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Links from GEO DataSets

Items: 20

1.

MicroRNAs of the RPE are essential for RPE differentiation and photoreceptor maturation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; synthetic construct
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL10740 GPL14613
14 Samples
Download data: CEL
Series
Accession:
GSE69883
ID:
200069883
2.

MicroRNAs of the RPE are essential for RPE differentiation and photoreceptor maturation (microRNA)

(Submitter supplied) Dysfunction of the retinal pigmented epithelium (RPE) results in degeneration of photoreceptors and vision loss and is correlated with common blinding disorders in humans. Although many protein-coding genes are known to be expressed in RPEs and important for their development and maintenance, virtually nothing is known about the in vivo roles of non-protein coding transcripts in RPEs. The expression patterns of microRNAs (miRNAs) have been analyzed in a variety of ocular tissues, and few were implicated to play role in RPE based on studies in cell lines. more...
Organism:
synthetic construct; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL14613
7 Samples
Download data: CEL
Series
Accession:
GSE69882
ID:
200069882
3.

MicroRNAs of the RPE are essential for RPE differentiation and photoreceptor maturation (mRNA)

(Submitter supplied) Dysfunction of the retinal pigmented epithelium (RPE) results in degeneration of photoreceptors and vision loss and is correlated with common blinding disorders in humans. Although many protein-coding genes are known to be expressed in RPEs and important for their development and maintenance, virtually nothing is known about the in vivo roles of non-protein coding transcripts in RPEs. The expression patterns of microRNAs (miRNAs) have been analyzed in a variety of ocular tissues, and few were implicated to play role in RPE based on studies in cell lines. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10740
7 Samples
Download data: CEL
Series
Accession:
GSE69881
ID:
200069881
4.

Analysis of the global retinal transcriptome of rod photoreceptor-specific Dicer1 conditional knockout mice and control littermates

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL16173 GPL17021
12 Samples
Download data
Series
Accession:
GSE55393
ID:
200055393
5.

RNAseq analysis of the global retinal transcriptome of rod photoreceptor-specific Dicer1 conditional knockout mice and control littermates

(Submitter supplied) We report RNAseq analysis of the transcriptome of retinas from mature rod-specific Dicer1 cKO mice and control littermates lacking Cre expression in order to better understand changes in gene regulation that could lead to retinal degeneration in cKO mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16173
6 Samples
Download data: TXT
Series
Accession:
GSE55377
ID:
200055377
6.

small RNAseq analysis of the global retinal transcriptome of rod photoreceptor-specific Dicer1 conditional knockout mice and control littermates

(Submitter supplied) We report RNAseq analysis of the transcriptome of retinas from mature rod-specific Dicer1 cKO mice and control littermates lacking Cre expression in order to better understand changes in gene regulation that could lead to retinal degeneration in cKO mice.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TXT
Series
Accession:
GSE55376
ID:
200055376
7.

Genetic profiling of developing human embryonic stem cell derived Retinal pigmented epithelium

(Submitter supplied) Age-related macular degeneration is a progressive disease resulting in impaired central vision. Degeneration of the retinal pigmented epithelial (RPE) monolayer is associated with the progression of the disease. To date no treatment is able to stop this progression, however new cell replacement studies using human embryonic stem cells (hESC) to generate RPE show a promising prospective. To improve cell replacement strategies a better understanding about the development of RPE cells is necessary. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
12 Samples
Download data: TXT
Series
Accession:
GSE85907
ID:
200085907
8.

Conditional knockdown of DNA methyltransferase-1 (Dnmt1) reveals a key role of retinal pigment epithelium integrity in photoreceptor outer segment morphogenesis

(Submitter supplied) To explore the epigenetic contribution to retinal development, we generated conditional knockout alleles of DNA methytransferase-1 (Dnmt1) mediated by Rx-Cre in mice. The results demonstrate a unique function of DNMT1-mediated DNA methylation in controlling RPE apicobasal polarity and neural retina differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
32 Samples
Download data: CEL
Series
Accession:
GSE43951
ID:
200043951
9.

Appropriately Differentiated ARPE-19 Cells Regain a Native Phenotype and Similar Gene Expression Profile

(Submitter supplied) The retinal pigment epithelial (RPE) cell line ARPE-19 provides a widely-used alternative to native RPE. However, retention of the native RPE phenotype becomes problematic after multiple passages. We wished to determine if suitable culture conditions and differentiation could restore RPE-appropriate gene expression to ARPE-19. ARPE-19 cells at passages p9 to p12, grown in DMEM containing high glucose and pyruvate with 1% fetal bovine serum, were differentiated for up to 4 months. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
10.

Comparison of mouse and human retinal pigment epithelium gene expression profiles reveals interspecies similarities and differences

(Submitter supplied) To determine mouse retinal pigment epithelium (RPE) specific gene expression, we compared the gene expression profile of the RPE to the gene expression of its adjacent layers: the choroid (CH) and photoreceptors (PR). We collected the tissues using the meticulous laser dissection microscopy. Next, we performed RNA isolation, amplification, labeling and hybridization against 44k Agilent microarrays. Compared RPE gene expression with CH gene expression, and with PR gene expression
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10333
9 Samples
Download data: TXT
Series
Accession:
GSE66916
ID:
200066916
11.

MicroRNA expression from ARPE-19 cells: control and PDTC treated.

