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<p>Gene Therapy advance online publication, September 25, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.149">doi:10.1038/gt.2008.149</a>
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<p>Authors: M L D Broekman, L A Tierney, C Benn, P Chawla, J H Cha
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<b>Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing</b>
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<p>Gene Therapy advance online publication, October 16, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.150">doi:10.1038/gt.2008.150</a>
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<p>Authors: H Y Chen, P Kathirvel, W C Yee
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<p>Gene Therapy advance online publication, October 16, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.152">doi:10.1038/gt.2008.152</a>
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<p>
<b>Controlled propagation of replication-competent Sindbis viral vector using suicide gene strategy</b>
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<p>Gene Therapy advance online publication, September 25, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.153">doi:10.1038/gt.2008.153</a>
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<p>Authors: J-C Tseng, G Daniels
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<p>
<b>Adenovirus serotype 35 vector-mediated transduction following direct administration into organs of nonhuman primates</b>
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<p>Gene Therapy advance online publication, September 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.154">doi:10.1038/gt.2008.154</a>
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<p>Authors: F Sakurai, S-i Nakamura, K Akitomo, H Shibata, K Terao, K Kawabata, T Hayakawa
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<dc:title>Adenovirus serotype 35 vector-mediated transduction following direct administration into organs of nonhuman primates</dc:title>
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<dc:creator>K Akitomo</dc:creator>
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<dc:creator>T Hayakawa</dc:creator>
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<p>
<b>The pros and cons of immunomodulatory IL-10 gene therapy with recombinant AAV in a Cftr&#8722;&#47;&#8722;-dependent allergy mouse model</b>
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<p>Gene Therapy advance online publication, September 25, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.156">doi:10.1038/gt.2008.156</a>
</p>
<p>Authors: C Mueller, S A Braag, A T Martino, Q Tang, M Campbell-Thompson
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]]></content:encoded>
<dc:title>The pros and cons of immunomodulatory IL-10 gene therapy with recombinant AAV in a Cftr&#8722;&#47;&#8722;-dependent allergy mouse model</dc:title>
<dc:creator>C Mueller</dc:creator>
<dc:creator>S A Braag</dc:creator>
<dc:creator>A T Martino</dc:creator>
<dc:creator>Q Tang</dc:creator>
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<dc:creator>T R Flotte</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.156</dc:identifier>
<dc:source>Gene Therapy advance online publication, September 25, 2008</dc:source>
<dc:date>September 25, 2008</dc:date>
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<p>
<b>An efficient rHSV-based complementation system for the production of multiple rAAV vector serotypes</b>
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<p>Gene Therapy advance online publication, October 16, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.158">doi:10.1038/gt.2008.158</a>
</p>
<p>Authors: W Kang, L Wang, H Harrell, J Liu, D L Thomas, T L Mayfield, M M Scotti, G J Ye, G Veres
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]]></content:encoded>
<dc:title>An efficient rHSV-based complementation system for the production of multiple rAAV vector serotypes</dc:title>
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<dc:creator>H Harrell</dc:creator>
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<dc:creator>D L Thomas</dc:creator>
<dc:creator>T L Mayfield</dc:creator>
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<dc:source>Gene Therapy advance online publication, October 16, 2008</dc:source>
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<p>
<b>Analysis of human immunodeficiency virus type 1 vector cis- and trans-acting elements production by means of Semliki Forest virus</b>
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<p>Gene Therapy advance online publication, November 27, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.159">doi:10.1038/gt.2008.159</a>
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<p>Authors: C Del Vecchio, A Calistri, G Lombardi, M Celegato, M A Biasolo, G Pal&#249;
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<dc:creator>M A Biasolo</dc:creator>
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<dc:source>Gene Therapy advance online publication, November 27, 2008</dc:source>
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<p>
<b>Re-targeted adenovirus vectors with dual specificity; binding specificities conferred by two different Affibody molecules in the fiber</b>
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<p>Gene Therapy advance online publication, October 23, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.160">doi:10.1038/gt.2008.160</a>
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<p>Authors: S Myhre, P Henning, M Friedman, S St&#229;hl, L Lindholm
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<dc:creator>L Lindholm</dc:creator>
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<p>
<b>Complete elimination of established neuroblastoma by synergistic action of &#947;-irradiation and DCs treated with rSeV expressing interferon-&#946; gene</b>
</p>
<p>Gene Therapy advance online publication, November 6, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.161">doi:10.1038/gt.2008.161</a>
</p>
<p>Authors: K Tatsuta, S Tanaka, T Tajiri, S Shibata, A Komaru, Y Ueda, M Inoue, M Hasegawa, S Suita, K Sueishi, T Taguchi
&amp; Y Yonemitsu</p>
]]></content:encoded>
<dc:title>Complete elimination of established neuroblastoma by synergistic action of &#947;-irradiation and DCs treated with rSeV expressing interferon-&#946; gene</dc:title>
<dc:creator>K Tatsuta</dc:creator>
<dc:creator>S Tanaka</dc:creator>
<dc:creator>T Tajiri</dc:creator>
<dc:creator>S Shibata</dc:creator>
<dc:creator>A Komaru</dc:creator>
<dc:creator>Y Ueda</dc:creator>
<dc:creator>M Inoue</dc:creator>
<dc:creator>M Hasegawa</dc:creator>
<dc:creator>S Suita</dc:creator>
<dc:creator>K Sueishi</dc:creator>
<dc:creator>T Taguchi</dc:creator>
<dc:creator>Y Yonemitsu</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.161</dc:identifier>
<dc:source>Gene Therapy advance online publication, November 6, 2008</dc:source>
<dc:date>November 6, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>November 6, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.162">
<title>A cell penetrating heme oxygenase protein protects heart graft against ischemia&#47;reperfusion injury</title>
<link>http://dx.doi.org/10.1038/gt.2008.162</link>
<content:encoded><![CDATA[

