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      <dc:title>Fishing anti(lymph)angiogenic drugs with zebrafish</dc:title>
      <dc:creator>García-Caballero, Melissa</dc:creator>
      <dc:creator>Rodríguez-Quesada, Ana María</dc:creator>
      <dc:creator>Medina-Torres, Miguel Ángel</dc:creator>
      <dc:creator>Mari-Beffa, Manuel</dc:creator>
      <dc:subject>Neovascularización</dc:subject>
      <dc:description>Zebrafish, an amenable small teleost fish with a complex mammal-like circulatory system, is being increasingly used for drug screening and toxicity studies. It combines the biological complexity of in vivo models with a higher-throughput screening capability compared with other available animal models.&#xd;
Externally growing, transparent embryos, displaying well-defined blood and lymphatic vessels, allow the inexpensive, rapid, and automatable evaluation of drug candidates that are able to inhibit neovascularisation. Here, we briefly review zebrafish as a model for the screening of anti(lymph) angiogenic drugs, with emphasis on the advantages and limitations of the different zebrafish-based in vivo assays.</dc:description>
      <dc:date>2018-10-19T07:38:40Z</dc:date>
      <dc:date>2018-10-19T07:38:40Z</dc:date>
      <dc:date>2018</dc:date>
      <dc:date>2018-10-19</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/16662</dc:identifier>
      <dc:identifier>10.1016/j.drudis.2017.10.018</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
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