All Stories

  1. Bictegravir in a fixed-dose tablet with emtricitabine and tenofovir alafenamide for the treatment of HIV infection: pharmacology and clinical implications
  2. Investigational drugs for the treatment of Zika virus infection: a preclinical and clinical update
  3. Erratum for Mesplède et al., “The R263K Dolutegravir Resistance-Associated Substitution Progressively Decreases HIV-1 Integration”
  4. Reply to Darcis and Berkhout
  5. Exploring an alternative explanation for the second phase of viral decay: Infection of short-lived cells in a drug-limited compartment during HAART
  6. Where are we with injectables against HIV infection and what are the remaining challenges?
  7. Investigational HIV integrase inhibitors in phase I and phase II clinical trials
  8. Antiviral Activity of Bictegravir and Cabotegravir against Integrase Inhibitor-Resistant SIVmac239 and HIV-1
  9. HIV-1 Resistance to Dolutegravir Is Affected by Cellular Histone Acetyltransferase Activity
  10. HIV drug resistance against strand transfer integrase inhibitors
  11. Differences among HIV-1 subtypes in drug resistance against integrase inhibitors
  12. The M184I/V and K65R nucleoside resistance mutations in HIV-1 prevent the emergence of resistance mutations against dolutegravir
  13. Will LEDGIN molecules be able to play a role in a cure for HIV infection?
  14. Might dolutegravir be part of a functional cure for HIV?1
  15. Effect on HIV-1 viral replication capacity of DTG-resistance mutations in NRTI/NNRTI resistant viruses
  16. Polymorphic substitution E157Q in HIV-1 integrase increases R263K-mediated dolutegravir resistance and decreases DNA binding activity
  17. Development of a G118R mutation in HIV-1 integrase following a switch to dolutegravir monotherapy leading to cross-resistance to integrase inhibitors
  18. The dolutegravir R263K resistance mutation in HIV-1 integrase is incompatible with the emergence of resistance against raltegravir
  19. Characterization of the Drug Resistance Profiles of Integrase Strand Transfer Inhibitors in Simian Immunodeficiency Virus SIVmac239
  20. HIV-1 Group O Resistance Against Integrase Inhibitors
  21. The Combination of the R263K and T66I Resistance Substitutions in HIV-1 Integrase Is Incompatible with High-Level Viral Replication and the Development of High-Level Drug Resistance
  22. Dolutegravir-Selected HIV-1 Containing the N155H and R263K Resistance Substitutions Does Not Acquire Additional Compensatory Mutations under Drug Pressure That Lead to Higher-Level Resistance and Increased Replicative Capacity
  23. Resistance against Integrase Strand Transfer Inhibitors and Relevance to HIV Persistence
  24. Dolutegravir maintains a durable effect against HIV replication in tissue culture even after drug washout
  25. The R263K substitution in HIV-1 subtype C is more deleterious for integrase enzymatic function and viral replication than in subtype B
  26. A resveratrol analog termed 3,3′,4,4′,5,5′-hexahydroxy-trans-stilbene is a potent HIV-1 inhibitor
  27. Structural Studies of the HIV-1 Integrase Protein: Compound Screening and Characterization of a DNA-Binding Inhibitor
  28. Dolutegravir inhibits HIV-1 Env evolution in primary human cells
  29. Combination of the R263K and M184I/V Resistance Substitutions against Dolutegravir and Lamivudine Decreases HIV Replicative Capacity
  30. Dolutegravir Resistance Mutation R263K Cannot Coexist in Combination with Many Classical Integrase Inhibitor Resistance Substitutions
  31. Identification of a dibenzocyclooctadiene lignan as a HIV-1 non-nucleoside reverse transcriptase inhibitor
  32. Simian-Tropic HIV as a Model To Study Drug Resistance against Integrase Inhibitors
  33. Differential Effects of the G118R, H51Y, and E138K Resistance Substitutions in Different Subtypes of HIV Integrase
  34. The dual CCR5 and CCR2 inhibitor cenicriviroc does not redistribute HIV into extracellular space: implications for plasma viral load and intracellular DNA decline
  35. The R262K Substitution Combined with H51Y in HIV-1 Subtype B Integrase Confers Low-Level Resistance against Dolutegravir
  36. Fitness Impaired Drug Resistant HIV-1 Is Not Compromised in Cell-to-Cell Transmission or Establishment of and Reactivation from Latency
  37. HIV-1 Group O Integrase Displays Lower Enzymatic Efficiency and Higher Susceptibility to Raltegravir than HIV-1 Group M Subtype B Integrase
  38. Exposure to Entry Inhibitors Alters HIV Infectiousness and Sensitivity to Broadly Neutralizing Monoclonal Antibodies
  39. Is Resistance to Dolutegravir Possible When This Drug Is Used in First-Line Therapy?
  40. Effect of HIV-1 Integrase Resistance Mutations When Introduced into SIVmac239 on Susceptibility to Integrase Strand Transfer Inhibitors
  41. Addition of E138K to R263K in HIV integrase increases resistance to dolutegravir, but fails to restore activity of the HIV integrase enzyme and viral replication capacity
  42. Integrase strand transfer inhibitors in the management of HIV-positive individuals
  43. Resistance mutations against dolutegravir in HIV integrase impair the emergence of resistance against reverse transcriptase inhibitors
  44. The M50I polymorphic substitution in association with the R263K mutation in HIV-1 subtype B integrase increases drug resistance but does not restore viral replicative fitness
  45. What if HIV were unable to develop resistance against a new therapeutic agent?
  46. Integrase Strand Transfer Inhibitors in HIV Therapy
  47. Biochemical Analysis of the Role of G118R-Linked Dolutegravir Drug Resistance Substitutions in HIV-1 Integrase
  48. Development of a fluorescence-based HIV-1 integrase DNA binding assay for identification of novel HIV-1 integrase inhibitors
  49. Productive Entry of HIV-1 during Cell-to-Cell Transmission via Dynamin-Dependent Endocytosis
  50. Automethylation of protein arginine methyltransferase 6 (PRMT6) regulates its stability and its anti-HIV-1 activity
  51. Viral fitness cost prevents HIV-1 from evading dolutegravir drug pressure
  52. Evolution of HIV integrase resistance mutations
  53. HIV Drug Resistance and the Advent of Integrase Inhibitors
  54. The development of novel HIV integrase inhibitors and the problem of drug resistance
  55. A high-throughput assay for HIV-1 integrase 3′-processing activity using time-resolved fluorescence
  56. Resistance to HIV integrase inhibitors
  57. HIV gp120 H375 Is Unique to HIV-1 Subtype CRF01_AE and Confers Strong Resistance to the Entry Inhibitor BMS-599793, a Candidate Microbicide Drug
  58. Characterization of the R263K Mutation in HIV-1 Integrase That Confers Low-Level Resistance to the Second-Generation Integrase Strand Transfer Inhibitor Dolutegravir