GSM2137617[Accession] - GEO DataSets

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Items: 3

Select item 2000807981.

RPTOR, a novel target of miR-155, regulates the fibrotic phenotype of cystic fibrosis lung epithelium by upregulating CTGF

(Submitter supplied) Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the most frequent of which is F508del-CFTR. CF is characterized by excessive secretion of pro-inflammatory chemokines into the airway lumen, inducing a highly inflammatory cellular phenotype. This process triggers fibrosis, causing airway destruction and leading to high morbidity and mortality. more...

Organism:: Homo sapiens

Type:: Expression profiling by array; Other

Platform:: GPL10558
9 Samples

Download data: TXT

Series

Accession:: GSE80798

ID:: 200080798

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000105582.

Illumina HumanHT-12 V4.0 expression beadchip

(Submitter supplied) The HumanHT-12 v4 Expression BeadChip provides high throughput processing of 12 samples per BeadChip without the need for expensive, specialized automation. The BeadChip is designed to support flexible usage across a wide-spectrum of experiments. The updated content on the HumanHT-12 v4 Expression BeadChips provides more biologically meaningful results through genome-wide transcriptional coverage of well-characterized genes, gene candidates, and splice variants. more...