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<title>Medical Xpress: PHYSorg news tagged with: genes and development</title>
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 <item>
     <title>Study IDs key protein for cell death, offers way to kill cancer cells by forcing them into programmed-death pathway</title>
   	 <description>When cells suffer too much DNA damage, they are usually forced to undergo programmed cell death, or apoptosis. However, cancer cells often ignore these signals, flourishing even after chemotherapy drugs have ravaged their DNA.</description>
     <link>http://medicalxpress.com/news/2013-05-ids-key-protein-cell-death.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 14 May 2013 06:27:15 EST</pubDate>
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     <title>Researchers discover that errors in RNA splicing lead to a class of neurological disorders </title>
   	 <description>(Medical Xpress)—Researchers have found that missteps in a basic cellular process, RNA splicing, is the culprit behind a class of rare neurological disorders manifested by intellectual disability and stunted development.</description>
     <link>http://medicalxpress.com/news/2013-03-errors-rna-splicing-class-neurological.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 29 Mar 2013 06:50:17 EST</pubDate>
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     <title>Cell reprogramming during liver regeneration</title>
   	 <description>During embryonic development, animals generate many different types of cells, each with a distinct function and identity.</description>
     <link>http://medicalxpress.com/news/2013-03-cell-reprogramming-liver-regeneration.html</link>
	 <category>Medical research</category>
	 <pubDate>Thu, 28 Mar 2013 12:06:25 EST</pubDate>
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     <title>Molecular master switch for pancreatic cancer identified, potential predictor of treatment outcome</title>
   	 <description>A recently described master regulator protein may explain the development of aberrant cell growth in the pancreas spurred by inflammation</description>
     <link>http://medicalxpress.com/news/2013-02-molecular-master-pancreatic-cancer-potential.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 12 Feb 2013 14:20:03 EST</pubDate>
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     <title>Researchers uncover novel role of BRCA1 in regulating the survival of skin stem cells</title>
   	 <description>Our DNA, which stores our genetic information, is constantly exposed to damage. If not properly repaired, DNA damage can lead to cell death. This, in turn, can  lead to tissue exhaustion and ageing, or induce mutations resulting in uncontrolled cell proliferation and cancer. Brca1 is a key gene that mediates DNA repair, and mutations in Brca1 lead to familial and sporadic breast and ovarian cancer in humans.</description>
     <link>http://medicalxpress.com/news/2013-01-uncover-role-brca1-survival-skin.html</link>
	 <category>Cancer</category>
	 <pubDate>Thu, 03 Jan 2013 07:59:49 EST</pubDate>
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     <title>Study offers clues to cause of kids' brain tumors</title>
   	 <description>(Medical Xpress)—Insights from a genetic condition that causes brain cancer are helping scientists better understand the most common type of brain tumor in children.</description>
     <link>http://medicalxpress.com/news/2012-11-clues-kids-brain-tumors.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 16 Nov 2012 07:42:49 EST</pubDate>
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     <title>Unlocking the destiny of a cell</title>
   	 <description>(Medical Xpress)— Scientists have discovered that breaking a biological signaling system in an embryo allows them to change the destiny of a cell. The findings could lead to new ways of making replacement organs.</description>
     <link>http://medicalxpress.com/news/2012-11-destiny-cell.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 01 Nov 2012 09:22:23 EST</pubDate>
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     <title>Researchers reveal how Trop2 protein drives tumor growth in prostate, other epithelial cancers</title>
   	 <description>(Medical Xpress)—Researchers led by Tanya Stoyanova and Dr. Owen Witte of UCLA's Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research have determined how a protein known as Trop2 drives the growth of tumor cells in prostate and other epithelial cancers.</description>
     <link>http://medicalxpress.com/news/2012-10-reveal-trop2-protein-tumor-growth.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 16 Oct 2012 07:33:15 EST</pubDate>
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     <title>Protein found to regulate red blood cell size and number</title>
   	 <description>The adult human circulatory system contains between 20 and 30 trillion red blood cells (RBCs), the precise size and number of which can vary from person to person. Some people may have fewer, but larger RBCs, while others may have a larger number of smaller RBCs. Although these differences in size and number may seem inconsequential, they raise an important question: Just what controls these characteristics of RBCs?</description>
     <link>http://medicalxpress.com/news/2012-08-protein-red-blood-cell-size.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 28 Aug 2012 18:23:09 EST</pubDate>
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</item>
<item>
