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  1. 1.   Engineering of glycerol dehydrogenase for improved activity towards 1, 3-butanediol
  2. Zhang, H. F.; Lountos, G. T.; Ching, C. B.; Jiang, R. R.
  3. Applied Microbiology and Biotechnology. 2010, Sep; 88(1): 117-124.
  1. 2.   PharmaGist: a webserver for ligand-based pharmacophore detection
  2. Schneidman-Duhovny, D.; Dror, O.; Inbar, Y.; Nussinov, R.; Wolfson, H. J.
  3. Nucleic Acids Research. 2008 36: W223-W228.
  1. 3.   Synthesis and applications of novel bis(ammonium) chiral ionic liquids derived from isomannide
  2. Kumar, V.; Olsen, C. E.; Schaffer, S. J. C.; Parmar, V. S.; Malhotra, S. V.
  3. Organic Letters. 2007, Sep; 9(20): 3905-3908.
  1. 4.   Synthesis of bicyclo 3.1.0 hexanes functionalized at the tip of the cyclopropane ring. Application to the synthesis of carbocyclic nucleosides
  2. Comin, M. J.; Parrish, D. A.; Deschamps, J. R.; Marquez, V. E.
  3. Organic Letters. 2006, Feb; 8(4): 705-708.
  1. 5.   (salen)Mn-III compounds as nonpeptidyl mimics of catalase. Mechanism-based tuning of catalase activity: A theoretical study
  2. Abashkin, Y. G.; Burt, S. K.
  3. Inorganic Chemistry. 2005, MAR 7; 44(5): 1425-1432.
  1. 7.   Enantioselective synthesis of metathesis-derived ureapeptoid macrocycles
  2. Wang, X. Z.; Burke, T. R.
  3. Synlett. 2004 (3): 469-472.
  1. 8.   Macrocyclization in the design of Grb2 SH2 domain-binding ligands exhibiting high potency in whole-cell systems
  2. Wei, C. Q.; Gao, Y.; Lee, K.; Guo, R.; Li, B. H.; Zhang, M. C.; Yang, D. J.; Burke, T. R.
  3. Journal of Medicinal Chemistry. 2003 46(2): 244-254.
  1. 9.   Synthesis and investigation of conformationally restricted analogues of lavendustin A as cytotoxic inhibitors of tubulin polymerization
  2. Mu, F. R.; Lee, D. J.; Pryor, D. E.; Hamel, E.; Cushman, M.
  3. Journal of Medicinal Chemistry. 2002 45(21): 4774-4785.
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