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Links from GEO DataSets

Items: 20

1.

Gene Profiling in the Livers of Wild-Type and PPARalpha-Null Mice Exposed to Perfluorooctanoic Acid (PFOA)

(Submitter supplied) Unlike the PPARalpha agonist W14,643, PFOA is capable of inducing effects independently of PPARa. Genes altered in the PPARalpha-null mouse following exposure to PFOA included those associated with fatty acid metabolism, inflammation, xenobiotic metabolism, and cell cycle progression. The specific signaling pathway(s) responsible for these effects is not readily apparent but it is conceivable that other members of the nuclear receptor superfamily such as PPARbeta/delta and CAR may be involved. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL2995
39 Samples
Download data
Series
Accession:
GSE9796
ID:
200009796
2.

Gene expression profiling in the lung and liver of low and high dose Perfluorooctanoic Acid exposed mouse fetuses

(Submitter supplied) Exposure to PFOA during gestation altered the expression of genes related to fatty acid catabolism in both the fetal liver and lung. In the fetal liver, the effects of PFOA were robust and also included genes associated with lipid transport, ketogenesis, glucose metabolism, lipoprotein metabolism, cholesterol biosynthesis, steroid metabolism, bile acid biosynthesis, phospholipid metabolism, retinol metabolism, proteosome activation, and inflammation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS3410 GDS3411
Platform:
GPL1261
59 Samples
Download data: CEL
Series
Accession:
GSE13044
ID:
200013044
3.
Full record GDS3411

Low doses of perfluorooctanoic acid effect on fetal liver and lung

Analysis of livers or lungs of fetuses dosed during gestation with up to 3 mg/(kg day) perfluorooctanoic acid (PFOA), an industrial chemical that induces growth deficits and mortality in murine neonates. Results provide insight into the molecular basis of PFOA-induced developmental toxicity.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 dose, 2 tissue sets
Platform:
GPL1261
Series:
GSE13044
29 Samples
Download data: CEL
DataSet
Accession:
GDS3411
ID:
3411
4.
Full record GDS3410

High doses of perfluorooctanoic acid effect on fetal liver and lung

Analysis of livers or lungs of fetuses dosed during gestation with up to 10 mg/(kg day) perfluorooctanoic acid (PFOA), an industrial chemical that induces growth deficits and mortality in murine neonates. Results provide insight into the molecular basis of PFOA-induced developmental toxicity.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 dose, 2 tissue sets
Platform:
GPL1261
Series:
GSE13044
30 Samples
Download data: CEL
DataSet
Accession:
GDS3410
ID:
3410
5.

Transcriptional response to PFOA in wild-type and PPARalpha-null mice

(Submitter supplied) Toxicogenomic Dissection of the Perfluorooctanoic Acid (PFOA) Transcript Profile in Mouse Liver: Evidence for the Involvement of Nuclear Receptors PPARalpha and CAR We performed a toxicogenomics dissection of the transcript profiles in the mouse liver after exposure to PFOA. We uncovered classes of genes that were regulated independently of PPARalpha. Some of these genes, including those involved in lipid metabolism, may be regulated by PPARbeta/delta or PPARgamma, whereas others, such as those involved in xenobiotic metabolism are likely regulated through CAR. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3407
Platform:
GPL1261
16 Samples
Download data: CEL
Series
Accession:
GSE9786
ID:
200009786
6.
Full record GDS3407

Perfluorooctanoic acid effect on livers lacking PPAR-alpha

Analysis of PPAR-alpha null livers from animals treated with perfluorooctanoic acid (PFOA), a member of a class of industrial chemicals called peroxisome proliferator chemicals. PFOA exposure is linked to cancer. Results provide insight into the role of PPAR-alpha in mediating the effects of PFOA.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE9786
16 Samples
Download data: CEL
DataSet
Accession:
GDS3407
ID:
3407
7.

