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1 cells and corneal epithelial cells regulates corneal angiogenesis.
2 F-induced (5%-57%) and VEGF-induced (3%-66%) corneal angiogenesis.
3 ts as a broad-spectrum negative regulator of corneal angiogenesis.
4 lly responsible for suppressing inflammatory corneal angiogenesis.
5 migration are initial events in PAF-promoted corneal angiogenesis.
6 the lack of TSP-1,2 and both TSPs on induced-corneal angiogenesis.
7 s TSP-1 and/or -2 resulted in no spontaneous corneal angiogenesis.
8 sly implanted Matrigel plugs, as well as rat corneal angiogenesis.
9 ration, and fibroblast growth factor-induced corneal angiogenesis.
10 , and basic fibroblast growth factor-induced corneal angiogenesis.
11 tic ring assay and a model of suture-induced corneal angiogenesis.
12 ctival injection of the morpholino-inhibited corneal angiogenesis and lymphangiogenesis, and suppress
14 We show that FOXC1 mutations also lead to corneal angiogenesis, and that mice homozygous for eithe
17 cularization, as well as models with induced corneal angiogenesis, are widely used to investigate the
20 ll migration and tube formation, and in vivo corneal angiogenesis assays, HRGP inhibited the antiangi
21 clude that activin A stimulates inflammatory corneal angiogenesis by increasing VEGF levels through a
22 exposure of the eyes to radiation suppressed corneal angiogenesis comparably to whole-body exposure.
27 aortic ring assay and promoted bFGF-induced corneal angiogenesis in vivo in a corneal pocket assay.
28 lary endothelial cell migration in vitro and corneal angiogenesis in vivo, and apparently act via bin
32 t loci (QTLs), which influence the extent of corneal angiogenesis induced by vascular endothelial gro
33 topical and systemic cyclosporin A (CsA) on corneal angiogenesis induced by xenotransplantation or b
34 Understanding the roles of Eph and ephrin in corneal angiogenesis may provide a therapeutic intervent
36 and this finding was confirmed by an in vivo corneal angiogenesis model and an ex vivo aortic ring as
41 SP-2, helps to suppress inflammation-induced corneal angiogenesis postnatally, implying that angiogen
43 st phase III study on a topical inhibitor of corneal angiogenesis showed that aganirsen eye drops sig
44 all TSP(-/-) mice had significantly greater corneal angiogenesis than those of control mice (P < 0.0
45 ings identify a role for FoxC1 in inhibiting corneal angiogenesis, thereby maintaining corneal transp
47 r supporting a role for MMP-9 in HSV-induced corneal angiogenesis was the observation that inhibition
48 area and density and extent of bFGF-induced corneal angiogenesis were determined in C57BL/6J, BALB/c
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