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Links from GEO DataSets

Items: 7

1.

The gene expression profile of humanized rat livers

(Submitter supplied) We investigated the transcriptome of repopualted human hepatocytes in humanized rat livers.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24688
2 Samples
Download data: XLSX
Series
Accession:
GSE162862
ID:
200162862
2.

RNA-seq transcriptional profiling in primary human hepatocyte(in vitro/in vivo) and Proliferting human hepatocyte(in vitro/in vivo)

(Submitter supplied) The source of human hepatocytes (HHs) is limited because of the shortage of donor organs and the difficulty to expand them in vitro. We developed a defined medium to expand HHs for about 10,000-fold in numbers. The proliferating HHs are bi-phenotypic, showing partially maintained hepatic features and additionally gained expression of progenitor-associated genes. Importantly, proliferating HHs extensively engraft in injured mouse livers at the level comparable to primary HHs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
22 Samples
Download data: TXT
3.

Expansion, in vivo-ex vivo cycling and genetic manipulation of primary human hepatocytes

(Submitter supplied) Primary human hepatocytes (PHH) are an essential tool for modeling drug metabolism and liver disease. However, variable plating efficiencies, short lifespan in culture and resistance to genetic manipulation have limited their use. Here we show that retrorsine improves human hepatocyte repopulation of chimeric mice to levels where poor donor PHH can be isolated for ex vivo cultures. Mouse-passaged (mp)PHH cultures overcome the marked donor-to-donor variability of cryopreserved PHH and remain functional for months, as demonstrated by metabolic assays and infection with hepatitis B virus and Plasmodium falciparum. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: TXT
4.

The whole genome effects of the PPARα agonist fenofibrate on livers of hepatocyte humanized mice

(Submitter supplied) The role of PPARα in gene regulation in mouse liver is well characterized. However, less is known about the effect of PPARα activation in human liver. The aim of the present study was to better characterize the impact of PPARα activation on gene regulation in human liver by combining transcriptomics with the use of hepatocyte humanized livers. To that end, chimeric mice containing hepatocyte humanized livers were given an oral dose of 300 mg/kg fenofibrate daily for 4 days. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platform:
GPL11532
6 Samples
Download data: CEL
Series
Accession:
GSE107041
ID:
200107041
5.

Conversion of mouse fibroblast to hepatocyte-like cells by defined factors

(Submitter supplied) Plasticity of differentiated cells has been proved by nuclear transfer, induced pluripotent cells and transdifferentiation. Here we show that by transduction of 3 factors (Hnf1alpha, Gata4, and Foxa3) and p19Arf inactivation, tail-tip fibroblasts can be converted to hepatocyte-like (iHep) cells, expressing hepatocyte marker genes, and acquiring many mature hepatocyte functions in vitro and in vivo.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
13 Samples
Download data: TXT
Series
Accession:
GSE23635
ID:
200023635
6.

Genomic and epigenomic characterization of regenerating hepatocytes

(Submitter supplied) To gain a deeper understanding of the genetic basis of liver repopulation after injury, we utilize an innovative technique to profile the expression changes and chromatin landscape during the regenerative response. We utilize the Fah-/- mouse, a model for hereditary tyrosinemia deficient in fumarylacetoacetate hydrolase (FAH), that undergoes repopulation with FAH-expressing hepatocytes. We employ translating ribosome affinity purification followed by RNA-sequencing (TRAP-seq) and assay for transposase accessible chromatin using sequencing (ATAC-seq) to specifically isolate regenerating hepatocytes and performed high-throughput sequencing to identify the dynamic genomic and epigenomic changes during liver repopulation.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21103 GPL17021
26 Samples
Download data: BIGWIG, XLS
Series
Accession:
GSE109466
ID:
200109466
7.

Impairment of host liver repopulation by transplanted hepatocytes in aged rats and the release by short-term growth hormone treatment

(Submitter supplied) By using high-density DNA microarrays, we analyzed the gene-expression profile of liver biopsies from young and aged donors Stock et al., accepted
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
2 Samples
Download data: CEL
Series
Accession:
GSE87889
ID:
200087889
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Supplemental Content

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