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Isolation of patient fibroblasts for reprogramming
Generation of foot-print free patient specific human induced pluripotent stem cells
CRISPR genome editing of hESCS and hiPSCs
Expression of genes of interest in hESCs and hiPSCs
Targeting to the AAVS1 locus in hESCs and hiPSCs
Differentiation of hESCs/hiPSCs to endothelial and mural cells
Targeted differentiation of patient derived hiPSCs
Formation of gastruloids
Generation of Vascular organoids
Generation of Retinal Organoids
Vascularisation of Organoids
Generation of anterior cruciate ligament
Drug and small molecule semi-high throughput screening of patient derived hiPSCs
Toxicology in human pluripotent and differentiated cell types
Endothelial barrier models to assess drug availability
Advanced imaging techniques
NeuroVascular Unit Parkinson’s Disease model
Internal Use
Partnership
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