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Links from GEO DataSets

Items: 20

1.

Investigate the role of Wnt/beta-catenin signaling in development of the exocrine pancreas

(Submitter supplied) beta-catenin is an essential mediator of canonical Wnt signaling and a central component of the cadherin-catenin epithelial adhesion complex. Dysregulation of beta-catenin expression has been described in pancreatic neoplasia. Newly published studies have suggested that beta-catenin is critical for normal pancreatic development although these reports reached somewhat different conclusions. In addition, the molecular mechanisms by which loss of beta-catenin affects pancreas development are not well understood. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE7430
ID:
200007430
2.

Beta-catenin hyperactivation in embryonic pancreas

(Submitter supplied) We used microarrays to detail the global programme of gene expression underlying beta catenin activation in embryonic pancreas.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
6 Samples
Download data: CEL
Series
Accession:
GSE82342
ID:
200082342
3.

Expression data from mouse embryonic stem cells

(Submitter supplied) Analysis of the transcriptome of ß-catenin flox/- mES cells in comparison with ß-catenin null mES cells or ß-catenin null mES cells stably transfected with an E-cadherin-α-catenin fusion protein. Expression assay was performed using the Affymetrix GeneChip Mouse Gene 1.0 ST array.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
9 Samples
Download data: CEL
Series
Accession:
GSE44543
ID:
200044543
4.

Expression data from mice neonatal pancreas (P1, same litter as control and Elastase-Cre mediated Pdx1cKO)

(Submitter supplied) During embryogenesis, exocrine and endocrine pancreatic tissues are formed in distinct regions within the branched ductal structure in mice. We previously reported that exocrine-specific inactivation of Pdx1, an indispensable gene for pancreatogenesis, by Elastase-Cre caused not only hypoplastic exocrine formation but also substantial endocrine defects resulting in diabetic phenotype, indicating the existence of exocrine-driven factor(s) that regulate proper endocrine development. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
5 Samples
Download data: CEL
Series
Accession:
GSE118665
ID:
200118665
5.

PERK role in the exocrine pancreas

(Submitter supplied) Molecular characterization of PERK's role in the mouse exocrine pancreas. Postnatal days 16, 19 and 32 were examined. Postnatal day 16 represents a stage immediately prior to severe cytological changes in the exPKO mice. Postnatal day 19 represents the initial stage of severe phenotypes in the exPKO mice. Postnatal day 32 represents the middle stage of severe phenotypes (about 2 wks from the initiation) in the exPKO mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
8 Samples
Download data
Series
Accession:
GSE4422
ID:
200004422
6.

Expression data from wildtype, MIST1-null, and induced MIST1 Mus musculus pancreata

(Submitter supplied) Although early developmental processes involve cell fate decisions that define the body axes and establish progenitor cell pools, development does not cease once cells are specified. Instead, most cells undergo specific maturation events where changes in the cell transcriptome ensure that the proper gene products are expressed to carry out unique physiological functions. Pancreatic acinar cells mature post-natally to handle an extensive protein synthetic load, establsih organized apical-basal polarity for zymogen granule trafficking, and assemble gap-junctions to perimt efficient cell-cell communication. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4341
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE34232
ID:
200034232
7.
Full record GDS4341

Transcription factor MIST1-null and MIST1-induced pancreas

Analysis of pancreas from C57BL/6 adults with Mist1-null phenotype rescued by tamoxifen-induced Mist1 expression. Embryonic knockout of Mist1 leads to acinar cell dysfunction, disrupting pancreatic function. Results provide insight into the role of Mist1 in regulating mature acinar properties.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 genotype/variation sets
Platform:
GPL6246
Series:
GSE34232
12 Samples
Download data: CEL
8.

Hippo Signaling Regulates Differentiation and Maintenance in the Exocrine Pancreas

(Submitter supplied) The Hippo signaling pathway has become recognized as a context-dependent regulator of cell proliferation, differentiation, and apoptosis in species ranging from Drosophila to human. In this study, we sought to understand whether Hippo signaling plays a role in pancreatic development and organ homeostasis.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
10 Samples
Download data: CEL, CHP
Series
Accession:
GSE44298
ID:
200044298
9.

