<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2020Cianfrocco_Wrong</id>
	<title>2020Cianfrocco Wrong - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2020Cianfrocco_Wrong"/>
	<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2020Cianfrocco_Wrong&amp;action=history"/>
	<updated>2026-06-13T12:16:54Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.2</generator>
	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2020Cianfrocco_Wrong&amp;diff=3626&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Cianfrocco, M. A. &amp; Kellogg, E. H. What Could Go Wrong? A Practical Guide to Single-Particle Cryo-EM: From Biochemistry to Atomic Models.  Journal of chemical...&quot;</title>
		<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2020Cianfrocco_Wrong&amp;diff=3626&amp;oldid=prev"/>
		<updated>2020-03-11T18:58:07Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Cianfrocco, M. A. &amp;amp; Kellogg, E. H. What Could Go Wrong? A Practical Guide to Single-Particle Cryo-EM: From Biochemistry to Atomic Models.  Journal of chemical...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
&lt;br /&gt;
Cianfrocco, M. A. &amp;amp; Kellogg, E. H.&lt;br /&gt;
What Could Go Wrong? A Practical Guide to Single-Particle Cryo-EM: From Biochemistry to Atomic Models. &lt;br /&gt;
Journal of chemical information and modeling, 2020 &lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Cryo-electron microscopy (cryo-EM) has enjoyed explosive recent growth due to revolutionary advances in hardware and software, resulting in a steady stream of long-awaited, high-resolution structures with unprecedented atomic detail. With this comes an increased number of microscopes, cryo-EM facilities, and scientists eager to leverage the ability to determine protein structures without crystallization. However, numerous pitfalls and considerations beset the path toward high-resolution structures and are not necessarily obvious from literature surveys. Here, we detail the most common misconceptions when initiating a cryo-EM project and common technical hurdles, as well as their solutions, and we conclude with a vision for the future of this exciting field.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://pubs.acs.org/doi/10.1021/acs.jcim.9b01178&lt;br /&gt;
&lt;br /&gt;
== Related software ==&lt;br /&gt;
&lt;br /&gt;
== Related methods ==&lt;br /&gt;
&lt;br /&gt;
== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
	</entry>
</feed>