Viral Vectors for Gene Therapy Methods and Protocols /
Corporate Author: | |
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Other Authors: | |
Format: | eBook |
Language: | English |
Published: |
Totowa, NJ :
Humana Press : Imprint: Humana,
2003.
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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.