<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>Leone DP</dc:creator>
  <dc:creator>Genoud S</dc:creator>
  <dc:creator>Atanasoski S</dc:creator>
  <dc:creator>Grausenburger R</dc:creator>
  <dc:creator>Berger P</dc:creator>
  <dc:creator>Metzger D</dc:creator>
  <dc:creator>Macklin WB</dc:creator>
  <dc:creator>Chambon P</dc:creator>
  <dc:creator>Suter U</dc:creator>
  <dc:date>2003</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Inducible transgenesis provides a valuable technique for the analysis of gene function in vivo. We report the generation and characterization of mouse lines carrying glia lineage-specific transgenes expressing an improved variant of the tamoxifen-inducible Cre recombinase, CreERT2, where the recombinase is fused to a mutated ligand binding domain of the human estrogen receptor. Using a PLP-CreERT2 transgene, we have generated mice that show specific inducible Cre function, as analyzed by cross-breeding experiments into the Rosa26 Cre-LacZ reporter line, in developing and adult Schwann cells, in mature myelinating oligodendrocytes, and in undifferentiated NG2-positive oligodendrocyte precursors in the adult. Using a P0Cx-CreERT2 transgene, we have also established mouse lines with inducible Cre function specifically in the Schwann cell lineage. These tamoxifen-inducible CreERT2 lines will allow detailed spatiotemporally controlled analysis of gene functions in loxP-based conditional mutant mice in both developing and adult Schwann cells and in the oligodendrocyte lineage.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/47091</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/s1044-7431(03)00029-0</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/12727441</dc:relation>
  <dc:source>Molecular and cellular neurosciences. - 2003</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals, Newborn</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Brain</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cell Lineage</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Dose-Response Relationship, Drug</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Female</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Fetus</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Gene Expression Regulation</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Genes, Reporter</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Integrases</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Lactation</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Mice, Transgenic</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Mutagenesis</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Oligodendroglia</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Peripheral Nervous System</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Protein Structure, Tertiary</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">Receptors, Estrogen</dc:subject>
  <dc:subject xmlns:ns20="xml" ns20:lang="en">Recombinant Fusion Proteins</dc:subject>
  <dc:subject xmlns:ns21="xml" ns21:lang="en">Schwann Cells</dc:subject>
  <dc:subject xmlns:ns22="xml" ns22:lang="en">Stem Cells</dc:subject>
  <dc:subject xmlns:ns23="xml" ns23:lang="en">Tamoxifen</dc:subject>
  <dc:subject xmlns:ns24="xml" ns24:lang="en">Transgenes</dc:subject>
  <dc:subject xmlns:ns25="xml" ns25:lang="en">Viral Proteins</dc:subject>
  <dc:title xmlns:ns26="xml" ns26:lang="en">Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
