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Links from GEO DataSets

Items: 20

1.

Expression data from lens epithelial cells (LECs) from Shumiya cataract rats (SCR) with or without cataract (Cat+ or Cat-)

(Submitter supplied) The Shumiya cataract rat (SCR) is a model for hereditary cataract. Two-third of these rats develop lens opacity within 10-11-weeks. Onset of cataract is attributed to the synergetic effect of lanosterol synthase (Lss) and farnesyl-diphosphate farnesyltransferase 1 (Fdft1) mutant alleles that lead to cholesterol deficiency in the lenses, which in turn adversely affects lens biology including the growth and differentiation of lens epithelial cells (LECs). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
2 Samples
Download data: CEL
Series
Accession:
GSE152616
ID:
200152616
2.

Glucocorticoid Induced Changes in Gene Expression in Human Lens Epithelial Cells

(Submitter supplied) Prolonged use of glucocorticoids can lead to the formation of a cataract, however the mechanism is not known. We recently reported the presence of the functional glucocorticoid receptor in immortalized cultured mammalian lens epithelial cells (Gupta & Wagner, Invest Ophthalmol Vis Sci 2003), but the short term biological effect of glucocorticoid action in lens epithelial cells is not known. This study seeks to examine glucocorticoid induced changes in global gene expression in LECs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1353
Platform:
GPL96
12 Samples
Download data
Series
Accession:
GSE3040
ID:
200003040
3.
Full record GDS1353

Glucocorticoid effect on lens epithelial cells: time course

Analysis of cultured immortalized lens epithelial cells (LEC) 4 and 16 hours after treatment with 1 uM dexamethasone, a glucocorticoid steroid hormone. Long-term glucocorticoid use can induce cataract formation. Results identify glucocorticoid targets and short-term effects of glucocorticoid on LECs
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 2 time sets
Platform:
GPL96
Series:
GSE3040
12 Samples
Download data
DataSet
Accession:
GDS1353
ID:
1353
4.

The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology

(Submitter supplied) Mutations of the RNA-granule component TDRD7 (OMIM: 611258) cause pediatric cataract in humans. Here, we applied an integrated approach to elucidate the molecular pathology of cataract in Tdrd7 targeted-knockout (Tdrd7-/-) mice. Tdrd7-/- animals precipitously develop lens fiber cell abnormalities early in life, suggesting a global-level breakdown/mis-regulation of key cellular processes. High-throughput RNA-sequencing followed by iSyTE-integrated bioinformatics-based analysis identified the molecular chaperone and cytoskeletal-modulator, HSPB1 (HSP27), among the high-priority down-regulated candidates in Tdrd7-/- lens. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE134384
ID:
200134384
5.

The influence of sex and age on the lens injury response

(Submitter supplied) The purpose of this study was to investigate/characterize age- and sex-dependent changes in transcriptomic profile in a mouse model of cataract surgery that mimics human cataract surgery. This surgery involves the removal of lens fiber cells (LFC) leaving behind the lens capsule and associated lens epithelial cells (LEC). The lens capsule and associated remnant LECs were harvested either following cataract surgery (0 hour) or 24 hours later. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
24 Samples
Download data: TXT, XLSX
Series
Accession:
GSE166619
ID:
200166619
6.

High-throughput transcriptomics of Celf1 conditional knockout lens identifies downstream networks linked to cataract pathology

(Submitter supplied) Celf1 germline or conditional deletion mouse mutants exhibit fully penetrant lens defects including cataract. To gain insight into gene expression changes underlying these lens defects Differential Gene Expression analysis was performed for lenses obtained from control and Celf1 conditional deletion mutant mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: CSV
Series
Accession:
GSE227293
ID:
200227293
7.

Celf1 and Postnatal Lens Microarray

(Submitter supplied) Celf1 germline or conditional deletion mouse mutants exhibit fully penetrant lens defects including cataract. To gain insight into gene expression changes underlying these lens defects, microarray comparison was performed for lenses obtained from control and Celf1 conditional deletion mutant mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
4 Samples
Download data: CSV
Series
Accession:
GSE225303
ID:
200225303
8.

Transcriptome profiling from Wild Type and Lss mutant (heterozygous and homozygous) lens at E14.5 reveals the potential pathways involved in cataract formation

(Submitter supplied) Congenital cataract is one of the leading causes of blindness in children worldwide. About one third of congenital cataracts are caused by genetic defects. Previous studies have identified LSS as a causal gene for congenital cataracts. However, its roles in lens development remains largely unknown. Here, we performed RNA-seq on the lens of WT and Lss mutant (heterozygous and homozygous )at E14.5, identified that cholesterol synthesis signaling pathways were significantly downregulated. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
9 Samples
Download data: TXT
Series
Accession:
GSE185143
ID:
200185143
9.

Microarray data of ICR lenses

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
19 Samples
Download data: CEL
Series
Accession:
GSE230323
ID:
200230323
10.

