Wild, M.; Hahn, F.; Brückner, N.; Schütz, M.; Wangen, C.; Wagner, S.; Sommerer, M.; Strobl, S.; Marschall, M.
Cyclin-Dependent Kinases (CDKs) and the Human Cytomegalovirus-Encoded CDK Ortholog pUL97 Represent Highly Attractive Targets for Synergistic Drug Combinations. Int. J. Mol. Sci. 2022, 23, 2493.
https://doi.org/10.3390/ijms23052493
AMA Style
Wild M, Hahn F, Brückner N, Schütz M, Wangen C, Wagner S, Sommerer M, Strobl S, Marschall M.
Cyclin-Dependent Kinases (CDKs) and the Human Cytomegalovirus-Encoded CDK Ortholog pUL97 Represent Highly Attractive Targets for Synergistic Drug Combinations. International Journal of Molecular Sciences. 2022; 23(5):2493.
https://doi.org/10.3390/ijms23052493
Chicago/Turabian Style
Wild, Markus, Friedrich Hahn, Nadine Brückner, Martin Schütz, Christina Wangen, Sabrina Wagner, Mona Sommerer, Stefan Strobl, and Manfred Marschall.
2022. "Cyclin-Dependent Kinases (CDKs) and the Human Cytomegalovirus-Encoded CDK Ortholog pUL97 Represent Highly Attractive Targets for Synergistic Drug Combinations" International Journal of Molecular Sciences 23, no. 5: 2493.
https://doi.org/10.3390/ijms23052493
APA Style
Wild, M., Hahn, F., Brückner, N., Schütz, M., Wangen, C., Wagner, S., Sommerer, M., Strobl, S., & Marschall, M.
(2022). Cyclin-Dependent Kinases (CDKs) and the Human Cytomegalovirus-Encoded CDK Ortholog pUL97 Represent Highly Attractive Targets for Synergistic Drug Combinations. International Journal of Molecular Sciences, 23(5), 2493.
https://doi.org/10.3390/ijms23052493