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Links from GEO DataSets

Items: 9

1.

Improved DNA methylation analysis via enrichment of demethylated cells expressing an X-inactivated GFP transgene

(Submitter supplied) The demethylating drug 5-aza-2’-deoxycytidine (5-aza-2dC) is frequently used to investigate the effect of global DNA demethylation on gene expression in cultured mammalian cells. Here, we utilize a novel method that uses the reactivation of an X-inactivated GFP transgene as a marker to enrich for cells that have undergone drug-induced demethylation. By combining it with microarray gene expression profiling, we demonstrate the method’s utility in identifying genes activated by global DNA demethylation. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Methylation profiling by array
Platform:
GPL1261
6 Samples
Download data
Series
Accession:
GSE4718
ID:
200004718
2.

Gene expression changes following demethylation by 5-aza-2'-deoxycytidine in primary mouse dermal fibroblasts

(Submitter supplied) DNA methylation can contribute to the stable transcriptional silencing of mammalian genes. Oftentimes, these genes are important developmental regulators, and their silencing in cell types where they are not supposed to be active is important for the phenotypic stability of the cells. To identify key developmental regulator genes whose expression in terminally differentiated cells may be inhibited by DNA methylation, mouse dermal fibroblasts were demethylated with 5-aza-2’-deoxycytidine, and changes in gene expression monitored by microarray analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Methylation profiling by array
Dataset:
GDS2044
Platform:
GPL1261
6 Samples
Download data
Series
Accession:
GSE4696
ID:
200004696
3.

Changes in gene expression in dermal fibroblasts following exposure to Et1 peptide

(Submitter supplied) To determine if aberrant activation of endothelin-1 (Et1) could lead to the dysregulation of many downstream genes, we exposed fibroblasts to exogenous ET1 peptide and assayed for transcriptional changes by microarray. Mouse dermal fibroblasts were treated with exogenous Et1 peptide for 24 hours. ET1 treatment resulted in significant expression changes — primarily downregulation — of a number of genes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1980
Platform:
GPL1261
6 Samples
Download data: CEL, EXP
Series
Accession:
GSE4695
ID:
200004695
4.
Full record GDS2044

DNA demethylation effect on dermal fibroblasts

Analysis of primary dermal fibroblasts treated with the DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine (Aza-dC) for 96 hours. This study seeks to identify developmental regulator genes whose expression in terminally differentiated cells is inhibited by DNA methylation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL1261
Series:
GSE4696
6 Samples
Download data
DataSet
Accession:
GDS2044
ID:
2044
5.
Full record GDS1980

Endothelin-1 effect on dermal fibroblasts

Anlaysis of primary dermal fibroblasts treated with exogenous endothelin-1 (ET1) peptide for 24 hours. ET1 has been implicated in the pathogenesis of fibrotic and inflammatory diseases. Results suggest that stable silencing of Et1 is important for the phenotypic stability of dermal fibroblasts.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL1261
Series:
GSE4695
6 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1980
ID:
1980
6.

Dexamethasone-resistant multiple myeloma cell line OPM1 treated with Dexamethasone and/or DAC

(Submitter supplied) To identify genes responsible for the synergistic effect of DAC with Dex, we performed cDNA microarray analyses using cDNA prepared from Dex-resistant OPM1 cells treated with/without Dex, DAC or DAC+Dex.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE14261
ID:
200014261
7.

Epigenetics of gene expression in human hepatoma cells

(Submitter supplied) Expression profiling the response to inhibition of DNA methylation and histone deacetylation. Comparison of expression in HepG2 cells treated with 5-aza-dC, Trichostatin A, both, or none (control) to change methylation and acetylation status. Background:DNA methylation and histone deacetylation are epigenetic mechanisms that play major roles in eukaryotic gene regulation. We hypothesize that many genes in the human hepatoma cell line HepG2 are regulated by DNA methylation and histone deacetylation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2213
Platform:
GPL570
16 Samples
Download data
Series
Accession:
GSE5230
ID:
200005230
8.
Full record GDS2213

Hepatoma cell response to inhibition of DNA methylation and histone deacetylation

Analysis of HepG2 hepatoma cells following treatment with 5-aza-2'-deoxycytidine (5-aza-dC) to inhibit DNA methylation, or trichostatin A (TSA) to inhibit histone deacetylation, or both. Results identify epigentically regulated genes in hepatoma cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 agent sets
Platform:
GPL570
Series:
GSE5230
16 Samples
Download data
9.

Genes that are differentially expressed by 5AZA treatment and DNMT1 knockdown in intestinal tumor organoid

(Submitter supplied) Gene expression profiles after treatment with the DNA methylation inhibitor 5-Aza-CdR and DNMT1 knockdown were analyzed in tumor organoids derived from ApcMin mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5642
4 Samples
Download data: TXT
Series
Accession:
GSE72768
ID:
200072768
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