U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 16

1.

Foxl1-Cre-marked Adult Hepatic Progenitors Have Clonogenic and Bi-Lineage Differentiation Potential - Time Course

(Submitter supplied) The winged helix transcription factor Foxl1 is a marker for progenitor cells and their descendants in the mouse liver in vivo. Here, we purify progenitor cells from Foxl1-Cre; RosaYFP mice and evaluate their proliferative and differentiation potential in vitro. Treatment of Foxl1-Cre; RosaYFP mice with 3,5-diethoxycarbonyl-1,4-dihydrocollidine diet led to an increase of the percentage of YFP-labeled Foxl1+ cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
26 Samples
Download data: TXT
Series
Accession:
GSE28890
ID:
200028890
2.

Foxl1-Cre-marked Adult Hepatic Progenitors Have Clonogenic and Bi-Lineage Differentiation Potential

(Submitter supplied) The winged helix transcription factor Foxl1 is a marker for progenitor cells and their descendants in the mouse liver in vivo. Here, we purify progenitor cells from Foxl1-Cre; RosaYFP mice and evaluate their proliferative and differentiation potential in vitro. Treatment of Foxl1-Cre; RosaYFP mice with 3,5-diethoxycarbonyl-1,4-dihydrocollidine diet led to an increase of the percentage of YFP-labeled Foxl1+ cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL10333 GPL4134
43 Samples
Download data: TXT
Series
Accession:
GSE28892
ID:
200028892
3.

Foxl1-Cre-marked Adult Hepatic Progenitors Have Clonogenic and Bi-Lineage Differentiation Potential - Differentiated vs Primary

(Submitter supplied) The winged helix transcription factor Foxl1 is a marker for progenitor cells and their descendants in the mouse liver in vivo. Here, we purify progenitor cells from Foxl1-Cre; RosaYFP mice and evaluate their proliferative and differentiation potential in vitro. Treatment of Foxl1-Cre; RosaYFP mice with 3,5-diethoxycarbonyl-1,4-dihydrocollidine diet led to an increase of the percentage of YFP-labeled Foxl1+ cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10333
17 Samples
Download data: TXT
Series
Accession:
GSE28891
ID:
200028891
4.

Prospective isolation of a bipotential clonogenic liver progenitor cell in adult mice

(Submitter supplied) The molecular identification of adult hepatic stem/progenitor cells has been hampered by the lack of truly specific markers. To isolate putative adult liver progenitor cells, we used cell surface-marking antibodies, including MIC1-1C3, to isolate subpopulations of liver cells from normal adult mice or those undergoing an oval cell response and tested their capacity to form bilineage colonies in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
16 Samples
Download data: TXT
Series
Accession:
GSE29121
ID:
200029121
5.

Search for markers for biphenotypic hepatocytes

(Submitter supplied) Comparson of Biphenotypic hepatocytes with Mature Hepatocytes
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10333
2 Samples
Download data: TXT
Series
Accession:
GSE78778
ID:
200078778
6.

Small molecule-mediated reprogramming of human hepatocytes into bipotent progenitor cells

(Submitter supplied) Currently, much effort is directed to the development of new cell sources for clinical therapy using cell fate conversion approaches by small molecules. Direct lineage reprogramming to a progenitor state has been reported in terminally differentiated rodent hepatocytes, yet remains a challenge in human hepatocytes. Human hepatocytes were isolated from healthy and diseased donor livers and reprogrammed into progenitor cells by two small molecules, A83-01 and CHIR99021 (AC), in the presence of EGF and HGF. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: TXT
Series
Accession:
GSE114643
ID:
200114643
7.

Transcriptional profiling of bipotential embryonic liver cells to identify liver progenitor cell surface markers.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL339 GPL1261
24 Samples
Download data: CEL
Series
Accession:
GSE6966
ID:
200006966
8.

Transcriptional profiling of bipotential embryonic liver cells to identify liver progenitor cell surface markers (430)

(Submitter supplied) The ability to purify to homogeneity a population of hepatic progenitor cells from adult liver is critical for their characterization prior to any therapeutic application. As a step in this direction, we have utilized gene profiling of a bipotential liver cell line from dpc 14 mouse embryonic liver to catalog genes expressed by liver progenitor cells. These cells, known as Bipotential Mouse Embryonic Liver (BMEL) cells, proliferate in an undifferentiated state and are capable of differentiating into hepatocyte-like and cholangiocyte-like cells in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE6957
ID:
200006957
9.

