All Stories

  1. New model integrates innate responses, PML‐NB formation, epigenetic control and reactivation from latency
  2. The Exonuclease Activity of Herpes Simplex Virus 1 UL12 Is Required for Production of Viral DNA That Can Be Packaged To Produce Infectious Virus
  3. ICP8 Filament Formation Is Essential for Replication Compartment Formation during Herpes Simplex Virus Infection
  4. The Putative Herpes Simplex Virus 1 Chaperone Protein UL32 Modulates Disulfide Bond Formation during Infection
  5. Recombination Promoted by DNA Viruses: Phage λ to Herpes Simplex Virus
  6. Structure of the Herpes Simplex Virus 1 Genome: Manipulation of Nicks and Gaps Can Abrogate Infectivity and Alter the Cellular DNA Damage Response
  7. New Herpes Simplex Virus Replication Targets
  8. Herpes Simplex Virus DNA Replication and Genome Maturation
  9. HSV-1 Protein Expression Using Recombinant Baculoviruses
  10. Herpes Simplex Virus Type 1 Single Strand DNA Binding Protein and Helicase/Primase Complex Disable Cellular ATR Signaling
  11. A short commentary on the review by Weller and Kuchta: the DNA helicase–primase complex as a target for herpes virus infection
  12. The DNA helicase–primase complex as a target for herpes viral infection
  13. Efficient Herpes Simplex Virus 1 Replication Requires Cellular ATR Pathway Proteins
  14. The HSV-1 Exonuclease, UL12, Stimulates Recombination by a Single Strand Annealing Mechanism
  15. DNA Mismatch Repair Proteins Are Required for Efficient Herpes Simplex Virus 1 Replication
  16. Disulfide Bond Formation Contributes to Herpes Simplex Virus Capsid Stability and Retention of Pentons
  17. Disulfide Bond Formation in the Herpes Simplex Virus 1 UL6 Protein Is Required for Portal Ring Formation and Genome Encapsidation
  18. Herpes Simplex Virus Reorganizes the Cellular DNA Repair and Protein Quality Control Machinery
  19. Herpes Simplex Virus Type 1 Helicase-Primase: DNA Binding and Consequent Protein Oligomerization and Primase Activation
  20. Physical Interaction between the Herpes Simplex Virus Type 1 Exonuclease, UL12, and the DNA Double-Strand Break-Sensing MRN Complex
  21. ATR and ATRIP Are Recruited to Herpes Simplex Virus Type 1 Replication Compartments Even though ATR Signaling Is Disabled
  22. DNA Virus Replication
  23. Herpes Simplex Virus Type 1 Immediate-Early Protein ICP22 Is Required for VICE Domain Formation during Productive Viral Infection
  24. Virus-Induced Chaperone-Enriched (VICE) Domains Function as Nuclear Protein Quality Control Centers during HSV-1 Infection
  25. Herpesvirus Genome Replication
  26. Oligomerization of ICP4 and Rearrangement of Heat Shock Proteins May Be Important for Herpes Simplex Virus Type 1 Prereplicative Site Formation
  27. Direct Interaction between the N- and C-Terminal Portions of the Herpes Simplex Virus Type 1 Origin Binding Protein UL9 Implies the Formation of a Head-to-Tail Dimer
  28. Enhanced Phosphorylation of Transcription Factor Sp1 in Response to Herpes Simplex Virus Type 1 Infection Is Dependent on the Ataxia Telangiectasia-Mutated Protein
  29. A Putative Leucine Zipper within the Herpes Simplex Virus Type 1 UL6 Protein Is Required for Portal Ring Formation
  30. A Mutation in the Human Herpes Simplex Virus Type 1 UL52 Zinc Finger Motif Results in Defective Primase Activity but Can Recruit Viral Polymerase and Support Viral Replication Efficiently
  31. Herpes simplex virus eliminates host mitochondrial DNA
  32. DNA Binding Activity of the Herpes Simplex Virus Type 1 Origin Binding Protein, UL9, Can Be Modulated by Sequences in the N Terminus: Correlation between Transdominance and DNA Binding
  33. Herpes Simplex Virus Type 1 DNA Polymerase Requires the Mammalian Chaperone Hsp90 for Proper Localization to the Nucleus
  34. Mutations in the Putative Zinc-Binding Motif of UL52 Demonstrate a Complex Interdependence between the UL5 and UL52 Subunits of the Human Herpes Simplex Virus Type 1 Helicase/Primase Complex
  35. Herpes Simplex Virus Type 1 Single-Strand DNA Binding Protein ICP8 Enhances the Nuclease Activity of the UL12 Alkaline Nuclease by Increasing Its Processivity
  36. Inhibition of the Herpes Simplex Virus Type 1 DNA Polymerase Induces Hyperphosphorylation of Replication Protein A and Its Accumulation at S-Phase-Specific Sites of DNA Damage during Infection
  37. Catalysis of Strand Exchange by the HSV-1 UL12 and ICP8 Proteins: Potent ICP8 Recombinase Activity is Revealed upon Resection of dsDNA Substrate by Nuclease
  38. The UL12.5 Gene Product of Herpes Simplex Virus Type 1 Exhibits Nuclease and Strand Exchange Activities but Does Not Localize to the Nucleus
  39. Recruitment of Cellular Recombination and Repair Proteins to Sites of Herpes Simplex Virus Type 1 DNA Replication Is Dependent on the Composition of Viral Proteins within Prereplicative Sites and Correlates with the Induction of the DNA Damage Response
