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The orphan nuclear receptor Nurr1 is responsive to non-steroidal anti-inflammatory drugs.

  • Read more about The orphan nuclear receptor Nurr1 is responsive to non-steroidal anti-inflammatory drugs.

A triple farnesoid X receptor and peroxisome proliferator-activated receptor α/δ activator reverses hepatic fibrosis in diet-induced NASH in mice.

  • Read more about A triple farnesoid X receptor and peroxisome proliferator-activated receptor α/δ activator reverses hepatic fibrosis in diet-induced NASH in mice.

Epigenetic modulation by targeting bromodomain containing protein 9 (BRD9): Its therapeutic potential and selective inhibition.

  • Read more about Epigenetic modulation by targeting bromodomain containing protein 9 (BRD9): Its therapeutic potential and selective inhibition.

Death by a Thousand Cuts â€" Combining Kinase Inhibitors for Selective Target Inhibition and Rational Polypharmacology.

  • Read more about Death by a Thousand Cuts â€" Combining Kinase Inhibitors for Selective Target Inhibition and Rational Polypharmacology.

Antecedent chromatin organization determines cGAS recruitment to ruptured micronuclei.

  • Read more about Antecedent chromatin organization determines cGAS recruitment to ruptured micronuclei.

Discovery of potent Plasmodium falciparum protein kinase 6 (PfPK6) inhibitors with a type II inhibitor pharmacophore.

  • Read more about Discovery of potent Plasmodium falciparum protein kinase 6 (PfPK6) inhibitors with a type II inhibitor pharmacophore.

SS148 and WZ16 inhibit the activities of nsp10-nsp16 complexes from all seven human pathogenic coronaviruses.

  • Read more about SS148 and WZ16 inhibit the activities of nsp10-nsp16 complexes from all seven human pathogenic coronaviruses.

Toward effective Atg8-based ATTECs: Approaches and perspectives.

  • Read more about Toward effective Atg8-based ATTECs: Approaches and perspectives.

Discovery and Characterization of BAY-805, a Potent and Selective Inhibitor of Ubiquitin-Specific Protease USP21.

  • Read more about Discovery and Characterization of BAY-805, a Potent and Selective Inhibitor of Ubiquitin-Specific Protease USP21.

Histone H4K20 monomethylation enables recombinant nucleosome methylation by PRMT1 in vitro.

  • Read more about Histone H4K20 monomethylation enables recombinant nucleosome methylation by PRMT1 in vitro.

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