. L., Mendes, P., Boogerd, F. C., & Westerhoff, H. V. (2013). A new regulatory principle for in vivo biochemistry: pleiotropic low affinity regulation by the adenine nucleotides--illustrated for the glycolytic enzymes of Saccharomyces cerevisiae. FEBS Letters, 587(17), 2860-2867. https://doi.org/10.1016/j.febslet.2013.07.013
  • Smallbone, K., Messiha, H. L., Carroll, K. M., Winder, C. L., Malys, N., Dunn, W. B., Murabito, E., Swainston, N., Dada, J. O., Khan, F., Pir, P., Simeonidis, E., Spasić, I., Wishart, J., Weichart, D., Hayes, N. W., Jameson, D., Broomhead, D. S., Oliver, S. G., ... Mendes, P. (2013). A model of yeast glycolysis based on a consistent kinetic characterisation of all its enzymes. FEBS Letters, 587(17), 2832-2841. https://doi.org/10.1016/j.febslet.2013.06.043
  • Geenen, S., du Preez, F. B., Snoep, J. L., Foster, A. J., Sarda, S., Kenna, J. G., Wilson, I. D., & Westerhoff, H. V. (2013). Glutathione metabolism modeling: a mechanism for liver drug-robustness and a new biomarker strategy. Biochimica et Biophysica Acta G General Subjects, 1830(10), 4943-59. https://doi.org/10.1016/j.bbagen.2013.04.014
  • Kolodkin, A., Sahin, N., Phillips, A., Hood, S. R., Bruggeman, F. J., Westerhoff, H. V., & Plant, N. (2013). Optimization of stress response through the nuclear receptor-mediated cortisol signalling network. Nature Communications, 4, 1792. https://doi.org/10.1038/ncomms2799
  • Thiele, I., Swainston, N., Fleming, R. M. T., Hoppe, A., Sahoo, S., Aurich, M. K., Haraldsdottir, H., Mo, M. L., Rolfsson, O., Stobbe, M. D., Thorleifsson, S. G., Agren, R., Bölling, C., Bordel, S., Chavali, A. K., Dobson, P., Dunn, W. B., Endler, L., Hala, D., ... Palsson, B. Ø. (2013). A community-driven global reconstruction of human metabolism. Nature Biotechnology, 31(5), 419-25. https://doi.org/10.1038/nbt.2488
  • Feldman-Salit, A., Hering, S., Messiha, H. L., Veith, N., Cojocaru, V., Sieg, A., Westerhoff, H. V., Kreikemeyer, B., Wade, R. C., & Fiedler, T. (2013). Regulation of the activity of lactate dehydrogenases from four lactic acid bacteria. The Journal of Biological Chemistry, 288(29), 21295-21306. https://doi.org/10.1074/jbc.M113.458265
  • van Zanten, M., Tessadori, F., Peeters, A. J. M., & Fransz, P. (2013). Environment-Induced Chromatin Reorganisation and Plant Acclimation. In G. Grafi, & N. Ohad (Eds.), Epigenetic Memory and Control in Plants (pp. 21-40). (Signaling and Communication in Plants; Vol. 18). Springer. https://doi.org/10.1007/978-3-642-35227-0_2
  • McLoughlin, F., Arisz, S. A., Dekker, H. L., Kramer, G., de Koster, C. G., Haring, M. A., Munnik, T., & Testerink, C. (2013). Identification of novel candidate phosphatidic acid-binding proteins involved in the salt-stress response of Arabidopsis thaliana roots. Biochemical Journal, 450(3), 573-581. https://doi.org/10.1042/BJ20121639
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