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Titlebook: Animal Cell Technology: Basic & Applied Aspects; Proceedings of the N K. Nagai,M. Wachi Conference proceedings 1998 Springer Science+Busine

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期刊全称Animal Cell Technology: Basic & Applied Aspects
期刊简称Proceedings of the N
影响因子2023K. Nagai,M. Wachi
视频video
学科分类Animal Cell Technology: Basic & Applied Aspects
图书封面Titlebook: Animal Cell Technology: Basic & Applied Aspects; Proceedings of the N K. Nagai,M. Wachi Conference proceedings 1998 Springer Science+Busine
影响因子Animal cell technology is a growing discipline of cell biologywhich aims not only to understand structures, functions and behaviorsof differentiated animal cells but also to uncover their abilities forindustrial and medical purposes. The goal of animal cell technologyincludes clonal expansion of differentiated cells with usefulabilities, optimization of their culture conditions on the industrialscale, modulation of their ability in order efficiently to producemedically and pharmaceutically important proteins, and application ofanimal cells to gene therapy and formation of artificial organs. ThisVolume gives the readers a complete review of the present state of theart in Japan, a country where this field is well advanced, as well asin Asia, Europe and the United States. The Proceedings will be usefulfor cell biologists, biochemists, molecular biologists, biochemicalengineers and those in other disciplines related to animal cellculture, working in academic environments as well as in thebiotechnology and pharmaceutical industries.
Pindex Conference proceedings 1998
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https://doi.org/10.1007/978-3-658-24822-2 maintaining their proper and sustainable functions. There are also many studies using such cell systems. The recent studies on immunocyte cultures reveal that cultured immunocytes provide adequate research systems for the investigations both of cytokine characterizations and their roles in immunobi
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https://doi.org/10.1007/978-3-322-81851-5ation mechanism in differentiated SFME cells was investigated SFME cells treated with 10% serum or with 10 ng/ml of TGF- β showed astrocytes-like phenotypes and lowered telomerase activity. These results indicate that telomerase activity is down-regulated with the differentiation of SFME cells into
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https://doi.org/10.1007/978-3-322-81851-5NS stem cells are potentially applicable for regeneration of damaged brain, such as in Parkinson’s Disease, or Alzheimer’s Disease. Recent studies have shown that mitogen and/or oncogene keep CNS stem cells proliferating. However, the long-term expansion of CNS stem cells needs a period of crisis, w
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Grundlagen des elektrischen Antriebs,c acid synthesis in the medium, during the construction of recombinant CHO cells. The results of selection of MTX tolerant cells when the MTX concentration was increased under 10 different stepwise conditions showed that the number of days required to obtain cells resistant to 1000 nM MTX depended o
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Echtzeitkommunikation und Ethernet/Internetmedia) and glucose-limited continuous cultivation (serum-free medium). Con A lectin blotting showed that N-linked glycosylation occurred under all the culture conditions used. The sugar composition of the oligosaccharide chain in each culture was studied using gas-chromatography and was found to be
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Echtzeitkommunikation und Ethernet/InternetRb, in the exit from cell cycle and the entry into cell-differentiation (1). During progression of cell cycle and differentiation, the activity of pRb is modulated in a phosphorylation/dephosphorylation dependent-manner. The activity of pRb is also regulated at gene expression level, and the express
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https://doi.org/10.1007/978-3-662-66217-5Verots S3 can be controlled by shifting the temperature. In this study, a stable hGH producing Verots S3 transformant was established, and the growth of the stable transformant of Verots S3 immobilized in porous carrier, Cellsnow, monitored by the glucose consumption rate, was observed faster than t
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Karl Kübler,Gerhard Krebser,Alexander Verllar carcinoma origin was established and investigated in its molecular genetic backgrounds. It was shown here that HBV DNA was integrated in eight different sites of the cellular DNA, in each of which HBV genome was rearranged, fragmented, and/or partly deleted. Complete HBV genome, as well as free
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