<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns="http://purl.org/rss/1.0/">
<channel rdf:about="http://www.nature.com/bjp/current_issue/rss">
<title>British Journal of Pharmacology</title>
<description/>
<link>http://www.nature.com/bjp/current_issue/</link>
<dc:publisher>Nature Publishing Group</dc:publisher>
<dc:language>en</dc:language>
<dc:rights>
Copyright &#169;  Nature Publishing Group</dc:rights>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:issn>0007-1188</prism:issn>
<prism:copyright>
Copyright &#169;  Nature Publishing Group</prism:copyright>
<prism:rightsAgent>permissions@nature.com</prism:rightsAgent>
<image rdf:resource="http://www.nature.com/aj/images/logos_b_o_w/bjp.gif"/>
<items>
<rdf:Seq>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.221"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.185"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.204"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.207"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.205"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.208"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.209"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.214"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.218"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.219"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.198"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.211"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.213"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.210"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.314"/>
<rdf:li rdf:resource="http://dx.doi.org/10.1038/bjp.2008.282"/>
</rdf:Seq>
</items>
</channel>
<image rdf:about="http://www.nature.com/aj/images/logos_b_o_w/bjp.gif">
<title>British Journal of Pharmacology</title>
<url>http://www.nature.com/aj/images/logos_b_o_w/bjp.gif</url>
<link>http://www.nature.com/bjp/</link>
</image>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.221">
<title>Brivaracetam: a rational drug discovery success story</title>
<link>http://dx.doi.org/10.1038/bjp.2008.221</link>
<content:encoded><![CDATA[

<p>
<b>Brivaracetam: a rational drug discovery success story</b>
</p>
<p>British Journal of Pharmacology 154, 1555 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.221">doi:10.1038/bjp.2008.221</a>
</p>
<p>Author: M A Rogawski</p>
]]></content:encoded>
<dc:title>Brivaracetam: a rational drug discovery success story</dc:title>
<dc:creator>M A Rogawski</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.221</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1555 (August 2008)</dc:source>
<dc:date>June 16, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 16, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1555</prism:startingPage>
<prism:endingPage>1557</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.185">
<title>Acetylcholine beyond neurons: the non-neuronal cholinergic system in humans</title>
<link>http://dx.doi.org/10.1038/bjp.2008.185</link>
<content:encoded><![CDATA[

<p>
<b>Acetylcholine beyond neurons: the non-neuronal cholinergic system in humans</b>
</p>
<p>British Journal of Pharmacology 154, 1558 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.185">doi:10.1038/bjp.2008.185</a>
</p>
<p>Authors: I Wessler
&amp; C J Kirkpatrick</p>
]]></content:encoded>
<dc:title>Acetylcholine beyond neurons: the non-neuronal cholinergic system in humans</dc:title>
<dc:creator>I Wessler</dc:creator>
<dc:creator>C J Kirkpatrick</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.185</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1558 (August 2008)</dc:source>
<dc:date>May 26, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>May 26, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1558</prism:startingPage>
<prism:endingPage>1571</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.204">
<title>Pharmacological targeting of the KIT growth factor receptor: a therapeutic consideration for mast cell disorders</title>
<link>http://dx.doi.org/10.1038/bjp.2008.204</link>
<content:encoded><![CDATA[

<p>
<b>Pharmacological targeting of the KIT growth factor receptor: a therapeutic consideration for mast cell disorders</b>
</p>
<p>British Journal of Pharmacology 154, 1572 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.204">doi:10.1038/bjp.2008.204</a>
</p>
<p>Authors: B M Jensen, C Akin
&amp; A M Gilfillan</p>
]]></content:encoded>
<dc:title>Pharmacological targeting of the KIT growth factor receptor: a therapeutic consideration for mast cell disorders</dc:title>
<dc:creator>B M Jensen</dc:creator>
<dc:creator>C Akin</dc:creator>
<dc:creator>A M Gilfillan</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.204</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1572 (August 2008)</dc:source>
<dc:date>May 26, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>May 26, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1572</prism:startingPage>
<prism:endingPage>1582</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.207">
<title>Gaddum and LSD: the birth and growth of experimental and clinical neuropharmacology research on 5-HT in the UK</title>
<link>http://dx.doi.org/10.1038/bjp.2008.207</link>
<content:encoded><![CDATA[

