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Links from GEO DataSets

Items: 20

1.

TNFa and LTB stimulated UM-SCC 46 gene expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18387
12 Samples
Download data: IDAT
Series
Accession:
GSE126905
ID:
200126905
2.

TNFα and LTβ stimulated UM-SCC 46 gene expression [TNF]

(Submitter supplied) To investigate the regulatory mechanisms and targets of the activation of NF-kB and inflammatory pathways, we treated HPV(-) head and neck cancer line UM-SCC 46 cells with TNFα and LTβ at different time points, and compared the gene expression by microarray. TNFα uniquely induced 172 genes, LTβ specifically induced 202 genes, while 155 genes were induced by both ligands. Total RNA samples were isolated from UM-SCC 46 cells after TNFα or LTβ treatment at different time points, and the gene expression were compared with untreated cell controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18387
6 Samples
Download data: IDAT, XLSX
Series
Accession:
GSE126904
ID:
200126904
3.

TNFα and LTβ stimulated UM-SCC 46 gene expression [LTB]

(Submitter supplied) To investigate the regulatory mechanisms and targets of the activation of NF-kappaB and inflammatory pathways, we treated HPV(-) head and neck cancer line UM-SCC 46 cells with TNFα and LTβ at different time points, and compared the gene expression by microarray. TNFα uniquely induced 172 genes, LTβ specifically induced 202 genes, while 155 genes were induced by both ligands. Total RNA samples were isolated from UM-SCC 46 cells after TNFα or LTβ treatment at different time points, and the gene expression were compared with untreated cell controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18387
6 Samples
Download data: IDAT, XLSX
Series
Accession:
GSE126903
ID:
200126903
4.

CDK12 mediated transcriptional regulation in U2OS cells

(Submitter supplied) While activation of canonical NF-κB signaling through the IKK complex is well studied, few regulators of NIK-dependent non-canonical p52 nuclear translocation have been identified. We discovered a novel role for cyclin dependent kinase 12 (CDK12) in transcriptionally regulating the non-canonical NF-κB pathway. High-content phenotypic screening identified a novel compound, 919278, which inhibits lymphotoxin β receptor (LTβR)- and FN14-dependent p52 nuclear translocation, but not TNFα receptor (TNFR)-mediated, canonical NF-κB p65 nuclear translocation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
56 Samples
Download data: TXT
Series
Accession:
GSE113926
ID:
200113926
5.

RelA and RelB-dependent transcriptome analysis in lymphotoxin-ß receptor stimulated mouse embryonic fibroblasts

(Submitter supplied) Background: Lymphotoxin signaling via the lymphotoxin-β receptor (LTβR) has been implicated in several biological processes, ranging from development of secondary lymphoid organs, maintenance of splenic tissue, host defense against pathogens, autoimmunity, and lipid homeostasis. The major transcription factor that is activated by LTβR crosslinking is NF-κB. Two signaling pathways have been described that result in the activation of classical p50-RelA and alternative p52-RelB NF-κB heterodimers. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5979
18 Samples
Download data: TXT
Series
Accession:
GSE11963
ID:
200011963
6.

Murine hepatocellular carcinoma of AlbLTa/b transgenic mice and age matched C57BL/6 mice - 18 months old.

(Submitter supplied) aCGH analysis of murine transgenic liver tissues affected with HCC, hybridized with age (18 months) and sex matched C57BL/6 mice. Moreover, 18months old C57BL/6 livers were hybridized with independent 18 months old C57BL/6 livers for control. Keywords: Array comparative genomic hybridization analysis (aCGH).
Organism:
Mus musculus
Type:
Genome variation profiling by array
Platform:
GPL8086
12 Samples
Download data: TXT
Series
Accession:
GSE14467
ID:
200014467
7.

Laser Capture Microdissection of Hyperlipidemic Mouse Aorta Atherosclerosis

(Submitter supplied) Atherosclerosis is a transmural chronic inflammatory condition of small and large arteries that is associated with adaptive immune responses at all disease stages. However, impacts of adaptive immune reactions on clinically apparent atherosclerosis such as intima lesion (plaque) rupture, thrombosis, myocardial infarction, and aneurysm largely remain to be identified. It is increasingly recognized that leukocyte infiltrates in plaque, media, and adventitia are distinct but their specific roles have not been defined. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8321
19 Samples
Download data: CEL
Series
Accession:
GSE21419
ID:
200021419
8.

