Viral Vectors for Gene Therapy Methods and Protocols /

Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Machida, Curtis A. (Editor)
Format: eBook
Language:English
Published: Totowa, NJ : Humana Press : Imprint: Humana, 2003.
Edition:1st ed. 2003.
Series:Methods in Molecular Medicine, 76
Subjects:
Online Access:https://doi.org/10.1385/1592593046
Table of Contents:
  • Use of the Herpes Simplex Viral Genome to Construct Gene Therapy Vectors
  • Construction of Multiply Disabled Herpes Simplex Viral Vectors for Gene Delivery to the Nervous System
  • Improved HSV-1 Amplicon Packaging System Using ICP27-Deleted, Oversized HSV-1 BAC DNA
  • Herpes Simplex Amplicon Vectors
  • Strategies to Adapt Adenoviral Vectors for Targeted Delivery
  • Use of Recombinant Adenovirus for Gene Transfer into the Rat Brain
  • Generation of Adenovirus Vectors Devoid of All Viral Genes by Recombination Between Inverted Repeats
  • Packaging Cell Lines for Generating Replication-Defective and Gutted Adenoviral Vectors
  • Improving the Transcriptional Regulation of Genes Delivered by Adenovirus Vectors
  • Targeted Integration by Adeno-Associated Virus
  • Development and Optimization of Adeno-Associated Virus Vector Transfer into the Central Nervous System
  • A Method for Helper Virus-Free Production of Adeno-Associated Virus Vectors
  • Novel Tools for Production and Purification of Recombinant Adeno-Associated Viral Vectors
  • Recombinant Adeno-Associated Viral Vector Types 4 and 5
  • Trans-Splicing Vectors Expand the Packaging Limits of Adeno-Associated Virus for Gene Therapy Applications
  • Generation of Retroviral Packaging and Producer Cell Lines for Large-Scale Vector Production with Improved Safety and Titer
  • An Ecdysone-Inducible Expression System for Use with Retroviruses
  • In Vivo Infection of Mice by Replication-Competent MLV-Based Retroviral Vectors
  • Development of Simian Retroviral Vectors for Gene Delivery
  • Self-Inactivating Lentiviral Vectors and a Sensitive Cre-loxP Reporter System
  • Lentiviral Vectors for Gene Transfer to the Central Nervous System
  • A Highly Efficient Gene Delivery System Derived from Feline Immunodeficiency Virus (FIV)
  • A Multigene Lentiviral Vector System Based on Differential Splicing
  • Production of Trans-Lentiviral Vector with Predictable Safety
  • Human Immunodeficiency Virus Type 1-Based Vectors for Gene Delivery to Human Hematopoietic Stem Cells
  • Semliki Forest Viral Vectors for Gene Transfer
  • Semliki Forest Virus (SFV) Vectors in Neurobiology and Gene Therapy
  • Semliki Forest Virus Vectors for Large-Scale Production of Recombinant Proteins
  • Development of Foamy Virus Vectors
  • Poxviral/Retroviral Chimeric Vectors Allow Cytoplasmic Production of Transducing Defective Retroviral Particles.