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Links from GEO DataSets

Items: 20

1.
Full record GDS170

Tumor suppressor protein p53 gene dosage effects

Analysis of tumor suppressor protein p53 gene dosage effects in HCT116 colorectal carcinoma-derived cell lines p53 -/-, +/- and +/+ at 0 and 12 hours. Cells with different numbers of functional TP53 alleles can be distinguished by gene expression profile.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 strain, 2 time sets
Platform:
GPL80
Series:
GSE90
12 Samples
Download data
2.

Expression profiling by p53 status

(Submitter supplied) Human colorectal carcinoma-derived cell lines, p53 -/-, +/-, +/+ at 0 and 12 hrs after growth arrest. Keywords = p53, expression, colon cancer, CSPG2 Keywords: repeat sample
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS170
Platform:
GPL80
12 Samples
Download data
Series
Accession:
GSE90
ID:
200000090
3.

RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation [ChIP-Seq]

(Submitter supplied) Cellular response to ionizing radiation involves activation of the p53-dependent pathways and activation of the atypical NF-κB pathway. Mechanisms of the crosstalk between these two transcriptional networks include (co)regulation of common gene targets. Novel genes potentially (co)regulated by p53 and NF-κB were found using high-throughput genomics screening in human osteosarcoma U2-OS cells irradiated with a high dose (4 and 10 Gy). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18460
3 Samples
Download data: BED, TXT
Series
Accession:
GSE110800
ID:
200110800
4.

RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation [RNA-Seq]

(Submitter supplied) Cellular response to ionizing radiation involves activation of the p53-dependent pathways and activation of the atypical NF-?B pathway. Mechanisms of the crosstalk between these two transcriptional networks include (co)regulation of common gene targets. Novel genes potentially (co)regulated by p53 and NF-?B were found using high-throughput genomics screening in human osteosarcoma U2-OS cells irradiated with a high dose (4 and 10 Gy). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
9 Samples
Download data: TXT
5.

Pro-inflammatory cytokine and high doses of ionizing radiation have similar effects on the expression of NF-kappaB-dependent genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18460 GPL16791 GPL9115
63 Samples
Download data: BED, TXT
Series
Accession:
GSE110387
ID:
200110387
6.

Head and neck squamous cell carcinoma cell lines (HNSCC) compared with normal keratinocytes

(Submitter supplied) Gene expression profiles of human HNSCC lines were compared with human normal keratinocytes by 24K cDNA microarray. The ten HNSCC analyzed are derived by the University of Michigan (UM-SCC), representing late stage SCC of different anatomic sites. Principle component analysis and hierarchical gene clustering classified ten cancer cell lines into two subsets, and associated each of the subsets with a distinctive p53 status. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6569
14 Samples
Download data: GPR
Series
Accession:
GSE10774
ID:
200010774
7.

Identification of SULF2 as a novel transcriptional target of p53 by use of integrated genomic analyses.

(Submitter supplied) Microarray analysis has been useful for identifying the targets of many transcription factors. However, gene expression changes in response to transcription factor perturbation reveal both direct transcriptional targets and secondary gene regulation. By integrating RNA interference, gene expression profiling, and chromatin immunoprecipitation technologies, we identified a set of 32 direct transcriptional targets of the tumor suppressor p53. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL4372 GPL3991 GPL6793
31 Samples
Download data: CEL
Series
Accession:
GSE15440
ID:
200015440
8.

p53 status and AAI gene expression response

(Submitter supplied) Human colon carcinoma cells (HCT116) differing in TP53 status were exposed to aristolochic acid I (AAI) (50 and 100 uM for up to 48 h), and their gene expression responses compared by cDNA microarray technology. Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4348
36 Samples
Download data: GPR
Series
Accession:
GSE10359
ID:
200010359
9.

Multiplex enhancer-reporter assays uncover unsophisticated p53 enhancer logic

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL21311
26 Samples
Download data: BW, TXT
Series
Accession:
GSE76657
ID:
200076657
10.

Multiplex enhancer-reporter assays uncover unsophisticated p53 enhancer logic [RNA-seq]

(Submitter supplied) Analysis of p53 binding sites using multiplex enhancer reporter assays, ChIP-seq data and RNA-seq data. Transcription factors establish and maintain the specific transcriptome of a cell by binding to genomic regulatory regions, thereby regulating the transcription of their target genes. Like many transcription factors, the DNA sequence-specific binding preferences of p53 are known. However, it remains largely unclear what distinguishes functional enhancers from other bound genomic regions that have no regulatory activity. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: TXT
11.

Multiplex enhancer-reporter assays uncover unsophisticated p53 enhancer logic [ChIP-seq]

(Submitter supplied) Analysis of p53 binding sites using multiplex enhancer reporter assays, ChIP-seq data and RNA-seq data. Transcription factors establish and maintain the specific transcriptome of a cell by binding to genomic regulatory regions, thereby regulating the transcription of their target genes. Like many transcription factors, the DNA sequence-specific binding preferences of p53 are known. However, it remains largely unclear what distinguishes functional enhancers from other bound genomic regions that have no regulatory activity. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BW
Series
Accession:
GSE76655
ID:
200076655
12.

