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Links from GEO DataSets

Items: 19

1.
Full record GDS1486

Serum response factor null mutation effect on neonatal cardiomyocytes

Analysis of serum response factor (SRF)-null neonatal cardiomyocytes. SRF is a transcriptional regulator required for mesodermal development and implicated in myogenesis. Results provide insight into the role of SRF in regulating genetic programs important for controlling cardiomyocyte function.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE3181
6 Samples
Download data
DataSet
Accession:
GDS1486
ID:
1486
2.

SRF-null neonatal cardiomyocytes

(Submitter supplied) Serum Response Factor (SRF) is a transcriptional regulator required for mesodermal development. Numerous studies have implicated SRF as a central regulator of muscle gene expression and myogenesis. In this present study we used a loss of function approach to delineate the role of SRF in cardiac myocyte gene expression and function. In SRF null neonatal cardiomyocytes, we observe severe defects in the contractile apparatus, including Z-disc and stress fiber formation, as well as mislocalization and/or attenuation of sarcomeric proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1486
Platform:
GPL1261
6 Samples
Download data
Series
Accession:
GSE3181
ID:
200003181
3.

Gene expression analysis in mice with heart muscle-specific repression of CELF activity (MHC-CELFdelta)

(Submitter supplied) Members of the CUG-BP, Elav-like family (CELF) regulate alternative splicing in the heart. In MHC-CELFdelta transgenic mice, CELF splicing activity is inhibited postnatally in heart muscle via expression of a nuclear dominant negative CELF protein under an a-myosin heavy chain promoter. MHC-CELFdelta mice develop dilated cardiomyopathy characterized by alternative splicing defects, enlarged hearts, and severe contractile dysfunction. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
12 Samples
Download data: TXT
Series
Accession:
GSE40677
ID:
200040677
4.

Next Generation Sequencing Quantitative Analysis of Srf-regulated Transcriptomes in mouse cardiomyocytes during cardiomyocyte maturation [exp2]

(Submitter supplied) The goal of this study is to analyze the impact of Srf overexpression on transcription during cardiomyocyte maturation in mouse
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE116030
ID:
200116030
5.

Genome-wide SRF occupancy on chromatin in mouse heart ventricles

(Submitter supplied) The goal of this study is to analyze genome-wide Srf binding to chromatin in mouse heart during heart maturation
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
7 Samples
Download data: BW
Series
Accession:
GSE109504
ID:
200109504
6.

Next Generation Sequencing Quantitative Analysis of Srf-regulated Transcriptomes in mouse cardiomyocytes during cardiomyocyte maturation [exp1]

(Submitter supplied) The goal of this study is to analyze the role of Srf in transcriptional analysis during cardiomyocyte maturation in mouse
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: TXT
Series
Accession:
GSE109425
ID:
200109425
7.

Genome-wide analysis of kainic acid-induced gene expression in dentate gyrus from CTR and SRF knockout mice.

(Submitter supplied) To identify genes regulated by SRF in response to increased neuronal activity whole-genome expression profiling (Illumina Mouse WG-6 microarrays) of kainic acid-induced genes were performed. We found that loss of SRF in DG leads to specific deficits in activity-induced gene expression. Identified genes functions are associated with synapse plasticity, epilepsy, outgrowth of neurites, behavior and MAPK signaling pathway.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17543
22 Samples
Download data: TXT
Series
Accession:
GSE60772
ID:
200060772
8.

SRF is required for neutrophil migration in response to inflammation

(Submitter supplied) RNA expression in Srf wildtype and knockout primary bone marrow derived mature neutrophils was determined via RNA sequencing
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE55090
ID:
200055090
9.

The influence of the deletion of Serum Response Factor in B cells

(Submitter supplied) Serum response factor (SRF), a MADS-box transcription factor, is essential for murine embryonic development and for the function of muscle cells and neurons. SRF and its transcriptional co-factors are broadly expressed. To determine the in vivo role of SRF in developing lymphocytes we specifically inactivated the murine Srf gene during T or B cell development using lymphocyte-specific Cre transgenic mouse lines. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2805
Platform:
GPL339
4 Samples
Download data: CEL
Series
Accession:
GSE7412
ID:
200007412
10.
Full record GDS2805

Serum response factor deficient B cells

Analysis of IgM+ IgD+ B cells lacking the Serum response factor (SRF) gene. SRF is a MADS-box transcription factor that is essential in embryonic development and in neuron and muscle cell function. Results provide insight into the role of SRF in lymphocyte development.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL339
Series:
GSE7412
4 Samples
Download data: CEL
DataSet
Accession:
GDS2805
ID:
2805
11.

