<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE104320" accession="SRP118980">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP118980</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA412362</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE104320</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>PP1-NIPP1 wild type and mutant overexpression in Flip-In™ T-Rex Hela cells</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>RNAi-seq of stable Flp-In™ T-Rex Hela cells that inducibly expressed PP1-NIPP1 and mutants. Overall design: Four cell types are investigated under two conditions in three independent experiments, resulting in 24 samples in total (i.e. 4x2x3). The four cell types are: (1) Flp-In™ T-Rex Hela cells with doxycycline-inducible EGFP transgene, (2) Flp-In™ T-Rex Hela cells with doxycycline-inducible EGFP-PP1-NIPP1 transgene, (3) Flp-In™ T-Rex Hela cells with doxycycline-inducible EGFP-PP1m-NIPP1 transgene (PP1 is mutated at Aa 64, i.e. D64A), (4) Flp-In™ T-Rex Hela cells with doxycycline-inducible EGFP-PP1-NIPP1m transgene (NIPP1 is mutated at the position AA 68-71, i.e. alanine mutation of NIPP1 residues 68-71). The two conditions are (1) not exposed to doxycycline, (2) treated with doxycycline. Three replicates are collected from three independent experiments.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE104320</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>29898919</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
