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<title>Medical Xpress: PHYSorg news tagged with: genomic medicine</title>
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<description>Medical Xpress internet news portal provides the latest news on Health and Medicine.</description>

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     <title>Scientists find potential therapeutic target for Cushing's disease</title>
   	 <description>Scientists at the Salk Institute for Biological Studies have identified a protein that drives the formation of pituitary tumors in Cushing's disease, a development that may give clinicians a therapeutic target to treat this potentially life-threatening disorder.</description>
     <link>http://medicalxpress.com/news/2013-05-scientists-potential-therapeutic-cushing-disease.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Tue, 07 May 2013 16:11:18 EST</pubDate>
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     <title>Sunshine hormone, vitamin D, may offer hope for treating liver fibrosis</title>
   	 <description>Liver fibrosis results from an excessive accumulation of tough, fibrous scar tissue and occurs in most types of chronic liver diseases. In industrialized countries, the main causes of liver injury leading to fibrosis include chronic hepatitis virus infection, excess alcohol consumption and, increasingly, nonalcoholic steatohepatitis (NASH).</description>
     <link>http://medicalxpress.com/news/2013-04-sunshine-hormone-vitamin-d-liver.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 25 Apr 2013 14:55:15 EST</pubDate>
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     <title>Science of genome-sequencing marks 10 years</title>
   	 <description>A decade after completion of the Human Genome Project on April 14, 2003, a top official of the National Institutes of Health surveyed the rarefied view from that mountaintop:</description>
     <link>http://medicalxpress.com/news/2013-04-science-genome-sequencing-years.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 15 Apr 2013 16:50:01 EST</pubDate>
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     <title>Scripps physicians call for change in cancer tissue handling</title>
   	 <description>Genetic sequencing technology is altering the way cancer is diagnosed and treated, but traditional specimen handling methods threaten to slow that progress.</description>
     <link>http://medicalxpress.com/news/2013-01-scripps-physicians-cancer-tissue.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 04 Jan 2013 13:09:32 EST</pubDate>
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     <title>When will genomic research translate into clinical care—and at what cost?</title>
   	 <description>Genomic research is widely expected to transform medicine, but progress has been slower than expected. While critics argue that the genomics &quot;promise&quot; has been broken – and that money might be better spent elsewhere—proponents say the deliberate pace underscores the complexity of the relationship between medicine and disease and, indeed, argues for more funding.</description>
     <link>http://medicalxpress.com/news/2013-01-genomic-clinical-careand.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 04 Jan 2013 12:59:59 EST</pubDate>
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     <title>Two new genetic mutations associated with Cowden syndrome</title>
   	 <description>Cleveland Clinic researchers from the Lerner Research Institute have uncovered two new genes associated with Cowden syndrome (CS) according to a new study, published today in the online version of the American Journal of Human Genetics.</description>
     <link>http://medicalxpress.com/news/2012-12-genetic-mutations-cowden-syndrome.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 13 Dec 2012 12:00:13 EST</pubDate>
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     <title>New genomics study shows ancestry could help solve disease riddles</title>
   	 <description>October 25, 2012 – Explosive advancement in human genome sequencing opens new possibilities for identifying the genetic roots of certain diseases and finding cures. However, so many variations among individual genomes exist that identifying mutations responsible for a specific disease has in many cases proven an insurmountable challenge. But now a new study by scientists at The Scripps Research Institute (TSRI), Scripps Health, and Scripps Translational Science Institute (STSI) reveals that by comparing the genomes of diseased patients with the genomes of people with sufficiently similar ancestries could dramatically simplify searches for harmful mutations, opening new treatment possibilities.</description>
     <link>http://medicalxpress.com/news/2012-10-genomics-ancestry-disease-riddles.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 25 Oct 2012 16:00:09 EST</pubDate>
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     <title>Personalized genomic medicine: How much can it really empower patients?</title>
