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<p>Gene Therapy advance online publication, April 2, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.35">doi:10.1038/gt.2009.35</a>
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<b>QuickMap: a public tool for large-scale gene therapy vector insertion site mapping and analysis</b>
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<p>Gene Therapy advance online publication, April 23, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.37">doi:10.1038/gt.2009.37</a>
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<b>Effects of ciliary muscle plasmid electrotransfer of TNF-&#945; soluble receptor variants in experimental uveitis</b>
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<b>Herpes simplex virus delivery to orthotopic rectal carcinoma results in an efficient and selective antitumor effect</b>
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<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.44">doi:10.1038/gt.2009.44</a>
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<dc:creator>A Khalaileh</dc:creator>
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<dc:creator>E Pikarsky</dc:creator>
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<dc:identifier>doi:10.1038/gt.2009.44</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
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<b>Asymmetry in siRNA design</b>
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<p>Gene Therapy advance online publication, April 30, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.45">doi:10.1038/gt.2009.45</a>
</p>
<p>Author: D Grimm</p>
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<dc:title>Asymmetry in siRNA design</dc:title>
<dc:creator>D Grimm</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.45</dc:identifier>
<dc:source>Gene Therapy advance online publication, April 30, 2009</dc:source>
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<b>Independent and high-level dual-gene expression in adult stem-progenitor cells from a single lentiviral vector</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.46">doi:10.1038/gt.2009.46</a>
</p>
<p>Authors: J Tian
                    &amp; S T Andreadis</p>
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<dc:title>Independent and high-level dual-gene expression in adult stem-progenitor cells from a single lentiviral vector</dc:title>
<dc:creator>J Tian</dc:creator>
<dc:creator>S T Andreadis</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.46</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
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<b>(Strept)avidin-displaying lentiviruses as versatile tools for targeting and dual imaging of gene delivery</b>
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<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.47">doi:10.1038/gt.2009.47</a>
</p>
<p>Authors: M U Kaikkonen, H P Lesch, J Pikkarainen, J K R&#228;ty, T Vuorio, T Huhtala, M Taavitsainen, T Laitinen, P Tuunanen, O Gr&#246;hn, A N&#228;rv&#228;nen, K J Airenne
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<dc:title>(Strept)avidin-displaying lentiviruses as versatile tools for targeting and dual imaging of gene delivery</dc:title>
<dc:creator>M U Kaikkonen</dc:creator>
<dc:creator>H P Lesch</dc:creator>
<dc:creator>J Pikkarainen</dc:creator>
<dc:creator>J K R&#228;ty</dc:creator>
<dc:creator>T Vuorio</dc:creator>
<dc:creator>T Huhtala</dc:creator>
<dc:creator>M Taavitsainen</dc:creator>
<dc:creator>T Laitinen</dc:creator>
<dc:creator>P Tuunanen</dc:creator>
<dc:creator>O Gr&#246;hn</dc:creator>
<dc:creator>A N&#228;rv&#228;nen</dc:creator>
<dc:creator>K J Airenne</dc:creator>
<dc:creator>S Yl&#228;-Herttuala</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.47</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
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<p>
<b>Excision repair cross-complementing 1 expression protects against ischemic injury following middle cerebral artery occlusion in the rat brain</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.48">doi:10.1038/gt.2009.48</a>
</p>
<p>Authors: K-Y He, S-Z Yang, D-H Shen, L-M Zhang, S-D Lu
                    &amp; F-Y Sun</p>
]]></content:encoded>
<dc:title>Excision repair cross-complementing 1 expression protects against ischemic injury following middle cerebral artery occlusion in the rat brain</dc:title>
<dc:creator>K-Y He</dc:creator>
<dc:creator>S-Z Yang</dc:creator>
<dc:creator>D-H Shen</dc:creator>
<dc:creator>L-M Zhang</dc:creator>
<dc:creator>S-D Lu</dc:creator>
<dc:creator>F-Y Sun</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.48</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
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<title>Lentiviral vectors with amplified &#946; cell-specific gene expression</title>
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<content:encoded><![CDATA[
            
<p>
<b>Lentiviral vectors with amplified &#946; cell-specific gene expression</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.49">doi:10.1038/gt.2009.49</a>
</p>
<p>Authors: K L Shaw, E Pais, S Ge, C Hardee, D Skelton, R P Hollis, G M Crooks
                    &amp; D B Kohn</p>
]]></content:encoded>
<dc:title>Lentiviral vectors with amplified &#946; cell-specific gene expression</dc:title>
<dc:creator>K L Shaw</dc:creator>
<dc:creator>E Pais</dc:creator>
<dc:creator>S Ge</dc:creator>
<dc:creator>C Hardee</dc:creator>
<dc:creator>D Skelton</dc:creator>
<dc:creator>R P Hollis</dc:creator>
<dc:creator>G M Crooks</dc:creator>
<dc:creator>D B Kohn</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.49</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 14, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.49</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.49</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.50">
<title>Subconjunctival gene delivery of the transcription factor GA-binding protein delays corneal neovascularization in a mouse model</title>
<link>http://dx.doi.org/10.1038/gt.2009.50</link>
<content:encoded><![CDATA[
            
