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1 accounted for an average of 40% of the total limbal epithelial cells.
2 proliferation, and intrastromal invasion by limbal epithelial cells.
3 tion of eyes retained morphologically normal limbal epithelial cells.
4 nces in glycogen content between corneal and limbal epithelial cells.
6 superior in vitro proliferative potential of limbal epithelial cells, and the transplanted limbal cel
8 ficiency, we developed cultivated autologous limbal epithelial cells (CALEC) using an innovative xeno
9 ring process utilizing cultivated autologous limbal epithelial cells (CALEC), the first xenobiotic-fr
10 stem cell deficiency (LSCD) with cultivated limbal epithelial cells (CLEC) from other countries, we
11 iated corneal epithelial cells, and SSEA4(-) limbal epithelial cells contain a higher proportion of l
12 the proliferation of stem/eTA cell-enriched limbal epithelial cells, contributing to expansion of th
15 t of these topographical features on corneal limbal epithelial cell differentiation has not been expl
17 cently, ex vivo cultivation and expansion of limbal epithelial cells has been performed utilizing AM
21 /beta-catenin pathway influences the fate of limbal epithelial cells, likely to be progenitor cells,
29 with limbal stem cell deficiency, cultivated limbal epithelial cell transplantation improves vision a
34 ained from a healthy area of the limbus, the limbal epithelial cells were cultured on a denuded human
35 thelial cells and immortalized human corneal limbal epithelial cells were cultured on the SF and denu
36 greatest number of Ki67-positive corneal and limbal epithelial cells were present at days 13 to 19, a