Mus musculus
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA128623 | ENA |
REPOSITORIES: ENA
Similar Datasets
Project description:Gene expression profiles of adult renal medullary endothelial cells isolated from TIE2-GFP transgenic mice using FACS. (GUDMAP Series ID: 35)
| PRJNA124071 | ENA
Project description:Gene expression profiles of E15.5 endothelial cells isolated from TIE2-GFP transgenic mice using FACS. (GUDMAP Series ID:38)
| PRJNA124503 | ENA
Project description:Gene expression profiles of adult glomerular endothelial cells isolated from TIE2-GFP transgenic mice using FACS. (GUDMAP Series ID: 42)
| PRJNA128445 | ENA
Project description:Gene expression profiles of E15.5 endothelial cells in the developing kidney isolated from TIE2-GFP transgenic mice using FACS. (GUDMAP Series ID: 21)
| PRJNA106729 | ENA
Project description:Gene expression profiles of E10.5 ureteric tip cells isolated from Hoxb7-GFP transgenic mice using FACS. (GUDMAP Series ID: 39)
| PRJNA126231 | ENA
Project description:Gene expression profiles of E10.5 ureteric trunk cells isolated from Hoxb7-GFP transgenic mice using FACS. (GUDMAP Series ID: 40)
| PRJNA127023 | ENA
Project description:Gene expression profiles of adult visceral epithelium (syn: podocyte layer) isolated from MafB-GFP transgenic mice using FACS. (GUDMAP Series ID: 31)
| PRJNA123643 | ENA
Project description:Deregulated retinal angiogenesis directly cause vision loss in many ocular diseases, such as diabetic retinopathy and retinopathy of prematurity. To identify endothelial-specific genes expressed in angiogenic retinal vessels, we purified genetically labeled endothelial cells from Tie2-GFP transgenic mice and performed gene expression profiling using DNA microarray. To find out genes associated with angiogenesis, comparisons of microarray data were carried out between GFP-negative non-endothelial retinal cells and GFP-positive retinal endothelial cells in angiogenic P8 retina. Eighteen arrays are included. Utilizing fluorescence-activated cell sorting (FACS), we isolated endothelial cells as GFP-positive cells from P8 retina in homozygous Tie2-GFP transgenic mice. GFP-negative cells were served as non-endothelial control. RNA extracts from sorted cells were amplified and then hybridized to Affymetrix MGU74v2 series arrays in triplicate.
2011-04-17 | E-GEOD-27238 | biostudies-arrayexpress
Project description:Gene expression profiles of E15.5 cap mesenchyme isolated from Six2 transgenic mice using FACS. (GUDMAP Series ID: 23)
| PRJNA112835 | ENA
Project description:The long term objective is to create an encyclopedia of the expression levels of all genes in multiple components of the developing kidney. The central thesis is straightforward. The combination of fluorescent activated cell sorting (FACS) plus microarray analysis offers a powerful, efficient and effective method for the creation of a global gene expression atlas of the developing kidney. Microarrays with essentially complete genome coverage can be used to quantitate expression levels of every gene in FACS isolated components of the developing kidney. The ensuing rapid read-out provides an expression atlas that is more sensitive, more economical and more complete than would be possible by in situ hybridizations alone. Tie2-GFP transgenic mice were utilized to isolate the endothelial cell population from the cortical region of adult kidneys. The cortical endothelial cells were isolated from kidneys using a combination of collagenase treatment, differential seiving, trypsin treatment and FACS. The RNA was isolated from purified endothelial cells and the gene expression profiles were determined by microarrays.
2010-07-30 | E-GEOD-22464 | biostudies-arrayexpress