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1 ld sores) and keratitis (inflammation of the cornea).
2 laced in the posterior chamber away from the cornea.
3 s such as decalcified ivory, fish scales, or cornea.
4 d maps of TCT and En/DMT of the central 6-mm cornea.
5 e with properties most similar to the native cornea.
6 on-invasive means of delivering siRNA to the cornea.
7 ickness (TCT) and En-DMT of the central 6-mm cornea.
8 ll deficiency (LSCD) were noted on the right cornea.
9 and the recruitment of mural cells into the cornea.
10 discriminate structural changes in a damaged cornea.
11 emination of virus to, and infection of, the cornea.
12 a resolution steepened the central posterior cornea.
13 events can lead to blinding scarring of the cornea.
14 mportant role in the pathogenicity of the KC cornea.
15 timulatory molecule CD80 but not CD86 in the cornea.
16 d in compound eyes incorporating a chitinous cornea.
17 ection, but also along the depth axis of the cornea.
18 eovascularization in the central 5 mm of the cornea.
19 therapy as a means of safely stiffening the cornea.
20 r in en face maps covering almost the entire cornea.
21 of the non-linear mechanical behavior of the cornea.
22 signaling in response to inflammation in the cornea.
23 e cellular and molecular organization of the cornea.
24 lpful in cases of iris defects and irregular corneas.
25 atoconus, subclinical keratoconus and normal corneas.
26 bit skin cells and in vivo in infected mouse corneas.
27 ratocytes both in culture and within ex vivo corneas.
28 nt iNKT cell subset in infected asymptomatic corneas.
29 ion in vitro and ex vivo in cultured porcine corneas.
30 had better DOF curves and DCNVA than normal corneas.
31 epithelial cells, respectively, in infected corneas.
32 requency shift of 4 MHz per decade in normal corneas.
33 but increased the opacity in HSV-1-infected corneas.
34 duced the development of hypoxia in infected corneas.
35 on the injury response in Mmp12(-/-) and WT corneas.
36 sted for differentiating normal from ectatic corneas.
37 ed in Mmp12(-/-) corneas as compared with WT corneas.
38 aired WST-D/NIR treated and untreated rabbit corneas.
39 erapy for stiffening pathologically weakened corneas.
40 ed area without the need for cadeveric donor corneas.
41 ated wolframin expression in human and mouse corneas.
42 come the global shortage of transplant-grade corneas.
43 ent diameters around the central part of the cornea (1, 2, and 3 mm) and reading elevation values at
44 randomized preclinical trial with 24 paired corneas, 1 was stored in OC and the other in ASM, using
45 s from 205 patients distributed in 82 normal corneas, 40 early-stage keratoconus and 83 established k
46 ift at the thinnest point compared to normal corneas (5.7072 +/- 0.0214 vs 5.7236 +/- 0.0146 GHz, P <
48 nerves in response to inflammation using the cornea, a normally avascular and densely innervated ocul
53 iate analysis suggested that a younger donor cornea age and higher donor endothelial cell count are a
57 rited disorders that affect any layer of the cornea and are usually progressive, bilateral conditions
60 and pro-inflammatory factors in the grafted cornea and draining lymph nodes (dLNs) were evaluated wi
61 p, with the most frequent in glaucoma (24%), cornea and external diseases (22%), and neuroophthalmolo
62 the dynamic biomechanical properties of the cornea and have been shown to be biomarkers of corneal d
63 h dextran (WST-D) to the epithelium-debrided cornea and illumination with Near Infrared (NIR), has be
64 nea (first, through the central point of the cornea and keratoconus apex; second, as the perpendicula
65 lamp biomicroscopy was used to evaluate the cornea and lens, and retinal vasculature was examined by
66 ing debridement of different portions of the cornea and limbus and applied them to the dual-fluoresce
69 vivo model using discs of porcine and human cornea and sclera (5 mm diameter) to assess penetration
72 y eyelids, eyelid edema, highly vascularized cornea and tarsal plates (TPs), slit eye, and increased
74 +), and NK1.1(+) T cells was observed in the cornea and TG of SPP-inducible knockout mice compared to
75 ion that stem cells exist within the central cornea and that their progeny have the capacity to migra
78 SPP mRNA was reduced by more than 93% in the cornea and trigeminal ganglia (TG) and by 99% in the liv
82 ior and posterior stroma in healed WST-D/NIR corneas and untreated controls revealed no obvious diffe
85 s, displacement of the thinnest point of the cornea, and the presence of posterior surface depression
86 of the iris is subject to refraction by the cornea, and thus an outside observer sees a virtual imag
87 genic levels of VEGF-A within HSV-1-infected corneas, and CD4(+) cell depletion promoted reinnervatio
88 ent of neutrophils infiltrating the infected corneas, and the depletion of neutrophils reduced the de
89 ssociated glycolytic genes in HSV-1 infected corneas, and the outcome of blocking hypoxia-inducible f
