Discovery of Ubiquitin Deamidases in the Pathogenic Arsenal of Legionella pneumophila. Read more about Discovery of Ubiquitin Deamidases in the Pathogenic Arsenal of Legionella pneumophila.
Structure activity relationship studies on rhodanines and derived enethiol inhibitors of metallo-β-lactamases. Read more about Structure activity relationship studies on rhodanines and derived enethiol inhibitors of metallo-β-lactamases.
The C-terminal extension landscape of naturally presented HLA-I ligands. Read more about The C-terminal extension landscape of naturally presented HLA-I ligands.
TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myeloma. Read more about TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myeloma.
Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype. Read more about Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype.
Identification and Structure-Activity Relationship of HDAC6 Zinc-Finger Ubiquitin Binding Domain Inhibitors. Read more about Identification and Structure-Activity Relationship of HDAC6 Zinc-Finger Ubiquitin Binding Domain Inhibitors.
Application of Integrated Drug Screening/Kinome Analysis to Identify Inhibitors of Gemcitabine-Resistant Pancreatic Cancer Cell Growth. Read more about Application of Integrated Drug Screening/Kinome Analysis to Identify Inhibitors of Gemcitabine-Resistant Pancreatic Cancer Cell Growth.
DOT1L inhibition attenuates graft-versus-host disease by allogeneic T cells in adoptive immunotherapy models. Read more about DOT1L inhibition attenuates graft-versus-host disease by allogeneic T cells in adoptive immunotherapy models.
BET bromodomain ligands: Probing the WPF shelf to improve BRD4 bromodomain affinity and metabolic stability. Read more about BET bromodomain ligands: Probing the WPF shelf to improve BRD4 bromodomain affinity and metabolic stability.
