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<title>Medical Xpress: PHYSorg news tagged with: viral vectors</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>Viral Vectors delivery new calcium pumps for ailing hearts</title>
   	 <description>(Medical Xpress)—A fresh round of trials to evaluate gene therapy for the heart is set to begin in a couple of weeks. The British Heart Foundation will be sponsoring the study, which seeks to replace defective calcium pump genes inside cells, with new ones delivered by a virus. The main trials will look at a group of around 200 patients worldwide, and a separate trial will look at 24 patients who already have a mechanical heart-assist device implanted.</description>
     <link>http://medicalxpress.com/news/2013-05-viral-vectors-delivery-calcium-ailing.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 01 May 2013 10:41:19 EST</pubDate>
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     <title>Recipe for large numbers of stem cells requires only one ingredient</title>
   	 <description>Stem cells and tissue-specific cells can be grown in abundance from mature mammalian cells simply by blocking a certain membrane protein, according to scientists at the University of Pittsburgh School of Medicine and the National Institutes of Health (NIH). Their experiments, reported today in Scientific Reports, also show that the process doesn't require other kinds of cells or agents to artificially support cell growth and doesn't activate cancer genes.</description>
     <link>http://medicalxpress.com/news/2013-04-recipe-large-stem-cells-requires.html</link>
	 <category>Medical research</category>
	 <pubDate>Wed, 17 Apr 2013 05:00:02 EST</pubDate>
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     <title>Researchers show that lipid nanoparticles are ideal for delivering genes and drugs</title>
   	 <description>Researchers from Basque Public University are using nanotechnology to develop new formulations that can be applied to drugs and gene therapy. Specifically, they are using nanoparticles to design systems for delivering genes and drugs; this helps to get the genes and drugs to the point of action so that they can produce the desired effect.</description>
     <link>http://medicalxpress.com/news/2013-02-lipid-nanoparticles-ideal-genes-drugs.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 28 Feb 2013 10:53:45 EST</pubDate>
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     <title>Mouse model could help identify viral vectors that may cause tumors</title>
   	 <description>Investigators at Nationwide Children's Hospital have identified a mouse model that could help evaluate the risk that viral vectors used in gene therapy might promote tumor formation as a side-effect. The study appears in Molecular Therapy. </description>
     <link>http://medicalxpress.com/news/2012-10-mouse-viral-vectors-tumors.html</link>
	 <category>Cancer</category>
	 <pubDate>Fri, 26 Oct 2012 09:00:01 EST</pubDate>
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     <title>New framework for more effective vaccine vectors</title>
   	 <description>Despite the development of new technologies for successful vaccination against contagious diseases and cancer, there is a lack of standard operation procedures (SOPs) and cross-comparison. European scientists built the framework for the systematic production, validation and comparison of effective vaccine vectors.</description>
     <link>http://medicalxpress.com/news/2012-09-framework-effective-vaccine-vectors.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 20 Sep 2012 08:28:00 EST</pubDate>
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     <title>Retina transplantation improved by manipulating recipient retinal microenvironment</title>
   	 <description>A research team in the United Kingdom has found that insulin-like growth factor (IGF1) impacts cell transplantation of photoreceptor precursors by manipulating the retinal recipient microenvironment, enabling better migration and integration of the cells into the adult mouse retina.</description>
     <link>http://medicalxpress.com/news/2012-07-retina-transplantation-recipient-retinal-microenvironment.html</link>
	 <category>Ophthalmology</category>
	 <pubDate>Wed, 11 Jul 2012 16:00:10 EST</pubDate>
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     <title>An economical, effective and biocompatible gene therapy strategy promotes cardiac repair</title>
