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

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