<?xml version="1.0" encoding="utf-8"?>
<?xml-stylesheet type="text/xsl" href="http://medicalxpress.com/tmpl/default/css/default/feedRSS.xsl"?>
<rss version="2.0" 
	xmlns:media="http://search.yahoo.com/mrss/">
<channel>
<title>Medical Xpress: PHYSorg news tagged with: genetic characteristics</title>
<link>http://medicalxpress.com/</link>
<language>en-us</language> 
<description>Medical Xpress internet news portal provides the latest news on Health and Medicine.</description>

 <item>
     <title>Breast cancer heterogeneity no barrier to predictive testing, study shows</title>
   	 <description>Breast cancers contain many different cell types with different patterns of gene expression, but a new study provides reassurance that this variability should not be a barrier to using gene expression tests to help tailor cancer treatments to individual patients.</description>
     <link>http://medicalxpress.com/news/2013-05-breast-cancer-heterogeneity-barrier.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 02 May 2013 09:21:30 EST</pubDate>
	 <guid isPermaLink="false">news286705284</guid>
	 
</item>
<item>
     <title>French patients keep HIV at bay despite stopping drugs (Update)</title>
   	 <description>A small French study of 14 HIV patients who have remained healthy for years after stopping drug treatment offers fresh evidence that early medical intervention may lead to a &quot;functional cure&quot; for AIDS, researchers said Thursday.</description>
     <link>http://medicalxpress.com/news/2013-03-french-patients-hiv-bay-drugs.html</link>
	 <category>HIV &amp; AIDS</category>
	 <pubDate>Thu, 14 Mar 2013 17:09:00 EST</pubDate>
	 <guid isPermaLink="false">news282499733</guid>
	 
</item>
<item>
     <title>Recon 2 modeling may help tailor treatments for patients with metabolic diseases, cancer</title>
   	 <description>An international team of researchers, including an investigator with the Virginia Bioinformatics Institute at Virginia Tech, has produced what may be the most comprehensive computer model of human metabolism yet developed.</description>
     <link>http://medicalxpress.com/news/2013-03-recon-tailor-treatments-patients-metabolic.html</link>
	 <category>Medical research</category>
	 <pubDate>Mon, 04 Mar 2013 10:05:09 EST</pubDate>
	 <guid isPermaLink="false">news281613903</guid>
	 
</item>
<item>
     <title>Study maps human metabolism in health and disease</title>
   	 <description>Scientists have produced an instruction manual for the human genome that provides a framework to better understand the relationship between an individual's genetic make-up and their lifestyle.</description>
     <link>http://medicalxpress.com/news/2013-03-human-metabolism-health-disease.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 03 Mar 2013 13:00:01 EST</pubDate>
	 <guid isPermaLink="false">news281521158</guid>
	 
</item>
<item>
     <title>Biomarker may identify neuroblastomas with sensitivity to BET bromodomain inhibitors</title>
   	 <description>Neuroblastoma, the most common malignant tumor of early childhood, is frequently associated with the presence of MYCN amplification, a genetic biomarker associated with poor prognosis. Researchers have determined that tumors containing MYCN amplification are sensitive to a new class of drugs, BET bromodomain inhibitors.</description>
     <link>http://medicalxpress.com/news/2013-02-biomarker-neuroblastomas-sensitivity-bromodomain-inhibitors.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 21 Feb 2013 10:32:14 EST</pubDate>
	 <guid isPermaLink="false">news280665121</guid>
	 
</item>
<item>
     <title>Researchers identify elusive taste stem cells</title>
   	 <description>Scientists at the Monell Center have identified the location and certain genetic characteristics of taste stem cells on the tongue. The findings will facilitate techniques to grow and manipulate new functional taste cells for both clinical and research purposes.</description>
     <link>http://medicalxpress.com/news/2013-02-elusive-stem-cells.html</link>
	 <category>Medical research</category>
	 <pubDate>Mon, 04 Feb 2013 00:20:01 EST</pubDate>
	 <guid isPermaLink="false">news279118489</guid>
	 
