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<title>Medical Xpress: PHYSorg news tagged with: genotyping</title>
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     <title>Large-scale genetic study defines relationship between primary sclerosing cholangitis and other autoimmune diseases</title>
   	 <description>For the first time, scientists show that a leading cause of liver transplant, primary sclerosing cholangitis (PSC), is a distinct disease from inflammatory bowel disease, opening up new avenues for specific PSC treatments.</description>
     <link>http://medicalxpress.com/news/2013-04-large-scale-genetic-relationship-primary-sclerosing.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 21 Apr 2013 13:00:17 EST</pubDate>
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     <title>Whole genome sequencing better at tracing TB outbreaks than standard test</title>
   	 <description>A new form of genetic testing of the bacteria that causes tuberculosis can provide better information on TB transmission and also trace TB outbreaks more accurately than the current standard test, according to a study from Germany published in this week's PLOS Medicine.</description>
     <link>http://medicalxpress.com/news/2013-02-genome-sequencing-tb-outbreaks-standard.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Tue, 19 Feb 2013 17:10:08 EST</pubDate>
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     <title>Mystery bleeding disorders could be unraveled by new research efforts</title>
   	 <description>(Medical Xpress)—Platelet disorders are heavily underdiagnosed, little understood and cannot be cured. University of Birmingham researchers and the Birmingham Platelet Group are running a UK-wide clinical trial 'Genotyping and platelet phenotyping' (GAPP) funded by the British Heart Foundation (BHF). The trial includes lab research by BHF-funded scientist Dr Yotis Senis in an effort to better identify patients and potentially to develop new treatments.</description>
     <link>http://medicalxpress.com/news/2013-02-mystery-disorders-unraveled-efforts.html</link>
	 <category>Medical research</category>
	 <pubDate>Mon, 11 Feb 2013 07:44:35 EST</pubDate>
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     <title>Patients with EGFR exon 20 insertions have poorer prognosis</title>
   	 <description>Exon 20 insertions are the third most common family of epidermal growth factor receptor (EGFR) mutations found in non–small-cell lung cancer (NSCLC). Little is known about cancers harboring these mutations aside from their lack of response to EGFR tyrosine kinase inhibitors, impairing the development of effective targeted therapies. A recent study published in the February 2013 issue of the International Association for the Study of Lung Cancer's (IASLC) Journal of Thoracic Oncology, concludes that patients with EGFR exon 20 insertions have similar clinical characteristics to those with common EGFR mutations, but a poorer prognosis.</description>
     <link>http://medicalxpress.com/news/2013-01-patients-egfr-exon-insertions-poorer.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 15 Jan 2013 11:16:49 EST</pubDate>
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     <title>Polygenic risk score helpful for women with familial breast CA</title>
   	 <description>(HealthDay)—For women affected by familial breast cancer, a polygenic risk score based on 22 genomic variants can identify women at high-risk of breast cancer, according to a study published in the Dec. 10 issue of the Journal of Clinical Oncology.</description>
     <link>http://medicalxpress.com/news/2012-12-polygenic-score-women-familial-breast.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 18 Dec 2012 18:30:01 EST</pubDate>
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     <title>Rare genetic mutation triples Alzheimer's risk</title>
   	 <description>A gene so powerful it nearly triples the risk of Alzheimer's disease has been discovered by an international team including researchers from Mayo Clinic. It is the most potent genetic risk factor for Alzheimer's identified in the past 20 years. The findings were reported Wednesday in the online edition of the New England Journal of Medicine.</description>
     <link>http://medicalxpress.com/news/2012-11-rare-genetic-mutation-triples-alzheimer.html</link>
	 <category>Alzheimer's disease &amp; dementia</category>
	 <pubDate>Wed, 14 Nov 2012 18:10:15 EST</pubDate>
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     <title>Genotyping IDs long-term risk of macular degeneration</title>
   	 <description>(HealthDay)—Genotyping of two genetic risk alleles can be used to estimate the long-term risk of early and late age-related macular degeneration (AMD), but knowing the phenotype is important in assessing risk when early AMD is present, according to a study published online Nov. 9 in the Archives of Ophthalmology.</description>
     <link>http://medicalxpress.com/news/2012-11-genotyping-ids-long-term-macular-degeneration.html</link>
	 <category>Ophthalmology</category>
	 <pubDate>Tue, 13 Nov 2012 18:10:04 EST</pubDate>
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     <title>Genotyping helps identify source of clinic infection outbreak</title>
