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Titlebook: Electron Tomography; Methods for Three-Di Joachim Frank Book 2006Latest edition Springer-Verlag New York 2006 biology.cell.cell biology.cry

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發(fā)表于 2025-3-26 23:47:52 | 只看該作者
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978-1-4419-2172-7Springer-Verlag New York 2006
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Introduction: Politics and Health,ame molecular assemblies after isolation. As with studies using single-particle cryoelectron microscopy, specimens smaller than 1 μ in size can be prepared for cryoelectron tomography by plunge-freezing (.). Cells or organelles can be rapidly frozen directly on an electron microscope grid in thin la
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發(fā)表于 2025-3-27 23:19:29 | 只看該作者
https://doi.org/10.1007/978-1-137-56618-8or of X-rays in matter to establish the conditions in which it is valid in radiography. In this chapter, we enquire whether it is valid in electron microscopy, where intuition might well lead us to suspect that it is not. Electron-specimen interactions are very different from those encountered in X-
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發(fā)表于 2025-3-28 03:24:05 | 只看該作者
Some SAS Descriptive Procedures well as the Fourier transform data of either the object or the projections. Both convolution back-projection and weighted back-projection algorithms are based on the same theory as Fourier reconstruction methods, whereas iterative methods normally do not take into account the Fourier relationships
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