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<title>SciBX: Science-Business eXchange</title>
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<title>A top-notch inhibitor</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/lLFsRAhTzag/scibx.2009.1649</link>
<description>The previously intractable Notch pathway looks to be opening as a Harvard team has described a way to specifically inhibit Notch signaling and UCSD researchers have identified a role for NOTCH3 in pulmonary arterial hypertension. Also, Aileron Therapeutics has moved the Harvard technology into preclinical programs for a range of indications beyond cancer.</description>
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<p>
<b>A top-notch inhibitor</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1649">doi:10.1038/scibx.2009.1649</a>
</p>
<p>Author: Tim Fulmer</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/lLFsRAhTzag" height="1" width="1"/>]]></content:encoded>
<dc:title>A top-notch inhibitor</dc:title>
<dc:creator>Tim Fulmer</dc:creator>
<dc:identifier>doi:10.1038/scibx.2009.1649</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
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<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Cover Story</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1649</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1651">
<title>gp130's sensitive side</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/N5u4aNt0v7w/scibx.2009.1651</link>
<description>Medical University Innsbruck researchers suggest that inhibiting the gp130 pathway could help manage certain types of pain as well as exert a therapeutic effect in cancer and inflammation. The key will be to block the pathway without disrupting the body's natural immune response.</description>
<content:encoded><![CDATA[

<p>
<b>gp130's sensitive side</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1651">doi:10.1038/scibx.2009.1651</a>
</p>
<p>Author: Lauren Martz</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/N5u4aNt0v7w" height="1" width="1"/>]]></content:encoded>
<dc:title>gp130's sensitive side</dc:title>
<dc:creator>Lauren Martz</dc:creator>
<dc:identifier>doi:10.1038/scibx.2009.1651</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1651</prism:doi>
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<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Targets and Mechanisms</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1651</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1650">
<title>APC mutants for ALS</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/-bPwWq-R26c/scibx.2009.1650</link>
<description>University of Rochester researchers suggest mutant forms of activated protein C could improve outcomes in ALS, and they point to a possible role of microglia in the etiology of the disease. The results could expand the number of indications addressed by ZZ Biotech's portfolio of APC mutants.</description>
<content:encoded><![CDATA[

<p>
<b>APC mutants for ALS</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1650">doi:10.1038/scibx.2009.1650</a>
</p>
<p>Author: Lev Osherovich</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/-bPwWq-R26c" height="1" width="1"/>]]></content:encoded>
<dc:title>APC mutants for ALS</dc:title>
<dc:creator>Lev Osherovich</dc:creator>
<dc:identifier>doi:10.1038/scibx.2009.1650</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
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<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Targets and Mechanisms</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1650</feedburner:origLink></item>
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<title>Warming up to lung transplants</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/XC_u9UtMpho/scibx.2009.1652</link>
<description>University of Toronto researchers have combined ex vivo IL-10 gene therapy with an organ preservation system from Vitrolife AB to repair damage in donor lungs and make them suitable for transplant. The approach could expand the supply of donor lungs and be applied to other donor organs.</description>
<content:encoded><![CDATA[

<p>
<b>Warming up to lung transplants</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1652">doi:10.1038/scibx.2009.1652</a>
</p>
<p>Author: Kai-Jye Lou</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/XC_u9UtMpho" height="1" width="1"/>]]></content:encoded>
<dc:title>Warming up to lung transplants</dc:title>
<dc:creator>Kai-Jye Lou</dc:creator>
<dc:identifier>doi:10.1038/scibx.2009.1652</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1652</prism:doi>
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<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Tools</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1652</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1653">
<title>MicroRNA-29b (miRNA-29b)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/5fWz4JPiuec/scibx.2009.1653</link>
<description>A study in cell culture and in mice suggests that miRNA-29b mimetics could help treat AML.</description>
<content:encoded><![CDATA[

