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1. Exploration of the P1 residue in 3CL protease inhibitors leading to the discovery of a 2-tetrahydrofuran P1 replacement

2. Classification of crystallization outcomes using deep convolutional neural networks

5. Combinatorial signaling by Twisted Gastrulation and Decapentaplegic

6. Exploration of the P1 Residue in CL Protease Inhibitors Leading to the Discovery of a Novel 2-Tetrahydrofuran P1 Replacement

11. A Teaching Conversation about Transformation.

12. Black Feminist Thought: Implications for a Transformative Women's Education.

16. Structural analyses reveal phosphatidyl inositols as ligands for the NR5 orphan receptors Sf-1 and LRH-1

21. Atomic structure of progesterone complexed with its receptor

23. An orally available, brain-penetrant CAMKK2 inhibitor reduces food intake in rodent model

25. Design of N‑Benzoxaborole Benzofuran GSK8175Optimization of Human Pharmacokinetics Inspired by Metabolites of a Failed Clinical HCV Inhibitor.

26. Design of N-Benzoxaborole Benzofuran GSK8175—Optimization of Human Pharmacokinetics Inspired by Metabolites of a Failed Clinical HCV Inhibitor

27. Structural Analysis of Rev-erbα Bound to NCoR Reveals a Unique Mechanism of Nuclear Receptor-Corepressor Interaction

32. A human fatty acid synthase inhibitor binds β-ketoacyl reductase in the keto-substrate site

38. FXR agonist activity of conformationally constrained analogs of GW 4064

42. Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064

43. Toward tuning electrical and optical properties in conjugated polymers using side chains: highly conductive heat-to-tail heteroatom-functionalized polythiophenes

44. Self-orienting head-to-tail poly(3-alkylthiophenes): new insights on structure-property relationships in conducting polymers

45. Small Molecule Agonists of the Orphan Nuclear Receptors Steroidogenic Factor-1 (SF-1, NR5A1) and Liver Receptor Homologue-1 (LRH-1, NR5A2)

48. Improving the developability profile of pyrrolidine progesterone receptor partial agonists

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