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Items: 1 to 20 of 315

1.

Immediate Early Response 2 (Ier2) overexpression effect in NIH 3T3 cells

(Submitter supplied) Analysis of Immediate Early Response 2 (Ier2)-inducible NIH 3T3 cells after Ier2 induction with RheoSwitch ligand RSL-1. Results provide insight into the function of Ier2 in NIH 3T3 mouse embryonal fibroblasts. Immediate early genes, including Ier2, are rapidly induced in quiescent cells by proliferation and migration-inducing stimuli. Microarray gene expression profiling was performed to identify differentially expressed genes following overexpression of Ier2 in NIH 3T3-Ier2 inducible cells after 24 hour induction of Ier2.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
12 Samples
Download data: CEL
Series
Accession:
GSE181200
ID:
200181200
2.

RIP-CHIP data from CNOT6L WT and KO hepatocytes

(Submitter supplied) mRNA poly(A) tail plays a key role in post-transcriptional regulation of gene expression, including mRNA decay and translation. Deadenylation is a rate-limiting step in mRNA decay, which is catalyzed by the CCR4-NOT complex. To identify mRNAs associated with the CCR4-NOT complex, we have done RIP-CHIP (RNA-immunoprecipitation followed by DNA microarray) using primary hepatocytes from CNOT6L wild-type and knockout mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE62365
ID:
200062365
3.

Tissue-specific metabolic reprogramming drives nutrient flux in diabetic complications

(Submitter supplied) Diabetes is associated with altered metabolism, but how altered metabolism contributes to the development of complications such as diabetic kidney disease is unknown. We used a systems approach with transcriptomics and mass spectrometry (MS)-based metabolomics to determine alterations in carbohydrate and lipid metabolism in kidney cortex tissue from 24-week-old BKS db/db diabetic mice and db/+ controls. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
10 Samples
Download data: CEL
Series
Accession:
GSE86300
ID:
200086300
4.

Dosage Compensation of an Aneuploid Genome in Mouse Spermatogenic Cells

(Submitter supplied) Autosomal trisomies and monosomies bring serious threats to embryonic development through transcriptional disarray primarily caused by the dosage effect of the aneuploid part of the genome. The present study compared the effect of a mouse viable 30 Mb segmental trisomy on the genome-wide transcriptional profile of somatic (liver) cells and male germ cells. While the 1.6-fold change in expression of triplicated genes reflected the gene dosage in liver cells, the extra copy was almost fully compensated in early pachytene spermatocytes, showing 1.18-fold increase. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
22 Samples
Download data: CEL
Series
Accession:
GSE54683
ID:
200054683
5.

Identification of stage specific genes associated with lupus nephritis and response to remission induction in NZB/W and NZM2410 mice

(Submitter supplied) The CEL files of this study are additional to the GSE32583 and GSE44691; they are microarrays of lupus nephritis NZBW mouse model at 30 wks old, or treated with CTX+CTLAIg+anti-CD154 (early and late after remission) or Ad-TACI-Ig+CTLA4Ig (late after remission) and NZM2410 treated with Ad-BAFF-R-Ig.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
32 Samples
Download data: CEL
Series
Accession:
GSE49898
ID:
200049898
6.

Expression data from lupus NZB/W and NZW/BXSB mouse prenephritic kidneys

(Submitter supplied) We defined the shared and unique features of systemic lupus erythematosus (SLE) nephritis in 2 mouse models of proliferative renal disease. We identified shared inflammatory mechanisms of SLE nephritis that can be therapeutically targeted. Some common mechanisms are shared with non-immune-mediated renal diseases, suggesting that new strategies to prevent tissue hypoxia and remodeling may be useful in SLE nephritis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
11 Samples
Download data: CEL, TXT
Series
Accession:
GSE44691
ID:
200044691
7.

