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Links from GEO DataSets

Items: 17

1.
Full record GDS253

Methylprednisolone effect on liver: time course

Expression profiling of liver from animals treated with methylprednisolone. Liver examined at various time points up to 72 hours following methylprednisolone treatment. Results provide insight into prednisone pharmacodynamics.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 17 time sets
Platform:
GPL85
Series:
GSE487
46 Samples
Download data: CEL
2.

PGA Rat Liver Methylprednisolone

(Submitter supplied) Summary: The liver is the major site of gluconeogenesis, fat processing and distribution, as well as drug and xenobiotic metabolism. Altered gene expression in the liver is centrally invovled in both the immuosuppressive and the energetic actions of corticosteroids. Hypothesis: That pharmacodynamics can be derived from expression profiling data. Specific Aim: The aim of this project is to identify distinct temporal patters of RNA expression in the liver of rats following a bolus dose of the corticosteroid methylprednisolone. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS253 GDS972
Platforms:
GPL341 GPL85
91 Samples
Download data: CEL
Series
Accession:
GSE487
ID:
200000487
3.
Full record GDS972

Methylprednisolone effect on liver: time course (RAE230A)

Expression profiling of liver from animals treated with methylprednisolone. Liver examined at various time points up to 168 hours following methylprednisolone treatment. Results provide insight into prednisone pharmacodynamics.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 11 time sets
Platform:
GPL341
Series:
GSE487
44 Samples
Download data: CEL
4.

Response of multiple genes to a chronic dose of corticosteroids in rat muscles

(Submitter supplied) Synthetic glucocorticoids are used therapeutically for a variety of conditions. Both the efficacy and toxicity of corticosteroids arise from their pharmacologically exaggerated effects on target and non-target tissues. For example, beneficial effects deriving from inhibition of the immune system are accompanied by toxic side effects that include hyperglycemia, dyslipidaemia, muscle wasting, fatty liver, and an increased risk of atherosclerosis. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS2688
Platform:
GPL341
44 Samples
Download data: CEL
Series
Accession:
GSE5101
ID:
200005101
5.

Pharmacogenomic effect of corticosteroid in skeletal muscle

(Submitter supplied) The aim of this project is to identify distinct temporal patterns of RNA expression in the skeletal muscle of rats following a bolus dose of the corticosteroid methylprednisolone. 51 RG_U34A chips were used over 17 time points. Keywords: other
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS256
Platform:
GPL85
51 Samples
Download data: CEL
Series
Accession:
GSE490
ID:
200000490
6.
Full record GDS2688

Skeletal muscle response to chronic corticosteroid exposure: time course

Analysis of skeletal muscles of adrenalectomized animals given methylprednisolone (MPL) at a constant rate of infusion for up to 7 days. Results compared to a time series experiment using a single dose of MPL. Results provide insight into the identity of genes regulated by MPL in both regimens.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 11 time sets
Platform:
GPL341
Series:
GSE5101
44 Samples
Download data: CEL
7.
Full record GDS256

Pharmacogenomic effect of corticosteroid in skeletal muscle

Temporal analysis of skeletal muscle response to corticosteroid methylprednisolone. Wistar rats injected with methylprednisolone and skeletal muscle analyzed at various time points up to 72 hours.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 17 time sets
Platform:
GPL85
Series:
GSE490
51 Samples
Download data: CEL
8.

Expression data from brain tissue of Rattus norvegicus treated with D-Serine

(Submitter supplied) d-serine is naturally present throughout the human body. It is also used as add-on therapy for treatment-refractory schizophrenia. d-Serine interacts with the strychnine-insensitive glycine binding site of NMDA receptor, and this interaction could lead to potentially toxic activity (i.e., excitotoxicity) in brain tissue. The transcriptomic changes that occur in the brain after d-serine exposure have not been fully explored. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS3643
Platform:
GPL1355
24 Samples
Download data: CEL
Series
Accession:
GSE10748
ID:
200010748
9.
Full record GDS3643

D-serine effect on the brain: dose response

Analysis of forebrains of animals treated with up to 500 mg/kg D-serine for 96 hours. D-serine is involved in many physiological processes through its interaction with the glycine binding site of the NMDA receptor. Results provide insight into the impact of D-serine exposure on neuronal functions.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 6 dose sets
Platform:
GPL1355
Series:
GSE10748
24 Samples
Download data: CEL
DataSet
Accession:
GDS3643
ID:
3643
10.

