<?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: molecular pathology</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>Researchers untangle molecular pathology of giant axonal neuropathy</title>
   	 <description>Giant axonal neuropathy (GAN) is a rare genetic disorder that causes central and peripheral nervous system dysfunction. GAN is known to be caused by mutations in the gigaxonin gene and is characterized by tangling and aggregation of neural projections, but the mechanistic link between the genetic mutation and the effects on neurons is unclear.</description>
     <link>http://medicalxpress.com/news/2013-04-untangle-molecular-pathology-giant-axonal.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Mon, 15 Apr 2013 12:00:08 EST</pubDate>
	 <guid isPermaLink="false">news285240172</guid>
	 
</item>
<item>
     <title>Are human genes patentable?</title>
   	 <description>(Medical Xpress)—On April 15, the Supreme Court will hear oral argument in Association for Molecular Pathology v. Myriad Genetics, a case that could answer the question, &quot;Under what conditions, if any, are isolated human genes patentable?&quot; Kevin Emerson Collins, JD, patent law expert and professor of law at Washington University in St. Louis, believes that layered uncertainties make this case an unusually difficult case in which to predict the outcome.</description>
     <link>http://medicalxpress.com/news/2013-04-human-genes-patentable.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 11 Apr 2013 17:44:31 EST</pubDate>
	 <guid isPermaLink="false">news284921064</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2013/genes.png" width="90" height="90" />
</item>
<item>
     <title>Advances in molecular testing offer new hope for lung cancer patients</title>
   	 <description>The emergence of molecular diagnostic testing in lung cancer offers new hope for patients battling the number one cancer killer in the United States and abroad. Now, for the first time after a decade of biomarker testing in lung cancer, a uniform approach for testing for the EGFR mutation and ALK rearrangement along with the availability of targeted therapies offer lung cancer patients the chance for improved quality of life and more time with their loved ones.</description>
     <link>http://medicalxpress.com/news/2013-04-advances-molecular-lung-cancer-patients.html</link>
	 <category>Cancer</category>
	 <pubDate>Wed, 03 Apr 2013 16:49:40 EST</pubDate>
	 <guid isPermaLink="false">news284226573</guid>
	 
</item>
<item>
     <title>Researchers define how a gene mutated in Parkinson's disease may normally function to ensure neuronal health</title>
   	 <description>(Medical Xpress)—Cell biologists studying Parkinson's disease are training their sights on mitochondria, the energy source of the cell, whose activity in neurons appears to go awry in this devastating neurodegenerative illness. A neuron needs its mitochondria to be healthy and mobile, particularly during their continual cycles of fission and fusion in which damaged bits are removed and healthy mitochondria are renewed.</description>
     <link>http://medicalxpress.com/news/2013-03-gene-mutated-parkinson-disease-function.html</link>
	 <category>Medical research</category>
	 <pubDate>Fri, 22 Mar 2013 10:00:05 EST</pubDate>
	 <guid isPermaLink="false">news283163411</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2013/6-5-4-3-2-1-researchersd.jpg" width="90" height="90" />
</item>
<item>
     <title>Protein central to cancer stem cell formation provides new potential target</title>
   	 <description>Researchers have identified a pivotal protein in a cellular transformation that makes a cancer cell more resistant to treatment and more capable of growing and spreading, making it an inviting new target for drug development.</description>
     <link>http://medicalxpress.com/news/2013-02-protein-central-cancer-stem-cell.html</link>
	 <category>Cancer</category>
	 <pubDate>Wed, 13 Feb 2013 14:30:01 EST</pubDate>
	 <guid isPermaLink="false">news279987024</guid>
	 
