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     <title>Researchers develop innovative method to detect genetic causes of complex diseases</title>
   	 <description>Computational biologists at Carnegie Mellon University have developed an analytical technique to detect the multiple genetic variations that contribute to complex disease syndromes such as diabetes, asthma and cancer, which are characterized by multiple clinical and molecular traits.</description>
     <link>http://www.physorg.com/news168843451.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Fri, 07 Aug 2009 06:10:01 EST</pubDate>
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     <title>Researchers uncover potential mechanisms to protect against genetic alterations, diseases</title>
   	 <description>Peering into the DNA of tiny yeast, researchers at the Moores Cancer Center at the University of California, San Diego and the San Diego Branch of the Ludwig Institute for Cancer Research have pinpointed a large number of genes that can prevent a type of genetic rearrangement that may lead to cancer and other diseases.</description>
     <link>http://www.physorg.com/news168786880.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Thu, 06 Aug 2009 14:15:17 EST</pubDate>
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     <title>Comprehensive look at rare leukemia finds relatively few genetic changes launch disease</title>
   	 <description>The most comprehensive analysis yet of the genome of childhood acute myeloid leukemia (AML) found only a few mistakes in the genetic blueprint, suggesting the cancer arises from just a handful of missteps, according to new findings from St. Jude Children's Research Hospital. The research appears in the July 27 online edition of the Proceedings of the National Academy of Sciences.</description>
     <link>http://www.physorg.com/news167935015.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Mon, 27 Jul 2009 18:40:01 EST</pubDate>
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     <title>Mouse Model Provides Clues to Human Language Development</title>
   	 <description>Scientists of the German Mouse Clinic at Helmholtz Zentrum Muenchen (Germany) have made a major contribution to understanding human language development. Using a comprehensive screening method, they studied a mouse model carrying a 'humanized version' of a key gene associated with human language. In the brains of the mice the researchers found alterations which may be closely linked to speech and language development. Their analyses comprise part of an international study led by the Leipzig Max Planck Institute for Evolutionary Anthropology. The findings have been published in the current issue of the renowned journal Cell.</description>
     <link>http://www.physorg.com/news165043680.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Wed, 24 Jun 2009 06:28:33 EST</pubDate>
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     <title>Displacing petroleum-derived butanol with plants</title>
   	 <description>As a chemical for industrial processes, butanol is used in everything from brake fluid, to paint thinners, to plastics. According to a University of Illinois researcher, butanol made from plant material could displace butanol made from petroleum, just not at the fuel pump.</description>
     <link>http://www.physorg.com/news150653472.html</link>
	 <category>Biology</category>
	 <pubDate>Thu, 08 Jan 2009 16:11:12 EST</pubDate>
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     <title>Scientists identify genomic causes of a certain type of leukemia relapse</title>
   	 <description>Scientists at St. Jude Children's Research Hospital have identified distinctive genetic changes in the cancer cells of children with acute lymphoblastic leukemia (ALL) that cause relapse. The finding offers a pathway to designing treatments for ALL relapse in children and, ultimately, in adults.</description>
     <link>http://www.physorg.com/news147015318.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Thu, 27 Nov 2008 13:35:18 EST</pubDate>
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     <title>Study finds association between male birth defect and certain genetic mutations</title>
   	 <description>A small percentage of males born with cryptorchidism (failure of one or both testicles to descend into the scrotum), the most frequent congenital birth defect in male children, are more likely to have genetic mutations, including for a syndrome that is a common genetic cause of infertility, according to a study in the November 19 issue of JAMA.</description>
     <link>http://www.physorg.com/news146243743.html</link>
	 <category>Medicine &amp; Health</category>
	 <pubDate>Tue, 18 Nov 2008 15:15:43 EST</pubDate>
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