Effects of histone acetyltransferase (HAT) and histone deacetylase (HDAC) inhibitors on proliferative, differentiative, and regenerative functions of Toll-like receptor 2 (TLR-2)-stimulated human dental pulp cells (hDPCs).
Sarah Hossam FahmyHolger JungbluthSøeren JepsenJochen WinterPublished in: Clinical oral investigations (2023)
Targeting hDPC nuclear function could be a promising option in the scope of the biological management of inflammatory pulp diseases.