     <title>Study suggests patients should be screened before receiving vemurafenib</title>
   	 <description>Different genetic mistakes driving skin cancer may affect  how patients respond to the drug vemurafenib, providing grounds to screen people with melanoma skin cancer before treatment, a new study by Cancer Research UK scientists suggests</description>
     <link>http://medicalxpress.com/news/2012-08-patients-screened-vemurafenib.html</link>
	 <category>Cancer</category>
	 <pubDate>Tue, 14 Aug 2012 04:39:40 EST</pubDate>
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     <title>Elimination of two ribosome subunits activates cell cycle control</title>
   	 <description>Alterations in the formation of ribosomes (the elements of the cell where proteins are made) cause the induction of p53 protein and cell cycle disruption. This process is crucial to understand fundamental biological processes and the emergence of various diseases. Now, scientists at the Bellvitge Biomedical Research Institute (IDIBELL) have found that this response is achieved independently, depending on which subunit of the ribosome (40S and 60S) is impaired, by the joint action of two proteins of the ribosome. The research results are published in the latest issue of the journal Genes and Development.</description>
     <link>http://medicalxpress.com/news/2012-05-ribosome-subunits-cell.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 22 May 2012 10:39:10 EST</pubDate>
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     <title>The influence of the mother: Maternal epigenetic inheritance</title>
   	 <description>(Medical Xpress) -- A study published in Genes and Development from scientists at the Friedrich Miescher Institute for Biomedical Research pinpoints the importance of maternal epigenetic influences during early embryogenesis in mammals. A chromatin regulatory complex in the oocyte ensures that the proper luggage of maternal transcripts and chromatin structures control the first steps in the formation of an embryo. In the absence of this epigenetic regulator the embryo fails to develop correctly.</description>
     <link>http://medicalxpress.com/news/2012-05-mother-maternal-epigenetic-inheritance.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 07 May 2012 08:58:44 EST</pubDate>
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     <title>Coordinating the circadian clock: Researchers find that molecular pair controls time-keeping and fat metabolism</title>
   	 <description>(PhysOrg.com) -- The 24-hour internal clock controls many aspects of human behavior and physiology, including sleep, blood pressure, and metabolism. Disruption in circadian rhythms leads to increased incidence of many diseases, including metabolic disease and cancer. Each cell of the body has its own internal timing mechanism, which is controlled by proteins that keep one another in check.</description>
     <link>http://medicalxpress.com/news/2012-04-circadian-clock-molecular-pair-time-keeping.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 04 Apr 2012 18:06:37 EST</pubDate>
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     <title>How protein networks stabilize muscle fibers: Same mechanism as for DNA</title>
   	 <description>The same mechanism that stabilises the DNA in the cell nucleus is also important for the structure and function of vertebrate muscle cells. This has been established by RUB-researchers led by Prof. Dr. Wolfgang Linke (Institute of Physiology) in cooperation with American and German colleagues. An enzyme attaches a methyl group to the protein Hsp90, which then forms a complex with the muscle protein titin. When the researchers disrupted this protein network through genetic manipulation in zebrafish the muscle structure partly disintegrated. The scientists have thus shown that methylation also plays a significant role outside the nucleus. They published their results in Genes and Development.</description>
     <link>http://medicalxpress.com/news/2012-01-protein-networks-stabilize-muscle-fibers.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 23 Jan 2012 12:55:02 EST</pubDate>
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     <title>Weill Institute researchers uncover basic cell pathway</title>
   	 <description>Although all cells in an organism have the same DNA, cells function differently based on the genes they express. While most studies of gene expression focus on activities in the cell's nucleus, a new Cornell study finds that processes outside the nucleus -- along the cell membrane -- also play important roles in gene expression.</description>
     <link>http://medicalxpress.com/news/2011-05-weill-uncover-basic-cell-pathway.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 24 May 2011 07:31:16 EST</pubDate>
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     <title>Cancer scientists discover new way breast cancer cells adapt to environmental stress</title>
   	 <description>An international research team led by Dr. Tak Mak, Director, The Campbell Family Institute for Breast Cancer Research at Princess Margaret Hospital (PMH), has discovered a new aspect of &quot;metabolic transformation&quot;, the process whereby tumour cells adapt and survive under conditions that would kill normal cells.</description>
     <link>http://medicalxpress.com/news/2011-05-cancer-scientists-breast-cells-environmental.html</link>
	 <category>Cancer</category>
	 <pubDate>Sun, 15 May 2011 11:38:25 EST</pubDate>
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