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1 uginosa invasion was explored using cultured rabbit corneal epithelial cells.
2 ovine corneas and in membranes from cultured rabbit corneal epithelial cells.
3                            Primary human and rabbit corneal epithelial cells and immortalized human c
4 ty, Kv channel types were sought in cultured rabbit corneal epithelial cells and in the intact rat co
5 e used for transient transduction of primary rabbit corneal epithelial cells, and the effect on cell
6 ing units) were added to primary cultures of rabbit corneal epithelial cells (approximately 10(5)/wel
7 ed parasites; CPE assays were performed with rabbit corneal epithelial cells as host cells; and the e
8                                           In rabbit corneal epithelial cells, both peroxisome prolife
9 n of Rho activity in the primary cultures of rabbit corneal epithelial cells by microinjecting them w
10                                              Rabbit corneal epithelial cells cultured in the presence
11                   Rho and ROCK activities in rabbit corneal epithelial cells in culture were inhibite
12                                              Rabbit corneal epithelial cells in culture were subjecte
13  Production of TGF-beta2 protein by cultured rabbit corneal epithelial cells is reduced by plating on
14                                            A rabbit corneal epithelial cell line SIRC was used to est
15                                              Rabbit corneal epithelial cells (RCECs) in culture were
16 tide-3 kinase (PI3K) activities in confluent rabbit corneal epithelial cells (RCECs).
17                                     RNA from rabbit corneal epithelial cells was probed for PAF-R exp
18                                 Immortalized rabbit corneal epithelial cells were cultured in 24-well
19                                              Rabbit corneal epithelial cells were grown to multilayer
20                                              Rabbit corneal epithelial cells were injured by scraping

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