<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE249433" accession="SRP476421">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP476421</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA1049030</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE249433</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Single-nucleus transcriptomic highlights sex differences in cardiac molecular signaling and identifies a novel cardiomyocyte population associated with CCNA2-mediated cardiac regeneration</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Adult mammalian hearts lack regenerative potential and this is a significant contributing cause of the extensive morbidity and mortality of cardiovascular disease.  We performed single nucleus RNA sequencing (snRNA-seq) to capture of cell diversity and gender-specific changes as well as identification of critical differentially expressed genes in cellular clusters throughout the heart. Overall design: Adult hearts isolated from female and male normal wild-type (both nontransgenic-nTG and CCNA2 constitutively expressing-Transgenic-Tg) mice.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE249433</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
