All Stories

  1. GSK2878175, a pan-genotypic non-nucleoside NS5B polymerase inhibitor, in healthy and treatment-naïve chronic hepatitis C subjects
  2. Pharmacokinetic Characteristics, Pharmacodynamic Effect and In Vivo Antiviral Efficacy of Liver-Targeted Interferon Alpha
  3. Plasma Pro-C3 (N-terminal type III collagen propeptide) predicts fibrosis progression in patients with chronic hepatitis C
  4. P1224 GSK2878175, A POTENT NON-NUCLEOSIDE INHIBITOR OF HCV NS5B WITH PAN-GENOTYPIC ACTIVITY
  5. O119 IN VIVO INHIBITION OF HBV ANTIGENEMIA AND VIREMIA BY ANTISENSE OLIGONUCLEOTIDES
  6. Novel Spiroketal Pyrrolidine GSK2336805 Potently Inhibits Key Hepatitis C Virus Genotype 1b Mutants: From Lead to Clinical Compound
  7. Hepatitis C Replication Inhibitors That Target the Viral NS4B Protein
  8. Discovery of a Potent Boronic Acid Derived Inhibitor of the HCV RNA-Dependent RNA Polymerase
  9. A Double-blind, randomized, placebo-controlled study to assess the safety, antiviral activity and pharmacokinetics of GSK2336805 when given as monotherapy and in combination with peginterferon alfa-2a and ribavirin in hepatitis C virus genotype 1-infected
  10. Preclinical Characterization of GSK2336805, a Novel Inhibitor of Hepatitis C Virus Replication That Selects for Resistance in NS5A
  11. Pharmacological disruption of hepatitis C NS5A protein intra- and intermolecular conformations
  12. In VitroCharacterization of GSK2485852, a Novel Hepatitis C Virus Polymerase Inhibitor
  13. Synthesis and antiviral activity of novel HCV NS3 protease inhibitors with P4 capping groups
  14. Discovery of Novel Urea-Based Hepatitis C Protease Inhibitors with High Potency against Protease-Inhibitor-Resistant Mutants
  15. Hepatitis C genotype 1a replicon improved through introduction of fitness mutations
  16. Discovery of novel P3-oxo inhibitor of hepatitis C virus NS3/4A serine protease
  17. HCV Inhibition Mediated Through the Nonstructural Protein 5A (NS5A) Replication Complex
  18. 764 IN VITRO PROFILING OF GSK2336805, A POTENT AND SELECTIVE INHIBITOR OF HCV NS5A
  19. 818 PRECLINICAL CHARACTERIZATION OF GSK2485852, A NOVEL HCV POLYMERASE INHIBITOR
  20. RDEA119/BAY 869766: A Potent, Selective, Allosteric Inhibitor of MEK1/2 for the Treatment of Cancer
  21. 577 POSTER Selective MEK Inhibitor RDEA119 exhibits efficacy in orthotopic hepatoma models and cytostatic potential in multiple cell based models of cancer
  22. A Novel NNRTI Class with Potent Anti-HIV Activity Against NNRTI-resistant Viruses
  23. Entecavir for Treatment of Hepatitis B Virus Displays No In Vitro Mitochondrial Toxicity or DNA Polymerase Gamma Inhibition
  24. Cyclic Monophosphate Prodrugs of Base-Modified 2′-C-Methyl Ribonucleosides as Potent Inhibitors of Hepatitis C Virus RNA Replication.
  25. Identification and Structure—Activity Relationships of Substituted Pyridones as Inhibitors of Pim-1 Kinase.
  26. 6-Hydrazinopurine 2′-methyl ribonucleosides and their 5′-monophosphate prodrugs as potent hepatitis C virus inhibitors
  27. Cyclic monophosphate prodrugs of base-modified 2′-C-methyl ribonucleosides as potent inhibitors of hepatitis C virus RNA replication
  28. Thiazolone-acylsulfonamides as novel HCV NS5B polymerase allosteric inhibitors: Convergence of structure-based drug design and X-ray crystallographic study
  29. Identification and structure–activity relationships of substituted pyridones as inhibitors of Pim-1 kinase
  30. Novel thiazolones as HCV NS5B polymerase allosteric inhibitors: Further designs, SAR, and X-ray complex structure
  31. Isothiazoles as active-site inhibitors of HCV NS5B polymerase
  32. A Novel Nonnucleoside Analogue That Inhibits Human Immunodeficiency Virus Type 1 Isolates Resistant to Current Nonnucleoside Reverse Transcriptase Inhibitors
  33. Identification of isothiazole-4-carboxamidines derivatives as a novel class of allosteric MEK1 inhibitors
  34. Structure-based design of a novel thiazolone scaffold as HCV NS5B polymerase allosteric inhibitors
  35. Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase
  36. Discovery of 3-hydroxy-4-carboxyalkylamidino-5-arylamino-isothiazoles as potent MEK1 inhibitors
  37. Novel Nonnucleoside Inhibitors That Select Nucleoside Inhibitor Resistance Mutations in Human Immunodeficiency Virus Type 1 Reverse Transcriptase
  38. Hepatitis B and D Protocols–Volume I: Detection, Genotypes, and Characterization. Robert K. Hamatake and Johnson Y.N. Lau, editors. Totowa, NJ: Humana Press, 2004, 374 pp., $125.00, hardcover. ISBN 1-58829-105-7.
  39. Hepatitis B and D Protocols–Volume II: Immunology, Model Systems, and Clinical Studies. Robert K. Hamatake and Johnson Y.N. Lau, editors. Totowa, NJ: Humana Press, 2004, 596 pp., $135.00, hardcover. ISBN 1-58829-108-1.
  40. Hepatitis B and D Protocols
  41. Hepatitis B and D Protocols
  42. The Rep Protein of Adeno-Associated Virus Type 2 Interacts with Single-Stranded DNA-Binding Proteins That Enhance Viral Replication
  43. HEP DART 2003: Frontiers in Drug Development for Viral Hepatitis
  44. Agents in clinical development for the treatment of chronic hepatitis B
  45. Antiviral Agents for Hepatitis Viruses
  46. De Novo Initiation of RNA Synthesis by the RNA-Dependent RNA Polymerase (NS5B) of Hepatitis C Virus
  47. Establishment of an in vitro Assay to Characterize Hepatitis C Virus NS3-4A Protease Trans-Processing Activity
  48. Characterization of monoclonal antibodies recognizing amino- and carboxy-terminal epitopes of the herpes simplex virus UL42 protein
  49. The herpes simplex virus type 1 DNA polymerase accessory protein, UL42, contains a functional protease-resistant domain
  50. DPB2, the gene encoding DNA polymerase II subunit B, is required for chromosome replication in Saccharomyces cerevisiae.
  51. Cloning DPB3 , the gene encoding the third subunit of DNA polymerase II of Saccharomyces cerevisiae
  52. A third essential DNA polymerase in S. cerevisiae
  53. The J gene of ?X174: Isolation and characterization of a J gene mutant
  54. In vitro synthesis of bacteriophage phi X174 by purified components.
  55. Morphogenesis of phi X174: in vitro synthesis of infectious phage from purified viral components.
  56. Role of DNA gyrase subunits in synthesis of bacteriophage phi X174 viral DNA.
  57. Isolation and identification of bacteriophage phi X174 prohead.