<p>
<b>Subconjunctival gene delivery of the transcription factor GA-binding protein delays corneal neovascularization in a mouse model</b>
</p>
<p>Gene Therapy advance online publication, May 7, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.50">doi:10.1038/gt.2009.50</a>
</p>
<p>Authors: K C Yoon, J A Bae, H J Park, S K Im, H J Oh, X H Lin, M Y Kim, J H Lee, S E Lee, K Y Ahn
                    &amp; K K Kim</p>
]]></content:encoded>
<dc:title>Subconjunctival gene delivery of the transcription factor GA-binding protein delays corneal neovascularization in a mouse model</dc:title>
<dc:creator>K C Yoon</dc:creator>
<dc:creator>J A Bae</dc:creator>
<dc:creator>H J Park</dc:creator>
<dc:creator>S K Im</dc:creator>
<dc:creator>H J Oh</dc:creator>
<dc:creator>X H Lin</dc:creator>
<dc:creator>M Y Kim</dc:creator>
<dc:creator>J H Lee</dc:creator>
<dc:creator>S E Lee</dc:creator>
<dc:creator>K Y Ahn</dc:creator>
<dc:creator>K K Kim</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.50</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 7, 2009</dc:source>
<dc:date>2009-05-07</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 7, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.50</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.50</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.51">
<title>Human neural stem cells overexpressing glial cell line-derived neurotrophic factor in experimental cerebral hemorrhage</title>
<link>http://dx.doi.org/10.1038/gt.2009.51</link>
<content:encoded><![CDATA[
            
<p>
<b>Human neural stem cells overexpressing glial cell line-derived neurotrophic factor in experimental cerebral hemorrhage</b>
</p>
<p>Gene Therapy advance online publication, June 25, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.51">doi:10.1038/gt.2009.51</a>
</p>
<p>Authors: H J Lee, I H Park, H J Kim
                    &amp; S U Kim</p>
]]></content:encoded>
<dc:title>Human neural stem cells overexpressing glial cell line-derived neurotrophic factor in experimental cerebral hemorrhage</dc:title>
<dc:creator>H J Lee</dc:creator>
<dc:creator>I H Park</dc:creator>
<dc:creator>H J Kim</dc:creator>
<dc:creator>S U Kim</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.51</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 25, 2009</dc:source>
<dc:date>2009-06-25</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 25, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.51</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.51</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.52">
<title>Long-term AAV vector gene and protein expression in mouse brain from a small pan-cellular promoter is similar to neural cell promoters</title>
<link>http://dx.doi.org/10.1038/gt.2009.52</link>
<content:encoded><![CDATA[
            
<p>
<b>Long-term AAV vector gene and protein expression in mouse brain from a small pan-cellular promoter is similar to neural cell promoters</b>
</p>
<p>Gene Therapy advance online publication, May 21, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.52">doi:10.1038/gt.2009.52</a>
</p>
<p>Authors: T Husain, M A Passini, M K Parente, N W Fraser
                    &amp; J H Wolfe</p>
]]></content:encoded>
<dc:title>Long-term AAV vector gene and protein expression in mouse brain from a small pan-cellular promoter is similar to neural cell promoters</dc:title>
<dc:creator>T Husain</dc:creator>
<dc:creator>M A Passini</dc:creator>
<dc:creator>M K Parente</dc:creator>
<dc:creator>N W Fraser</dc:creator>
<dc:creator>J H Wolfe</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.52</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 21, 2009</dc:source>
<dc:date>2009-05-21</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 21, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.52</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.52</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.53">
<title>Shortened ALK1 regulatory fragment maintains a specific activity in arteries feeding ischemic tissues</title>
<link>http://dx.doi.org/10.1038/gt.2009.53</link>
<content:encoded><![CDATA[
            
<p>
<b>Shortened ALK1 regulatory fragment maintains a specific activity in arteries feeding ischemic tissues</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.53">doi:10.1038/gt.2009.53</a>
</p>
<p>Authors: X Li, Y Yonenaga
                    &amp; T Seki</p>
]]></content:encoded>
<dc:title>Shortened ALK1 regulatory fragment maintains a specific activity in arteries feeding ischemic tissues</dc:title>
<dc:creator>X Li</dc:creator>
<dc:creator>Y Yonenaga</dc:creator>
<dc:creator>T Seki</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.53</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 14, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.53</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.53</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.54">
<title>Efficient nonviral Sleeping Beauty transposon-based TCR gene transfer to peripheral blood lymphocytes confers antigen-specific antitumor reactivity</title>
<link>http://dx.doi.org/10.1038/gt.2009.54</link>
<content:encoded><![CDATA[
            
