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Links from GEO DataSets

Items: 8

1.

Dysregulation of amino acid metabolism upon rapid depletion of cap-binding protein eIF4E [aro10_screen]

(Submitter supplied) Protein synthesis is metabolically costly, and the level of translation must match nutrient availability and cellular needs. Overall protein synthesis levels are modulated by regulating translation initiation. The cap-binding protein eIF4E—the earliest contact between mRNAs and the translation machinery—serves as one point of control, but its contributions to mRNA-specific translation regulation remain poorly understood. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
8 Samples
Download data: TXT
Series
Accession:
GSE231756
ID:
200231756
2.

Dysregulation of amino acid metabolism upon rapid depletion of cap-binding protein eIF4E

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL27812 GPL21656
40 Samples
Download data: TXT
Series
Accession:
GSE231759
ID:
200231759
3.

Dysregulation of amino acid metabolism upon rapid depletion of cap-binding protein eIF4E [RNA-Seq]

(Submitter supplied) Protein synthesis is metabolically costly, and the level of translation must match nutrient availability and cellular needs. Overall protein synthesis levels are modulated by regulating translation initiation. The cap-binding protein eIF4E—the earliest contact between mRNAs and the translation machinery—serves as one point of control, but its contributions to mRNA-specific translation regulation remain poorly understood. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21656 GPL27812
16 Samples
Download data: TXT
Series
Accession:
GSE231758
ID:
200231758
4.

Dysregulation of amino acid metabolism upon rapid depletion of cap-binding protein eIF4E [pcl5_screen]

(Submitter supplied) Protein synthesis is metabolically costly, and the level of translation must match nutrient availability and cellular needs. Overall protein synthesis levels are modulated by regulating translation initiation. The cap-binding protein eIF4E—the earliest contact between mRNAs and the translation machinery—serves as one point of control, but its contributions to mRNA-specific translation regulation remain poorly understood. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27812
16 Samples
Download data: TXT
Series
Accession:
GSE231757
ID:
200231757
5.

Capture and identification of the eIF4E:mRNA interactome in human cells

(Submitter supplied) Here we develop a novel methodology, capCLIP, to capture and identify mRNA interactions with the major cellular cap-binding protein eIF4E.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: BED, NARROWPEAK, TSV
Series
Accession:
GSE138473
ID:
200138473
6.

Translation initiation factor 4E confers primary human cells with neoplastic properties

(Submitter supplied) Deregulation of translational control is an obligatory step in oncogenesis; however, this step has not been addressed by prior genomic and transcriptional profiling studies of cancer biology. Here we simulate the translational deregulation found in cancer by ectopically over expressing translation initiation factor eIF4E in primary human mammary epithelial cells; and examine its impact on cell biology and the pattern of ribosomal recruitment to mRNA genome wide. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4454
9 Samples
Download data: CEL
Series
Accession:
GSE6043
ID:
200006043
7.

PAR-CLIP of RBM4 and HIF-2a

(Submitter supplied) To identify which mRNAs bind to RBM4/HIF-2a
Organism:
Homo sapiens
Type:
Other
Platform:
GPL9115
2 Samples
Download data: TXT
Series
Accession:
GSE36247
ID:
200036247
8.

The eukaryotic translation initiation factor eIF4E elevates steady-state m7G capping of coding and noncoding transcripts

(Submitter supplied) Methyl-7-guanosine (m7G) “capping” of coding and some noncoding RNAs is critical for their maturation and subsequent activity. Here, we discovered that eukaryotic translation initiation factor 4E(eIF4E), itself a cap-binding protein, drives the expression of the capping machinery and the increased capping efficiency of ∼100 coding and noncoding RNAs. This dataset collects transcriptomic data for quantitative cap immunoprecipitation (CapIP) assay in eIF4E-Flag or vector stable U2Os cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
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