<p>
<b>Gaddum and LSD: the birth and growth of experimental and clinical neuropharmacology research on 5-HT in the UK</b>
</p>
<p>British Journal of Pharmacology 154, 1583 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.207">doi:10.1038/bjp.2008.207</a>
</p>
<p>Author: A R Green</p>
]]></content:encoded>
<dc:title>Gaddum and LSD: the birth and growth of experimental and clinical neuropharmacology research on 5-HT in the UK</dc:title>
<dc:creator>A R Green</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.207</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1583 (August 2008)</dc:source>
<dc:date>May 26, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>May 26, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1583</prism:startingPage>
<prism:endingPage>1599</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.205">
<title>Regional haemodynamic responses to adenosine receptor activation vary across time following lipopolysaccharide treatment in conscious rats</title>
<link>http://dx.doi.org/10.1038/bjp.2008.205</link>
<content:encoded><![CDATA[

<p>
<b>Regional haemodynamic responses to adenosine receptor activation vary across time following lipopolysaccharide treatment in conscious rats</b>
</p>
<p>British Journal of Pharmacology 154, 1600 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.205">doi:10.1038/bjp.2008.205</a>
</p>
<p>Authors: L Jolly, J E March, P A Kemp, T Bennett
&amp; S M Gardiner</p>
]]></content:encoded>
<dc:title>Regional haemodynamic responses to adenosine receptor activation vary across time following lipopolysaccharide treatment in conscious rats</dc:title>
<dc:creator>L Jolly</dc:creator>
<dc:creator>J E March</dc:creator>
<dc:creator>P A Kemp</dc:creator>
<dc:creator>T Bennett</dc:creator>
<dc:creator>S M Gardiner</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.205</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1600 (August 2008)</dc:source>
<dc:date>May 26, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>May 26, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1600</prism:startingPage>
<prism:endingPage>1610</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.208">
<title>Isolated porcine bronchi provide a reliable model for development of bronchodilator anti-muscarinic agents for human use</title>
<link>http://dx.doi.org/10.1038/bjp.2008.208</link>
<content:encoded><![CDATA[

<p>
<b>Isolated porcine bronchi provide a reliable model for development of bronchodilator anti-muscarinic agents for human use</b>
</p>
<p>British Journal of Pharmacology 154, 1611 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.208">doi:10.1038/bjp.2008.208</a>
</p>
<p>Authors: G D'Agostino, A M Condino, L Gioglio, F Zonta, M Tonini
&amp; A Barbieri</p>
]]></content:encoded>
<dc:title>Isolated porcine bronchi provide a reliable model for development of bronchodilator anti-muscarinic agents for human use</dc:title>
<dc:creator>G D'Agostino</dc:creator>
<dc:creator>A M Condino</dc:creator>
<dc:creator>L Gioglio</dc:creator>
<dc:creator>F Zonta</dc:creator>
<dc:creator>M Tonini</dc:creator>
<dc:creator>A Barbieri</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.208</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1611 (August 2008)</dc:source>
<dc:date>June 2, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 2, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1611</prism:startingPage>
<prism:endingPage>1618</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.209">
<title>Pathology-specific effects of the IKur&#47;Ito&#47;IK,ACh blocker AVE0118 on ion channels in human chronic atrial fibrillation</title>
<link>http://dx.doi.org/10.1038/bjp.2008.209</link>
<content:encoded><![CDATA[

<p>
<b>Pathology-specific effects of the IKur&#47;Ito&#47;IK,ACh blocker AVE0118 on ion channels in human chronic atrial fibrillation</b>
</p>
<p>British Journal of Pharmacology 154, 1619 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.209">doi:10.1038/bjp.2008.209</a>
</p>
<p>Authors: T Christ, E Wettwer, N Voigt, O H&#225;la, S Radicke, K Matschke, A V&#225;rro, D Dobrev
&amp; U Ravens</p>
]]></content:encoded>
<dc:title>Pathology-specific effects of the IKur&#47;Ito&#47;IK,ACh blocker AVE0118 on ion channels in human chronic atrial fibrillation</dc:title>
<dc:creator>T Christ</dc:creator>
<dc:creator>E Wettwer</dc:creator>
<dc:creator>N Voigt</dc:creator>
<dc:creator>O H&#225;la</dc:creator>
<dc:creator>S Radicke</dc:creator>
<dc:creator>K Matschke</dc:creator>
<dc:creator>A V&#225;rro</dc:creator>
<dc:creator>D Dobrev</dc:creator>
<dc:creator>U Ravens</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.209</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1619 (August 2008)</dc:source>
<dc:date>June 9, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 9, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1619</prism:startingPage>
<prism:endingPage>1630</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.214">
<title>Vasorelaxation induced by prostaglandin E2 in human pulmonary vein: role of the EP4 receptor subtype</title>
<link>http://dx.doi.org/10.1038/bjp.2008.214</link>
<content:encoded><![CDATA[

