<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE137412" accession="SRP221585">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP221585</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA565396</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE137412</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>RNA-Seq in LPS and Dex+LPS treated bone marrow-derived macrophages</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Wild-type bone marrow-derived macrophages (BMDMs) were treated with vehicle (0.1% EtOH/D-PBS), 6h 100 ng/ml lipopolysaccharide (LPS) or 16h 1uM dexamethasone (Dex) and 6h 100 ng/ml LPS (Dex+LPS) and mRNA expression analysed by RNA-Seq. Overall design: We profiled mRNA expression by RNA-Seq in BMDMs form wild-type C57BL/6 mice treated with either vehicle (0.1% EtOH) for 16h, 6h LPS (0.1% EtOH, 100ng/ml LPS) or 16h Dex+6h LPS (1 uM Dex, 100ng/ml LPS).Three biological replicates were sequenced per treatment.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE137412</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>33567280</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
