| License: Creative Commons Attribution 4.0 PDF - Published Version (5MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-351739
- DOI to cite this document:
- 10.5283/epub.35173
Abstract
Induced pluripotent stem cell (iPSC)-derived retinal pigment epithelium (RPE) has widely been appreciated as a promising tool to model human ocular disease emanating from primary RPE pathology. Here, we describe the successful reprogramming of adult human dermal fibroblasts to iPSCs and their differentiation to pure expandable RPE cells with structural and functional features characteristic for ...
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