Viral vectors for gene therapy : methods and protocols /
| Other Authors: | |
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| Format: | Book |
| Language: | English |
| Published: |
Totowa, N.J. :
Humana Press,
[2003]
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| Series: | Methods in molecular medicine ;
76. |
| Subjects: |
Table of Contents:
- Use of the herpes simplex viral genome to construct gene therapy vectors
- Construction of mutiply 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 : evaluation of gene transfer efficiency, toxicity, and inflammatory and immune reactions
- Generation of adenovirus vectors devoid of all virus 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
- Recombinant adeno-associated viral vector types 4 and 5 : preparation and application for CNS gene transfer
- 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 : application in lysosomal storage disease animal models
- 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