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<title>Medical Xpress: PHYSorg news tagged with: genetic origins</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>Researchers discover new therapy for fragile X chromosome syndrome</title>
   	 <description>Researchers at the University of the Basque Country (UPV/EHU) and the Achucarro neurosciences centre have discovered a new therapy for the fragile X chromosome syndrome. This new therapy proposes the modulation of the cerebral endocannabinoid system in order to ameliorate the symptoms of the disease. &quot;Clearly, a cure as such is not going to be achieved, as it involves a disease of genetic origin, but the fact that, by manipulating in a certain way at a cerebral level in order to obtain an improvement in the symptoms of the disease is something highly positive&quot;, stated Ms Susana Mato, researcher at the Department of Neurosciences at the UPV/EHU and at the Achucarro centre. This scientific finding has just been published in Nature Medicine.</description>
     <link>http://medicalxpress.com/news/2013-04-therapy-fragile-chromosome-syndrome.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 10 Apr 2013 09:17:02 EST</pubDate>
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     <title>New obesity, height genes identified</title>
   	 <description>(Medical Xpress)—Busselton residents and researchers from The University of Western Australia have helped a worldwide scientific collaboration identify new genes associated with height and obesity.</description>
     <link>http://medicalxpress.com/news/2013-04-obesity-height-genes.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 08 Apr 2013 06:47:33 EST</pubDate>
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     <title>EU releases 144 mn euro for new rare disease research</title>
   	 <description>The European Union on Thursday pledged 144 million euros of fresh funding for research on rare diseases that currently affect some 30 million Europeans, the majority of them children.</description>
     <link>http://medicalxpress.com/news/2013-02-eu-mn-euro-rare-disease.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 28 Feb 2013 04:50:01 EST</pubDate>
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     <title>Large-scale Japanese genomics project finds eight new loci linked to atopic dermatitis</title>
   	 <description>Around one in ten Japanese school children suffer from a debilitating form of eczema known as atopic dermatitis (AD). Despite clear signs that the condition is heritable, the genetic origins of the disease have remained elusive. Now, in a study of about 3,300 Japanese individuals with AD and some 15,000 unaffected controls, researchers have discovered eight new loci with ties to the chronic inflammatory skin disorder, a finding that could lead to new treatment options, particularly for Japanese people.</description>
     <link>http://medicalxpress.com/news/2013-02-large-scale-japanese-genomics-loci-linked.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 22 Feb 2013 08:40:01 EST</pubDate>
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     <title>Following the footprints of positive selection</title>
   	 <description>For decades, the human genome could only tell us what we already suspected about the evolution of certain traits. Researchers were able to trace the genetic origin stories of lactose tolerance (as opposed to lactose intolerance), malaria resistance, and more only after observing these successful traits in specific populations. Now, the study of positive selection – the ability to determine which genetic changes have conferred an evolutionary advantage – has reached a turning point: the genome itself can be used as a starting point to guide scientists to important genetic locations, leading to hypotheses about human health and disease.</description>
     <link>http://medicalxpress.com/news/2013-02-footprints-positive.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 15 Feb 2013 10:50:01 EST</pubDate>
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     <title>Researchers identify genetic root to early-onset prostate cancer</title>
   	 <description>Prostate cancer is often considered an elderly man's disease, and little is known about the approximately 2% of cases that arise in men who are aged 50 years or younger. Research published in the February 11th issue of the Cell Press journal Cancer Cell uncovers the genetic origin of such early-onset prostate cancer. The findings could help in the development of new diagnostic, prognostic, therapeutic, and prevention strategies for the disease.</description>
     <link>http://medicalxpress.com/news/2013-02-genetic-root-early-onset-prostate-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 11 Feb 2013 12:00:05 EST</pubDate>
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     <title>First Alzheimer's case has full diagnosis 106 years later</title>
   	 <description>(Medical Xpress)—More than a hundred years after Alois Alzheimer identified Alzheimer's disease in a patient an analysis of that original patient's brain has revealed the genetic origin of their condition.</description>
     <link>http://medicalxpress.com/news/2013-01-alzheimer-case-full-diagnosis-years.html</link>
	 <category>Alzheimer's disease &amp; dementia</category>
	 <pubDate>Wed, 09 Jan 2013 06:28:38 EST</pubDate>
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     <title>Inherited retinal disease research may lead to treatment</title>