   	 <description>Researchers from East Carolina University used a new technique of genotyping to identify the source of a hematology clinic outbreak of Mycobacterium mucogenicum, a gram-positive, acid-fast bacteria found in tap water. This is the first outbreak of M. mucogenicum in an ambulatory care setting; five other outbreaks have been reported in hospital settings since 1995. The study was published in the November issue of Infection Control and Hospital Epidemiology, the journal of the Society for Healthcare Epidemiology of America.</description>
     <link>http://medicalxpress.com/news/2012-10-genotyping-source-clinic-infection-outbreak.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Fri, 05 Oct 2012 11:31:41 EST</pubDate>
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     <title>Metabolic MAGIC: Meta-analyses reveal new genetic regions influencing blood glucose traits</title>
   	 <description>Researchers have identified 38 new genetic regions that are associated with glucose and insulin levels in the blood. This brings the total number of genetic regions associated with glucose and insulin levels to 53, over half of which are associated with type 2 diabetes.</description>
     <link>http://medicalxpress.com/news/2012-08-metabolic-magic-meta-analyses-reveal-genetic.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 12 Aug 2012 13:00:27 EST</pubDate>
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     <title>Report highlights child deaths from post-surgery codeine use</title>
   	 <description>(HealthDay) -- Researchers have identified three previously unreported instances of severe opioid-induced toxicity in children following adenotonsillectomy for obstructive sleep apnea syndrome, according to a case report published online April 9 in Pediatrics.</description>
     <link>http://medicalxpress.com/news/2012-04-highlights-child-deaths-post-surgery-codeine.html</link>
	 <category>Sleep apnea</category>
	 <pubDate>Mon, 09 Apr 2012 13:50:02 EST</pubDate>
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     <title>World's first bedside genetic test gets green light by Lancet</title>
   	 <description>Developed in Canada and conducted by researchers from the University of Ottawa Heart Institute, in partnership with Spartan Bioscience, the world's first bedside genetic test has received acknowledgment by The Lancet, the world's leading general medical journal.</description>
     <link>http://medicalxpress.com/news/2012-03-world-bedside-genetic-green-lancet.html</link>
	 <category>Cardiology</category>
	 <pubDate>Thu, 29 Mar 2012 11:21:58 EST</pubDate>
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     <title>Eat fish, build up brainpower</title>
   	 <description>Can pregnant women help boost their children's brainpower by eating fish? The findings of a study, presented in the American Journal of Clinical Nutrition, show how children born to women who consumed more fish during their pregnancies demonstrated improved outcomes in tests for verbal intelligence, fine motor skills and prosocial behavior.</description>
     <link>http://medicalxpress.com/news/2012-01-fish-brainpower.html</link>
	 <category>Health</category>
	 <pubDate>Tue, 10 Jan 2012 10:53:43 EST</pubDate>
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     <title>Study participants at risk for Alzheimer's talk about their genetic test results</title>
   	 <description>If you had a family history of developing Alzheimer's disease, would you take a genetic test that would give you more information about your chances?</description>
     <link>http://medicalxpress.com/news/2011-12-alzheimers-genetic-results.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Mon, 12 Dec 2011 11:21:46 EST</pubDate>
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     <title>Study finds specific gene linked to cold sore susceptibility</title>
   	 <description>Investigators have identified a human chromosome containing a specific gene associated with susceptibility to herpes simplex labialis (HSL), the common cold sore. Published in the Journal of Infectious Diseases and now available online, the study looks at how several genes may affect the severity of symptoms and frequency of this common infection. The findings, if confirmed, could have implications for the development of new drugs to treat outbreaks.</description>
     <link>http://medicalxpress.com/news/2011-10-specific-gene-linked-cold-sore.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Fri, 28 Oct 2011 04:28:41 EST</pubDate>
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     <title>New discovery brings customized tuberculosis therapies based on genotype closer to reality</title>
   	 <description>Are you genetically predisposed to tuberculosis? Scientists may now be able to answer this question and doctors may be able to adjust their therapeutic approach based on what they learn. That's because new research presented in the Journal of Leukocyte Biology  suggests that two frequent mutations in an immune system gene called TLR1 are responsible for cellular changes that ultimately make us less likely to resist the disease.</description>
     <link>http://medicalxpress.com/news/2011-08-discovery-customized-tuberculosis-therapies-based.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Mon, 01 Aug 2011 11:50:23 EST</pubDate>
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