<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE131263" accession="SRP198487">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP198487</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA543087</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE131263</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Next Generation Sequencing Analysis of Prenatal Chlorpyrifos Exposure embryonic kidneys</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Purpose: In order to study signaling pathway changes of prenatal chlorpyrifos exposure embryonic kidney development Methods: By using RNA-seq, we studied the transcriptome of E12.5, E14.5, E16.5 and E18.5 prenatal chlorpyrifos exposure embryonic kidneys and DMSO exposure (control) embryonic kidneys Results: We show that Notch signaling pathway and aquaporin family had high expression in chlorpyrifos exposure E18.5 kidney. The nephron progenitor markers had low expression in chlorpyrifos exposure embryonic kidneys Overall design: ICR mice aged 8 weeks were bred using timed matings, the pregnant mice were randomly divided into two groups. Chlorpyrifos (96% purity) was dissolved in dimethyl sulfoxide (DMSO), and CPF 5mg/kg was injected subcutaneously daily in CPF group during gestation day 7.5-11.5. The controls were injected with isovolumetric DMSO at the same time. We collected E12.5, E14.5, E16.5 and E18.5 mouse embryonic kidneys for RNA-seq of the two groups respectively.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE131263</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>32715474</ID>
        </XREF_LINK>
      </STUDY_LINK>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>33987351</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
