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Links from GEO DataSets

Items: 10

1.
Full record GDS3789

Coronary artery disease response to exercise: CD133+ cells

Analysis of CD133+ endothelial progenitor cells of coronary artey disease (CAD) patients after 3 months of exercise. Bone marrow derived progenitor cells with endothelial differentiation potential are fewer in CAD. Results provide insight into the impact of exercise on CD133+ cells of CAD patients.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 14 individual, 2 protocol sets
Platform:
GPL570
Series:
GSE18608
24 Samples
Download data: CEL
2.

Transcriptional Profiling of CD133+ Cells in Coronary Artery Disease and Effects of Exercise on Gene Expression

(Submitter supplied) Bone marrow-derived progenitor cells are under investigation for cardiovascular repair, but may be altered by disease. We identified 82 differentially expressed genes in CD133+ cells from patients with coronary artery disease (CAD) versus controls, of which 59 were found to be up-regulated and 23 down-regulated. These genes were found to be involved in carbohydrate metabolism, cellular development and signaling, molecular transport and cell differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3789
Platform:
GPL570
24 Samples
Download data: CEL
Series
Accession:
GSE18608
ID:
200018608
3.

Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas.

(Submitter supplied) Background: Gliomas are the most common type of primary brain tumours, and in this group glioblastomas (GBMs) are the higher-grade gliomas with fast progression and unfortunate prognosis. Two major aspects of glioma biology that contributes to its awful prognosis are the formation of new blood vessels through the process of angiogenesis and the invasion of glioma cells. Despite of advances, two-year survival for GBM patients with optimal therapy is less than 30%. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
16 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE18015
ID:
200018015
4.

CD133+ and CD133- cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3904
40 Samples
Download data: GPR
Series
Accession:
GSE9980
ID:
200009980
5.

Expression profiling basal and luminal prostate epithelial cells

(Submitter supplied) Immuno-stained (keratin 14+ basal marker) frozen prostate sections were subjected to laser-guided microdissection to isolate basal and luminal epithelial prostate cells for expression profiling. RNA was amplified using the AmpTec TRinucleotide kit (AmpTec GmBH). Expression profiling performed using the Invitrogen post-labelling kit and the CRUK whole genome array (WGA) gene set. Keywords: repeat sample
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3904
10 Samples
Download data: GPR
Series
Accession:
GSE9966
ID:
200009966
6.

CD133+ and CD133- expression profiles of benign and HRPC cells

(Submitter supplied) Epithelial cell cultures derived from benign and HRPC tissue biopsies were expanded in culture for 2-3 weeks. CD133+ and CD133- cells were isolated using the miltenyi magnetic bead system after adherence to collagen. CD133+ and CD133- RNA was isolated and amplified using the RiboAmp HS kit and expression profiling performed using the CRUK WGA gene set. Keywords: Tumour vs normal comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3904
28 Samples
Download data: GPR
Series
Accession:
GSE9962
ID:
200009962
7.

Benign Uncultured CD133+ vs CD133-

(Submitter supplied) 6 benign TURP samples taken directly from patients were subjected to collagen digestion overnight. Epithelial cells isolated were adhered to collagen for 15 minutes. Adherent cells were passed through a magnetic bead column and cells positive for CD133 antibody were double selected. RNA was extracted from CD133+ and CD133- cells from each patient and amplified using the RiboAmp HS RNA amplification system. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3904
12 Samples
Download data: GPR
Series
Accession:
GSE9935
ID:
200009935
8.

Gene epression profile in human BM-MSC

(Submitter supplied) Gene expression profiles of human BM-MSC isolated form normal donor to elucidate potential molecular network for clinical application
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE19471
ID:
200019471
9.

Expression profiling of GIST: CD133 is associated with KIT exon 11 deletion, gastric location and poor prognosis

(Submitter supplied) Background & Aims: In gastrointestinal stromal tumors (GIST) KIT exon 11 deletions are associated with poor prognosis. The aim of this study was to determine the gene expression profile of GIST carrying KIT exon 11 deletions and to identify genes associated with poor prognosis. Methods: Expression profiling was performed on 9 tumors with KIT exon 11 deletions and 7 without KIT exon 11 mutations using oligonucleotide microarrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5345
21 Samples
Download data: TXT
Series
Accession:
GSE14755
ID:
200014755
10.

Impact of exercise training on endothelial transcriptional profiles in healthy swine: A genome-wide microarray analysis

(Submitter supplied) While the salutary effects of exercise training on conduit artery endothelial cells have been reported in animals and humans with cardiovascular risk factors or disease, whether a healthy endothelium is alterable with exercise training is less certain. The purpose of this study was to evaluate the impact of exercise training on transcriptional profiles in normal endothelial cells using a genome-wide microarray analysis. more...
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL3533
29 Samples
Download data: CEL
Series
Accession:
GSE26663
ID:
200026663
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