<p>
<b>A cell penetrating heme oxygenase protein protects heart graft against ischemia&#47;reperfusion injury</b>
</p>
<p>Gene Therapy advance online publication, November 6, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.162">doi:10.1038/gt.2008.162</a>
</p>
<p>Authors: J Ma, C K Lau, A Obed, A Dada, A Doenecke, S T Fan, H J Schlitt
&amp; T Y Tsui</p>
]]></content:encoded>
<dc:title>A cell penetrating heme oxygenase protein protects heart graft against ischemia&#47;reperfusion injury</dc:title>
<dc:creator>J Ma</dc:creator>
<dc:creator>C K Lau</dc:creator>
<dc:creator>A Obed</dc:creator>
<dc:creator>A Dada</dc:creator>
<dc:creator>A Doenecke</dc:creator>
<dc:creator>S T Fan</dc:creator>
<dc:creator>H J Schlitt</dc:creator>
<dc:creator>T Y Tsui</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.162</dc:identifier>
<dc:source>Gene Therapy advance online publication, November 6, 2008</dc:source>
<dc:date>November 6, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>November 6, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.164">
<title>Role of TLR3 in the immunogenicity of replicon plasmid-based vaccines</title>
<link>http://dx.doi.org/10.1038/gt.2008.164</link>
<content:encoded><![CDATA[

<p>
<b>Role of TLR3 in the immunogenicity of replicon plasmid-based vaccines</b>
</p>
<p>Gene Therapy advance online publication, December 4, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.164">doi:10.1038/gt.2008.164</a>
</p>
<p>Authors: S S Diebold, O Schulz, L Alexopoulou, W W Leitner, R A Flavell
&amp; C Reis e Sousa</p>
]]></content:encoded>
<dc:title>Role of TLR3 in the immunogenicity of replicon plasmid-based vaccines</dc:title>
<dc:creator>S S Diebold</dc:creator>
<dc:creator>O Schulz</dc:creator>
<dc:creator>L Alexopoulou</dc:creator>
<dc:creator>W W Leitner</dc:creator>
<dc:creator>R A Flavell</dc:creator>
<dc:creator>C Reis e Sousa</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.164</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 4, 2008</dc:source>
<dc:date>December 4, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 4, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.165">
<title>Neural stem cells target intracranial glioma to deliver an oncolytic adenovirus in vivo</title>
<link>http://dx.doi.org/10.1038/gt.2008.165</link>
<content:encoded><![CDATA[