Microarray data from 4-, 8-, and 10-week-old ICR lenses

(Submitter supplied) Analysis of gene expression changes during cortical cataract progression in ICR.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
12 Samples
Download data: CEL
Series
Accession:
GSE230322
ID:
200230322
11.

Microarray data of ICR lenses at each week of age

(Submitter supplied) Analysis of gene expression changes during cataract progression.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
7 Samples
Download data: CEL
Series
Accession:
GSE230320
ID:
200230320
12.

Comparison of expression data of 2 & 4- months old CRYAAN101D versus CRYAAWT lenses

(Submitter supplied) To understand the global view of dysregulated genes and pathwyas in CRYAAN101D lenses, RNA sequencing of 2 & 4 months old CRYAAWT and CRYAAN101D lenses was carried out.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: XLSX
Series
Accession:
GSE57959
ID:
200057959
13.

Effect of Atm Inhibitor on Galactose-Induced Cataract in Rat Lens

(Submitter supplied) Analysis of gene expression changes in galactose-induced cataracts when an Atm inhibitors is added. A total of six samples were analyzed: a sample without induced turbidity (control), three samples in which turbidity was induced by galactose (galactose), and a sample with ATM inhibitor added (KU55933 or AZD0156).
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
6 Samples
Download data: CEL
Series
Accession:
GSE194074
ID:
200194074
14.

Microarray data of lenses with glutamate

(Submitter supplied) The addition of Glutamate to the lens induced by galactose eliminated the white clouding formed and showed a therapeutic effect. Genes regulated by Glutamate addition were identified by microarray analysis. A total of seven samples were used in this analysis: two samples without galactose (control), three samples with galactose (galactose) and two samples with Glutamate (Glutamate).
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
7 Samples
Download data: CEL
Series
Accession:
GSE227475
ID:
200227475
15.

Microarray data of lenses with 2ME2

(Submitter supplied) The addition of 2ME2 (HIF-1 inhibitor) to rat model of galactose-induced cataract decreased opacity and therapeutic effect. Genes regulated by 2ME2 addition were identified by microarray analysis. A total of 7 samples were analyzed: samples with no cataract (Control_Day4, Control_Day6), samples with cataract (Galactose-1, Galactose-2, Galactose-3), samples with decreased lens opacity (2ME2, 2ME2-2)
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
7 Samples
Download data: CEL
Series
Accession:
GSE240617
ID:
200240617
16.

Therapeutic Effect of Histone Acetyltransferase Inhibitors on Galactose-Induced Cataract in Rats

(Submitter supplied) We investigated the therapeutic effects of histone acetyltransferase (HAT) inhibitors on cataracts using an ex vivo model of galactose-induced cataracts in the rat lens.Among the tested HAT inhibitors, TH1834 was the only inhibitor that could completely reverse white opacities once formed in the lens. Combination treatment with C646/CPTH2 and CBP30/CPTH2 also had therapeutic effects. To identify the genes regulated by HAT inhibitors, we conducted microarray analysis of treated and untreated cataract samples.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
13 Samples
Download data: CEL
Series
Accession:
GSE186248
ID:
200186248
17.

Rat ex vivo cataract model using DNA damage inducer

(Submitter supplied) By adding MMS or Bleomycin, a DNA damage inducing agent, to the removed rat lens and culturing it, opacity was formed in the lens. To investigate genes whose expression fluctuates when DNA damage is inflicted and causes lens opacity, microarray analysis was performed.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17117
5 Samples
Download data: CEL
Series
Accession:
GSE194317
ID:
200194317
18.

Developmental timecourse of mouse ocular lens and whole embryo control

(Submitter supplied) Identification of genes involved in ocular birth defects remains a challenge. To facilitate the identification of genes associated with cataract, we developed iSyTE (integrated Systems Tool for Eye gene discovery; http://bioinformatics.udel.edu/Research/iSyTE). iSyTE contains microarray gene expression profiles of the mouse embryonic lens as it transitions from the stage of placode invagination to that of vesicle formation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS4452 GDS4453
Platform:
GPL1261
19 Samples
Download data: CEL
Series
Accession:
GSE32334
ID:
200032334
19.
Full record GDS4453

Wild type embryonic tooth germ tissue

Analysis of laser capture microdissected tooth germ tissue from ICR E13.5 embryos and matched whole embryo body (WB, without tooth germ) controls representing stages E11.5, E12.5, and E13.5. Results provide insight into molecular mechanisms underlying tooth development.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 development stage, 2 tissue sets
Platform:
GPL1261
Series:
GSE32334
6 Samples
Download data: CEL
20.
Full record GDS4452

Wild type embryonic lens development

Analysis of lens from ICR embryos at 3 key developmental stages in the transition from E10.5 lens placode invagination to E12.5 lens primary fiber cell differentiation and matched whole embryo body (WB, minus ocular tissue) controls. Results provide insight into molecular basis of lens development.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 development stage, 2 tissue sets
Platform:
GPL1261
Series:
GSE32334
13 Samples
Download data: CEL
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