This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Santini, C., Pellei, M., Gandin, V., Porchia, M., Tisato, F., Marzano, C. (2014) Advances in copper complexes as anticancer agents. Chem Rev 114:815–862.SantiniC.PelleiM.GandinV.PorchiaM.TisatoF.MarzanoC.2014Advances in copper complexes as anticancer agents114815862Search in Google Scholar
Li, D.D., Zhang, N., Dai, L.L., Yang, Z.B, Tao, Z.W. (2016). Synthesis, DNA binding, nuclease activity and cytotoxic studies of a wheel-shaped octanuclear copper(II) complex based on 1,2,4-triazole. Appl Organometal Chem 30:346–353.LiD.D.ZhangN.DaiL.L.YangZ.B.TaoZ.W.2016Synthesis, DNA binding, nuclease activity and cytotoxic studies of a wheel-shaped octanuclear copper(II) complex based on 1,2,4-triazole30346353Search in Google Scholar
Qi, J.X., Liang, S.C., Gou, Y.,, Zhang Z.L., Zhou, Z.P., Yang, F., Liang, H. (2015) Synthesis of four binuclear copper(II) complexes: structure, anticancer properties and anticancer mechanism. Eur J Med Chem 96:360–368.QiJ.X.LiangS.C.GouY.ZhangZ.L.ZhouZ.P.YangF.LiangH.2015Synthesis of four binuclear copper(II) complexes: structure, anticancer properties and anticancer mechanism96360368Search in Google Scholar
Denoyer D, Masaldan S, La Fontaine S, Cater M.A (2015). Targeting copper in cancer therapy: ‘copper that cancer’. Metallomics 7:1459–1476.DenoyerDMasaldanSLa FontaineSCaterM.A2015Targeting copper in cancer therapy: ‘copper that cancer’714591476Search in Google Scholar
Lintnerová L, Valentová J, Herich P, Kožíšek J, Devínsky F (2018). Synthesis and antiradical activity of novel copper(II) complexes of long chain reduced Schiff base ligands. Monatsh Chem – Chem Mon 149:901–911.LintnerováLValentováJHerichPKožíšekJDevínskyF2018Synthesis and antiradical activity of novel copper(II) complexes of long chain reduced Schiff base ligands149901911Search in Google Scholar
Cole, K. D., Tellez, C. M. (2002). Separation of large circular DNA by electrophoresis in agarose gels. Biotechnology progress 18(1):82–87.ColeK. D.TellezC. M.2002Separation of large circular DNA by electrophoresis in agarose gels1818287Search in Google Scholar
Kumar, A., et al.(2012). Cu (II) complexes of glyco-iminoaromatic conjugates in DNA binding, plasmid cleavage and cell cytotoxicity. J Chem Sci 124(6):1217–1228.KumarA.2012Cu (II) complexes of glyco-iminoaromatic conjugates in DNA binding, plasmid cleavage and cell cytotoxicity124612171228Search in Google Scholar
Bitacura, J. G. (2018). The Use of Baker’s Yeast in the Resazurin Reduction Test: A Simple, Low-Cost Method for Determining Cell Viability in Proliferation and Cytotoxicity Assays. J Microbio. Biol Educ 19 (2):19–87. DOI: https://doi.org/10.1128/jmbe.v19i2.1599BitacuraJ. G.2018The Use of Baker’s Yeast in the Resazurin Reduction Test: A Simple, Low-Cost Method for Determining Cell Viability in Proliferation and Cytotoxicity Assays1921987https://doi.org/10.1128/jmbe.v19i2.1599Open DOISearch in Google Scholar
Botstein, D., Cherviz, S.A., Cherry, J.M. (1997). Yeast as a model organism. Science 277(5330):1259–1260.BotsteinD.ChervizS.A.CherryJ.M.1997Yeast as a model organism277533012591260Search in Google Scholar
Borra, R.C., Lotufo, M.A., Gagioti, S.M., Barros, F.D.M., Andrade, P.M. (2009). A simple method to measure cell viability in proliferation and cytotoxicity assays. Braz Oral Res 23(3):255–262.BorraR.C.LotufoM.A.GagiotiS.M.BarrosF.D.M.AndradeP.M.2009A simple method to measure cell viability in proliferation and cytotoxicity assays233255262Search in Google Scholar
Matuo, R., Sousa, F.G., Soares, D.G., Bonatto, D., Saffi, J., Escargueil, A.E., Larsen, A.K., Henriques, J.A. (2012). Saccharomyces cerevisiae as a model system to study the response to anticancer agents. Cancer Chemother Pharmacol 70:491–502.MatuoR.SousaF.G.SoaresD.G.BonattoD.SaffiJ.EscargueilA.E.LarsenA.K.HenriquesJ.A.2012Saccharomyces cerevisiae as a model system to study the response to anticancer agents70491502Search in Google Scholar