Meiotic Consequences of Genetic Extension of Unsynapsed Autosomal Chromatin

(Submitter supplied) We investigated the influence of extension of autosomal asynapsis on expression profiles during spermatogenesis. We used the mouse autosomal translocation T(16;17)43H (abbreviated T43H) and t12 haplotype, a natural variant of Chr 17 encompassing four adjacent non-overlapping inversions proximal to the T43H translocation breakpoint, as a model. The presence of t12 haplotype in trans to the T43H translocation resulted in stringent spermatogenic block and in more complete silencing of genes surrounding the T43H translocation break. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
18 Samples
Download data: CEL
Series
Accession:
GSE29177
ID:
200029177
8.

Immunopathogenesis of renal inflammation during the progression, remission and relapse of renal disease in the NZB/W murine lupus model

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
100 Samples
Download data: CEL
Series
Accession:
GSE50038
ID:
200050038
9.

Distinct translational control in CD4+ T-cell subsets

(Submitter supplied) Regulatory T cells expressing the transcription factor Foxp3 play indispensable roles for the induction and maintenance of immunological self-tolerance and immune homeostasis. Genome-wide mRNA expression-studies have defined canonical signatures of T-cell subsets. Changes in steady-state mRNA levels do, however, often not reflect those of corresponding proteins due to post-transcriptional mechanisms including mRNA translation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
16 Samples
Download data: CEL
Series
Accession:
GSE45401
ID:
200045401
10.

Human and mouse lupus nephritis cross-species transcriptional analysis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL14663 GPL7546
150 Samples
Download data: CEL
Series
Accession:
GSE32592
ID:
200032592
11.

Expression data from lupus NZB/W, NZM2410, NZW/BXSB mouse kidneys prenephritic and nephritic.

(Submitter supplied) Nephritis (LN) is a serious manifestation of SLE. Therapeutic studies in mouse LN models do not always predict outcomes of human therapeutic trials, raising concerns about the human relevance of these models. In this study we used an unbiased transcriptional network approach to define similarities and differences between three lupus models and human LN. Affymetrix-based expression profiles were analyzed using Genomatix Bibliosphere software and transcriptional networks were compared using the Tool for Approximate LargE graph matching (TALE). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
57 Samples
Download data: CEL, TXT
Series
Accession:
GSE32583
ID:
200032583
12.

Expression data from macrophages isolated from lupus NZB/W mouse kidneys prenephritic, nephritic or after complete remission.

(Submitter supplied) Renal infiltration with mononuclear cells is associated with poor prognosis in SLE. A renal macrophage/dendritic cell signature is associated with onset of nephritis in NZB/W mice and immune modulating therapies can reverse this signature and the associated renal damage despite ongoing immune complex deposition. Our findings suggest that mononuclear phagocytes with an aberrant activation profile contribute to tissue damage in lupus nephritis by mediating both local inflammation and excessive tissue remodeling. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4194
Platform:
GPL7546
17 Samples
Download data: CEL
Series
Accession:
GSE27045
ID:
200027045
13.
Full record GDS4194

NZB/W model of systemic lupus erythematosus: renal macrophages

Analysis of F4/80hi renal macrophages isolated at an early stage of lupus, during lupus nephritis, and after induction of remission. The infiltrating F4/80hi cells are associated with renal damage. Results provide insight into mechanisms by which F4/80hi macrophages contribute to lupus nephritis.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 tissue sets
Platform:
GPL7546
Series:
GSE27045
17 Samples
Download data: CEL
14.

PDGF-BB modulates hematopoiesis and tumor angiogenesis by inducing erythropoietin production in stromal cells.

(Submitter supplied) The platelet-derived growth factor (PDGF) signaling system contributes to tumor angiogenesis and vascular remodeling. Here, we show PDGF-BB markedly induces erythropoietin (EPO) mRNA and protein expression by targeting the PDGFR-beta+ stromal and perivascular compartments. In mouse tumor models, PDGF-BB-induced EPO promotes tumor growth via two mechanisms: 1) paracrine stimulation of tumor angiogenesis by directly inducing endothelial cell proliferation, migration, sprouting and tube formation; and 2) endocrine stimulation of extramedullary hematopoiesis leading to increased oxygen perfusion and protection against tumor-associated anemia. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
6 Samples
Download data: CEL
Series
Accession:
GSE33717
ID:
200033717
15.

