27 results on '"Winters, Michael"'
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2. Two-component irreversible adsorption with pore diffusion control – Experimental verification of a theory for protein adsorption on core–shell resins
3. Impact of aluminum adjuvants on the stability of pneumococcal polysaccharide-protein conjugate vaccines
4. Theory of two-component irreversible adsorption with pore diffusion control
5. Immunogenicity of PCV24, an expanded pneumococcal conjugate vaccine, in adult monkeys and protection in mice
6. Immunogenicity differences of a 15-valent pneumococcal polysaccharide conjugate vaccine (PCV15) based on vaccine dose, route of immunization and mouse strain
7. Balancing noise sensitivity, response latency, and posture accuracy for a computer-assisted canine posture training system
8. Dynamic structural changes during complement C3 activation analyzed by hydrogen/deuterium exchange mass spectrometry
9. Discovery and optimization of a novel series of pyrazolyltetrahydropyran N-type calcium channel (Cav 2.2) blockers for the treatment of pain
10. Erratum to “Discovery of N-arylpyrroles as agonists of GPR120 for the treatment of type II diabetes” Bioorg. Med. Chem. Lett. 28 (2018) [841–846]
11. Discovery of N-arylpyrroles as agonists of GPR120 for the treatment of type II diabetes
12. Discovery of novel benzo[b]thiophene tetrazoles as non-carboxylate GPR40 agonists
13. Design, synthesis and SAR of a novel series of heterocyclic phenylpropanoic acids as GPR120 agonists
14. Discovery and SAR of a novel series of 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles as N-type calcium channel inhibitors
15. Discovery and SAR of novel tetrahydropyrrolo[3,4-c]pyrazoles as inhibitors of the N-type calcium channel
16. The discovery and SAR of cyclopenta[b]furans as inhibitors of CCR2
17. Synthesis of substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles by intramolecular nitrilimine cycloaddition
18. A novel series of pyrazolylpiperidine N-type calcium channel blockers
19. Itk kinase inhibitors: Initial efforts to improve the metabolical stability and the cell activity of the benzimidazole lead
20. Discovery, SAR and X-ray structure of 1 H-benzimidazole-5-carboxylic acid cyclohexyl-methyl-amides as inhibitors of inducible T-cell kinase (Itk)
21. 5-Aminomethyl-1 H-benzimidazoles as orally active inhibitors of inducible T-cell kinase (Itk)
22. Carboxylic acid bioisosteres acylsulfonamides, acylsulfamides, and sulfonylureas as novel antagonists of the CXCR2 receptor
23. Hit-to-lead studies on benzimidazole inhibitors of ITK: Discovery of a novel class of kinase inhibitors
24. Discovery and SAR of novel [1,6]Naphthyridines as potent inhibitors of spleen tyrosine kinase (SYK)
25. Corrigendum to “Discovery, SAR and X-ray structure of 1 H-benzimidazole-5-carboxylic acid cyclohexyl-methyl-amides as inhibitors of inducible T-cell kinase (Itk)” [Bioorg. Med. Chem. Lett. 18 (2008) 5545–5549]
26. New N- and O-arylations with phenylboronic acids and cupric acetate
27. New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
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