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		<description>RSC - Photochem. Photobiol. Sci. latest articles</description>
		<link>http://xlink.rsc.org/jumptojournal.cfm?journal_code=PP</link>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
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		<dc:creator>The Royal Society of Chemistry</dc:creator>
		<dc:description>Royal Society of Chemistry - Photochem. Photobiol. Sci. latest articles</dc:description>
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			<rdf:Seq><rdf:li rdf:resource="http://xlink.rsc.org/?DOI=b9pp00052f&amp;RSS=1"/>
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	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00052f&amp;RSS=1"><title>Mechanism of aerobic visible light formic acid oxidation catalyzed by poly(tri-s-triazine) modified titania</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00052f&amp;RSS=1</link>
		<description>The visible light formic acid oxidation catalyzed by poly(tri-s-triazine)-modified titania involves both oxidative and reductive pathways.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2010/b9pp00052f-ga.gif"/&gt;
	&lt;/p&gt;Dariusz Mitoraj, Radim Beranek, Horst Kisch &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Dariusz Mitoraj, Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00052f&lt;br/&gt;
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		<dc:title>Mechanism of aerobic visible light formic acid oxidation catalyzed by poly(tri-s-triazine) modified titania</dc:title>
		<dc:creator>Dariusz Mitoraj</dc:creator>
		<dc:creator>Radim Beranek </dc:creator><dc:creator>Horst Kisch </dc:creator><dc:identifier>10.1039/b9pp00052f</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00052f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-12</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00052f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00051h&amp;RSS=1"><title>Immunosuppressive ultraviolet-A radiation inhibits the development of skin memory CD8 T cells</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00051h&amp;RSS=1</link>
		<description>UVA does not affect CD8 T cell expansion in draining lymph nodes, but it can inhibit the development of peripheral memory CD8 T cells in a model of systemic immunosuppression.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2010/b9pp00051h-ga.gif"/&gt;
	&lt;/p&gt;Sabita Rana, Linda J. Rogers, Gary M. Halliday &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Sabita Rana, Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00051h&lt;br/&gt;
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		<dc:title>Immunosuppressive ultraviolet-A radiation inhibits the development of skin memory CD8 T cells</dc:title>
		<dc:creator>Sabita Rana</dc:creator>
		<dc:creator>Linda J. Rogers </dc:creator><dc:creator>Gary M. Halliday </dc:creator><dc:identifier>10.1039/b9pp00051h</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00051h</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-11-06</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00051h</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00068b&amp;RSS=1"><title>The role of Nrf2 in ultraviolet A mediated heme oxygenase 1 induction in human skin fibroblasts</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00068b&amp;RSS=1</link>
		<description>Silencing of Nrf2 reduces basal and UVA-induced HO-1 protein levels.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2010/b9pp00068b-ga.gif"/&gt;
	&lt;/p&gt;Julia L. Zhong, Gavin P. Edwards, Chintan Raval, Haibin Li, Rex M. Tyrrell &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Julia L. Zhong, Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00068b&lt;br/&gt;
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		<dc:title>The role of Nrf2 in ultraviolet A mediated heme oxygenase 1 induction in human skin fibroblasts</dc:title>
		<dc:creator>Julia L. Zhong</dc:creator>
		<dc:creator>Gavin P. Edwards </dc:creator><dc:creator>Chintan Raval </dc:creator><dc:creator>Haibin Li </dc:creator><dc:creator>Rex M. Tyrrell </dc:creator><dc:identifier>10.1039/b9pp00068b</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00068b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-28</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00068b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00037b&amp;RSS=1"><title>Photochemical investigation of a photochromic diarylethene compound that can be used as a wide range actinometer</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00037b&amp;RSS=1</link>
