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Links from GEO DataSets

Items: 20

1.

MicroRNA expression profiling of zebrafish heart regeneration

(Submitter supplied) Cardiovascular disease is the leading cause of morbidity and mortality in the Western world due to a limited regenerative capacity. In lieu of new muscle synthesis, the human heart replaces necrotic tissue with deposition of a non-contractile scar. In contrast, the adult zebrafish is endowed with a remarkable regenerative capacity, capable of de novo cardiomyocyte (CM) creation and scar tissue resolution when challenged with an acute injury. more...
Organism:
Danio rerio
Type:
Non-coding RNA profiling by array
Platform:
GPL21083
6 Samples
Download data: TXT
Series
Accession:
GSE74494
ID:
200074494
2.

siRNA knockdown of neonatal rat cardiac myocytes and fibroblasts

(Submitter supplied) Primary neonatal rat cardiac myocytes or fibroblasts were isolated and subjected to siRNA mediated Yap knockdown
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24782
12 Samples
Download data: XLSX
Series
Accession:
GSE112464
ID:
200112464
3.

RNAseq of regenerating yap mutant zebrafish hearts

(Submitter supplied) A Yap knockout zebrafish line was used to observe how loss of Yap affects cardiac regeneration.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24776
12 Samples
Download data: XLSX
Series
Accession:
GSE112452
ID:
200112452
4.

Single-cell analysis uncovers that metabolic reprogramming is essential for cardiomyocyte proliferation in the regenerating heart.

(Submitter supplied) While the heart regenerates poorly in mammals, efficient heart regeneration occurs in certain amphibian and fish species. Zebrafish has been used extensively to study heart regeneration, resulting in a model in which preexisting cardiomyocytes dedifferentiate and reinitiate proliferation to replace the lost myocardium. However, there is limited knowledge about the cellular processes that occur in this rare population of proliferating cardiomyocytes during heart regeneration. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20828
4 Samples
Download data: CSV, TSV
Series
Accession:
GSE139218
ID:
200139218
5.

In vivo activation of a conserved microRNA program induces robust mammalian heart regeneration

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Danio rerio; Rattus norvegicus
Type:
Non-coding RNA profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL14613 GPL18694
7 Samples
Download data: CEL
Series
Accession:
GSE62389
ID:
200062389
6.

In vivo activation of a conserved microRNA program induces robust mammalian heart regeneration (RNA-Seq)

(Submitter supplied) Heart failure is a leading cause of mortality and morbidity in the developed world, partly because mammals lack the ability to regenerate heart tissue. Whether this is due to evolutionary loss of regenerative mechanisms present in other organisms or to an inability to activate such mechanisms is currently unclear. Here, we decipher mechanisms underlying heart regeneration in adult zebrafish and show that the molecular regulators of this response are conserved in mammals. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
2 Samples
Download data: TXT
Series
Accession:
GSE62387
ID:
200062387
7.

In vivo activation of a conserved microRNA program induces robust mammalian heart regeneration (array)

(Submitter supplied) Heart failure is a leading cause of mortality and morbidity in the developed world, partly because mammals lack the ability to regenerate heart tissue. Whether this is due to evolutionary loss of regenerative mechanisms present in other organisms or to an inability to activate such mechanisms is currently unclear. Here, we decipher mechanisms underlying heart regeneration in adult zebrafish and show that the molecular regulators of this response are conserved in mammals. more...
Organism:
synthetic construct; Danio rerio
Type:
Non-coding RNA profiling by array
Platform:
GPL14613
5 Samples
Download data: CEL
Series
Accession:
GSE62386
ID:
200062386
8.

Regulation of microRNA during cardiomyocyte maturation in sheep

(Submitter supplied) Background: There is a limited capacity to repair damage in the mammalian heart after birth, which is primarily due to the inability of cardiomyocytes to proliferate after birth. This is in contrast to zebrafish and salamander, in which cardiomyocytes retain the ability to proliferate throughout life and can regenerate their heart after significant damage. Recent studies in zebrafish and rodents implicate microRNAs (miRNAs) in the regulation of genes responsible for cardiac cell cycle progression and regeneration, in particular, miR-133a, the miR-15 family, miR-199a and miR-590. more...
Organism:
Ovis aries
Type:
Non-coding RNA profiling by array
Platform:
GPL20132
12 Samples
Download data: TXT
Series
Accession:
GSE68496
ID:
200068496
9.

Identification of targets of Vegfc signaling during cardiac regeneration in zebrafish

(Submitter supplied) Purpose:to identify with transcriptomic analysis, gene targets of Vegfc signaling during cardiac regeneration in zebrafish. Results: We were able to identify several differential expressed genes, many of which encode for immune related genes, as well as ECM components.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20828
4 Samples
Download data: TXT
Series
Accession:
GSE168175
ID:
200168175
10.

Tp53 suppression promotes cardiomyocyte proliferation during zebrafish heart regeneration

(Submitter supplied) Transcriptome sequencing of uninjured and regenerating (7dpi) tp53M214K and tp53WT ventricles.
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24776
12 Samples
Download data: TXT
Series
Accession:
GSE146859
ID:
200146859
11.

Fast revascularization of the injured area is essential to support zebrafish heart regeneration

(Submitter supplied) To better understand the possible mechanisms that vegfaa mutants display to compensate for the lack of vegfaa, we performed transcriptomic profiling of vegfaa+/+ and vegfaa-/- ventricles. Total RNA was isolated from hearts extracted from vegfaa+/+ and vegfaa-/- fish (8 months old) pooling 4 hearts per sample.
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL20686
2 Samples
Download data: TXT
Series
Accession:
GSE78945
ID:
200078945
12.