<p>
<b>Efficient nonviral Sleeping Beauty transposon-based TCR gene transfer to peripheral blood lymphocytes confers antigen-specific antitumor reactivity</b>
</p>
<p>Gene Therapy advance online publication, June 4, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.54">doi:10.1038/gt.2009.54</a>
</p>
<p>Authors: P D Peng, C J Cohen, S Yang, C Hsu, S Jones, Y Zhao, Z Zheng, S A Rosenberg
                    &amp; R A Morgan</p>
]]></content:encoded>
<dc:title>Efficient nonviral Sleeping Beauty transposon-based TCR gene transfer to peripheral blood lymphocytes confers antigen-specific antitumor reactivity</dc:title>
<dc:creator>P D Peng</dc:creator>
<dc:creator>C J Cohen</dc:creator>
<dc:creator>S Yang</dc:creator>
<dc:creator>C Hsu</dc:creator>
<dc:creator>S Jones</dc:creator>
<dc:creator>Y Zhao</dc:creator>
<dc:creator>Z Zheng</dc:creator>
<dc:creator>S A Rosenberg</dc:creator>
<dc:creator>R A Morgan</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.54</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 4, 2009</dc:source>
<dc:date>2009-06-04</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 4, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.54</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.54</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.55">
<title>Visualization of in vivo electroporation-mediated transgene expression in experimental tumors by optical and magnetic resonance imaging</title>
<link>http://dx.doi.org/10.1038/gt.2009.55</link>
<content:encoded><![CDATA[
            
<p>
<b>Visualization of in vivo electroporation-mediated transgene expression in experimental tumors by optical and magnetic resonance imaging</b>
</p>
<p>Gene Therapy advance online publication, May 21, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.55">doi:10.1038/gt.2009.55</a>
</p>
<p>Authors: W Aung, S Hasegawa, M Koshikawa-Yano, T Obata, H Ikehira, T Furukawa, I Aoki
                    &amp; T Saga</p>
]]></content:encoded>
<dc:title>Visualization of in vivo electroporation-mediated transgene expression in experimental tumors by optical and magnetic resonance imaging</dc:title>
<dc:creator>W Aung</dc:creator>
<dc:creator>S Hasegawa</dc:creator>
<dc:creator>M Koshikawa-Yano</dc:creator>
<dc:creator>T Obata</dc:creator>
<dc:creator>H Ikehira</dc:creator>
<dc:creator>T Furukawa</dc:creator>
<dc:creator>I Aoki</dc:creator>
<dc:creator>T Saga</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.55</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 21, 2009</dc:source>
<dc:date>2009-05-21</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 21, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.55</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.55</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.56">
<title>Ad5&#47;3-9HIF-&#916;24-VEGFR-1-Ig, an infectivity enhanced, dual-targeted and antiangiogenic oncolytic adenovirus for kidney cancer treatment</title>
<link>http://dx.doi.org/10.1038/gt.2009.56</link>
<content:encoded><![CDATA[
            
<p>
<b>Ad5&#47;3-9HIF-&#916;24-VEGFR-1-Ig, an infectivity enhanced, dual-targeted and antiangiogenic oncolytic adenovirus for kidney cancer treatment</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.56">doi:10.1038/gt.2009.56</a>
</p>
<p>Authors: K Guse, I Diaconu, M Rajecki, M Sloniecka, T Hakkarainen, A Ristim&#228;ki, A Kanerva, S Pesonen
                    &amp; A Hemminki</p>
]]></content:encoded>
<dc:title>Ad5&#47;3-9HIF-&#916;24-VEGFR-1-Ig, an infectivity enhanced, dual-targeted and antiangiogenic oncolytic adenovirus for kidney cancer treatment</dc:title>
<dc:creator>K Guse</dc:creator>
<dc:creator>I Diaconu</dc:creator>
<dc:creator>M Rajecki</dc:creator>
<dc:creator>M Sloniecka</dc:creator>
<dc:creator>T Hakkarainen</dc:creator>
<dc:creator>A Ristim&#228;ki</dc:creator>
<dc:creator>A Kanerva</dc:creator>
<dc:creator>S Pesonen</dc:creator>
<dc:creator>A Hemminki</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.56</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 14, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.56</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.56</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.57">
<title>Gene transfer using bovine adeno-associated virus in the guinea pig cochlea</title>
<link>http://dx.doi.org/10.1038/gt.2009.57</link>
<content:encoded><![CDATA[
            
<p>
<b>Gene transfer using bovine adeno-associated virus in the guinea pig cochlea</b>
</p>
<p>Gene Therapy advance online publication, May 21, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.57">doi:10.1038/gt.2009.57</a>
</p>
<p>Authors: S B Shibata, G Di Pasquale, S R Cortez, J A Chiorini
                    &amp; Y Raphael</p>
]]></content:encoded>
<dc:title>Gene transfer using bovine adeno-associated virus in the guinea pig cochlea</dc:title>
<dc:creator>S B Shibata</dc:creator>
<dc:creator>G Di Pasquale</dc:creator>
<dc:creator>S R Cortez</dc:creator>
<dc:creator>J A Chiorini</dc:creator>
<dc:creator>Y Raphael</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.57</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 21, 2009</dc:source>
<dc:date>2009-05-21</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 21, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.57</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.57</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.58">
<title>Analysis of neuronal proliferation, migration and differentiation in the postnatal brain using equine infectious anemia virus-based lentiviral vectors</title>
<link>http://dx.doi.org/10.1038/gt.2009.58</link>
<content:encoded><![CDATA[
            
