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  1. 1.   Antineoplastic agents. 445. Synthesis and evaluation of structural modifications of (Z)- and (E)-combretastatin A-4
  2. Pettit, G. R.; Rhodes, M. R.; Herald, D. L.; Hamel, E.; Schmidt, J. M.; Pettitt, R. K.
  3. Journal of Medicinal Chemistry. 2005, JUN 16; 48(12): 4087-4099.
  1. 2.   Anthocyanidins inhibit activator protein 1 activity and cell transformation: structure-activity relationship and molecular mechanisms
  2. Hou, D. X.; Kai, K.; Li, J. J.; Lin, S. G.; Terahara, N.; Wakamatsu, M.; Fujii, M.; Young, M. R.; Colburn, N.
  3. Carcinogenesis. 2004 25(1): 29-36.
  1. 3.   Interaction of novel thiocolchicine analogs with the tubulin isoforms from bovine brain
  2. Banerjee, A.; Kasmala, L. T.; Hamel, E.; Sun, L.; Lee, K. H.
  3. Biochemical and Biophysical Research Communications. 1999 254(2): 334-337.
  1. 4.   Biosynthesis of radiolabeled curacin A and its rapid and apparently irreversible binding to the colchicine site of tubulin
  2. Verdier-Pinard, P.; Sitachitta, N.; Rossi, J. V.; Sackett, D. L.; Gerwick, W. H.; Hamel, E.
  3. Archives of Biochemistry and Biophysics. 1999 370(1): 51-58.
  1. 5.   Structure-Activity Analysis of the Interaction of Curacin a, the Potent Colchicine Site Antimitotic Agent, With Tubulin and Effects of Analogs On the Growth of Mcf-7 Breast Cancer Cells
  2. Verdier-Pinard, P.; Lai, J. Y.; Yoo, H. D.; Yu, J. R.; Marquez, B.; Nagle, D. G.; Nambu, M.; White, J. D.; Falck, J. R.; Gerwick, W. H.; Day, B. W.; Hamel, E.
  3. Molecular Pharmacology. 1998 53(1): 62-76.
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