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Links from GEO DataSets

Items: 5

1.
Full record GDS494

Cystic fibrosis pathology and 4-phenylbutyrate (HG-U133B)

Effect of 1mM 4-phenylbutyrate (PBA) at 0, 12 and 24 hours in cystic fibrosis bronchial epithelial model cell line IB3-1. PBA modulates heat shock protein and promotes trafficking of deltaF508 cystic fibrosis transmembrane conductance regulator (CFTR).
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 time sets
Platform:
GPL97
Series:
GSE620
11 Samples
Download data: CEL
DataSet
Accession:
GDS494
ID:
494
2.

Gene expression profile analysis of 4-phenylbutyrate treatment of IB3-1 bronchial epithelial cell line

(Submitter supplied) Most individuals with cystic fibrosis (CF) carry one or two mutations that result in a maturation defect of the full-length CFTR protein. The deltaF508 mutation results in a mutant protein that is degraded by the proteasome instead of progressing to the apical membrane where it functions as a cyclic AMP-regulated chloride channel. 4 phenylbutyrate modulates heat shock protein expression and promotes trafficking of deltaF508 thus permitting maturation and membrane insertion. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS493 GDS494
Platforms:
GPL96 GPL97
22 Samples
Download data: CEL
Series
Accession:
GSE620
ID:
200000620
3.
Full record GDS493

Cystic fibrosis pathology and 4-phenylbutyrate (HG-U133A)

Effect of 1mM 4-phenylbutyrate (PBA) at 0, 12 and 24 hours in cystic fibrosis bronchial epithelial model cell line IB3-1. PBA modulates heat shock protein and promotes trafficking of deltaF508 cystic fibrosis transmembrane conductance regulator (CFTR).
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 time sets
Platform:
GPL96
Series:
GSE620
11 Samples
Download data: CEL
DataSet
Accession:
GDS493
ID:
493
4.

Effect of TGF-beta1 on the miRNome in CFBE41o- cells stably transduced with Wild Type (WT)-CFTR and F508del-CFTR

(Submitter supplied) The purpose of this study was to explore miRNA mediated Transforming Growth Factor (TGF)-β1 regulation of F508del Cystic Fibrosis Transmembrane Conductance regulator (CFTR). To fulfill this goal, miRNA sequencing was done to see miRNA landscape in Cystic Fibrosis Bronchial Epithelial (CFBE) Cells with homozygous WT-CFTR and F508del mutated CFTR in response to TGFβ1 treatment.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: XLSX
5.

CFTR dependent response

(Submitter supplied) Wild-type and dF508 CFTR mutant human bronchial epithelial cells were uninfected or infected for 3 hours at an MOI of 30-50 with P.aeruginosa strain PAO1. Each cell line was tested in 4 replicates. Each replicate consists of 4 data sets: 2 sets of duplicate spots on 2 arrays. The two arrays in each replicate were dye-swapped pairs where the opposite dye was used for each sample in the second array. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1883
32 Samples
Download data
Series
Accession:
GSE2357
ID:
200002357
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Supplemental Content

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