The effects of perfluorooctanoate on high fat diet induced non-alcoholic fatty liver disease in mice

(Submitter supplied) We reported the hepatic gene expression profiling in mice treated by perfluorooctanoate (PFOA) and high fat diet (HFD). Chronic HFD treatment was associated with gene expression changes in cholesterol biosynthetic process, lipid metabolic process, extracellular matrix, and inflammatory response pathways. Many chemokine related genes including Ccl2, Ccr2, Ccl3l3, Cx3cl1, Cx3cr1, Cxcl14, and toll-like receptor (TLR) related genes including Tlr2, Tlr7, Tlr8, Tlr13 were all significant upregulated comparing vehicle-treated HFD-fed mice to control diet (CD)-fed mice, suggesting their roles in the development of steatohepatitis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
16 Samples
Download data: TXT
Series
Accession:
GSE119441
ID:
200119441
8.

Expression data from wild-type and PPARalpha-null mice exposed to perfluorooctane sulfonate (PFOS)

(Submitter supplied) Perfluorooctane sulfonate (PFOS) is a perfluoroalkyl acid (PFAA) and a persistent environmental contaminant found in the tissues of humans and wildlife. Although blood levels of PFOS have begun to decline, health concerns remain because of the long half-life of PFOS in humans. Like other PFAAs, such as perfluorooctanoic acid (PFOA), PFOS is an activator of peroxisome proliferator-activated receptor-alpha (PPARα) and exhibits hepatocarcinogenic potential in rodents. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
30 Samples
Download data: CEL
Series
Accession:
GSE22871
ID:
200022871
9.

Detailed transcriptomics analysis of the effect of dietary fatty acids on gene regulation in the murine heart [superseries]

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL7440 GPL1261
59 Samples
Download data: CEL
Series
Accession:
GSE30649
ID:
200030649
10.

Detailed transcriptomics analysis of the effect of the PPARalpha agonist Wy14,643 on gene regulation in the murine heart

(Submitter supplied) Fatty acids comprise the primary energy source for the heart and are mainly taken up via hydrolysis of circulating triglyceride-rich lipoproteins. While most of the fatty acids entering the cardiomyocyte are oxidized, a small portion is involved in altering gene transcription to modulate cardiometabolic functions. So far, no in vivo model has been developed enabling study of the transcriptional effects of specific fatty acids in the intact heart. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7440
4 Samples
Download data: CEL
Series
Accession:
GSE30553
ID:
200030553
11.

Detailed transcriptomics analysis of the effect of dietary fatty acids on gene regulation in the murine heart.

(Submitter supplied) Fatty acids comprise the primary energy source for the heart and are mainly taken up via hydrolysis of circulating triglyceride-rich lipoproteins. While most of the fatty acids entering the cardiomyocyte are oxidized, a small portion is involved in altering gene transcription to modulate cardiometabolic functions. So far, no in vivo model has been developed enabling study of the transcriptional effects of specific fatty acids in the intact heart. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
55 Samples
Download data: CEL
Series
Accession:
GSE30495
ID:
200030495
12.

Analysis of the Heat Shock Response in Mouse Liver Reveals Transcriptional Dependence on the Nuclear Receptor PPARα

(Submitter supplied) The nuclear receptor peroxisome proliferator-activated receptor alpha (PPARα) regulates responses to chemical or physical stress in part by altering expression of genes involved in proteome maintenance. Many of these genes are also transcriptionally regulated by heat shock (HS) through activation by HS factor-1 (HSF1). We hypothesized that there are interactions on a genetic level between PPARα and the HS response mediated by HSF1. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
24 Samples
Download data: CEL, CHP
Series
Accession:
GSE14869
ID:
200014869
13.

Transcriptional profilling of liver from C57BL/6 wildtype and PPARα-knockout mice treated with PFOA and GenX after 20 weeks of high-fat diet

(Submitter supplied) Perfluoroalkyl substances (PFAS) are man-made chemicals with suspected endocrine-disrupting properties. Exposure to perfluorooctanoic acid (PFOA) has been linked to disturbed metabolism via the liver, although the exact mechanism is not clear. Moreover, information on the metabolic effects of the new PFAS alternative GenX is limited. We tested whether low-dose exposure to PFOA and GenX induces metabolic disturbances, including NAFLD, dyslipidemia, and glucose tolerance in mice and studied the involvement of PPARα. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
32 Samples
Download data: RDATA, TXT
Series
Accession:
GSE212294
ID:
200212294
14.

