This SuperSeries is composed of the SubSeries listed below.
Overall design: Refer to individual Series
| Accession | PRJNA517443; GEO: GSE125752 |
| Type | Umbrella project |
| Publications | Mzoughi S et al., "PRDM15 loss of function links NOTCH and WNT/PCP signaling to patterning defects in holoprosencephaly.", Sci Adv, 2020 Jan;6(2):eaax9852 |
| Submission | Registration date: 28-Jan-2019
Chromatin, Epigenetics & Differentiation, Institute of Molecular and Cell Biology |
| Relevance | Superseries |
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 34 |
| Publications |
| PubMed | 1 |
| PMC | 1 |
| Other datasets |
| BioSample | 34 |
| GEO DataSets | 5 |
PRDM15 loss-of-function causes brain malformations through defective embryonic anterior-posterior patterning encompasses the following 4 sub-projects:
| Project Type | Number of Projects |
| Epigenomics | 2 |
BioProject
accession | Organism | Title |
|---|
| PRJNA517445 | Mus musculus | Identification of PRDM15 cistrome in the mouse ESCs (Chromatin, Epigenetics &...) | | PRJNA517446 | Mus musculus | Identification of PRDM15 cistrome in the mouse embryo (6.5 d.p.c) (Chromatin, Epigenetics &...) |
|
| Transcriptome or Gene expression | 2 |
|