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.
Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery. Read more about Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery.
Crystal structures explain functional differences in the two actin depolymerization factors of the malaria parasite. Read more about Crystal structures explain functional differences in the two actin depolymerization factors of the malaria parasite.
3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands. Read more about 3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.