<p>
<b>Vasorelaxation induced by prostaglandin E2 in human pulmonary vein: role of the EP4 receptor subtype</b>
</p>
<p>British Journal of Pharmacology 154, 1631 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.214">doi:10.1038/bjp.2008.214</a>
</p>
<p>Authors: N Foudi, L Kotelevets, L Louedec, G Les&#233;che, D Henin, E Chastre
&amp; X Norel</p>
]]></content:encoded>
<dc:title>Vasorelaxation induced by prostaglandin E2 in human pulmonary vein: role of the EP4 receptor subtype</dc:title>
<dc:creator>N Foudi</dc:creator>
<dc:creator>L Kotelevets</dc:creator>
<dc:creator>L Louedec</dc:creator>
<dc:creator>G Les&#233;che</dc:creator>
<dc:creator>D Henin</dc:creator>
<dc:creator>E Chastre</dc:creator>
<dc:creator>X Norel</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.214</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1631 (August 2008)</dc:source>
<dc:date>June 2, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 2, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1631</prism:startingPage>
<prism:endingPage>1639</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.218">
<title>Hypercholesterolaemia exacerbates ventricular remodelling after myocardial infarction in the rat: role of angiotensin II type 1 receptors</title>
<link>http://dx.doi.org/10.1038/bjp.2008.218</link>
<content:encoded><![CDATA[

<p>
<b>Hypercholesterolaemia exacerbates ventricular remodelling after myocardial infarction in the rat: role of angiotensin II type 1 receptors</b>
</p>
<p>British Journal of Pharmacology 154, 1640 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.218">doi:10.1038/bjp.2008.218</a>
</p>
<p>Authors: M M&#261;czewski, J M&#261;czewska
&amp; M Duda</p>
]]></content:encoded>
<dc:title>Hypercholesterolaemia exacerbates ventricular remodelling after myocardial infarction in the rat: role of angiotensin II type 1 receptors</dc:title>
<dc:creator>M M&#261;czewski</dc:creator>
<dc:creator>J M&#261;czewska</dc:creator>
<dc:creator>M Duda</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.218</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1640 (August 2008)</dc:source>
<dc:date>June 9, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 9, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1640</prism:startingPage>
<prism:endingPage>1648</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.219">
<title>CO-MP4, a polyethylene glycol-conjugated haemoglobin derivative and carbon monoxide carrier that reduces myocardial infarct size in rats</title>
<link>http://dx.doi.org/10.1038/bjp.2008.219</link>
<content:encoded><![CDATA[

<p>
<b>CO-MP4, a polyethylene glycol-conjugated haemoglobin derivative and carbon monoxide carrier that reduces myocardial infarct size in rats</b>
</p>
<p>British Journal of Pharmacology 154, 1649 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.219">doi:10.1038/bjp.2008.219</a>
</p>
<p>Authors: K D Vandegriff, M A Young, J Lohman, A Bellelli, M Samaja, A Malavalli
&amp; R M Winslow</p>
]]></content:encoded>
<dc:title>CO-MP4, a polyethylene glycol-conjugated haemoglobin derivative and carbon monoxide carrier that reduces myocardial infarct size in rats</dc:title>
<dc:creator>K D Vandegriff</dc:creator>
<dc:creator>M A Young</dc:creator>
<dc:creator>J Lohman</dc:creator>
<dc:creator>A Bellelli</dc:creator>
<dc:creator>M Samaja</dc:creator>
<dc:creator>A Malavalli</dc:creator>
<dc:creator>R M Winslow</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.219</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1649 (August 2008)</dc:source>
<dc:date>June 9, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 9, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1649</prism:startingPage>
<prism:endingPage>1661</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.198">
<title>Anti-convulsive and anti-epileptic properties of brivaracetam (ucb 34714), a high-affinity ligand for the synaptic vesicle protein, SV2A</title>
<link>http://dx.doi.org/10.1038/bjp.2008.198</link>
<content:encoded><![CDATA[

