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Links from GEO DataSets

Items: 20

1.

Triazole Antifungal Toxicogenomics: rat_repro_Testis

(Submitter supplied) The modes of triazole reproductive toxicity have been characterized by an observed increased in serum testosterone and reduced insemination and fertility indices. The key events involved in the disruption in testosterone homeostasis and reduced fertility remain unclear. Gene expression analysis was conducted on liver and testis from Wistar Han IGS rats fed myclobutanil (M: 500, 2000 ppm), propiconazole (P: 500, 2500 ppm), or triadimefon (T: 500, 1800 ppm) from gestation day six to postnatal day 92. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
34 Samples
Download data: CEL
Series
Accession:
GSE10412
ID:
200010412
2.

Triazole Antifungal Toxicogenomics: rat_repro_Liver

(Submitter supplied) The modes of triazole reproductive toxicity have been characterized by an observed increased in serum testosterone and reduced insemination and fertility indices. The key events involved in the disruption in testosterone homeostasis and reduced fertility remain unclear. Gene expression analysis was conducted on liver and testis from Wistar Han IGS rats fed myclobutanil (M: 500, 2000 ppm), propiconazole (P: 500, 2500 ppm), or triadimefon (T: 500, 1800 ppm) from gestation day six to postnatal day 92. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
35 Samples
Download data: CEL
Series
Accession:
GSE10411
ID:
200010411
3.

Triazole Antifungal Toxicogenomics: human_primary_hepatocytes_CellzDirect

(Submitter supplied) The triazole antifungals myclobutanil (MYC), propiconazole (PPZ) and triadimefon (TDF) [Propiconazole CASNR 60207-90-1; Triadimefon CASNR 43121-43-3; Myclobutanil CASNR 88671-89-0] all disrupt steroid hormone homeostasis and cause varying degrees of hepatic toxicity. To identify biological pathways consistently activated across various study designs, gene expression profiling was conducted on livers from rats following acute, repeated dose, or prenatal to adult exposures. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
43 Samples
Download data: CEL
Series
Accession:
GSE10410
ID:
200010410
4.

Triazole Antifungal Toxicogenomics: Iconix3_Triazoles

(Submitter supplied) The modes of triazole reproductive toxicity have been characterized by an observed increased in serum testosterone and reduced insemination and fertility indices. The key events involved in the disruption in testosterone homeostasis and reduced fertility remain unclear. Gene expression analysis was conducted on liver from Sprague Dawley rats dosed with myclobutanil (300 mg/kg/day), propiconazole (300 mg/kg/day), or triadimefon (175 mg/kg/day) for 72 hours. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
12 Samples
Download data: CEL
Series
Accession:
GSE10409
ID:
200010409
5.

Triazole Antifungal Toxicogenomics: GeneLogic_Triazoles

(Submitter supplied) The modes of triazole reproductive toxicity have been characterized by an observed increased in serum testosterone and reduced insemination and fertility indices. The key events involved in the disruption in testosterone homeostasis and reduced fertility remain unclear. Gene expression analysis was conducted on liver from Sprague Dawley rats dosed with myclobutanil (300 mg/kg/day) or triadimefon (175 mg/kg/day) for 6, 24 or 336 hours. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
45 Samples
Download data: CEL
Series
Accession:
GSE10408
ID:
200010408
6.

Triazole Antifungal Toxicogenomics: rat_primary_hepatocyte_CellzDirect

(Submitter supplied) The triazole antifungals myclobutanil (MYC), propiconazole (PPZ) and triadimefon (TDF) all disrupt steroid hormone homeostasis and cause varying degrees of hepatic toxicity. To identify biological pathways consistently activated across various study designs, gene expression profiling was conducted on livers from rats following acute, repeated dose, or prenatal to adult exposures. To explore conservation of responses across species, gene expression from these rat in vivo studies were also compared to in vitro data from rat and human primary hepatocytes exposed to MYC, PPZ, or TDF. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
35 Samples
Download data: CEL
Series
Accession:
GSE9387
ID:
200009387
7.

Hepatic transcriptome of rats treated with vehicle or fipronil (3 mg/kg/d per os for 14 days)

(Submitter supplied) Fipronil (CAS #: 120068-37-3), a widely used insecticide, has been described as a thyroid disruptor in rat inducing a marked increase in thyroxine (T4) clearance resulting in a decrease in T4 plasma concentration. These effects seem to require the bioactivation of fipronil via its biotransformation into fipronil sulfone by cytochromes P450 (CYP). Here, we hypothesized that fipronil-induced thyroid disruption may, at least in part, result from the induction of hepatic enzymes involved in the metabolism of thyroid hormones. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL7294
15 Samples
Download data: TXT
Series
Accession:
GSE39378
ID:
200039378
8.

Discrimination of Tumorigenic Triazole Conazoles from Phenobarbital by Transcriptional Analyses of Mouse Liver

(Submitter supplied) The goal of this study was to apply transcriptional analyses to hepatic tissues from mice exposed to PB, propiconazole (Pro) or triadimefon (Tri) at tumorigenic exposure levels to reveal similarities and differences in response among these treatments.The goal of this study was to apply transcriptional analyses to hepatic tissues from mice exposed to PB, propiconazole (Pro) or triadimefon (Tri) at tumorigenic exposure levels to reveal similarities and differences in response among these treatments.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
38 Samples
Download data: CEL
Series
Accession:
GSE16777
ID:
200016777
9.

