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<title>Medical Xpress: PHYSorg news tagged with: gene discovery</title>
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 <item>
     <title>Twin research comes of age</title>
   	 <description>Thanks to thousands of volunteer twins, scientists have discovered over 400 novel genes associated with over 30 diseases over the last two decades, marking a golden era in genetic discovery.</description>
	  <link>http://medicalxpress.com/news/2013-06-twin-age.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 07 Jun 2013 07:36:55 EST</pubDate>
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     <title>Gene signature can predict who will survive chemotherapy</title>
   	 <description>An eight gene 'signature' can predict length of relapse-free survival after chemotherapy, finds new research in Biomed Central's open access journal BMC Medicine.</description>
	  <link>http://medicalxpress.com/news/2013-04-gene-signature-survive-chemotherapy.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 15 Apr 2013 20:00:01 EST</pubDate>
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     <title>High-throughput sequencing shows potentially hundreds of gene mutations related to autism</title>
   	 <description>Genomic technology has revolutionized gene discovery and disease understanding in autism, according to an article published in the December 20 issue of the journal Neuron.</description>
	  <link>http://medicalxpress.com/news/2012-12-high-throughput-sequencing-potentially-hundreds-gene.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 19 Dec 2012 14:33:25 EST</pubDate>
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     <title>Genetic technology detects CHARGE syndrome in prenatal sample</title>
   	 <description>Brief Report in the December 6, 2012 issue of the New England Journal of Medicine (NEJM) focuses on findings from Cynthia Morton, PhD, director of Cytogenetics at Brigham and Women's Hospital and senior study author, and colleagues on a prenatal case study involving a new, balanced translocation (a genetic abnormality caused by chromosomal rearrangements) between chromosomes 6 and 8.</description>
	  <link>http://medicalxpress.com/news/2012-12-genetic-technology-syndrome-prenatal-sample.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 06 Dec 2012 07:15:38 EST</pubDate>
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     <title>Researchers find genetic cause for body tremors</title>
   	 <description>Researchers at the University of Montreal and its affiliated CHU Sainte-Justine and CHUM hospitals have linked some cases of Essential Tremor (ET) to a specific genetic problem. ET is the most common movement disorder, becoming increasingly frequent with increasing age, which is characterized by an involuntary shaking movement (tremor) that occurs with motion, particularly when doing precise fine movement. The researchers will be publishing their findings tomorrow in The American Journal of Human Genetics.</description>
	  <link>http://medicalxpress.com/news/2012-08-genetic-body-tremors.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 02 Aug 2012 12:00:21 EST</pubDate>
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<item>
     <title>Stanford researcher discusses new AHA call for tougher regulation of genetic testing</title>
   	 <description>Rapid advances in genetic disease research that are transforming how we diagnose and treat illness require new safeguards to protect patients from the misuse of these technologies and realize their full potential, according to new American Heart Association policy recommendations.</description>
	  <link>http://medicalxpress.com/news/2012-05-stanford-discusses-aha-tougher-genetic.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 30 May 2012 08:29:27 EST</pubDate>
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<item>
     <title>Researchers identify genes that may help in ovarian cancer diagnosis and prognosis</title>
   	 <description>Scientists from Duke University Medical Center have determined that genes acting as molecular &quot;on/off&quot; switches can define clinically relevant molecular subtypes of ovarian cancer, providing ideal potential targets for use in clinical prognostic and diagnostic testing. These bimodal genes can define tumor subtypes that have different overall prognoses and respond to different therapeutic regimens. The researchers' results are published in the May issue of The Journal of Molecular Diagnostics.</description>
	  <link>http://medicalxpress.com/news/2012-04-genes-ovarian-cancer-diagnosis-prognosis.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 09 Apr 2012 10:24:35 EST</pubDate>
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</item>
<item>
     <title>Researchers find clues to common birth defect in gene expression data</title>
   	 <description>Researchers at MassGeneral Hospital for Children (MGHfC), The Jackson Laboratory and other institutes have uncovered 27 new candidate genes for congenital diaphragmatic hernia (CDH), a common and often deadly birth defect.</description>
	  <link>http://medicalxpress.com/news/2012-02-clues-common-birth-defect-gene.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 06 Feb 2012 15:00:12 EST</pubDate>
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<item>
     <title>From genomic data to new cancer drug</title>
   	 <description>New discoveries about follicular lymphoma, a currently intractable form of cancer, highlight the power of functional genomics in cancer gene discovery. A report in the Oct 28th issue of Cell demonstrates how genetic insights can be translated directly into therapies.</description>
	  <link>http://medicalxpress.com/news/2011-10-genomic-cancer-drug.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 27 Oct 2011 13:05:37 EST</pubDate>
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     <title>Study discovers new genes for rare inherited diseases</title>
   	 <description>An international team of researchers has identified two new genes connected with hereditary renal diseases.</description>
	  <link>http://medicalxpress.com/news/2011-09-genes-rare-inherited-diseases.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 06 Sep 2011 10:01:13 EST</pubDate>
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<item>
     <title>A gene discovery in truffle dogs sheds new light on the mechanisms of childhood epilepsy</title>
   	 <description>A new epilepsy gene, LGI2, has been found in the Lagotto Romagnolo dogs, known from their gift for truffle hunting. The gene discovery made by Professor Hannes Lohi and his research group at the University of Helsinki and the Folkh&amp;#228;lsan Research Center offers a new candidate gene for human benign childhood epilepsies characterized by seizure remission. The research will be published in the prestigious scientific journal PLoS Genetics.</description>
	  <link>http://medicalxpress.com/news/2011-07-gene-discovery-truffle-dogs-mechanisms.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 28 Jul 2011 17:00:04 EST</pubDate>
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