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Viral Vectors for Gene Therapy: Methods and Protocols Book by Curtis A Machida

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Laatst bijgewerkt op 22 jan 2024 21:56:48 CETAlle herzieningen bekijkenAlle herzieningen bekijken

Specificaties

Objectstaat
Goed: Een boek dat is gelezen, maar zich in goede staat bevindt. De kaft is zeer minimaal beschadigd ...
Pages
592
Publication Date
2002-10-07
ISBN
9781588290199
Subject Area
Science, Medical
Publication Name
Viral Vectors for Gene Therapy : Methods and Protocols
Item Length
9.3 in
Publisher
Humana Press
Subject
Clinical Medicine, Life Sciences / Virology, Life Sciences / Genetics & Genomics, Genetics
Series
Methods in Molecular Medicine Ser.
Publication Year
2002
Type
Textbook
Format
Hardcover
Language
English
Author
Curtis A. Machida
Item Width
6.1 in
Item Weight
41.6 Oz
Number of Pages
Xvi, 592 Pages

Over dit product

Product Information

Over thirty chapters detail the use of herpes viruses, adenoviruses, adeno-associated viruses, simple and complex retroviruses, including lentiviruses, and other virus systems for vector development and gene transfer. These protocols will enable the researcher to develop, construct and use virus vectors for gene transfer and gene therapy.

Product Identifiers

Publisher
Humana Press
ISBN-10
1588290190
ISBN-13
9781588290199
eBay Product ID (ePID)
2230439

Product Key Features

Author
Curtis A. Machida
Publication Name
Viral Vectors for Gene Therapy : Methods and Protocols
Format
Hardcover
Language
English
Subject
Clinical Medicine, Life Sciences / Virology, Life Sciences / Genetics & Genomics, Genetics
Series
Methods in Molecular Medicine Ser.
Publication Year
2002
Type
Textbook
Subject Area
Science, Medical
Number of Pages
Xvi, 592 Pages

Dimensions

Item Length
9.3 in
Item Width
6.1 in
Item Weight
41.6 Oz

Additional Product Features

LCCN
2002-075944
Intended Audience
Scholarly & Professional
Series Volume Number
76
Number of Volumes
1 Vol.
Lc Classification Number
Rb155-155.8
Reviews
"This text would be very good for someone who can appreciate the many and varied practical aspects of performing a gene therapy study. I would certainly recommend it to anyone I knew working in the gene therapy field as a book to compare and contrast practical approaches and requirements for various viral vectors." - Pharmaceutical Research
Table of Content
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.
Copyright Date
2003
Dewey Decimal
616/.042
Dewey Edition
21
Illustrated
Yes

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