Cite
Curcumin is a tight-binding inhibitor of the most efficient human daunorubicin reductase--Carbonyl reductase 1.
MLA
Hintzpeter, Jan, et al. “Curcumin Is a Tight-Binding Inhibitor of the Most Efficient Human Daunorubicin Reductase--Carbonyl Reductase 1.” Chemico-Biological Interactions, vol. 234, June 2015, pp. 162–68. EBSCOhost, https://doi.org/10.1016/j.cbi.2014.12.019.
APA
Hintzpeter, J., Hornung, J., Ebert, B., Martin, H.-J., & Maser, E. (2015). Curcumin is a tight-binding inhibitor of the most efficient human daunorubicin reductase--Carbonyl reductase 1. Chemico-Biological Interactions, 234, 162–168. https://doi.org/10.1016/j.cbi.2014.12.019
Chicago
Hintzpeter, Jan, Jan Hornung, Bettina Ebert, Hans-Jörg Martin, and Edmund Maser. 2015. “Curcumin Is a Tight-Binding Inhibitor of the Most Efficient Human Daunorubicin Reductase--Carbonyl Reductase 1.” Chemico-Biological Interactions 234 (June): 162–68. doi:10.1016/j.cbi.2014.12.019.