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Links from GEO DataSets

Items: 20

1.

CELF1, and RNA binding protein, regulates transcript networks in cultured embryonic cardiomyocytes.

(Submitter supplied) We report on the regulation of transcripts following siRNA-mediated depletion of an RNA binding protein, CELF1, in primary chicken embryonic cardiomyocytes in culture.
Organism:
Gallus gallus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16133
6 Samples
Download data: TXT
Series
Accession:
GSE67360
ID:
200067360
2.

Functional Antagonism Between CELF and Mbnl Proteins in Cytoplasm and Nucleus [RNA Bind-N-Seq]

(Submitter supplied) The CUG-BP and ETR-3-like factor 1 (Celf1) RNA binding protein plays an important role in heart and muscle development, and is over-expressed in the disease myotonic dystrophy. Celf1 has known roles in regulation of RNA splicing, RNA stability, and protein translation. To identify transcriptome-wide targets of the Celf1 protein, we performed CLIP-seq against Celf1 using the 3B1 antibody, in myoblasts, heart tissue, and muscle tissue.
Organism:
synthetic construct
Type:
Other
Platform:
GPL15228
7 Samples
Download data: XLSX
Series
Accession:
GSE67337
ID:
200067337
3.

Functional Antagonism Between CELF and Mbnl Proteins in Cytoplasm and Nucleus

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; synthetic construct
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL13112 GPL15228 GPL9250
40 Samples
Download data: BED
Series
Accession:
GSE61893
ID:
200061893
4.

Functional Antagonism Between CELF and Mbnl Proteins in Cytoplasm and Nucleus [CLIP-seq]

(Submitter supplied) The CUG-BP and ETR-3-like factor 1 (Celf1) RNA binding protein plays an important role in heart and muscle development, and is over-expressed in the disease myotonic dystrophy. Celf1 has known roles in regulation of RNA splicing, RNA stability, and protein translation. To identify transcriptome-wide targets of the Celf1 protein, we performed CLIP-seq against Celf1 using the 3B1 antibody, in myoblasts, heart tissue, and muscle tissue.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BED, TXT
Series
Accession:
GSE61892
ID:
200061892
5.

Functional Antagonism Between CELF and Mbnl Proteins in Cytoplasm and Nucleus [hearts]

(Submitter supplied) The CUG-BP and ETR-3-like factor 1 (Celf1) RNA binding protein plays an important role in heart and muscle development, and is over-expressed in the disease myotonic dystrophy. Celf1 has known roles in regulation of RNA splicing, RNA stability, and protein translation. To identify transcriptome-wide targets of the Celf1 protein in heart, we performed RNA-Seq of polyA+ RNA from mice inducibly expressing Celf1 in the muscle.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9250
15 Samples
Download data: TXT
Series
Accession:
GSE61891
ID:
200061891
6.

Functional Antagonism Between CELF and Mbnl Proteins in Cytoplasm and Nucleus [muscle]

(Submitter supplied) The CUG-BP and ETR-3-like factor 1 (Celf1) RNA binding protein plays an important role in heart and muscle development, and is over-expressed in the disease myotonic dystrophy. Celf1 has known roles in regulation of RNA splicing, RNA stability, and protein translation. To identify transcriptome-wide targets of the Celf1 protein in heart, we performed RNA-Seq of polyA+ RNA from mice inducibly expressing Celf1 in the muscle.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9250
15 Samples
Download data: TXT
Series
Accession:
GSE61890
ID:
200061890
7.

Regulation of the mouse heart transcriptome by Celf1

(Submitter supplied) The CUG-BP and ETR-3-like factor 1 (Celf1) RNA binding protein plays an important role in heart and muscle development, and is over-expressed in the disease myotonic dystrophy. Celf1 has known roles in regulation of RNA splicing, RNA stability, and protein translation. To identify transcriptome-wide targets of the Celf1 protein in heart, we performed RNA-Seq of polyA+ RNA from mice inducibly expressing Celf1 in the heart.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9250
15 Samples
Download data: TXT
Series
Accession:
GSE56185
ID:
200056185
8.

Neonatal cardiac dysfunction and transcriptome changes caused by the absence of Celf1

(Submitter supplied) The RNA binding protein Celf1 regulates alternative splicing in the nucleus and mRNA stability and translation in the cytoplasm. Celf1 is strongly down-regulated during mouse postnatal heart development. Its re-induction in adults induced severe heart failure and reversion to fetal splicing and gene expression patterns. However, the impact of Celf1 depletion on cardiac transcriptional and posttranscriptional dynamics in neonates has not been addressed. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
5 Samples
Download data: TXT
Series
Accession:
GSE85646
ID:
200085646
9.

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
10.