<p>
<b>MicroRNA-29b (miRNA-29b)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1653">doi:10.1038/scibx.2009.1653</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/5fWz4JPiuec" height="1" width="1"/>]]></content:encoded>
<dc:title>MicroRNA-29b (miRNA-29b)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1653</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1653</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1653</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1653</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1654">
<title>Mdm2 p53 binding protein homolog (MDM2)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/fVoTcjewoFs/scibx.2009.1654</link>
<description>In vitro and mouse studies suggest that antagonizing MDM2 could help treat chemotherapy-resistant neuroblastoma.</description>
<content:encoded><![CDATA[

<p>
<b>Mdm2 p53 binding protein homolog (MDM2)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1654">doi:10.1038/scibx.2009.1654</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/fVoTcjewoFs" height="1" width="1"/>]]></content:encoded>
<dc:title>Mdm2 p53 binding protein homolog (MDM2)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1654</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1654</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1654</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1654</feedburner:origLink></item>
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<title>Integrin α5 (CD49e); radixin (RDX); Ras homolog gene family member (RHOA)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/mSNqvWUur-8/scibx.2009.1655</link>
<description>In vitro and mouse studies suggest that inhibiting CD49e, RDX or RHOA could help prevent breast cancer metastasis.</description>
<content:encoded><![CDATA[

<p>
<b>Integrin &#945;5 (CD49e); radixin (RDX); Ras homolog gene family member (RHOA)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1655">doi:10.1038/scibx.2009.1655</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/mSNqvWUur-8" height="1" width="1"/>]]></content:encoded>
<dc:title>Integrin α5 (CD49e); radixin (RDX); Ras homolog gene family member (RHOA)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1655</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1655</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1655</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1655</feedburner:origLink></item>
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<title>Mucosa associated lymphoid tissue lymphoma translocation gene 1 (MALT1)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/f2TAS33_eq4/scibx.2009.1656</link>
<description>A study in cell culture suggests that inhibiting the protease MALT1 could help treat diffuse large B cell lymphoma.</description>
<content:encoded><![CDATA[

<p>
<b>Mucosa associated lymphoid tissue lymphoma translocation gene 1 (MALT1)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1656">doi:10.1038/scibx.2009.1656</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/f2TAS33_eq4" height="1" width="1"/>]]></content:encoded>
<dc:title>Mucosa associated lymphoid tissue lymphoma translocation gene 1 (MALT1)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1656</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1656</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1656</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1656</feedburner:origLink></item>
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<title>Microtubules</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/HBJw4ylK4XE/scibx.2009.1657</link>
<description>An in vitro and cell culture study suggests that zampanolide, a macrolide compound isolated from a Tongan sea sponge, could help treat cancer.</description>
<content:encoded><![CDATA[

<p>
<b>Microtubules</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1657">doi:10.1038/scibx.2009.1657</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/HBJw4ylK4XE" height="1" width="1"/>]]></content:encoded>
<dc:title>Microtubules</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1657</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1657</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1657</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1657</feedburner:origLink></item>
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<title>Notch transcription factor complex</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/gS99SBOCrV0/scibx.2009.1658</link>
<description>A study in mice and in cell culture suggests that an α-helical peptide antagonist of the notch transcriptional complex could help treat cancer.</description>
<content:encoded><![CDATA[

<p>
<b>Notch transcription factor complex</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1658">doi:10.1038/scibx.2009.1658</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/gS99SBOCrV0" height="1" width="1"/>]]></content:encoded>
<dc:title>Notch transcription factor complex</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1658</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1658</prism:doi>
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<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1658</feedburner:origLink></item>
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<title>Estrogen receptor</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/UML4XW_pNIU/scibx.2009.1659</link>
<description>A study in mice suggests that selective estrogen receptor antagonists could help treat and prevent cervical cancer.</description>
<content:encoded><![CDATA[

<p>
<b>Estrogen receptor</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1659">doi:10.1038/scibx.2009.1659</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/UML4XW_pNIU" height="1" width="1"/>]]></content:encoded>
<dc:title>Estrogen receptor</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1659</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1659</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1659</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1659</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1660">
<title>Janus kinase 2 (JAK2); histone deacetylase (HDAC)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/nz7rvUKwZok/scibx.2009.1660</link>
<description>In vitro studies suggest that combining HDAC inhibitors with JAK2 inhibitors could help treat myeloproliferative cancers.</description>
<content:encoded><![CDATA[

