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This research led to the subsequent emergence of telomerase as a potential target for the development of anticancer drugs.
Thus, the E protein is an attractive target for the development of antiviral agents.
SHP2 is a potential target for the development of novel therapies for SHP2-dependent cancers.
As such, this enzyme could be a target for the development of future anti-virulence therapies.
Histone deacetylases (HDACs) enzyme is a promising target for the development of anticancer drugs.
As such, galanin receptors provide an attractive target for the development of novel anticonvulsant drugs.
NS5B is a major target for the development of antiviral compounds directed against HCV.
Human DNA topoisomerase IIα (htIIα) is a validated target for the development of novel anticancer agents.
Metabotropic glutamate receptors (mGluRs) constitute an attractive target for the development of potential neuroprotective agents.
Thus, protease 3C is an optimal target for the development of anti-HRV agents.
Therefore, FabG represents an appealing target for the development of new antimicrobial agents.
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