<?xml version="1.0" encoding="utf-8"?>
<?xml-stylesheet type="text/xsl" href="http://medicalxpress.com/tmpl/default/css/default/feedRSS.xsl"?>
<rss version="2.0" 
	xmlns:media="http://search.yahoo.com/mrss/">
<channel>
<title>Medical Xpress: PHYSorg news tagged with: enzymatic activity</title>
<link>http://medicalxpress.com/</link>
<language>en-us</language> 
<description>Medical Xpress internet news portal provides the latest news on Health and Medicine.</description>

 <item>
     <title>Cold winters freezing out breast cancer treatment</title>
   	 <description>For women diagnosed with a form of breast cancer known as estrogen receptor positive (ER+) breast cancer, tamoxifen is an essential drug used in the treatment and prevention of recurring breast cancer. Currently, tamoxifen is used in a one-size-fits-all approach where the same dose is prescribed for every patient. New research at Lawson Health Research Institute has found that in addition to patient-specific genetic factors, lack of exposure to vitamin D during the long winter months affects the body's ability to metabolize the drug.</description>
     <link>http://medicalxpress.com/news/2013-04-cold-winters-breast-cancer-treatment.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 18 Apr 2013 14:30:01 EST</pubDate>
	 <guid isPermaLink="false">news285512979</guid>
	 
</item>
<item>
     <title>Study shows additional role for abiraterone in blocking tumor growth in CRPC</title>
   	 <description>As part of an EU-supported IMI-PREDECT consortium (http://www.predect.eu), a Dutch study showed that anti-androgenic properties of the drug abiraterone may provide an additional mechanism of action in blocking tumour growth of castration resistant prostate cancer (CRPC).</description>
     <link>http://medicalxpress.com/news/2013-03-additional-role-abiraterone-blocking-tumor.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 15 Mar 2013 03:00:02 EST</pubDate>
	 <guid isPermaLink="false">news282499173</guid>
	 
</item>
<item>
     <title>Elusive substrate protein identified in the most common form of heritable rickets</title>
   	 <description>(Medical Xpress)—Diagnosed in toddlers, X-linked hypophosphatemia (XLH) is the most common form of heritable rickets, in which soft bones bend and deform, and tooth abscesses develop because infections penetrate soft teeth that are not properly calcified.  Researchers at McGill University and the Federal University of Sao Paulo have identified that osteopontin, a major bone and tooth substrate protein, plays a role in XLH. Their discovery may pave the way to effectively treating this rare disease.</description>
     <link>http://medicalxpress.com/news/2013-02-elusive-substrate-protein-common-heritable.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 20 Feb 2013 08:40:05 EST</pubDate>
	 <guid isPermaLink="false">news280569805</guid>
	 
</item>
<item>
     <title>The same genetic defect causes Pompe disease in both humans and dogs</title>
   	 <description>Pompe disease, a severe glycogen storage disease appearing in Lapphunds is caused by a genetic defect in acid α-glucosidase gene. The same genetic mutation also causes the equivalent disease in humans. Based on this finding, canine Pompe disease can now be diagnosed with a genetic test.</description>
     <link>http://medicalxpress.com/news/2013-02-genetic-defect-pompe-disease-humans.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 15 Feb 2013 14:40:03 EST</pubDate>
	 <guid isPermaLink="false">news280158933</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2013/thesamegenet.jpg" width="90" height="90" />
</item>
<item>
     <title>Loss of essential blood cell gene leads to anemia</title>
   	 <description>Researchers at Brigham and Women's Hospital (BWH) have discovered a new gene that regulates hemoglobin synthesis during red blood cell formation. The findings advance the biomedical community's understanding and treatment of human anemias and mitochondrial disorders.</description>
     <link>http://medicalxpress.com/news/2012-11-loss-essential-blood-cell-gene.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 07 Nov 2012 13:00:07 EST</pubDate>
	 <guid isPermaLink="false">news271507940</guid>
	 
</item>
<item>
     <title>Researchers identify gene that leads to myopia (nearsightedness)</title>
   	 <description>A Ben-Gurion University of the Negev research group led by Prof. Ohad Birk has identified a gene whose defect specifically causes myopia or nearsightedness.</description>
     <link>http://medicalxpress.com/news/2011-09-gene-myopia-nearsightedness.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 01 Sep 2011 12:31:53 EST</pubDate>
	 <guid isPermaLink="false">news234099102</guid>
	 
</item>


</channel>
</rss>