<p>
<b>Janus kinase 2 (JAK2); histone deacetylase (HDAC)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1660">doi:10.1038/scibx.2009.1660</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/nz7rvUKwZok" height="1" width="1"/>]]></content:encoded>
<dc:title>Janus kinase 2 (JAK2); histone deacetylase (HDAC)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1660</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1660</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1660</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1660</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1661">
<title>Wingless-type MMTV integration site family member 5A (WNT5A)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/JKi8jP-tmR0/scibx.2009.1661</link>
<description>A study in cell culture identified an N-butyloxycarbonyl hexapeptide inhibitor of WNT5A that could help prevent melanoma-associated metastasis.</description>
<content:encoded><![CDATA[

<p>
<b>Wingless-type MMTV integration site family member 5A (WNT5A)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1661">doi:10.1038/scibx.2009.1661</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/JKi8jP-tmR0" height="1" width="1"/>]]></content:encoded>
<dc:title>Wingless-type MMTV integration site family member 5A (WNT5A)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1661</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1661</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1661</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1661</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1662">
<title>Angiotensin-converting enzyme (ACE); endothelin converting enzyme 1 (ECE1); membrane metallo-endopeptidase (MME; NEP; CD10)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/RC5SQBbn1DQ/scibx.2009.1662</link>
<description>In vitro and rat studies suggest that dual ACE and ECE1 inhibitors could help treat hypertension.</description>
<content:encoded><![CDATA[

<p>
<b>Angiotensin-converting enzyme (ACE); endothelin converting enzyme 1 (ECE1); membrane metallo-endopeptidase (MME; NEP; CD10)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1662">doi:10.1038/scibx.2009.1662</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/RC5SQBbn1DQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Angiotensin-converting enzyme (ACE); endothelin converting enzyme 1 (ECE1); membrane metallo-endopeptidase (MME; NEP; CD10)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1662</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1662</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1662</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1662</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1663">
<title>Not applicable</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/mA_aSKGcUnM/scibx.2009.1663</link>
<description>In vitro and rat studies suggest that losartan-antioxidant hybrid compounds are more effective than losartan at controlling hypertension.</description>
<content:encoded><![CDATA[

<p>
<b>Not applicable</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1663">doi:10.1038/scibx.2009.1663</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/mA_aSKGcUnM" height="1" width="1"/>]]></content:encoded>
<dc:title>Not applicable</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1663</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1663</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1663</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1663</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1664">
<title>Androgen receptor</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/1B7YwcS-ngw/scibx.2009.1664</link>
<description>Studies in mice suggest that inhibiting the androgen receptor could improve wound healing.</description>
<content:encoded><![CDATA[

<p>
<b>Androgen receptor</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1664">doi:10.1038/scibx.2009.1664</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/1B7YwcS-ngw" height="1" width="1"/>]]></content:encoded>
<dc:title>Androgen receptor</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1664</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1664</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1664</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1664</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1665">
<title>Syntaxin binding protein 2 (STXBP2; MUNC18–2)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/bNNEVK_6gck/scibx.2009.1665</link>
<description>Genetic studies in humans identified mutations in STXBP2 that could be biomarkers of the hematological disorder familial hemophagocytic lymphohistiocytosis type 5.</description>
<content:encoded><![CDATA[

<p>
<b>Syntaxin binding protein 2 (STXBP2; MUNC18&#8211;2)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1665">doi:10.1038/scibx.2009.1665</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/bNNEVK_6gck" height="1" width="1"/>]]></content:encoded>
<dc:title>Syntaxin binding protein 2 (STXBP2; MUNC18–2)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1665</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1665</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1665</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1665</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1666">
<title>C-type lectin domain family 7 member A (CLEC7A; DECTIN1)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/-zcGOKWtv6E/scibx.2009.1666</link>
<description>Genetic studies identified a mutation in DECTIN1 that could help predict susceptibility to recurrent mucocutaneous fungal infections.</description>
<content:encoded><![CDATA[