Hoxd genes and fiber type-specific markers specify adult mouse muscle type in a diet-independent way

(Submitter supplied) Introduction: The mouse skeletal muscle is composed of four distinct fiber types that differ in contractile function, number of mitochondria and metabolism. Every muscle group has a specific composition and distribution of the four fiber types. Until now, three genes (CnA, PGC1α and PPARδ) are identified that are involved in the generation of more oxidative muscle types. In the present study we searched for novel genes that are involved in specifying different muscle types. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
40 Samples
Download data: CEL
Series
Accession:
GSE18127
ID:
200018127
16.

A high fat diet causes obesity and insulin resistance in mice, but induces small changes in the muscle transcriptome

(Submitter supplied) An 8-week high fat palm oil diet causes obesity and insulin resistance in C57BL/6J mice, but induces only small changes in the muscle transcriptome. Introduction: The metabolic syndrome (MS) is a cluster of metabolic abnormalities linked to an increased risk of type 2 diabetes and cardiovascular diseases. Two major characteristics of the MS are obesity and insulin resistance. In the present study we investigated the effect of obesity and insulin resistance on the mouse muscle transcriptome. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4015
Platform:
GPL7546
30 Samples
Download data: CEL
Series
Accession:
GSE17576
ID:
200017576
17.
Full record GDS4015

High fat diet effect on C57BL/6J quadriceps muscle

Analysis of skeletal muscle of C57BL/6J males fed a high fat diet (HFD) for 8 weeks to induce obesity and insulin resistance. Results provide insight into the molecular mechanisms underlying the development of diet-induced obesity and insulin resistance.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 growth protocol, 2 time sets
Platform:
GPL7546
Series:
GSE17576
30 Samples
Download data: CEL
DataSet
Accession:
GDS4015
ID:
4015
18.

c-Met confers protection against chronic liver tissue damage and fibrosis progression after bile-duct-ligation in mice

(Submitter supplied) The HGF/c-Met system is an essential inducer of hepatocyte growth and proliferation. Although a fundamental role for the HGF receptor c-Met has been demonstrated in acute liver regeneration its cell specific role in hepatocytes during chronic liver injury and fibrosis progression has not been determined yet. In order to better characterize the role of c-Met in hepatocytes we generated a hepatocyte-specific c-Met knockout mouse (c-Met∆hepa) using the Cre-loxP system and studied its relevance after bile-duct ligation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7546
12 Samples
Download data: CEL
Series
Accession:
GSE13992
ID:
200013992
19.

[Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/projects/geo/info/geo_affy.html June 03, 2009: annotation table updated with netaffx build 28 June 07, 2012: annotation table updated with netaffx build 32 June 23, 2016: annotation table updated with netaffx build 35 Protocol: see manufacturer's web site All probe sets represented on the GeneChip Mouse Expression Set 430 are included on the GeneChip Mouse Genome 430 2.0 Array. more...
Organism:
Mus musculus
601 DataSets
4538 Series
40 Related Platforms
58877 Samples
Download data
Platform
Accession:
GPL1261
ID:
100001261
20.

Affymetrix GeneChip Mouse Genome 430 2.0 Array [CDF: Mm_ENTREZG_10]

(Submitter supplied) CDF file was created by Microarray Lab at the Molecular and Behavioral Neuroscience Institute at the University of Michigan. Oligonucleotide probes on GeneChips were reorganized based on the latest genome and transcriptome information. In this particular case the Entrez Gene database (build: Jun 28, 2007) was used as source. For the CDF file based on Entrez Gene: A probe must hit only one genomic location; Probes that can be mapped to the same target sequence in the correct direction are grouped together in the same probe set; Each probe set must contain at least three oligonucleotide probes and probes in a set are ordered according to their location in the corresponding exon. more...
Organism:
Mus musculus
2 DataSets
16 Series
1 Related Platform
295 Samples
Download data: TAR
Platform
Accession:
GPL7546
ID:
100007546
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