Search Results - "Patterson, A.V"

  • Showing 1 - 16 results of 16
Refine Results
  1. 1
  2. 2

    uvrB gene deletion enhances SOS chromotest sensitivity for nitroreductases that preferentially generate the 4-hydroxylamine metabolite of the anti-cancer prodrug CB1954 by Prosser, G.A., Patterson, A.V., Ackerley, D.F.

    Published in Journal of biotechnology (01-10-2010)
    “…CB1954 is an anti-cancer prodrug that can be reduced at either of two nitro groups to form cytotoxic metabolites. We describe here two efficient and previously…”
    Get full text
    Journal Article
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10

    Discovery and evaluation of Escherichia coli nitroreductases that activate the anti-cancer prodrug CB1954 by Prosser, G.A., Copp, J.N., Syddall, S.P., Williams, E.M., Smaill, J.B., Wilson, W.R., Patterson, A.V., Ackerley, D.F.

    Published in Biochemical pharmacology (01-03-2010)
    “…Gene-directed enzyme prodrug therapy (GDEPT) aims to achieve highly selective tumor-cell killing through the use of tumor-tropic gene delivery vectors coupled…”
    Get full text
    Journal Article
  11. 11

    Toward a high-throughput screening platform for directed evolution of enzymes that activate genotoxic prodrugs by Copp, J.N., Williams, E.M., Rich, M.H., Patterson, A.V., Smaill, J.B., Ackerley, D.F.

    Published in Protein engineering, design and selection (01-10-2014)
    “…Engineering of enzymes to more efficiently activate genotoxic prodrugs holds great potential for improving anticancer gene or antibody therapies. We report the…”
    Get full text
    Journal Article
  12. 12

    Targeted mutagenesis of the Vibrio fischeri flavin reductase FRase I to improve activation of the anticancer prodrug CB1954 by Swe, P.M., Copp, J.N., Green, L.K., Guise, C.P., Mowday, A.M., Smaill, J.B., Patterson, A.V., Ackerley, D.F.

    Published in Biochemical pharmacology (15-09-2012)
    “…Phase I/II cancer gene therapy trials of the Escherichia coli nitroreductase NfsB in partnership with the prodrug CB1954…”
    Get full text
    Journal Article
  13. 13
  14. 14
  15. 15

    Cytotoxicity of the bioreductive agent RH1 and its lack of interaction with radiation by Kim, Joo-Young, West, C.M.L., Valentine, H., Ward, T.H., Patterson, A.V., Stratford, I.J., Roberts, S.A., Hendry, J.H.

    Published in Radiotherapy and oncology (01-03-2004)
    “…RH1 is a new bioreductive agent that was developed as a cytotoxic agent with selectivity for tumour cells expressing high levels of the enzyme DT-diaphorase…”
    Get full text
    Journal Article
  16. 16