<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE106389" accession="SRP123271">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP123271</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA416696</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE106389</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>RNAseq anaysis of ventral striatum cholinergic cells of p11 cKO mice</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Purpose: To identify gene expression changes in cholinergic neurons of the ventral striatum of p11 cKO mice Method: Translating Ribosome Affinity Purification (TRAP) to isolate RNA from ChAT+ cells and, cDNA synthesisi and next generation RNAseq using Illumina Hiseq sequencer. Results: Biostatistical analysis identified 113 genes that were altered by p11. 59 genes were up-regulated and 54 down-regulated. Overall design: 6 ventral striata from 3 ChAT bacTRAP mice   were pooled for one translating ribosome affinity purification sample. We used mice that were ChAT BacTRAP crossed with ChAT Cre and p11 fl/fl and littermates without Cre as controls.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE106389</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>30638901</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
