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Links from GEO DataSets

Items: 20

1.

Effects of Glucocorticoids in Epidermal Keratinocytes

(Submitter supplied) Glucocorticoids (GCs) have a long history of use as therapeutic agents for numerous skin diseases. Surprisingly, their specific molecular effects are largely unknown. To characterize GC action in epidermis, we compared the transcriptional profiles of primary human keratinocytes untreated and treated with dexamethasone (DEX) for 1, 4, 24, 48 and 72 hours using large-scale microarray analyses. The majority of genes were found regulated only after 24 hours and remained regulated throughout the treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5208
Platform:
GPL8300
20 Samples
Download data: CEL
Series
Accession:
GSE26487
ID:
200026487
2.
Full record GDS5208

Dexamethasone effect on epidermal keratinocytes in vitro: time course

Analysis of cultured epidermal keratinocytes treated with the synthetic glucocorticoid (GC) dexamethasone for up to 72 hours. GCs are used as therapeutic agents for skin conditions. Results provide insight into the molecular response of the epidermis to GCs.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 5 time sets
Platform:
GPL8300
Series:
GSE26487
20 Samples
Download data: CEL
DataSet
Accession:
GDS5208
ID:
5208
3.

Human epidermal keratinocytes treated with retinoic acid or thyroid hormone

(Submitter supplied) Targets of Retinoic Acid (RA) were identified in primary human epidermal keratinocytes grown in the presence or absence of all-trans retinoic acid for 1, 4, 24, 48 and 72 hours. Targets of Thyroid Hormone (T3) were identified in primary human epidermal keratinocytes grown in the presence or absence of the hormone; same controls as for RA.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE22298
ID:
200022298
4.

IL-1 treatment of human epidermal keratinocytes

(Submitter supplied) Interleukin-1 is a proinflammatory and immunomodulatory cytokine that plays a crucial role in inflammatory diseases of the skin, including bacterial infections, bullous diseases, UV damage and especially psoriasis. To characterize the molecular effects of IL-1 in epidermis, we defined the transcriptional changes in human epidermal keratinocytes 1, 4, 24, and 48 h after treatment with IL-1a. IL-1 significantly regulated 388 genes, including genes associated with proteolysis, adhesion, signal transduction, proliferation, and epidermal differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3011
Platform:
GPL571
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE9120
ID:
200009120
5.
Full record GDS3011

Interleukin-1 effect on epidermal keratinocytes: time course

Analysis of epidermal keratinocytes at various time points up to 48 hours post-interleukin-1 (IL-1) treatment. IL-1 is a proinflammatory and immunomodulatory cytokine that plays a role in inflammatory diseases of the skin. Results provide insight into gene products that mediate the effects of IL-1.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL571
Series:
GSE9120
8 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS3011
ID:
3011
6.

Epidermal keratinocytes and IFNg, TNFa and IL1 treatment

(Submitter supplied) Cultured epidermal keratinocyte controls used for IFNg, TNFa and IL1 treatment. Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1846
Platform:
GPL8300
9 Samples
Download data: CEL, EXP
Series
Accession:
GSE440
ID:
200000440
7.
Full record GDS1846

Interferon gamma effect on keratinocytes: time course

Analysis of keratinocytes treated with interferon gamma (IFN-gamma) for up to 48 hours. IFN-gamma is a multifunctional, immunomodulatory cytokine with cell type-specific antiviral activities. Results provide insight into molecular processes regulated by IFN-gamma in keratinocytes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL8300
Series:
GSE440
9 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1846
ID:
1846
8.

TNF & Parthenolide treatment of keratinocytes

(Submitter supplied) Cultured keratinocytes treated with TNFa in the presence or absence of NFkB inhibitor; time course 1, 4, 24 & 48 hrs. Keywords = Epidermis Keywords = skin Keywords = keratinocytes Keywords = inflammation Keywords = NFkB Keywords = TNFa Keywords: time-course
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1289
Platform:
GPL8300
16 Samples
Download data: CEL, EXP
Series
Accession:
GSE2489
ID:
200002489
9.
Full record GDS1289

TNFalpha effect on epidermal keratinocytes in the presence of NF-kappa B inhibitor: time course

Analysis of epidermal keratinocytes treated with TNFalpha in the presence of 10 uM parthenolide, an NF-kappa B inhibitor. Cells examined at various time points up to 48 hours following TNFalpha treatment. Results identify NF-kappa B-dependent subset of TNFalpha-regulated genes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 agent, 4 time sets
Platform:
GPL8300
Series:
GSE2489
16 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1289
ID:
1289
10.

Targets of Ephrin-A signaling in epidermal keratinocytes

(Submitter supplied) Both ephrins and their receptors are membrane bound, restricting their interactions to the sites of direct cell-to-cell interfaces. They are widely expressed, often co-expressed and regulate developmental processes, cell adhesion, motility, survival, proliferation, and differentiation. Both tumor suppressor and oncogene activities are ascribed to EFNs and Ephs in various contexts. A major conundrum regarding the EFN/Eph system concerns their large number and functional redundancy, given the promiscuous cross-activation of ligands and receptors and the overlapping intracellular signaling pathways. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
6 Samples
Download data: CEL
Series
Accession:
GSE26521
ID:
200026521
11.