<p>
<b>Neural stem cells target intracranial glioma to deliver an oncolytic adenovirus in vivo</b>
</p>
<p>Gene Therapy advance online publication, December 11, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.165">doi:10.1038/gt.2008.165</a>
</p>
<p>Authors: M A Tyler, I V Ulasov, A M Sonabend, S Nandi, Y Han, S Marler, J Roth
&amp; M S Lesniak</p>
]]></content:encoded>
<dc:title>Neural stem cells target intracranial glioma to deliver an oncolytic adenovirus in vivo</dc:title>
<dc:creator>M A Tyler</dc:creator>
<dc:creator>I V Ulasov</dc:creator>
<dc:creator>A M Sonabend</dc:creator>
<dc:creator>S Nandi</dc:creator>
<dc:creator>Y Han</dc:creator>
<dc:creator>S Marler</dc:creator>
<dc:creator>J Roth</dc:creator>
<dc:creator>M S Lesniak</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.165</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 11, 2008</dc:source>
<dc:date>December 11, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 11, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.167">
<title>Generation of optimized and urokinase-targeted oncolytic Sendai virus vectors applicable for various human malignancies</title>
<link>http://dx.doi.org/10.1038/gt.2008.167</link>
<content:encoded><![CDATA[

<p>
<b>Generation of optimized and urokinase-targeted oncolytic Sendai virus vectors applicable for various human malignancies</b>
</p>
<p>Gene Therapy advance online publication, November 27, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.167">doi:10.1038/gt.2008.167</a>
</p>
<p>Authors: H Kinoh, M Inoue, A Komaru, Y Ueda, M Hasegawa
&amp; Y Yonemitsu</p>
]]></content:encoded>
<dc:title>Generation of optimized and urokinase-targeted oncolytic Sendai virus vectors applicable for various human malignancies</dc:title>
<dc:creator>H Kinoh</dc:creator>
<dc:creator>M Inoue</dc:creator>
<dc:creator>A Komaru</dc:creator>
<dc:creator>Y Ueda</dc:creator>
<dc:creator>M Hasegawa</dc:creator>
<dc:creator>Y Yonemitsu</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.167</dc:identifier>
<dc:source>Gene Therapy advance online publication, November 27, 2008</dc:source>
<dc:date>November 27, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>November 27, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.168">
<title>Antigen-specific humoral tolerance or immune augmentation induced by intramuscular delivery of adeno-associated viruses encoding CTLA4-Ig-antigen fusion molecules</title>
<link>http://dx.doi.org/10.1038/gt.2008.168</link>
<content:encoded><![CDATA[

<p>
<b>Antigen-specific humoral tolerance or immune augmentation induced by intramuscular delivery of adeno-associated viruses encoding CTLA4-Ig-antigen fusion molecules</b>
</p>
<p>Gene Therapy advance online publication, November 27, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.168">doi:10.1038/gt.2008.168</a>
</p>
<p>Authors: G J Logan, L Wang, M Zheng, S L Ginn, R L Coppel
&amp; I E Alexander</p>
]]></content:encoded>
<dc:title>Antigen-specific humoral tolerance or immune augmentation induced by intramuscular delivery of adeno-associated viruses encoding CTLA4-Ig-antigen fusion molecules</dc:title>
<dc:creator>G J Logan</dc:creator>
<dc:creator>L Wang</dc:creator>
<dc:creator>M Zheng</dc:creator>
<dc:creator>S L Ginn</dc:creator>
<dc:creator>R L Coppel</dc:creator>
<dc:creator>I E Alexander</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.168</dc:identifier>
<dc:source>Gene Therapy advance online publication, November 27, 2008</dc:source>
<dc:date>November 27, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>November 27, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.169">
<title>A Kunjin replicon vector encoding granulocyte macrophage colony-stimulating factor for intra-tumoral gene therapy</title>
<link>http://dx.doi.org/10.1038/gt.2008.169</link>
<content:encoded><![CDATA[

