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Links from GEO DataSets

Items: 16

1.

Differentially expressed genes in normal gastric mucosa and gastric cancer tissues

(Submitter supplied) To identify the differentially expressed genes in normal gastric mucosa and gastric cancer tissues, we employed the microarray profiling analysis. Genes with greater than 2-fold change and P-value <0.05 were identified as differentially expressed genes. From this dataset, we obtained differentially expressed genes by cluster analysis and enriched GOs was identified by Gene set enrichment analysis (GSEA) analysis, microtubule GO was one of the most enriched GOs, and the gene KIF14 was selected to go on to the next step in the study.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
20 Samples
Download data: CEL
Series
Accession:
GSE118897
ID:
200118897
2.

A Transcriptomic Analysis of NET1 (a RhoA GEF Exchange Factor) in AGS Gastric Cancer Cells

(Submitter supplied) Stable knockdown of NET1, a RhoGEF, was achieved in AGS Gastric Cancer cells. This gene is known to be overexpressed in the disease. Knockdown was achieved using lentiviral shRNA particles. Gene expression was compared between knockdown and scrambled shRNA treated control cells. Cells were treated with and without LPA, a known activator of RhoA.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4196
Platform:
GPL571
12 Samples
Download data: CEL
Series
Accession:
GSE26309
ID:
200026309
3.
Full record GDS4196

Lysophosphatidic acid effect on RhoA GEF Exchange Factor NET1-deficient, AGS gastric adenocarcinoma cells

Analysis of AGS gastric cancer (GC) cells depleted of NET1, a guanine exchange factor (GEF) for RhoA, and treated with lysophosphatidic acid, a RhoA activator. NET1 is up-regulated in GC and drives its aggressive phenotype. Results provide insight into the role of NET1 in GC.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 3 genotype/variation sets
Platform:
GPL571
Series:
GSE26309
12 Samples
Download data: CEL
4.

RNA Binding protein KPNA2 promotes the progress of gastric cancer by regulating alternative splicing of related genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
10 Samples
Download data
Series
Accession:
GSE201420
ID:
200201420
5.

RNA Binding protein KPNA2 promotes the progress of gastric cancer by regulating alternative splicing of related genes [RIP-seq]

(Submitter supplied) RNA binding proteins (RBPs) took a critical part in genome regulation. kpna2, as an essential member of the RBP family, was found to be highly expressed and associated with lymph node metastasis in gastric cancer (GC). Transcriptional sequencing data were used to find that KPNA2 primarily regulated alternative 5' splice site (A5SS), alternative 3'splice site (A3SS), exon skipping (ES) and cassette exon. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
4 Samples
Download data: TXT
Series
Accession:
GSE201419
ID:
200201419
6.

RNA Binding protein KPNA2 promotes the progress of gastric cancer by regulating alternative splicing of related genes [RNA-seq]

(Submitter supplied) RNA binding proteins (RBPs) took a critical part in genome regulation. kpna2, as an essential member of the RBP family, was found to be highly expressed and associated with lymph node metastasis in gastric cancer (GC). Transcriptional sequencing data were used to find that KPNA2 primarily regulated alternative 5' splice site (A5SS), alternative 3'splice site (A3SS), exon skipping (ES) and cassette exon. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
6 Samples
Download data: TXT
Series
Accession:
GSE201418
ID:
200201418
7.

HOXC10 Overexpression Promotes Cell Proliferation and Migration through Regulation of CST1 Expression in Gastric Cancer

(Submitter supplied) This study propose HOXC10 overexpression by reduced DNA methylation promotes gastric cancer progression through regulation of CST1 and S100P.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: TXT
8.

LncRNA/mRNA expression profiling for 10 human samples

(Submitter supplied) By using the method of “small samples for high throughput screening + large samples for validation”, to find the risk-related long non-coding RNAs and encoding-genes in gastric cancer. To improve the level of clinical diagnosis and treatment of gastric cancer by studying the biological function and its molecular mechanism of these molecules
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL15314
10 Samples
Download data: TXT
Series
Accession:
GSE51308
ID:
200051308
9.

