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Titlebook: Gene Therapy; Principles and Appli Thomas Blankenstein Book 1999 Birkh?user Verlag 1999 DNA.HIV.bacteria.biotechnology.cancer.gene expressi

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發(fā)表于 2025-3-21 19:25:03 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Gene Therapy
副標(biāo)題Principles and Appli
編輯Thomas Blankenstein
視頻videohttp://file.papertrans.cn/382/381966/381966.mp4
圖書封面Titlebook: Gene Therapy; Principles and Appli Thomas Blankenstein Book 1999 Birkh?user Verlag 1999 DNA.HIV.bacteria.biotechnology.cancer.gene expressi
描述K. Sikora Gene therapy is one of the fastest developing areas in modern medical research. Transcending the classical preclinical and clinical disciplines, it is likely to have far- reaching consequences in the practice of medicine, as we enter the next millennium. Currently, there are over 200 seperate active clinical trials with over 2,500 patients entered. These studies involve over 20 countries and include patients with a wide range of diseases, including cancer, HIV infection; cystic fibrosis (CF), haemophilia, diabetes, immune deficiencies, metabolic disorders, ischaemic heart disease and arthritis. Gene therapy can be defined as the deliberate transfer of DNA for therapeutic purposes. There is a further implication that only specific sequences containing rel- evant genetic information are used; otherwise, transplantation procedures involving bone marrow, kidney or liver could be considered a form of gene therapy. The con- cept of transfer of genetic information as a practical clinical tool arose from the gene-cloning technology, developed during the 1970s. Without the ability to isolate and replicate defined genetic sequences, it would be impossible to produce purified materi
出版日期Book 1999
關(guān)鍵詞DNA; HIV; bacteria; biotechnology; cancer; gene expression; gene therapy; genes
版次1
doihttps://doi.org/10.1007/978-3-0348-7011-5
isbn_softcover978-3-0348-7013-9
isbn_ebook978-3-0348-7011-5
copyrightBirkh?user Verlag 1999
The information of publication is updating

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https://doi.org/10.1007/978-3-030-27621-8t is likely that modifications of both the vector and packaging lines should result in even higher titer, targetable viruses with elevated and/or regulated gene expression. Thus, it is likely that retroviral vectors will continue to be the vector of choice for many gene therapy applications.
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Staatsbürgerrechte und soziale Klassen 1996]. After in-fection, the Ad vector expresses the transgene in the nucleus of replicating and non-replicating cells in an epi-chromosomal fashion, where the duration of gene expres-sion is transient over time [Rosenfeld et al., 1991; Kass-Eissler et al., 1994; Smith et al., 1993; Engelhard et al., 1994; Yang et al., 1994a, b].
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Gene Transfection Using Particle Bombardmentwith transfection efficiencies of 1–15%. In this article, we summarize the characteristics of this approach, present our preliminary results and discuss possible future application of this gene transfer technology.
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