Multiplex enhancer-reporter assays uncover unsophisticated p53 enhancer logic [STARR-seq]

(Submitter supplied) Analysis of p53 binding sites using multiplex enhancer reporter assays, ChIP-seq data and RNA-seq data. Transcription factors establish and maintain the specific transcriptome of a cell by binding to genomic regulatory regions, thereby regulating the transcription of their target genes. Like many transcription factors, the DNA sequence-specific binding preferences of p53 are known. However, it remains largely unclear what distinguishes functional enhancers from other bound genomic regions that have no regulatory activity. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
10 Samples
Download data: TXT
13.

Multiplex enhancer-reporter assays uncover unsophisticated p53 enhancer logic [CHEQ-seq]

(Submitter supplied) Analysis of p53 binding sites using multiplex enhancer reporter assays, ChIP-seq data and RNA-seq data. Transcription factors establish and maintain the specific transcriptome of a cell by binding to genomic regulatory regions, thereby regulating the transcription of their target genes. Like many transcription factors, the DNA sequence-specific binding preferences of p53 are known. However, it remains largely unclear what distinguishes functional enhancers from other bound genomic regions that have no regulatory activity. more...
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL21311 GPL11154
12 Samples
Download data: TXT
Series
Accession:
GSE76653
ID:
200076653
14.

Response of p53 isogenic colorectal cancer panel to 12 Gy gamma irradiation

(Submitter supplied) Though targeted homologous recombination, we developed a panel of matched colorectal cancer cell lines that differ only with respect to their endogenous TP53 status. We then used these lines to define the genes whose expression was altered following DNA damage induced by ionizing radiation. Transcriptome analyses revealed a consistent upregulation of polo-like kinase I (PLK1) as well as other genes controlling the G2/M transition in the cells whose TP53 genes were inactivated compared to those with wild type (wt ) TP53 genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
13 Samples
Download data: TXT
Series
Accession:
GSE13886
ID:
200013886
15.

Mouse model of Osteosarcoma

(Submitter supplied) expression analysis from a genetically engineered mouse model of osteosarcoma determine the expression profile of mouse osteosarcoma Keywords: disease state analysis
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
26 Samples
Download data: CEL
Series
Accession:
GSE9460
ID:
200009460
16.

Profiling of p53-responsive genes in human breast cancer cells harboring endogenous ts-p53 E285K

(Submitter supplied) The ts-p53 E285K protein is a rare p53 mutant with temperature-sensitive (ts) loss of function characteristics. In cancer cells, which express ts-p53 E285K intriniscally, endogenous wild type p53 activity is reconstituted by appropriate cultivation temperature (permissive condition). At non-appropriate cultivation temperature (restrictive condition) this p53 mutant is inactive. The present study took advantage of this mechanism and employed IPH-926 lobular breast cancer cells and BT-474 ductal breast cancer cells, which both harbor endogenous ts-p53 E285K, for the transcriptional profiling of p53-responsive genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
18 Samples
Download data: CEL
Series
Accession:
GSE35006
ID:
200035006
17.

Gene Expression Profiles of Multiple Myeloma

(Submitter supplied) Samples in this series are pre-treatment bone marrow aspirates from multiple myeloma patients. Keywords = Multiple Myeloma, Bone Marrow, Pre-Treatment Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
559 Samples
Download data
Series
Accession:
GSE2658
ID:
200002658
18.

Hierarchy of mono- and bi-allelic TP53 alterations in Multiple Myeloma cell fitness

(Submitter supplied) Comparison of the TP53 wild-type myeloma cell line AMO1 with the CRISPR/Cas9 engineered AMO1 cell line named UMC901. UMC901 harbors bi-allelic alterations to TP53: TP53 del/mut. Analysis of impact of TP53 alterations on gene transcription and identification of affected pathways by transcriptome-wide differential gene expression analysis.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: CSV
Series
Accession:
GSE132340
ID:
200132340
19.

Expression data from CIC wild type and knockout cell lines

(Submitter supplied) Type I low-grade gliomas (LGGs), characterized by 1p/19q co-deletions and IDH1/2 mutations, show superior overall survival compared to other gliomas. Approximately 70% of cases harbour mutations in the Capicua (CIC) gene, whose product is a transcriptional repressor whose transcriptional network has yet to be extensively studied in human cells. To address this, we developed CIC knockout cell lines and used transcriptome analyses to study the consequences of CIC loss. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
6 Samples
Download data: CEL
Series
Accession:
GSE80359
ID:
200080359
20.

NCI cDNA microarray-human 60 cell lines

(Submitter supplied) We used cDNA microarrays to explore the variation in expression of approximately 8,000 unique genes among the 60 cell lines used in the National Cancer Institute's screen for anti-cancer drugs. Keywords: parallel sample
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1761
Platform:
GPL1290
64 Samples
Download data
Series
Accession:
GSE2003
ID:
200002003
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