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5. Discovery of VU0467319: an M1 Positive Allosteric Modulator Candidate That Advanced into Clinical Trials.

8. Displacement of WDR5 from Chromatin by a WIN Site Inhibitor with Picomolar Affinity

9. Supplementary Figure 2 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

10. Supplementary Figure 7 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

11. Supplementary Figure 4 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

12. Supplementary Figure 5 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

13. Supplementary Figure 3 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

14. Supplementary Figure 6 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

15. Supplementary Figure 1 from Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

16. Prostate Cancer Progression Relies on the Mitotic Kinase Citron Kinase

19. TheSLC1A1/EAAT3 Dicarboxylic Amino Acid Transporter is an Epigenetically Dysregulated Nutrient Carrier that Sustains Oncogenic Metabolic Programs

20. VU0477573: Partial Negative Allosteric Modulator of the Subtype 5 Metabotropic Glutamate Receptor with In Vivo Efficacy

21. Discovery of Small-Molecule Nonfluorescent Inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pair

23. 361 WDR5 represents a therapeutically exploitable target for cancer stem cells in glioblastoma

26. Advancing Biological Understanding and Therapeutics Discovery with Small-Molecule Probes

27. Biased mGlu5-Positive Allosteric Modulators Provide In Vivo Efficacy without Potentiating mGlu5 Modulation of NMDAR Currents

28. WDR5 represents a therapeutically exploitable target for cancer stem cells in glioblastoma

29. Biotransformation of a Novel Positive Allosteric Modulator of Metabotropic Glutamate Receptor Subtype 5 Contributes to Seizure-Like Adverse Events in Rats Involving a Receptor Agonism-Dependent Mechanism

31. Unique Signaling Profiles of Positive Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 Determine Differences in In Vivo Activity

33. Functional Impact of Allosteric Agonist Activity of Selective Positive Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 in Regulating Central Nervous System Function

34. Discovery of Novel Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 Reveals Chemical and Functional Diversity and In Vivo Activity in Rat Behavioral Models of Anxiolytic and Antipsychotic Activity

36. WDR5 represents a therapeutically exploitable target for cancer stem cells in glioblastoma

37. Structure-Based Optimization of ML300-Derived, Noncovalent Inhibitors Targeting the Severe Acute Respiratory Syndrome Coronavirus 3CL Protease (SARS-CoV-2 3CLpro)

38. Discovery and Structure-Based Optimization of Potent and Selective WDR5 Inhibitors Containing a Dihydroisoquinolinone Bicyclic Core

39. Structure-Based Optimization of ML300-Derived, Noncovalent Inhibitors Targeting the Severe Acute Respiratory Syndrome Coronavirus 3CL Protease (SARS-CoV-2 3CLpro).

41. Identification of second-generation P2X3 antagonists for treatment of pain

42. Discovery of WD Repeat-Containing Protein 5 (WDR5)–MYC Inhibitors Using Fragment-Based Methods and Structure-Based Design

43. Discovery and Structure-Based Optimization of Potent and Selective WD Repeat Domain 5 (WDR5) Inhibitors Containing a Dihydroisoquinolinone Bicyclic Core

45. Discovery and Optimization of Salicylic Acid-Derived Sulfonamide Inhibitors of the WD Repeat-Containing Protein 5–MYC Protein–Protein Interaction

47. Structure-Based Optimization of ML300-Derived, Noncovalent Inhibitors Targeting the Severe Acute Respiratory Syndrome Coronavirus 3CL Protease (SARS-CoV-2 3CLpro)

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