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Links from GEO DataSets

Items: 11

1.

RNA-seq on LX-2 cells treated with conditioned medium from either HCT116Vector or HCT116FGFBP1 cells

(Submitter supplied) To define the global effects of tumor cell-derived FGFBP1 on the phenotype modifications of HSCs
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
6 Samples
Download data: XLS
Series
Accession:
GSE208084
ID:
200208084
2.

RNA-seq in LX-2Vector and LX-2FAP cells

(Submitter supplied) To investigate the underlying mechanism by which FAPα in HSCs promoted tumor cell EMT
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
6 Samples
Download data: TXT
Series
Accession:
GSE208091
ID:
200208091
3.

RNA-seq performed on LSECs obtained from bevacizumab-sensitive and -resistant HCT116 CRCLM xenografts

(Submitter supplied) To determine the differentially-expressed endothelial genes in explants from the bevacizumab-sensitive and -resistant explants
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
6 Samples
Download data: TXT
Series
Accession:
GSE207976
ID:
200207976
4.

Effect of overexpression of TRPM8 on gene expression of tumor pericytes

(Submitter supplied) RNA-sequencing for 6 samples
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
6 Samples
Download data: XLSX
Series
Accession:
GSE216780
ID:
200216780
5.

Whole transcriptome analysis of HK1EBV exosome-treated fibroblasts.

(Submitter supplied) We aimed to investigate whether EBV exosomes will affect gene expression in primary fibroblasts. By obtaining normalized read counts of genes generated from RNA-sequencing, we compared the transcriptomic alterations between fibroblasts treated with HK1EBV exosomes and untreated fibroblasts.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
3 Samples
Download data: TXT
Series
Accession:
GSE197560
ID:
200197560
6.

Reducing metastases stiffness by targeting fibroblasts improves therapeutic outcome in colorectal cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
34 Samples
Download data
Series
Accession:
GSE145432
ID:
200145432
7.

Reducing metastases stiffness by targeting fibroblasts improves therapeutic outcome in colorectal cancer [Tissue]

(Submitter supplied) Analysis of colorectal primary tumors (pTU) and liver metastases (LM) tissue samples from patients and identify corresponding gene expression signatures
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
22 Samples
Download data: TXT
Series
Accession:
GSE145429
ID:
200145429
8.

Reducing metastases stiffness by targeting fibroblasts improves therapeutic outcome in colorectal cancer [Cells]

(Submitter supplied) Analysis of primary fibroblasts isolated from human colorectal primary tumors(CAFs) and liver metastases(MAFs) and identify corresponding gene expression signatures
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
Series
Accession:
GSE145428
ID:
200145428
9.

Neutrophils expressing lysyl oxidase-like 4 protein are present in colorectal cancer liver metastases resistant to anti-angiogenic therapy

(Submitter supplied) Colorectal cancer liver metastases (CRCLM) that present with a replacement histopathological growth pattern (HGP) are resistant to neoadjuvant anti-angiogenic therapy. Surrogate biomarkers are not available to preoperatively identifypatients with these tumors. Here we identify differentially expressed genes between CRCLM with a replacement HGP and those with a desmoplastic HGP using RNA sequencing.We demonstrate that LOXL4 is transcriptionally upregulated in replacement HGP CRCLM compared with desmoplastic HGP CRCLM and the adjacent normal liver. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
30 Samples
Download data: XLSX
Series
Accession:
GSE151165
ID:
200151165
10.

Induction of hepatocellular carcinoma through activation of stromal cells in Pdgf-c transgenic mice

(Submitter supplied) Liver cirrhosis is a strong risk factor for the development of hepatocellular carcinoma (HCC), yet the mechanisms by which cirrhosis predisposes patients to tumorigenesis are not well understood. Transgenic mice expressing platelet-derived growth factor C (Pdgf-c) under the control of the albumin promoter provide a unique animal model that mimics the step-wise disease progression in humans from fibrosis to HCC. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5320
Platform:
GPL6246
16 Samples
Download data: CEL
Series
Accession:
GSE38199
ID:
200038199
11.
Full record GDS5320

Platelet-derived growth factor C transgenic model of hepatocellular carcinoma: liver stromal cells

Analysis of liver stroma from 8.8-week-old PDGF-C transgenics wherein PDGF-C is ectopically expressed in hepatocytes. The transgenics develop progressive liver fibrosis with a high incidence of HCC. Results provide insight into PDGF-C-driven molecular changes in liver stroma contributing to HCC.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE38199
16 Samples
Download data: CEL
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