Titlebook: Cellular Nanomachines; From Discovery to St Bhanu P. Jena Book 2020 Springer Nature Switzerland AG 2020 nanomachines.electron microscopy.at

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Sandip Das,Ulf Lagercrantz,Martin Lascouxt release during cell secretion could only be possible via a plasma membrane structure capable of preventing the complete merger or collapse of secretory vesicles into the cell plasma membrane. Cup-shaped plasma membrane-embedded lipoprotein structure called . was first discovered in 1996 in live pa

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Bird Migration and Offshore Wind Turbinesand thus the transport process through the nuclear pore complex is energy-dependent. Since the nuclear pore complex is the gateway to the genome, the number of nuclear pore complexes varies during the different stages of the cell cycle. For example, between G1 and G2 phase of the cell cycle, the num

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Chaperonin: Protein Folding Machinery in Cells,units. Each subunit is composed of three domains, including an ATP-binding domain. The binding of ATP leads to the establishment of a hydrophilic cage for protein folding. Mutations in genes encoding chaperones, or changes in the expression levels of chaperones, have been identified to result in a w

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Nuclear Pore: A Bidirectional Transport Machinery,and thus the transport process through the nuclear pore complex is energy-dependent. Since the nuclear pore complex is the gateway to the genome, the number of nuclear pore complexes varies during the different stages of the cell cycle. For example, between G1 and G2 phase of the cell cycle, the num

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