<p>
<b>Analysis of neuronal proliferation, migration and differentiation in the postnatal brain using equine infectious anemia virus-based lentiviral vectors</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.58">doi:10.1038/gt.2009.58</a>
</p>
<p>Authors: B V Jacquet, M Patel, M Iyengar, H Liang, B Therit, R Salinas-Mondragon, C Lai, J C Olsen, E S Anton
                    &amp; H T Ghashghaei</p>
]]></content:encoded>
<dc:title>Analysis of neuronal proliferation, migration and differentiation in the postnatal brain using equine infectious anemia virus-based lentiviral vectors</dc:title>
<dc:creator>B V Jacquet</dc:creator>
<dc:creator>M Patel</dc:creator>
<dc:creator>M Iyengar</dc:creator>
<dc:creator>H Liang</dc:creator>
<dc:creator>B Therit</dc:creator>
<dc:creator>R Salinas-Mondragon</dc:creator>
<dc:creator>C Lai</dc:creator>
<dc:creator>J C Olsen</dc:creator>
<dc:creator>E S Anton</dc:creator>
<dc:creator>H T Ghashghaei</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.58</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.58</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.58</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.59">
<title>A muscle-targeting peptide displayed on AAV2 improves muscle tropism on systemic delivery</title>
<link>http://dx.doi.org/10.1038/gt.2009.59</link>
<content:encoded><![CDATA[
            
<p>
<b>A muscle-targeting peptide displayed on AAV2 improves muscle tropism on systemic delivery</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.59">doi:10.1038/gt.2009.59</a>
</p>
<p>Authors: C-Y Yu, Z Yuan, Z Cao, B Wang, C Qiao, J Li
                    &amp; X Xiao</p>
]]></content:encoded>
<dc:title>A muscle-targeting peptide displayed on AAV2 improves muscle tropism on systemic delivery</dc:title>
<dc:creator>C-Y Yu</dc:creator>
<dc:creator>Z Yuan</dc:creator>
<dc:creator>Z Cao</dc:creator>
<dc:creator>B Wang</dc:creator>
<dc:creator>C Qiao</dc:creator>
<dc:creator>J Li</dc:creator>
<dc:creator>X Xiao</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.59</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.59</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.59</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.60">
<title>Chitosan&#8211;plasmid nanoparticle formulations for IM and SC delivery of recombinant FGF-2 and PDGF-BB or generation of antibodies</title>
<link>http://dx.doi.org/10.1038/gt.2009.60</link>
<content:encoded><![CDATA[
            
<p>
<b>Chitosan&#8211;plasmid nanoparticle formulations for IM and SC delivery of recombinant FGF-2 and PDGF-BB or generation of antibodies</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.60">doi:10.1038/gt.2009.60</a>
</p>
<p>Authors: M Jean, F Smaoui, M Lavertu, S M&#233;thot, L Bouhdoud, M D Buschmann
                    &amp; A Merzouki</p>
]]></content:encoded>
<dc:title>Chitosan&#8211;plasmid nanoparticle formulations for IM and SC delivery of recombinant FGF-2 and PDGF-BB or generation of antibodies</dc:title>
<dc:creator>M Jean</dc:creator>
<dc:creator>F Smaoui</dc:creator>
<dc:creator>M Lavertu</dc:creator>
<dc:creator>S M&#233;thot</dc:creator>
<dc:creator>L Bouhdoud</dc:creator>
<dc:creator>M D Buschmann</dc:creator>
<dc:creator>A Merzouki</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.60</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 14, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.60</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.60</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.61">
<title>Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse</title>
<link>http://dx.doi.org/10.1038/gt.2009.61</link>
<content:encoded><![CDATA[
            
<p>
<b>Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse</b>
</p>
<p>Gene Therapy advance online publication, May 21, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.61">doi:10.1038/gt.2009.61</a>
</p>
<p>Authors: T K Park, Z Wu, S Kjellstrom, Y Zeng, R A Bush, P A Sieving
                    &amp; P Colosi</p>
]]></content:encoded>
<dc:title>Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse</dc:title>
<dc:creator>T K Park</dc:creator>
<dc:creator>Z Wu</dc:creator>
<dc:creator>S Kjellstrom</dc:creator>
<dc:creator>Y Zeng</dc:creator>
<dc:creator>R A Bush</dc:creator>
<dc:creator>P A Sieving</dc:creator>
<dc:creator>P Colosi</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.61</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 21, 2009</dc:source>
<dc:date>2009-05-21</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 21, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.61</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.61</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.62">
<title>siRNA silencing of keratinocyte-specific GFP expression in a transgenic mouse skin model</title>
<link>http://dx.doi.org/10.1038/gt.2009.62</link>
<content:encoded><![CDATA[
            