<p>
<b>A Kunjin replicon vector encoding granulocyte macrophage colony-stimulating factor for intra-tumoral gene therapy</b>
</p>
<p>Gene Therapy advance online publication, December 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.169">doi:10.1038/gt.2008.169</a>
</p>
<p>Authors: D Hoang-Le, L Smeenk, I Anraku, G P Pijlman, X J Wang, J de Vrij, W J Liu, T T Le, W A Schroder, A A Khromykh
&amp; A Suhrbier</p>
]]></content:encoded>
<dc:title>A Kunjin replicon vector encoding granulocyte macrophage colony-stimulating factor for intra-tumoral gene therapy</dc:title>
<dc:creator>D Hoang-Le</dc:creator>
<dc:creator>L Smeenk</dc:creator>
<dc:creator>I Anraku</dc:creator>
<dc:creator>G P Pijlman</dc:creator>
<dc:creator>X J Wang</dc:creator>
<dc:creator>J de Vrij</dc:creator>
<dc:creator>W J Liu</dc:creator>
<dc:creator>T T Le</dc:creator>
<dc:creator>W A Schroder</dc:creator>
<dc:creator>A A Khromykh</dc:creator>
<dc:creator>A Suhrbier</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.169</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 18, 2008</dc:source>
<dc:date>December 18, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 18, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.170">
<title>Tailoring the AAV vector capsid for gene therapy</title>
<link>http://dx.doi.org/10.1038/gt.2008.170</link>
<content:encoded><![CDATA[

<p>
<b>Tailoring the AAV vector capsid for gene therapy</b>
</p>
<p>Gene Therapy advance online publication, December 4, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.170">doi:10.1038/gt.2008.170</a>
</p>
<p>Authors: L H Vandenberghe, J M Wilson
&amp; G Gao</p>
]]></content:encoded>
<dc:title>Tailoring the AAV vector capsid for gene therapy</dc:title>
<dc:creator>L H Vandenberghe</dc:creator>
<dc:creator>J M Wilson</dc:creator>
<dc:creator>G Gao</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.170</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 4, 2008</dc:source>
<dc:date>December 4, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 4, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.171">
<title>Foamy virus as a gene transfer vector to the central nervous system</title>
<link>http://dx.doi.org/10.1038/gt.2008.171</link>
<content:encoded><![CDATA[

<p>
<b>Foamy virus as a gene transfer vector to the central nervous system</b>
</p>
<p>Gene Therapy advance online publication, December 4, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.171">doi:10.1038/gt.2008.171</a>
</p>
<p>Authors: A V Caprariello, R H Miller
&amp; S M Selkirk</p>
]]></content:encoded>
<dc:title>Foamy virus as a gene transfer vector to the central nervous system</dc:title>
<dc:creator>A V Caprariello</dc:creator>
<dc:creator>R H Miller</dc:creator>
<dc:creator>S M Selkirk</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.171</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 4, 2008</dc:source>
<dc:date>December 4, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 4, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.172">
<title>Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic &#946;-cells to correct diabetes in allogeneic mice</title>
<link>http://dx.doi.org/10.1038/gt.2008.172</link>
<content:encoded><![CDATA[

<p>
<b>Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic &#946;-cells to correct diabetes in allogeneic mice</b>
</p>
<p>Gene Therapy advance online publication, December 25, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.172">doi:10.1038/gt.2008.172</a>
</p>
<p>Authors: T Kojaoghlanian, A Joseph, A Follenzi, J H Zheng, M Leiser, N Fleischer, M S Horwitz, T P DiLorenzo
&amp; H Goldstein</p>
]]></content:encoded>
<dc:title>Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic &#946;-cells to correct diabetes in allogeneic mice</dc:title>
<dc:creator>T Kojaoghlanian</dc:creator>
<dc:creator>A Joseph</dc:creator>
<dc:creator>A Follenzi</dc:creator>
<dc:creator>J H Zheng</dc:creator>
<dc:creator>M Leiser</dc:creator>
<dc:creator>N Fleischer</dc:creator>
<dc:creator>M S Horwitz</dc:creator>
<dc:creator>T P DiLorenzo</dc:creator>
<dc:creator>H Goldstein</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.172</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 25, 2008</dc:source>
<dc:date>December 25, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 25, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.173">
<title>Transduction of human neural progenitor cells with foamy virus vectors for differentiation-dependent gene expression</title>
<link>http://dx.doi.org/10.1038/gt.2008.173</link>
<content:encoded><![CDATA[

