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Items: 3

1.

Impaired attenuation of pluripotency enhancers at the onset of neural crest formation in ARID1B haploinsufficient Coffin-Siris patients

(Submitter supplied) De-novo ARID1B haploinsufficient mutations cause many developmental disorders characterized by neurological and craniofacial phenotypes, including Coffin-Siris Syndrome. ARID1B and its paralog ARID1A encode for mutually exclusive subunits of the BAF chromatin remodeler, yet their role in cell-fate determination is poorly understood. We discovered a novel neural crest configuration of the BAF complex (ARID1B-BAF), which includes ARID1B, SMARCA4, and eight additional subunits. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
73 Samples
Download data: BED, BW, TXT, XLSX
Series
Accession:
GSE169654
ID:
200169654

PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector

2.

Illumina NextSeq 500 (Homo sapiens)

Organism:
Homo sapiens
12606 Series
343788 Samples
Download data
Platform
Accession:
GPL18573
ID:
100018573

3.

CTRL_LINE2_iPSC_ARID1B

Organism:
Homo sapiens
Source name:
Control_Line_2 (GM23716 line)
Platform:
GPL18573
Series:
GSE169654
Download data: BW
Sample
Accession:
GSM5530975
ID:
305530975

SRA Run Selector

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db=gds|term=GSM5530975[Accession]|query=1|qty=2|blobid=MCID_67497c0986d4ad4f7f6357ff|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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