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 BB technique was performed on ex vivo human
corneoscleral buttons using a depth-sensing needle, base
6 A total of 1748
corneoscleral buttons were harvested from 10,265 decease
7 The dissected
corneoscleral buttons were immersed in OCT media and fro
8 Organ cultured human
corneoscleral buttons were studied.
9 Porcine corneal strips (8 x 4 mm) and
corneoscleral complexes were cross-linked using 1 to 100
10 cohols (BNAs) may be useful as pharmacologic
corneoscleral cross-linking agents.
11 bility of using these agents for therapeutic
corneoscleral cross-linking.
12 Human donor
corneoscleral (
CS) tissue containing the intact aqueous
13 The extra peripheral
corneoscleral data gained from OCT characterization of o
14 Thirty EDML were stripped from
corneoscleral discs and placed in a well plate containin
15 mm(2) vs 2,129 +/- 222 cells/mm(2) for the 5
corneoscleral discs of the control group.
16 lls/mm(2) vs 2,129 222 cells/mm(2) for the 5
corneoscleral discs of the control group.
17 An additional 5
corneoscleral discs were also placed in the same medium
18 The average ECD of the 30
corneoscleral discs, which later underwent stripping, wa
19 The average ECD of the 30
corneoscleral discs, which later underwent stripping, wa
20 rior-superior meridians of five normal human
corneoscleral discs.
21 To determine the incidence of positive
corneoscleral donor rim fungal cultures after keratoplas
22 he growth effect of VIP on TM cells in situ,
corneoscleral explants in organ cultures were first trea
23 e total cell number in the TM in LTP-treated
corneoscleral explants were increased by VIP.
24 ary human trabecular meshwork (TM) cells and
corneoscleral explants were stimulated with either dexam
25 the most effective VIP concentration, bovine
corneoscleral explants were treated with 0 (control) and
26 secretion of ANGPTL7 protein by TM cells and
corneoscleral explants.
27 in subconfluent cultures and in LTP-treated
corneoscleral explants.
28 nd three other ocular cells (ciliary muscle,
corneoscleral fibroblast, and lamina cribrosa) were cult
29 The
corneoscleral HBV DNA of 170 corneas (113 donors) was qu
30 00) and negative predictive value (1.00) for
corneoscleral HBV DNA.
31 al sagittal height (CS), iris diameter (ID),
corneoscleral junction angle (CSJ), and scleral radius (
32 Corneoscleral junction angle, corneal diameter, corneal
33 es, there was a tangential transition at the
corneoscleral junction.
34 ions of the cornea and cross-sections of the
corneoscleral junctions.
35 Corneoscleral limbal dissection of >/=6 clock hours duri
36 P = .11), and mean number of clock hours of
corneoscleral limbal dissection owing to wide tumor exci
37 N prevents LSCD in cases requiring extensive
corneoscleral limbal dissection.
38 and 47% of them originated from preexisting
corneoscleral limbus capillaries.
39 radiation was applied for 360 degrees of the
corneoscleral limbus in C57BL/6 normal mice and for 180
40 lculated by counting the nerve trunks at the
corneoscleral limbus of the entire cornea.
41 scans, approximately 35 microm) of the nasal
corneoscleral limbus were performed before and 1 hour af
42 ients to assess microscopic structure of the
corneoscleral limbus, in all quadrants.
43 located in the basal epithelial layer of the
corneoscleral limbus, represent essential components of
44 by and persistently associated with dilated
corneoscleral lymphatics.
45 this model suggests that, at least in part,
corneoscleral mechanics drive angle opening rather than
46 eparate TM beam regions within the uveal and
corneoscleral meshwork for image acquisition pairs of AF
47 to autofluorescent TM structures and filled
corneoscleral meshwork pores.
48 asty (ALK) (n = 127, 35.1%), or a peripheral
corneoscleral patch graft (n = 93, 25.7%) most commonly
49 apid progressive astigmatism attributable to
corneoscleral pigment accumulation.
50 30 minutes, CF labeled mainly the uveal and
corneoscleral regions.
51 and of the trabecular meshwork (TM) in human
corneoscleral rim tissues, with little collateral damage
52 qRT-PCR detected CHIKV RNA in
corneoscleral rims from 4 patients: 1 patient was viremi
53 A was detected in 80.0%, 9.2%, and 0% of the
corneoscleral rims in each group.
54 Corneoscleral rims retained after corneal transplantatio
55 Hepatitis B virus (HBV) DNA extracted from
corneoscleral rims was quantified by polymerase chain re
56 Human CBSM cells isolated from donor
corneoscleral rims were incubated for 24 hours with cont
57 Human donor
corneoscleral rims were sectioned immediately before int
58 Serum specimens and
corneoscleral rims were subjected to quantitative revers
59 The
corneoscleral shape profile analyzed from cross-sectiona
60 ructural organization and composition of the
corneoscleral shell (CSS) determine the biomechanical be
61 Nine human
corneoscleral specimens unsuitable for transplantation w
62 nly performed surgeries were corneal suture,
corneoscleral suture, and evisceration.
63 Fresh human
corneoscleral tissue was mounted on an artificial anteri
64 tern of PG-EP(4) receptors was determined in
corneoscleral tissues of human donor eyes and in culture
65 In the adjacent
corneoscleral TM, beams were thicker and coalesced as pl
66 ogical mechanisms in CSS and the efficacy of
corneoscleral treatments.
67 The iris-free procedure of
corneoscleral trephination developed by his contemporary