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1. Sulfopin is a covalent inhibitor of Pin1 that blocks Myc-driven tumors in vivo

2. Identification of a potent and selective covalent Pin1 inhibitor

3. Development and Characterization of Selective FAK Inhibitors and PROTACs with In Vivo Activity

6. Identification of a potent and selective covalent Pin1 inhibitor

8. Sulfopin, a selective covalent inhibitor of Pin1, blocks Myc-driven tumor initiation and growthin vivo

9. Development and Characterization of a Wee1 Kinase Degrader

10. Discovery of Covalent CDK14 Inhibitors with Pan-TAIRE Family Specificity

12. A Chemoproteomic Strategy for Direct and Proteome-Wide Covalent Inhibitor Target-Site Identification

13. Arsenic targets Pin1 and cooperates with retinoic acid to inhibit cancer-driving pathways and tumor-initiating cells

14. Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation

15. A Chemoproteomic Approach to Query the Degradable Kinome Using a Multi-kinase Degrader

16. Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation

18. Front Cover: Development and Characterization of Selective FAK Inhibitors and PROTACs with In Vivo Activity (ChemBioChem 19/2023).

19. Pharmacological perturbation of CDK9 using selective CDK9 inhibition or degradation

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