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Items: 4

1.

HIC2 represses BCL11A transcription to regulate hemoglobin switching during development (ChIP-Seq)

(Submitter supplied) The switch from fetal to adult hemoglobin production has been studied in great depth in part because of its relevance to the treatment of hemolobinopathies. Transcription factor BCL11A, which is essential for repression of the fetal beta-type globin (γ-globin) genes after birth, is largely controlled at the level of transcription but the mechanism of BCL11A developmental control is unknown. Here, using a CRISPR-Cas9 screen in human erythroblasts, we identify transcription factor HIC2 as a repressor of BCL11A transcription. more...
Organism:
Mus musculus; Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL30173 GPL30172
27 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE173584
ID:
200173584
2.

HIC2 represses BCL11A transcription to regulate hemoglobin switching during development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by array; Other
Platforms:
GPL30172 GPL30173
65 Samples
Download data: BED, BIGWIG, TSV
Series
Accession:
GSE173587
ID:
200173587
3.

NextSeq 2000 (Mus musculus)

Platform
Accession:
GPL30172
ID:
100030172
4.

ChIP-Seq G1E-ER4 cells hHIC2-OE HA ChIP-seq rep2

Organism:
Mus musculus
Source name:
G1E-ER4 cells
Platform:
GPL30172
Series:
GSE173584 GSE173587
Download data: BED, BIGWIG
Sample
Accession:
GSM5271229
ID:
305271229
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Supplemental Content

db=gds|term=GSM5271229[Accession]|query=1|qty=3|blobid=MCID_66e169ee3683c757ca4cbe6c|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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