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Links from GEO DataSets

Items: 20

1.
Full record GDS4313

Foregut endoderm and combined heart mesoderm and head tissue from E8.5 embryos

Analysis of foregut endoderm and mesoderm/ectoderm from early somite-stage embryos. Foregut definitive endoderm is the precursor of many tissues such as liver, pancreas, oesophagus. Results provide insight into molecular mechanisms underlying early development of the foregut definitive endoderm.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 tissue sets
Platform:
GPL1261
Series:
GSE36453
4 Samples
Download data: CEL
DataSet
Accession:
GDS4313
ID:
4313
2.

Identification of endoderm-specific genes in mouse embryos

(Submitter supplied) The foregut definitive endoderm is the precursor of many tissues including the liver, pancreas, thyroid, lungs, trachea and oesophagus. However, networks and pathways involved in the early development of the definitive endoderm of mammals are not well studied. To identify genes with potential roles in the early development of the foregut definitive endoderm in mouse embryos, we performed microarray analysis to compare the gene expression profile of foregut endoderm and non-endodermal tissues from early somite-stage mouse embryos.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4313
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE36453
ID:
200036453
3.

Sin3a regulates epithelial progenitor cell fate during lung development

(Submitter supplied) Comparison of global transcription profiles in mouse E12.5 embryonic lung from Shh-Cre;Sin3a flox/+ control with Shh-Cre;Sin3a flox/flox revealed a large change genes due to loss of Sin3a in early lung development.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE94306
ID:
200094306
4.

Single cell sequencing of dissected mouse foreguts at embryonic day 8.5 to 9.5

(Submitter supplied) Single cell sequencing of dissected mouse foreguts at embryonic day 8.5 to 9.5
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE136689
ID:
200136689
5.

Transcriptomic changes in the mouse foregut comparing Gli2,3 double mutant to heterozygous controls

(Submitter supplied) We dissected foreguts from Gli2-/-,Gli3-/- and Gli2+/-,Gli3+/- mouse embryos at embryonic day 9.5. Three foreguts were obtained for each group and each foregut was individually processed for bulk RNA extraction and library preparation. Sequencing results identified Gli positively and negatively regulated genes in the foreguts.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: XLSX
Series
Accession:
GSE136687
ID:
200136687
6.

Hedgehog-regulated genes in the chick coelomic epithelium

(Submitter supplied) In the experimental group, the coelomic cavity of HHStage 12-13 chick embryos was electroporated with a plasmid expressing PatchedDLoop2 (a dominant negative hedgehog pathway inhibitor) and GFP. In the control group, a plasmid expressing GFP alone was electroporated. After 14 hours, embryos were dissociated into single cells, FACS sorted, and processed for RNAseq.
Organism:
Gallus gallus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19005
9 Samples
Download data: CSV
Series
Accession:
GSE147540
ID:
200147540
7.

Gene expression pattern between Wild-type and Setd2 knockout mESCs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL1261 GPL11002
8 Samples
Download data: CEL
Series
Accession:
GSE54933
ID:
200054933
8.

Quantitative Analysis of Wild Type(wt) and Setd2 knockout(ko) mESCs Transcriptomes [RNA-Seq]

(Submitter supplied) Purpose: This study aimed at exploring the deregulated genes in setd2 knockout mESCs compared with wt, more particularly to find the mechanism controlled by setd2,which was required for endoderm differentiation. Methods: Setd2 wt and ko mESCs were generated by deep sequencing, using Illumina GAIIx. Using Avadis NGS (version:1.3) software to analyze the sequence reads that passed quality filter to acquire the expression level of all genes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
2 Samples
Download data: TXT
Series
Accession:
GSE54932
ID:
200054932
9.

Comparison of gene expression pattern between Wild-type and Setd2 knockout mESCs [Affymetrix]

(Submitter supplied) SETD2/HYPB has been known as a histone H3K36 specific methyltransferase. However, its roles in physiology such as development and cellular function remain unclear. In this study, using mESCs as cellular model, we show that Setd2 mainly regulates differentiation of murine embryonic stem cells (mESCs) towards primitive endoderm. This study aimed at exploring how did Setd2 regulate primitive endoderm. differentiation. We used microarrays to detail the global programme of gene expression controled by setd2, which is required for endoderm differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE54931
ID:
200054931
10.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development [scRNA_RA_titration]

(Submitter supplied) Developmental defects affecting the pharynx and derived tissues can be found in a variety of syndromes, including DiGeorge, 22q11 deletion, CHARGE and Otofaciocervical syndromes. The associated malformations and dysfunctions of pharynx-derived tissues precipitate phenotypes ranging from malformed features and endocrine disorders to severe immunodeficiency, some of which are associated with high morbidity or elaborate treatment and health care costs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
4 Samples
Download data: H5
Series
Accession:
GSE230563
ID:
200230563
11.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development II

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154
40 Samples
Download data: BIGWIG, NARROWPEAK, TXT
Series
Accession:
GSE222443
ID:
200222443
12.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development [RNA-seq]

