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Links from GEO DataSets

Items: 10

1.
Full record GDS5253

miR-24 overexpression effect on HepG2 liver cells

Analysis of HepG2 liver cells overexpressing miR-24. miR-24 is upregulated during the terminal differentiation of various types of cells. HepG2 cells have low endogenous miR-24 levels. Results identify target genes of miR-24.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL5104
Series:
GSE17828
4 Samples
Download data
2.

Control HepG2 vs miR-24 HepG2 cells

(Submitter supplied) miR-24 targets were identified in this study using mRNA microarrays. Combined with Bioinformatics, our results show that miR-24 regulates cell cycle and DNA repair.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5253
Platform:
GPL5104
4 Samples
Download data: TXT
Series
Accession:
GSE17828
ID:
200017828
3.

Response of quiescent human fibroblasts to miR-22 overexpression

(Submitter supplied) Quiescent human fibroblasts (2091) were transfected with 100nM mature miR-22 RNA duplexes. Cells were collected 24 hours after miR-22 transfection.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16359
4 Samples
Download data: GPR
Series
Accession:
GSE42788
ID:
200042788
4.

Mechanisms of terminal erythroid differentiation defect in EKLF-deficient mice

(Submitter supplied) EKLF is a Krüppel-like transcription factor identified as a transcriptional activator and chromatin modifier in erythroid cells. EKLF-deficient (Eklf -/-) mice die at day 14.5 of gestation from severe anemia. In this study, we demonstrate that early progenitor cells fail to undergo terminal erythroid differention in Eklf -/- embryos. To discover potential EKLF target genes responsible for the failure of erythropoiesis, transcriptional profiling was performed with RNA from wild type and Eklf -/- early erythroid progenitor cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE36618
ID:
200036618
5.

ChIP-chip from lymph node-derived primary lymphocytes with anti-E2F2 and anti-SV40TAg

(Submitter supplied) E2F2 is essential for the maintenance of T lymphocyte quiescence. To identify the full set of E2F2 target genes, and to gain further understanding of the role of E2F2 in transcriptional regulation, we have performed ChIP-chip analyses across the genome of lymph node-derived T lymphocytes. Here we show that during quiescence, E2F2 binds the promoters of a large number of genes involved in DNA metabolism and cell cycle regulation, concomitant with their transcriptional silencing.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL18145
6 Samples
Download data: GFF, PAIR, TXT
Series
Accession:
GSE53888
ID:
200053888
6.

Gene expression microarray during Human NK cell development; 1-, 7- and 14-day cultured cells after differentiation induction

(Submitter supplied) To identify differentially expressed genes during human NK cell development, we performed mRNA arrays analysis by using total RNA isolated from 1-, 7- or 14-day cultured cells after the addition of medium supplemented with IL-15 in HSCs isolated from human umbilical cord blood (UCB).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
2 Samples
Download data: TXT
Series
Accession:
GSE47521
ID:
200047521
7.

A microRNA network regulates proliferative timing and extracellular matrix synthesis during cellular quiescence in fibroblasts

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL8227 GPL6480
22 Samples
Download data: TXT
Series
Accession:
GSE42614
ID:
200042614
8.

A microRNA network regulates proliferative timing and extracellular matrix synthesis during cellular quiescence in fibroblasts [mRNA]

(Submitter supplied) Background: Although quiescence—reversible cell-cycle arrest—is a key part in the life history and fate of many mammalian cell types, the mechanisms of gene regulation in quiescent cells are poorly understood. We sought to clarify the role of microRNAs as regulators of the cellular functions of quiescent human fibroblasts. Results: Using microarrays, we discovered that the expression of the majority of profiled microRNAs differed between proliferating and quiescent fibroblasts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
4 Samples
Download data: TXT
Series
Accession:
GSE42613
ID:
200042613
9.

A microRNA network regulates proliferative timing and extracellular matrix synthesis during cellular quiescence in fibroblasts [miRNA]

(Submitter supplied) Background: Although quiescence—reversible cell-cycle arrest—is a key part in the life history and fate of many mammalian cell types, the mechanisms of gene regulation in quiescent cells are poorly understood. We sought to clarify the role of microRNAs as regulators of the cellular functions of quiescent human fibroblasts. Results: Using microarrays, we discovered that the expression of the majority of profiled microRNAs differed between proliferating and quiescent fibroblasts. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8227
18 Samples
Download data: TXT
Series
Accession:
GSE42593
ID:
200042593
10.

The 3’-UTR of MYC couples RNA polymerase II function to ribonucleotide levels

(Submitter supplied) Deregulated expression of MYC enhances glutamine utilization and renders cell survival dependent on an external supply of glutamine, an observation termed “glutamine addiction”. Surprisingly, human colon cancer cells, which express high levels of MYC due to mutations in the WNT pathway, are not glutamine-addicted but undergo a reversible cell cycle arrest upon glutamine deprivation. We show here that glutamine deprivation suppresses endogenous MYC expression via the 3’-UTR of the MYC mRNA, enabling escape from apoptosis. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
9 Samples
Download data: BEDGRAPH
Series
Accession:
GSE86556
ID:
200086556
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