Leveraging crowdsourcing to facilitate the discovery of new medicines. Read more about Leveraging crowdsourcing to facilitate the discovery of new medicines.
Normalizing molecular docking rankings using virtually generated decoys. Read more about Normalizing molecular docking rankings using virtually generated decoys.
Structural and histone binding ability characterizations of human PWWP domains. Read more about Structural and histone binding ability characterizations of human PWWP domains.
PRC2 complexes with JARID2, MTF2, and esPRC2p48 in ES cells to modulate ES cell pluripotency and somatic cell reprogramming. Read more about PRC2 complexes with JARID2, MTF2, and esPRC2p48 in ES cells to modulate ES cell pluripotency and somatic cell reprogramming.
Comparative structural analysis of lipid binding START domains. Read more about Comparative structural analysis of lipid binding START domains.
A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells. Read more about A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cells.
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Read more about Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.
Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolines. Read more about Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolines.
Critical role for a stage-specific actin in male exflagellation of the malaria parasite. Read more about Critical role for a stage-specific actin in male exflagellation of the malaria parasite.
High-throughput kinase profiling: a more efficient approach toward the discovery of new kinase inhibitors. Read more about High-throughput kinase profiling: a more efficient approach toward the discovery of new kinase inhibitors.
