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		<title>Gene Therapy</title>
		<link>http://sujithkpillai.wordpress.com/2006/10/18/gene-therapy/</link>
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		<pubDate>Wed, 18 Oct 2006 11:33:37 +0000</pubDate>
		<dc:creator>sujithkpillai</dc:creator>
				<category><![CDATA[Science]]></category>

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		<description><![CDATA[What is gene therapy? Genes, which are carried on chromosomes, are the basic physical and functional units of heredity. Genes are specific sequences of bases that encode instructions on how to make proteins. Although genes get a lot of attention, it’s the proteins that perform most life functions and even make up the majority of [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sujithkpillai.wordpress.com&amp;blog=418263&amp;post=6&amp;subd=sujithkpillai&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<h3><strong>What is gene therapy?</strong></h3>
<p>Genes, which are carried on chromosomes, are the basic physical and functional    units of heredity. Genes are specific sequences of bases that encode instructions    on how to make proteins. Although genes get a lot of attention, it’s the    proteins that perform most life functions and even make up the majority of cellular    structures. When genes are altered so that the encoded proteins are unable to    carry out their normal functions, genetic disorders can result.</p>
<p>Gene therapy is a technique for correcting defective genes responsible for    disease development. Researchers may use one of several approaches for correcting    faulty genes:</p>
<ul>
<li>A normal gene may be inserted into a nonspecific location within the genome      to replace a nonfunctional gene. This approach is most common.</li>
<li>An abnormal gene could be swapped for a normal gene through homologous recombination.</li>
<li>The abnormal gene could be repaired through selective reverse mutation,      which returns the gene to its normal function.</li>
<li>The regulation (the degree to which a gene is turned on or off) of a particular      gene could be altered.</li>
</ul>
<h3><a title="work" name="work"></a>Working Of Gene Therapy</h3>
<p>For correcting the defective genes responsible for    disease by replacing an healthy one with that. There are so many methods to replace the defective genes. Currently, the most common vector is a virus that has been genetically    altered to carry normal human DNA.</p>
<p>Some of the different types of viruses used as gene therapy vectors:</p>
<ul>
<li><strong>Retroviruses</strong> &#8211; A class of viruses that can create double-stranded      DNA copies of their RNA genomes. These copies of its genome can be integrated      into the chromosomes of host cells. Human immunodeficiency virus (HIV) is      a retrovirus.</li>
<li><strong>Adenoviruses</strong> &#8211; A class of viruses with double-stranded DNA genomes      that cause respiratory, intestinal, and eye infections in humans. The virus      that causes the common cold is an adenovirus.</li>
<li><strong>Adeno-associated viruses</strong> &#8211; A class of small, single-stranded DNA      viruses that can insert their genetic material at a specific site on chromosome      19.</li>
<li><strong>Herpes simplex viruses</strong> &#8211; A class of double-stranded DNA viruses that      infect a particular cell type, neurons. Herpes simplex virus type 1 is a common      human pathogen that causes cold sores.</li>
</ul>
<p>Besides virus-mediated gene-delivery systems, there are several non viral options    for gene delivery. The simplest method is the direct introduction of therapeutic    DNA into target cells. This approach is limited in its application because it    can be used only with certain tissues and requires large amounts of DNA.</p>
<p>Another nonviral approach involves the creation of an artificial lipid sphere    with an aqueous core. This liposome, which carries the therapeutic DNA, is capable    of passing the DNA through the target cell&#8217;s membrane.</p>
<p>Researchers also are experimenting with introducing a 47th (artificial human)    chromosome into target cells. This chromosome would exist autonomously alongside    the standard 46 &#8211;not affecting their workings or causing any mutations. It    would be a large vector capable of carrying substantial amounts of genetic code,    and scientists anticipate that, because of its construction and autonomy, the    body&#8217;s immune systems would not attack it. A problem with this potential method    is the difficulty in delivering such a large molecule to the nucleus of a target    cell.</p>
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		<title>Human Genome Project (HGP)</title>
		<link>http://sujithkpillai.wordpress.com/2006/10/18/human-genome-project-hgp/</link>
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		<pubDate>Wed, 18 Oct 2006 11:03:47 +0000</pubDate>
		<dc:creator>sujithkpillai</dc:creator>
				<category><![CDATA[Science]]></category>

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		<description><![CDATA[The Human Genome Project (HGP) is a project to map and sequence the 3 billion nucleotides contained in the human genome and to identify all the genes present in it. There are currently two human genome projects: the first is the international HGP which is being produced by a group of international government bodies and [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=sujithkpillai.wordpress.com&amp;blog=418263&amp;post=5&amp;subd=sujithkpillai&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>The <strong>Human Genome Project</strong> (HGP) is a project to map and sequence the 3 billion nucleotides contained in the human genome and to identify all the genes present in it. There are currently two human genome projects: the first is the international HGP which is being produced by a group of international government bodies and organizations, and the second by a private company Celera Genomics.</p>
<p>This researches begun formally in 1990, the U.S. Human Genome Project was a 13-year effort          coordinated by the U.S. Department of Energy and the National Institutes          of Health. The project originally was planned to last 15 years, but rapid          technological advances accelerated the completion date to 2003. Project          goals          were to</p>
<ul>
<li><em>identify</em> all the approximately 20,000-25,000 genes in human DNA,</li>
<li><em>determine</em> the sequences of the 3 billion chemical base pairs            that make up human DNA,</li>
<li><em>store</em> this information in databases,</li>
<li><em>improve</em> tools for data analysis,</li>
<li><em>transfer</em> related technologies to the private sector, and</li>
<li><em>address</em> the ethical, legal, and social issues (ELSI) that may            arise from the project.</li>
</ul>
<p><font size="+1"><strong>What&#8217;s a genome?</strong></font></p>
<ul>
<li>A <strong>genome</strong> is all the DNA in an organism, including its genes. Genes carry information for making all the proteins required by all organisms. These proteins determine, among other things, how the organism looks, how well its body metabolizes food or fights infection, and sometimes even how it behaves.</li>
<li>DNA is made up of four similar chemicals called nucleotides (adenine(A),Guanine(G),Thymine(T) and Cytosine(C) )are the basic and functional units of DNA that are repeated millions or billions of times throughout a genome. The human genome, for example, has 3 billion pairs of bases.</li>
</ul>
<p>More information just visit</p>
<p><a href="http://www.ornl.gov/sci/techresources/Human_Genome/project/info.shtml">http://www.ornl.gov/sci/techresources/Human_Genome/project/info.shtml</a></p>
<p><a href="http://www.ornl.gov/sci/techresources/Human_Genome/project/info.shtml"></a><a href="http://jgi.doe.gov/education/how/">http://jgi.doe.gov/education/how/ </a></p>
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