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Titlebook: Cell Biology of Extracellular Matrix; Second Edition Elizabeth D. Hay Book 1991 Springer Science+Business Media New York 1991 Embryo.biolog

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書(shū)目名稱Cell Biology of Extracellular Matrix
副標(biāo)題Second Edition
編輯Elizabeth D. Hay
視頻videohttp://file.papertrans.cn/223/222759/222759.mp4
圖書(shū)封面Titlebook: Cell Biology of Extracellular Matrix; Second Edition Elizabeth D. Hay Book 1991 Springer Science+Business Media New York 1991 Embryo.biolog
描述In the ten-year interval since the first edition of this volume went to press, our knowledge of extracellular matrix (ECM) function and structure has enor- mously increased. Extracellular matrix and cell-matrix interaction are now routine topics in the meetings and annual reviews sponsored by cell biology societies. Research in molecular biology has so advanced the number of known matrix molecules and the topic of gene structure and regulation that we won- dered how best to incorporate the new material. For example, we deliberated over the inclusion of chapters on molecular genetics. We decided that with judicious editing we could present the recent findings in molecular biology within the same cell biology framework that was used for the first edition, using three broad headings: what is extracellular matrix, how is it made, and what does it do for cells? Maintaining control over the review of literature on the subject of ECM was not always an easy task, but we felt it was essential to production of a highly readable volume, one compact enough to serve the the student as an introduction and the investigator as a quick update on graduate the important recent discoveries. The first
出版日期Book 1991
關(guān)鍵詞Embryo; biology; cell; cell biology; genetics; glycoprotein; membrane; metabolism; molecular biology; molecul
版次1
doihttps://doi.org/10.1007/978-1-4615-3770-0
isbn_softcover978-1-4613-6680-5
isbn_ebook978-1-4615-3770-0
copyrightSpringer Science+Business Media New York 1991
The information of publication is updating

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https://doi.org/10.1007/978-94-010-3514-9tro studies of isolated type I collagen and procollagen have indicated that much of the assembly process of a collagen fibril can be explained by physicochemical forces, often described as “self-assembly.” Light microscopic studies of type I collagen-rich tissues reveal a variety of architectures ra
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Introductory Remarksontinues to interact with its own ECM products, and with the ECM produced by other cells. At the cell surface, matrix receptors link the ECM to the cell interior; the metabolism and fate of the cell, its shape, and many of its other properties are continuously related to and dependent on the composi
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Proteoglycanseeks, and cell surface PGs generally have half-lives of only a few hours. Changes in the metabolism and structure of PGs can have profound effects on the pathobiology of many diseases. This chapter, then, summarizes current concepts and problems relating to biosynthesis, catabolism, and pathology of
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Matrix Assemblytro studies of isolated type I collagen and procollagen have indicated that much of the assembly process of a collagen fibril can be explained by physicochemical forces, often described as “self-assembly.” Light microscopic studies of type I collagen-rich tissues reveal a variety of architectures ra
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Extracellular Matrix Degradationo cell migration. In contrast to the involution reaction, lysis associated with cell motility is a limited reaction that leaves the bulk of the matrix intact and is directed only at the “structural kingpins,” those molecules that constitute a barrier to cell displacement. Cell growth, division, and
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