All Stories

  1. Generation of an Oncolytic Herpes Simplex Viral Vector Completely Retargeted to the GDNF Receptor GFRα1 for Specific Infection of Breast Cancer Cells
  2. Protocol Optimization for the Production of the Non-Cytotoxic JΔNI5 HSV Vector Deficient in Expression of Immediately Early Genes
  3. Point Mutations in Retargeted gD Eliminate the Sensitivity of EGFR/EGFRvIII-Targeted HSV to Key Neutralizing Antibodies
  4. Herpes Simplex Virus Vectors for Gene Transfer to the Central Nervous System
  5. Cellular Antisilencing Elements Support Transgene Expression from Herpes Simplex Virus Vectors in the Absence of Immediate Early Gene Expression
  6. A Novel Oncolytic Herpes Simplex Virus Design based on the Common Overexpression of microRNA-21 in Tumors
  7. Deletion of the Virion Host Shut-off Gene Enhances Neuronal-Selective Transgene Expression from an HSV Vector Lacking Functional IE Genes
  8. Engineered HSV vector achieves safe long-term transgene expression in the central nervous system
  9. Syncytial Mutations Do Not Impair the Specificity of Entry and Spread of a Glycoprotein D Receptor-Retargeted Herpes Simplex Virus
  10. Constitutive Expression of GATA4 Dramatically Increases the Cardiogenic Potential of D3 Mouse Embryonic Stem Cells
  11. Development of an oncolytic HSV vector fully retargeted specifically to cellular EpCAM for virus entry and cell-to-cell spread
  12. An HSV-based library screen identifies PP1α as a negative TRPV1 regulator with analgesic activity in models of pain
  13. Moving toward a gene therapy for Huntington’s disease
  14. CAR-Engineered NK Cells Targeting Wild-Type EGFR and EGFRvIII Enhance Killing of Glioblastoma and Patient-Derived Glioblastoma Stem Cells
  15. Herpes simplex viral-vector design for efficient transduction of nonneuronal cells without cytotoxicity
  16. Use of miRNA Response Sequences to Block Off-target Replication and Increase the Safety of an Unattenuated, Glioblastoma-targeted Oncolytic HSV
  17. Oncolytic HSV virotherapy in murine sarcomas differentially triggers an antitumor T-cell response in the absence of virus permissivity
  18. Effective Treatment of an Orthotopic Xenograft Model of Human Glioblastoma Using an EGFR-retargeted Oncolytic Herpes Simplex Virus
  19. Expression of HSV-1 receptors in EBV-associated lymphoproliferative disease determines susceptibility to oncolytic HSV
  20. Novel Mutations in gB and gH Circumvent the Requirement for Known gD Receptors in Herpes Simplex Virus 1 Entry and Cell-to-Cell Spread
  21. Gene therapy for the treatment of chronic peripheral nervous system pain
  22. Inhibition of Indoleamine-2,3-dioxygenase (IDO) in Glioblastoma Cells by Oncolytic Herpes Simplex Virus
  23. Mechanism of HSV infection through soluble adapter-mediated virus bridging to the EGF receptor
  24. Bispecific Adapter-Mediated Retargeting of a Receptor-Restricted HSV-1 Vector to CEA-Bearing Tumor Cells
  25. A Double Mutation in Glycoprotein gB Compensates for Ineffective gD-Dependent Initiation of Herpes Simplex Virus Type 1 Infection
  26. Ectopic matrix metalloproteinase-9 expression in human brain tumor cells enhances oncolytic HSV vector infection
  27. A Herpes Simplex Virus Vector System for Expression of Complex Cellular cDNA Libraries
  28. Equine herpesvirus type 1 (EHV-1) utilizes microtubules, dynein, and ROCK1 to productively infect cells
  29. Design and application of oncolytic HSV vectors for glioblastoma therapy
  30. Generation of Herpesvirus Entry Mediator (HVEM)-Restricted Herpes Simplex Virus Type 1 Mutant Viruses: Resistance of HVEM-Expressing Cells and Identification of Mutations That Rescue Nectin-1 Recognition
  31. Chk2 is required for HSV-1 ICP0-mediated G2/M arrest and enhancement of virus growth
  32. Equine Herpesvirus 1 Enters Cells by Two Different Pathways, and Infection Requires the Activation of the Cellular Kinase ROCK1
  33. Characterization of soluble glycoprotein D-mediated herpes simplex virus type 1 infection
  34. Soluble V Domain of Nectin-1/HveC Enables Entry of Herpes Simplex Virus Type 1 (HSV-1) into HSV-Resistant Cells by Binding to Viral Glycoprotein D
  35. Herpes Simplex Virus Targeting to the EGF Receptor by a gD-Specific Soluble Bridging Molecule
  36. Equine Herpesvirus 1 Utilizes a Novel Herpesvirus Entry Receptor
  37. Combination gene therapy for glioblastoma involving herpes simplex virus vector-mediated codelivery of mutant IκBα and HSV thymidine kinase
  38. Enhanced efficacy of conditionally replicating herpes simplex virus (G207) combined with 5-fluorouracil and surgical resection in peritoneal cancer dissemination models
  39. Treatment of rat gliosarcoma brain tumors by HSV-based multigene therapy combined with radiosurgery
  40. Double suicide gene therapy using a replication defective herpes simplex virus vector reveals reciprocal interference in a malignant glioma model
  41. Herpesvirus-Mediated Systemic Delivery of Nerve Growth Factor
  42. Pseudotyping of Glycoprotein D-Deficient Herpes Simplex Virus Type 1 with Vesicular Stomatitis Virus Glycoprotein G Enables Mutant Virus Attachment and Entry
  43. Effective Treatment of Experimental Glioblastoma by HSV Vector-Mediated TNFα and HSV-tk Gene Transfer in Combination with Radiosurgery and Ganciclovir Administration
  44. Pseudotyping of Glycoprotein D-Deficient Herpes Simplex Virus Type 1 with Vesicular Stomatitis Virus Glycoprotein G Enables Mutant Virus Attachment and Entry
  45. Connexin 43-Enhanced Suicide Gene Therapy Using Herpesviral Vectors
  46. U1 small nuclear RNA-promoted exon selection requires a minimal distance between the position of U1 binding and the 3' splice site across the exon.
  47. Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  48. U1 snRNA promotes the selection of nearby 5' splice sites by U6 snRNA in mammalian cells.
  49. Suppression of mammalian 5' splice-site defects by U1 small nuclear RNAs from a distance.
  50. Expression of the H-ras proto-oncogene is controlled by alternative splicing
  51. A point mutation in the last intron responsible for increased expression and transforming activity of the c-Ha-ras oncogene
  52. "Retroposon" insertion into the cellular oncogene c-myc in canine transmissible venereal tumor.
  53. Rearrangement of the oncogene c-mos in mouse myeloma NSI and hybridomas
  54. Organization and evolution of immunoglobulin VH gene subgroups.
  55. Simple DNA sequences in homologous flanking regions near immunoglobulin VHgenes: a role in gene interaction?
  56. Diversity of germ-line immunoglobulin VH genes
  57. Cloning and sequence of the cDNA corresponding to the variable region of immonoglobin heavy chain MPC11