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BET inhibition disrupts transcription but retains enhancer-promoter contact.

  • Read more about BET inhibition disrupts transcription but retains enhancer-promoter contact.

Large-scale survey and database of high affinity ligands for peptide recognition modules.

  • Read more about Large-scale survey and database of high affinity ligands for peptide recognition modules.

Inhibition of the SUV4-20 H1 histone methyltransferase increases frataxin expression in Friedreich's ataxia patient cells.

  • Read more about Inhibition of the SUV4-20 H1 histone methyltransferase increases frataxin expression in Friedreich's ataxia patient cells.

Identification of small molecule allosteric modulators of 5,10-methylenetetrahydrofolate reductase (MTHFR) by targeting its unique regulatory domain.

  • Read more about Identification of small molecule allosteric modulators of 5,10-methylenetetrahydrofolate reductase (MTHFR) by targeting its unique regulatory domain.

Development of a potent and selective chemical probe for the pleiotropic kinase CK2.

  • Read more about Development of a potent and selective chemical probe for the pleiotropic kinase CK2.

Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2.

  • Read more about Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2.

Drugging the 'undruggable' MYCN oncogenic transcription factor: Overcoming previous obstacles to impact childhood cancers.

  • Read more about Drugging the 'undruggable' MYCN oncogenic transcription factor: Overcoming previous obstacles to impact childhood cancers.

Rational Design and Synthesis of Selective PRMT4 Inhibitors: a New Chemotype for Development of Cancer Therapeutics.

  • Read more about Rational Design and Synthesis of Selective PRMT4 Inhibitors: a New Chemotype for Development of Cancer Therapeutics.

Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2.

  • Read more about Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2.

Substrate reduction therapy for inborn errors of metabolism.

  • Read more about Substrate reduction therapy for inborn errors of metabolism.

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