(Submitter supplied) The cultured cell line ARPE-19 is frequently employed in studies of rpe function. Here we have identified the microRNAs expressed in RPE cells in the presence and absence of PDTC (pyrrolidine dithiocarbamate), an antioxidant.
Organism:
Danio rerio; Caenorhabditis elegans; Homo sapiens; Mus musculus; Drosophila melanogaster; Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL10724
2 Samples
Download data: TXT
Series
Accession:
GSE23107
ID:
200023107
12.

Gene expression profiles of DKO172 cells expressing DICER1 wildtype or hotspot mutants

(Submitter supplied) DICER1 plays a critical role in microRNA (miRNA) biogenesis. Recurrent somatic “hotspot” mutations at four mental binding sites within the RNase IIIb domain of DICER1, were identified in ovarian sex cord-stromal tumors and have since been described in other pediatric tumors. In this study, we identified and characterized DICER1 hotspot mutations in endometrial cancers derived from The Cancer Genome Atlas (TCGA) and our local tumor bank. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
12 Samples
Download data: TXT
Series
Accession:
GSE65092
ID:
200065092
13.

DGCR8 is required for microRNA maturation

(Submitter supplied) To determine whether DGCR8 is required for maturation of all miRNAs, we performed miRNA microarray analysis. Using RNA from wild-type ES cells as our reference sample, we observed a global loss of miRNAs in DGCR8 knockout cells, but normal levels of expression in DGCR8 heterozygous cells. The similarity in expression levels between wild-type and heterozygous cells suggests that DGCR8 is not limiting in the maintenance of steady-state levels of miRNAs in ES cells. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL4690
9 Samples
Download data: GPR
Series
Accession:
GSE6586
ID:
200006586
14.

Gene expression profiles of ovarian Sertoli-Leydig cell tumors

(Submitter supplied) Analysis of the global gene expression in ovarian Sertoli-Leydig cell tumor samples with or without DICER1 RNase IIIb domain mutation
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14951
8 Samples
Download data: TXT
Series
Accession:
GSE71160
ID:
200071160
15.

Identification of miRNA signatures during the differentiation of hESCs into retinal pigment epithelial cells

(Submitter supplied) Retinal pigment epithelium (RPE) cells can be obtained through in vitro differentiation of both embryonic stem cell (ESC) and induced pluripotent stem cells (iPSC) for cell replacement therapy. We have previously identified 87 signature genes relevant to RPE cell differentiation and function through transcriptome analysis of both human ESC- and iPSC-derived RPE as well as normal fetal RPE. Here, we profiled miRNA expression through small RNA-seq in human ESCs and their RPE derivatives. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
10 Samples
Download data: TXT
Series
Accession:
GSE37686
ID:
200037686
16.

ChIP-seq analysis of SOX9 in hES-RPE cells

(Submitter supplied) SOX9 binding sites were profiled in RPE cells generated from human embryonic stem cells (hES-RPE)
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: BED
Series
Accession:
GSE114305
ID:
200114305
17.

Identification and characterization of FGF2-dependent mRNA:microRNA networks during lens fiber cell differentiation

(Submitter supplied) Background: FGF signaling controls numerous processes during cell lineage specification, organogenesis and terminal differentiation. In lens, FGF signaling was implicated as the key pathway that controls lens fiber cell differentiation, but little is known about its full range and spectrum of regulated genes. Results: Herein, we employed rat lens epithelial explant system and performed RNA and microRNA expression profiling in cells induced to differentiate by FGF2. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS5604
Platform:
GPL1355
10 Samples
Download data: CEL
Series
Accession:
GSE50604
ID:
200050604
18.
Full record GDS5604

Fibroblast growth factor 2 effect on lens epithelia explant cultures: time course

Analysis of lens explant cultures grown overnight in the presence of 5 ng/mL FGF2 to promote proliferation and survival, then treated with 100 ng/mL FGF2 for up to 24hr to induce differentiation. Results provide insight into the molecular basis of FGF2-induced lens fiber cell differentiation.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 growth protocol, 5 time sets
Platform:
GPL1355
Series:
GSE50604
10 Samples
Download data: CEL
19.

Gene Expression Profiling of Zebrafish Embryonic Retinal Pigment Epithelium in vivo.

(Submitter supplied) Eye development and photoreceptor maintenance requires the retinal pigment epithelium (RPE), a thin layer of cells that underlies the neural retina. Despite its importance, RPE development has not been studied by a genomic approach. A microarray expression profiling methodology was established in this study for studying RPE development. The intact retina with RPE attached was dissected from developing embryos, and differentially expressed genes in RPE were inferred by comparing the dissected tissues with retinas without RPE using microarray and statistical analyses. more...
Organism:
Danio rerio
Type:
Expression profiling by array
Dataset:
GDS2556
Platform:
GPL1319
6 Samples
Download data: CEL, DAT
Series
Accession:
GSE5048
ID:
200005048
20.
Full record GDS2556

Embryonic retinal pigment epithelium

Analysis of microdissected embryonic retinas with or without the retinal pigment epithelium (RPE). The RPE is a thin layer of cells that underlies the neural retina and supports the function and development of photoreceptors. Results provide insight into the development of the RPE.
Organism:
Danio rerio
Type:
Expression profiling by array, count, 2 tissue sets
Platform:
GPL1319
Series:
GSE5048
6 Samples
Download data: CEL, DAT
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