Expression data from gastric cancer and paried normal tissues

(Submitter supplied) Gastric cancer (GC) is one of the most common cancer worldwide. Specific and reliable molecular markers are limited; it is critical to identify new biomarkers for GC to aid in early diagnosis, treatment strategy, and prognosis evaluation. Microarray technology makes it possible to measure the expression levels of thousands of genes, and identifying meaningful and useful molecular targets from these large data.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
20 Samples
Download data: CEL
Series
Accession:
GSE79973
ID:
200079973
10.

Genomic copy number aberrations of 11 gastric cancer cell lines

(Submitter supplied) Genomic copy number aberrations of 11 gastric cancer cell lines were analyzed by 244k CGH array from Agilent Technologies. Based on this results, we separated the 11 cell lines into 2 groups, with and without copy number increase at chromosome 20q13
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
11 Samples
Download data: TXT
Series
Accession:
GSE67604
ID:
200067604
11.

DUSP5P1 promotes gastric cancer metastasis and platinum drug resistance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
5 Samples
Download data: TXT, XLSX
Series
Accession:
GSE213582
ID:
200213582
12.

DUSP5P1 promotes gastric cancer metastasis and platinum drug resistance [ChIRP-seq]

(Submitter supplied) We elucidated the functional significance and molecular mechanisms of DUSP5P1 lncRNA (dual specificity phosphatase 5 pseudogene 1) in gastric carcinogenesis. We demonstrated that gastric cancer (GC) patients with high DUSP5P1 expression had shortened survival in two independent cohorts. DUSP5P1 promoted GC cell migration and invasion in vitro and metastasis in vivo. Mechanistically, DUSP5P1 activated ARHGAP5 transcription by directly binding to the promoter of ARHGAP5 with a binding motif of TATGTG. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
3 Samples
Download data: TXT
Series
Accession:
GSE213581
ID:
200213581
13.

DUSP5P1 promotes gastric cancer metastasis and platinum drug resistance [RNA-seq]

(Submitter supplied) We elucidated the functional significance and molecular mechanisms of DUSP5P1 lncRNA (dual specificity phosphatase 5 pseudogene 1) in gastric carcinogenesis. We demonstrated that gastric cancer (GC) patients with high DUSP5P1 expression had shortened survival in two independent cohorts. DUSP5P1 promoted GC cell migration and invasion in vitro and metastasis in vivo. Mechanistically, DUSP5P1 activated ARHGAP5 transcription by directly binding to the promoter of ARHGAP5 with a binding motif of TATGTG. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: XLSX
Series
Accession:
GSE213560
ID:
200213560
14.

RNA-Seq and ChIP-Seq: cell lines

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL18573
16 Samples
Download data: BED
Series
Accession:
GSE137316
ID:
200137316
15.

Genome-wide H3K4me2 distribution comparison between Positive and Negative A375 (Human skin melanoma cell line)

(Submitter supplied) Purpose: Characterizing the epigenetic differences between the positive and negative cells by using histone modification (h3k4me2- Active loci)
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: BED, TXT
Series
Accession:
GSE137315
ID:
200137315
16.

Triangular Correlation (TrC) between cancer aggressiveness, cell uptake capability and cell deformability

(Submitter supplied) The malignancy potential is correlated with mechanical deformability of the cancer cells. Therefore, mechanical properties of individual patient cells can contribute essential knowledge in cancer diagnostics and in precision therapies. However, clinical applications are limited by lack of current knowledge and of reliable and robust cell mechanical tests. In a comprehensive study, we found a Triangular Correlation (TrC) between cell deformability, phagocytic like capacity, and cancer aggressiveness. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: XLSX
Series
Accession:
GSE135193
ID:
200135193
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