<?xml version="1.0"?>
<rss version="2.0">
   <channel>
      <title>Research Article by Urooj Morris</title>
      <link>https://padlet.com/uroojmorris/926qowyyuyzo</link>
      <description>Targeting mitochondrial oxidation phosphorylation eradicates therapy-resistant chronic myeloid leukaemia stem cell.</description>
      <language>en-us</language>
      <pubDate>2017-11-28 14:39:49 UTC</pubDate>
      <lastBuildDate>2024-05-27 12:46:07 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
      <image>
         <url></url>
      </image>
      <item>
         <title>The Research Article </title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210927095</link>
         <description><![CDATA[<div>Kuntz, EM, 2017. Targeting mitochondrial oxidative phosphorylation eradicates therapy-resistant chronic myeloid leukemia stem cells. <em>Nature Medicine</em>, [Online]. 23, 1234-1240. Available at: <a href="https://www.nature.com/articles/nm.4399">https://www.nature.com/articles/nm.4399</a> [Accessed 27 November 2017].<br>Improvements of this article:<br>Have clear sections for each part of the report.<br>Have more paitents to test this on as only 4 CML patients were used. <br><br></div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-28 14:52:42 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210927095</guid>
      </item>
      <item>
         <title>Aims </title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210936958</link>
         <description><![CDATA[<div>The aim of the research article is to investigate if targeting mitochondrial oxidation phosphorylation eradicates therapy-resistant chronic myeloid leukaemia stem cells.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-28 15:06:07 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210936958</guid>
      </item>
      <item>
         <title>Methods </title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210939059</link>
         <description><![CDATA[<div>Liquid chromatography-mass spec was used to metabolically profile CD34+ and CD34- by the steady state of metabolites central to glucose, nucleotide, amino acid, fatty acid, and energy metabolism. This was done because stem cells can exhibit opposite/ corresponding traits. <br>Mice were also used to study the invivo engraftment of CD34+ CML cells.</div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-28 15:08:53 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210939059</guid>
      </item>
      <item>
         <title>Results</title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210941876</link>
         <description><![CDATA[<div>Figure 1a,b show that the imatinib treatment targets differentiated CD34- CML cells for apoptosis, leading to enrichment of primative CD34+.<br>Figure 1c,d. Show that imatinib in line with resistence of CML stem cells to tyrosine kinase inhibitors treatment, colony-forming capacity of CD34+ cells is not affected. </div>]]></description>
         <enclosure url="https://padletuploads.blob.core.windows.net/prod/233993787/a214893b229509d2b29dabc60d052191/biomed_cw_cml.jpg" />
         <pubDate>2017-11-28 15:12:37 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210941876</guid>
      </item>
      <item>
         <title>Conclusion </title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210942755</link>
         <description><![CDATA[<div>Primitive CML cells rely on upregulated metabolism for their survival as they are highly susceptible to inhibition of oxidative phosphorylation, whereas normal CD34+ are not.  Also the combination treatment of imatinib and tigecycline (antibody that inbibits mitochondrial protein translation) eradicates  CML LSCs.  </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-28 15:13:48 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210942755</guid>
      </item>
      <item>
         <title>Discussion</title>
         <author>uroojmorris</author>
         <link>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210943305</link>
         <description><![CDATA[<div>In culture, proliferating untreated CD34+ chronic myeloid leukaemia cells rapidly lose surface CD34 expansion. Imatinib treatment primarily targets the differentiated CD34- CML cells for apoptosis, therefore leading to enrichment of more primitive CD34+ cells. </div>]]></description>
         <enclosure url="" />
         <pubDate>2017-11-28 15:14:35 UTC</pubDate>
         <guid>https://padlet.com/uroojmorris/926qowyyuyzo/wish/210943305</guid>
      </item>
   </channel>
</rss>