<p>
<b>Transduction of human neural progenitor cells with foamy virus vectors for differentiation-dependent gene expression</b>
</p>
<p>Gene Therapy advance online publication, December 4, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.173">doi:10.1038/gt.2008.173</a>
</p>
<p>Authors: I Rothenaigner, S Kramer, M Meggendorfer, A Rethwilm
&amp; R Brack-Werner</p>
]]></content:encoded>
<dc:title>Transduction of human neural progenitor cells with foamy virus vectors for differentiation-dependent gene expression</dc:title>
<dc:creator>I Rothenaigner</dc:creator>
<dc:creator>S Kramer</dc:creator>
<dc:creator>M Meggendorfer</dc:creator>
<dc:creator>A Rethwilm</dc:creator>
<dc:creator>R Brack-Werner</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.173</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 4, 2008</dc:source>
<dc:date>December 4, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 4, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.174">
<title>AAV2&#47;1-TNFR:Fc gene delivery prevents periodontal disease progression</title>
<link>http://dx.doi.org/10.1038/gt.2008.174</link>
<content:encoded><![CDATA[

<p>
<b>AAV2&#47;1-TNFR:Fc gene delivery prevents periodontal disease progression</b>
</p>
<p>Gene Therapy advance online publication, December 11, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.174">doi:10.1038/gt.2008.174</a>
</p>
<p>Authors: J A Cirelli, C H Park, K MacKool, M Taba, K H Lustig, H Burstein
&amp; W V Giannobile</p>
]]></content:encoded>
<dc:title>AAV2&#47;1-TNFR:Fc gene delivery prevents periodontal disease progression</dc:title>
<dc:creator>J A Cirelli</dc:creator>
<dc:creator>C H Park</dc:creator>
<dc:creator>K MacKool</dc:creator>
<dc:creator>M Taba</dc:creator>
<dc:creator>K H Lustig</dc:creator>
<dc:creator>H Burstein</dc:creator>
<dc:creator>W V Giannobile</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.174</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 11, 2008</dc:source>
<dc:date>December 11, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 11, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.176">
<title>Human adipose tissue-derived mesenchymal stromal cells as vehicles for tumor bystander effect: a model based on bioluminescence imaging</title>
<link>http://dx.doi.org/10.1038/gt.2008.176</link>
<content:encoded><![CDATA[

<p>
<b>Human adipose tissue-derived mesenchymal stromal cells as vehicles for tumor bystander effect: a model based on bioluminescence imaging</b>
</p>
<p>Gene Therapy advance online publication, December 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.176">doi:10.1038/gt.2008.176</a>
</p>
<p>Authors: M Vilalta, I R D&#233;gano, J Bag&#243;, E Aguilar, S S Gambhir, N Rubio
&amp; J Blanco</p>
]]></content:encoded>
<dc:title>Human adipose tissue-derived mesenchymal stromal cells as vehicles for tumor bystander effect: a model based on bioluminescence imaging</dc:title>
<dc:creator>M Vilalta</dc:creator>
<dc:creator>I R D&#233;gano</dc:creator>
<dc:creator>J Bag&#243;</dc:creator>
<dc:creator>E Aguilar</dc:creator>
<dc:creator>S S Gambhir</dc:creator>
<dc:creator>N Rubio</dc:creator>
<dc:creator>J Blanco</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.176</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 18, 2008</dc:source>
<dc:date>December 18, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 18, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.177">
<title>Identification of the murine firefly luciferase-specific CD8 T-cell epitopes</title>
<link>http://dx.doi.org/10.1038/gt.2008.177</link>
<content:encoded><![CDATA[

<p>
<b>Identification of the murine firefly luciferase-specific CD8 T-cell epitopes</b>
</p>
<p>Gene Therapy advance online publication, January 8, 2009. <a href="http://dx.doi.org/10.1038/gt.2008.177">doi:10.1038/gt.2008.177</a>
</p>
<p>Authors: M P Limberis, C L Bell
&amp; J M Wilson</p>
]]></content:encoded>
<dc:title>Identification of the murine firefly luciferase-specific CD8 T-cell epitopes</dc:title>
<dc:creator>M P Limberis</dc:creator>
<dc:creator>C L Bell</dc:creator>
<dc:creator>J M Wilson</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.177</dc:identifier>
<dc:source>Gene Therapy advance online publication, January 8, 2009</dc:source>
<dc:date>January 8, 2009</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>January 8, 2009</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.178">
<title>Cellular tropism and transduction properties of seven adeno-associated viral vector serotypes in adult retina after intravitreal injection</title>
<link>http://dx.doi.org/10.1038/gt.2008.178</link>
<content:encoded><![CDATA[

