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Links from GEO DataSets

Items: 13

1.
Full record GDS2932

TGF-beta effect on normal and tumor cell lines: time course

Analysis of normal lung epithelial HPL1D cells and lung adenocarcinoma A549 cells treated with TGF-beta for up to 12 hours. TGF-beta inhibits growth and promotes apoptosis in normal epithelial cells but acts as a pro-tumor cytokine by promoting tumour angiogenesis, immune-escape, and metastasis.
Organism:
Homo sapiens
Type:
Expression profiling by array, log2 ratio, 2 cell line, 3 time sets
Platform:
GPL3515
Series:
GSE7436
12 Samples
Download data
2.

Profiling of genes regulated by TGF-beta in lung carcinoma (A549) and immortalized lung epithelial (HPL1D)cells.

(Submitter supplied) TGF-beta is one of the key cytokines implicated in various disease processes including cancer. TGF-beta inhibits growth and promotes apoptosis in normal epithelial cells and in contrast, acts as a pro-tumour cytokine by promoting tumour angiogenesis, immune-escape and metastasis. It is not clear if various actions of TGF-beta on normal and tumour cells are due to differential gene regulations. Hence we studied the regulation of gene expression by TGF-beta in normal and cancer cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2932
Platform:
GPL3515
12 Samples
Download data
Series
Accession:
GSE7436
ID:
200007436
3.

Gene expression profiling of human gliomas and human glioblastoma cell lines

(Submitter supplied) To identify signaling pathways that are differentially regulated in human gliomas, a microarray analysis on 30 brain tumor samples (12 primary glioblastomas (GBM), 3 secondary glioblastomas (GBM-2), 8 astrocytomas (Astro) and 7 oligodendrogliomas (Oligo)) and on 5 glioblastoma cell lines (LN018, LN215, LN229, LN319 and BS149) was performed. Normal brain tissue (NB) and normal human astrocytes (NHA) were used as a control. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4467 GDS4468
Platform:
GPL570
45 Samples
Download data: CEL
Series
Accession:
GSE15824
ID:
200015824
4.
Full record GDS4468

Glioblastoma cell lines: LN018, LN215, LN229, LN319 and BS149

Analysis of 5 glioblastoma cell lines (LN018, LN215, LN229, LN319 and BS149). Results provide insight into molecular mechanisms underlying glioblastoma multiforme and other aggressive brain cancers.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 5 cell line sets
Platform:
GPL570
Series:
GSE15824
10 Samples
Download data: CEL
DataSet
Accession:
GDS4468
ID:
4468
5.
Full record GDS4467

Primary and secondary brain tumors: glioblastomas, astrocytomas and oligodendrogliomas

Analysis of primary glioblastomas (GBM), astrocytomas, oligodendrogliomas and secondary GBM brain tumors. MNK1 kinase upregulation observed in primary GBM brain tumors. Results identifiy signaling pathways differentially regulated in gliomas.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 5 cell type, 8 other, 3 tissue sets
Platform:
GPL570
Series:
GSE15824
35 Samples
Download data: CEL
DataSet
Accession:
GDS4467
ID:
4467
6.

Epigenetic events in early breast cancer

(Submitter supplied) Subpopulations of primary Human Mammary Epithelial Cells (HMEC) have the unique ability to escape a period of growth arrest and continue to proliferate. These cells, called post-selection or variant cells (vHMEC), share features with premalignant breast cancer lesions, including p16INK4A promoter hypermethylation. Epigenetic silencing of tumour suppressor genes through DNA methylation and histone modification is an early event in tumorigenesis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3348
6 Samples
Download data: TXT
Series
Accession:
GSE8007
ID:
200008007
7.

Biocompatibility and Discovery of the Potential Applications of Magnetite (Fe3O4) Nanoparticles

(Submitter supplied) A Transcriptomics Approach to Study the Biocompatibility and Finding out the Potential Applications of Magnetite (Fe3O4) Nanoparticles Here in this study, we examine the molecular effects of uptake of Fe3O4 nanoparticles using a whole genome microarray study in human epithelial cancer cell line. 38 genes (55%) out of 69 downregulated genes were found to be associated with TGF-beta or BMP signaling including six genes, Id1, Id2, Id3, Caspase-9, Smad6 and SMAD7, important negative regulators of these signaling pathways involved in development and tumorigenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
6 Samples
Download data: TXT
Series
Accession:
GSE15248
ID:
200015248
8.

Hog1 ChIP Chip

(Submitter supplied) Yeast Hog1-3HA ChIP-Chip in triplicate Keywords: ChIP-Chip
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL1689
3 Samples
Download data
Series
Accession:
GSE4862
ID:
200004862
9.

Gene expression analysis of peritoneal mesotheliomas following chemical treatment in F344 rats

(Submitter supplied) This study was performed to characterize the gene expression profile of rat peritoneal mesothelioma (RPM) formation following treatment of Fischer 344 rats with o-nitrotoluene (o-NT) or bromochloracetic acid (BCA). Keywords: Rat, Mesotheliomas, Bromochloractetic acid, o-Nitrotoluene, Carcinogenesis, Microarray
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS2051
Platform:
GPL890
16 Samples
Download data: TIFF, TXT
Series
Accession:
GSE4682
ID:
200004682
10.
Full record GDS2051

Peritoneal mesotheliomas induced by o-nitrotoluene and bromochloracetic acid: dose response

Analysis of peritoneal mesotheliomas induced by various concentrations of o-nitrotoluene (o-NT) or bromochloracetic acid (BCA). o-NT is a high production chemical. BCA is a by-product of drinking water disinfection. Results provide insight into the mechanisms underlying mesothelioma formation.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, log10 ratio, 2 agent, 5 dose sets
Platform:
GPL890
Series:
GSE4682
16 Samples
Download data: TIFF, TXT
DataSet
Accession:
GDS2051
ID:
2051
11.

Expression data from mouse limb tendon cells during development.

(Submitter supplied) We have undertaken a screen of mouse limb tendon cells in order to identify molecular pathways involved in tendon development. Mouse limb tendon cells were isolated based on Scleraxis (Scx) expression at different stages of development: E11.5, E12.5 and E14.5 Microarray comparisons were carried out between tendon progenitor and differentiated stages.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5642
Platform:
GPL1261
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE54207
ID:
200054207
12.
Full record GDS5642

Tendon development: embryonic limb tendon cells

Analysis of tendon cells isolated by FACS from forelimbs of embryonic day 11.5, E12.5 and E14.5 scleraxis (Scx)-GFP embryos. Basic helix-loop-helix transcription factor Scx is a specific tendon and ligament marker. Results provide insight into molecular pathways involved in tendon development.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age sets
Platform:
GPL1261
Series:
GSE54207
9 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS5642
ID:
5642
13.

Transcriptional profiling of a novel pro-angiogenic small molecule phthalimide neovascular factor 1 (PNF1)

(Submitter supplied) We generated the transcriptional regulatory footprint of phthalimide neovascular factor 1 (PNF1)—a novel synthetic small molecule that exhibits significant in vitro endothelial potency and significant in vivo microvascular network expansion—by performing comparative microarray analysis on PNF1-stimulated (versus control) human microvascular endothelial cells (HMVEC) spanning 1-48 h post-supplementation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
14 Samples
Download data: CEL
Series
Accession:
GSE17119
ID:
200017119
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