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Links from GEO DataSets

Items: 15

1.
Full record GDS5367

miR-542-3p overexpression effect on TP53 wild-type osteosarcoma cell line

Analysis of U2OS osteosarcoma cells overexpressing miR-542-3p. U2OS contains wild-type p53 tumor suppressor TP53. Results provide insight into the function of miR-542-3p and its role in regulating the expression and function of p53.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 protocol sets
Platform:
GPL10558
Series:
GSE47363
6 Samples
Download data
2.

The impact of miR-542-3p on gene expression profile in U2OS cells

(Submitter supplied) Analysis of gene expression change in U2OS cells expression synthetic miR-542-3p mimics.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5367
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE47363
ID:
200047363
3.

The Six1 oncoprotein represses translation of p53 via concomitant regulation of RPL26 and microRNA-27a

(Submitter supplied) TP53 is mutated in 50% of all cancers, and is often functionally compromised in cancers where it is not mutated. We demonstrate that the pro-tumorigenic/metastatic Six1 homeoprotein decreases p53 levels through a mechanism that does not involve the negative regulator of p53, MDM2. Instead, Six1 regulates p53 via a dual mechanism involving upregulation of microRNA-27a and downregulation of the ribosomal protein L26 (RPL26), a positive regulator of p53 translation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
5 related Platforms
377 Samples
Download data
Series
Accession:
GSE65677
ID:
200065677
4.

The Six1 oncoprotein represses translation of p53 via concomitant regulation of RPL26 and microRNA-27a

(Submitter supplied) TP53 is mutated in 50% of all cancers, and is often functionally compromised in cancers where it is not mutated. We demonstrate that the pro-tumorigenic/metastatic Six1 homeoprotein decreases p53 levels through a mechanism that does not involve the negative regulator of p53, MDM2. Instead, Six1 regulates p53 via a dual mechanism involving upregulation of microRNA-27a and downregulation of the ribosomal protein L26 (RPL26), a positive regulator of p53 translation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11537
6 Samples
Download data: CEL
Series
Accession:
GSE65200
ID:
200065200
5.

Comparison of miRNA expression in HT29-tsp53 cells cultured at the permissive and restrictive temperatures

(Submitter supplied) The p53 tumour suppressor is a transcription factor that can regulate the expression of numerous genes encoding either proteins or microRNAs (miRNAs). The predominant outcomes of a typical p53 response are the initiation of apoptotic cascades and the activation of cell cycle checkpoints. HT29-tsp53 cells express a temperature sensitive variant of p53 and in the absence of exogenous DNA damage, these cells preferentially undergo G1 phase cell cycle arrest at the permissive temperature that correlates with increased expression of the cyclin-dependent kinase inhibitor p21WAF1. more...
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
6 Samples
Download data: CEL
Series
Accession:
GSE76576
ID:
200076576
6.

Integrative genomic analysis in HCC samples

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL6801 GPL10558 GPL570
80 Samples
Download data: CEL, IDAT
Series
Accession:
GSE109361
ID:
200109361
7.

Integrative genomic analysis in HCC samples [SNP]

(Submitter supplied) We integrated the copy number data with gene expression data from the same HCC samples, and identified fifteen putative driver genes with recurrently genomic aberrations and their associated modules in HCC. We further confirmed empirically that three putative driver genes (MYH10, CEP104 and RRS1) play significant roles in tumor initiation and progression of HCC. Notably, we demonstrated that RRS1 regulates the MDM2-P53 pathway and promotes tumor progression by retaining RPL11 in the nucleolus in HCC. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL6801
62 Samples
Download data: CEL, TXT
Series
Accession:
GSE109360
ID:
200109360
8.

Integrative genomic analysis in HCC samples [RRS1]

(Submitter supplied) We integrated the copy number data with gene expression data from the same HCC samples, and identified fifteen putative driver genes with recurrently genomic aberrations and their associated modules in HCC. We further confirmed empirically that three putative driver genes (MYH10, CEP104 and RRS1) play significant roles in tumor initiation and progression of HCC. Notably, we demonstrated that RRS1 regulates the MDM2-P53 pathway and promotes tumor progression by retaining RPL11 in the nucleolus in HCC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: IDAT
Series
Accession:
GSE109359
ID:
200109359
9.

Integrative genomic analysis in HCC samples [MYH]

(Submitter supplied) We integrated the copy number data with gene expression data from the same HCC samples, and identified fifteen putative driver genes with recurrently genomic aberrations and their associated modules in HCC. We further confirmed empirically that three putative driver genes (MYH10, CEP104 and RRS1) play significant roles in tumor initiation and progression of HCC. Notably, we demonstrated that RRS1 regulates the MDM2-P53 pathway and promotes tumor progression by retaining RPL11 in the nucleolus in HCC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE109358
ID:
200109358
10.

Integrative genomic analysis in HCC samples [CEP104]

(Submitter supplied) We integrated the copy number data with gene expression data from the same HCC samples, and identified fifteen putative driver genes with recurrently genomic aberrations and their associated modules in HCC. We further confirmed empirically that three putative driver genes (MYH10, CEP104 and RRS1) play significant roles in tumor initiation and progression of HCC. Notably, we demonstrated that RRS1 regulates the MDM2-P53 pathway and promotes tumor progression by retaining RPL11 in the nucleolus in HCC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE109357
ID:
200109357
11.

Expression profiling of RBM38-knocked down and control MCF7 cells with and without doxorubicin treatment

(Submitter supplied) Gene expression analysis of MCF-7 cells transfected with a scramble or RBM38 siRNA and incubated with or without doxorubicin. The hypothesis tested in the present study was to assess the impact of RBM38 depletion on gene expression of normal growing and doxorubicin-stressed MCF-7 cells. Results provide information about doxorubicin and/or RBM38-responsive genes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
8 Samples
Download data: TXT
Series
Accession:
GSE32301
ID:
200032301
12.

RNA-seq for siRpl14+siDux/siRpl11

(Submitter supplied) Bulk RNA-seq were performed on E14 cells knockdown with siRNA; siRpl14+siDux; siRpl14+siRpl11
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
22 Samples
Download data: TXT
Series
Accession:
GSE185232
ID:
200185232
13.

RNA-seq for siRNA 48h

(Submitter supplied) Bulk RNA-seq were performed on E14 cells knockdown with siRNA
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
15 Samples
Download data: TXT
Series
Accession:
GSE179124
ID:
200179124
14.

E14 cells knockdown with siRNA or shRNA

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
12 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE167182
ID:
200167182
15.

ATAC-seq for E14 cells knockdown with siRNA or shRNA

(Submitter supplied) ATAC-seq was performed on cells E14 cells knockdown with siRNA or shRNA
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: BW
Series
Accession:
GSE167177
ID:
200167177
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Supplemental Content

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