<p>
<b>siRNA silencing of keratinocyte-specific GFP expression in a transgenic mouse skin model</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.62">doi:10.1038/gt.2009.62</a>
</p>
<p>Authors: E Gonzalez-Gonzalez, H Ra, R P Hickerson, Q Wang, W Piyawattanametha, M J Mandella, G S Kino, D Leake, A A Avilion, O Solgaard, T C Doyle, C H Contag
                    &amp; R L Kaspar</p>
]]></content:encoded>
<dc:title>siRNA silencing of keratinocyte-specific GFP expression in a transgenic mouse skin model</dc:title>
<dc:creator>E Gonzalez-Gonzalez</dc:creator>
<dc:creator>H Ra</dc:creator>
<dc:creator>R P Hickerson</dc:creator>
<dc:creator>Q Wang</dc:creator>
<dc:creator>W Piyawattanametha</dc:creator>
<dc:creator>M J Mandella</dc:creator>
<dc:creator>G S Kino</dc:creator>
<dc:creator>D Leake</dc:creator>
<dc:creator>A A Avilion</dc:creator>
<dc:creator>O Solgaard</dc:creator>
<dc:creator>T C Doyle</dc:creator>
<dc:creator>C H Contag</dc:creator>
<dc:creator>R L Kaspar</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.62</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.62</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.62</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.63">
<title>Adenovirus-mediated gene transfer of fibromodulin inhibits neointimal hyperplasia in an organ culture model of human saphenous vein graft disease</title>
<link>http://dx.doi.org/10.1038/gt.2009.63</link>
<content:encoded><![CDATA[
            
<p>
<b>Adenovirus-mediated gene transfer of fibromodulin inhibits neointimal hyperplasia in an organ culture model of human saphenous vein graft disease</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.63">doi:10.1038/gt.2009.63</a>
</p>
<p>Authors: P Ranjzad, H K Salem
                    &amp; P A Kingston</p>
]]></content:encoded>
<dc:title>Adenovirus-mediated gene transfer of fibromodulin inhibits neointimal hyperplasia in an organ culture model of human saphenous vein graft disease</dc:title>
<dc:creator>P Ranjzad</dc:creator>
<dc:creator>H K Salem</dc:creator>
<dc:creator>P A Kingston</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.63</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.63</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.63</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.64">
<title>Non-cell-autonomous effects of vector-expressed regulatory RNAs in mammalian heart cells</title>
<link>http://dx.doi.org/10.1038/gt.2009.64</link>
<content:encoded><![CDATA[
            
<p>
<b>Non-cell-autonomous effects of vector-expressed regulatory RNAs in mammalian heart cells</b>
</p>
<p>Gene Therapy advance online publication, June 11, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.64">doi:10.1038/gt.2009.64</a>
</p>
<p>Authors: E Kizana, E Cingolani
                    &amp; E Marb&#225;n</p>
]]></content:encoded>
<dc:title>Non-cell-autonomous effects of vector-expressed regulatory RNAs in mammalian heart cells</dc:title>
<dc:creator>E Kizana</dc:creator>
<dc:creator>E Cingolani</dc:creator>
<dc:creator>E Marb&#225;n</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.64</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 11, 2009</dc:source>
<dc:date>2009-06-11</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 11, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.64</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.64</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.65">
<title>Development of fiber-substituted adenovirus vectors containing foreign peptides in the adenovirus serotype 35 fiber knob</title>
<link>http://dx.doi.org/10.1038/gt.2009.65</link>
<content:encoded><![CDATA[
            
<p>
<b>Development of fiber-substituted adenovirus vectors containing foreign peptides in the adenovirus serotype 35 fiber knob</b>
</p>
<p>Gene Therapy advance online publication, June 11, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.65">doi:10.1038/gt.2009.65</a>
</p>
<p>Authors: H Matsui, F Sakurai, S Kurachi, K Tashiro, K Sugio, K Kawabata, K Yamanishi
                    &amp; H Mizuguchi</p>
]]></content:encoded>
<dc:title>Development of fiber-substituted adenovirus vectors containing foreign peptides in the adenovirus serotype 35 fiber knob</dc:title>
<dc:creator>H Matsui</dc:creator>
<dc:creator>F Sakurai</dc:creator>
<dc:creator>S Kurachi</dc:creator>
<dc:creator>K Tashiro</dc:creator>
<dc:creator>K Sugio</dc:creator>
<dc:creator>K Kawabata</dc:creator>
<dc:creator>K Yamanishi</dc:creator>
<dc:creator>H Mizuguchi</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.65</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 11, 2009</dc:source>
<dc:date>2009-06-11</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 11, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.65</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.65</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.66">
<title>Therapeutic silencing of an endogenous gene by siRNA cream in an arthritis model mouse</title>
<link>http://dx.doi.org/10.1038/gt.2009.66</link>
<content:encoded><![CDATA[
            
