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Titlebook: Gene Therapy for Cancer; Kelly K. Hunt,Stephan A. Vorburger,Stephen G. Swis Book 2007 Humana Press 2007 angiogenesis.apoptosis.cancer trea

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https://doi.org/10.1007/978-3-540-73616-5als for cancer to date. In an ex vivo setting, conventional replication-defective oncoretrovirus vectors can reliably and efficiently achieve permanent gene transfer which is selective for dividing cells; however, successful application of these vectors in vivo has been difficult because of their re
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https://doi.org/10.1007/978-94-010-9169-5led to identify a suitable virus, which though unable to cause disease, retained the capability to replicate in cancer cells. In principal, the productive growth of the virus would kill or lyse malignant cells and the newly minted viral progeny would spread the infection, resulting ultimately in the
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Properties of Canonical Transformations,0s that a resurrection of the interest in the ability of certain viruses to preferentially replicate in malignant cells and less so in normal cells occurred, the curiosity being to evaluate whether these agents could be useful in cancer therapy regimes. It was following these reports, demonstrating
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https://doi.org/10.1007/978-1-4612-4236-9tial application of parvovirus-based vectors in cancer gene therapy. Unique characteristics of paroviruses such as nonpathogenicity, antioncogenicity, and methods of efficient recombinant vector production have drawn more attention toward utilizing parvovirus-based vectors in cancer gene therapy. Al
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Current, Resistance and Circuits, the target cancer cells and high transduction of nontarget normal organs. To address these issues, we have been working on “retargeting” of Ad vectors via transductional or transcriptional targeting. Transductional targeting has been achieved with application of various bridging moieties, genetical
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Lefteris Tsoulfidis,Persefoni Tsalikiin molecular biology that have allowed relatively easy manipulation of the viral genome, a number of different viruses have been evaluated and shown to have promise as anticancer agents. Of these, herpes simplex virus (HSV) has been perhaps the most intensively investigated. Several strains of repli
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Mathematical Functions and Techniquesficacy. It focuses on two approaches for delivery of cytokine genes to achieve effective therapy; . delivery using adenoviral vectors also termed “active vaccination,” and cell based approaches using specific immune cells modified with cytokine genes. These approaches have potential advantages for p
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