(Submitter supplied) Developmental defects affecting the pharynx and derived tissues can be found in a variety of syndromes, including DiGeorge, 22q11 deletion, CHARGE and Otofaciocervical syndromes. The associated malformations and dysfunctions of pharynx-derived tissues precipitate phenotypes ranging from malformed features and endocrine disorders to severe immunodeficiency, some of which are associated with high morbidity or elaborate treatment and health care costs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
8 Samples
Download data: TXT
Series
Accession:
GSE222442
ID:
200222442
13.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development [ChIP-seq]

(Submitter supplied) Developmental defects affecting the pharynx and derived tissues can be found in a variety of syndromes, including DiGeorge, 22q11 deletion, CHARGE and Otofaciocervical syndromes. The associated malformations and dysfunctions of pharynx-derived tissues precipitate phenotypes ranging from malformed features and endocrine disorders to severe immunodeficiency, some of which are associated with high morbidity or elaborate treatment and health care costs. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL18573
25 Samples
Download data: BIGWIG, NARROWPEAK
Series
Accession:
GSE222441
ID:
200222441
14.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development [ATAC-seq]

(Submitter supplied) Developmental defects affecting the pharynx and derived tissues can be found in a variety of syndromes, including DiGeorge, 22q11 deletion, CHARGE and Otofaciocervical syndromes. The associated malformations and dysfunctions of pharynx-derived tissues precipitate phenotypes ranging from malformed features and endocrine disorders to severe immunodeficiency, some of which are associated with high morbidity or elaborate treatment and health care costs. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
7 Samples
Download data: BIGWIG, NARROWPEAK
Series
Accession:
GSE222439
ID:
200222439
15.

Using human pluripotent stem cells to dissect the molecular basis of human pharyngeal endoderm development [scRNA-Seq]

(Submitter supplied) Developmental defects affecting the pharynx and derived tissues can be found in a variety of syndromes, including DiGeorge, 22q11 deletion, CHARGE and Otofaciocervical syndromes. The associated malformations and dysfunctions of pharynx-derived tissues precipitate phenotypes ranging from malformed features and endocrine disorders to severe immunodeficiency, some of which are associated with high morbidity or elaborate treatment and health care costs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TXT
Series
Accession:
GSE221616
ID:
200221616
16.

An RNAi Screen for Skin Morphogenesis Unravels The Complexities of Rho GTPase Networks

(Submitter supplied) During embryogenesis, antagonism and synergy between developmental signaling pathways dictate cell fate decisions. How these circuits orchestrate the complex cellular remodeling needed for tissue morphogenesis remains poorly understood. As effectors of cytoskeletal dynamics, Rho GTPases and their regulators are likely to be involved. However, their daunting complexity has hindered progress in dissecting their functions. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
6 Samples
Download data: TXT
Series
Accession:
GSE123047
ID:
200123047
17.

Identification of the genes exhibiting differential expression along the dorsoventral axis in the tracheoesophageal anlagen.

(Submitter supplied) During development, morphogenetic movement occur that separate the single tube of tracheoesophageal anlagen to the esophagus on the dorsal side and trachea and lung on the ventral side. In this process, signaling factors from the mesoderm induce the function and structure that is specific for esophagus or respiratory system in the lining endoderm. In order to elucidate the mechanism of demarcating these two regions and identify factors that involved in the dorsal and ventral specific inductions, we attempted to identify genes that show different expression in the dorsal and ventral regions using a microarray.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE118641
ID:
200118641
18.

Characterization of the mid-foregut transcriptome identifies genes regulated during lung bud induction.

(Submitter supplied) To identify genes expressed during initiation of lung organogenesis, we generated transcriptional profiles of the prospective lung region of the mouse foregut (mid-foregut) microdissected from embryos at three developmental stages between embryonic day 8.5 (E8.5) and E9.5. This period spans from lung specification of foregut cells to the emergence of the primary lung buds. We identified a number of known and novel genes that are temporally regulated as the lung bud forms. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
9 Samples
Download data: CEL
Series
Accession:
GSE19873
ID:
200019873
19.

Chromatin and tissue plasticity precede commitment to intestinal differentiation during endoderm development

(Submitter supplied) Intestinal differentiation during endoderm development We used RNA-sequencing to profile gene expression changes during the embryonic development of the gastrointestinal tract.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
74 Samples
Download data: TXT
Series
Accession:
GSE115541
ID:
200115541
20.

Identification of the central intermediate in the extra-embryonic to embryonic endoderm transition through single cell transcriptomics

(Submitter supplied) An increasing number of studies suggests that embryonic development is a highly plastic process and that lineage specification can proceed via alternative routes not encompassed in canonically defined germ layers. Despite these recent revisions to fate maps, the differentiation of pluripotent stem cells (PSCs) to specific lineages tends to continue to focus on defined germ layer differentiation. Thus although recent studies suggest that the visceral organs originate from both embryonic and extra-embryonic lineages, PSC differentiation has focused on generating definitive and gut endoderm solely via an embryonic trajectory. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
75 Samples
Download data: TXT
Series
Accession:
GSE164464
ID:
200164464
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