		<description>The thermally stable isomers 1a and 1b interconvert photochemically in acetonitrile. The photochemistry, wide spectral absorption range (240-700 nm) and high fatigue resistance make 1 suitable as a simple reusable chemical actinometer, especially for the visible (400-620 nm), where few other actinometers are available.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00037b-ga.gif"/&gt;
	&lt;/p&gt;Andre Ribeiro Santos, Roberto Ballardini, Peter Belser, Maria Teresa Gandolfi, Vijay Mahadevan Iyer, Luca Moggi &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Andre Ribeiro Santos, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00037b&lt;br/&gt;
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		<dc:title>Photochemical investigation of a photochromic diarylethene compound that can be used as a wide range actinometer</dc:title>
		<dc:creator>Andre Ribeiro Santos</dc:creator>
		<dc:creator>Roberto Ballardini </dc:creator><dc:creator>Peter Belser </dc:creator><dc:creator>Maria Teresa Gandolfi </dc:creator><dc:creator>Vijay Mahadevan Iyer </dc:creator><dc:creator>Luca Moggi </dc:creator><dc:identifier>10.1039/b9pp00037b</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00037b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-28</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00037b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00054b&amp;RSS=1"><title>Photophysical properties and photodynamic activity of octacationic oxotitanium(iv) phthalocyanines</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00054b&amp;RSS=1</link>
		<description>Both singlet oxygen and hydroxyl radicals participate in bacterial cell killing and oxidation of organic substrates photosensitized by octacationic oxotitanium phthalocyanines in aqueous solutions.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00054b-ga.gif"/&gt;
	&lt;/p&gt;Nina Kuznetsova, Dmitry Makarov, Olga Yuzhakova, Anton Strizhakov, Yana Roumbal, Ludmila Ulanova, Alexander Krasnovsky, Oleg Kaliya &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Nina Kuznetsova, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00054b&lt;br/&gt;
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		<dc:title>Photophysical properties and photodynamic activity of octacationic oxotitanium(iv) phthalocyanines</dc:title>
		<dc:creator>Nina Kuznetsova</dc:creator>
		<dc:creator>Dmitry Makarov </dc:creator><dc:creator>Olga Yuzhakova </dc:creator><dc:creator>Anton Strizhakov </dc:creator><dc:creator>Yana Roumbal </dc:creator><dc:creator>Ludmila Ulanova </dc:creator><dc:creator>Alexander Krasnovsky </dc:creator><dc:creator>Oleg Kaliya </dc:creator><dc:identifier>10.1039/b9pp00054b</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00054b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-26</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00054b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00063a&amp;RSS=1"><title>Enhanced efficiency of the visible-light photocatalytic hydrogen generation by the ruthenium tris(2,2[prime or minute]-bipyridyl)-methyl viologen system in the presence of cucurbit[n]urils</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00063a&amp;RSS=1</link>
		<description>The efficiency of photocatalytic H2 generation increases when cucurbiturils are present in solution. The efficiency enhancement is CB[6] &lt; CB[7] &lt; CB[8].</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00063a-ga.gif"/&gt;
	&lt;/p&gt;Claudia Gomes Silva, Maykel de Miguel, Belen Ferrer, Mercedes Alvaro, Hermenegildo Garcia &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Claudia Gomes Silva, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00063a&lt;br/&gt;
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		<dc:title>Enhanced efficiency of the visible-light photocatalytic hydrogen generation by the ruthenium tris(2,2[prime or minute]-bipyridyl)-methyl viologen system in the presence of cucurbit[n]urils</dc:title>
		<dc:creator>Claudia Gomes Silva</dc:creator>
		<dc:creator>Maykel de Miguel </dc:creator><dc:creator>Belen Ferrer </dc:creator><dc:creator>Mercedes Alvaro </dc:creator><dc:creator>Hermenegildo Garcia </dc:creator><dc:identifier>10.1039/b9pp00063a</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00063a</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-26</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00063a</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00053d&amp;RSS=1"><title>Pyrearinus termitilluminans larval click beetle luciferase: active site properties, structure and function relationships and comparison with other beetle luciferases</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00053d&amp;RSS=1</link>
