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Structural Basis for EPC1-Mediated Recruitment of MBTD1 into the NuA4/TIP60 Acetyltransferase Complex.

  • Read more about Structural Basis for EPC1-Mediated Recruitment of MBTD1 into the NuA4/TIP60 Acetyltransferase Complex.

The RESOLUTE consortium: unlocking SLC transporters for drug discovery.

  • Read more about The RESOLUTE consortium: unlocking SLC transporters for drug discovery.

New Insights into 4-Anilinoquinazolines as Inhibitors of Cardiac Troponin I-Interacting Kinase (TNNi3K).

  • Read more about New Insights into 4-Anilinoquinazolines as Inhibitors of Cardiac Troponin I-Interacting Kinase (TNNi3K).

Importance of Quantifying Drug-Target Engagement in Cells.

  • Read more about Importance of Quantifying Drug-Target Engagement in Cells.

Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding.

  • Read more about Crystal structure of DRIK1, a stress-responsive receptor-like pseudokinase, reveals the molecular basis for the absence of ATP binding.

Telomere dysfunction cooperates with epigenetic alterations to impair murine embryonic stem cell fate commitment.

  • Read more about Telomere dysfunction cooperates with epigenetic alterations to impair murine embryonic stem cell fate commitment.

CDK12 inhibition reduces abnormalities in cells from patients with myotonic dystrophy and in a mouse model.

  • Read more about CDK12 inhibition reduces abnormalities in cells from patients with myotonic dystrophy and in a mouse model.

L-thyroxin and the non-classical thyroid hormone TETRAC are potent activators of PPARγ.

  • Read more about L-thyroxin and the non-classical thyroid hormone TETRAC are potent activators of PPARγ.

Therapeutic targeting of p300/CBP HAT domain for the treatment of NUT midline carcinoma.

  • Read more about Therapeutic targeting of p300/CBP HAT domain for the treatment of NUT midline carcinoma.

Discovery of a First-in-class Protein Arginine Methyltransferase 6 (PRMT6) Covalent Inhibitor.

  • Read more about Discovery of a First-in-class Protein Arginine Methyltransferase 6 (PRMT6) Covalent Inhibitor.

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