<p>
<b>Anti-convulsive and anti-epileptic properties of brivaracetam (ucb 34714), a high-affinity ligand for the synaptic vesicle protein, SV2A</b>
</p>
<p>British Journal of Pharmacology 154, 1662 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.198">doi:10.1038/bjp.2008.198</a>
</p>
<p>Authors: A Matagne, D-G Margineanu, B Kenda, P Michel
&amp; H Klitgaard</p>
]]></content:encoded>
<dc:title>Anti-convulsive and anti-epileptic properties of brivaracetam (ucb 34714), a high-affinity ligand for the synaptic vesicle protein, SV2A</dc:title>
<dc:creator>A Matagne</dc:creator>
<dc:creator>D-G Margineanu</dc:creator>
<dc:creator>B Kenda</dc:creator>
<dc:creator>P Michel</dc:creator>
<dc:creator>H Klitgaard</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.198</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1662 (August 2008)</dc:source>
<dc:date>May 26, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>May 26, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1662</prism:startingPage>
<prism:endingPage>1671</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.211">
<title>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</title>
<link>http://dx.doi.org/10.1038/bjp.2008.211</link>
<content:encoded><![CDATA[

<p>
<b>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</b>
</p>
<p>British Journal of Pharmacology 154, 1672 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.211">doi:10.1038/bjp.2008.211</a>
</p>
<p>Authors: D De Filippis, A Russo, A D'Amico, G Esposito, P Concetta, M Cinelli, G Russo
&amp; T Iuvone</p>
]]></content:encoded>
<dc:title>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</dc:title>
<dc:creator>D De Filippis</dc:creator>
<dc:creator>A Russo</dc:creator>
<dc:creator>A D'Amico</dc:creator>
<dc:creator>G Esposito</dc:creator>
<dc:creator>P Concetta</dc:creator>
<dc:creator>M Cinelli</dc:creator>
<dc:creator>G Russo</dc:creator>
<dc:creator>T Iuvone</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.211</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1672 (August 2008)</dc:source>
<dc:date>June 16, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 16, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1672</prism:startingPage>
<prism:endingPage>1679</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.213">
<title>Regulation of two-pore-domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein</title>
<link>http://dx.doi.org/10.1038/bjp.2008.213</link>
<content:encoded><![CDATA[

<p>
<b>Regulation of two-pore-domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein</b>
</p>
<p>British Journal of Pharmacology 154, 1680 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.213">doi:10.1038/bjp.2008.213</a>
</p>
<p>Authors: J Gierten, E Ficker, R Bloehs, K Schl&#246;mer, S Kath&#246;fer, E Scholz, E Zitron, C Kiesecker, A Bauer, R Becker, H A Katus, C A Karle
&amp; D Thomas</p>
]]></content:encoded>
<dc:title>Regulation of two-pore-domain (K2P) potassium leak channels by the tyrosine kinase inhibitor genistein</dc:title>
<dc:creator>J Gierten</dc:creator>
<dc:creator>E Ficker</dc:creator>
<dc:creator>R Bloehs</dc:creator>
<dc:creator>K Schl&#246;mer</dc:creator>
<dc:creator>S Kath&#246;fer</dc:creator>
<dc:creator>E Scholz</dc:creator>
<dc:creator>E Zitron</dc:creator>
<dc:creator>C Kiesecker</dc:creator>
<dc:creator>A Bauer</dc:creator>
<dc:creator>R Becker</dc:creator>
<dc:creator>H A Katus</dc:creator>
<dc:creator>C A Karle</dc:creator>
<dc:creator>D Thomas</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.213</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1680 (August 2008)</dc:source>
<dc:date>June 2, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 2, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1680</prism:startingPage>
<prism:endingPage>1690</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.210">
<title>Pharmacodynamic interaction of warfarin with cranberry but not with garlic in healthy subjects</title>
<link>http://dx.doi.org/10.1038/bjp.2008.210</link>
<content:encoded><![CDATA[

