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Links from GEO DataSets

Items: 10

1.

SENP3-mediated host defense response contains HBV replication and restores protein synthesis

(Submitter supplied) Certain organs are capable of containing the replication of various types of viruses. In the liver, infection of Hepatitis B virus (HBV), the etiological factor of Hepatitis B and hepatocellular carcinoma (HCC), often remains asymptomatic and leads to a chronic carrier state. Here we investigated how hepatocytes contain HBV replication and promote their own survival by orchestrating a translational defense mechanism via the stress-sensitive SUMO-2/3-specific peptidase SENP3. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
2 Samples
Download data: CSV
2.

Hepatitis B virus deregulates cell cycle to promote viral replication and a premalignant phenotype

(Submitter supplied) Hepatitis B virus (HBV) infection is a major health problem worldwide and chronically infected individuals are at high risk of developing cirrhosis and hepatocellular carcinoma (HCC). The molecular mechanisms whereby HBV causes HCC are largely unknown. By using a biologically relevant system of HBV infection of primary human hepatocytes (PHHs), we studied how HBV perturbs gene expressions and signaling pathways of infected hepatocytes, and whether these effects are relevant to productive HBV infection and HBV-associated HCC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE118295
ID:
200118295
3.

Expression data from CD8alpha positive dendritic cells

(Submitter supplied) We screened a number of interferon inducible genes that may be involved in impeding HBV replication and found an anti-HBV activity in ISG20. ISG20 is an IFN-inducible 3’- to 5’-exonuclease, that degrades DNA and RNA and reduces antigen production in hepatocyte-derived cells A range of candidate genes whose expression was dependent on type I IFN stimulation were identified by gene arrays
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE75690
ID:
200075690
4.

Changes of microRNA expression levels in HBV-infected human primary hepatocytes

(Submitter supplied) Human primary hepatocytes isolated from chimeric mice were infected with HBV for 7 days. The comprehensive changes of miRNA levels were determined by miRNA array.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL17061
2 Samples
Download data: TXT
Series
Accession:
GSE55929
ID:
200055929
5.

Changes of mRNA expression levels in HBV-infected human primary hepatocytes and those cells treated with bionanocapsules containing microRNA-93.

(Submitter supplied) Human primary hepatocytes isolated from chimeric mice were infected with HBV for 7 days. The comprehensive changes of mRNA levels were determined by mRNA array. Also, microRNA93 was delivered into those cells using bionanocapsules to determine the effects of rescue expression of miR93 in HBV replicating cells, because we found that miR93 expression level was downregulated in HBV-infected hepatocytes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13915
4 Samples
Download data: TXT
Series
Accession:
GSE55928
ID:
200055928
6.

Hepatitis B virus-mediated alterations to the primary hepatocyte transcriptome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18694 GPL20084
35 Samples
Download data
Series
Accession:
GSE68113
ID:
200068113
7.

Hepatitis B virus-mediated alterations to the primary hepatocyte transcriptome [Full Set]

(Submitter supplied) Purpose: Chronic infection with hepatitis B virus is the leading global risk factor for the development of liver cancer. A large body of research has shown the many effects an HBV infection has on cellular physiology, particularly on pathways that may be involved in the development of HBV-associated diseases. Unfortunately, a significant portion of this research has been done in systems that may not mimic what is seen in a primary hepatocyte, and is not done on a transcriptome-wide scale. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
23 Samples
Download data: TXT
Series
Accession:
GSE68112
ID:
200068112
8.

Hepatitis B virus-mediated alterations to the primary hepatocyte transcriptome [24 and 48 h]

(Submitter supplied) Purpose: Chronic infection with hepatitis B virus is the leading global risk factor for the development of liver cancer. A large body of research has shown the many effects an HBV infection has on cellular physiology, particularly on pathways that may be involved in the development of HBV-associated diseases. Unfortunately, a significant portion of this research has been done in systems that may not mimic what is seen in a primary hepatocyte, and is not done on a transcriptome-wide scale. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
12 Samples
Download data: TXT
Series
Accession:
GSE66566
ID:
200066566
9.

Expression data from HepG2-NTCP and Huh-106 cell lines

(Submitter supplied) Microarray data to compare the gene expression in HepG2-NTCP and Huh-106 cell lines Knowledge of HBV virus-host interactions is still limited. Here, we performed a genome-wide gain-of-function screen using weakly permissive Huh-106 cells to uncover novel HBV host factors.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE132638
ID:
200132638
10.

Gene expression response to HBV infection in PHH

(Submitter supplied) Hepatitis B virus (HBV) is known for its ability to interact with the host cell DNA methylation machinery. In HBV-infected hepatocytes, this interaction leads to chronic liver diseases, including hepatocellular carcinoma (HCC). We studied the extent of genomic changes induced by natural HBV infection in human primary hepatocytes. Transcriptome and methylome profiles were obtained at different time points post-infection to identify HBV-specific alterations. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
20 Samples
Download data: TXT
Series
Accession:
GSE72068
ID:
200072068
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