Transcriptional Profiling of Adult Male Rat Liver and Testis following 14 Day Myclobutanil Exposure

(Submitter supplied) We report the RNAseq-based transcriptome profiles of adult male rat liver and testis following 14 day exposure to myclobutanil. A treatment-related change in mRNA levels were observed in both liver and testis.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
48 Samples
Download data: TXT
Series
Accession:
GSE139098
ID:
200139098
10.

Ciprofibrate stimulated gene expression in rats

(Submitter supplied) Samples and RNA preparation: The series is composed of 4 hybridizations for analysis of differentially expressed genes in the liver of ciprofibrate dosed vs. control rats. Rats (200-250 g) were given (by gastric intubation) tap water (control group, n=5) or ciprofibrate (50 mg/kg body weight, once daily for 60 days, n=4). Liver total RNA extraction was performed first by ultracentrifugation on a cesium chloride cushion and then using TRIZOL Reagent (GIBCO BRL Life Technologies, New York, NY). more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL264
4 Samples
Download data
Series
Accession:
GSE335
ID:
200000335
11.

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
12.
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
13.

Expression data from adult Rattus liver

(Submitter supplied) Activation of the pregnane X receptor (NR1I2) by drugs and other xenobiotics stimulates (or suppresses) expression of numerous genes involved in the metabolic elimination of foreign compounds and some toxic endogenous substrates. We used microarray analysis to identify genes whose expression in rat liver was significantly altered by pregnenolone 16alpha-carbonitrile (PCN) treatment. Keywords: a single ip injection of PCN (100 mg/kg), 8 h treatment
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS2093 GDS2094
Platforms:
GPL341 GPL342
19 Samples
Download data
Series
Accession:
GSE4959
ID:
200004959
14.
Full record GDS2094

Pregnane X receptor agonist effect on the liver (RAE230B)

Analysis of livers of animals treated with pregnenolone 16alpha-carbonitrile (PCN), a pregnane X receptor (NR1I2) agonist. NR1I2 is a member of the nuclear receptor family of ligand-activated transcription factors, and regulates the transcription of genes encoding xenobiotic metabolizing enzymes.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL342
Series:
GSE4959
9 Samples
Download data
15.
Full record GDS2093

Pregnane X receptor agonist effect on the liver (RAE230A)

Analysis of livers of animals treated with pregnenolone 16alpha-carbonitrile (PCN), a pregnane X receptor (NR1I2) agonist. NR1I2 is a member of the nuclear receptor family of ligand-activated transcription factors, and regulates the transcription of genes encoding xenobiotic metabolizing enzymes.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL341
Series:
GSE4959
10 Samples
Download data
16.

Gut microbiota regulate xenobiotic metabolism in the liver

(Submitter supplied) Germ-free (GF) mice can be used as a powerful tool to investigate the role of the intestinal commensal flora in metabolism and immune tolerance. In this study we have used whole genome transcriptome analyses to compare expression levels systemically in liver of germ-free mice and specific pathogen free (SPF) mice. Keywords: Mouse liver tissue germ-free or specific pathogen free vs universal mouse reference Specific Pathogens Excluded from the SPF mice: Virus 1. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8146
8 Samples
Download data: GPR
Series
Accession:
GSE14689
ID:
200014689
17.

Sex Specific Transciption in Mouse Tissues

(Submitter supplied) Sex Specific Transciption in Mouse Hypothalamus, Liver, Kidney, Ovary and Testis. For each somatic tissue there are 3 biological samples from different pools comprised of 10 animals for each sex each with a technical replicate. For each of the reproductive tissues there are 3 biological samples from different pools comprised of 10 animals with a technical replicate for each. Keywords = Mouse sex-specific transcription, gonad specific gene expression Keywords: other
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS565
Platform:
GPL339
48 Samples
Download data
Series
Accession:
GSE1148
ID:
200001148
18.

Sex Specific Transciption in Human Hypothalamus

(Submitter supplied) Sex Specific Transciption in Human Hypothalamus between 7 male biological samples (2 technical replicates of each) and 5 female biological samples (2 technical replicates of 4 of these). Keywords = human hypothalamus, sex-specific transcription Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS564
Platform:
GPL96
23 Samples
Download data
Series
Accession:
GSE1147
ID:
200001147
19.
Full record GDS565

Sex specific transcription in somatic and reproductive tissues

Analysis of sex specific transcription in somatic and reproductive tissues. Hypothalamus, liver, kidney, ovary, and testis tissues pooled from 10 different animals examined.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 gender, 5 tissue sets
Platform:
GPL339
Series:
GSE1148
48 Samples
Download data
DataSet
Accession:
GDS565
ID:
565
20.
Full record GDS564

Sex specific transcription in hypothalamus

Examination of sex specific transcription in hypothalamus using postmortem samples from individuals averaging 70 years of age.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 gender sets
Platform:
GPL96
Series:
GSE1147
23 Samples
Download data
DataSet
Accession:
GDS564
ID:
564
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