David C. ClarkeEducationPh.D. Chemical Engineering. University of Colorado at Boulder (2008) M.Sc. Kinesiology. University of Waterloo, Waterloo, ON, Canada (2002) B.Sc. (Honours) Kinesiology. Laurentian University, Sudbury, ON, Canada (2000) Research InterestsI am interested in studying mammalian cell signal transduction using quantitative approaches. Within this theme, my postdoctoral research involves the following projects: 1) constrained fuzzy logic modeling of hepatocellular carcinoma cell signaling, 2) mixed modeling techniques for statistical analysis of multiplexed cell signaling data and 3) investigating biological and statistical reasons underlying a paradox of systems biology in which everything seems to regulate everything. PublicationsPeer-reviewed Publications Clarke, D. C. and Liu, X. (2008). Decoding the quantitative nature of Transforming Growth Factor-β signaling. Trends in Cell Biology. 18(9): 430-42. Zhu, S., Wang, W., Clarke, D. C., Liu, X. (2007). Activation of Mps1 promotes Transforming Growth Factor-β-independent Smad signaling. Journal of Biological Chemistry. 282(25): 18327-18338. Clarke, D. C., Betterton, M. D., Liu, X. (2006). Systems theory of Smad signaling. Systems Biology (Stevenage). 153(6): 412-424. Clarke, D. C., Miskovic, D., Han, X.-X., Calles-Escandon, J., Glatz, J. F. C., Luiken, J. J. F. P., Heikkila, J. J., Bonen, A. (2004). Overexpression of membrane-associated fatty acid binding protein (FABPpm) in vivo increases fatty acid sarcolemmal transport and metabolism. Physiological Genomics. 17: 31-37. Book Chapters Lay Publications |