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      <subfield code="a">dc</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Gualda Manzano, Emilio José</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Moreno, Nuno</subfield>
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      <subfield code="c">2015-08</subfield>
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      <subfield code="a">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;
perspectives</subfield>
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      <subfield code="a">Fundação para a Ciência e Tecnologia, grant SFRH/BD/80717/2011</subfield>
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      <subfield code="a">Postprint (published version)</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Àrees temàtiques de la UPC::Ciències de la visió::Òptica física::Llum</subfield>
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      <subfield code="a">Fluorescence.</subfield>
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      <subfield code="a">Fluorescence microscopy</subfield>
   </datafield>
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      <subfield code="a">Fluorescència</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">3D volume rendering of invertebrates using light-sheet fluorescence microscopy</subfield>
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