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
LEADER 03379nam a22002895i 4500
001 978-1-59259-304-0
005 20190618111533.0
007 cr nn 008mamaa
008 100301s2003 xxu| s |||| 0|eng d
020 |a 9781592593040 
024 7 |a 10.1385/1592593046  |2 doi 
040 |a Sistema de Bibliotecas del Tecnológico de Costa Rica 
245 1 0 |a Viral Vectors for Gene Therapy  |b Methods and Protocols /  |c edited by Curtis A. Machida. 
250 |a 1st ed. 2003. 
260 # # |a Totowa, NJ :  |b Humana Press :  |b Imprint: Humana,  |c 2003. 
300 |a XVI, 592 p.  |b online resource. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Methods in Molecular Medicine,  |v 76 
505 0 |a 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. 
650 0 |a Human genetics. 
650 1 4 |a Human Genetics. 
700 1 |a Machida, Curtis A.  |e editor. 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
856 4 0 |u https://doi.org/10.1385/1592593046