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Links from GEO DataSets

Items: 20

1.

Tmem88a Mediates GATA-dependent Specification of Cardiomyocyte Progenitors by Restricting Canonical WNT Signaling

(Submitter supplied) We sequenced mRNA from zebrafish wild-type embryos, gata5 morphants, gata6 morphants, and gata5/6 morphants at bud and 6-somite developmental stages to identify genes co-operatively regulated by gata5 and gata6 during cardiomyocyte progenitor specification.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15583
16 Samples
Download data: TSV
Series
Accession:
GSE44026
ID:
200044026
2.

TMEM88 knockdown during human embryonic stem cell cardiac differentiation

(Submitter supplied) TMEM88 is indispensable for heart development and acts in the pre-cardiac mesoderm to specify lineage commitment of the cardiovascular progenitor cell through inhibition of Wnt signaling.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5077
Platform:
GPL10558
4 Samples
Download data: TXT
Series
Accession:
GSE43805
ID:
200043805
3.
Full record GDS5077

Transmembrane protein 88 depletion effect on stem cell cardiac differentiation in vitro

Analysis of RUES2 stem cells first depleted for transmembrane protein 88 (TMEM88) and then induced to differentiate into cardiac cells. RUES cells examined at day 5 of differentitation. Results provide insight into the role of TMEM 88 in cardiac cell differentiation.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 other, 2 protocol sets
Platform:
GPL10558
Series:
GSE43805
4 Samples
Download data
DataSet
Accession:
GDS5077
ID:
5077
4.

Comparison of cardiomyocyte transcripts after knockdown of Gata4 in zebrafish embryos

(Submitter supplied) The Gata4 transcription factor is essential for normal heart development, but the molecular basis for its function remain poorly understood. We profiled at the whole genome level transcript changes in cardiomyocytes when Gata4 is depleted from zebrafish embryos. Our objective was to elucidate the cardiomyocyte-specific molecular program functioning downstream of Gata4 in order to better understand the role of Gata4 in cardiac morphogenesis.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL14875 GPL9319
6 Samples
Download data: TXT, WIG
Series
Accession:
GSE44233
ID:
200044233
5.

Two Forkhead transcription factors regulate cardiac progenitor specification by controlling the expression of receptors of the fibroblast growth factor and Wnt signaling pathways

(Submitter supplied) Cardiogenesis involves multiple biological processes acting in concert during development, a coordination achieved by the regulation of diverse cardiac genes by a finite set of transcription factors (TFs). Previous work from our laboratory identified the roles of two Forkhead TFs, Checkpoint suppressor homologue (CHES-1-like) and Jumeau (Jumu) in governing cardiac progenitor cell divisions by regulating Polo kinase activity. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL1322
9 Samples
Download data: CEL
Series
Accession:
GSE65439
ID:
200065439
6.

Two Forkhead transcription factors regulate the division of cardiac progenitor cells by a Polo-dependent pathway - II

(Submitter supplied) The development of a complex organ requires the specification of appropriate numbers of each of its constituent cell types, as well as their proper differentiation and correct positioning relative to each other. During Drosophila cardiogenesis, all three of these processes are controlled by jumeau (jumu) and Checkpoint suppressor homologue (CHES-1-like), two genes encoding forkhead transcription factors that we discovered utilizing an integrated genetic, genomic and computational strategy for identifying novel genes expressed in the developing Drosophila heart. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL1322
6 Samples
Download data: CEL
Series
Accession:
GSE34946
ID:
200034946
7.

An integrated strategy for analyzing the unique developmental program of different myoblast subtypes

(Submitter supplied) An important but largely unmet challenge in understanding the mechanisms that govern formation of specific organs is to decipher the complex and dynamic genetic programs exhibited by the diversity of cell types within the tissue of interest. Here, we use an integrated genetic, genomic and computational strategy to comprehensively determine the molecular identities of distinct myoblast subpopulations within the Drosophila embryonic mesoderm at the time that cell fates are initially specified. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Dataset:
GDS1739
Platform:
GPL72
54 Samples
Download data: CEL
Series
Accession:
GSE3854
ID:
200003854
8.
Full record GDS1739

Primary mesodermal cells from various mutants perturbed for muscle development

Analysis of primary mesodermal cells from mutant embryos perturbed for the development of founder cells, fusion-competent myoblasts, or both myoblast types. 12 mutant genotypes examined. Results identify candidate myoblast subpopulation-specific genes and provide insight into embryonic myogenesis.
Organism:
Drosophila melanogaster
Type:
Expression profiling by array, transformed count, 13 genotype/variation, 3 other, 2 protocol sets
Platform:
GPL72
Series:
GSE3854
54 Samples
Download data: CEL
DataSet
Accession:
GDS1739
ID:
1739
9.

The flow responsive transcription factor Klf2 is required for myocardial wall integrity by modulating Fgf signaling

(Submitter supplied) Complex interplay between cardiac tissues is crucial for their integrity. The flow responsive transcription factor KLF2, which is expressed in the endocardium, is vital for cardiovascular development but its exact role remains to be defined. To this end, we mutated both klf2 paralogues in zebrafish, and while single mutants exhibit no obvious phenotypes, double mutants display a novel phenotype of cardiomyocyte extrusion towards the abluminal side. more...
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL19785
2 Samples
Download data: TXT
Series
Accession:
GSE122137
ID:
200122137
10.

Comparison of tbx5-positive ventricular cardiomyoctes with the rest of ventricular cardiomyocytes from adult zebrafish hearts

(Submitter supplied) In vertebrates, the heart has two main layers of cardiac muscle, a peripheral compact layer and an internal trabecular layer. Little is known on the differerences in gene expression between both layers. In zebrafish the outer layer is named cortical layer and the internal also trabecular layer. Here we used a double transgenic line labelling with GFP tbx5-positive cells and cardiomyoctes with nuclear DsRed (nucDsRed) to distinguish cortical from trabecular myocardium. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18413
8 Samples
Download data: XLS
Series
Accession:
GSE87596
ID:
200087596
11.