Srf is essential for mesodermal cell migration during elongation of the embryonic body axis

(Submitter supplied) Timecourse analysis of SRF dependent genes in the nascent mesoderm of mouse embryos. Srf was conditionally deleted by a T::cre driver and the three embryonic stages analyzed represent embryos before onset of the phenotype (E8.5) and progressive appearance of the phenotype (E8.75 and E9.0).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
24 Samples
Download data: TXT
Series
Accession:
GSE44406
ID:
200044406
12.

Disruption of the Circadian Clock within the Cardiomyocyte

(Submitter supplied) Disruption of the Circadian Clock within the Cardiomyocyte Influences Myocardial Contractie Function, Metabolism, and Gene Expression Virtually every mammalian cell, including cardiomyocytes, possesses an intrinsic circadian clock. The role of this transcriptionally-based molecular mechanism in cardiovascular biology is poorly understood. We hypothesized that the circadian clock within the cardiomyocyte influences diurnal variations in myocardial biology. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6333
130 Samples
Download data: XLS
Series
Accession:
GSE10045
ID:
200010045
13.

Serum Response Factor binding in Dstn-corn1 mutant and WT murine cornea

(Submitter supplied) We report the application of chromatin immunoprecipitation sequencing to identify binding sites of the transcription factor serum response factor (SRF) in the cornea of WT and Dstn-corn1 mutant mice
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BW, TXT, XLS
Series
Accession:
GSE54209
ID:
200054209
14.

Gene expression data from Dstncorn1 mutant, rescued and WT cornea after genetic ablation of Srf from the corneal epithelium

(Submitter supplied) The purpose of this study is to characterize gene expression changes that occur when conditional knock-out of Srf rescues mutant phenotypes in the cornea of Dstncorn1 mice. This study uses a unique model combining genetic and genomic approaches to identify genes that are regulated by SRF.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE49688
ID:
200049688
15.

RNA sequencing in iAM-1 differentiated cells and RnSbk2 knockdown

(Submitter supplied) RNA sequencing in iAM-1 differentiated cells and RnSbk2 knockdown
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25947
12 Samples
Download data: XLSX
Series
Accession:
GSE186626
ID:
200186626
16.

RNA sequencing of iAM-1 cells at different stages during one cycle of differentiation and subsequent dedifferentiation

(Submitter supplied) RNA sequencing of iAM-1 cells at different stages during one cycle of differentiation and subsequent dedifferentiation
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22396
36 Samples
Download data: XLSX
Series
Accession:
GSE164763
ID:
200164763
17.

Alkaline nucleoplasm facilitates contractile gene expression in the mammalian heart

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL22396 GPL20084
21 Samples
Download data
Series
Accession:
GSE196439
ID:
200196439
18.

Alkaline nucleoplasm facilitates contractile gene expression in the mammalian heart [ChIP-seq]

(Submitter supplied) Cardiac contractile strength is recognised as highly pH-sensitive, but less is known about the influence of pH on cardiac gene expression, which may be relevant during changes in myocardial metabolism or vascularization in development or disease. We sought evidence for pH-responsive cardiac genes and a context in which this has physiological relevance. pHLIP, a peptide-based reporter of acidity, revealed a non-uniform pH landscape in early-postnatal myocardium, dissipating in later life. more...
Organism:
Rattus norvegicus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20084
6 Samples
Download data: TXT
Series
Accession:
GSE196438
ID:
200196438
19.

Alkaline nucleoplasm facilitates contractile gene expression in the mammalian heart [RNA-seq]

(Submitter supplied) Cardiac contractile strength is recognised as highly pH-sensitive, but less is known about the influence of pH on cardiac gene expression, which may be relevant during changes in myocardial metabolism or vascularization in development or disease. We sought evidence for pH-responsive cardiac genes and a context in which this has physiological relevance. pHLIP, a peptide-based reporter of acidity, revealed a non-uniform pH landscape in early-postnatal myocardium, dissipating in later life. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22396
15 Samples
Download data: TXT
Series
Accession:
GSE196437
ID:
200196437
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