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Titlebook: Cell Engineering; Mohamed Al-Rubeai Book 1999 Springer Science+Business Media Dordrecht 1999 Expression.Tissue Engineering.Translation.cel

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发表于 2025-3-21 16:15:33 | 显示全部楼层 |阅读模式
书目名称Cell Engineering
编辑Mohamed Al-Rubeai
视频videohttp://file.papertrans.cn/223/222811/222811.mp4
丛书名称Cell Engineering
图书封面Titlebook: Cell Engineering;  Mohamed Al-Rubeai Book 1999 Springer Science+Business Media Dordrecht 1999 Expression.Tissue Engineering.Translation.cel
描述Integrating advances in molecular biology into bioprocessespresents a continuous challenge to scientists and bioengineers. Thisseries is conceived to help meet this challenge. It examines andassesses the feasibility of new approaches for the modification ofcellular function such as gene expression, protein processing,secretion, glycosylation, immortalisation, proliferation, andapoptosis as well as the systematic study of the metabolicgenotype-phenotype relationship. The series provides detailedcoverage of the methodology for improving cellular properties of cellsused in the production of biopharmaceuticals, gene and cell therapiesand tissue engineering. It also seeks to explain the cellularmechanisms underlying .in vitro. physiological activity andproductivity. .This volume, which is based on presentations at the `European Workshopon Animal Cell Engineering‘ held in Costa Brava, Spain, contains acollection of chapters relating to cellular function and modificationby leading authorities in several different areas of basic researchand the biopharmaceutical industry.
出版日期Book 1999
关键词Expression; Tissue Engineering; Translation; cells; cellular mechanisms; gene expression; phenotype; regula
版次1
doihttps://doi.org/10.1007/978-0-585-37971-5
isbn_softcover978-90-481-5254-4
isbn_ebook978-0-585-37971-5Series ISSN 1389-6946 Series E-ISSN 2542-9515
issn_series 1389-6946
copyrightSpringer Science+Business Media Dordrecht 1999
The information of publication is updating

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High Yield Expression of Recombinant Proteins Requiring Proteolytic Maturation: Use of the Endoprotylation, phosphorylation, acetylation, sulfation, β-hydroxylation, γ-carboxylation and disulphide-bond formation. In addition, the generation of biologically active molecules may require post-translational proteolytic processing. In this case the protein is synthesised as an inactive precursor molec
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The Regulation of Apoptosis in Animal Cells, necessitates a measured amount of cell deletion as does homeostatic maintenance and protection of the organism from pathogens. The process whereby a cell orchestrates its own destruction is now referred to as . or . (PCD). Apoptosis is a phrase originally employed to denote a collective set of feat
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Inhibition of Apoptosis In Mammalian Cell Culture,es could be attenuated . for use as vaccines initiated attempts to develop large scale cultures of mammalian cells. In the 1970’s, two discoveries led to the expanded use of such cultures: (1) the advent of recombinant DNA technology meant that cell lines could be engineered to overexpress heterolog
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Control of Mammalian Cell Proliferation as an Important Strategy in Cell Culture Technology, Cancerex regulatory network which orchestrates the global changes of cycling cells in a temporal and spatial manner. Based on such mechanistic research, cell-cycle regulatory circuits came to be perceived as a fundamental program which stands at the center of multicellular life, since the cell-cycle machi
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Development of an IRF-1 Based Proliferation Control System,ation of the oocyte that divides and proliferates until the animal reaches its mature size. Further cell growth is tightly controlled. Proliferation and cell death are balanced to keep the total cell mass essentially constant, while the synthesis and secretion of cellular products continues. Despite
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Factors Involved In The Cell Cycle Arrest Of Adult Rat Cardiomyocytes,d the body. Therefore, it is more likely to fail despite the fact that it has more muscle. O. carried by the blood is essential to maintain life. If the left ventricle weakens, the body suffers from O. deficit. A failing left ventricle will also fail to keep pace with the right ventricle, which is f
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Immortalization of Hepatocytes through Targeted Deregulation of the Cell Cycle,s of liver toxicology and pathology, in recombinant protein technology and in gene therapy and medicine. The requirements of these disciplines will define the parameters for selecting an immortalization strategy and will ultimately pass judgement on the success of newly created cell lines.
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