<p>
<b>C-type lectin domain family 7 member A (CLEC7A; DECTIN1)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1666">doi:10.1038/scibx.2009.1666</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/-zcGOKWtv6E" height="1" width="1"/>]]></content:encoded>
<dc:title>C-type lectin domain family 7 member A (CLEC7A; DECTIN1)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1666</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1666</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1666</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1666</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1667">
<title>HCV NS3 protease</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/dO8N7dT2X2o/scibx.2009.1667</link>
<description>In vitro and rat studies identified macrocyclic HCV NS3 protease inhibitors that could help treat HCV.</description>
<content:encoded><![CDATA[

<p>
<b>HCV NS3 protease</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1667">doi:10.1038/scibx.2009.1667</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/dO8N7dT2X2o" height="1" width="1"/>]]></content:encoded>
<dc:title>HCV NS3 protease</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1667</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1667</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1667</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1667</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1668">
<title>Not applicable</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/l546if-4xAY/scibx.2009.1668</link>
<description>In vitro and in vivo studies suggest that a rhodacyanine analog could help treat visceral leishmaniasis.</description>
<content:encoded><![CDATA[

<p>
<b>Not applicable</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1668">doi:10.1038/scibx.2009.1668</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/l546if-4xAY" height="1" width="1"/>]]></content:encoded>
<dc:title>Not applicable</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1668</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1668</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1668</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1668</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1669">
<title>Histone cluster 4, H4 (HIST4H4)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/UBKfj63h1NA/scibx.2009.1669</link>
<description>Studies in cell culture and in mice suggest that blocking HIST4H4 could help treat sepsis.</description>
<content:encoded><![CDATA[

<p>
<b>Histone cluster 4, H4 (HIST4H4)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1669">doi:10.1038/scibx.2009.1669</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/UBKfj63h1NA" height="1" width="1"/>]]></content:encoded>
<dc:title>Histone cluster 4, H4 (HIST4H4)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1669</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1669</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1669</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1669</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1670">
<title>Solute carrier family 6 member 3 (SLC6A3; DAT1)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/RJi8jyv87QY/scibx.2009.1670</link>
<description>Genetic association studies identified two loci that could help predict resistance to TB.</description>
<content:encoded><![CDATA[

<p>
<b>Solute carrier family 6 member 3 (SLC6A3; DAT1)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1670">doi:10.1038/scibx.2009.1670</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/RJi8jyv87QY" height="1" width="1"/>]]></content:encoded>
<dc:title>Solute carrier family 6 member 3 (SLC6A3; DAT1)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1670</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1670</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1670</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1670</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1671">
<title>Muscarinic acetylcholine receptor M1 (CHRM1; HM1)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/9fc7SQDLMNE/scibx.2009.1671</link>
<description>In vitro and mouse studies suggest that benzylquinolone carboxylic acid (BQCA) activates HM1 and could help treat cognitive impairment.</description>
<content:encoded><![CDATA[

<p>
<b>Muscarinic acetylcholine receptor M1 (CHRM1; HM1)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1671">doi:10.1038/scibx.2009.1671</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/9fc7SQDLMNE" height="1" width="1"/>]]></content:encoded>
<dc:title>Muscarinic acetylcholine receptor M1 (CHRM1; HM1)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1671</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1671</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1671</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1671</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1672">
<title>NMDA receptor NR2A subtype (GRIN2A; NR2A)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/EZVmzd5l6rE/scibx.2009.1672</link>
<description>Studies in mice suggest that blocking phosphorylation of NR2A could help treat depression.</description>
<content:encoded><![CDATA[

<p>
<b>NMDA receptor NR2A subtype (GRIN2A; NR2A)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1672">doi:10.1038/scibx.2009.1672</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/EZVmzd5l6rE" height="1" width="1"/>]]></content:encoded>
<dc:title>NMDA receptor NR2A subtype (GRIN2A; NR2A)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1672</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1672</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1672</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1672</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1673">
<title>Not applicable</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/vN-cz0CesZ0/scibx.2009.1673</link>
<description>Studies in rats suggest that analogs of valproic acid could help treat neuropathic pain and epilepsy.</description>
<content:encoded><![CDATA[

