Viral Vectors for Gene Therapy Methods and Protocols - Machida, Curtis A.; SpringerLink (Online service) (Totowa, NJ : Humana Press : Imprint: Humana, 2003)
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.
Keywords: Human genetics; Human Genetics