</item>
<item>
     <title>A key gene for brain development</title>
   	 <description>(Medical Xpress)—Neurobiologists at the Research institute of Molecular Pathology (IMP) in Vienna have discovered one of the key genes required to make a brain. Mutations in this gene, called TUBB5, cause neurodevelopmental disease in children.</description>
     <link>http://medicalxpress.com/news/2012-12-key-gene-brain.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 14 Dec 2012 07:17:37 EST</pubDate>
	 <guid isPermaLink="false">news274691841</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2012/akeygeneforb.jpg" width="90" height="90" />
</item>
<item>
     <title>How the brain forms categories</title>
   	 <description>Neurobiologists at the Research Institute of Molecular Pathology (IMP) in Vienna investigated how the brain is able to group external stimuli into stable categories. They found the answer in the discrete dynamics of neuronal circuits. The journal Neuron publishes the results in its current issue.</description>
     <link>http://medicalxpress.com/news/2012-10-brain-categories.html</link>
	 <category>Neuroscience</category>
	 <pubDate>Sat, 20 Oct 2012 06:38:33 EST</pubDate>
	 <guid isPermaLink="false">news269933819</guid>
	 <media:thumbnail url="http://s.ph-cdn.com/newman/gfx/news/tmb/2012/345tertretr.jpg" width="90" height="90" />
</item>
<item>
     <title>AMP reports on possibilities, challenges, and applications of next-generation sequencing</title>
   	 <description>Bethesda, MD, October 18, 2012 The Association for Molecular Pathology (AMP) published the report of the Whole Genome Analysis (WGA) Working Group of the AMP Clinical Practice Committee in the November 2012 issue of The Journal of Molecular Diagnostics (JMD).</description>
     <link>http://medicalxpress.com/news/2012-10-amp-possibilities-applications-next-generation-sequencing.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 18 Oct 2012 15:53:30 EST</pubDate>
	 <guid isPermaLink="false">news269794400</guid>
	 
</item>
<item>
     <title>Aurora-A hinders tumor-suppressor to allow chemotherapy resistance</title>
   	 <description>A protein abundantly found in treatment-resistant cancers holds an important tumor-suppressor out of the cell nucleus, where it would normally detect DNA damage and force defective cells to kill themselves, a team of scientists reports in the current Cancer Cell.</description>
     <link>http://medicalxpress.com/news/2012-02-aurora-a-hinders-tumor-suppressor-chemotherapy-resistance.html</link>
	 <category>Cancer</category>
	 <pubDate>Mon, 27 Feb 2012 15:25:36 EST</pubDate>
	 <guid isPermaLink="false">news249578450</guid>
	 
</item>
<item>
     <title>AMP presented testimony to the Patent and Trademark Office requesting moratorium on human gene patenting</title>
   	 <description>Today, the Association for Molecular Pathology (AMP) asked the U.S. Patent and Trademark Office (USPTO) to place a moratorium on the issuing of patents on human genes during testimony presented at an Agency hearing on genetic diagnostic testing. AMP is the lead plaintiff of 20 plaintiffs in an American Civil Liberties Union (ACLU) sponsored lawsuit challenging the validity of patents on two hereditary breast and ovarian cancer genes, BRCA1 and BRCA2. AMP joined the litigation because of its members' first hand view of the harmful effects of gene patents on patients with genetic diseases and their at-risk family members. &quot;Every day, AMP members witness the ability of genetic testing to better patients' lives and improve their health. Unfortunately, they also experience firsthand the challenges imposed by gene patents that interfere with the practice of medicine and limit their treatment decisions,&quot; said Mary Williams, Executive Director of AMP.</description>
     <link>http://medicalxpress.com/news/2012-02-amp-testimony-patent-trademark-office.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 16 Feb 2012 13:28:07 EST</pubDate>
	 <guid isPermaLink="false">news248621216</guid>
	 
</item>
<item>
     <title>U.S. Supreme Court petitioned to review AMP, et al. lawsuit on gene patents</title>
   	 <description>The American Civil Liberties Union and the Public Patent Foundation have petitioned the U.S. Supreme Court to hear Association for Molecular Pathology v. U.S. Patent and Trademark Office, a case that challenges the validity of patents on two human genes associated with hereditary breast and ovarian cancer.</description>
     <link>http://medicalxpress.com/news/2011-12-supreme-court-petitioned-amp-al.html</link>
	 <category>Other</category>
	 <pubDate>Thu, 15 Dec 2011 13:21:06 EST</pubDate>
	 <guid isPermaLink="false">news243177656</guid>
	 