   	 <description>Dr Changfa Guo, Professor Chunsheng Wang and their co-investigators from Zhongshan hospital Fudan University, Shanghai, China have established a novel hyperbranched poly(amidoamine) (hPAMAM) nanoparticle based hypoxia regulated vascular endothelial growth factor (HRE-VEGF) gene therapy strategy which is an excellent substitute for the current expensive and uncontrollable VEGF gene delivery system. This discovery, reported in the June 2012 issue of Experimental Biology and Medicine, provides an economical, feasible and biocompatible gene therapy strategy for cardiac repair.</description>
     <link>http://medicalxpress.com/news/2012-07-economical-effective-biocompatible-gene-therapy.html</link>
	 <category>Medical research</category>
	 <pubDate>Fri, 06 Jul 2012 13:30:18 EST</pubDate>
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     <title>The neurological basis for fear and memory</title>
   	 <description>Fear conditioning using sound and taste aversion, as applied to mice, have revealed interesting information on the basis of memory allocation.</description>
     <link>http://medicalxpress.com/news/2012-06-neurological-basis-memory.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Mon, 18 Jun 2012 13:25:16 EST</pubDate>
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     <title>Study using stem cell therapy shows promise in fight against HIV</title>
   	 <description>UC Davis Health System researchers are a step closer to launching human clinical trials involving the use of an innovative stem cell therapy to fight the virus that causes AIDS.</description>
     <link>http://medicalxpress.com/news/2012-05-stem-cell-therapy-hiv.html</link>
	 <category>HIV &amp; AIDS</category>
	 <pubDate>Wed, 02 May 2012 11:07:53 EST</pubDate>
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     <title>Transforming scar tissue into beating hearts: The next instalment</title>
   	 <description>The latest research developments to reprogram scar tissue resulting from myocardial infarction (MI) into viable heart muscle cells, were presented at the Frontiers in CardioVascular Biology (FCVB) 2012 meeting, held 30 March to 1 April at the South Kensington Campus of Imperial College in London.</description>
     <link>http://medicalxpress.com/news/2012-04-scar-tissue-hearts.html</link>
	 <category>Cardiology</category>
	 <pubDate>Sun, 01 Apr 2012 12:35:46 EST</pubDate>
	 <guid isPermaLink="false">news252502521</guid>
	 
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     <title>Can nerve growth factor gene therapy prevent diabetic heart disease?</title>
   	 <description>Diabetes is a major risk factor for cardiovascular disease and can reduce blood supply to the heart tissue and damage cardiac cells, resulting in heart failure. New research has investigated if nerve growth factor (NGF) gene therapy can prevent diabetic heart failure and small vascular disease in mice.</description>
     <link>http://medicalxpress.com/news/2011-12-nerve-growth-factor-gene-therapy.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Tue, 20 Dec 2011 16:00:04 EST</pubDate>
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     <title>Advances in delivery of therapeutic genes to treat brain tumors</title>
   	 <description>Novel tools and methods for delivering therapeutic genes to cells in the central nervous system hold great promise for the development of new treatments to combat incurable neurologic diseases. Five of the most exciting developments in this rapidly advancing field are presented in a series of articles in the June issue of Human Gene Therapy, a peer-reviewed journal published by Mary Ann Liebert, Inc. </description>
     <link>http://medicalxpress.com/news/2011-06-advances-delivery-therapeutic-genes-brain.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 27 Jun 2011 15:53:44 EST</pubDate>
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     <title>Gene therapy success depends on ability to advance viral delivery vectors to commercialization</title>
   	 <description>Many gene therapy strategies designed to deliver a normal copy of a gene to cells carrying a disease-causing genetic mutation rely on a modified virus to transfer the gene product into affected tissues. One technology platform that is well suited for in vivo delivery of genes is based on adeno-associated viruses (AAV).  As these novel therapies move closer to commercialization, so do the methods for large-scale production and efficient delivery of AAV vectors, which are documented in a series of articles published online ahead of print in Human Gene Therapy, a peer-reviewed journal published by Mary Ann Liebert, Inc.</description>
     <link>http://medicalxpress.com/news/2011-05-gene-therapy-success-ability-advance.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 18 May 2011 13:09:59 EST</pubDate>
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