<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE260517" accession="SRP492414">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP492414</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA1081921</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE260517</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Development of MAPT S305 mutation models exhibiting elevated 4R tau expression, resulting in altered neuronal and astrocytic function [bulkRNA-seq]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We have developed a panel of isogenic iPSC lines carrying MAPT splice-site mutations S305S, S305I or S305N, derived from four different donors. All three mutations significantly increased the proportion of 4R tau expression in iPSC-neurons and astrocytes, with up to 80% 4R transcripts in S305N neurons from as early as 4 weeks of differentiation. Overall design: We performed bulk RNA-sequencing on isogenic sets of MAPT S305 mutation iPSC-neurons at 4, 6 and 8 weeks of differentiation, as well as iPSC-astrocytes</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE260517</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA1171846</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
