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Links from GEO DataSets

Items: 20

1.

Sensors, Pathways and Transcription factors regulating IR-induced inflammatory transcriptional output

(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:
GPL13112
266 Samples
Download data: BEDGRAPH
Series
Accession:
GSE100963
ID:
200100963
2.

Sensors, Pathways and Transcription factors regulating IR-induced inflammatory transcriptional output [RNA-seq data set 2]

(Submitter supplied) RNA-seq of mRNA from five stimulation time point (LipidA, 100ng/ml) of bone marrow-derived macrophages from C57Bl/6 mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
10 Samples
Download data: BEDGRAPH
Series
Accession:
GSE103903
ID:
200103903
3.

Sensors, Pathways and Transcription factors regulating IR-induced inflammatory transcriptional output [ChIP-seq]

(Submitter supplied) Radiation induced interferon response is mediated by IRF1 but not by the IRF3. Phosphorylated p53 binds strongly within 1kb of TTS of p53 dependent genes that are potently induced by ionizing radiation.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
15 Samples
Download data: BEDGRAPH
Series
Accession:
GSE100962
ID:
200100962
4.

Sensors, Pathways and Transcription factors regulating IR-induced inflammatory transcriptional output [RNA-seq data set 1]

(Submitter supplied) Bone marrow-derived macrophages derived from C57Bl/6, Myd88-/- and Trif-/-, Ifnar-/-, Atm-/-, Sting-/-, Scid, Irf3-/-, Irf1-/-, p53-/-, Nrf2-/-mice were irradiated with 6Gray ioninzing radiation; C57Bl/6 macrophages were Irradiated in the presence of MAPK inhibitors or Reactive Oxygen Species Scavenger (N-Acetyl Cysteine), Two biological replicates were generated for each time point. RNA samples were collected at 0 (unirradiated), 0.5, 1, 2, 6, and 24h post irradiation except where ever mentioned.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
241 Samples
Download data: BEDGRAPH
Series
Accession:
GSE100961
ID:
200100961
5.

Expression data from 5 human cell lines exposed to IR (5 Gy)

(Submitter supplied) The cellular response to DNA damage is vital for maintaining genomic stability and preventing undue cell death or cancer formation. The DNA damage response (DDR), most robustly mobilized by double-strand breaks (DSBs), rapidly activates an extensive signaling network that affects numerous cellular systems, leading to cell survival or programmed cell death. A major component of the DDR is the widespread modulation of gene expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
75 Samples
Download data: CEL, CHP
Series
Accession:
GSE30240
ID:
200030240
6.

Ionizing Radiation Induced Gene and micro RNA Expression Alterations in Human Peripheral Blood Mononuclear Cells

(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:
GPL16770 GPL14550
56 Samples
Download data: TXT
Series
Accession:
GSE55955
ID:
200055955
7.

Ionizing Radiation Induced micro RNA Expression Alterations in Human Peripheral Blood Mononuclear Cells

(Submitter supplied) Ionizing Radition is known to cause cell damage. Human peripheral blood mononuclear cells have long been used to study radiation induced gene expression profiling. Whithin this study we evaluated gene and microRNA expression alterations of human PBMC irradiated with 60 Gy g-ray. Cells were cultured for 2, 4 and 20h after irradiation before RNA was isolated and Agilent Human microRNA Microarrays was performed.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL16770
28 Samples
Download data: TXT
Series
Accession:
GSE55954
ID:
200055954
8.

Ionizing Radiation Induced Gene Expression Alterations in Human Peripheral Blood Mononuclear Cells

(Submitter supplied) Ionizing Radition is known to cause cell damage. Human peripheral blood mononuclear cells have long been used to study radiation induced gene expression profiling. Within this study we evaluated gene and microRNA expression alterations of human PBMC irradiated with 60 Gy g-ray. Cells were cultured for 2, 4 and 20h after irradiation before RNA was isolated and Agilent whole human GenomeOligo Microarray was performed.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14550
28 Samples
Download data: TXT
Series
Accession:
GSE55953
ID:
200055953
9.