</item>
<item>
     <title>DNA analysis reveals genetic variants that make individuals susceptible to form of glaucoma prevalent in Asian countries</title>
   	 <description>Glaucoma is the leading cause of irreversible blindness in the world. A form known as primary open angle glaucoma (POAG) predominantly affects Europeans and Africans, whereas primary closed angle glaucoma (PACG) mostly affects Asians. Despite the high levels of blindness caused by PACG in Asian countries, scientists lacked the information that could confirm the disease's genetic basis and provide a starting point to tackle the problem.</description>
     <link>http://medicalxpress.com/news/2013-01-dna-analysis-reveals-genetic-variants.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 30 Jan 2013 07:20:05 EST</pubDate>
	 <guid isPermaLink="false">news278749743</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2013/eyediseaseop.jpg" width="90" height="90" />
</item>
<item>
     <title>Lung cancer patients with pockets of resistance prolong disease control by 'weeding the garden'</title>
   	 <description>The central skill of cancer is its ability to mutate – that's how it became cancerous in the first place. Once it's started down that path, it's not so difficult for a cancer cell to mutate again and again. This means that different tumors within a single patient or even different areas within the same cancerous deposit may develop different genetic characteristics. This heterogeneity helps cancer escape control by new, targeted cancer therapy drugs.</description>
     <link>http://medicalxpress.com/news/2012-12-lung-cancer-patients-pockets-resistance.html</link>
	 <category>Cancer</category>
	 <pubDate>Sat, 01 Dec 2012 06:12:23 EST</pubDate>
	 <guid isPermaLink="false">news273564734</guid>
	 
</item>
<item>
     <title>Gene variations linked to lung cancer susceptibility in Asian women</title>
   	 <description>An international group of scientists has identified three genetic regions that predispose Asian women who have never smoked to lung cancer. The finding provides further evidence that risk of lung cancer among never-smokers, especially Asian women, may be associated with certain unique inherited genetic characteristics that distinguishes it from lung cancer in smokers.</description>
     <link>http://medicalxpress.com/news/2012-11-gene-variations-linked-lung-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Sun, 11 Nov 2012 13:13:06 EST</pubDate>
	 <guid isPermaLink="false">news271861968</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2012/86fujvk.jpg" width="90" height="91" />
</item>
<item>
     <title>Biological markers increase clinical trial success rate of new breast cancer drugs</title>
   	 <description>Using biological markers—genetic characteristics that are associated with some patients with breast cancer—can increase the success rate of clinical trials for breast cancer drugs by almost 50 per cent, says new research from the University of Toronto Mississauga.</description>
     <link>http://medicalxpress.com/news/2012-10-biological-markers-clinical-trial-success.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 01 Oct 2012 12:51:48 EST</pubDate>
	 <guid isPermaLink="false">news268314695</guid>
	 
</item>
<item>
     <title>BGI develops whole exome sequencing analysis of FFPE DNA samples to boost biomedicine</title>
   	 <description>BGI Tech Solutions announced today that they have achieved whole exome sequencing analysis of total degraded DNA as low as 200 ng from formalin fixed paraffin embedded (FFPE) samples. This advancement enables researchers to efficiently uncover the genetic information from FFPE disease samples such as cancers and infectious diseases, with the advantages of high reliability, accuracy and fast turnaround time.</description>
     <link>http://medicalxpress.com/news/2012-09-bgi-exome-sequencing-analysis-ffpe.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 18 Sep 2012 09:51:55 EST</pubDate>
	 <guid isPermaLink="false">news267180706</guid>
	 
</item>
<item>
     <title>New approach for efficient analysis of emerging genetic data</title>
   	 <description>(Medical Xpress)—With the ability to sequence human genes comes an onslaught of raw material about the genetic characteristics that distinguish us, and wading through these reserves of data poses a major challenge for life scientists. Researchers at Roswell Park Cancer Institute (RPCI) and the Center for Human Genome Variation at Duke University Medical Center (DUMC) have developed an approach for analyzing data that can help researchers studying genetic factors in disease to quickly cull out relevant genetic patterns and identify variants that lead to particular disorders.</description>
     <link>http://medicalxpress.com/news/2012-09-approach-efficient-analysis-emerging-genetic.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 06 Sep 2012 09:26:47 EST</pubDate>
	 <guid isPermaLink="false">news266142401</guid>
	 