</item>
<item>
     <title>AMP opposes exclusive licensing of NIH proteomics patent</title>
   	 <description>The Association for Molecular Pathology (AMP) opposed the National Institutes of Health (NIH) proposal to exclusively license the subject matter of a cancer-related proteonomics patent application filed by the Agency. AMP's written remarks were submitted to NIH in response to a request for comments in the Federal Register Notice entitled, &quot;Prospective Grant of Exclusive License: The Development of a Companion Diagnostic Kit for Predicting Therapeutic Efficacy of Anti-Cancer Agents.&quot; The proposed license grants exclusive worldwide rights to use the relationships between levels of three proteins, PTEN, Akt, and mTOR and cancers of the breast, lung, and kidney. Under the terms of the prospective agreement, the licensor could provide laboratory test services and/or sell test kits.</description>
     <link>http://medicalxpress.com/news/2011-11-amp-opposes-exclusive-nih-proteomics.html</link>
	 <category>Other</category>
	 <pubDate>Tue, 22 Nov 2011 11:58:29 EST</pubDate>
	 <guid isPermaLink="false">news241185497</guid>
	 
</item>
<item>
     <title>Proposed NIH genetic testing registry lacks clarity, understates costs</title>
   	 <description>The Association for Molecular Pathology (AMP) submitted comments to the National Institutes of Health (NIH), in which the Association voiced concerns about the proposed Genetic Testing Registry (GTR) as currently designed, and requested that NIH take clarity and cost into consideration when designing a test registry.</description>
     <link>http://medicalxpress.com/news/2011-10-nih-genetic-registry-lacks-clarity.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 28 Oct 2011 10:16:08 EST</pubDate>
	 <guid isPermaLink="false">news239015756</guid>
	 
</item>
<item>
     <title>Association for Molecular Pathology comments on proposed changes to the common rule</title>
   	 <description>Yesterday, the Association for Molecular Pathology (AMP) submitted comments on the Advanced Notice of Proposed Rulemaking (ANPRM) called, Human Subjects Research Protections: Enhancing Protections for Research Subjects and Reducing Burden, Delay, and Ambiguity for Investigators. AMP commends the agency for its efforts to streamline the regulations to facilitate participation in research while maintaining the high level of protections research subjects deserve and expect. The Association also supports the creation of an excused category of studies and modifies the rule to allow a multi-site study to rely on a single institutional review board (IRB). However, AMP believes that this should not be mandatory and asks that the final rule deem this change to be optional.</description>
     <link>http://medicalxpress.com/news/2011-10-association-molecular-pathology-comments-common.html</link>
	 <category>Other</category>
	 <pubDate>Wed, 26 Oct 2011 11:03:30 EST</pubDate>
	 <guid isPermaLink="false">news238845803</guid>
	 
</item>
<item>
     <title>FDA draft guidance document may limit patient access to tests</title>
   	 <description>The Association for Molecular Pathology (AMP) submitted comments to the US Food and Drug Administration on the draft guidance document titled, &quot;Commercially Distributed In Vitro Diagnostic Products Labeled for Research Use Only or Investigational Use Only: Frequently Asked Questions.&quot; AMP is very concerned that this guidance could compromise the quality of patient care by severely reducing the availability of certain reagents and laboratory developed testing services that have become the standard of care for many diseases or conditions. Specifically, if enforced in its broadest sense without sufficient accommodations for low test volume or sufficient time for manufacturers to achieve submission compliance, the draft guidance document could result in reduced availability of testing services would limit a healthcare provider's ability to manage patient care, and ultimately limit patient access to new or improved molecular tests.</description>
     <link>http://medicalxpress.com/news/2011-08-fda-guidance-document-limit-patient.html</link>
	 <category>Medications</category>
	 <pubDate>Tue, 30 Aug 2011 11:40:52 EST</pubDate>
	 <guid isPermaLink="false">news233923187</guid>
	 
</item>
<item>
     <title>AMP releases statement on diagnostics in drug labels</title>
   	 <description>Today, the Association for Molecular Pathology (AMP) released its new position statement on the appropriate manner to reference diagnostic tests in drug labels. The association also met with officials from the United States Food and Drug Administration that participate in the effort to draft guidance documents for co-developed products and companion diagnostics to inform them of its new position statement.</description>
     <link>http://medicalxpress.com/news/2011-05-amp-statement-diagnostics-drug.html</link>
	 <category>Medications</category>
	 <pubDate>Mon, 16 May 2011 11:10:01 EST</pubDate>
	 <guid isPermaLink="false">news224761676</guid>
	 
</item>


</channel>
</rss>
