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Status |
Public on Jun 22, 2021 |
Title |
Wdr5 |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Expression profiling by high throughput sequencing
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Summary |
This SuperSeries is composed of the SubSeries listed below.
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Overall design |
Refer to individual Series
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Citation(s) |
- Li Q, Mao F, Zhou B, Huang Y et al. p53 Integrates Temporal WDR5 Inputs during Neuroectoderm and Mesoderm Differentiation of Mouse Embryonic Stem Cells. Cell Rep 2020 Jan 14;30(2):465-480.e6. PMID: 31940490
- Li Q, Huang Y, Xu J, Mao F et al. p53 inactivation unmasks histone methylation-independent WDR5 functions that drive self-renewal and differentiation of pluripotent stem cells. Stem Cell Reports 2021 Nov 9;16(11):2642-2658. PMID: 34715053
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Submission date |
Jun 21, 2021 |
Last update date |
Dec 02, 2021 |
Contact name |
Rajesh C Rao |
E-mail(s) |
rajeshr@umich.edu
|
Organization name |
University of Michigan
|
Street address |
1000 Wall Street
|
City |
Ann Arbor |
State/province |
Michigan |
ZIP/Postal code |
48105 |
Country |
USA |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
|
Samples (43)
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This SuperSeries is composed of the following SubSeries:
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GSE178551 |
Chromatin accessibility profiling of mouse embryonic stem cells and embryonic bodies using SFEBq differentiation methods upon Wdr5 and P53 deletion with or without WT or mutant hWDR5 rescue |
GSE178552 |
Genome profiling of WDR5 and H3K4me3 binding in mouse embryonic stem cells |
GSE178554 |
Genome profiling of MAX binding in mouse embryonic bodies using SFEBq differentiation methods |
GSE178555 |
Transcriptome of Wdr5 and (or) p53 double knockout ESCs and embryoid bodies |
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Relations |
BioProject |
PRJNA739648 |