<p>
<b>Cellular tropism and transduction properties of seven adeno-associated viral vector serotypes in adult retina after intravitreal injection</b>
</p>
<p>Gene Therapy advance online publication, December 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.178">doi:10.1038/gt.2008.178</a>
</p>
<p>Authors: M Hellstr&#246;m, M J Ruitenberg, M A Pollett, E M E Ehlert, J Twisk, J Verhaagen
&amp; A R Harvey</p>
]]></content:encoded>
<dc:title>Cellular tropism and transduction properties of seven adeno-associated viral vector serotypes in adult retina after intravitreal injection</dc:title>
<dc:creator>M Hellstr&#246;m</dc:creator>
<dc:creator>M J Ruitenberg</dc:creator>
<dc:creator>M A Pollett</dc:creator>
<dc:creator>E M E Ehlert</dc:creator>
<dc:creator>J Twisk</dc:creator>
<dc:creator>J Verhaagen</dc:creator>
<dc:creator>A R Harvey</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.178</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 18, 2008</dc:source>
<dc:date>December 18, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 18, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.179">
<title>A phase I trial of intratumoral administration of recombinant oncolytic adenovirus overexpressing HSP70 in advanced solid tumor patients</title>
<link>http://dx.doi.org/10.1038/gt.2008.179</link>
<content:encoded><![CDATA[

<p>
<b>A phase I trial of intratumoral administration of recombinant oncolytic adenovirus overexpressing HSP70 in advanced solid tumor patients</b>
</p>
<p>Gene Therapy advance online publication, December 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.179">doi:10.1038/gt.2008.179</a>
</p>
<p>Authors: J-L Li, H-L Liu, X-R Zhang, J-P Xu, W-K Hu, M Liang, S-Y Chen, F Hu
&amp; D-T Chu</p>
]]></content:encoded>
<dc:title>A phase I trial of intratumoral administration of recombinant oncolytic adenovirus overexpressing HSP70 in advanced solid tumor patients</dc:title>
<dc:creator>J-L Li</dc:creator>
<dc:creator>H-L Liu</dc:creator>
<dc:creator>X-R Zhang</dc:creator>
<dc:creator>J-P Xu</dc:creator>
<dc:creator>W-K Hu</dc:creator>
<dc:creator>M Liang</dc:creator>
<dc:creator>S-Y Chen</dc:creator>
<dc:creator>F Hu</dc:creator>
<dc:creator>D-T Chu</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.179</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 18, 2008</dc:source>
<dc:date>December 18, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 18, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
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<item rdf:about="http://dx.doi.org/10.1038/gt.2008.180">
<title>Interleukin-6 small interfering RNA improved the herpes simplex virus-induced systemic inflammation in vivo Behcet&#8217;s disease-like mouse model</title>
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<p>
<b>Interleukin-6 small interfering RNA improved the herpes simplex virus-induced systemic inflammation in vivo Behcet&#8217;s disease-like mouse model</b>
</p>
<p>Gene Therapy advance online publication, December 18, 2008. <a href="http://dx.doi.org/10.1038/gt.2008.180">doi:10.1038/gt.2008.180</a>
</p>
<p>Authors: J Shim, H O Byun, Y D Lee, E S Lee
&amp; S Sohn</p>
]]></content:encoded>
<dc:title>Interleukin-6 small interfering RNA improved the herpes simplex virus-induced systemic inflammation in vivo Behcet&#8217;s disease-like mouse model</dc:title>
<dc:creator>J Shim</dc:creator>
<dc:creator>H O Byun</dc:creator>
<dc:creator>Y D Lee</dc:creator>
<dc:creator>E S Lee</dc:creator>
<dc:creator>S Sohn</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.180</dc:identifier>
<dc:source>Gene Therapy advance online publication, December 18, 2008</dc:source>
<dc:date>December 18, 2008</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>December 18, 2008</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
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<item rdf:about="http://dx.doi.org/10.1038/gt.2008.181">
<title>An adenoviral vector-based mucosal vaccine is effective in protection against botulism</title>
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<content:encoded><![CDATA[