<p>
<b>Therapeutic silencing of an endogenous gene by siRNA cream in an arthritis model mouse</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.66">doi:10.1038/gt.2009.66</a>
</p>
<p>Authors: M Takanashi, K Oikawa, K Sudo, M Tanaka, K Fujita, A Ishikawa, S Nakae, R L Kaspar, M Matsuzaki, M Kudo
                    &amp; M Kuroda</p>
]]></content:encoded>
<dc:title>Therapeutic silencing of an endogenous gene by siRNA cream in an arthritis model mouse</dc:title>
<dc:creator>M Takanashi</dc:creator>
<dc:creator>K Oikawa</dc:creator>
<dc:creator>K Sudo</dc:creator>
<dc:creator>M Tanaka</dc:creator>
<dc:creator>K Fujita</dc:creator>
<dc:creator>A Ishikawa</dc:creator>
<dc:creator>S Nakae</dc:creator>
<dc:creator>R L Kaspar</dc:creator>
<dc:creator>M Matsuzaki</dc:creator>
<dc:creator>M Kudo</dc:creator>
<dc:creator>M Kuroda</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.66</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.66</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.66</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.67">
<title>Transgene-specific host responses in cutaneous gene therapy: the role of cells expressing the transgene</title>
<link>http://dx.doi.org/10.1038/gt.2009.67</link>
<content:encoded><![CDATA[
            
<p>
<b>Transgene-specific host responses in cutaneous gene therapy: the role of cells expressing the transgene</b>
</p>
<p>Gene Therapy advance online publication, May 14, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.67">doi:10.1038/gt.2009.67</a>
</p>
<p>Authors: Z Zhang, C Kuscu
                    &amp; S Ghazizadeh</p>
]]></content:encoded>
<dc:title>Transgene-specific host responses in cutaneous gene therapy: the role of cells expressing the transgene</dc:title>
<dc:creator>Z Zhang</dc:creator>
<dc:creator>C Kuscu</dc:creator>
<dc:creator>S Ghazizadeh</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.67</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 14, 2009</dc:source>
<dc:date>2009-05-14</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 14, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.67</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.67</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.68">
<title>PML has a predictive role in tumor cell permissiveness to interferon-sensitive oncolytic viruses</title>
<link>http://dx.doi.org/10.1038/gt.2009.68</link>
<content:encoded><![CDATA[
            
<p>
<b>PML has a predictive role in tumor cell permissiveness to interferon-sensitive oncolytic viruses</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.68">doi:10.1038/gt.2009.68</a>
</p>
<p>Authors: P T Sobol, J L Hummel, R M Rodrigues
                    &amp; K L Mossman</p>
]]></content:encoded>
<dc:title>PML has a predictive role in tumor cell permissiveness to interferon-sensitive oncolytic viruses</dc:title>
<dc:creator>P T Sobol</dc:creator>
<dc:creator>J L Hummel</dc:creator>
<dc:creator>R M Rodrigues</dc:creator>
<dc:creator>K L Mossman</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.68</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.68</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.68</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.69">
<title>In vitro analysis of cidofovir and genetically engineered TK expression as potential approaches for the intervention of ColoAd1-based treatment of cancer</title>
<link>http://dx.doi.org/10.1038/gt.2009.69</link>
<content:encoded><![CDATA[
            
<p>
<b>In vitro analysis of cidofovir and genetically engineered TK expression as potential approaches for the intervention of ColoAd1-based treatment of cancer</b>
</p>
<p>Gene Therapy advance online publication, May 21, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.69">doi:10.1038/gt.2009.69</a>
</p>
<p>Authors: M Bauzon, F Jin, P Kretschmer
                    &amp; T Hermiston</p>
]]></content:encoded>
<dc:title>In vitro analysis of cidofovir and genetically engineered TK expression as potential approaches for the intervention of ColoAd1-based treatment of cancer</dc:title>
<dc:creator>M Bauzon</dc:creator>
<dc:creator>F Jin</dc:creator>
<dc:creator>P Kretschmer</dc:creator>
<dc:creator>T Hermiston</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.69</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 21, 2009</dc:source>
<dc:date>2009-05-21</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 21, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.69</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.69</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.70">
<title>Translational stability for sickle gene therapy</title>
<link>http://dx.doi.org/10.1038/gt.2009.70</link>
<content:encoded><![CDATA[
            
<p>
<b>Translational stability for sickle gene therapy</b>
</p>
<p>Gene Therapy advance online publication, June 25, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.70">doi:10.1038/gt.2009.70</a>
</p>
<p>Author: M C Walters</p>
]]></content:encoded>
<dc:title>Translational stability for sickle gene therapy</dc:title>
<dc:creator>M C Walters</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.70</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 25, 2009</dc:source>
<dc:date>2009-06-25</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 25, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.70</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.70</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.71">
<title>Systemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders</title>
<link>http://dx.doi.org/10.1038/gt.2009.71</link>
<content:encoded><![CDATA[
            
