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Items: 6

1.

ChIP-seq analysis of H3K27ac in K562 cells with shRNA-mediated depeltion of TFAM expression

(Submitter supplied) The developing erythroid cells require highly coordinated gene expression and metabolism. By comparing the proteomic and transcriptomic changes in human hematopoietic stem/progenitor cells (HSPCs) and lineage-committed erythroid progenitors (ProEs), and uncover pathways related to mitochondrial biogenesis enhanced through post-transcriptional regulation. Two principal mitochondrial factors TFAM and PHB2 are tightly regulated at the protein level and indispensable for mitochondria and erythropoiesis. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: BED, WIG
Series
Accession:
GSE86864
ID:
200086864

PubMed Full text in PMC Similar studies SRA Run Selector

2.

Illumina NextSeq 500 (Homo sapiens)

Organism:
Homo sapiens
12044 Series
332532 Samples
Download data
Platform
Accession:
GPL18573
ID:
100018573

3.

Input_K562

Organism:
Homo sapiens
Source name:
Human K562 cells
Platform:
GPL18573
Series:
GSE86864 GSE86912
Download data: WIG
Sample
Accession:
GSM2309713
ID:
302309713

SRA Run Selector

4.

H3K27ac_K562_TFAM-sh2

Organism:
Homo sapiens
Source name:
Human K562 cells
Platform:
GPL18573
Series:
GSE86864 GSE86912
Download data: BED, WIG
Sample
Accession:
GSM2309712
ID:
302309712

SRA Run Selector

5.

H3K27ac_K562_TFAM-sh1

Organism:
Homo sapiens
Source name:
Human K562 cells
Platform:
GPL18573
Series:
GSE86864 GSE86912
Download data: BED, WIG
Sample
Accession:
GSM2309711
ID:
302309711

SRA Run Selector

6.

H3K27ac_K562_shNT

Organism:
Homo sapiens
Source name:
Human K562 cells
Platform:
GPL18573
Series:
GSE86864 GSE86912
Download data: BED, WIG
Sample
Accession:
GSM2309710
ID:
302309710

SRA Run Selector

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db=gds|term=GSE86864[Accession]|query=1|qty=2|blobid=MCID_666aca204f49d52cd289b4e6|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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