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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Gualda Manzano, Emilio José</mods:namePart>
               </mods:name>
               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Moreno, Nuno</mods:namePart>
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               <mods:originInfo>
                  <mods:dateIssued encoding="iso8601">2015-08</mods:dateIssued>
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               <mods:abstract>Light-Sheet Fluorescence Microscopy (LSFM) has recently emerged as the technique of choice for obtaining&#xd;
high quality 3D images of whole organisms with low photo-damage and fast acquisition rates. Unlike&#xd;
conventional optical microscopy or scanning electron microscopy systems it offers the possibility of&#xd;
obtaining multi-views of the sample by rotating it. Here we show that the use of light sheet microscopy for&#xd;
the analysis of invertebrates provides a fair compromise compared to scanning electron microscopy (SEM) in&#xd;
terms of resolution but avoiding some its drawbacks such as sample preparation or limited three-dimensional&#xd;
perspectivesFundação para a Ciência e Tecnologia, grant SFRH/BD/80717/2011Postprint (published version)</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/3.0/es/ Open Access Attribution-NonCommercial-NoDerivs 3.0 Spain</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Àrees temàtiques de la UPC::Ciències de la visió::Òptica física::Llum</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Fluorescence.</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Fluorescence microscopy</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Fluorescència</mods:topic>
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               <mods:titleInfo>
                  <mods:title>3D volume rendering of invertebrates using light-sheet fluorescence microscopy</mods:title>
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