<p>
<b>Systemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders</b>
</p>
<p>Gene Therapy advance online publication, May 28, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.71">doi:10.1038/gt.2009.71</a>
</p>
<p>Authors: B M Koppanati, J Li, X Xiao
                    &amp; P R Clemens</p>
]]></content:encoded>
<dc:title>Systemic delivery of AAV8 in utero results in gene expression in diaphragm and limb muscle: treatment implications for muscle disorders</dc:title>
<dc:creator>B M Koppanati</dc:creator>
<dc:creator>J Li</dc:creator>
<dc:creator>X Xiao</dc:creator>
<dc:creator>P R Clemens</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.71</dc:identifier>
<dc:source>Gene Therapy advance online publication, May 28, 2009</dc:source>
<dc:date>2009-05-28</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>May 28, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.71</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.71</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.72">
<title>Double E1B 19&#8201;kDa- and E1B 55&#8201;kDa-deleted oncolytic adenovirus in combination with radiotherapy elicits an enhanced anti-tumor effect</title>
<link>http://dx.doi.org/10.1038/gt.2009.72</link>
<content:encoded><![CDATA[
            
<p>
<b>Double E1B 19&#8201;kDa- and E1B 55&#8201;kDa-deleted oncolytic adenovirus in combination with radiotherapy elicits an enhanced anti-tumor effect</b>
</p>
<p>Gene Therapy advance online publication, June 4, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.72">doi:10.1038/gt.2009.72</a>
</p>
<p>Authors: J Kim, P-H Kim, J Y Yoo, A-R Yoon, H J Choi, J Seong, I-W Kim, J-H Kim
                    &amp; C-O Yun</p>
]]></content:encoded>
<dc:title>Double E1B 19&#8201;kDa- and E1B 55&#8201;kDa-deleted oncolytic adenovirus in combination with radiotherapy elicits an enhanced anti-tumor effect</dc:title>
<dc:creator>J Kim</dc:creator>
<dc:creator>P-H Kim</dc:creator>
<dc:creator>J Y Yoo</dc:creator>
<dc:creator>A-R Yoon</dc:creator>
<dc:creator>H J Choi</dc:creator>
<dc:creator>J Seong</dc:creator>
<dc:creator>I-W Kim</dc:creator>
<dc:creator>J-H Kim</dc:creator>
<dc:creator>C-O Yun</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.72</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 4, 2009</dc:source>
<dc:date>2009-06-04</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 4, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.72</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.72</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.75">
<title>Redirecting human CD4&#43;CD25&#43; regulatory T cells from the peripheral blood with pre-defined target specificity</title>
<link>http://dx.doi.org/10.1038/gt.2009.75</link>
<content:encoded><![CDATA[
            
<p>
<b>Redirecting human CD4&#43;CD25&#43; regulatory T cells from the peripheral blood with pre-defined target specificity</b>
</p>
<p>Gene Therapy advance online publication, June 25, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.75">doi:10.1038/gt.2009.75</a>
</p>
<p>Authors: A A Hombach, D Kofler, G Rappl
                    &amp; H Abken</p>
]]></content:encoded>
<dc:title>Redirecting human CD4&#43;CD25&#43; regulatory T cells from the peripheral blood with pre-defined target specificity</dc:title>
<dc:creator>A A Hombach</dc:creator>
<dc:creator>D Kofler</dc:creator>
<dc:creator>G Rappl</dc:creator>
<dc:creator>H Abken</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.75</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 25, 2009</dc:source>
<dc:date>2009-06-25</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 25, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.75</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.75</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.76">
<title>An immobilized nanoparticle-based platform for efficient gene knockdown of targeted cells in the circulation</title>
<link>http://dx.doi.org/10.1038/gt.2009.76</link>
<content:encoded><![CDATA[
            
<p>
<b>An immobilized nanoparticle-based platform for efficient gene knockdown of targeted cells in the circulation</b>
</p>
<p>Gene Therapy advance online publication, June 25, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.76">doi:10.1038/gt.2009.76</a>
</p>
<p>Authors: Z Huang
                    &amp; M R King</p>
]]></content:encoded>
<dc:title>An immobilized nanoparticle-based platform for efficient gene knockdown of targeted cells in the circulation</dc:title>
<dc:creator>Z Huang</dc:creator>
<dc:creator>M R King</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.76</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 25, 2009</dc:source>
<dc:date>2009-06-25</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 25, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.76</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.76</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.77">
<title>CR1&#47;2 is an important suppressor of Adenovirus-induced innate immune responses and is required for induction of neutralizing antibodies</title>
<link>http://dx.doi.org/10.1038/gt.2009.77</link>
<content:encoded><![CDATA[
            
<p>
<b>CR1&#47;2 is an important suppressor of Adenovirus-induced innate immune responses and is required for induction of neutralizing antibodies</b>
</p>
<p>Gene Therapy advance online publication, June 25, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.77">doi:10.1038/gt.2009.77</a>
</p>
<p>Authors: S S Seregin, Y A Aldhamen, D M Appledorn, N J Schuldt, A J McBride, M Bujold, S S Godbehere
                    &amp; A Amalfitano</p>
]]></content:encoded>
<dc:title>CR1&#47;2 is an important suppressor of Adenovirus-induced innate immune responses and is required for induction of neutralizing antibodies</dc:title>
<dc:creator>S S Seregin</dc:creator>
<dc:creator>Y A Aldhamen</dc:creator>
<dc:creator>D M Appledorn</dc:creator>
<dc:creator>N J Schuldt</dc:creator>
<dc:creator>A J McBride</dc:creator>
<dc:creator>M Bujold</dc:creator>
<dc:creator>S S Godbehere</dc:creator>
<dc:creator>A Amalfitano</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.77</dc:identifier>
<dc:source>Gene Therapy advance online publication, June 25, 2009</dc:source>
<dc:date>2009-06-25</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>June 25, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.77</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.77</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.79">
<title>Immunological priming potentiates non-viral anti-inflammatory gene therapy treatment of neuropathic pain</title>
<link>http://dx.doi.org/10.1038/gt.2009.79</link>
<content:encoded><![CDATA[
            
