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Status |
Public on Apr 03, 2019 |
Title |
RNA sequencing of WT and AICDA KO iPCS clones |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
We report AICDA facilitates naïve pluripotency of mouse iPSCs by suppressing FGF/ERK signaling. In the absence of AICDA iPSCs fail to achive naïve pluripotent state and display chracteristics of EpiSCs and are primed for differentiation.
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Overall design |
IPSC clones from WT and AICDA KO fibroblasts were reprogrammed using OSKM.
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Contributor(s) |
Kumar R, Evans T |
Citation(s) |
31021461 |
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Submission date |
Apr 02, 2019 |
Last update date |
Oct 08, 2019 |
Contact name |
Ritu Kumar |
E-mail(s) |
rik2002@med.cornell.edu
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Organization name |
Weill Cornell Medicine
|
Department |
Surgery
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Street address |
1300 York Avenue
|
City |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE129223 |
The Cytosine Deaminase AICDA Regulates FGF/ERK Signaling to Achieve the Naïve Pluripotent State During Reprogramming. |
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Relations |
BioProject |
PRJNA530409 |
SRA |
SRP190136 |