Transcriptional profiling of bipotential embryonic liver cells to identify liver progenitor cell surface markers (430A)

(Submitter supplied) The ability to purify to homogeneity a population of hepatic progenitor cells from adult liver is critical for their characterization prior to any therapeutic application. As a step in this direction, we have utilized gene profiling of a bipotential liver cell line from dpc 14 mouse embryonic liver to catalog genes expressed by liver progenitor cells. These cells, known as Bipotential Mouse Embryonic Liver (BMEL) cells, proliferate in an undifferentiated state and are capable of differentiating into hepatocyte-like and cholangiocyte-like cells in vitro. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
12 Samples
Download data: CEL
Series
Accession:
GSE6942
ID:
200006942
10.

Human hepatocyte metaplasia in injured humanized mouse livers

(Submitter supplied) The goal of this experiment was to test whether human hepatocytes could give rise to biliary-like progenitor cells in an in vivo context. Here Fah-/- Il2ry-/- Rag2-/-NOD mouse livers were humanized with human hepatocytes. Only hepatocytes engraft in the Fah-/- mouse at detectable levels in this model. Then animals were given chronic liver injury with 0.1% ddc. After injury we measured human-specific transcripts to determine whether the phenotype of the human cells had changed. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL13112 GPL16512
13 Samples
Download data: TXT
Series
Accession:
GSE58679
ID:
200058679
11.

Hepatocyte ductal metaplasia in chronic mouse liver injury

(Submitter supplied) Expression profiling of hepatocytes-derived ductal cells with properties intermediate between mature hepatocytes and cholangiocytes
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
14 Samples
Download data: TXT
Series
Accession:
GSE55552
ID:
200055552
12.

Human embryonic stem cells as a tool to study hepatocyte differentiation

(Submitter supplied) The availability of pluripotent stem cells offers the possibility of using such cells to model hepatic disease and development. With this in mind, we previously established a protocol that facilitates the differentiation of both human embryonic stem cells and induced pluritpotent cells into cells with hepatocyte characteristics. The use of highly defined culture conditions and the avoidance of feeder cells or embryoid bodies allowed synchronous and reproducible differentiation to occur. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3926
Platform:
GPL570
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE25417
ID:
200025417
13.
Full record GDS3926

HNF4A deficiency effect on embryonic stem cell model of hepatocyte differentiation

Analysis of H9 (WAO9) embryonic stem (ES) cells subjected to hepatic differentiation protocol. ES-derived hepatocytes depleted of nuclear hormone receptor HNF4A also examined. Results provide insight into the role of HNF4A during the formation of hepatocytes from pluripotent stem cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 development stage, 2 genotype/variation, 4 time sets
Platform:
GPL570
Series:
GSE25417
12 Samples
Download data: CEL, CHP
14.

Global gene expression analysis for mouse embryonic fibroblasts (MEFs), induced hepatocyte-like (iHep) cells and adult mouse hepatocytes.

(Submitter supplied) In order to characterize iHep cells more precisely, we conducted global gene expression analyses using microarrays to compare among the gene expression profiles of MEFs, iHep cells and adult mouse hepatocytes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
7 Samples
Download data: TXT
Series
Accession:
GSE29725
ID:
200029725
15.

SOX9+/PTF1A+ Cells Define the Tip Progenitor Cells of the Human Fetal Pancreas of the Second Trimester

(Submitter supplied) Significant progress has been made in recent years in characterizing human multipotent progenitor cells (hMPCs) of the early pancreas; however, the identity and persistence of these cells during the second trimester, after the initiation of branching morphogenesis, remain elusive. Additionally, studies on hMPCs have been hindered by few isolation methods that allow for the recovery of live cells. Here, we investigated the tip progenitor domain in the branched epithelium of human fetal pancreas between 13.5 and 17.5 gestational weeks by immunohistological staining. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
1 Sample
Download data: CSV
Series
Accession:
GSE141087
ID:
200141087
16.

Gene expression profile of the stomach from an AGR2 null mouse

(Submitter supplied) The in vivo function of AGR2 was examined by generating an AGR2 null mouse. The mice died prematurely due to hyperplasia and dysplasia of the glandular stomach. Gene expression profiling was performed to compare differences in transcription between wild-type and null AGR2 mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8389
2 Samples
Download data: TXT
Series
Accession:
GSE40062
ID:
200040062
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_662a1ad4862bea0a3fc4e24d|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center