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46 results on '"Mason, Stephen W."'

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1. JNJ-7184, a respiratory syncytial virus inhibitor targeting the connector domain of the viral polymerase

2. Preclinical characterization of an intravenous coronavirus 3CL protease inhibitor for the potential treatment of COVID19

4. Discovery of Novel Small-Molecule HIV-1 Replication Inhibitors That Stabilize Capsid Complexes

7. An oral SARS-CoV-2 M pro inhibitor clinical candidate for the treatment of COVID-19

8. An Oral SARS-CoV-2 Mpro Inhibitor Clinical Candidate for the Treatment of COVID-19

9. Discovery of a Novel Inhibitor of Coronavirus 3CL Protease for the Potential Treatment of COVID-19

10. Modified Alphavirus-Vesiculovirus Hybrid Vaccine Vectors for Homologous Prime-Boost Immunotherapy of Chronic Hepatitis B

13. Clinical Trial of the Anti-PD-L1 Antibody BMS-936559 in HIV-1 Infected Participants on Suppressive Antiretroviral Therapy

16. Transcriptional antitermination

19. Virus-like vesicles expressing multiple antigens for immunotherapy of chronic hepatitis B

22. Safety and efficacy of anti-PD-L1 therapy in the woodchuck model of HBV infection

23. Aligning Potency and Pharmacokinetic Properties for Pyridine-Based NCINIs

24. Blockade of the PD-1 axis alone is not sufficient to activate HIV-1 virion production from CD4+ T cells of individuals on suppressive ART.

25. Inhibition of HIV-1 capsid assembly: Optimization of the antiviral potency by site selective modifications at N1, C2 and C16 of a 5-(5-furan-2-yl-pyrazol-1-yl)-1H-benzimidazole scaffold

27. Identification of BI-C, a Novel HIV-1 Non-Catalytic Site Integrase Inhibitor

28. Minimizing the Contribution of Enterohepatic Recirculation to Clearance in Rat for the NCINI Class of Inhibitors of HIV

29. Distinct Effects of Two HIV-1 Capsid Assembly Inhibitor Families That Bind the Same Site within the N-Terminal Domain of the Viral CA Protein

30. Discovery of BI 224436, a Noncatalytic Site Integrase Inhibitor (NCINI) of HIV-1

32. Novel Inhibitor Binding Site Discovery on HIV-1 Capsid N-Terminal Domain by NMR and X-ray Crystallography

33. Inside Cover: Monitoring Binding of HIV-1 Capsid Assembly Inhibitors Using19F Ligand-and15N Protein-Based NMR and X-ray Crystallography: Early Hit Validation of a Benzodiazepine Series (ChemMedChem 3/2013)

34. Monitoring Binding of HIV-1 Capsid Assembly Inhibitors Using19F Ligand-and15N Protein-Based NMR and X-ray Crystallography: Early Hit Validation of a Benzodiazepine Series

35. Inhibitors of Respiratory Syncytial Virus Replication Target Cotranscriptional mRNA Guanylylation by Viral RNA-Dependent RNA Polymerase

36. Distinct Effects of Two HIV-1 Capsid Assembly Inhibitor Families That Bind the Same Site within the N-Terminal Domain of the Viral CA Protein

37. Inhibitors of Respiratory Syncytial Virus Replication Target Cotranscriptional mRNA Guanylylation by Viral RNA-Dependent RNA Polymerase

40. A novel inhibitor-binding site on the HIV-1 capsid N-terminal domain leads to improved crystallization via compound-mediated dimerization.

44. RNA polymerase I transcription termination: similar mechanisms are employed by yeast and mammals11Edited by M. Yaniv

45. Discovery of a Novel Inhibitor of Coronavirus 3CL Protease for the Potential Treatment of COVID-19.

46. Monitoring binding of HIV-1 capsid assembly inhibitors using (19)F ligand-and (15)N protein-based NMR and X-ray crystallography: early hit validation of a benzodiazepine series.

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