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Shifting the selectivity of pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors towards the salt-inducible kinase (SIK) subfamily.

  • Read more about Shifting the selectivity of pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors towards the salt-inducible kinase (SIK) subfamily.

NMR resonance assignment of a fibroblast growth factor 8 splicing isoform b.

  • Read more about NMR resonance assignment of a fibroblast growth factor 8 splicing isoform b.

Editorial: The next generation of tools and technologies for studying human neurons in a dish.

  • Read more about Editorial: The next generation of tools and technologies for studying human neurons in a dish.

A Small Step Toward Generalizability: Training a Machine Learning Scoring Function for Structure-Based Virtual Screening.

  • Read more about A Small Step Toward Generalizability: Training a Machine Learning Scoring Function for Structure-Based Virtual Screening.

A novel BRET-based assay to investigate binding and residence times of unmodified ligands to the human lysosomal ion channel TRPML1 in intact cells.

  • Read more about A novel BRET-based assay to investigate binding and residence times of unmodified ligands to the human lysosomal ion channel TRPML1 in intact cells.

Structure-Based Development of Isoform-Selective Inhibitors of Casein Kinase 1ε vs Casein Kinase 1δ.

  • Read more about Structure-Based Development of Isoform-Selective Inhibitors of Casein Kinase 1ε vs Casein Kinase 1δ.

Open drug discovery in Alzheimer's disease.

  • Read more about Open drug discovery in Alzheimer's disease.

Identification of inhibitors for the trans-membrane Trypanosoma cruzi eIF2α kinase relevant for parasite proliferation.

  • Read more about Identification of inhibitors for the trans-membrane Trypanosoma cruzi eIF2α kinase relevant for parasite proliferation.

Structural insights into a regulatory mechanism of FIR RRM1-FUSE interaction.

  • Read more about Structural insights into a regulatory mechanism of FIR RRM1-FUSE interaction.

Structure-Based Discovery of Inhibitors of the SARS-CoV-2 Nsp14 N7-Methyltransferase.

  • Read more about Structure-Based Discovery of Inhibitors of the SARS-CoV-2 Nsp14 N7-Methyltransferase.

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