Rat liver response to Clofibrate, DEHP or VPA

(Submitter supplied) The project had 2 goals: 1) To evaluate the transcriptional response of 3 prototypical toxicants (Clofibrate, VPA, and DEHP) on rat lever. 2) To evaluate the impact pooling samples has on data analysis. Keywords = Clofibrate Keywords = Diethylhexyl phthalate Keywords = Phthalic acid bis(2-ethylhexyl ester) Keywords = Sodium Valproate Keywords = Valproic Acid Keywords = VPA Keywords = vehicle Keywords: other
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS1451
Platform:
GPL85
94 Samples
Download data: CEL, CHP, EXP
Series
Accession:
GSE2303
ID:
200002303
11.
Full record GDS1451

Toxicants effect on liver: pooled and individual sample comparison

Analysis of livers of Sprague-Dawley males at various time points up to 168 hours after treatment with clofibrate, diethylhexylphthalate, or valproic acid. Expression profiles from pooled and individual samples compared. Results provide insight into the impact of pooling on experimental analysis.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 3 agent, 2 protocol, 4 time sets
Platform:
GPL85
Series:
GSE2303
94 Samples
Download data: CEL, CHP, EXP
DataSet
Accession:
GDS1451
ID:
1451
12.

Rat exposure to RDX (3mg/kg or 18mg/kg; 0, 4, 24, 48 hr)

(Submitter supplied) RDX (Hexahydro-1,3,5-trinitro-1,3,5-triazine) is a synthetic, high-impact, relatively stable explosive that has been in use since WWII. Exposure to RDX can occur either occupationally or through ordnance that lays unexploded on training ranges. The toxicology of RDX is dominated by acute tonic-clonic seizures at high doses, which remit when exposure is removed and internal RDX levels decrease. Sub-chronic studies have revealed few other toxic effects. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS5282 GDS5283
Platform:
GPL1355
48 Samples
Download data: CEL
Series
Accession:
GSE12196
ID:
200012196
13.
Full record GDS5283

Hexahydro-1,3,5-trinitro-1,3,5-triazine effect on the liver: dose response and time course

Analysis of livers of males for up to 48 hours after treatment with a single, oral, nonseizure-inducing dose of 3 or 18 mg/kg hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). RDX is a synthetic, high-impact, stable explosive. Results provide insight into the acute effects of RDX on the liver.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 2 dose, 4 time sets
Platform:
GPL1355
Series:
GSE12196
24 Samples
Download data: CEL
DataSet
Accession:
GDS5283
ID:
5283
14.
Full record GDS5282

Hexahydro-1,3,5-trinitro-1,3,5-triazine effect on the brain: dose response and time course

Analysis of cerebral cortices of males for up to 48 hours after treatment with an oral, nonseizure-inducing dose of 3 or 18 mg/kg hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). RDX is a synthetic, high-impact, stable explosive. Results provide insight into the acute effects of RDX on the brain.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 2 dose, 4 time sets
Platform:
GPL1355
Series:
GSE12196
24 Samples
Download data: CEL
DataSet
Accession:
GDS5282
ID:
5282
15.

Rat Kidney Methylprednisolone

(Submitter supplied) Summary: To identify distinct temporal patterns of mRNA expression in the kidney of rats following a bolus dose of the corticosteroid methylprednisolone. Hypothesis: That prednisone pharmacodynamics can be derived from expression profiling data. Keywords: other
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS964 GDS965
Platforms:
GPL341 GPL85
63 Samples
Download data: CEL
Series
Accession:
GSE1721
ID:
200001721
16.
Full record GDS965

Methylprednisolone effect on kidney: time course (RG-U34A)

Expression profiling of kidneys from animals treated with methylprednisolone. Kidneys examined at various time points up to 6 hours following methylprednisolone treatment. Results provide insight into prednisone pharmacodynamics.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 3 time sets
Platform:
GPL85
Series:
GSE1721
10 Samples
Download data: CEL
17.
Full record GDS964

Methylprednisolone effect on kidney: time course (RAE230A)

Expression profiling of kidneys from animals treated with methylprednisolone. Kidneys examined at various time points up to 72 hours following methylprednisolone treatment. Results provide insight into prednisone pharmacodynamics.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 agent, 17 time sets
Platform:
GPL341
Series:
GSE1721
53 Samples
Download data: CEL
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