<p>
<b>Immunological priming potentiates non-viral anti-inflammatory gene therapy treatment of neuropathic pain</b>
</p>
<p>Gene Therapy advance online publication, July 2, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.79">doi:10.1038/gt.2009.79</a>
</p>
<p>Authors: E Sloane, S Langer, B Jekich, J Mahoney, T Hughes, M Frank, W Seibert, G Huberty, B Coats, J Harrison, D Klinman, S Poole, S Maier, K Johnson, R Chavez, L R Watkins, L Leinwand
                    &amp; E Milligan</p>
]]></content:encoded>
<dc:title>Immunological priming potentiates non-viral anti-inflammatory gene therapy treatment of neuropathic pain</dc:title>
<dc:creator>E Sloane</dc:creator>
<dc:creator>S Langer</dc:creator>
<dc:creator>B Jekich</dc:creator>
<dc:creator>J Mahoney</dc:creator>
<dc:creator>T Hughes</dc:creator>
<dc:creator>M Frank</dc:creator>
<dc:creator>W Seibert</dc:creator>
<dc:creator>G Huberty</dc:creator>
<dc:creator>B Coats</dc:creator>
<dc:creator>J Harrison</dc:creator>
<dc:creator>D Klinman</dc:creator>
<dc:creator>S Poole</dc:creator>
<dc:creator>S Maier</dc:creator>
<dc:creator>K Johnson</dc:creator>
<dc:creator>R Chavez</dc:creator>
<dc:creator>L R Watkins</dc:creator>
<dc:creator>L Leinwand</dc:creator>
<dc:creator>E Milligan</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.79</dc:identifier>
<dc:source>Gene Therapy advance online publication, July 2, 2009</dc:source>
<dc:date>2009-07-02</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>July 2, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.79</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.79</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.83">
<title>Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome</title>
<link>http://dx.doi.org/10.1038/gt.2009.83</link>
<content:encoded><![CDATA[
            
<p>
<b>Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome</b>
</p>
<p>Gene Therapy advance online publication, July 2, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.83">doi:10.1038/gt.2009.83</a>
</p>
<p>Authors: Z Zeier, A Kumar, K Bodhinathan, J A Feller, T C Foster
                    &amp; D C Bloom</p>
]]></content:encoded>
<dc:title>Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome</dc:title>
<dc:creator>Z Zeier</dc:creator>
<dc:creator>A Kumar</dc:creator>
<dc:creator>K Bodhinathan</dc:creator>
<dc:creator>J A Feller</dc:creator>
<dc:creator>T C Foster</dc:creator>
<dc:creator>D C Bloom</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.83</dc:identifier>
<dc:source>Gene Therapy advance online publication, July 2, 2009</dc:source>
<dc:date>2009-07-02</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>July 2, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.83</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.83</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2009.84">
<title>Ultrasound-targeted microbubble destruction enhances AAV-mediated gene transfection in human RPE cells in vitro and rat retina in vivo</title>
<link>http://dx.doi.org/10.1038/gt.2009.84</link>
<content:encoded><![CDATA[
            
<p>
<b>Ultrasound-targeted microbubble destruction enhances AAV-mediated gene transfection in human RPE cells in vitro and rat retina in vivo</b>
</p>
<p>Gene Therapy advance online publication, July 2, 2009. <a href="http://dx.doi.org/10.1038/gt.2009.84">doi:10.1038/gt.2009.84</a>
</p>
<p>Authors: H L Li, X Z Zheng, H P Wang, F Li, Y Wu
                    &amp; L F Du</p>
]]></content:encoded>
<dc:title>Ultrasound-targeted microbubble destruction enhances AAV-mediated gene transfection in human RPE cells in vitro and rat retina in vivo</dc:title>
<dc:creator>H L Li</dc:creator>
<dc:creator>X Z Zheng</dc:creator>
<dc:creator>H P Wang</dc:creator>
<dc:creator>F Li</dc:creator>
<dc:creator>Y Wu</dc:creator>
<dc:creator>L F Du</dc:creator>
<dc:identifier>doi:10.1038/gt.2009.84</dc:identifier>
<dc:source>Gene Therapy advance online publication, July 2, 2009</dc:source>
<dc:date>2009-07-02</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>July 2, 2009</prism:publicationDate>
<prism:doi>10.1038/gt.2009.84</prism:doi>
<prism:url>http://dx.doi.org/10.1038/gt.2009.84</prism:url>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
</rdf:RDF>
