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Links from GEO DataSets

Items: 14

1.

ATAC sequencing of developing cone photoreceptors

(Submitter supplied) We determined the accessible genome of postmitotic cone photoreceptors in the central region of the mouse retina on postnatal days P3, P6, and P10. At eachtimepoint we isolated GFP-labeled cells from three different Chrnb4-GFP mice (biological triplicates) using fluorescence-activated cell sorting. We then acquired reads of regions of accessible DNA of the sorted cones using ATAC sequencing. Our data set contained 9 samples.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
9 Samples
Download data: BED, CSV
Series
Accession:
GSE97535
ID:
200097535
2.

RNA sequencing and ATAC sequencing of developing cone photoreceptors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
48 Samples
Download data
Series
Accession:
GSE97536
ID:
200097536
3.

RNA sequencing of developing cone photoreceptors

(Submitter supplied) We determined the transcriptomes of postmitotic cone photoreceptors in the central region of the mouse retina every day between birth (P0) and eye opening (P12). At each postnatal day we isolated GFP-labeled cells from three different Chrnb4-GFP mice (biological triplicates) using fluorescence-activated cell sorting. We then acquired the transcriptomes of the sorted cones using next generation RNA sequencing. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
39 Samples
Download data: CSV
Series
Accession:
GSE97534
ID:
200097534
4.

Differential expression of genes in Fezf2KO mouse retina and control retina

(Submitter supplied) To analyze roles of transcription factor Fezf2 in retinal development, knockout mouse of Fezf2 was generated, and gene expression pattern of Fezf2-KO retina and control retina was examined by RNA-seq.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE101700
ID:
200101700
5.

In vivo function of NR2E3 in establishing photoreceptor identity during mammalian retinal development

(Submitter supplied) Rod and cone photoreceptors in mammalian retina are generated from common pool(s) of neuroepithelial progenitors. NRL, CRX and NR2E3 are key transcriptional regulators that control photoreceptor differentiation. Mutations in NR2E3, a rod-specific orphan nuclear receptor, lead to loss of rods, increased density of S-cones, and supernormal S-cone-mediated vision in humans. To better understand its in vivo function, NR2E3 was expressed ectopically in the Nrl-/- retina, where post-mitotic precursors fated to be rods develop into functional S-cones similar to the human NR2E3 disease. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2455
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE5338
ID:
200005338
6.
Full record GDS2455

Photoreceptor-specific nuclear receptor NR2E3 ectopic expression effect on NRL null retinas

Analysis of 4 week-old neural retinal leucine zipper (NRL) null retinas expressing photoreceptor-specific nuclear receptor (NR2E3) from the cone-rod homeobox (CRX) promoter. NRL, NR2E3, and CRX control photoreceptor differentiation. Results provide insight into the molecular function of NR2E3.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 strain sets
Platform:
GPL1261
Series:
GSE5338
8 Samples
Download data: CEL
7.

Epigenomic Landscapes of Retinal Rods and Cones

(Submitter supplied) Both rod and cone photoreceptors are critical for mammalian vision yet they have important functional differences. In this study, we investigate patterns of DNA methylation and chromatin accessibility in mouse rods and cones. Unexpectedly, we find that a substantial fraction of hypo-methylated regions in the rod methylome are in inaccessible chromatin. These regions show marks of active regulatory regions earlier in neuronal development and could remain undermethylated in adult rods due to their highly compact chromatin. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL13112 GPL17021
33 Samples
Download data: BW, TAR, TXT
Series
Accession:
GSE72550
ID:
200072550
8.

Expression profiling of the developing and mature Nrl -/- mouse retina (Yoshida et al. 2004, HMG)

(Submitter supplied) The rod photoreceptor-specific neural retina leucine zipper protein Nrl is essential for rod differentiation and plays a critical role in regulating gene expression. In the mouse retina, rods account for 97% of the photoreceptors; however, in the absence of Nrl (Nrl-/-), no rods are present and a concomitant increase in cones is observed. Using mouse GeneChips (Affymetrix), we have generated expression profiles of the wild-type and Nrl-/- retina at three time-points representing distinct stages of photoreceptor differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2936
Platform:
GPL81
24 Samples
Download data: CEL
Series
Accession:
GSE8972
ID:
200008972
9.
Full record GDS2936

Neural retina leucine zipper deficiency effect on retinas: time course

Analysis of retinas of mutants lacking the rod photoreceptor-specific neural retina leucine zipper protein (Nrl), at up to 2 months of age. In the absence of Nrl, rods are missing and cones increase in number. Results provide insight into the differences between the two photoreceptor subtypes.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE8972
24 Samples
Download data: CEL
DataSet
Accession:
GDS2936
ID:
2936
10.

MiRNAs 182 and 183 are necessary to maintain adult cone photoreceptor outer segments and visual function

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL6246 GPL13112
42 Samples
Download data: CEL, TXT
Series
Accession:
GSE58501
ID:
200058501
11.

MicroRNA expression profile in mouse cone photoreceptors at P60 [miRNA-seq]

(Submitter supplied) The outer segments of cones serve as light detectors for daylight color vision, and their dysfunction leads to human blindness conditions. We show that the cone-specific disruption of DiGeorge Syndrome Critical Region Gene 8 (DGCR8) in adult mice led to the loss of miRNAs and the loss of outer segments, resulting in photoreceptors with significantly reduced light responses. Using next-generation sequencing of RNA from isolated wild type P60 cones, we determine the most highly expressed miRNAs as candidates for controlling outer segment maintenance. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE58500
ID:
200058500
12.

Expression data of wild type and C-DGCR8 KO cones at different timepoints [RNA-seq]

(Submitter supplied) We have analyzed gene expression in cone photoreceptors isolated from wild type and C-DGCR8 (DiGeorge Syndrome Critical Region Gene 8) KO mice at five different time points to get a mechanistic inside into the altered molecular pathways after microRNAs depletion.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
20 Samples
Download data: TXT
Series
Accession:
GSE58498
ID:
200058498
13.

Expression data of wild type and C-DGCR8 KO cones at different timepoints [array]

(Submitter supplied) We have analyzed gene expression in cone photoreceptors isolated from wild type and C-DGCR8 (DiGeorge Syndrome Critical Region Gene 8) KO mice at five different time points to get a mechanistic inside into the altered molecular pathways after microRNAs depletion.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
20 Samples
Download data: CEL
Series
Accession:
GSE58493
ID:
200058493
14.

Analysis of Wild Type and Top2b-/- Retinal Transcriptomes

(Submitter supplied) Purpose: Identify Top2b-dependent genes by comparing retinal transcriptome profiling (RNA-seq) Methods: Retinal mRNA profiles of neonatal (postnatal day 0 and 6) wild-type (WT) and Topoisomerase IIbeta (Top2b) conditional knockout (Top2b−/−, or cKO) mice were generated using the SOLiD System (Applied Biosystems). Data analysis was performed according to published protocols (Trapnell et al., 2012) with minor modifications. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10010
4 Samples
Download data: DIFF
Series
Accession:
GSE86187
ID:
200086187
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