Vegetally localised Vrtn functions as a novel repressor to modulate bmp2b transcription during dorsoventral patterning in zebrafish

(Submitter supplied) The vegetal pole cytoplasm represents a crucial source of maternal dorsal determinants for patterning the dorsoventral axis of the early embryo. Removal of the vegetal yolk in the zebrafish fertilised egg before the completion of the first cleavage results in embryonic ventralisation, but removal of this part at the two-cell stage leads to embryonic dorsalisation. How this is achieved remains unknown. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL14875
2 Samples
Download data: TXT
Series
Accession:
GSE103090
ID:
200103090
12.

GATA factors efficiently direct cardiac fate from ESCs

(Submitter supplied) Gata5 efficiently promotes cardiomyocyte fate from murine ESCs.By removing serum from the culture conditions, GATA4 and GATA6 are each also able to efficiently promote cardiogenesis in ESC derivatives, with some distinctions. Thus, GATA factors can function in ESC derivatives upstream of other cardiac transcription factors to direct specification of progenitors with cardiac potential. We used microarray to compared the global gene expression of Gata5-induced cardiac cells with other growth factor directed ESC-derived cardiac cells
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
1 Sample
Download data: CEL, CHP
Series
Accession:
GSE43831
ID:
200043831
13.

An orthologous epigenetic gene expression signature derived from differentiating embryonic stem cells identifies regulators of cardiogenesis

(Submitter supplied) We report a time course of RNA-seq data from wild-type embryonic stem cells and embryonic stem cells in which the cardiogenic transcription factors ZNF503, ZEB2 and NKX2-5 are depleted with shRNAs differentiating along the cardiac lineage.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
34 Samples
Download data: TXT
Series
Accession:
GSE69618
ID:
200069618
14.

Whole transcriptome analysis of reaggregated embryoid bodies treated with IWR-1

(Submitter supplied) We identified distict mesodermal sub-populations based on Endoglin (Eng) and Flk1 expression in Brachyury (Bry) positive cells. By using whole-transcriptome analysis, we further characterized these populations and how they changed when Wnt pathway is inhibited
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: XLS
Series
Accession:
GSE85855
ID:
200085855
15.

Genome wide analysis of SMAD1 binding in mouse mesodermal cells treated or not with the WNT inhibitor IWR1

(Submitter supplied) Using chromatin-immunoprecipitation followed by next-generation sequencing, we studied the effect of WNT pathway inhibition of the binding of SMAD1 in mouse mesodermal cells from Embryoid Bodies (EB) cultures. The WNT inhibitor IWR1 (or the vehicle control DMSO) were added in day 3 EB cultures and cells were collected 24h later for ChIP assay.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE85797
ID:
200085797
16.

Expression data comparing wild-type and spt mutant zebrafish tissues at two developmental time points.

(Submitter supplied) Mesoderm differentiation in zebrafish relies on a complex interaction between transcription factors and signaling pathways. Tbx16 is a t-box transcription factor involved in this interaction. Here, we examine downstream targets of tbx16 in the intermediate mesoderm at the 4/5-somite stage and tail mesoderm at the 21-somite stage by comparing wild-type tissues with tissues from the tbx16 mutant, spadetail (spt).
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL1319
11 Samples
Download data: CEL
Series
Accession:
GSE19955
ID:
200019955
17.

Transcriptional profiling of embryonic zebrafish expressing a mutant TNNT2

(Submitter supplied) Transcriptional profiling of embryonic zebrafish injected with a control morpholino or a morpholino that causes exclusion of TNNT2 exon 13.
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL6457
4 Samples
Download data: TXT
Series
Accession:
GSE20179
ID:
200020179
18.

Characterization of Wnt-Tcf functions during Ciona heart development

(Submitter supplied) To assay Tcf functions during early cardiopharyngeal specification, bulk RNAseq were performed to profile the FACS-purified cardiopharyngeal lineage cells isolated from 15 and 18hpf Ciona larvae with CRISPR/Cas9-mediated Tcf mutagenesis.
Organism:
Ciona robusta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23563
8 Samples
Download data: TXT
Series
Accession:
GSE123295
ID:
200123295
19.

Single-cell transcriptomic analysis of embryonic vasculogenesis identifies the conversion of Etv2-deficient vascular progenitors into skeletal muscle

(Submitter supplied) During vertebrate embryogenesis, vascular endothelial cells originate in the lateral plate mesoderm (LPM) next to the progenitors of skeletal muscle. It is currently not clear what prevents vascular progenitors from responding to the adjacent signals that promote muscle development. An ETS transcription factor Etv2 functions as an evolutionarily conserved master regulator of vasculogenesis. Here we performed single-cell transcriptomic analysis of hematovascular development in wild-type and etv2 mutant zebrafish embryos. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18413
2 Samples
Download data: TXT, ZIP
Series
Accession:
GSE142484
ID:
200142484
20.

Cohesin composition and dosage independently affect early development in zebrafish

(Submitter supplied) Cohesin, a chromatin-associated protein complex with four core subunits (Smc1a, Smc3, Rad21 and either Stag1 or 2), has a central role in cell proliferation and gene expression in metazoans. Human developmental disorders termed “cohesinopathies” are characterised by germline mutations in cohesin or its regulators that do not entirely eliminate cohesin function. However, it is not clear if mutations in individual cohesin subunits have independent developmental consequences. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18413
2 Samples
Download data: MTX, TSV
Series
Accession:
GSE248952
ID:
200248952
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