Comparison of gene expression in AhR WT (+/+) and AhR KO (-/-) primary mouse keratinocytes

(Submitter supplied) The AhR is a ligand activated transcription factor that may be important in normal skin physiology. We compared gene expression profiles between AhR Wt and AhR KO primary mouse keratinocyte cultures. We identified 391 genes that were differentially expressed with a 1.5 fold cutoff and p<.05, and identified the AhR as an important regulator of genes involved in normal epidermal differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
7 Samples
Download data: CEL
Series
Accession:
GSE62490
ID:
200062490
12.

Microarray of Dexamethasone-treated primary chondrocytes identifies downstream targets of glucocorticoid signalling

(Submitter supplied) Background: Glucocorticoids (GCs) are widely used anti-inflammatory drugs. While useful in clinical practice, patients taking GCs often suffer from skeletal side effects including growth retardation and decreased bone quality in adults. On a physiological level, GCs have been implicated in the regulation of chondrogenesis and osteoblast differentiation, as well as maintaining homeostasis in cartilage and bone. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2802
Platform:
GPL1261
12 Samples
Download data: CEL, CHP, EXP
Series
Accession:
GSE7683
ID:
200007683
13.
Full record GDS2802

Dexamethasone effect on fetal chondrocytes in vitro: time course

Analysis of primary cultured fetal chondrocytes treated with pharmacological doses of dexamethasone (DEX) for 6 and 24 hours. DEX is a synthetic glucorticoid (GC) receptor agonist. Results provide insight into the effects of pharmacological GC on chondrocytes.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 2 time sets
Platform:
GPL1261
Series:
GSE7683
12 Samples
Download data: CEL, CHP, EXP
14.

ZNF750 in late keratinocyte differentiation

(Submitter supplied) Disrupted skin barrier due to altered keratinocyte differentiation is common in pathologic conditions such as atopic dermatitis, ichthyosis and psoriasis. However, the molecular cascades governing keratinocyte terminal differentiation are still poorly understood. We have previously demonstrated that a dominant mutation in ZNF750 leads to a clinical phenotype that reminiscent of psoriasis and seborrheic dermatitis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4599
Platform:
GPL6244
6 Samples
Download data: CEL
Series
Accession:
GSE38039
ID:
200038039
15.
Full record GDS4599

ZNF750 silencing effect on differentiated keratinocytes

Analysis of ZNF750-silenced HaCaT keratinocytes (KCs) at day 12 of calcium-induced differentiation. ZNF750 knockdown in HaCaT KCs leads to sustained cell proliferation and decreased apoptosis. Results provide insight into molecular mechanisms underlying keratinocyte terminal differentiation.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 protocol sets
Platform:
GPL6244
Series:
GSE38039
6 Samples
Download data: CEL
16.

Transcriptional signature of wounded keratinocytes reveals selective roles for ERK1/2, P38 and PI3K signalling pathways

(Submitter supplied) Covering denuded dermal surface after injury requires migration, proliferation and differentiation of skin keratinocytes. To clarify the major traits controlling these intermingled biological events, we surveyed the genomic modifications occurring during the course of a scratch closure of cultured human keratinocytes. Using a DNA microarray approach, we report the identification of 161 new markers of epidermal repair. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1521
36 Samples
Download data: TXT
Series
Accession:
GSE6820
ID:
200006820
17.

Expression of proinflammatory genes in epidermal keratinocytes is regulated by the hydration status.

(Submitter supplied) We hypothesized that treatment of the injured skin with occlusion limits TEWL and results in a phenotype of epithelial response that more closely resembles mucosa. Here we addressed whether different hydration conditions change gene expression patterns in epidermis using microarray study in rabbit partial-thickness incisional wound. Microarray on epidermis showed that global expression patterns of the genes in full occluded vs. more...
Organism:
Oryctolagus cuniculus
Type:
Expression profiling by array
Platform:
GPL11170
30 Samples
Download data: TXT
Series
Accession:
GSE42653
ID:
200042653
18.

SP600125 effect on keratinocytes

(Submitter supplied) In inflamed tissue, normal signal transduction pathways are altered by extracellular signals. For example, the JNK pathway is activated in psoriatic skin, which makes it an attractive target for treatment. To define comprehensively the JNK-regulated genes in human epidermal keratinocytes, we compared the transcriptional profiles of control and JNK inhibitor-treated keratinocytes, using DNA microarrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2081
Platform:
GPL8300
8 Samples
Download data
Series
Accession:
GSE4828
ID:
200004828
19.
Full record GDS2081

Jun kinase inhibition effect on keratinocytes: time course

Analysis of keratinocytes at various time points up to 48 hours following treatment with the Jun kinase (JNK) inhibitor SP600125. SP600125 is a reversible ATP-competitive inhibitor specific for the three isoforms of JNK. Results identify JNK-regulated genes in epidermal keratinocytes.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL8300
Series:
GSE4828
8 Samples
Download data
DataSet
Accession:
GDS2081
ID:
2081
20.

microRNA expression in human keratinocytes from infant, adult and ederly skin

(Submitter supplied) We want to identifiy microRNAs modulated by aging in human primary keratinocytes prepared from skin samples from individuals of various age
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL21572
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE101493
ID:
200101493
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