93 of the cornea has been found and keratoconus corneas are statistically significantly different from n
100 y measuring mechanical properties of porcine corneas based on volumetric deformation following varyin
102 stically significantly different from normal corneas, but for precise differentiating of keratoconus
103 lacrimal drainage) 0.071% penetrated porcine cornea by 60 min and 0.0002% penetrated human cornea and
104 timulated microenvironment remodeling in the cornea by promoting the paracrine action of secreted int
105 parallel with a partial reinnervation of the cornea by TRPM8(+) fibers and with an increase in basal
107 Herpes simplex virus type 1 (HSV-1)-infected corneas can develop a blinding immunoinflammatory condit
108 an sulfate epitopes were majorly observed in cornea, cartilage and brain; and mainly involved in embr
110 s of HSV-1-infected WT mice, the symptomatic corneas CD1d KO mice, with iNKT cell deficiency, had inc
111 Seven of 16 (43.7%) eyes with N-PCG had a cornea clear enough at presentation for a goniotomy comp
114 erence in the virus titer recovered from the cornea comparing vaccinated mice, HSV-1 0DeltaNLS-vaccin
115 ann- correlated intraocular pressure (IOPg), cornea-compensated IOP (IOPcc) using the ORA, and centra
119 subclinical edema (n = 16), in <=42% of FECD corneas deemed not to have edema (n = 62), and in <=5% o
124 nclude that the cells that develop the mouse cornea do not require a primary stroma for cell migratio
129 by projecting two perpendicular axes onto a cornea (first, through the central point of the cornea a
130 oscopy, we investigated the developing mouse cornea, focusing on the invading cells, the extracellula
131 nced salt solution) to the de-epithelialized cornea for 30 minutes, followed by irradiation with a 6
133 mically or photochemically cross-linking the cornea for therapy presents a unique approach to managin
136 ose of this study was to investigate whether corneas from donors >=80 years old are suitable for Desc
138 els of HSV-1 gene expression were similar in corneas from HSV-CD80-infected and parental virus-infect
139 ed a useful model for differentiating normal corneas from the clinically normal eyes of patients with
141 on (AMD), diabetic retinopathy, glaucoma, or cornea guttata (aOR, 1.35; P = 0.006); use of Trypan blu
144 t impact on optic neuropathy, dose to 20% of cornea had the largest impact on neovascular glaucoma, a
150 , that the outer edge (limbus) of live human corneas has a substantially lower bulk modulus compared
153 geometric and volumetric characterization of cornea in pediatric patients with early and mild KC usin
155 first measurement of shear modulus in human corneas in vivo using optical coherence elastography (OC
156 be the non-linear mechanical behavior of the cornea, in order to characterize the capability of the n
157 ging therapies to replace the need for donor corneas include pre-formed biosynthetic buttons and in s
159 is an immune response to the lens following cornea injury involving the lens-associated MAGP1-rich c
161 rneal nociceptors.SIGNIFICANCE STATEMENT The cornea is a richly innervated and highly sensitive tissu
166 domly selected from 312 patients with normal corneas; Keratoconus group, including 1 eye randomly sel
167 topically to mice eyes penetrated across all cornea layers and resulted in a significant reduction of
168 Still, topical modulation of Piezo2 in the cornea may be useful to selectively relief unpleasant se
176 both as a function of IOP in ex vivo porcine cornea, obtaining values consistent with both tensile an
177 stem cells of non-skin origin (e.g. that of cornea, oesophagus, vagina, bladder, prostate) that expr
178 nd circular actin fibers associated with the corneas of A. irradians that may represent muscles whose
179 the predominant iNKT cell subset in infected corneas of asymptomatic B6 mice (with little to no corne
181 s of wild-type (WT) B6 mice, the symptomatic corneas of CD1d KO mice, which lack iNKT cells, showed (
184 e number of CD4(+) T cells was lower, in the corneas of HSV-CD80-infected mice than in mice infected
186 nalysis detected 75 known HSV-1 genes in the corneas of mice infected with HSV-CD80 or parental virus
187 to no corneal herpetic disease), compared to corneas of symptomatic mice (with severe corneal herpeti
188 a), TNFalpha, and TLR4 were evaluated in the corneas of the mice with fungal infection and the contro
189 antification of IL-1beta and TNFalpha in the corneas of the mice with fungal infection was determined
190 s has implications for the proposed calcitic corneas of trilobites, which we posit are artefacts of p
191 xt generation RNA sequencing from individual corneas of two distinct patient populations - one from t
198 oocyte), tissues (Xenopus epithelium and rat cornea), organs (Xenopus gills and mouse skin) and appen
199 virus, but multiple factors are involved in cornea pathology in response to ocular virus challenge.