<p>
<b>Pharmacodynamic interaction of warfarin with cranberry but not with garlic in healthy subjects</b>
</p>
<p>British Journal of Pharmacology 154, 1691 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.210">doi:10.1038/bjp.2008.210</a>
</p>
<p>Authors: M I Mohammed Abdul, X Jiang, K M Williams, R O Day, B D Roufogalis, W S Liauw, H Xu
&amp; A J McLachlan</p>
]]></content:encoded>
<dc:title>Pharmacodynamic interaction of warfarin with cranberry but not with garlic in healthy subjects</dc:title>
<dc:creator>M I Mohammed Abdul</dc:creator>
<dc:creator>X Jiang</dc:creator>
<dc:creator>K M Williams</dc:creator>
<dc:creator>R O Day</dc:creator>
<dc:creator>B D Roufogalis</dc:creator>
<dc:creator>W S Liauw</dc:creator>
<dc:creator>H Xu</dc:creator>
<dc:creator>A J McLachlan</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.210</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1691 (August 2008)</dc:source>
<dc:date>June 2, 2008</dc:date>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:publicationDate>June 2, 2008</prism:publicationDate>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1691</prism:startingPage>
<prism:endingPage>1700</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.314">
<title>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</title>
<link>http://dx.doi.org/10.1038/bjp.2008.314</link>
<content:encoded><![CDATA[

<p>
<b>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</b>
</p>
<p>British Journal of Pharmacology 154, 1701 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.314">doi:10.1038/bjp.2008.314</a>
</p>
<p>Authors: D De Filippis, A Russo, A D'Amico, G Esposito, C Pietropaolo, M Cinelli, G Russo
&amp; T Iuvone</p>
]]></content:encoded>
<dc:title>Cannabinoids reduce granuloma-associated angiogenesis in rats by controlling transcription and expression of mast cell protease-5</dc:title>
<dc:creator>D De Filippis</dc:creator>
<dc:creator>A Russo</dc:creator>
<dc:creator>A D'Amico</dc:creator>
<dc:creator>G Esposito</dc:creator>
<dc:creator>C Pietropaolo</dc:creator>
<dc:creator>M Cinelli</dc:creator>
<dc:creator>G Russo</dc:creator>
<dc:creator>T Iuvone</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.314</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1701 (August 2008)</dc:source>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1701</prism:startingPage>
<prism:endingPage>1701</prism:endingPage>
</item>
<item rdf:about="http://dx.doi.org/10.1038/bjp.2008.282">
<title>Anti-inflammatory effects of dimemorfan on inflammatory cells and LPS-induced endotoxin shock in mice</title>
<link>http://dx.doi.org/10.1038/bjp.2008.282</link>
<content:encoded><![CDATA[

<p>
<b>Anti-inflammatory effects of dimemorfan on inflammatory cells and LPS-induced endotoxin shock in mice</b>
</p>
<p>British Journal of Pharmacology 154, 1702 (August 2008). <a href="http://dx.doi.org/10.1038/bjp.2008.282">doi:10.1038/bjp.2008.282</a>
</p>
<p>Authors: Y-H Wang, Y-C Shen, J-F Liao, C-H Lee, C-Y Chou, K-T Liou
&amp; Y-C Chou</p>
]]></content:encoded>
<dc:title>Anti-inflammatory effects of dimemorfan on inflammatory cells and LPS-induced endotoxin shock in mice</dc:title>
<dc:creator>Y-H Wang</dc:creator>
<dc:creator>Y-C Shen</dc:creator>
<dc:creator>J-F Liao</dc:creator>
<dc:creator>C-H Lee</dc:creator>
<dc:creator>C-Y Chou</dc:creator>
<dc:creator>K-T Liou</dc:creator>
<dc:creator>Y-C Chou</dc:creator>
<dc:identifier>doi:10.1038/bjp.2008.282</dc:identifier>
<dc:source>British Journal of Pharmacology 154, 1702 (August 2008)</dc:source>
<prism:publicationName>British Journal of Pharmacology</prism:publicationName>
<prism:volume>154</prism:volume>
<prism:number>8</prism:number>
<prism:startingPage>1702</prism:startingPage>
<prism:endingPage>1702</prism:endingPage>
</item>
</rdf:RDF>
