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1 ome trabecular cell loss was observed in the corneoscleral and uveal regions of the perfused treated
2 esent in most trabecular cells of the uveal, corneoscleral, and juxtacanalicular regions but only var
3 rom human donors (n = 19) and organ-cultured corneoscleral buttons (n = 10) obtained after Descemet's
4                                        Fresh corneoscleral buttons from human donors (n = 19) and org
5                                The dissected corneoscleral buttons were immersed in OCT media and fro
6                         Organ cultured human corneoscleral buttons were studied.
7        Porcine corneal strips (8 x 4 mm) and corneoscleral complexes were cross-linked using 1 to 100
8 cohols (BNAs) may be useful as pharmacologic corneoscleral cross-linking agents.
9 bility of using these agents for therapeutic corneoscleral cross-linking.
10                                  Human donor corneoscleral (CS) tissue containing the intact aqueous
11                         The extra peripheral corneoscleral data gained from OCT characterization of o
12 rior-superior meridians of five normal human corneoscleral discs.
13       To determine the incidence of positive corneoscleral donor rim fungal cultures after keratoplas
14 he growth effect of VIP on TM cells in situ, corneoscleral explants in organ cultures were first trea
15 e total cell number in the TM in LTP-treated corneoscleral explants were increased by VIP.
16 ary human trabecular meshwork (TM) cells and corneoscleral explants were stimulated with either dexam
17 the most effective VIP concentration, bovine corneoscleral explants were treated with 0 (control) and
18 secretion of ANGPTL7 protein by TM cells and corneoscleral explants.
19  in subconfluent cultures and in LTP-treated corneoscleral explants.
20 nd three other ocular cells (ciliary muscle, corneoscleral fibroblast, and lamina cribrosa) were cult
21 al sagittal height (CS), iris diameter (ID), corneoscleral junction angle (CSJ), and scleral radius (
22                                              Corneoscleral junction angle, corneal diameter, corneal
23 es, there was a tangential transition at the corneoscleral junction.
24 ions of the cornea and cross-sections of the corneoscleral junctions.
25                                              Corneoscleral limbal dissection of >/=6 clock hours duri
26  P = .11), and mean number of clock hours of corneoscleral limbal dissection owing to wide tumor exci
27 N prevents LSCD in cases requiring extensive corneoscleral limbal dissection.
28  and 47% of them originated from preexisting corneoscleral limbus capillaries.
29 radiation was applied for 360 degrees of the corneoscleral limbus in C57BL/6 normal mice and for 180
30 lculated by counting the nerve trunks at the corneoscleral limbus of the entire cornea.
31 scans, approximately 35 microm) of the nasal corneoscleral limbus were performed before and 1 hour af
32 ients to assess microscopic structure of the corneoscleral limbus, in all quadrants.
33  by and persistently associated with dilated corneoscleral lymphatics.
34  this model suggests that, at least in part, corneoscleral mechanics drive angle opening rather than
35 eparate TM beam regions within the uveal and corneoscleral meshwork for image acquisition pairs of AF
36  to autofluorescent TM structures and filled corneoscleral meshwork pores.
37 asty (ALK) (n = 127, 35.1%), or a peripheral corneoscleral patch graft (n = 93, 25.7%) most commonly
38 apid progressive astigmatism attributable to corneoscleral pigment accumulation.
39  30 minutes, CF labeled mainly the uveal and corneoscleral regions.
40 and of the trabecular meshwork (TM) in human corneoscleral rim tissues, with little collateral damage
41                qRT-PCR detected CHIKV RNA in corneoscleral rims from 4 patients: 1 patient was viremi
42                                              Corneoscleral rims retained after corneal transplantatio
43         Human CBSM cells isolated from donor corneoscleral rims were incubated for 24 hours with cont
44                                  Human donor corneoscleral rims were sectioned immediately before int
45                          Serum specimens and corneoscleral rims were subjected to quantitative revers
46                                          The corneoscleral shape profile analyzed from cross-sectiona
47 ructural organization and composition of the corneoscleral shell (CSS) determine the biomechanical be
48                                   Nine human corneoscleral specimens unsuitable for transplantation w
49                                  Fresh human corneoscleral tissue was mounted on an artificial anteri
50 tern of PG-EP(4) receptors was determined in corneoscleral tissues of human donor eyes and in culture
51                              In the adjacent corneoscleral TM, beams were thicker and coalesced as pl
52 ogical mechanisms in CSS and the efficacy of corneoscleral treatments.
53                   The iris-free procedure of corneoscleral trephination developed by his contemporary

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