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1 HD CAV-2 vectors to treat diseases affecting corneal keratocytes.
2 SMA expression induced by TGFbeta1 in rabbit corneal keratocytes.
3 ression of Ctnnb1(DeltaE3) mutant protein in corneal keratocytes.
4        Recent studies have shown that rabbit corneal keratocytes abundantly express two water-soluble
5 c differences between anterior and posterior corneal keratocytes after stimulation with the profibrot
6                                As they do in corneal keratocytes and endothelial cells, K+ channels d
7 he present study has previously reported for corneal keratocytes and endothelial cells.
8 is a useful marker for the identification of corneal keratocytes and for documenting their response t
9                                    Embryonic corneal keratocytes and sensory nerve fibers grow and di
10                   Serum-free cultured rabbit corneal keratocytes and TGFbeta (5 ng/mL) induced myofib
11                                              Corneal keratocytes are able to differentiate normally a
12 ta show that, even at late embryonic stages, corneal keratocytes are not terminally differentiated, b
13 ication between corneal epithelial cells and corneal keratocytes as well as vascular endothelial cell
14  tissues of E13.5 embryos, and restricted to corneal keratocytes at E14.5 and thereafter.
15 dult eyes, keratocan mRNA can be detected in corneal keratocytes, but not in scleral cells.
16 inally, this work demonstrates that cultured corneal keratocytes can act as a model for the study of
17                                  TKT loss in corneal keratocytes can be induced by PDGF or bFGF and t
18 were nontoxic to the cornea and entered into corneal keratocyte cytoplasm.
19           An R124H mutation in primary human corneal keratocytes derived from a GCD2 patient was corr
20 In this study, to strengthen the notion that corneal keratocyte-derived Wnt/beta-catenin signaling re
21             In contrast to epithelial cells, corneal keratocytes did not express IL-1RII mRNA.
22 rowth factor (TGF)-beta-dependence of feline corneal keratocyte differentiation into alpha-smooth mus
23 nscriptional repressor, efficiently inhibits corneal keratocyte differentiation to myofibroblasts in
24 experiments show that anterior and posterior corneal keratocytes exhibit different sensitivities to t
25 rosis is caused in part by the activation of corneal keratocytes from a native mechanically quiescent
26 he role of glucose in the behaviour of human corneal keratocytes has been overlooked.
27                                              Corneal keratocytes have a remarkable ability to heal th
28  that human corneal epithelial cells but not corneal keratocytes have evolved the capacity to dampen
29 of this study was to determine whether human corneal keratocyte (HCKs) in culture synthesize these ch
30 entify oxidative stress levels between human corneal keratocytes (HCKs), fibroblasts (HCFs) and kerat
31                                              Corneal keratocytes in basal media within compressed mat
32 all, mutant beta-catenin accumulation in the corneal keratocytes inhibited corneal epithelial stratif
33 at activation of ICl(LPA) by LPA in cultured corneal keratocytes is receptor mediated and that ICl(LP
34 1P) on Cl(-) currents (ICl(LPA)) in cultured corneal keratocytes isolated from the corneas of New Zea
35 pha-galactosyl glycoconjugates were found in corneal keratocytes, lens fibers, and retinal vascular e
36    Apoptosis was noted in the deeper central corneal keratocytes located anteriorly and posteriorly t
37 ted cAMP can inhibit TGFbeta1-induced rabbit corneal keratocyte-myofibroblast transformation.
38 eratocan and lumican expression in activated corneal keratocytes observed during corneal stromal woun
39                        The results show that corneal keratocytes occupy a significantly greater tissu
40 g activity was significantly elevated in the corneal keratocytes of the Dox-induced mutant mice, comp
41 nd contractility, we cultured primary rabbit corneal keratocytes on flexible substrata of varying sti
42                                       Rabbit corneal keratocytes (RCKs) were treated with EGF, TGF-be
43  endothelial (RCEn) cells, as well as rabbit corneal keratocytes (RCKs) were used.
44 at genetic deletion of beta-catenin in mouse corneal keratocytes resulted in precocious corneal epith
45       Human corneal epithelial cells but not corneal keratocytes synthesize both membrane and soluble
46 in expression is a characteristic feature of corneal keratocytes that is lost when cells are phenotyp
47               In culture, TGFbeta caused cat corneal keratocytes to differentiate into alphaSMA-posit
48 d subcellular pattern of force generation in corneal keratocytes treated with TGF-beta1.
49                                Primary human corneal keratocytes under serum-free conditions were use
50 osis in healing corneal wounds, and in vitro corneal keratocytes up-regulate expression of several fi
51 zed beta-catenin mutant (Ctnnb1(DeltaE3)) in corneal keratocytes via a doxycycline (Dox)-inducible co
52 GFBI mutation in GCD patient-derived primary corneal keratocytes via homology-directed repair (HDR).
53 ell culture model of freshly isolated rabbit corneal keratocytes was used.
54                      Primary isolated rabbit corneal keratocytes were cultured in serum-free medium.
55                                 Normal human corneal keratocytes were isolated from donor corneas of
56                                       Rabbit corneal keratocytes were plated within standard bovine o
57                                       Rabbit corneal keratocytes were seeded within collagen matrices