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Items: 3

1.

The complex etiology of autism spectrum disorder due to missense mutations of CHD8

(Submitter supplied) CHD8 is an ATP-dependent chromatin-remodeling factor encoded by the most frequently mutated gene in individuals with autism spectrum disorder (ASD). Although many studies have examined the consequences of CHD8 haploinsufficiency in cells and mice, few have focused on missense mutations, the most common type of CHD8 alteration in ASD patients. We here characterized CHD8 missense mutations in ASD patients according to six prediction scores and experimentally examined the effects of such mutations on the biochemical activities of CHD8, neural differentiation of embryonic stem cells, and mouse behavior. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
70 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE227579
ID:
200227579
2.

Illumina NovaSeq 6000 (Mus musculus)

Platform
Accession:
GPL24247
ID:
100024247
3.

WT NPC RNA-seq replicate 2

Organism:
Mus musculus
Source name:
Neural progenitor cell
Platform:
GPL24247
Series:
GSE227579
Download data
Sample
Accession:
GSM7103364
ID:
307103364
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db=gds|term=GSM7103364[Accession]|query=1|qty=2|blobid=MCID_666d2b96909a3d46ada2c95c|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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