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Castaño-Díez D., Al-Amoudi A., Glynn A.M., Seybert A., and Frangakis A.S. Fiducial-less alignment of cryo-sections. J Struct Biol 159 (2007) 413-423
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Intact carboxysomes in a cyanobacterial cell visualized by hilbert differential contrast transmission electron microscopy
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Kaneko Y., Danev R., Nagayama K., and Nakamoto H. Intact carboxysomes in a cyanobacterial cell visualized by hilbert differential contrast transmission electron microscopy. J Bacteriol 188 (2006) 805-808
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Kaneko, Y.1
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Single particle analysis based on Zernike phase contrast transmission electron microscopy
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Danev R., and Nagayama K. Single particle analysis based on Zernike phase contrast transmission electron microscopy. J Struct Biol 161 (2008) 211-218
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Direct electron imaging in electron microscopy with monolithic active pixel sensors
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Deptuch G., Besson A., Rehak P., Szelezniak M., Wall J., Winter M., and Zhu Y. Direct electron imaging in electron microscopy with monolithic active pixel sensors. Ultramicroscopy 107 (2007) 674-684
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Prerequisites for a Cc/Cs-corrected ultrahigh-resolution TEM
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Haider M., Müller H., Uhlemann S., Zach J., Loebau U., and Hoeschen R. Prerequisites for a Cc/Cs-corrected ultrahigh-resolution TEM. Ultramicroscopy 108 (2008) 167-178
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Haider, M.1
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46
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Electron tomography of swollen rigor fibers of insect flight muscle reveals a short and variably angled S2 domain
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3-D reconstructions of a highly organized insect muscle allow the identification of functional intermediates in the behavior of myosin cross-bridges. Here, both classification and averaging are used to improve the SNR of different states in the mechanochemical cross-bridge cycle.
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Liu J., Wu S., Reedy M.C., Winkler H., Lucaveche C., Cheng Y., Reedy M.K., and Taylor K.A. Electron tomography of swollen rigor fibers of insect flight muscle reveals a short and variably angled S2 domain. J Mol Biol 362 (2006) 844-860. 3-D reconstructions of a highly organized insect muscle allow the identification of functional intermediates in the behavior of myosin cross-bridges. Here, both classification and averaging are used to improve the SNR of different states in the mechanochemical cross-bridge cycle.
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J Mol Biol
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Liu, J.1
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Taylor, K.A.8
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47
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Electron tomographic analysis of somatic cell plate formation in meristematic cells of Arabidopsis preserved by high-pressure freezing
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ET of serial sections of RF/FSF material allows the assembly of informative models that show the relationships between phragmoplast microtubules and the vesicles that assemble to form the cell plate that will separate two dividing plant cells.
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Segui-Simarro J.M., Austin J.R., White E.A., and Staehelin L.A. Electron tomographic analysis of somatic cell plate formation in meristematic cells of Arabidopsis preserved by high-pressure freezing. Plant Cell 16 (2004) 836-856. ET of serial sections of RF/FSF material allows the assembly of informative models that show the relationships between phragmoplast microtubules and the vesicles that assemble to form the cell plate that will separate two dividing plant cells.
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Segui-Simarro, J.M.1
Austin, J.R.2
White, E.A.3
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48
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33749239641
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Katanin disrupts the microtubule lattice and increases polymer number in C. elegans meiosis
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ET of RF/FSF nematode embryos provides both the overview to see spindle microtubule organization (not shown here) and the details of katanin action as it helps to sever these polymers.
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Srayko M.T., O'Toole E., Hyman A.A., and Muller-Reichert T. Katanin disrupts the microtubule lattice and increases polymer number in C. elegans meiosis. Curr Biol 16 (2006) 1944-1949. ET of RF/FSF nematode embryos provides both the overview to see spindle microtubule organization (not shown here) and the details of katanin action as it helps to sever these polymers.
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Curr Biol
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Srayko, M.T.1
O'Toole, E.2
Hyman, A.A.3
Muller-Reichert, T.4
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49
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53749093685
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Nanoscale architecture of endoplasmic reticulum export sites and of Golgi membranes as determined by electron tomography
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ET of sections cut from hydrophilic plastic-embedded plant cells allow the application of antibodies for labeling of specific enzymes in the Golgi complex. Although antibody binding is limited to the surface of each section, the use of ET allows the tracking of membranes and the assembly of a 3-D model in which the position of the label can be visualized.
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Staehelin L.A., and Kang B.H. Nanoscale architecture of endoplasmic reticulum export sites and of Golgi membranes as determined by electron tomography. Plant Physiol 147 (2008) 1454-1468. ET of sections cut from hydrophilic plastic-embedded plant cells allow the application of antibodies for labeling of specific enzymes in the Golgi complex. Although antibody binding is limited to the surface of each section, the use of ET allows the tracking of membranes and the assembly of a 3-D model in which the position of the label can be visualized.
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(2008)
Plant Physiol
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Staehelin, L.A.1
Kang, B.H.2
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