<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE261632" accession="SRP495308">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP495308</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA1088141</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE261632</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Mutant p53 dysregulates gene transcription in hematopoietic stem and progenitor cells [RNA-seq 1]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We found that p53 mutant hematopoietic stem and progenitor cells are resistant to iL-1? treatment through altering inflammatory response. Overall design: To determine the mechanism by which mutant p53 HSPCs are resistant to IL-1ß, we performed RNA-seq in wild type and mutant p53 LSKs treated with 10 ng/ml of IL-1ß or PBS in vitro.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE261632</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA1088138</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
