个人简历

2005年获武汉大学药学院硕士学位，毕业后赴暨南大学药学院工作。2012年在新加坡南洋理工大学化学与生物化学系获博士学位，毕业后在南洋理工大学从事博士后研究。2013年加入江南大学食品学院工作，任副教授、硕士生导师；2017年1月调入江南大学药学院工作。

研究领域

核酸纳米生物技术；DNA结构与功能研究

近期论文

[1] Yang, Z.Q.*; Jiang T.Y.; Zhong, H.S.; Kang Y. Bulge Oligonucleotide as an Inhibitory Agent of Bacterial Topoisomerase I. J. Enzyme. Inhib. Med. Ch., 2018, 33,319-323.
[2] Yang, Z.Q.*; Jiang T.Y.; Zhong, H.S.; Liu, Y.F. Portion mismatch in duplex oligonucleotides as inhibitors of bacterial topoisomerase I. RSC Adv., 2016, 6, 107572-107576.
[3] Yang, Z.Q.*; Tang X.S.; Liu, Y.F. Enhanced performance of dye-sensitized solar cells with fluorine doped nanocrystalline TiO2 as photoanode. Electrochim. Acta, 2015, 186, 151-156.
[4] Yang, Z.Q.*; Liu, Y.F. Truncated Au decahedron by the time induced truncating. Nanosci. Nanotech. Lett., 2015, 7(8), 685-689.
[5] Yang, Z.Q.*; Chen, W.W.; Zu, Z.Q.; Zang, Z.Q.; Yang, Y.C; Tang, X.S. Facile synthesis and photoluminescence characterization of AgInZnS hollow nanoparticles. Mater. Lett., 2015, 151, 89-92.
[6] Yang, Z.Q.; Li, D.W.; Guo, J.J.; Shao, F.W.; Li, T.H. Intrinsic curvature in duplex DNA inhibits Human Topoisomerase I. Bioorg. Med. Chem. Lett., 2012, 22(3), 1322-1325.
[7] Yang, Z.Q.; Li, D.W.; Li, T.H. Design and synthesis of catenated rings based on toroidal DNA structures. Chem.Comm., 2011, 47 (43), 11930 -11932.
[8] Yang, Z.Q.; Li, D.W.; Hiew, S.H.; Ng, T.T.M.; Yuan, W.X.; Su, H.B.; Shao, F.W.; Li, T.H. Recognition of forcible curvature in circular DNA by human topoisomerase I. Chem.Comm., 2011, 47 (40), 11309-11311.
[9] Li, D.W.; Li, W.L.; Wang, Q.; Yang, Z.Q.*; Hou, Z.J. Concise Synthesis of Cannabisin G. Bioorg. Med. Chem. Lett., 2010, 20(17), 5095-5098.[10] Wong, W. C.; Zhuang, J.Y.; Ng, L.L.S.; New, L.L.L.; Hiew, S.H.; Guo, J.J.; Yang, Z.Q.*; Li, T.H Conformational organizations of G-quadruplexes composed of d(G4Tn)3G4. Bioorg. Med. Chem. Lett., 2010, 20, 4689-4692.
[11] Yang, Z.Q.; Sun, P.; Chen, W.M. 3D-QSAR Analysis on Pyrrolopyridine analogs as Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 (MK-2) inhibitors. Lett. Drug Des. Discovery, 2007, 4(8), 557-561.[12] Yang, Z.Q.; Sun, P. 3D-QSAR study of Potent Inhibitor of Phosphodiesterase-4 by using CoMFA approach. Int. J. Mol. Sci. 2007, 8(7), 714-722.