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Titlebook: Cell Immortalization; Alvaro Macieira-Coelho Book 2000 Springer-Verlag Berlin Heidelberg 2000 Cell immortalization.Krebs.Seneszenz.aging.b

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书目名称Cell Immortalization
编辑Alvaro Macieira-Coelho
视频videohttp://file.papertrans.cn/223/222830/222830.mp4
概述This is the first book which comprehensively deals with cell immortalization and its relationship with cancer, aging, homeostasis, and the development of organs and organisms
丛书名称Progress in Molecular and Subcellular Biology
图书封面Titlebook: Cell Immortalization;  Alvaro Macieira-Coelho Book 2000 Springer-Verlag Berlin Heidelberg 2000 Cell immortalization.Krebs.Seneszenz.aging.b
描述The problem of the long-term proliferation of cells is a seminal one. It has always been a hot subject in biology, a source of far-reaching hypotheses, even more so now when explanations for the mechanisms of cell prolifera­ tive mortality or immortality seem within our reach. A question which is still debated is whether an infinite division potential can be a normal trait or is always the result of modifications leading to abnormal cell growth and escape from homeostasis. In general, investigators have been advocates of one of the two extremes, universal limited or unlim­ ited normal proliferative potential. Since the long-term proliferative potential of cells concerns regulation of development, regeneration of tissues, and homeostatic control of cell growth, in brief survival of living organisms, and since the regulation of these processes is so different along the evolutionary scale, it is not surpris­ ing that there does not seem to be any universal trait. The question of whether cells are endowed with finite or infinite prolifera­ tive phenotypes has to be seen using the perspective of comparative biology.
出版日期Book 2000
关键词Cell immortalization; Krebs; Seneszenz; aging; biology; cancer; cell; cell division; evolution; gene; mortalit
版次1
doihttps://doi.org/10.1007/978-3-662-06227-2
isbn_softcover978-3-642-08491-1
isbn_ebook978-3-662-06227-2Series ISSN 0079-6484 Series E-ISSN 2197-8484
issn_series 0079-6484
copyrightSpringer-Verlag Berlin Heidelberg 2000
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Clonal Life Cycle of , in the Context of Evolutionally Acquired Mortality,ght would exceed the weight of the earth (6 × 10. g), even if the weight of a single bacterium is underestimated at 10. g (10. × 10. = 10.). Our body, consisting of on the order of 10. cells, all of which have been derived from a single cell (a fertilized egg) would be attained by only 43 cell divis
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Telomeres and Cell Division Potential,ich DNA repeat sequences (Blackburn 1991) and specific telomere binding proteins (Zhong et al. 1992; Cardenas et al. 1993; Shore 1994; Chong et al. 1995; Broccoli et al. 1997). All vertebrate chromosome terminal sequences consist of TTAGGG hexanucleotide repeats (reading 5’–3’ centromere to telo-mer
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Cellular Mortality and Immortalization: A Complex Interplay of Multiple Gene Functions,mited number (depending on the cell type) of divisions and reach an irreversibly growth arrested, but viable stage. The age of cells is determined by the number of times cells divide rather than the calendar time elapsed. The restricted replicative capacity of normal cells which confers them the mor
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