http://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&feed=atom&action=historyTeam:Heidelberg/Project - Revision history2024-03-29T07:37:32ZRevision history for this page on the wikiMediaWiki 1.16.5http://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=208124&oldid=prevNaoiwamoto at 03:50, 28 October 20102010-10-28T03:50:21Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cells and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div><br></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cells and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows <ins class="diffchange diffchange-inline">- </ins>for the first time <ins class="diffchange diffchange-inline">- </ins>to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (<ins class="diffchange diffchange-inline"><i></ins>in vitro<ins class="diffchange diffchange-inline"></i></ins>) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div><br></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><div class="t3">Graphical abstract</div><br></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><div class="t3">Graphical abstract</div><br></div></td></tr>
</table>Naoiwamotohttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=208072&oldid=prevNaoiwamoto at 03:48, 28 October 20102010-10-28T03:48:51Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian <del class="diffchange diffchange-inline">cell </del>and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div><br></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian <ins class="diffchange diffchange-inline">cells </ins>and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div><br></div></td></tr>
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</table>Naoiwamotohttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=207908&oldid=prevThomasU at 03:42, 28 October 20102010-10-28T03:42:31Z<p></p>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><div style="font-weight:bold">The circle of gene regulation</div></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><p>In living systems, gene expression is regulated by the interaction of miRNAs with the endogenous transcripts. The iGEM Team Heidelberg 2010 developed an fine-tuning regulatory mechanism of gene expression by miTuner, an auxiliary system employing both endogenous and exogenous miRNAs. Gene delivery by AAVs furthermore supports and enhances the efficiency of the fine-tuning regulation. </p></ins></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site strength in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div><<ins class="diffchange diffchange-inline">br</ins>></div></td></tr>
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</table>ThomasUhttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=206702&oldid=prevOla at 03:10, 28 October 20102010-10-28T03:10:13Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site <del class="diffchange diffchange-inline">strenght </del>in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA binding site <ins class="diffchange diffchange-inline">strength </ins>in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></div></td></tr>
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</table>Olahttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=206684&oldid=prevOla at 03:09, 28 October 20102010-10-28T03:09:53Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA <del class="diffchange diffchange-inline">activity </del>in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA <ins class="diffchange diffchange-inline">binding site strenght </ins>in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></div></td></tr>
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</table>Olahttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=202631&oldid=prevThomasU at 00:36, 28 October 20102010-10-28T00:36:40Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline">=Abstract=</del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><div <ins class="diffchange diffchange-inline">class</ins>="<ins class="diffchange diffchange-inline">t3</ins>"><ins class="diffchange diffchange-inline">miBricks</ins>: <ins class="diffchange diffchange-inline">DNA </ins>is <ins class="diffchange diffchange-inline">not enough</ins></div></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><div <del class="diffchange diffchange-inline">id</del>="<del class="diffchange diffchange-inline">wrapperheadline</del>"><del class="diffchange diffchange-inline">iGEM Heidelberg Mission 2010</del>: <del class="diffchange diffchange-inline">miBricks</div><br><br></del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline"><div id="projectabstract">The key to successful gene therapy </del>is <del class="diffchange diffchange-inline">integration of tissue specificity and fine-tuned target gene expression. iGEM Team Heidelberg 2010 unlocks the world of synthetic microRNAs. We engineered a toolkit for standardized measurements of interactions between artificial miRNAs and their binding sites. Thus, the expression level of any gene of choice could be arbitrarily adjusted by employing the corresponding binding site design. To produce tissue specific miRNA gene shuttles, we developed an evolution-based method for synthesis of new adeno associated viruses. In the future, miBricks could open the doors to new Synthetic Biology based medical approaches. </del></div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><div id="projectabstract">The iGEM Team Heidelberg 2010 unlocks the entirely new field of synthetic mi(cro)RNA technologies for mammalian cell and tissue engineering. By combining novel miRNA-based tools and protocols with cell-specific viral delivery systems our technology allows for the first time to use RNAi for rationally engineering gene regulation in targeted cells and organs. The two most prominent technologies we developed are a new measurement standard for real-time detection/quantification of miRNA activity in living cells (miMeasure) as well as a synthetic miRNA expression kit (miTuner) that allows to precisely repress (fully or partly) and thus fine-regulate any desired target gene. The rational design of this miRNA expression kit is accomplished by a novel computational model for miRNA-based gene silencing termed miBEAT. The miRNA technology is accompanied by a novel gene delivery technology based on re-designed Adeno-associated viruses (AAV) that were molecularly engineered and evolved to specifically deliver our miRNA expression kit to hepatocytes. The rationally designed synthetic miRNA expression kits were successfully validated in cultured, transformed or primary liver cells and then transferred into an adult mouse model. We thereby demonstrate that our miRNA expression kit is able to specifically fine tune the expression level of target genes both in cell culture (in vitro) and importantly also in the liver of mice (<i>in vivo</i>). In summary, we show that this technology allows the precise, predictable and quantitative adjustment of mammalian gene expression levels. Our work fosters the introduction of synthetic biology based technologies into the rapidly emerging field of personalized biomedicine.</div></ins></div></td></tr>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><div style="font-weight:bold">The circle of gene regulation</div></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><p>Fine-tuning of gene expression was achieved by application of miRNAs, both endo- and exogenous ones, as well as by the use of AAVs.</p></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><img src="https://static.igem.org/mediawiki/2010/2/26/RegCircle.png"/></ins></div></td></tr>
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</table>ThomasUhttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=168945&oldid=prevOla at 23:42, 26 October 20102010-10-26T23:42:18Z<p></p>
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</table>Olahttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=135106&oldid=prevKleinsorg at 17:32, 24 October 20102010-10-24T17:32:09Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>{{:Team:Heidelberg/Pagetop|<del class="diffchange diffchange-inline">home</del>}}</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>{{:Team:Heidelberg/Pagetop|<ins class="diffchange diffchange-inline">project</ins>}}</div></td></tr>
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</table>Kleinsorghttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=129003&oldid=prevAlejandroHD at 01:54, 24 October 20102010-10-24T01:54:34Z<p></p>
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</table>AlejandroHDhttp://2010.igem.org/wiki/index.php?title=Team:Heidelberg/Project&diff=128992&oldid=prevAlejandroHD at 01:52, 24 October 20102010-10-24T01:52:20Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline">This page </del>is <del class="diffchange diffchange-inline">still under construction</del>.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><div id="wrapperheadline">iGEM Heidelberg Mission 2010: miBricks</div><br><br></ins></div></td></tr>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><div id="projectabstract">The key to successful gene therapy </ins>is <ins class="diffchange diffchange-inline">integration of tissue specificity and fine-tuned target gene expression</ins>. <ins class="diffchange diffchange-inline">iGEM Team Heidelberg 2010 unlocks the world of synthetic microRNAs. We engineered a toolkit for standardized measurements of interactions between artificial miRNAs and their binding sites. Thus, the expression level of any gene of choice could be arbitrarily adjusted by employing the corresponding binding site design. To produce tissue specific miRNA gene shuttles, we developed an evolution-based method for synthesis of new adeno associated viruses. In the future, miBricks could open the doors to new Synthetic Biology based medical approaches. </div></ins></div></td></tr>
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</table>AlejandroHD