<p>
<b>Not applicable</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1673">doi:10.1038/scibx.2009.1673</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/vN-cz0CesZ0" height="1" width="1"/>]]></content:encoded>
<dc:title>Not applicable</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1673</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1673</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1673</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1673</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1674">
<title>Adenosine A2A receptor (ADORA2A)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/RyOI5xLnEe0/scibx.2009.1674</link>
<description>Studies in rats suggest that agonizing ADORA2A could help treat neuropathic pain.</description>
<content:encoded><![CDATA[

<p>
<b>Adenosine A2A receptor (ADORA2A)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1674">doi:10.1038/scibx.2009.1674</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/RyOI5xLnEe0" height="1" width="1"/>]]></content:encoded>
<dc:title>Adenosine A2A receptor (ADORA2A)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1674</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1674</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1674</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1674</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1675">
<title>IL-6; IL-6 signal transducer (IL-6ST; gp130; CD130)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/0doOBHcIgm0/scibx.2009.1675</link>
<description>Studies in mice suggest that inhibiting gp130 could help treat pain.</description>
<content:encoded><![CDATA[

<p>
<b>IL-6; IL-6 signal transducer (IL-6ST; gp130; CD130)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1675">doi:10.1038/scibx.2009.1675</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/0doOBHcIgm0" height="1" width="1"/>]]></content:encoded>
<dc:title>IL-6; IL-6 signal transducer (IL-6ST; gp130; CD130)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1675</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1675</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1675</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1675</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1676">
<title>Protein kinase Cδ (PRKCD); Src homology protein tyrosine phosphatase 1 (SHP-1; SHPTP1; PTPN6)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/QB6xgn2ZRK4/scibx.2009.1676</link>
<description>A study in cell culture and in mice suggests that antagonizing PKCD and SHP-1 could help treat diabetic retinopathy.</description>
<content:encoded><![CDATA[

<p>
<b>Protein kinase C&#948; (PRKCD); Src homology protein tyrosine phosphatase 1 (SHP-1; SHPTP1; PTPN6)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1676">doi:10.1038/scibx.2009.1676</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/QB6xgn2ZRK4" height="1" width="1"/>]]></content:encoded>
<dc:title>Protein kinase Cδ (PRKCD); Src homology protein tyrosine phosphatase 1 (SHP-1; SHPTP1; PTPN6)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1676</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1676</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1676</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1676</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1677">
<title>CD80 (B7–1); cytotoxic T lymphocyte–associated protein 4 (CTLA4; CTLA-4; CD152)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/ZvIuFhPME3k/scibx.2009.1677</link>
<description>A study in cell culture suggests that antagonizing B7–1 on myeloid dendritic cells (DCs) could help treat inflammation associated with emphysema.</description>
<content:encoded><![CDATA[

<p>
<b>CD80 (B7&#8211;1); cytotoxic T lymphocyte&#8211;associated protein 4 (CTLA4; CTLA-4; CD152)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1677">doi:10.1038/scibx.2009.1677</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/ZvIuFhPME3k" height="1" width="1"/>]]></content:encoded>
<dc:title>CD80 (B7–1); cytotoxic T lymphocyte–associated protein 4 (CTLA4; CTLA-4; CD152)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1677</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1677</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1677</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1677</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1678">
<title>Serum amyloid P component (SAP; APCS)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/8hoD73bgyd0/scibx.2009.1678</link>
<description>Studies in mice suggest that SAP could be useful for treating kidney fibrosis.</description>
<content:encoded><![CDATA[

<p>
<b>Serum amyloid P component (SAP; APCS)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1678">doi:10.1038/scibx.2009.1678</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/8hoD73bgyd0" height="1" width="1"/>]]></content:encoded>
<dc:title>Serum amyloid P component (SAP; APCS)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1678</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1678</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1678</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Therapeutics</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1678</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1679">
<title>Adoptive therapy to treat autoimmune diseases using engineered antigen-specific Tregs</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/j9Pkxm-hqlQ/scibx.2009.1679</link>
<description>Adoptive therapy using Tregs engineered to target a specific antigen could help treat autoimmune diseases.</description>
<content:encoded><![CDATA[