</item>
<item>
     <title>BGI achieves next-gen sequencing analysis of FFPE DNA as low as 200 ng</title>
   	 <description>BGI, the world's largest genomics organization, reported that it can use next-generation sequencing to analyze DNA as low as 200 ng from formalin-fixed paraffin-embedded (FFPE) samples. This advancement enables researchers to easily identify the genetic details and pathology mechanism of FFPE disease samples, especially for some rare tumors, with higher accuracy and reliability than existing techniques.</description>
     <link>http://medicalxpress.com/news/2012-03-bgi-next-gen-sequencing-analysis-ffpe.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 08 Mar 2012 10:52:41 EST</pubDate>
	 <guid isPermaLink="false">news250426351</guid>
	 
</item>
<item>
     <title>Single-cell sequencing leads to a new era of cancer research</title>
   	 <description>BGI, the world's largest genomics organization, developed single-cell genome sequencing technology and published two research papers for cancer single-cell sequencing in the research journal Cell. In the papers, which were published today in the same issue of Cell, BGI researchers applied their new single-cell sequencing (SCS) method to identify the genetic characteristics of essential thrombocythemia (ET, a kind of blood neoplasm) and clear cell renal cell carcinoma (ccRCC, a typical kidney cancer), and demonstrated that single cell analyses of highly heterogeneous tissues provide much clearer intratumoral genetic pictures and developmental history than previous bulk tissue sequencing.</description>
     <link>http://medicalxpress.com/news/2012-03-single-cell-sequencing-era-cancer.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 02 Mar 2012 10:47:05 EST</pubDate>
	 <guid isPermaLink="false">news249907619</guid>
	 
</item>
<item>
     <title>Lawson research team working to personalize cancer care</title>
   	 <description>The Lawson Translational Cancer Research Team (LTCRT) of the Lawson Health Research Institute is one of five groups participating in a new study that seeks to personalize cancer drug treatment.</description>
     <link>http://medicalxpress.com/news/2011-12-lawson-team-personalize-cancer.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 12 Dec 2011 13:00:03 EST</pubDate>
	 <guid isPermaLink="false">news242916553</guid>
	 
</item>
<item>
     <title>When well-known flu strains 'hook up' dangerous progeny can result</title>
   	 <description>A new University of Maryland-led study finds that 'sex' between the virus responsible for the 2009 flu pandemic (H1N1) and a common type of avian flu virus (H9N2) can produce offspring -- new combined flu viruses -- with the potential for creating a new influenza pandemic.</description>
     <link>http://medicalxpress.com/news/2011-07-well-known-flu-strains-dangerous-progeny.html</link>
	 <category>Diseases, Conditions, Syndromes</category>
	 <pubDate>Wed, 13 Jul 2011 12:36:44 EST</pubDate>
	 <guid isPermaLink="false">news229779385</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2011/whenwellknow.jpg" width="90" height="90" />
</item>
<item>
     <title>Zebrafish models identify high-risk genetic features in leukemia patients</title>
   	 <description>Leukemia is the most common childhood cancer; it also occurs in adults. Now researchers working with zebrafish at Huntsman Cancer Institute (HCI) at the University of Utah have identified previously undiscovered high-risk genetic features in T-cell acute lymphocytic leukemia (T-ALL), according to an article published online May 9, 2011, in the cancer research journal Oncogene. When compared to samples from human patients with T-ALL, these genetic characteristics allowed scientists to predict which patients may have more aggressive forms of the disease that either recur after remission or do not respond to treatment.</description>
     <link>http://medicalxpress.com/news/2011-05-zebrafish-high-risk-genetic-features-leukemia.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 10 May 2011 12:32:01 EST</pubDate>
	 <guid isPermaLink="false">news224249478</guid>
	 
</item>


</channel>
</rss>
