1                                              RCECs were grown in membrane filters to exhibit tight ba

2                                              RCECs were grown on membrane filters to exhibit tight ba

3          Apparent permeability of GSH across RCEC layers was approximately eight times higher in the

4                    GSH is transported across RCEC membranes by both Na(+)-dependent and -independent

5 indicated net absorption of L-cystine across RCECs.

6              Cellular uptake of L-cystine by RCECs occurred through both Na(+)-dependent and -indepen

7 ultured retinal capillary endothelial cells (RCECs) and in db/db mice treated with lovastatin.

8             Rabbit corneal epithelial cells (RCECs) in culture were arrested in the G(0) phase of the

9 ltured rabbit conjunctival epithelial cells (RCECs).

10 ltured rabbit conjunctival epithelial cells (RCECs).

11 n confluent rabbit corneal epithelial cells (RCECs).

12                                  In cultured RCECs, hypoxia and high glucose upregulated mRNA and pro

13 s significantly elevated in primary cultured RCECs treated for 24 hours with various concentrations (

14 ter a 24-hour incubation of primary cultured RCECs with an NO donor, S-nitroso-N-acetylpenicillamine

15 ved by Western blot analysis of lysates from RCECs treated with 0.25 mM SNAP for 24 hours.

16            Simian virus (SV)-40-immortalized RCECs were cultured in the presence and absence of EGF a

17 neration, HIF-1alpha, and VEGF expression in RCECs.

18 ing is involved in cell cycle progression in RCECs, possibly by upregulation of cyclin-D1 and -D3 and

19 -independent amino acid transport systems in RCECs.

20 phase and led to a decrease in the number of RCECs entering the S phase between 12 and 24 hours from

21 egulated during EGF-induced proliferation of RCECs and to determine whether there is any cross-talk b

22                             Depolarizing the RCEC membrane potential decreased GSH efflux into either