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2. Uncovering the Nonnegligible Mechanism of Degrading Structural Extracellular Polymeric Substances for Nitrate Removal in Psychrophilic (15 °C) Waste-Activated Sludge Fermentation

4. Correction to “Discovery of RORγ Allosteric Fluorescent Probes and Their Application: Fluorescence Polarization, Screening, and Bioimaging”

5. Discovery of RORγ Allosteric Fluorescent Probes and Their Application: Fluorescence Polarization, Screening, and Bioimaging

6. Insight into Janus kinases specificity: From molecular architecture to cancer therapeutics

8. Genome assembly of autotetraploid Actinidia arguta highlights adaptive evolution and enables dissection of important economic traits

11. Design and Synthesis 1H-Pyrrolo[2,3-b]pyridine Derivatives as FLT3 Inhibitors for the Treatment of Acute Myeloid Leukemia

16. Preclinical characterization of danatinib as a novel FLT3 inhibitor with excellent efficacy against resistant acute myeloid leukemia

19. Aging rate, environmental risk and production efficiency of the low-density polyethylene (LDPE) films with contrasting thickness in irrigated region

20. An SAR Study on a Class of 6-(Trifluoromethyl)-pyridine Derivatives as RORγt Inverse Agonists

21. Glucose status within dark-grown etiolated cotyledons determines seedling de-etiolation upon light irradiation

25. Natural products as potential lead compounds to develop new antiviral drugs over the past decade

28. Can shallow-incorporated organic mulching replace plastic film mulching for irrigated maize production systems in arid environments?

29. Scaffold-hopping of Linifanib to Design 6-Phenylisoxazolo[3,4-b]pyridin-3-amine Derivatives as FLT3 Inhibitors for Treating Acute Myeloid Leukemia

36. Synthesis and Biological Evaluation of 2-Amino-1-phenyl-benzimidazole Derivatives as BACE1 Inhibitors

38. Intraoperative Low-Dose S-Ketamine Reduces Depressive Symptoms in Patients with Crohn’s Disease Undergoing Bowel Resection: A Randomized Controlled Trial

41. Discovery of 4‐(4‐aminophenyl)‐6‐phenylisoxazolo[3,4‐ b ]pyridine‐3‐amine derivatives as novel FLT3 covalent inhibitors for the intervention of acute myeloid leukemia

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