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Pim Kinase Inhibitors Evaluated with a Single-Molecule Engineered Nanopore Sensor.

  • Read more about Pim Kinase Inhibitors Evaluated with a Single-Molecule Engineered Nanopore Sensor.

Tankyrase 1 Inhibitors with Drug-like Properties Identified by Screening a DNA-Encoded Chemical Library.

  • Read more about Tankyrase 1 Inhibitors with Drug-like Properties Identified by Screening a DNA-Encoded Chemical Library.

MemProtMD: Automated Insertion of Membrane Protein Structures into Explicit Lipid Membranes.

  • Read more about MemProtMD: Automated Insertion of Membrane Protein Structures into Explicit Lipid Membranes.

Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2.

  • Read more about Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2.

Mechanisms underlying clinical efficacy of Angiotensin II type 2 receptor (AT2R) antagonist EMA401 in neuropathic pain: clinical tissue and in vitro studies.

  • Read more about Mechanisms underlying clinical efficacy of Angiotensin II type 2 receptor (AT2R) antagonist EMA401 in neuropathic pain: clinical tissue and in vitro studies.

Biochemical characterization of FIKK8-a unique protein kinase from the malaria parasite Plasmodium falciparum and other apicomplexans.

  • Read more about Biochemical characterization of FIKK8-a unique protein kinase from the malaria parasite Plasmodium falciparum and other apicomplexans.

Structural Basis for the Specificity of Human NUDT16 and Its Regulation by Inosine Monophosphate.

  • Read more about Structural Basis for the Specificity of Human NUDT16 and Its Regulation by Inosine Monophosphate.

Assessment of a method to characterize antibody selectivity and specificity for use in immunoprecipitation.

  • Read more about Assessment of a method to characterize antibody selectivity and specificity for use in immunoprecipitation.

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies.

  • Read more about Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies.

Beating the odds: BETs in disease.

  • Read more about Beating the odds: BETs in disease.

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