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Titlebook: Viral Vectors for Gene Therapy; Methods and Protocol Curtis A. Machida Book 2003 Humana Press 2003

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Thomas W. Dubensky Jr.,Sybille L. Sauter a comparison of the strengths and weaknesses of the different bodies of literature. It is shown that no one approach makes an effort to relate systematically the hybridization of subsidiary production systems to the impact of both the strategic and institutional distance and to strategic choices at
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1543-1894 for the construction, development, and use of viral vectors for gene transfer and gene therapy. I would like to thank the many chapter authors for their contributions. They are all experts in v978-1-61737-308-4978-1-59259-304-0Series ISSN 1543-1894 Series E-ISSN 1940-6037
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Andres Hurtado-Lorenzo,Anne David,Clare Thomas,Maria G. Castro,Pedro R. Lowenstein
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Semyon Rubinchik,Jan Woraratanadharm,Jennifer Schepp,Jian-yun Dong
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Strategies to Adapt Adenoviral Vectors for Targeted Delivery,ing can be achieved at the level of capsid binding or at later transduction events by the use of tissue-specific promoters (.–.). Targeting at the level of binding is preferred because even the interaction of cells with empty capsids leads to toxic effects (.), however a combination of both strategi
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