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Combinatorial Anticancer Drug Screen Identifies Off-Target Effects of Epigenetic Chemical Probes.

  • Read more about Combinatorial Anticancer Drug Screen Identifies Off-Target Effects of Epigenetic Chemical Probes.

Identification of Histone Peptide Binding Specificity and Small-Molecule Ligands for the TRIM33α and TRIM33β Bromodomains.

  • Read more about Identification of Histone Peptide Binding Specificity and Small-Molecule Ligands for the TRIM33α and TRIM33β Bromodomains.

CDK11 regulates pre-mRNA splicing by phosphorylation of SF3B1.

  • Read more about CDK11 regulates pre-mRNA splicing by phosphorylation of SF3B1.

Identification and Utilization of a Chemical Probe to Interrogate the Roles of PIKfyve in the Lifecycle of β-Coronaviruses.

  • Read more about Identification and Utilization of a Chemical Probe to Interrogate the Roles of PIKfyve in the Lifecycle of β-Coronaviruses.

A small molecule antagonist of SMN disrupts the interaction between SMN and RNAP II.

  • Read more about A small molecule antagonist of SMN disrupts the interaction between SMN and RNAP II.

Development and Characterization of Type I, Type II, and Type III LIM-Kinase Chemical Probes.

  • Read more about Development and Characterization of Type I, Type II, and Type III LIM-Kinase Chemical Probes.

Fragment-based discovery of orphan nuclear receptor Nur77/NGFI-B ligands.

  • Read more about Fragment-based discovery of orphan nuclear receptor Nur77/NGFI-B ligands.

ChemBioPort: an online portal to navigate the structure, function and chemical inhibition of the human proteome.

  • Read more about ChemBioPort: an online portal to navigate the structure, function and chemical inhibition of the human proteome.

Identification of Novel 2,4,5-Trisubstituted Pyrimidines as Potent Dual Inhibitors of Plasmodial PfGSK3/PfPK6 with Activity against Blood Stage Parasites In Vitro.

  • Read more about Identification of Novel 2,4,5-Trisubstituted Pyrimidines as Potent Dual Inhibitors of Plasmodial PfGSK3/PfPK6 with Activity against Blood Stage Parasites In Vitro.

Covalent Modification of Bromodomain Proteins by Peptides Containing a DNA Damage-Induced, Histone Post-Translational Modification.

  • Read more about Covalent Modification of Bromodomain Proteins by Peptides Containing a DNA Damage-Induced, Histone Post-Translational Modification.

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