		<description>The green-emitting Pyrearinus termitilluminans larval click beetle luciferase was expressed, purified and characterized. Among beetle luciferases, it displays the most blue-shifted bioluminescence spectrum, as well as a high catalytic constant, thermal stability and sustained luminescence.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00053d-ga.gif"/&gt;
	&lt;/p&gt;A. J. Silva Neto, V. Scorsato, F. G. C. Arnoldi, V. R. Viviani &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
A. J. Silva Neto, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00053d&lt;br/&gt;
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		<dc:title>Pyrearinus termitilluminans larval click beetle luciferase: active site properties, structure and function relationships and comparison with other beetle luciferases</dc:title>
		<dc:creator>A. J. Silva Neto</dc:creator>
		<dc:creator>V. Scorsato </dc:creator><dc:creator>F. G. C. Arnoldi </dc:creator><dc:creator>V. R. Viviani </dc:creator><dc:identifier>10.1039/b9pp00053d</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00053d</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00053d</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00086k&amp;RSS=1"><title>Drug efflux transporters, MRP1 and BCRP, affect the outcome of hypericin-mediated photodynamic therapy in HT-29 adenocarcinoma cells</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00086k&amp;RSS=1</link>
		<description>Stimulation of MRP1 and BCRP expression by hypericin per se affected its accumulation and therefore HY-PDT efficiency, however this undesired effect was eliminated by pre-treatment with proadifen.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00086k-ga.gif"/&gt;
	&lt;/p&gt;Rastislav Jendzelovsky, Jaromir Mikes, Jan Koval', Karel Soucek, Jirina Prochazkova, Martin Kello, Veronika Sackova, Jirina Hofmanova, Alois Kozubik, Peter Fedorocko &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Rastislav Jendzelovsky, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00086k&lt;br/&gt;
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		<dc:title>Drug efflux transporters, MRP1 and BCRP, affect the outcome of hypericin-mediated photodynamic therapy in HT-29 adenocarcinoma cells</dc:title>
		<dc:creator>Rastislav Jendzelovsky</dc:creator>
		<dc:creator>Jaromir Mikes </dc:creator><dc:creator>Jan Koval' </dc:creator><dc:creator>Karel Soucek </dc:creator><dc:creator>Jirina Prochazkova </dc:creator><dc:creator>Martin Kello </dc:creator><dc:creator>Veronika Sackova </dc:creator><dc:creator>Jirina Hofmanova </dc:creator><dc:creator>Alois Kozubik </dc:creator><dc:creator>Peter Fedorocko </dc:creator><dc:identifier>10.1039/b9pp00086k</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00086k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-23</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00086k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00081j&amp;RSS=1"><title>Effect of bridgehead substitution on the fluorescence quenching of 2,3-diazabicyclo[2.2.2]oct-2-enes by solvents and antioxidants</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00081j&amp;RSS=1</link>
		<description>Simple bridgehead substitution in bicyclic azoalkanes allows the fine-tuning of fluorescent probes for antioxidants with respect to their reactivity, selectivity, and nucleophilicity.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00081j-ga.gif"/&gt;
	&lt;/p&gt;Roland Meyer, Xiangyang Zhang, Werner M. Nau &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Roland Meyer, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00081j&lt;br/&gt;
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		<dc:title>Effect of bridgehead substitution on the fluorescence quenching of 2,3-diazabicyclo[2.2.2]oct-2-enes by solvents and antioxidants</dc:title>
		<dc:creator>Roland Meyer</dc:creator>
		<dc:creator>Xiangyang Zhang </dc:creator><dc:creator>Werner M. Nau </dc:creator><dc:identifier>10.1039/b9pp00081j</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00081j</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00081j</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00041k&amp;RSS=1"><title>Cucurbituril complexes cross the cell membrane</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00041k&amp;RSS=1</link>
		<description>Host-guest complexes based on CB[7] and CB[8] with strong binding constants can enter tumoral cells as determined by fluorescence microscopy.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00041k-ga.gif"/&gt;
	&lt;/p&gt;Pedro Montes-Navajas, Maria Gonzalez-Bejar, J. C. Scaiano, Hermenegildo Garcia &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Pedro Montes-Navajas, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00041k&lt;br/&gt;
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		<dc:title>Cucurbituril complexes cross the cell membrane</dc:title>
