
Gene Therapy Methods
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Content
- Front Cover
- Gene Therapy Methods
- Copyright Page
- Table of Contents
- Contributors to Volume 346
- Preface
- Volumes in Series
- Section I: Nonviral
- Chapter 1. Gene Therapy for Hypertension: The Preclinical Data
- Chapter 2. Oligonucleotide-Mediated Site-Directed Gene Repair
- Chapter 3. Stabilized Plasmid-Lipid Particles: A Systemic Gene Therapy Vector
- Chapter 4. Enhancing Direct in Vivo Transfection with Nuclease Inhibitors and Pulsed Electrical Fields
- Chapter 5. Hydrodynamics-Based Transfection: Simple and Efficient Method for Introducing and Expressing Transgenes in Animals by Intravenous Injection of DNA
- Chapter 6. Bioplex Technology: Novel Synthetic Gene Delivery System Based on Peptides Anchored to Nucleic Acids
- Chapter 7. Surgical Procedures for Intravascular Delivery of Plasmid DNA to Organs
- Chapter 8. Direct Gene Transfer into Mouse Heart
- Section II: Adenovirus
- Chapter 9. Myoblast-Mediated Gene Transfer for Therapeutic Angiogenesis
- Chapter 10. Use of Phage Display to Identify Novel Peptides for Targeted Gene Therapy
- Chapter 11. Helper-Dependent Adenoviral Vectors
- Chapter 12. Gene Transfer Methods for Transplantation
- Chapter 13. Generation and Growth of Gutted Adenoviral Vectors
- Chapter 14. Adenovirus-Mediated Gene Transfer for Cardiovascular and Renal Diseases
- Chapter 15. Gene Transfer to Blood Vessels Using Adenoviral Vectors
- Chapter 16. Rearrangements in Adenoviral Genomes Mediated by Inverted Repeats
- Chapter 17. High-Capacity, Helper-Dependent, "Gutless" AdenoviralVectors for Gene Transfer into Brain
- Chapter 18. Gene Therapy Methods in Cardiovascular Diseases
- Section III: Adeno-Associated Virus
- Chapter 19. Gene Delivery to Cardiac Muscle
- Chapter 20. Recombinant AAV-Mediated Gene Delivery Using Dual Vector Heterodimerization
- Chapter 21. Designing and Characterizing Hammerhead Ribozymes for Use in AAV Vector-Mediated Retinal Gene Therapies
- Chapter 22. Adeno-Associated Viral Vector-Mediated Gene Therapy of Ischemia-Induced Neuronal Death
- Chapter 23. Recombinant Adeno-Associated Viral Vector Production Using Stable Packaging and Producer Cell Lines
- Chapter 24. Streamlined Large-Scale Production of Recombinant Adeno-Associated Virus (rAAV) Vectors
- Section IV: Lentivirus
- Chapter 25. Gene Transfer to the Brain Using Feline Immunodeficiency Virus-Based Lentivirus Vectors
- Chapter 26. Generation of HIV-1 Derived Lentiviral Vectors
- Chapter 27. Design, Production, Safety, Evaluation, and Clinical Applications of Nonprimate Lentiviral Vectors
- Chapter 28. Gene Transfer to Airway Epithelia Using Feline Immunodeficiency Virus-Based Lentivirus Vectors
- Chapter 29. Transduction of a Gene Expression Cassette Using Advanced Generation Lentiviral Vectors
- Chapter 30. Construction, Purification, and Characterization of Adenovirus Vectors Expressing Apoptosis- Inducing Transgenes
- Section V: Retrovirus
- Chapter 31. Ligand-Inducible Transgene Regulation for Gene Therapy
- Chapter 32. Large-Scale Production of Retroviral Vectors for Systemic Gene Delivery
- Chapter 33. Oncoretroviral and Lentiviral Vector-Mediated Gene Therapy
- Section VI: Other Strategies
- Chapter 34. HSV-1 Amplicon Vectors
- Chapter 35. Microencapsulation of Genetically Engineered Cells for Cancer Therapy
- Chapter 36. HVJ (Hemagglutinating Virus of Japan
- Sendai Virus)-Liposome Method
- Chapter 37. Gene Transfer with Foamy Virus Vectors
- Chapter 38. Infectious Epstein-Barr Virus Vectors for Episomal Gene Therapy
- Author Index
- Subject Index
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