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Links from GEO DataSets

Items: 13

1.

RNA levels in wild-type and HIF1α-mutant MCF7 cells in normoxia (21% O2), and in hypoxia (1% O2) for 3 h or 24 h

(Submitter supplied) We report the generation of CRISPR/Cas9-engineered MCF7 human breast cancer cells that lack functional HIF1α. We show that the HIF1α-dependent transcriptional response to hypoxia is severely impaired in HIF1α-mutant MCF7 cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
18 Samples
Download data: TXT
2.

HIF1alpha drives early induction of pluripotency through reprogramming of glycolytic metabolism

(Submitter supplied) Gene expression analyis of two neonatal fibroblasts (BJ and HFF1), one adult dermal fibroblasts (NFH2), two BJ-derived human iPSCs (iB4 and iB5), two HFF1-derived iPSCs (iPS 2 and iPS4), four NFH2-derived iPSCs (OiPS3, OiPS6, OiPS8, OiPS16), one amniotic fluid cells and three derived iPSCs (lines 4, 5, 6, 10, and 41), two human ES cells (H1 and H9), neonatal fibroblasts transduced with the four retroviral factors (OKSM) after 24h, 48h, and 72h, neonatal fibroblasts treated with EDHB for 24h, 48h, and 72h, neonatal fibroblasts transduced with four factors and treated with EDHB for 24h, 48h, and 72h, neonatal fibroblasts knocked down for HIF1A (HIF1-KD) and for a scrambled sequence (SCR-KD)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
48 Samples
Download data: TXT
Series
Accession:
GSE37709
ID:
200037709
3.

Short-term hypoxia synergizes with interleukin 15 priming in driving glycolytic gene transcription and supports human natural killer cell activities.

(Submitter supplied) Natural killer (NK) cells induce apoptosis in infected and transformed cells and produce immunoregulatory cytokines. At this, NK cells operate in inflammatory and tumor environments low in oxygen (hypoxic) and with immunosuppressive properties. In vitro studies of NK cells are, however, commonly performed in ambient air (normoxia). We evaluated the immediate impact of short-term hypoxia on various intrinsic activities of resting and IL-15 primed NK cells and determined underlying transcriptional pathway regulations using a 2 × 2 factorial design. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
20 Samples
Download data: CEL
Series
Accession:
GSE70214
ID:
200070214
4.

HIF1a-dependent glycolytic pathway orchestrates a metabolic checkpoint for the differentiation of TH17 and Treg cells

(Submitter supplied) Upon antigen stimulation, the bioenergetic demands of T cells increase dramatically over the resting state. Although a role for the metabolic switch to glycolysis has been suggested to support increased anabolic activities and facilitate T cell growth and proliferation, whether cellular metabolism controls T cell lineage choices remains poorly understood. Here we report that the glycolytic pathway is actively regulated during the differentiation of inflammatory TH17 and Foxp3-expressing regulatory T cells (Treg), and controls cell fate determination. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
6 Samples
Download data: CEL
Series
Accession:
GSE29765
ID:
200029765
5.

SIRT3 opposes metabolic reprogramming of cancer cells through HIF1a destabilization

(Submitter supplied) Tumor cells exhibit aberrant metabolism characterized by high glycolysis even in the presence of oxygen. This metabolic reprogramming, known as the Warburg effect, provides tumor cells with the substrates and redox potential required for the generation of biomass. Here, we show that the mitochondrial NAD-dependent deacetylase SIRT3 is a crucial regulator of the Warburg effect. SIRT3 loss promotes a metabolic profile consistent with high glycolysis required for anabolic processes in vivo and in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4058
Platform:
GPL1261
10 Samples
Download data: CEL
Series
Accession:
GSE27309
ID:
200027309
6.
Full record GDS4058

SIRT3 knockout effect on brown adipose tissue

Analysis of brown adipose tissue of sirtuin SIRT3 knockout 129Sv males. SIRT3 is a crucial regulator of the Warburg effect, a metabolic reprogramming that provides tumor cells with the substrates required for biomass generation. Results provide insight into the role of SIRT3 in tumorigenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE27309
10 Samples
Download data: CEL
7.

Mitochondrial mutations in cigarette smoke extract-chronically treated human oral OKF6 cells

(Submitter supplied) The objective of this study was to analyze the mitochondrial mutations induced by chronic cigarette smoke extract treatment in human oral immortal OKF6 cells. The objective of this study was to analyze the mitochondrial mutations induced by chronic cigarette smoke extract treatment in human oral immortal OKF6 cells.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10983
2 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE24414
ID:
200024414
8.

RNA-sequencing data from PLC/PRF/5 cells with NC or USP22 knockdown (shUSP22) under hypoxic condition

(Submitter supplied) We use RNA-sequencing to evaluate the effect of USP22 knockdown on the gene changes in HCC cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
4 Samples
Download data: TXT
Series
Accession:
GSE133858
ID:
200133858
9.

Hypoxia and dimethyloxalylglycine (DMOG) downregulates tryptophan-2,3-dioxygenase (TDO2) expression in GBM cells

(Submitter supplied) The tryptophan degrading enzyme TDO2 is downregulated upon HIF1alpha stabilization by exposure to both hypoxia as well as chemical hypoxia mimetics such as DMOG in glioblastoma cell line A172.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
16 Samples
Download data: CEL, XLSX
Series
Accession:
GSE138535
ID:
200138535
10.

Interleukin-17 governs hypoxic adaptation of injured epithelium

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21103 GPL24247
20 Samples
Download data: H5, TAR
Series
Accession:
GSE166950
ID:
200166950
11.

Interleukin-17 governs hypoxic adaptation of injured epithelium [CITE-seq & single-cell RNA-seq]

(Submitter supplied) To define the composition of “first responder” lymphocytes that may engage in crosstalk with injured epithelium we profiled the lymphoytes from unwounded health skin and skin from different time points after wounding with CITE-seq and single-cell RNA-sequencing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
2 Samples
Download data: H5
Series
Accession:
GSE166949
ID:
200166949
12.

Interleukin-17 governs hypoxic adaptation of injured epithelium [spatial transcriptomics]

(Submitter supplied) To define the gene signature and spatial architecture of the skin after injury, we performed spatial transcriptomics from mouse unwounded and wounded skin.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
6 Samples
Download data: H5, TAR
Series
Accession:
GSE166948
ID:
200166948
13.

Interleukin-17 governs hypoxic adaptation of injured epithelium [bulk RNA-seq]

(Submitter supplied) RORgt deficency impaired wound re-epithelialization. We adopted low-input RNA-seq of purified wound epithelium to explore the underlying epithelial cell functional difference between wild type and RORgt deficient mice during wound healing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: CSV
Series
Accession:
GSE166946
ID:
200166946
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