ATR inhibition potentiates ionizing radiation-induced interferon response via cytosolic nucleic acid-sensing pathways

(Submitter supplied) Mechanistic understanding of how ionizing radiation induces type I interferon signaling and how to amplify this signaling module should help to maximize the efficacy of radiotherapy. In the current study, we report that inhibitors of the DNA damage response kinase ATR can significantly potentiate ionizing radiation-induced innate immune responses. Using a series of mammalian knockout cell lines, we demonstrate that, surprisingly, both the cGAS/STING-dependent DNA-sensing pathway and the MAVS-dependent RNA-sensing pathway are responsible for type I interferon signaling induced by ionizing radiation in the presence or absence of ATR inhibitors. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: XLSX
10.

Microarray analysis of gene expression in ATM-deficient MEFs

(Submitter supplied) The expression of interferon-related genes was more enhanced in irradiated ATM-deficient mouse embryonic fibroblasts (MEFs) than in irradiated ATM wild-type MEFs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
12 Samples
Download data: TXT
Series
Accession:
GSE23116
ID:
200023116
11.

IR-response in Atm-/- and control lymph nodes

(Submitter supplied) The DNA damage response network modulates a wide array of signaling pathways, including DNA repair, cell cycle checkpoints, apoptotic pathways and numerous stress signals. The ATM protein kinase, functionally missing in patients with the human genetic disorder ataxia-telangiectasia (A-T), is a master regulator of this network when the inducing DNA lesions are double strand breaks. The ATM gene is also frequently mutated in sporadic cancers of lymphoid origin. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1544
Platform:
GPL81
14 Samples
Download data: CEL
Series
Accession:
GSE2118
ID:
200002118
12.
Full record GDS1544

Ionizing radiation effect on lymphoid tissue of ATM protein kinase deficient mutants

Analysis of lymph nodes from ATM-deficient males exposed to ionizing radiation (IR). ATM regulates the cellular network induced by DNA double-strand breaks and is often mutated in lymphoid tumors. Results identify parallel induction of ATM-dependent pro- and antiapoptotic signals in response to IR.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 stress, 3 time sets
Platform:
GPL81
Series:
GSE2118
14 Samples
Download data: CEL
DataSet
Accession:
GDS1544
ID:
1544
13.

Role of NFBD1 in global gene expression

(Submitter supplied) NFBD1 (nuclear factor with BRCT domains 1), also known as MDC1 (mediator of DNA damage signaling 1), is a protein involved in the ATM signaling pathway in response to DNA damage. In addition to a role in signaling, NFBD1 possesses transactivation activity, suggesting that it may influence transcription. Furthermore, NFBD1 affects p53-mediated transcription in the presence of the DNA damaging agent adriamycin. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
30 Samples
Download data: TXT
Series
Accession:
GSE23010
ID:
200023010
14.

Identification of novel gene targets and functions of p21-activated kinase 1 during DNA damage by gene expression profiling

(Submitter supplied) The purpose of the study was to identify new PAK1 targets in response to ionizing radiation with putative role in the DNA damage response. We examined the effect of IR on the gene expression patterns in the murine embryonic fibroblasts with or without Pak1 using microarray.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
12 Samples
Download data: CEL
Series
Accession:
GSE47503
ID:
200047503
15.

MEK1/2 inhibitors unlock the constrained interferon response in macrophages through IRF1 signaling

(Submitter supplied) Analysis of bone-marrow derived macrophages (BMDMs) stimulated with single or combinatorial TLR agonist and MEK1/2 inhibitor in wild-type and Irf1-/- macrophages. Results provide insights into the versatile but yet uncharacterized roles of IRF1 in TLR-MEK1/2-ERK MAPK signaling.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL20775
10 Samples
Download data: CEL, XLSX
Series
Accession:
GSE123512
ID:
200123512
16.

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
17.

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
18.

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:
GPL16791 GPL9115 GPL18460
63 Samples
Download data: BED, TXT
Series
Accession:
GSE110387
ID:
200110387
19.

Primary macrophage response to L. monocytogenes and bacteria-derived ligands

(Submitter supplied) Transcriptional profiling of macrophages (of various genetic backgrounds) infected with L. monocytogenes or transfected with purified ligands Keywords: Timecourse, cell type comparison, bacteria strain comparison, drug comparison, ligand comparison.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5137
81 Samples
Download data: GPR
Series
Accession:
GSE8104
ID:
200008104
20.

WT macrophage response to transfected bacterial ligands

(Submitter supplied) Transcriptional profiling of WT macrophages transfected with L. monocytogenes genomic DNA, synthetic MDP, or both Keywords: Ligand comparison.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5137
8 Samples
Download data: GPR
Series
Accession:
GSE8103
ID:
200008103
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