200 ed in vaccinated mice challenged with HSV-1, cornea pathology was mixed with a reduction in neovascul
201 oducibility were similar in all subgroups of cornea patients, excluding the DES group, for which repr
204 sruption of the basement membrane in wounded corneas prompted an increase in the abundance of IL-1bet
209 nprecedented endothelial cell quality: no OC corneas remained suitable for transplantation, but one-t
211 t early during ocular herpesvirus infection, cornea-resident IFN-gamma-producing PLZF(lo)RORgammat(lo
212 is study, we examined the protective role of cornea-resident iNKT cell subsets using the mouse model
214 HSV-1) keratitis, we found that infection of corneas resulted in subsequent infection of ocular gland
215 can occur during microbial infection of the cornea, resulting in potentially permanent visual defici
216 transmission electron tomography on four KC corneas showed the degeneration of microfibrils within t
217 higher SP-A1 and thinner CCT (thin and stiff corneas) showed accelerated RNFL thinning by 0.72 mum/ye
218 ye morphology is similar in both species and cornea size relative to eye size (C:A ratio) is intermed
223 This study analyzed sex differences among cornea specialists with regards to academic rank, schola
225 ly definite edema (n = 15), in >=81% of FECD corneas suspicious for subclinical edema (n = 16), in <=
227 Nitrate and nitrite levels were higher in cornea than in other eye parts, while lens contained the
228 igher isolation rate of S. aureus from their cornea than those with a single episode (p < 0.01) and a
232 bust antiviral CD4(+) T cell response in the cornea that was associated with protective immunity agai
233 ises after triple DMEK particularly occur in corneas that are flatter centrally than the periphery be
235 ting of keratoconus stages (including normal corneas) the method is currently neither specific nor se
236 ssociated with the optical properties of the cornea, the absence of any large-scale changes following
238 cus on assessing the center of this diseased cornea, there is growing evidence of peripheral involvem
243 ng factors that predispose clinically normal corneas to aberrant fibrosis post surgery and the role o
244 AS) OCT tube parameters, including posterior cornea-to-tube tip distance, tube angle-to-posterior cor
248 asticity mapping of individual layers in the cornea using non-destructive elastography techniques adv
252 ent (A2) took place earlier in time, and the cornea was moving faster during A2 in the OEs than in th
256 est and lowest corneal point in all measured cornea was stronger for subjects with a peripheral corne
258 ssion of Krt12, Krt14 and Pax6 in the mutant corneas was not altered after overexpression of Ctnnb1(D
259 A higher SP-A1, suggestive of a stiffer cornea, was associated with a faster rate of RNFL thinni
261 evoked by von Frey filaments applied on the cornea were lower in Piezo2-deficient mice compared with
264 ce of scar in keratoconic and nonkeratoconic corneas were all associated with an increased risk of po
265 l keratoplasty and participants with healthy corneas were assessed around noon the day before surgery
267 Three, 7 and 14 days after the treatment, corneas were collected and stained with FITC-conjugated
278 ed as conjunctival extensions onto the clear cornea, were diagnosed upon slit-lamp examination and on
279 e virus reactivates and migrates back to the cornea, where it restimulates the immune response, leadi
281 nd DeltaNp63 was downregulated in the mutant corneas, which was associated with reduced corneal epith
282 d neurotrophic factor levels in diabetic rat corneas, which were partially restored by fenofibrate tr
283 uorescence staining was decreased in patient corneas, while KEAP1, which helps to degrade NRF2, was i
284 l collagen architecture of wounded embryonic corneas, whilst identifying temporal and spatial changes
285 multifactorial, degenerative disease of the cornea whose pathogenesis and underlying transcriptomic
286 show that treating the burnt surface of the cornea with collagenase effectively restores the tissue'
287 ncreasing biomechanical inhomogeneity in the cornea with keratoconus progression and biomechanical as
288 iffness plays a critical role in shaping the cornea with respect to intraocular pressure and physical
290 g pachymetry and posterior elevation maps of corneas with a range of severity of FECD were evaluated
291 raphic features were all present in all FECD corneas with clinically definite edema (n = 15), in >=81
292 ferences were observed when comparing normal corneas with early-stage keratoconus/ in variables of th
298 lation with slope in the central part of the cornea (with a radius of 1 mm) ranging from 0.48 (p < 0.
299 y and sympathetic nerve landscape within the cornea, with implications for the treatment of blinding