Mouse aorta smooth muscle cells differentiate into lymphoid tissue organizers upon combined TNFR1/LTBR NF-kB signaling

(Submitter supplied) Cultured mouse aorta endothelial cells (from 8-12 weeks old C57BL/6J mice, passage 2-3) were exposed to phosphate buffered saline (control) or a combination of TNFalpha plus agonistic alpha-LTßR antibody for 24 hours as described in Lötzer et al. 2009. Arterioscler. Thromb. Vasc. Biol., in press. Total RNA was extracted and microarrays were prepared.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3810
Platform:
GPL1261
5 Samples
Download data: CEL
Series
Accession:
GSE19139
ID:
200019139
9.

Mouse aorta smooth muscle cells differentiate into lymphoid tissue organizers upon combined TNFR1/LTBR NF-kB signaling

(Submitter supplied) Mouse aorta smooth muscle cells (SMCs) express TNF receptor superfamily member 1A (TNFR1) and lymphotoxin ß receptor (LTßR). Circumstantial evidence has linked the SMC LTßR to tertiary lymphoid organogenesis in diseased aortae of hyperlipidemic mice. Here, we explored potential roles of TNFR1 and LTßR activation in cultured SMCs. TNFR1 signaling by TNF activated the classical RelA NF-κB pathway, whereas LTßR signaling by agonistic anti LTßR antibody activated both the classical RelA and alternative RelB NF-κB pathways. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3809
Platform:
GPL1261
21 Samples
Download data: CEL
Series
Accession:
GSE15062
ID:
200015062
10.
Full record GDS3810

TNF receptor and lymphotoxin beta -receptor activation effect on aortic endothelial cells in vitro

Analysis of cultured aortic endothelial cells stimulated with a combination of tumor necrosis factor (TNF) and α-LTßR antibody for 24 hours. Unlike similarly-treated aortic smooth muscle cells (SMCs), the endothelial cells did not differentiate into a lymphoid tissue organizer (LTO) phenotype.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL1261
Series:
GSE19139
5 Samples
Download data: CEL
11.
Full record GDS3809

TNF receptor and lymphotoxin beta -receptor activation effect on aortic smooth muscle cells in vitro: time course

Analysis of cultured aortic smooth muscle cells (SMCs) stimulated with a combination of tumor necrosis factor (TNF) and α-LTβR monoclonal antibody for up to 24 hours. SMCs stimulated by TNF/α-LTβR mAb, but not with either agent alone, differentiate into lymphoid tissue organizer (LTO)-like cells
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 agent, 3 time sets
Platform:
GPL1261
Series:
GSE15062
21 Samples
Download data: CEL
12.

The NF-kB genomic landscape in lymphoblastoid B-cells

(Submitter supplied) The nuclear factor kB (NF-kB) subunits RelA, RelB, c-Rel, p50 and p52 are each critical for B-cell development and function. To systematically characterize their responses to canonical and non-canonical NF-kB pathways activity, we performed ChIP-seq analysis in lymphoblastoid B-cells. We found a surprisingly complex NF-kB binding landscape, which did not readily reflect the two NF-kB pathway paradigm. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
10 Samples
Download data: TDF
Series
Accession:
GSE55105
ID:
200055105
13.

Ectodysplasin regulates the lymphotoxin-beta pathway for hair differentiation

(Submitter supplied) To find developmental stage specific genes controled by EDA Keywords: development or differentiation design,genetic modification design
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL2551 GPL2550
36 Samples
Download data: TIFF, TXT
Series
Accession:
GSE6952
ID:
200006952
14.

p100 deficiency alone is insufficient for full activation of the alternative NF-κB pathway: TNF signaling cooperates with p52-RelB activation in the transcriptional regulation of the enpp2/autotaxin promoter

(Submitter supplied) Background: Constitutive activation of the alternative NF-κB pathway leads to marginal zone B cell expansion and disorganized spleen microarchitecture. Furthermore, uncontrolled alternative NF-κB signaling results in the development and progression of cancer. We aimed here to learn about the mechanisms how does the constitutively active alternative NF-κB pathway exert its effects in these malignant processes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8063
10 Samples
Download data: TXT
Series
Accession:
GSE30317
ID:
200030317
15.