Prrx1b restricts fibrosis and promotes Nrg1-dependent cardiomyocyte proliferation during zebrafish heart regeneration

(Submitter supplied) Fibroblasts are activated to repair the heart following injury. Fibroblast activation in the mammalian heart leads to a permanent fibrotic scar that impairs cardiac function. In other organisms, such as zebrafish, cardiac injury is followed by transient fibrosis and scar-free regeneration. The mechanisms that drive scarring versus scar-free regeneration are not well understood. Here, we show that the homeobox-containing transcription factor Prrx1b is required for scar-free regeneration of the zebrafish heart as the loss of Prrx1b results in excessive fibrosis and impaired cardiomyocyte proliferation. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20828
4 Samples
Download data: CSV, TSV
Series
Accession:
GSE153170
ID:
200153170
13.

Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways

(Submitter supplied) The mammalian heart has poor regenerative capacity following injury. In contrast, certain lower vertebrates such as zebrafish retain a robust capacity for regeneration into adult life. Here we use an integrated approach to identify evolutionary conserved regenerative miRNA-dependant regulatory circuits in the heart. We identified novel miRNA-dependant networks involved in critical biological pathways, which are differentially utilized between the infarcted mouse heart and the regenerating zebrafish heart.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9250
6 Samples
Download data: TXT
Series
Accession:
GSE51019
ID:
200051019
14.

Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways

(Submitter supplied) The mammalian heart has poor regenerative capacity following injury. In contrast, certain lower vertebrates such as zebrafish retain a robust capacity for regeneration into adult life. Here we use an integrated approach to identify evolutionary conserved regenerative miRNA-dependant regulatory circuits in the heart. We identified novel miRNA-dependant networks involved in critical biological pathways, which are differentially utilized between the infarcted mouse heart and the regenerating zebrafish heart.
Organism:
Danio rerio
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9319
8 Samples
Download data: TXT
Series
Accession:
GSE51018
ID:
200051018
15.

Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Danio rerio
Type:
Expression profiling by array; Non-coding RNA profiling by high throughput sequencing
4 related Platforms
34 Samples
Download data: CEL
Series
Accession:
GSE51014
ID:
200051014
16.

Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways

(Submitter supplied) The mammalian heart has poor regenerative capacity following injury. In contrast, certain lower vertebrates such as zebrafish retain a robust capacity for regeneration into adult life. Here we use an integrated approach to identify evolutionary conserved regenerative miRNA-dependant regulatory circuits in the heart. We identified novel miRNA-dependant networks involved in critical biological pathways, which are differentially utilized between the infarcted mouse heart and the regenerating zebrafish heart.
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL1319
8 Samples
Download data: CEL
Series
Accession:
GSE51013
ID:
200051013
17.

Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways

(Submitter supplied) The mammalian heart has poor regenerative capacity following injury. In contrast, certain lower vertebrates such as zebrafish retain a robust capacity for regeneration into adult life. Here we use an integrated approach to identify evolutionary conserved regenerative miRNA-dependant regulatory circuits in the heart. We identified novel miRNA-dependant networks involved in critical biological pathways, which are differentially utilized between the infarcted mouse heart and the regenerating zebrafish heart.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10740
12 Samples
Download data: CEL
Series
Accession:
GSE51012
ID:
200051012
18.

­runx1 controls zebrafish heart regeneration by promoting scar deposition as well as inhibiting myocardial proliferation and survival

(Submitter supplied) Runx1 is a transcription factor that plays a key role in determining the proliferative and differential state of multiple cell types, during both development and adulthood. Here, we report how runx1 is specifically upregulated at the injury site during zebrafish heart regeneration, but unexpectedly, absence of runx1 results in enhanced regeneration. Using single cell sequencing, we found that the wild-type injury site consists of Runx1-positive endocardial cells and thrombocytes that express smooth muscle and collagen genes without differentiating into myofibroblasts. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18413
3 Samples
Download data: H5
Series
Accession:
GSE138181
ID:
200138181
19.

Antagonistic roles of TGF-β ligands during cardiac regeneration in zebrafish

(Submitter supplied) we are comparing sham-injured zebrafish heart samples with 4 days post cryoinjured zebrafish heart samples.
Organism:
Danio rerio
Type:
Expression profiling by array
Platform:
GPL14664
1 Sample
Download data: TXT
Series
Accession:
GSE89259
ID:
200089259
20.

RNA sequencing analyses of grl/hey2-overexpressing hearts and control hearts, as well as grl/hey2-deficient hearts and wild-type hearts following ventricular resection at 7 dpa

(Submitter supplied) As Grl/Hey2 directly binds DNA through E box motifs and mediates transcription repression, we aim to gain insights into potential target genes of Grl/Hey2 during heart regeneration. We performed RNA-seq analyses using total RNAs collected from 4-HT-treated Tg(cmlc2:creER;cmlc2:nRSGG) hearts and Tg(cmlc2:nRSGG) control hearts, as well as grl5nt-/- mutant hearts and wild-type hearts following ventricular resection at 7 dpa. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23085
12 Samples
Download data: XLS, XLSX
Series
Accession:
GSE129499
ID:
200129499
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