<p>
<b>An adenoviral vector-based mucosal vaccine is effective in protection against botulism</b>
</p>
<p>Gene Therapy advance online publication, January 8, 2009. <a href="http://dx.doi.org/10.1038/gt.2008.181">doi:10.1038/gt.2008.181</a>
</p>
<p>Authors: Q Xu, M E Pichichero, L L Simpson, Md Elias, L A Smith
&amp; M Zeng</p>
]]></content:encoded>
<dc:title>An adenoviral vector-based mucosal vaccine is effective in protection against botulism</dc:title>
<dc:creator>Q Xu</dc:creator>
<dc:creator>M E Pichichero</dc:creator>
<dc:creator>L L Simpson</dc:creator>
<dc:creator>Md Elias</dc:creator>
<dc:creator>L A Smith</dc:creator>
<dc:creator>M Zeng</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.181</dc:identifier>
<dc:source>Gene Therapy advance online publication, January 8, 2009</dc:source>
<dc:date>January 8, 2009</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>January 8, 2009</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.182">
<title>Gene delivery to human adult and embryonic cell-derived stem cells using biodegradable nanoparticulate polymeric vectors</title>
<link>http://dx.doi.org/10.1038/gt.2008.182</link>
<content:encoded><![CDATA[

<p>
<b>Gene delivery to human adult and embryonic cell-derived stem cells using biodegradable nanoparticulate polymeric vectors</b>
</p>
<p>Gene Therapy advance online publication, January 8, 2009. <a href="http://dx.doi.org/10.1038/gt.2008.182">doi:10.1038/gt.2008.182</a>
</p>
<p>Authors: F Yang, J J Green, T Dinio, L Keung, S-W Cho, H Park, R Langer
&amp; D G Anderson</p>
]]></content:encoded>
<dc:title>Gene delivery to human adult and embryonic cell-derived stem cells using biodegradable nanoparticulate polymeric vectors</dc:title>
<dc:creator>F Yang</dc:creator>
<dc:creator>J J Green</dc:creator>
<dc:creator>T Dinio</dc:creator>
<dc:creator>L Keung</dc:creator>
<dc:creator>S-W Cho</dc:creator>
<dc:creator>H Park</dc:creator>
<dc:creator>R Langer</dc:creator>
<dc:creator>D G Anderson</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.182</dc:identifier>
<dc:source>Gene Therapy advance online publication, January 8, 2009</dc:source>
<dc:date>January 8, 2009</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
<prism:publicationDate>January 8, 2009</prism:publicationDate>
<prism:volume>aop</prism:volume>
<prism:number>current</prism:number>
</item>
<item rdf:about="http://dx.doi.org/10.1038/gt.2008.183">
<title>Progress and Prospects: The design and production of plasmid vectors</title>
<link>http://dx.doi.org/10.1038/gt.2008.183</link>
<content:encoded><![CDATA[

<p>
<b>Progress and Prospects: The design and production of plasmid vectors</b>
</p>
<p>Gene Therapy advance online publication, January 8, 2009. <a href="http://dx.doi.org/10.1038/gt.2008.183">doi:10.1038/gt.2008.183</a>
</p>
<p>Authors: D R Gill, I A Pringle
&amp; S C Hyde</p>
]]></content:encoded>
<dc:title>Progress and Prospects: The design and production of plasmid vectors</dc:title>
<dc:creator>D R Gill</dc:creator>
<dc:creator>I A Pringle</dc:creator>
<dc:creator>S C Hyde</dc:creator>
<dc:identifier>doi:10.1038/gt.2008.183</dc:identifier>
<dc:source>Gene Therapy advance online publication, January 8, 2009</dc:source>
<dc:date>January 8, 2009</dc:date>
<prism:publicationName>Gene Therapy</prism:publicationName>
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