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Links from GEO DataSets

Items: 9

1.

Gene Expression in wild type and CCR5 knockout mice with lung metastasis

(Submitter supplied) We have shown that C57BL/6J CCR5 knockout mice develop 30.4% ± 8.6% fewer B16 F10 lung nodules compared to wild type mice after the intravenous injection of 100,000 B16 F10 cells. We sought to understand this phenomenon by comparing gene expression in the lungs of these mice at 6, 24, and 48 hours after tumor injection.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4840
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE51422
ID:
200051422
2.
Full record GDS4840

C-C Chemokine receptor 5 deficient lungs with melanoma metastasis: time course

Analysis of lungs from CCR5-deficient mutants 6 to 48 hrs after tail vein injection with B16-F10 melanoma cells. Lungs of CCR5-deficient mutants develop fewer metastatic nodules than in wild type animals. Results provide insight into the molecular mechanisms underlying CCR5-dependent metastasis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 3 time sets
Platform:
GPL1261
Series:
GSE51422
6 Samples
Download data: CEL
3.

Lentiviral shRNA library screen to identify growth-related genes in malignant melanoma

(Submitter supplied) Little is known about genes that promote melanoma cell growth and proliferation. siRNAs may be used to address the role of individual genesin these processes. RNAi library screens were used in the past to gain a comprehensive overview of all genes involved in cell growth, proliferation, migration and other cellular processes. A large-scale loss-of-function screen for eight different melanoma cell lines was performed using a pooled lentiviral shRNA library (GeneNet Human 50K lentiviral shRNA Library,cat#SI206B-1, System Biosciences) to identify genes relevant for melanoma cell growth and proliferation. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL17118
16 Samples
Download data: CEL, TXT
Series
Accession:
GSE46675
ID:
200046675
4.

Tumor-infiltrating monocytic myeloid-derived suppressor cells mediate CCR5-dependent recruitment of regulatory T cells favoring tumor growth

(Submitter supplied) Analysis of MDSC subsets from naive blood and RMA-S blood and RMA-S tumor, respectively. Tumor-infiltrating MO-MDSCs changed their expression pattern compared to blood and exhibited high levels of chemokines
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6105
18 Samples
Download data: CSV, TXT
Series
Accession:
GSE41620
ID:
200041620
5.

DMEM treated WT and PKBa -/- MEFs

(Submitter supplied) Mouse embryonic fibroblasts (MEFs) were generated from 13.5-day-old embryos obtained from heterozygous PKBa mice intercrosses (Yang et al., 2003). Briefly, after dissection of head and visceral organs for genotyping, embryos were minced and trypsinized for 30 min at 37°C. Embryonic fibroblasts were then plated and maintained in Dulbecco’s Modified Eagle Medium (DMEM) with 10% foetal calf serum (FCS) (Life Technologies), 100 units/ml of penicillin and 100 mg/ml of streptomycin at 37°C in an atmosphere of 5% CO2. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1784
Platform:
GPL339
36 Samples
Download data
Series
Accession:
GSE2746
ID:
200002746
6.
Full record GDS1784

Protein kinase B alpha knockout effect on adipogenesis: time course

Analysis of protein kinase B alpha (PKBalpha) knockout embryonic fibroblasts (MEFs) following treatment with a standard induction cocktail to induce differentiation into adipocytes. Cells examined up to 48 hours following treatment. Results provide insight into the role of PKBalpha in adipogenesis.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 5 time sets
Platform:
GPL339
Series:
GSE2746
36 Samples
Download data
DataSet
Accession:
GDS1784
ID:
1784
7.

Bone-marrow-derived mesenchymal stem cells promote breast cancer metastasis

(Submitter supplied) tumor microenviroment facilitates metastatic spread by eliciting reversible changes in the phenotypes of cancer cells Keywords: expression analysis of breast tumor samples
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
22 Samples
Download data: CEL, DCP
Series
Accession:
GSE8977
ID:
200008977
8.

miRNA expression profile of cells and exosomes

(Submitter supplied) We hypothesized that miRNAs in the bone maroow mesenchymal stem cells (BM-MSC)-derived exosomes contributed to the phenotype change of breast cancer cells through exosome transfer. We analyzed the miRNA expression signature in BM-MSC-derived exosomes. We compared the miRNA expression levels in exosomes between BM-MSCs and adult fibroblasts (as a control).
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL15446
8 Samples
Download data: TXT
Series
Accession:
GSE58027
ID:
200058027
9.

Gene expression signatures for breast cancer cells metastatic to bone marrow

(Submitter supplied) To clarify and compare gene expression profile of each cell line, we have employed microarray expression profiling. The expression of many genes was similar in MM231-D3H2LN-GFP-BM2 cells parental cells, MM231-D3H2LN-GFP cells; however, the expression of genes related to the cell cycle was decreased in the BM2 cells compared with the parental cells. We also confirmed that the global gene expression patterns of the CD44+ and CD44- MM231-D3H2LN-GFP-BM2 cells were similar, although some genes which encode proteins that breast cancer cell dormancy, such as SRC and ERBB2 were increased and decreased, respectively, in the CD44- population.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16699
4 Samples
Download data: TXT
Series
Accession:
GSE57921
ID:
200057921
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