232 results on '"Yang, Shyh-Ming"'
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2. Triple combination of BET plus PI3K and NF-κB inhibitors exhibit synergistic activity in adult T-cell leukemia/lymphoma
3. Supplementary Figure S1 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
4. Data from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
5. Supplementary Table 3 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
6. Supplementary Table 2 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
7. Supplementary Table 1 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
8. Supplementary Table 4 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
9. Supplementary Table 5 from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
10. Supplementary Data Legends from RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
11. RALDH1 Inhibition Shows Immunotherapeutic Efficacy in Hepatocellular Carcinoma
12. Discovery of endoplasmic reticulum calcium stabilizers to rescue ER-stressed podocytes in nephrotic syndrome
13. Supplementary Table 5 from Predicting Novel Therapies and Targets: Regulation of Notch3 by the Bromodomain Protein BRD4
14. Supplementary Materials from Predicting Novel Therapies and Targets: Regulation of Notch3 by the Bromodomain Protein BRD4
15. Data from Predicting Novel Therapies and Targets: Regulation of Notch3 by the Bromodomain Protein BRD4
16. Supplementary Table 4 from Predicting Novel Therapies and Targets: Regulation of Notch3 by the Bromodomain Protein BRD4
17. Inhibition of YAP/TAZ-driven TEAD activity prevents growth of NF2-null schwannoma and meningioma
18. A widely-applicable high-throughput cellular thermal shift assay (CETSA) using split Nano Luciferase
19. DDB2 represses ovarian cancer cell dedifferentiation by suppressing ALDH1A1
20. Retro Drug Design: From Target Properties to Molecular Structures
21. Inhibition of YAP/TAZ-driven TEAD activity prevents growth of NF2-null schwannoma and meningioma.
22. CN470 is a BET/CBP/p300 multi-bromodomain inhibitor and has an anti-tumor activity against MLL-rearranged acute lymphoblastic leukemia
23. A Genome-Edited ERα-HiBiT Fusion Reporter Cell Line for the Identification of ERα Modulators Via High-Throughput Screening and CETSA
24. A quinazoline‐based bromodomain inhibitor, CN210 , ameliorates indomethacin‐induced ileitis in mice by inhibiting inflammatory cytokine expression
25. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome
26. Synthesis of polycyclic and 4,5-diacylthiophene-2-carboxylates via intramolecular Friedel–Crafts alkylations and unusual autooxidative fragmentation of the derivatives obtained from the samarium diiodide-promoted coupling reactions of thiophene-2-carboxylate with carbonyl compounds
27. Lead optimization and efficacy evaluation of quinazoline-based BET family inhibitors for potential treatment of cancer and inflammatory diseases
28. Pyrazole-Based Lactate Dehydrogenase Inhibitors with Optimized Cell Activity and Pharmacokinetic Properties
29. Abstract 1745: Application of BET/CBP/p300 multi-bromodomain inhibitors as a novel therapeutic strategy for MLL-rearranged acute lymphoblastic leukemia
30. Abstract 5957: Roles for the cancer stem cell marker Aldh1A1 in Merlin null nervous system tumors
31. Ameliorative effect of a quinazoline-based bromodomain inhibitor, CN210, on experimentally-induced Crohn’s disease-like murine ileitis via inhibition of inflammatory cytokine expression
32. Coupling reactions and coupling-alkylations of thiophenecarbaldehydes promoted by samarium diiodide
33. Chapter 4 Application of silicon-assisted intramolecular cross-coupling in total synthesis of (+)-brasilenyne
34. Indolecarbonyl coupling reactions promoted by samarium diiodide: application to the synthesis of indole-fused compounds
35. Sequential ring-closing metathesis/Pd-catalyzed, Si-assisted cross-coupling reactions: general synthesis of highly substituted unsaturated alcohols and medium-sized rings containing a 1,3- cis– cis diene unit
36. Discovery and lead identification of quinazoline-based BRD4 inhibitors
37. Ameliorative effect of a novel BET inhibitor CN210 on experimentally-induced murine Crohn's disease-like ileitis via inhibition of inflammatory cytokine expression
38. Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol
39. Predicting Novel Therapies and Targets: Regulation of Notch3 by the Bromodomain Protein BRD4
40. Author response: Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol
41. Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol
42. Discovery of Orally Bioavailable, Quinoline-Based Aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitors with Potent Cellular Activity
43. Correction: A High-Content Assay Enables the Automated Screening and Identification of Small Molecules with Specific ALDH1A1-Inhibitory Activity
44. Discovery and Optimization of Potent, Cell-Active Pyrazole-Based Inhibitors of Lactate Dehydrogenase (LDH)
45. Crystal Structure of LCAT Bound to a Small Molecule Allosteric Activator Reveals its Active Conformation
46. A High-Content Assay Enables the Automated Screening and Identification of Small Molecules with Specific ALDH1A1-Inhibitory Activity
47. 4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable stearoyl-CoA desaturase-1 (SCD1) inhibitors: Part 2. Pyridazine-based analogs
48. A High-Throughput Screen Identifies 2,9-Diazaspiro[5.5]Undecanes as Inducers of the Endoplasmic Reticulum Stress Response with Cytotoxic Activity in 3D Glioma Cell Models
49. 4-Bicyclic heteroaryl-piperidine derivatives as potent, orally bioavailable Stearoyl-CoA desaturase-1 (SCD1) inhibitors. Part 1: Urea-based analogs
50. A High-Throughput Screen Identifies 2,9-Diazaspiro[5.5]Undecanes as Inducers of the Endoplasmic Reticulum Stress Response with Cytotoxic Activity in 3D Glioma Cell Models
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