   	 <description>Inherited retinal disease is a major cause of vision impairment in early life - and a researcher at The University of Western Australia hopes a study in which he was involved will contribute towards the development of a drug-based treatment.</description>
     <link>http://medicalxpress.com/news/2013-01-inherited-retinal-disease-treatment.html</link>
	 <category>Medical research</category>
	 <pubDate>Tue, 08 Jan 2013 05:59:10 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>Confirmation of nitisinone efficacy for life-threatening liver disease</title>
   	 <description>A consortium of Quebec researchers coordinated by the Medical Genetics Service of the Sainte-Justine UHC has just published the findings of a 25-year study on the treatment of tyrosinemia, a life-threatening liver disease of genetic origin, which is screened at birth in the province of Quebec, where it is much more frequent than anywhere else in the world. &quot;After five years of treatment, no trace of the disease can be detected in the liver of newborns who were treated with nitisinone starting from the first month of life,&quot; states Dr. Grant Mitchell of the Sainte-Justine UHC and the University of Montreal, who is the senior author of a study published in Molecular Genetics and Metabolism in September 2012.</description>
     <link>http://medicalxpress.com/news/2012-10-nitisinone-efficacy-life-threatening-liver-disease.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Wed, 31 Oct 2012 16:18:21 EST</pubDate>
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     <title>Global genome effort seeks genetic roots of disease</title>
   	 <description>By decoding the genomes of more than 1,000 people whose homelands stretch from Africa and Asia to Europe and the Americas, scientists have compiled the largest and most detailed catalog yet of human genetic variation. The massive resource will help medical researchers find the genetic roots of rare and common diseases in populations worldwide.</description>
     <link>http://medicalxpress.com/news/2012-10-global-genome-effort-genetic-roots.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 31 Oct 2012 14:46:31 EST</pubDate>
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     <title>Major genetic discovery explains 10 percent of aortic valve disease</title>
   	 <description>Researchers at the Sainte-Justine University Hospital Center and University of Montreal have identified genetic origins in 10% of an important form of congenital heart diseases by studying the genetic variability within families.</description>
     <link>http://medicalxpress.com/news/2012-09-major-genetic-discovery-percent-aortic.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 28 Sep 2012 04:45:42 EST</pubDate>
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     <title>Step forward in research into new treatments for brain edema</title>
   	 <description>Cerebral edemas are accumulations of fluid into the intra- or extracellular spaces of the brain and it can result from several factors such as stroke or head trauma, among others.</description>
     <link>http://medicalxpress.com/news/2012-03-treatments-brain-edema.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Mon, 19 Mar 2012 11:39:58 EST</pubDate>
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     <title>Golden retrievers help scientists track human disease genes</title>
   	 <description>A team of EU-funded researchers has successfully identified a gene that triggers a skin disorder in dogs - and the findings could have implications for humans who also suffer from the condition. Whether it manifests in golden retrievers or in humans, the disease ichthyosis has the same common genetic basis; therefore, any new bounds made in understanding the condition in dogs are applicable to humans too. No molecular cause for ichthyosis has previously been identified. </description>
     <link>http://medicalxpress.com/news/2012-01-golden-scientists-track-human-disease.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 31 Jan 2012 07:55:07 EST</pubDate>
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     <title>Genome-wide study reveals 3 new susceptibility loci for adult asthma in Japanese population</title>
   	 <description>Researchers at the RIKEN Center for Genomic Medicine (CGM), together with colleagues at Kyoto University, Tsukuba University, Harvard University, and other medical institutions have identified three new loci associated with susceptibility to adult asthma in the Japanese population. The findings appear in Nature Genetics and derive from a genome-wide study of 4836 Japanese individuals.</description>
     <link>http://medicalxpress.com/news/2011-07-genome-wide-reveals-susceptibility-loci-adult.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 31 Jul 2011 13:20:01 EST</pubDate>
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     <title>New study sheds light on evolution of 2009 pandemic influenza A(H1N1) virus in Japan</title>
   	 <description>Analysis of mutations of the 2009 pandemic influenza A(H1N1) virus by researchers at the RIKEN Omics Science Center (OSC) has revealed major genetic differences between the virus in its early phase of infection in Japan and in its peak phase. While yielding valuable clues on the genetic origins of drug resistance, the findings also pave the way toward the development of new diagnostic kits for detecting and preventing the spread of global pandemic diseases.</description>
     <link>http://medicalxpress.com/news/2011-04-evolution-pandemic-influenza-ah1n1-virus.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Mon, 25 Apr 2011 18:20:00 EST</pubDate>
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