<p>
<b>Adoptive therapy to treat autoimmune diseases using engineered antigen-specific Tregs</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1679">doi:10.1038/scibx.2009.1679</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/j9Pkxm-hqlQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Adoptive therapy to treat autoimmune diseases using engineered antigen-specific Tregs</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1679</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1679</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1679</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Techniques</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1679</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1680">
<title>Glycoprotein 2 (GP2)-targeted antigens as mucosal vaccines</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/RIunD2NXuTY/scibx.2009.1680</link>
<description>GP2-targeted antigen delivery could be useful for developing mucosal vaccines against a variety of pathogens.</description>
<content:encoded><![CDATA[

<p>
<b>Glycoprotein 2 (GP2)-targeted antigens as mucosal vaccines</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1680">doi:10.1038/scibx.2009.1680</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/RIunD2NXuTY" height="1" width="1"/>]]></content:encoded>
<dc:title>Glycoprotein 2 (GP2)-targeted antigens as mucosal vaccines</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1680</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1680</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1680</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Techniques</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1680</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1681">
<title>IL-10–expressing adult neural stem cells for treatment of autoimmune encephalitis and multiple sclerosis (MS)</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/ohqtyW_O04A/scibx.2009.1681</link>
<description>Expression of anti-inflammatory IL-10 in adult neural stem cells could improve the ability of implanted cells to treat autoimmune encephalitis and MS.</description>
<content:encoded><![CDATA[

<p>
<b>IL-10&#8211;expressing adult neural stem cells for treatment of autoimmune encephalitis and multiple sclerosis (MS)</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1681">doi:10.1038/scibx.2009.1681</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/ohqtyW_O04A" height="1" width="1"/>]]></content:encoded>
<dc:title>IL-10–expressing adult neural stem cells for treatment of autoimmune encephalitis and multiple sclerosis (MS)</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1681</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1681</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1681</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Techniques</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1681</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/scibx.2009.1682">
<title>Near-infrared imaging of β-amyloid (Aβ) deposits with curcumin-derived compounds</title>
<link>http://feeds.nature.com/~r/scibx/rss/current/~3/Jj5cXSiO-98/scibx.2009.1682</link>
<description>A curcumin-derived imaging agent could help detect Aβ aggregates to diagnose Alzheimer's disease (AD).</description>
<content:encoded><![CDATA[

<p>
<b>Near-infrared imaging of &#946;-amyloid (A&#946;) deposits with curcumin-derived compounds</b>
</p>
<p>SciBX: Science-Business eXchange 2, (2009). <a href="http://dx.doi.org/10.1038/scibx.2009.1682">doi:10.1038/scibx.2009.1682</a>
</p>
<img src="http://feeds.feedburner.com/~r/scibx/rss/current/~4/Jj5cXSiO-98" height="1" width="1"/>]]></content:encoded>
<dc:title>Near-infrared imaging of β-amyloid (Aβ) deposits with curcumin-derived compounds</dc:title>
<dc:identifier>doi:10.1038/scibx.2009.1682</dc:identifier>
<dc:source>SciBX: Science-Business eXchange 2, (2009)</dc:source>
<dc:date>2009-11-19</dc:date>
<prism:publicationName>SciBX: Science-Business eXchange</prism:publicationName>
<prism:publicationDate>2009-11-19</prism:publicationDate>
<prism:doi>10.1038/scibx.2009.1682</prism:doi>
<prism:url>http://dx.doi.org/10.1038/scibx.2009.1682</prism:url>
<prism:volume>2</prism:volume>
<prism:number>45</prism:number>
<prism:section>Distillery: Techniques</prism:section>
<feedburner:origLink>http://dx.doi.org/10.1038/scibx.2009.1682</feedburner:origLink></item>
</rdf:RDF>
