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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180418</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180419" accession="SRX7186773">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186773</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180419</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180419: 2526-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692988">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692988</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180419</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180419</ID>
          <LABEL>GSM4180419</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180419</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180420" accession="SRX7186774">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186774</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180420</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180420: 2571-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692989">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692989</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180420</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180420</ID>
          <LABEL>GSM4180420</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180420</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180421" accession="SRX7186775">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186775</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180421</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180421: 2572-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692990">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692990</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180421</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180421</ID>
          <LABEL>GSM4180421</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180421</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180422" accession="SRX7186776">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186776</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180422</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180422: 2722-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692991">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692991</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180422</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180422</ID>
          <LABEL>GSM4180422</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180422</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180423" accession="SRX7186777">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186777</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180423</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180423: 2728-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692992">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692992</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180423</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180423</ID>
          <LABEL>GSM4180423</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180423</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180424" accession="SRX7186778">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186778</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180424</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180424: 2731-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692993">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692993</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180424</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180424</ID>
          <LABEL>GSM4180424</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180424</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180425" accession="SRX7186779">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186779</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180425</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180425: 2403-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692994">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692994</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180425</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180425</ID>
          <LABEL>GSM4180425</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180425</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180426" accession="SRX7186780">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186780</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180426</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180426: 2404-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692995</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180426</ID>
          <LABEL>GSM4180426</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180426</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180427" accession="SRX7186781">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186781</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180427</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180427: 2408-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692996</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180427</ID>
          <LABEL>GSM4180427</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180427</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180428" accession="SRX7186782">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186782</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180428</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180428: 2527-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692997</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180428</ID>
          <LABEL>GSM4180428</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180428</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180429" accession="SRX7186783">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186783</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180429</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180429: 2543-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692998</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180429</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180429</ID>
          <LABEL>GSM4180429</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180429</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180430" accession="SRX7186784">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186784</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180430</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180430: 2547-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5692999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5692999</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180430</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180430</ID>
          <LABEL>GSM4180430</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180430</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180431" accession="SRX7186785">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186785</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180431</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180431: 2573-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693000</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180431</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180431</ID>
          <LABEL>GSM4180431</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180431</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180432" accession="SRX7186786">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186786</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180432</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180432: 2717-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693001</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180432</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180432</ID>
          <LABEL>GSM4180432</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180432</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180433" accession="SRX7186787">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186787</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180433</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180433: 2403-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180433</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180433</ID>
          <LABEL>GSM4180433</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180433</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180434" accession="SRX7186788">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186788</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180434</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180434: 2404-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180434</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180434</ID>
          <LABEL>GSM4180434</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180434</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180435" accession="SRX7186789">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186789</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180435</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180435: 2408-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180435</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180435</ID>
          <LABEL>GSM4180435</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180435</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180436" accession="SRX7186790">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186790</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180436</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180436: 2527-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180436</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180436</ID>
          <LABEL>GSM4180436</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180436</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180437" accession="SRX7186791">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186791</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180437</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180437: 2543-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180437</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180437</ID>
          <LABEL>GSM4180437</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180437</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180438" accession="SRX7186792">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186792</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180438</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180438: 2547-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180438</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180438</ID>
          <LABEL>GSM4180438</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180438</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180439" accession="SRX7186793">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186793</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180439</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180439: 2573-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180439</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180439</ID>
          <LABEL>GSM4180439</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180439</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180440" accession="SRX7186794">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186794</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180440</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180440: 2717-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180440</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180440</ID>
          <LABEL>GSM4180440</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180440</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180441" accession="SRX7186795">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186795</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180441</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180441: 2411-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180441</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180441</ID>
          <LABEL>GSM4180441</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180441</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180442" accession="SRX7186796">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186796</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180442</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180442: 2412-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180442</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180442</ID>
          <LABEL>GSM4180442</LABEL>
        </XREF_LINK>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180442</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180443" accession="SRX7186797">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186797</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180443</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180443: 2415-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180443</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180443</ID>
          <LABEL>GSM4180443</LABEL>
        </XREF_LINK>
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    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180443</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180444" accession="SRX7186798">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186798</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180444</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180444: 2420-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180444</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180444</ID>
          <LABEL>GSM4180444</LABEL>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180444</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180445" accession="SRX7186799">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX7186799</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180445</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180445: 2531-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM4180445</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180445</ID>
          <LABEL>GSM4180445</LABEL>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180445</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180446" accession="SRX7186800">
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      <PRIMARY_ID>SRX7186800</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180446</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180446: 2532-CA1; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693015</PRIMARY_ID>
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        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180446</ID>
          <LABEL>GSM4180446</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180446</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180447" accession="SRX7186801">
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      <PRIMARY_ID>SRX7186801</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180447</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180447: 2411-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693016</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
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        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180447</ID>
          <LABEL>GSM4180447</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM4180447</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM4180448" accession="SRX7186802">
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      <PRIMARY_ID>SRX7186802</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180448</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180448: 2412-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693017</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180448</ID>
          <LABEL>GSM4180448</LABEL>
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    </EXPERIMENT_LINKS>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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      <PRIMARY_ID>SRX7186803</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM4180449</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM4180449: 2415-DG; Rattus norvegicus; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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    </STUDY_REF>
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      <DESIGN_DESCRIPTION/>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS5693018</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX7186804</PRIMARY_ID>
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    <TITLE>GSM4180450: 2420-DG; Rattus norvegicus; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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          <PRIMARY_ID>SRS5693019</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
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      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>304180450</ID>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX7186805</PRIMARY_ID>
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    <TITLE>GSM4180451: 2531-DG; Rattus norvegicus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP230638" refname="GSE140685">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS5693020">
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          <PRIMARY_ID>SRS5693020</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
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          <DB>gds</DB>
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          <LABEL>GSM4180451</LABEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX7186806</PRIMARY_ID>
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    <TITLE>GSM4180452: 2532-DG; Rattus norvegicus; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP230638</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS5693021</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hippocampi were collected 48 hours after a seventh injection. Rats were anesthetized with isoflurane and swiftly decapitated. The brains were rapidly removed and one hippocampus was subdivided into CA1 and dentate gyrus (DG) for RNA sequencing. All brain samples were flash frozen in liquid nitrogen and were stored at -80 C. Sequencing libraries were constructed using the library preparation kit Ion Total RNA-Seq kit v2 (Thermo Fisher, Cat# 4475936). Ion Xpress barcodes (Thermo Fisher, catalog number4475485) were added for multiplex sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
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          <DB>gds</DB>
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</EXPERIMENT_SET>