Gene expression changes in liver tissues from alcohol treated PPARa-null mice

(Submitter supplied) transcriptomic changes in wild typw and PPARa-null mice fed the Lieber-Decarli liquid diet with or without alcohol for up to four months to identify biomarkers for the early stage of alcohol induced liver damage. Mice were sampled after 1, 2 and 4 months treatment.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
48 Samples
Download data: TXT
Series
Accession:
GSE54034
ID:
200054034
15.

PPARalpha-mediated effects of dietary lipids on intestinal barrier gene expression

(Submitter supplied) Background: The selective absorption of nutrients and other food constituents in the small intestine is mediated by a group of transport proteins and metabolic enzymes, often collectively called ‘intestinal barrier proteins’. An important receptor that mediates the effects of dietary lipids on gene expression is the peroxisome proliferator-activated receptor alpha (PPARα), which is abundantly expressed in enterocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
35 Samples
Download data: CEL
Series
Accession:
GSE9533
ID:
200009533
16.

Validation of a genomics-based hypothetical adverse outcome pathway: 2,4-dinitrotoluene perturbs PPAR signaling impairing energy metabolism and decreasing exercise endurance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platforms:
GPL17621 GPL17622 GPL17554
72 Samples
Download data
Series
Accession:
GSE50170
ID:
200050170
17.

Real-time quantitative PCR analysis of fatty acid metabolism genes of liver tissue from wild-type and PPARα (-/-) mice exposed to 2,4-dinitrotoluene (glucose)

(Submitter supplied) 2,4-dinitrotoluene (2,4-DNT), a nitroaromatic used in industrial and explosive manufacturing processes, is known to contaminate artillery ranges, demilitarization areas and munitions manufacturing facilities. Previous transcriptomic and lipidomic studies identified energy metabolism as a principle biochemical process affected by 2,4-DNT where up-stream effects on PPARα signaling were hypothesized as themolecular initiating event for these effects. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL17622
24 Samples
Download data: XLS
Series
Accession:
GSE50169
ID:
200050169
18.

Real-time quantitative PCR analysis of fatty acid metabolism genes of liver tissue from wild-type and PPARα (-/-) mice exposed to 2,4-dinitrotoluene (fatty acid)

(Submitter supplied) 2,4-dinitrotoluene (2,4-DNT), a nitroaromatic used in industrial and explosive manufacturing processes, is known to contaminate artillery ranges, demilitarization areas and munitions manufacturing facilities. Previous transcriptomic and lipidomic studies identified energy metabolism as a principle biochemical process affected by 2,4-DNT where up-stream effects on PPARα signaling were hypothesized as themolecular initiating event for these effects. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL17621
24 Samples
Download data: XLS
Series
Accession:
GSE50168
ID:
200050168
19.

Real-time quantitative PCR analysis of fatty acid metabolism genes of liver tissue from wild-type and PPARa (-/-) mice exposed to 2,4-dinitrotoluene (PPARa)

(Submitter supplied) 2,4-dinitrotoluene (2,4-DNT), a nitroaromatic used in industrial and explosive manufacturing processes, is known to contaminate artillery ranges, demilitarization areas and munitions manufacturing facilities. Previous transcriptomic and lipidomic studies identified energy metabolism as a principle biochemical process affected by 2,4-DNT where up-stream effects on PPARα signaling were hypothesized as themolecular initiating event for these effects. more...
Organism:
Mus musculus
Type:
Expression profiling by RT-PCR
Platform:
GPL17554
24 Samples
Download data: XLS
Series
Accession:
GSE50167
ID:
200050167
20.

PPARa siRNA-Treated Expression Profiles Uncover the Causal Sufficiency Network for Compound-Induced Liver Hypertrophy

(Submitter supplied) Approaches for discovering mechanisms of action and for identifying molecular biomarkers in biomedical research are evolving today, as the growing symbiosis with computational sciences becomes more widely appreciated than ever. In fact, the combination of various new technologies has been pushing forward both frontiers. Here, we present an example of the combined use of in vivo siRNA knock-down technology, genome-wide gene expression profiling, and computational reasoning to unveil regulatory causal relationships and the sufficiency network of identified genes for compound-induced toxicity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4696
20 Samples
Download data
Series
Accession:
GSE6622
ID:
200006622
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