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Links from GEO DataSets

Items: 14

1.
Full record GDS2088

Transcription factor p63 inactivation effect on squamous cells (HG-U133 2.0)

Analysis of squamous cell lines following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 cell line, 2 cell type, 2 protocol sets
Platform:
GPL570
Series:
GSE4975
6 Samples
Download data
DataSet
Accession:
GDS2088
ID:
2088
2.

Expression data from p63 siRNA in squamous cell lines

(Submitter supplied) p63, a homologue of the tumor suppressor p53, is critical for the development and maintenance of squamous epithelia. p63 is specifically expressed in the basal layers of stratified epithelial tissues, and is considered to be a specific marker for cells of this type. The role of p63 in tumorigenesis remains poorly defined. Numerous studies have highlighted the oncogenic potential of the predominant p63 isoform, ΔNp63α; however, data suggests that other p63 proteins can act as tumor suppressors or alter the metastatic potential of tumors. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2086 GDS2087 GDS2088
Platforms:
GPL96 GPL97 GPL570
14 Samples
Download data
Series
Accession:
GSE4975
ID:
200004975
3.
Full record GDS2087

Transcription factor p63 inactivation effect on squamous cells (HG-U133B)

Analysis of squamous cells following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 cell line, 2 cell type, 2 protocol sets
Platform:
GPL97
Series:
GSE4975
4 Samples
Download data
DataSet
Accession:
GDS2087
ID:
2087
4.
Full record GDS2086

Transcription factor p63 inactivation effect on squamous cells (HG-U133A)

Analysis of squamous cells following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 cell line, 2 cell type, 2 protocol sets
Platform:
GPL96
Series:
GSE4975
4 Samples
Download data
DataSet
Accession:
GDS2086
ID:
2086
5.

Expression data from oral squamous cell carcinoma (OSCC)-derived cell lines and normal oral keratinocytes

(Submitter supplied) Oral squamous cell carcinoma (OSCC) is a lethal disease and early death usually occurs as a result of local invasion and regional lymph node metastases. We used microarrays to identify down or upregulated genes in OSCCs compared with non-malignant controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4560
Platforms:
GPL96 GPL570
11 Samples
Download data: CEL, CHP
Series
Accession:
GSE31853
ID:
200031853
6.
Full record GDS4560

Oral squamous cell carcinoma-derived cell lines

Analysis of oral squamous cell carcinoma (OSCC)-derived cell lines. OSCC is a lethal disease with early death typically occurring as a result of local invasion and regional lymph node metastases. Results provide insight the molecular mechanisms underlying OSCC.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 9 cell line sets
Platform:
GPL96
Series:
GSE31853
9 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS4560
ID:
4560
7.

TGFβ/mutant-p53 jointly controlled genes

(Submitter supplied) TGFβ ligands act as tumor suppressors in early stage tumors but are paradoxically diverted into potent prometastatic factors in advanced cancers. The molecular nature of this switch remains enigmatic. We now show that TGFβ-dependent cell migration, invasion and metastasis are empowered by mutant-p53. To investigate the specific gene expression program by which mutant-p53 and TGFβ control invasion and metastasis in breast cancer cells, we compared the TGFβ transcriptomic profile of control and mutant-p53 depleted MDA-MB-231 cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE14491
ID:
200014491
8.

Genes modulated by miR-205 in DU145 prostate cancer cells

(Submitter supplied) The study was aimed at identifying genes directly or indirectly regulated by miR-205 in the prostate. To this purpose, DU145 prostate cancer cells, which express miR-205 at very low levels, were transfected with miR-205 synthetic precursor and consequent alterations of gene expression analyzed using a microarray approach. Keywords: comparison betweed cells exposed to different miRNA precursors
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3634
Platform:
GPL6104
8 Samples
Download data: TXT
Series
Accession:
GSE11701
ID:
200011701
9.
Full record GDS3634

miR-205 expression effect on prostate cancer cell line

Analysis of DU145 prostate cancer cells with restored miR-205 expression. miR-205 expression is lower in prostate cancer cell lines than in normal cell lines, as well as in prostate tumors than in matched normal prostate tissues. Results provide insight into the role of miR-205 in prostate cancer.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL6104
Series:
GSE11701
8 Samples
Download data: TXT
DataSet
Accession:
GDS3634
ID:
3634
10.

Depletion of ZNF185 causes delay of keratinocyte differentiation

(Submitter supplied) Development of epidermis includes a complicated program of keratinocyte differentiation. Here we study a new membrane LIM-domain containing Zn-finger protein ZNF185 which is expressed in upper layers of human skin and is up-regulated during keratinocyte differentiation in vitro. Interestingly, depletion of ZNF185 causes delay of keratinocyte differentiation with decreased levels of FLG, LOR, LCEs expression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17077
8 Samples
Download data: TXT
Series
Accession:
GSE102613
ID:
200102613
11.

Cross-regulation between Notch and p63 in keratinocyte commitment to differentiation

(Submitter supplied) Notch signaling promotes commitment of keratinocytes to differentiation and suppresses tumorigenesis. p63, a p53 family member, has been implicated in establishment of the keratinocyte cell fate and/or maintenance of epithelial self-renewal. Here we show that p63 expression is suppressed by Notch1 activation in both mouse and human keratinocytes through a mechanism independent of cell cycle withdrawal and requiring down-modulation of selected interferon-responsive genes, including IRF7 and/or IRF3. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL571 GPL339
4 Samples
Download data
Series
Accession:
GSE5229
ID:
200005229
12.

Epigenetic regulation of iASPP-p63 feedback loop in cutaneous squamous cell carcinoma

(Submitter supplied) Keratinocyte skin cancer, comprising cutaneous squamous (cSCC) and basal cell carcinoma, is the most common malignancy in the UK. P53 is frequently mutated in cSCC. iASPP is a key inhibitor of p53 and NF-kB signalling pathways and has been documented as highly expressed in several types of human cancer. We have previously identified an autoregulatory feedback loop between iASPP and p63, which is critical in epidermal homeostasis. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19730
6 Samples
Download data: TXT
Series
Accession:
GSE123189
ID:
200123189
13.

ChIP-seq of p63 and RNA-seq of knockdown and overexpression of p63

(Submitter supplied) We performed ChIP-seq of p63 in ME-180 cell line and RNA-seq of knockdown and overexpression of p63
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
14.

Gene expression profiles induced by knockdown and overexpression of p63 variants in MCF-10A mammary epithelial cell line

(Submitter supplied) p63 is critical for epithelial development yet little is known about the transcriptional programmes it regulates. The p63 transactivating (TA) isoforms contain an amino-terminal exon that encodes a p53-like transactivation domain, whereas ΔN-isoforms lack this domain but contain the common DNA binding domain (DBD), suggesting that TAp63 and ΔNp63 isoforms may have opposing functions. By characterising transcriptional changes and cellular effects following modulation of p63 expression, we have defined a vital role for p63 in cellular adhesion. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
15 Samples
Download data: CEL
Series
Accession:
GSE20286
ID:
200020286
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