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Links from GEO DataSets

Items: 9

1.
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
2.

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
3.

Gene expression profiles in mouse embryonic fibroblasts (MEFs) derived from BCL11B-KO mice

(Submitter supplied) The differentiation of preadipocytes into adipocytes is controlled by several transcription factors, including peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT/enhancer-binding protein α (C/EBPα), which are known as master regulators of adipogenesis. BCL11B is a zinc finger-type transcription factor that regulates the development of the skin and central nervous and immune systems. Here, we found that BCL11B was expressed in the white adipose tissue (WAT), particularly the subcutaneous WAT and that BCL11B−/− mice had a reduced amount of subcutaneous WAT. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL
Series
Accession:
GSE83980
ID:
200083980
4.

Adipose Tissue MicroRNAs as Regulators of CCL2 Production in Human Obesity (differentiation data)

(Submitter supplied) We used an unbiased systems biology approach to study the regulation of gene expression in human adipose tissue focusing on inflammation. We show that microRNAs play a major role as regulators of CCL2 production in obesity.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
36 Samples
Download data: CEL
Series
Accession:
GSE25910
ID:
200025910
5.

Adipose Tissue MicroRNAs as Regulators of CCL2 Production in Human Obesity [miRNA data]

(Submitter supplied) We used an unbiased systems biology approach to study the regulation of gene expression in human adipose tissue focusing on inflammation. We show that microRNAs play a major role as regulators of CCL2 production in obesity.
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
56 Samples
Download data: CEL
Series
Accession:
GSE25470
ID:
200025470
6.

Adipose Tissue MicroRNAs as Regulators of CCL2 Production in Human Obesity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; synthetic construct
Type:
Methylation profiling by array; Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL6244 GPL8786
148 Samples
Download data: CEL
Series
Accession:
GSE25402
ID:
200025402
7.

Adipose Tissue MicroRNAs as Regulators of CCL2 Production in Human Obesity [gene expression]

(Submitter supplied) We used an unbiased systems biology approach to study the regulation of gene expression in human adipose tissue focusing on inflammation. We show that microRNAs play a major role as regulators of CCL2 production in obesity.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
56 Samples
Download data: CEL
Series
Accession:
GSE25401
ID:
200025401
8.

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
9.
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
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