ACVR1 Mutations in DIPG: Lessons Learned from FOP. Read more about ACVR1 Mutations in DIPG: Lessons Learned from FOP.
(R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells. Read more about (R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells.
The Crystal Structure of the RhoA : AKAP-Lbc DH-PH Domain Complex. Read more about The Crystal Structure of the RhoA : AKAP-Lbc DH-PH Domain Complex.
A unique inhibitor binding site in ERK1/2 is associated with slow binding kinetics. Read more about A unique inhibitor binding site in ERK1/2 is associated with slow binding kinetics.
Identification and structure-function analysis of sub-family selective G protein-coupled receptor kinase inhibitors. Read more about Identification and structure-function analysis of sub-family selective G protein-coupled receptor kinase inhibitors.
Structural basis for selective binding of m(6)A RNA by the YTHDC1 YTH domain. Read more about Structural basis for selective binding of m(6)A RNA by the YTHDC1 YTH domain.
OOMMPPAA: A tool to aid directed synthesis by the combined analysis of activity and structural data. Read more about OOMMPPAA: A tool to aid directed synthesis by the combined analysis of activity and structural data.
Structure and function of the nucleosome-binding PWWP domain. Read more about Structure and function of the nucleosome-binding PWWP domain.
Stimulation of Hepatic Apolipoprotein A-I Production by Novel Thieno-Triazolodiazepines: Roles of the Classical Benzodiazepine Receptor, PAF Receptor, and Bromodomain Binding. Read more about Stimulation of Hepatic Apolipoprotein A-I Production by Novel Thieno-Triazolodiazepines: Roles of the Classical Benzodiazepine Receptor, PAF Receptor, and Bromodomain Binding.