Transcriptome modulation of ventricles, cardiomyocytes and cardiac fibroblasts during postnatal mouse development

(Submitter supplied) During development the fetal heart undergoes a rapid and dramatic transition to adult function through transcriptional and post-transcriptional mechanisms, including alternative splicing (AS). We performed deep RNA-sequencing for high-resolution analysis of transcriptome changes during postnatal mouse heart development using RNA from ventricles and freshly isolated cardiomyocytes (CM) and cardiac fibroblasts (CF). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
13 Samples
Download data: TXT
Series
Accession:
GSE49906
ID:
200049906
11.

High-throughput transcriptomics of Celf1 conditional knockout lens identifies downstream networks linked to cataract pathology

(Submitter supplied) Celf1 germline or conditional deletion mouse mutants exhibit fully penetrant lens defects including cataract. To gain insight into gene expression changes underlying these lens defects Differential Gene Expression analysis was performed for lenses obtained from control and Celf1 conditional deletion mutant mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: CSV
Series
Accession:
GSE227293
ID:
200227293
12.

Celf1 and Postnatal Lens Microarray

(Submitter supplied) Celf1 germline or conditional deletion mouse mutants exhibit fully penetrant lens defects including cataract. To gain insight into gene expression changes underlying these lens defects, microarray comparison was performed for lenses obtained from control and Celf1 conditional deletion mutant mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
4 Samples
Download data: CSV
Series
Accession:
GSE225303
ID:
200225303
13.

CELF1 upregulates MMP gene expression to regulate cataract development

(Submitter supplied) As a multifunctional RBP, CELF1 is known to preferentially binds to GU-rich elements (GREs) predominantly located in 3’ untranslated regions(UTRs) of target mRNA to regulate various post-transcriptional process. However, the targeted genes that regulated by CELF1 during cataractogenesis remains unknown. In present study,the function of CELF1 in SRA01/04 cells was investigated with CELF1 overexpression, the expression of MMPs was regulated by CELF1.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20795
6 Samples
Download data: TXT
14.

Gene expression changes in human melanoma cell lines compared to primary melanocytes

(Submitter supplied) Gene expression changes in 3 human melanoma cell lines were compared to freshly isolated normal primary melanocytes
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TXT
15.

Systems analysis identifies melanoma-enriched pro-oncogenic networks controlled by the RNA binding protein CELF1

(Submitter supplied) Melanomas are well-known for their altered mRNA expression profiles. Yet, the specific contribution of mRNA binding proteins (mRBPs) to melanoma development remains unclear. Here we identify a cluster of melanoma-enriched genes under the control of CUGBP Elav-like family member 1 (CELF1). CELF1 was discovered with a distinct prognostic value in melanoma after mining the genomic landscape of the 692 known mRBPs across different cancer types. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10635
12 Samples
Download data: GPR
Series
Accession:
GSE83678
ID:
200083678
16.

Gene expression comparison in control and DEK oncogene depleted human melanoma cell lines

(Submitter supplied) Gene expression SK-Mel-103 melanoma cell line to find genes controled by DEK oncogene
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
3 Samples
Download data: TXT
Series
Accession:
GSE83614
ID:
200083614
17.

CUGBP1 RNA immunoprecipitation and sequencing (RIP-seq) in SK-Mel-103 and UACC-62 melanoma cell lines

(Submitter supplied) Identification of the mRNAs bound by CUGBP1 in melanoma cells
Organism:
Homo sapiens
Type:
Other
Platform:
GPL10999
6 Samples
Download data: TXT
18.

mRNAseq in control (WT) and Nes:Cre_Qk cKO

(Submitter supplied) We sequenced mRNA from mouse E14.5 embryonic cortex to compare gene expression level and alternative splicing events between 2 control (WT) and 2 Qk cKO. A set of tissue specific splicing factors are thought to govern alternative splicing events during neural progenitors (NPC) to neuron transition by regulating neuron specific exons. Here we proposed one such a factor, RNA-binding protein Qki5, which is specifically expressed in neural stem cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
4 Samples
Download data: TXT
Series
Accession:
GSE123927
ID:
200123927
19.

RNAseq in control and shQk KD mouse neural stem cells, and Qki5 CLIP in E14.5 mouse brain

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL16417 GPL17021
7 Samples
Download data: BED, BEDGRAPH, TXT
Series
Accession:
GSE103248
ID:
200103248
20.

Qki5 CLIP in E14.5 mouse brain

(Submitter supplied) Mouse brains at E14.5 wild-type were subjected to HITS-CLIP to identify Qki5-binding positions on RNA.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16417
1 Sample
Download data: BED, BEDGRAPH
Series
Accession:
GSE103247
ID:
200103247
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