   	 <description>Personalized genomic medicine is hailed as a revolution that will empower patients to take control of their own health care, but it could end up taking control away from patients and limiting their treatment choices, concludes an article in the Hastings Center Report. A commentary responding to the article, by the editorial director of Health and Family at Consumer Reports, also appears in the journal.</description>
     <link>http://medicalxpress.com/news/2012-10-personalized-genomic-medicine-empower-patients.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 15 Oct 2012 16:52:02 EST</pubDate>
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     <title>50-hour whole genome sequencing provides rapid diagnosis for children with genetic disorders</title>
   	 <description>Today investigators at Children's Mercy Hospitals and Clinics in Kansas City reported the first use of whole genome information for diagnosing critically ill infants. As reported in Science Translational Medicine, the team describes STAT-Seq, a whole genome sequencing approach - from blood sample to returning results to a physician - in about 50 hours. Currently, testing even a single gene takes six weeks or more.</description>
     <link>http://medicalxpress.com/news/2012-10-hour-genome-sequencing-rapid-diagnosis.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 03 Oct 2012 14:00:05 EST</pubDate>
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     <title>Study shows vitamin E may decrease cancer risk in Cowden syndrome patients</title>
   	 <description>Cleveland Clinic researchers have discovered that vitamin E may prevent cancer in patients with an under-recognized genetic disorder.</description>
     <link>http://medicalxpress.com/news/2012-09-vitamin-decrease-cancer-cowden-syndrome.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 17 Sep 2012 16:12:03 EST</pubDate>
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     <title>Personalized genomic medicine faces many hurdles</title>
   	 <description>When the human genome project was completed in 2003, some expected it to herald a new age of personalized genomic medicine, but the resulting single &quot;reference&quot; sequence has significant shortcomings for these applications and does not account for the actual variability in the human population, as reported in a study published July 11 in the open access journal PLoS ONE.</description>
     <link>http://medicalxpress.com/news/2012-07-personalized-genomic-medicine-hurdles.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 11 Jul 2012 17:00:10 EST</pubDate>
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     <title>Cleveland Clinic researcher discovers genetic cause of thyroid cancer</title>
   	 <description>Cleveland Clinic researchers have discovered three genes that increase the risk of thyroid cancer, which is has the largest incidence increase in cancers among both men and women.</description>
     <link>http://medicalxpress.com/news/2011-12-cleveland-clinic-genetic-thyroid-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 23 Dec 2011 09:55:37 EST</pubDate>
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     <title>Pinpointing asthma susceptibility in Japanese adults</title>
   	 <description>A team of geneticists has identified five specific gene regions associated with asthma susceptibility among Japanese adults. Mayumi Tamari of the RIKEN Center for Genomic Medicine, Yokohama, led the research.</description>
     <link>http://medicalxpress.com/news/2011-12-asthma-susceptibility-japanese-adults.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 22 Dec 2011 08:40:01 EST</pubDate>
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     <title>Genetic link to Barrett's esophagus, esophageal cancer discovered</title>
   	 <description>Mutations in three genes have been identified that are more prevalent in patients with esophageal cancer and Barrett esophagus, a premalignant metaplasia (change in cells or tissue) caused by chronic gastroesophageal reflux disease (GERD), according to preliminary research reported in the July 27 issue of JAMA.</description>
     <link>http://medicalxpress.com/news/2011-07-genetic-link-barrett-esophagus-esophageal.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 26 Jul 2011 16:00:07 EST</pubDate>
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     <title>Genetic variant linked to development of liver cancer in hepatitis C virus carriers</title>
   	 <description>A genome-wide study by researchers at the RIKEN Center for Genomic Medicine, Hiroshima University Hospital and Sapporo-Kosei General Hospital has identified a genetic variant associated with the development of liver cancer in chronic hepatitis C virus carriers. The findings are based on a study of 3,312 Japanese individuals and appear in the journal Nature Genetics.</description>
     <link>http://medicalxpress.com/news/2011-07-genetic-variant-linked-liver-cancer.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 03 Jul 2011 13:00:01 EST</pubDate>
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