		<dc:creator>Pedro Montes-Navajas</dc:creator>
		<dc:creator>Maria Gonzalez-Bejar </dc:creator><dc:creator>J. C. Scaiano </dc:creator><dc:creator>Hermenegildo Garcia </dc:creator><dc:identifier>10.1039/b9pp00041k</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00041k</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00041k</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00018f&amp;RSS=1"><title>Demetalation kinetics of natural chlorophylls purified from oxygenic photosynthetic organisms: effect of the formyl groups conjugated directly to the chlorin [small pi]-macrocycle</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00018f&amp;RSS=1</link>
		<description>Demetalation kinetics of chlorophyll (Chl) d possessing 3-formyl group was slower than that of Chl a possessing 3-vinyl group, but faster than that of Chl b possessing 7-formyl group.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00018f-ga.gif"/&gt;
	&lt;/p&gt;Yuki Hirai, Hitoshi Tamiaki, Shigenori Kashimura, Yoshitaka Saga &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Yuki Hirai, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00018f&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Demetalation kinetics of natural chlorophylls purified from oxygenic photosynthetic organisms: effect of the formyl groups conjugated directly to the chlorin [small pi]-macrocycle</dc:title>
		<dc:creator>Yuki Hirai</dc:creator>
		<dc:creator>Hitoshi Tamiaki </dc:creator><dc:creator>Shigenori Kashimura </dc:creator><dc:creator>Yoshitaka Saga </dc:creator><dc:identifier>10.1039/b9pp00018f</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00018f</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00018f</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00023b&amp;RSS=1"><title>Encapsulation of 2-(4[prime or minute]-N,N-dimethylamino)phenylimidazo[4,5-b]pyridine in [small beta]-cyclodextrin: effect on H-bond-induced intramolecular charge transfer emission</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00023b&amp;RSS=1</link>
		<description>DMAPIP-b/[small beta]-CD inclusion complex emits dual fluorescence with enhanced normal and ICT emission due to reduced polarity experienced by DMAPIP-b inside the cavity and hydrogen bonding of pyridine nitrogen with water.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2009/b9pp00023b-ga.gif"/&gt;
	&lt;/p&gt;Nihar Dash, Francis A. S. Chipem, G. Krishnamoorthy &lt;br/&gt;
(Paper from Photochem. Photobiol. Sci.)&lt;br/&gt;
Nihar Dash, Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00023b&lt;br/&gt;
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&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry</content:encoded>
		<dc:title>Encapsulation of 2-(4[prime or minute]-N,N-dimethylamino)phenylimidazo[4,5-b]pyridine in [small beta]-cyclodextrin: effect on H-bond-induced intramolecular charge transfer emission</dc:title>
		<dc:creator>Nihar Dash</dc:creator>
		<dc:creator>Francis A. S. Chipem </dc:creator><dc:creator>G. Krishnamoorthy </dc:creator><dc:identifier>10.1039/b9pp00023b</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2009, DOI: 10.1039/b9pp00023b</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00023b</dc:identifier>
	</item>
	<item rdf:about="http://xlink.rsc.org/?DOI=b9pp00012g&amp;RSS=1"><title>Is the action spectrum for the UV-induced production of previtamin D3 in human skin correct?</title>
		<link>http://xlink.rsc.org/?DOI=b9pp00012g&amp;RSS=1</link>
		<description>Doubts regarding the accuracy of the "official" action spectrum for the UV-induced conversion of 7-dehydrocholesterol to previtamin D3 in human skin are explained, and their implications discussed.</description><content:encoded>&lt;p&gt;&lt;img align="center" src="http://www.rsc.org/ejga/PP/2010/b9pp00012g-ga.gif"/&gt;
	&lt;/p&gt;Mary Norval, Lars Olof Bjorn, Frank R. de Gruijl &lt;br/&gt;
(Perspective from Photochem. Photobiol. Sci.)&lt;br/&gt;
Mary Norval, Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00012g&lt;br/&gt;
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		<dc:title>Is the action spectrum for the UV-induced production of previtamin D3 in human skin correct?</dc:title>
		<dc:creator>Mary Norval</dc:creator>
		<dc:creator>Lars Olof Bjorn </dc:creator><dc:creator>Frank R. de Gruijl </dc:creator><dc:identifier>10.1039/b9pp00012g</dc:identifier>
		<dc:source>Photochem. Photobiol. Sci., 2010, DOI: 10.1039/b9pp00012g</dc:source>
		<dc:format>html/pdf</dc:format>
		<dc:date>2009-10-19</dc:date>
		<dc:publisher>The Royal Society of Chemistry</dc:publisher>
		<dc:rights>Copyright (c) 2010 The Royal Society of Chemistry</dc:rights>
		<dc:identifier>DOI 10.1039/b9pp00012g</dc:identifier>
	</item>
</rdf:RDF>
