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Titlebook: Cell Biology and Biotechnology; Novel Approaches to Melvin S. Oka,Randall G. Rupp Conference proceedings 1993 Springer Science+Business Me

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書目名稱Cell Biology and Biotechnology
副標題Novel Approaches to
編輯Melvin S. Oka,Randall G. Rupp
視頻videohttp://file.papertrans.cn/223/222735/222735.mp4
叢書名稱Serono Symposia USA
圖書封面Titlebook: Cell Biology and Biotechnology; Novel Approaches to  Melvin S. Oka,Randall G. Rupp Conference proceedings 1993 Springer Science+Business Me
描述.Cell Biology and Biotechnology: Novel Approaches to . .Increased Cellular Productivity. contains the proceedings of the symposium by the same name held in Cambridge, Massachusetts, January 30 - February 2, 1992. State-of-the-art research is presented on: the IGF-1 Receptor and Gene Expression During the Cell Cycle; Attachment Control of Fibroplast Proliferation; Cell Biology and Serum-Free Mouse Embryo Cells; Immunoglobulin Production Stimulating Factors; Erythropoietin Control of Programmed Death in Erythroid Progenitors; Prohormone Processing Enzymes and Protein Production; Control of Translation Initiation by Phosphorylation; Protein Retention in the Endoplasmic Reticulum Mediated by GPR78; Molecular Approaches Towards Manipulating the Expression of the Glucose Related Proteins in Mammalian Cells; Protein Folding in the Endoplasmic Reticulum; Sorting of Membrane Proteins in the Endocytic and Exocytic Pathways; CIS-Acting Elements Which Regulate Immunoglobulin Gene Transcription.
出版日期Conference proceedings 1993
關(guān)鍵詞Expression; Glucose; biology; biotechnology; cell; cell biology; cell cycle; enzyme; enzymes; gene; gene expre
版次1
doihttps://doi.org/10.1007/978-1-4684-9418-1
isbn_softcover978-1-4684-9420-4
isbn_ebook978-1-4684-9418-1
copyrightSpringer Science+Business Media New York 1993
The information of publication is updating

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Erythropoietin Control of Programmed Death in Erythroid Progenitors,r human BFU-E. How the BFU-E arise by “commitment” to erythroid differentiation of pluripotent hematopoietic cells is not understood. . (CFU-E) are intermediate in their level of differentiation, giving rise to colonies of 8–32 erythroblasts after 2 days of culture for murine CFU-E and 7 days for hu
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Prohormone Processing Enzymes and Protein Production,nd the like). Furthermore, an important feature that distinguishes the regulated from the constitutive pathway is the requirement for a specific extracellular signal before stored proteins within the coated secretory granules may be released into the external milieu of the cell. Proteins that are co
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Attachment Control of Fibroblast Proliferation,factors to maintain cell cycle progression throughout most of Gl (4, 5). Fibroblasts leave the cell cycle and enter a quiescent, G0 state when growth factors are removed from nutrient-containing medium (4, 6). Reentry into the cell cycle requires stimulation of the G0/G1 transition, and these events
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Erythropoietin Control of Programmed Death in Erythroid Progenitors,new erythrocytes (RBCs) appear in the circulation. The manner by which new RBCs are formed has been surmised by in vitro culture of bone marrow or spleen cells in semisolid medium in the presence of EPO. In such cultures, colonies of erythroblasts arise from committed erythroid progenitor cells that
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Control of Translation Initiation by Phosphorylation,t determine its intrinsic “strength” or efficiency—features that remain constant over time—and (ii) the effectiveness of the translational machinery to translate the mRNA—a condition that may be temporally modulated. Furthermore, we can focus on translational control either of a single species of mR
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