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Kate Fynes

Researcher at University College London

Publications -  5
Citations -  577

Kate Fynes is an academic researcher from University College London. The author has contributed to research in topics: Retinal pigment epithelium & Induced pluripotent stem cell. The author has an hindex of 5, co-authored 5 publications receiving 400 citations. Previous affiliations of Kate Fynes include University of London & UCL Institute of Ophthalmology.

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Journal ArticleDOI

Engineering Efficient Retinal Pigment Epithelium Differentiation From Human Pluripotent Stem Cells

TL;DR: By monitoring the emergence of pigmented cells over time, it is shown how the cell line, passaging method, passage number, and seeding density have a significant and reproducible effect on the RPE yield.
Journal ArticleDOI

Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC).

TL;DR: It is shown that BEST1 is expressed more abundantly in peripheral RPE compared to central RPE and is also expressed in cells of the developing retina during human eye development, suggesting that higher levels of mislocalised BEST1 expression in the periphery could provide a mechanism that leads to the distinct clinical phenotype observed in ADVIRC patients.
Book ChapterDOI

Stem cell-derived retinal pigment epithelium transplantation for treatment of retinal disease.

TL;DR: This chapter examines some of these initial proof-of-principle studies for the replacement of RPE cells in age-related macular degeneration (AMD) patients, and goes on to review the use of pluripotent stem cells as a source for RPE replacement in a number of current AMD clinical trials.
Journal ArticleDOI

The differential effects of 2% oxygen preconditioning on the subsequent differentiation of mouse and human pluripotent stem cells

TL;DR: The impact of low oxygen preconditioning was to prime human cells for ectodermal lineage commitment during subsequent EB differentiation, with significant upregulation of Nestin and β3-tubulin.