<?xml version="1.0" encoding="UTF-8"?>
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  <STUDY center_name="GEO" alias="GSE124005" accession="SRP173890">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP173890</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA510746</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE124005</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Genomic instability in the naturally and prematurely aged myocardium [RNA-Seq]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Our data demonstrate that genomic instability does not evidently contribute to naturally aging of the mouse heart and support the contention that the endogenous DNA repair machinery is remarkably active to maintain genomic integrity in cardiac cells throughout life. Overall design: Investigation of variants in RNAseq for four different accelerated aging mouse models as well as natural aging at 3 different time points, each with 4 replicates.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE124005</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34465617</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA510744</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
