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Items: 4

1.

Impaired CHD6 function links misregulation of autophagy and DNA damage response to premature ageing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
55 Samples
Download data: BED, BW, TDF, TXT
Series
Accession:
GSE161120
ID:
200161120
2.

Impaired CHD6 function links misregulation of autophagy and DNA damage response to premature ageing [RNA-Seq]

(Submitter supplied) Members of the Chromodomain-Helicase-DNA binding (CHD) protein family are chromatin remodelers critically implicated in human pathologies. CHD6 is the least studied member of this family, and we were motivated to dissect its in-cell roles by discovering a mutated CHD6 allele in a patient suffering from the rare Hallermann-Streiff premature aging syndrome (HSS). We generated isogenic iPSC lines carrying (or not) this single point mutation in the CHD6 SANT/SLIDE domain, which allow studying HSS-relevant cell identities. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
32 Samples
Download data: BW, TXT
3.

Illumina HiSeq 4000 (Homo sapiens)

Platform
Accession:
GPL20301
ID:
100020301
4.

S27

Organism:
Homo sapiens
Source name:
iPSCs_monoallelic mutant 1_control
Platform:
GPL20301
Series:
GSE135832 GSE161120
Download data: BW, TXT
Sample
Accession:
GSM4034929
ID:
304034929
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db=gds|term=GSM4034929[Accession]|query=1|qty=2|blobid=MCID_675b1c6d1fc51b7b012c284d|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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