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Links from GEO DataSets

Items: 6

1.
Full record GDS4492

FHH.Pkhd1 model of autosomal recessive polycystic kidney disease

Analysis of kidneys from 30 day-old males representing SD, FHH, PCK, and FHH.Pkhd1 strains. The FHH.Pkhd1 strain carries the PCK Pkhd1 mutation but is resistant to the development of ARPKD. Results provide insight into the molecular mechanisms that modulate ARPKD disease progression and severity.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, transformed count, 4 strain sets
Platform:
GPL1355
Series:
GSE33056
12 Samples
Download data: CEL
2.

Expression data from polycystic kidney disease susceptible and resistant rat strains

(Submitter supplied) To facilitate the search for genetic modifiers that modulate ARPKD disease progression and severity, we sought to generate a congenic rat model that carries the PCK Pkhd1 mutation but is resistant to the development of ARPKD. We transferred the Pkhd1 mutation from the PCK rat onto the genetic background of the FHH (Fawn-Hooded Hypertensive) rat. This newly developed strain, called FHH.Pkhd1, showed significant amelioration of renal disease, and delayed onset of biliary abnormalities. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS4492
Platform:
GPL1355
12 Samples
Download data: CEL
Series
Accession:
GSE33056
ID:
200033056
3.

Global gene expression profiling in PPAR-γ agonist-treated kidneys in an orthologous rat model of human autosomal recessive polycystic kidney disease

(Submitter supplied) Kidneys are enlarged by aberrant proliferation of tubule epithelial cells leading to the formation of numerous cysts, nephron loss, and interstitial fibrosis in polycystic kidney disease (PKD). Pioglitazone (PIO), a PPAR-γ agonist, decreased cell proliferation, interstitial fibrosis and inflammation, and ameliorated PKD progression in PCK rats. To examine the genetic mechanisms in this efficacy, we analyzed changes in global gene expression. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL4135
2 Samples
Download data: TXT
Series
Accession:
GSE35167
ID:
200035167
4.

MALDI imaging MS reveals candidate lipid markers of polycystic kidney disease

(Submitter supplied) Autosomal recessive polycystic kidney disease is a severe, monogenetically inherited kidney and liver disease and PCK rats carrying the orthologous mutant gene serve as a model of human disease. We combined selective MALDI imaging of sulfated kidney lipids and Fisher discriminant analysis of imaging data sets for identification of candidate lipid markers of progressive disease in PCK rats. Our study highlights strong increases in lower mass lipids as main classifiers of cystic disease. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL17378
12 Samples
Download data: CEL
Series
Accession:
GSE48357
ID:
200048357
5.

An organoids-on-a-chip model of human ARPKD

(Submitter supplied) Microarray of kidney organoids derived from PKHD1 mutant human pluripotent stem cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13915
6 Samples
Download data: TXT
Series
Accession:
GSE190272
ID:
200190272
6.

Genome-wide analysis of perinatal effect of nitric oxide (NO) donor molsidomine on the kidneys of Fawn-Hooded Hypertensive (FHH) rats at different ages

(Submitter supplied) Microarray was performed on kidneys in molsidomine-treated FHH rats in order to gain understanding why perinatal treatment with molsidomine in FHH was beneficial in FHH offspring (e.g. lower blood pressure and less renal damage)
Organism:
Rattus norvegicus
Type:
Genome variation profiling by SNP array
Platform:
GPL6101
62 Samples
Download data: TXT
Series
Accession:
GSE27725
ID:
200027725
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