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International Journal of Cancer|June 30, 2020
Histone deacetylase inhibition prevents the growth of primary and metastatic osteosarcomaJeremy J McGuire, Niveditha Nerlakanti, Chen Hao Lo, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|August 25, 2016
Catechol-based matrix metalloproteinase inhibitors with additional antioxidative activityMarilena Tauro, Antonio Laghezza, Fulvio Loiodice, et al.Pharmaceuticals (Basel, Switzerland)|June 5, 2020
Bone-Seeking Matrix Metalloproteinase Inhibitors for the Treatment of Skeletal MalignancyAntonio Laghezza, Luca Piemontese, Leonardo Brunetti, et al.Cancer Research|October 17, 2025
PRDM16 Regulates Prostate Cancer Cell Dormancy and Prevents Bone Metastatic OutgrowthMostafa M Nasr, Bishoy Wadie, Tao Li, et al.European Journal of Medicinal Chemistry|December 16, 2014
Design, synthesis and biological evaluation of a class of bioisosteric oximes of the novel dual peroxisome proliferator-activated receptor α/γ ligand LT175Luca Piemontese, Giuseppe Fracchiolla, Antonio Carrieri, et al.Chemmedchem|February 27, 2016
Structure-Based Design of Microsomal Prostaglandin E2 Synthase-1 (mPGES-1) Inhibitors using a Virtual Fragment Growing Optimization SchemeGianluigi Lauro, Paolo Tortorella, Alessia Bertamino, et al.Haematologica|December 5, 2024
Acid ceramidase controls proteasome inhibitor resistance and is a novel therapeutic target for the treatment of relapsed/refractory multiple myelomaRyan T Bishop, Tao Li, Praneeth Sudalagunta, et al.Molecular Cancer Therapeutics|March 25, 2017
Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer TherapeuticsStuart W Ember, Que T Lambert, Norbert Berndt, et al.Research Square|August 20, 2025
Unc-51 Like Kinase 3 (ULK3) is essential for autophagy and cell survival in multiple myelomaMarilena Tauro, Tao Li, Praneeth R Sudalagunta, et al.Pageof 2