Similar studies for GEO DataSets (Select 2901) - GEO DataSets

Select item 29011.

Tsc2 tumor suppressor gene mutant kidney response to genotoxic and non-genotoxic carcinogens: time course

Analysis of kidneys of Eker males treated for up to 14 days with the genotoxic carcinogen aristolochic acid (AA) or the non-genotoxic carcinogen ochratoxin A (OTA). The Eker rat, heterozygous mutant for the tuberous sclerosis 2 (Tsc2) tumor suppressor gene, is a model to study renal carcinogenesis.

Organism:: Rattus norvegicus

Type:: Expression profiling by array, count, 5 agent, 2 genotype/variation, 4 time sets

Platform:: GPL341
Series:: GSE5923
84 Samples

Download data

DataSet

Accession:: GDS2901

ID:: 2901

Select item 2000059232.

Expression data from Aristolochic Acid and Ochratoxin A treated Tsc2 mutant (Eker) and corresponding wild type rats

(Submitter supplied) Renal gene expression profiles of Eker and wild type rats, gavaged with AA or OTA, respectively for 1, 3, 7 or 14 days We used Affymetrix RAE230A microarrays for the analysis of early gene expression changes in the renal cortex_ outer medulla of carcinogen treated Eker and corresponding wild type rats Keywords: time course

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Dataset:: GDS2901
Platform:: GPL341
84 Samples

Download data

Series

Accession:: GSE5923

ID:: 200005923

Select item 2000106083.

Gene expression data from renal preneoplastic lesions

(Submitter supplied) Microarrays were used to analyse gene expression underlying early tumourigenesis in Eker rats. Distinct classes of up- and downregulated genes were identified in different preneoplasic lesion vs. microdissected normal (healthy) renal tubules. Laser capture microdissected renal basophilic atypical tubule (bAT) and basophilic atypical hyperplasia (bAH) and healthy tissue (HT) of 6-months aristolochic acid (AA)- and ochratoxin A (OTA)-treated and control (C) male Eker rats were isolated for RNA extraction and microarray analysis in order to investigate gene expression profiles induced by AA and OTA as well as to differentiate pathways specific for the bAT to bAH progression. more...

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL1355
29 Samples

Download data: CEL

Series

Accession:: GSE10608

ID:: 200010608

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2001604194.

DNA copy number alterations in radiation-induced rat renal carcinomas

(Submitter supplied) To investigate DNA copy number changes in rat renal carcinomas induced by ionizing radiation.

Organism:: Rattus norvegicus

Type:: Genome variation profiling by array

Platform:: GPL21089
8 Samples

Download data: TXT

Series

Accession:: GSE160419

ID:: 200160419

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2000028525.

Ochratoxin A study on rat liver and kidney gene expression

(Submitter supplied) Ochratoxin A gene expression profiling in liver and kidney, with time points of exposure from 7 days to 12 motnhs Keywords: timecourse

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL85
67 Samples

Download data: CEL, EXP

Series

Accession:: GSE2852

ID:: 200002852

Select item 2000872786.

Gene expression changes of tert-butyl alchol-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with tert-butyl alchol, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL19135
12 Samples

Download data: TXT

Series

Accession:: GSE87278

ID:: 200087278

Select item 2000872767.

Gene expression changes of o-nitroanisole-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with o-nitroanisole, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL19135
6 Samples

Download data: TXT

Series

Accession:: GSE87276

ID:: 200087276

Select item 2000872758.

Gene expression changes of o-anthranilic acid-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with o-anthranilic acid, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL19135
6 Samples

Download data: TXT

Series

Accession:: GSE87275

ID:: 200087275

Select item 2000872749.

Gene expression changes of o-anisidine hydrochloride-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with o-anisidine hydrochloride, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL19135
6 Samples

Download data: TXT

Series

Accession:: GSE87274

ID:: 200087274

Select item 20008727210.

Gene expression changes of cisplatin-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with cisplatin, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL22435
12 Samples

Download data: TXT

Series

Accession:: GSE87272

ID:: 200087272

Select item 20008727111.

Gene expression changes of 4,4'-thiobis(6-tert-butyl-m-cresol)-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with 4,4'-thiobis(6-tert-butyl-m-cresol), and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL22435
6 Samples

Download data: TXT

Series

Accession:: GSE87271

ID:: 200087271

Select item 20008727012.

Gene expression changes of tris(2-chloroethyl)phosphate-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with tris(2-chloroethyl)phosphate, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL19135
6 Samples

Download data: TXT

Series

Accession:: GSE87270

ID:: 200087270

Select item 20008726913.

Gene expression changes of tricresyl phosphate-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with tricresyl phosphate, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL22435
6 Samples

Download data: TXT

Series

Accession:: GSE87269

ID:: 200087269

Select item 20008726814.

Gene expression changes of sulfone bis(p-chlorophenyl)-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with sulfone bis(p-chlorophenyl), and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL22435
6 Samples

Download data: TXT

Series

Accession:: GSE87268

ID:: 200087268

Select item 20008726715.

Gene expression changes of potassium bromate-induced in renal cortex of rats

(Submitter supplied) This study is to develop a short term and highly accurate prediction method of renal carcinogenicity based on gene expression profile of rats administrated by carcinogens. We conducted 28 days-repeated dose experiments in male SD rats with potassium bromate, and the gene expression profiles of renal cortex were analyzed using custom microarrays.

Organism:: Rattus norvegicus

Type:: Expression profiling by array

Platform:: GPL22435
6 Samples

Download data: TXT

Series

Accession:: GSE87267

ID:: 200087267

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