|
Status |
Public on Nov 08, 2023 |
Title |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms |
Organisms |
Mus musculus; synthetic construct |
Experiment type |
Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing Other
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
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Overall design |
Refer to individual Series
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|
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Citation(s) |
37963072 |
NIH grant(s) |
Grant ID |
Grant title |
Affiliation |
Name |
R01 EY012543 |
CRX AND ITS REGULATORY NETWORK IN RETINAL DEGENERATIONS |
WASHINGTON UNIVERSITY |
SHIMING CHEN |
R01 EY032136 |
Understanding and treating CRX-linked retinopathies |
WASHINGTON UNIVERSITY |
SHIMING CHEN |
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|
Submission date |
Jan 24, 2023 |
Last update date |
Dec 06, 2023 |
Contact name |
Shiming Chen |
E-mail(s) |
chenshiming@wustl.edu
|
Phone |
314-747-4351
|
Organization name |
Washington University in St Louis
|
Department |
Department of Ophthalmology & Visual Sciences
|
Lab |
Shiming Chen, Ph.D.
|
Street address |
517 South Euclid Avenue
|
City |
Saint Louis |
State/province |
Missouri |
ZIP/Postal code |
63110 |
Country |
USA |
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|
Platforms (2) |
GPL17769 |
Illumina MiSeq (synthetic construct) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
|
Samples (68)
|
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This SuperSeries is composed of the following SubSeries: |
GSE223439 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [RNA-seq] |
GSE223657 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [ChIP-seq] |
GSE223658 |
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [Spec-seq] |
|
Relations |
BioProject |
PRJNA927048 |