<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Inderbitzin D</dc:creator>
  <dc:creator>Stoupis C</dc:creator>
  <dc:creator>Sidler D</dc:creator>
  <dc:creator>Gass M</dc:creator>
  <dc:creator>Candinas D</dc:creator>
  <dc:date>2007</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Because of superior soft-tissue contrast compared to other imaging techniques, non-invasive abdominal magnetic resonance imaging (MRI) is ideal for monitoring organ regeneration, tissue repair, cancer stage, and treatment effects in a wide variety of experimental animal models. Currently, sophisticated MR protocols, including technically demanding procedures for motion artefact compensation, achieve an MRI resolution limit of &lt; 100 microm under ideal conditions. However, such a high spatial resolution is not required for most experimental rodent studies. This article describes both a detailed imaging protocol for MR data acquisition in a ubiquitously and commercially available 1.5 T MR unit and 3-dimensional volumetry of organs, tissue components, or tumors. Future developments in MR technology will allow in vivo investigation of physiological and pathological processes at the cellular and even the molecular levels. Experimental MRI is crucial for non-invasive monitoring of a broad range of biological processes and will further our general understanding of physiology and disease.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/131611</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ymeth.2007.03.010</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/17720563</dc:relation>
  <dc:source>Methods (San Diego, Calif.). - 2007</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Abdomen</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Artifacts</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Body Size</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Carcinoma, Hepatocellular</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Clinical Protocols</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Echo-Planar Imaging</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Image Enhancement</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Image Interpretation, Computer-Assisted</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Magnetic Resonance Imaging</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Mice, Inbred BALB C</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Rats</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Rats, Inbred ACI</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Reproducibility of Results</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Rodentia</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Time Factors</dc:subject>
  <dc:title xmlns:ns19="xml" ns19:lang="en">Abdominal magnetic resonance imaging in small rodents using a clinical 1.5 T MR scanner.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