A NIK-SIX signaling axis controls inflammation by targeted silencing of noncanonical NF-κB

(Submitter supplied) The non-canonical NF-κB signaling cascade is essential for lymphoid organogenesis, B-cell maturation, osteoclast differentiation, and inflammation in mammals, whereas dysfunction of this system is associated with human diseases, including immunological disorders and cancer. While controlled expression of NF-κB Inducing Kinase (NIK) is the rate-limiting step in non-canonical NF-κB activation, mechanisms of inhibition remain largely unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
20 Samples
Download data: FPKM_TRACKING, TXT
16.

Type 3 innate lymphoid cells direct goblet cell differentiation via the LT-LTβR pathway during Listeria infection

(Submitter supplied) As a specialized subset of intestinal epithelial cells (IECs), goblet cells (GCs) play an important role during the antibacterial response via mucin production. However, the regulatory mechanisms involved in GC differentiation and function during infection, particularly the role of immune cell-IEC crosstalk, remain largely unknown. Here, using VillinΔLtbr conditional knockout mice, we demonstrate that LTβR, expressed on IECs, is required for GC hyperplasia and mucin 2 (MUC2) expression during Listeria infection for host defense but not homeostatic maintenance in the naïve state. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
5 Samples
Download data: CSV
Series
Accession:
GSE150071
ID:
200150071
17.

RNA-seq Analysis of Transcriptomes in β-Gal-overexpressing, NIK-overexpressing, and NIK(KA)-overexpressing αTC1-6 cells

(Submitter supplied) Purpose: The goal of this study is to determine the molecular mechanisms involved in the NIK regulation of α cell function. Methods: mRNA profiles of β-Gal control, NIK, and NIK(KA) overexpressed αTC1-6 cells were generated by deep sequencing using an Illumina Hiseq platform. Paired-end clean reads were aligned to the mouse reference genome(Ensemble_GRCm38.89) with TopHat (version 2.0.12), and the aligned reads were used to quantify mRNA expression by using HTSeq-count (version 0.6.1). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
3 Samples
Download data: XLSX
Series
Accession:
GSE112511
ID:
200112511
18.

RNA-seq of NIK Kockdown and control cells in lung metastatic human breast cancer cells established from MDA-MB-231 by orthotopic xenograft model

(Submitter supplied) Orthotopic xenograft (OX) model can mimics early process of spontaneous metastasis comparing than intra-cardiac injection (ICI) or tail vein injection (TVI) model. However, many gene signatures in orthotopic breast cancer metastasis have not yet been studied in detail. Here we have established new highly lung metastatic breast cancer cells from MDA-MB231 by OX model.Comparative analysis between Parent cells (MDA-MB231) and the highly lung metastatic breast cancer cells (LM05) revealed that Non-canonical NF-κB pathway was constitutively activated by NIK up-regulation in protein level. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28038
6 Samples
Download data: CSV
19.

Constitutive Activation of NF-kB Inducing Kinase (NIK) in the Mesenchymal Lineage Drives Spontaneous Soft Tissue Sarcoma

(Submitter supplied) Aberrant NF-kB signaling fuels tumor growth in multiple human cancer types including both hematologic and solid malignancies. Chronic elevated alternative NF-kB signaling can be modeled in transgenic mice upon activation of a conditional NF-kB-inducing kinase (NIK) allele lacking the regulatory TRAF3 binding domain (NT3). Here, we report that expression of NT3 in the mesenchymal lineage with Osterix (Osx/Sp7)-Cre or Fibroblast Specific Protein (Fsp1)-Cre caused subcutaneous, soft tissue tumors. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: TSV
Series
Accession:
GSE158479
ID:
200158479
20.

Conditional Activation of NF-kB Inducing Kinase (NIK) in the Osteolineage Enhances both Basal and Loading-Induced Bone Formation

(Submitter supplied) Studies from global loss-of-function mutants suggest that alternative NF-kB downstream of NF-kB inducing kinase (NIK) is a cell-intrinsic negative regulator of osteogenesis. However, the interpretation of the osteoblast and/or osteocyte contribution to the bone phenotype is complicated by simultaneous osteoclast defects in these models. Therefore, we turned to a transgenic mouse model to investigate the direct role of NIK in the osteolineage. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
16 Samples
Download data: TXT
Series
Accession:
GSE133212
ID:
200133212
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