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(shū)目名稱Cell Biology and Biotechnology影響因子(影響力)




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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

MERIT

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