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Items: 4

1.

Alterations in GRHL2-OVOL2-ZEB1 Axis and Aberrant Activation of Wnt Signaling Lead to Altered Gene Transcription in Posterior Polymorphous Corneal Dystrophy

(Submitter supplied) To investigate the molecular basis of posterior polymorphous corneal dystrophy (PPCD) by examining the transcriptome in an affected individuals with an OVOL2 promoter mutation c.307T>C (PPCD1).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
2 Samples
Download data: XLS
Series
Accession:
GSE126487
ID:
200126487
2.

Illumina HiSeq 3000 (Homo sapiens)

Platform
Accession:
GPL21290
ID:
100021290
3.

Control 223 (C7)

Organism:
Homo sapiens
Source name:
ex vivo corneal endothelium
Platform:
GPL21290
Series:
GSE126487
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Sample
Accession:
GSM3602449
ID:
303602449
4.

PPCD CDDL 91 (P7)

Organism:
Homo sapiens
Source name:
ex vivo corneal endothelium
Platform:
GPL21290
Series:
GSE126487
Download data
Sample
Accession:
GSM3602448
ID:
303602448
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Supplemental Content

db=gds|term=GSE126487[Accession]|query=1|qty=2|blobid=MCID_6102d8f9329f403f702cef90|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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