40 results on '"Zhu, Jin-Yi"'
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2. A Girl with PRRT2 Mutation Presenting with Benign Familial Infantile Seizures Followed by Autistic Regression
3. Data from Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics
4. Supplementary Tables S4, S5 from Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics
5. Supplementary Tables S1-S3 and Figures S1-S11 from Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics
6. Molecular glue CELMoD compounds are allosteric regulators of cereblon conformation
7. Functional Consequence of Covalent Reaction of Phosphoenolpyruvate with UDP-N-acetylglucosamine 1-Carboxyvinyltransferase (MurA)
8. Differential BET Bromodomain Inhibition by Dihydropteridinone and Pyrimidodiazepinone Kinase Inhibitors
9. Structural Basis of Inhibitor Selectivity in the BRD7/9 Subfamily of Bromodomains
10. Comparative Study on Two Solutions of 3-RPS Parallel Mechanism Pose
11. Molecular Basis for the N-Terminal Bromodomain-and-Extra-Terminal-Family Selectivity of a Dual Kinase–Bromodomain Inhibitor
12. Structural Basis of ALDH1A2 Inhibition by Irreversible and Reversible Small Molecule Inhibitors
13. Structure-Activity Studies ofN-Butyl-1-deoxynojirimycin (NB-DNJ) Analogues: Discovery of Potent and Selective Aminocyclopentitol Inhibitors of GBA1 and GBA2
14. Structural Basis of Wee Kinases Functionality and Inactivation by Diverse Small Molecule Inhibitors
15. Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations
16. Correction to BET Bromodomain Inhibitors with One-Step Synthesis Discovered from Virtual Screen
17. BET Bromodomain Inhibitors with One-Step Synthesis Discovered from Virtual Screen
18. Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics
19. Back Cover: Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET‐BRET (ChemMedChem 23/2016)
20. Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET‐BRET
21. Discovery of Diverse Small-Molecule Inhibitors of Mammalian Sterile20-like Kinase 3 (MST3)
22. Structure-Activity Studies of N-Butyl-1-deoxynojirimycin ( NB-DNJ) Analogues: Discovery of Potent and Selective Aminocyclopentitol Inhibitors of GBA1 and GBA2.
23. Abstract 3643: Targeting the acetyl-lysine binding site of BRD4 with dual nanomolar BET-JAK2 inhibitors: A new anticancer therapeutic strategy
24. Stability of the Human Hsp90-p50Cdc37 Chaperone Complex against Nucleotides and Hsp90 Inhibitors, and the Influence of Phosphorylation by Casein Kinase 2
25. Acetyl-lysine Binding Site of Bromodomain-Containing Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors
26. Structural Basis of ALDH1A2 Inhibition by Irreversible and Reversible Small Molecule Inhibitors
27. Development of o-Chlorophenyl Substituted Pyrimidines as Exceptionally Potent Aurora Kinase Inhibitors
28. Structure of theArchaeoglobus fulgidusorphan ORF AF1382 determined by sulfur SAD from a moderately diffracting crystal
29. A Novel Approach to the Discovery of Small-Molecule Ligands of CDK2
30. Abstract 3902: Development of Aurora A inhibitors withortho-halophenyl substituted pyrimidines: Unusual potency, SAR and X-ray crystallography studies.
31. Abstract 2942: RKI-1447, a potent ROCK inhibitor with anti-tumor and anti-invasive activities in breast cancer
32. Abstract 3904: Pyridylthiazole-based ureas as inhibitors of Rho-associated protein kinases
33. Synthesis and Evaluation of Eight- and Four-Membered Iminosugar Analogues as Inhibitors of Testicular Ceramide-Specific Glucosyltransferase, Testicular β-Glucosidase 2, and Other Glycosidases
34. Fragment-Based and Structure-Guided Discovery and Optimization of Rho Kinase Inhibitors
35. A Novel Mechanism by Which Small Molecule Inhibitors Induce the DFG Flip in Aurora A
36. Pyridylthiazole-based ureas as inhibitors of Rho associated protein kinases (ROCK1 and 2)
37. Crystal structure of a novel non‐Pfam protein AF1514 from Archeoglobus fulgidus DSM 4304 solved by S‐SAD using a Cr X‐ray source
38. Development of o-ChlorophenylSubstituted Pyrimidines as Exceptionally Potent Aurora Kinase Inhibitors.
39. Structure of the Archaeoglobus fulgidus orphan ORF AF1382 determined by sulfur SAD from a moderately diffracting crystal.
40. Fragment-Based and Structure-GuidedDiscovery andOptimization of Rho Kinase Inhibitors.
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