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