  40. Point Mutations in Exon I of the Herpes Simplex Virus Putative Terminase Subunit, UL15, Indicate that the Most Conserved Residues Are Essential for Cleavage and Packaging
  41. Existence of Transdominant and Potentiating Mutants of UL9, the Herpes Simplex Virus Type 1 Origin-Binding Protein, Suggests that Levels of UL9 Protein May Be Regulated during Infection
  42. The Role of DNA Recombination in Herpes Simplex Virus DNA Replication
  43. The Herpes Simplex Virus Type 1 Alkaline Nuclease and Single-Stranded DNA Binding Protein Mediate Strand Exchange In Vitro
  44. Recruitment of Polymerase to Herpes Simplex Virus Type 1 Replication Foci in Cells Expressing Mutant Primase (UL52) Proteins
  45. Helicase Motif Ia Is Involved in Single-Strand DNA-Binding and Helicase Activities of the Herpes Simplex Virus Type 1 Origin-Binding Protein, UL9
  46. The Product of the UL12.5 Gene of Herpes Simplex Virus Type 1 Is Not Essential for Lytic Viral Growth and Is Not Specifically Associated with Capsids
  47. The UL6 Gene Product Forms the Portal for Entry of DNA into the Herpes Simplex Virus Capsid
  48. Interactions of Herpes Simplex Virus Type 1 with ND10 and Recruitment of PML to Replication Compartments
  49. Herpes Simplex Virus DNA Cleavage and Packaging Proteins Associate with the Procapsid prior to Its Maturation
  50. A tale of two HSV-1 helicases: Roles of phage and animal virus helicases in DNA replication and recombination
  51. Evidence for Controlled Incorporation of Herpes Simplex Virus Type 1 UL26 Protease into Capsids
  52. Isolation of Herpes Simplex Virus Procapsids from Cells Infected with a Protease-Deficient Mutant Virus
  53. Functional Conservations of the Alkaline Nuclease of Herpes Simplex Type 1 and Human Cytomegalovirus
  54. The Exonuclease Activity of HSV-1 UL12 Is Required forin VivoFunction
  55. Genetic Analysis of the UL15 Gene Locus for the Putative Terminase of Herpes Simplex Virus Type 1
  56. The Herpes Simplex Virus Type 1 UL6 Protein Is Essential for Cleavage and Packaging but Not for Genomic Inversion
  57. Intracellular Localization of the Herpes Simplex Virus Type-1 Origin Binding Protein, UL9
  58. Replacement of Gly815 in Helicase Motif V Alters the Single-stranded DNA-dependent ATPase Activity of the Herpes Simplex Virus Type 1Helicase-Primase
  59. The Herpes Simplex Virus Type 1 Transactivator ICP0 Mediates Aberrant Intracellular Localization of the Viral Helicase/Primase Complex Subunits
  60. The Product of a 1.9-kb mRNA Which Overlaps the HSV-1 Alkaline Nuclease Gene (UL12) Cannot Relieve the Growth Defects of a Null Mutant
  61. Phase I trial of valaciclovir, the L-valyl ester of acyclovir, in patients with advanced human immunodeficiency virus disease.
  62. Herpes Simplex Virus 1 Alkaline Nuclease Is Required for Efficient Egress of Capsids from the Nucleus
  63. Genetic analysis of the herpes simplex virus type 1 UL9 gene: Isolation of a lacZ insertion mutant and expression in eukaryotic cells
  64. The Herpes Simplex Virus Type 1 Alkaline Nuclease is Not Essential for Viral DNA Synthesis: Isolation and Characterization of a lacZ Insertion Mutant
  65. Herpes simplex virus type 1 mutants for the origin-binding protein induce DNA amplification in the absence of viral replication
  66. A herpes simplex virus ribonucleotide reductase deletion mutant is defective for productive acute and reactivatable latent infections of mice and for replication in mouse cells
  67. Herpes Simplex Virus Ribonucleotide Reductase Mutants Are Hypersensitive to Acyclovir
  68. Herpes simplex virus ribonucleotide reductase mutants are hypersensitive to acyclovir.
  69. Herpes simplex virus 1 helicase-primase: a complex of three herpes-encoded gene products.
  70. UL5, A protein required for HSV DNA synthesis: Genetic analysis, overexpression in Escherichia coli, and generation of polyclonal antibodies
  71. Factor(s) present in herpes simplex virus type 1-infected cells can compensate for the loss of the large subunit of the viral ribonucleotide reductase: characterization of an ICP6 deletion mutant
  72. Genetic and phenotypic characterization of mutants in four essential genes that map to the left half of HSV-1 UL DNA
  73. Sequence and mapping analyses of the herpes simplex virus DNA polymerase gene predict a C-terminal substrate binding domain.
  74. Mutations in the herpes simplex virus major DNA-binding protein gene leading to altered sensitivity to DNA polymerase inhibitors
  75. Genetics of Herpes Simplex Virus.
  76. Genetics of Herpes Simplex Virus
  77. Genetic analysis of temperature-sensitive mutants of HSV-1: The combined use of complementation and physical mapping for cistron assignment
  78. Correlation of Transient Accumulation of Linear Unintegrated Viral DNA and Transient Cell Killing by Avian Leukosis and Reticuloendotheliosis Viruses
  79. Cleavage and Packaging of Herpes Simplex Virus 1 DNA