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	<title>2004Henderson Review - Revision history</title>
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	<updated>2026-05-24T19:52:23Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2004Henderson_Review&amp;diff=1758&amp;oldid=prev</id>
		<title>WikiSysop at 15:49, 16 April 2009</title>
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		<updated>2009-04-16T15:49:07Z</updated>

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&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
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Henderson R (2004) Realizing the potential of electron cryo-microscopy.&lt;br /&gt;
Q Rev Biophys 37:3–13&lt;br /&gt;
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[http://scholar.google.com/scholar?hl=en&amp;amp;lr=&amp;amp;newwindow=1&amp;amp;cites=7161228452335788130 Cited by]&lt;br /&gt;
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== Abstract ==&lt;br /&gt;
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Structural analysis by electron microscopy of biological macromolecules or macromolecular assemblies embedded in rapidly frozen, vitreous ice has made great advances during the last few years. Electron cryo-microscopy, or cryo-EM, can now be used to analyse the structures of molecules arranged in the form of two-dimensional crystals, helical arrays or as single particles with or without symmetry. Although it has been possible, using crystalline or helical specimens, to reach a resolution adequate to build atomic models (4 A), there is every hope this will soon also be possible with single particles. Small and large single particles present different obstacles to progress.&lt;br /&gt;
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== Keywords ==&lt;br /&gt;
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Review, electron microscopy&lt;br /&gt;
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== Links ==&lt;br /&gt;
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Article http://www.ncbi.nlm.nih.gov/pubmed/17390603&lt;br /&gt;
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== Related software ==&lt;br /&gt;
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== Related methods ==&lt;br /&gt;
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== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
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