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Titlebook: Cell Cycle and Cell Differentiation; J. Reinert,Howard Holtzer Book 1975 Springer-Verlag Berlin Heidelberg 1975 DNA.Zelldifferenzierung.bi

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書(shū)目名稱(chēng)Cell Cycle and Cell Differentiation
編輯J. Reinert,Howard Holtzer
視頻videohttp://file.papertrans.cn/223/222796/222796.mp4
叢書(shū)名稱(chēng)Results and Problems in Cell Differentiation
圖書(shū)封面Titlebook: Cell Cycle and Cell Differentiation;  J. Reinert,Howard Holtzer Book 1975 Springer-Verlag Berlin Heidelberg 1975 DNA.Zelldifferenzierung.bi
描述It is instructive to compare the response of biologists to the two themes that comprise the title of this volume. The concept of the cell cycle-in contra- distinction to cell division-is a relatively recent one. Nevertheless biologists of all persuasions appreciate and readily agree on the central problems in this area. Issues ranging from mechanisms that initiate and integrate the synthesis of chro- mosomal proteins and DNA during S-phase of mitosis to the manner in which assembly of microtubules and their interactions lead to the segregation of metaphase chromosomes are readily followed by botanists and zoologists, as well as by cell and molecular biologists. These problems are crisp and well-defined. The current state of "cell differentiation" stands in sharp contrast. This, one of the oldest problems in experimental biology, almost defies definition today. The difficulties arise not only from a lack of pertinent information on the regulatory mechanisms, but also from conflicting basic concepts in this field. One of the ways in which this situation might be improved would be to find a broader experimental basis, including a better understanding of the relationship between the ce
出版日期Book 1975
關(guān)鍵詞DNA; Zelldifferenzierung; biology; cell; cell cycle; cell differentiation; cell division; chromosome; protei
版次1
doihttps://doi.org/10.1007/978-3-540-37390-2
isbn_softcover978-3-662-21693-4
isbn_ebook978-3-540-37390-2Series ISSN 0080-1844 Series E-ISSN 1861-0412
issn_series 0080-1844
copyrightSpringer-Verlag Berlin Heidelberg 1975
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https://doi.org/10.1007/978-981-10-3599-9oducing red blood cell. Available evidence will be presented which indicates that this transition requires the “exposure” of the globin genes so that they become available for binding by RNA polymerase. Additional experiments will show that the proper rate of DNA chain elongation is required for the
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https://doi.org/10.1007/978-981-10-3599-9re remainder of the embryo. More importantly, it is the characteristic . (rather than properties which all neurons share to the exclusion of non-neural cells) that enables them to associate selectively and to assemble the synaptic circuits which are the substrates of macroscopic brain function. Neur
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Innovation Competition and Strategy,veloping cell systems, with proliferation of cells taking place in an orderly programmed fashion. The complexity of the nervous system apparently derives from genetic and environmental influences which not only direct proliferation of the various cell types, but also control subsequent cell migratio
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https://doi.org/10.1007/978-981-10-4118-1ytodifferentiation can be divided into two phases (., 1950; ., 1967). First, cells become committed or determined for particular developmental fates, often without showing overt signs of specialization. Once established, determination can persist even in the absence of the factors that initiated the
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