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1. Fish-hunting cone snail disrupts prey’s glucose homeostasis with weaponized mimetics of somatostatin and insulin

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3. 5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology

4. Ligand selectivity hotspots in serotonin GPCRs

7. Somatostatin venom analogs evolved by fish-hunting cone snails:From prey capture behavior to identifying drug leads

8. (S)-2-Mercaptohistidine: A First Selective Orthosteric GluK3 Antagonist

9. Somatostatin venom analogs evolved by fish-hunting cone snails: From prey capture behavior to identifying drug leads

10. Somatostatin venom analogs evolved by fish-hunting cone snails: From prey capture behavior to identifying drug leads

11. Curses or Cures:A Review of the Numerous Benefits Versus the Biosecurity Concerns of Conotoxin Research

14. Design and Synthesis of 2,3-trans-Proline Analogues as Ligands for Ionotropic Glutamate Receptors and Excitatory Amino Acid Transporters

15. New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III

16. New insights into the structure-activity-relationship of selective excitatory amino acid transporter subtype 1 (EAAT1) inhibitors UCPH-101 and UCPH-102

19. New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III

20. Bioavailability Studies and in vitro Profiling of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitor UCPH-102

21. New Insight into the Structure-Activity Relationships of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors UCPH-101 and UCPH-102

22. 5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology.

23. Venom-inspired somatostatin receptor 4 (SSTR4) agonists as new drug leads for peripheral pain conditions.

24. Identification and Structure-Activity Relationship Study of Imidazo[1,2- a ]pyridine-3-amines as First Selective Inhibitors of Excitatory Amino Acid Transporter Subtype 3 (EAAT3).