Comparison of Hox6 mutant and control E12.5 mouse pancreas

(Submitter supplied) Hox genes are critical developmental transcription factor. We found that in mice with disrupted expression of Hoxa6, Hoxb6 and Hoxc6 there is significantly disrupted endocrine pancreas development. We used microarray analysis to probe for possible molecular mechanisms involed in Hox6 signaling in pancreas development.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE68390
ID:
200068390
10.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21103 GPL13112
32 Samples
Download data: BW
Series
Accession:
GSE91056
ID:
200091056
11.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance [ChIP-seq batch3]

(Submitter supplied) Aberrant activation of embryonic signaling pathways is frequent in pancreatic ductal adenocarcinoma (PDA) making developmental regulators therapeutically attractive. Here, we demonstrate diverse functions for PDX1, a transcription factor indispensable for pancreas development, in the progression from normal exocrine cells to metastatic PDA. We identify a critical role for PDX1 in maintaining acinar cell identity, thus resisting the formation of PanIN-derived PDA. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BW
Series
Accession:
GSE91055
ID:
200091055
12.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance [ChIP-seq batch2]

(Submitter supplied) Aberrant activation of embryonic signaling pathways is frequent in pancreatic ductal adenocarcinoma (PDA) making developmental regulators therapeutically attractive. Here, we demonstrate diverse functions for PDX1, a transcription factor indispensable for pancreas development, in the progression from normal exocrine cells to metastatic PDA. We identify a critical role for PDX1 in maintaining acinar cell identity, thus resisting the formation of PanIN-derived PDA. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: BW
Series
Accession:
GSE91054
ID:
200091054
13.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance [ChIP-seq batch1]

(Submitter supplied) Aberrant activation of embryonic signaling pathways is frequent in pancreatic ductal adenocarcinoma (PDA) making developmental regulators therapeutically attractive. Here, we demonstrate diverse functions for PDX1, a transcription factor indispensable for pancreas development, in the progression from normal exocrine cells to metastatic PDA. We identify a critical role for PDX1 in maintaining acinar cell identity, thus resisting the formation of PanIN-derived PDA. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BW
Series
Accession:
GSE91053
ID:
200091053
14.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance [RNA-seq]

(Submitter supplied) Aberrant activation of embryonic signaling pathways is frequent in pancreatic ductal adenocarcinoma (PDA) making developmental regulators therapeutically attractive. Here, we demonstrate diverse functions for PDX1, a transcription factor indispensable for pancreas development, in the progression from normal exocrine cells to metastatic PDA. We identify a critical role for PDX1 in maintaining acinar cell identity, thus resisting the formation of PanIN-derived PDA. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
24 Samples
Download data: XLSX
Series
Accession:
GSE91052
ID:
200091052
15.

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance

(Submitter supplied) Aberrant activation of embryonic signaling pathways is frequent in pancreatic ductal adenocarcinoma (PDA) making developmental regulators therapeutically attractive. Here, we demonstrate diverse functions for PDX1, a transcription factor indispensable for pancreas development, in the progression from normal exocrine cells to metastatic PDA. We identify a critical role for PDX1 in maintaining acinar cell identity, thus resisting the formation of PanIN-derived PDA. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
3 Samples
Download data: TXT
Series
Accession:
GSE90775
ID:
200090775
16.

Genome-wide analysis of gene expression from islets of different sizes in response to in vivo serpin B13 mAB treatment

(Submitter supplied) By using oligonucleotide microarray-based technology as a tool for rapid mapping of unique differences in gene expression, we found that inhibiting serpin B13 in BALB/c mice treated with a mAb according to our protocol resulted in the upregulation of relatively few genes, including several Reg genes, which have been implicated in β-cell proliferation.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17543
6 Samples
Download data: IDAT, TXT
Series
Accession:
GSE125151
ID:
200125151
17.

Lamin A/C ablation in pancreatic acinar cells

(Submitter supplied) Lamin A/C was ablated in pancreatic acinar cells using Elastase1 driven, Cre-ErT mediated, LoxP recombination, causing excision of exons 10 and 11 of the Lmna gene
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
8 Samples
Download data: CEL
Series
Accession:
GSE97396
ID:
200097396
18.

Global activation of embryonic colon gene expression in murine colon tumor models and human colorectal cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL3899 GPL570
226 Samples
Download data
Series
Accession:
GSE5261
ID:
200005261
19.

Large-scale deployment of embryonic gene programming in human and murine colon cancer: a new target for intervention.

(Submitter supplied) Goal of the experiment: To identify and understand the overall transcriptional programming of human colorectal cancer tumors by evaluating gene expression profiles of tumors from four murine models, and comparing and contrasting these to the developing stages of the mouse embryonic colon. Experiment description: Colorectal cancer results from multiple genetic and epigenetic events that produce variable histologies and clinical outcomes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
105 Samples
Download data: TXT
Series
Accession:
GSE5206
ID:
200005206
20.

Mouse models of human colon cancer and mouse colon development

(Submitter supplied) Goal of the experiment: To identify transcriptional patterns across tumors from colorectal cancer murine models and normal mouse colon samples at different developmental stages. Experiment description: Colorectal cancer (CRC) results from multiple genetic and epigenetic events that produce variable histologies and clinical outcomes. To identify gene regulatory programs that underlie colon tumorigenesis, we profiled gene expression in 39 mouse colon tumors from four independent mouse models and compared this to mouse colon embryonic development, as well as with 100 human colon carcinomas. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL3899
79 Samples
Download data
Series
Accession:
GSE5204
ID:
200005204
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