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Links from GEO DataSets

Items: 8

1.

Assessing kidney injury induced by mercuric chloride in guinea pigs with in vivo and in vitro experiments [in vitro]

(Submitter supplied) In this study we tested the ability to predict organ injury from in vitro transcriptomics data at early time points after exposure to mercury chloride (12 and 24 hours). We selected mercury chloride, a compound extensively used in animal studies for its ability to cause acute kidney damage.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28437
30 Samples
Download data: TXT
Series
Accession:
GSE226311
ID:
200226311
2.

Assessing kidney injury induced by mercuric chloride in guinea pigs with in vivo and in vitro experiments

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28437
60 Samples
Download data: TXT
Series
Accession:
GSE226313
ID:
200226313
3.

Assessing kidney injury induced by mercuric chloride in guinea pigs with in vivo and in vitro experiments [in vivo]

(Submitter supplied) In this study we tested the ability to predict organ injury from in vivo transcriptomics data in male Hartley guinea pigs at early time points after exposure to mercury chloride (9 and 33 hours). We selected mercury chloride, a compound extensively used in animal studies for its ability to cause acute kidney damage.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28437
30 Samples
Download data: TXT
Series
Accession:
GSE226312
ID:
200226312
4.

In vivo transcriptomic responses to mercury chloride exposure in rat kidney tissue

(Submitter supplied) In this study we tested the ability to predict organ injury from transcriptomics data in Sprague-Dawley rats at early time points after exposure to mercury chloride (10 and 34 hours). We selected mercury chloride, a compound extensively used in animal studies for its ability to cause acute kidney and liver damage.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23945
30 Samples
Download data: TXT
Series
Accession:
GSE147248
ID:
200147248
5.

In vivo transcriptomic responses to thioacetamide exposure in guinea pig liver tissue

(Submitter supplied) In this study we tested the ability to predict organ injury from transcriptomic data in Hartley guinea pigs at early time points after exposure to thioacetamide (9 and 33 hours). We selected thioacetamide, a compound extensively used in animal studies for its ability to cause liver damage.
Organism:
Cavia porcellus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28437
30 Samples
Download data: TXT
Series
Accession:
GSE169545
ID:
200169545
6.

In vivo transcriptomic responses to thioacetamide exposure in rat liver, kidney, and heart tissue

(Submitter supplied) In this study we tested the ability to predict organ injury from transcriptomics data in Sprague-Dawley rats at early time points after exposure to thioacetmide (8 and 24 hours). We selected thioacetamide, an organosulfur compound extensively used in animal studies as a hepatotoxin and carcinogen for its ability to cause acute liver damage.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14844
90 Samples
Download data: TXT
Series
Accession:
GSE120195
ID:
200120195
7.

In vitro transcriptomic responses to thioacetamide-S-oxide exposure in Sprague-Dawley rat primary hepatocytes, renal tube epithelial, and cardiomyocytes

(Submitter supplied) In this study we tested the ability to predict organ injury endpoints from in vitro transcriptomics responses at early time points (9 and 24 hours) after to thioacetamide-S-oxide treatment, the toxic metabolite of thioacetamide. Thioacetamide, an organosulfur compound, have been extensively used in animal studies as a hepatotoxin and carcinogen for its ability to cause acute liver damage.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25947
90 Samples
Download data: TXT
Series
Accession:
GSE134569
ID:
200134569
8.

Ischemic vs. nephrotoxic acute renal failure, early time points (2h and 8h)

(Submitter supplied) Acute renal failure (ARF) has high morbidity and mortality. In animal ARF models, effective treatments must be administered before or shortly after the insult, limiting their clinical potential. We used microarrays to identify early biomarkers that distinguish ischemic from nephrotoxic ARF, or that detect both injury types. We compared rat kidney transcriptomes 2 and 8 hours after ischemia/reperfusion and after mercuric chloride. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL2774
36 Samples
Download data
Series
Accession:
GSE3219
ID:
200003219
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Supplemental Content

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