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1 Heterozygotes have no corneal disease.
2 n tear fluid derived from virally associated corneal disease.
3 loss of neurotrophic support contributes to corneal disease.
4 growth of fungal hyphae and the severity of corneal disease.
5 F. solani keratitis, a potentially blinding corneal disease.
6 located posterior chamber IOL in 1 case with corneal disease.
7 lenses of patients with contact lens-related corneal disease.
8 successful cataract surgery in patients with corneal disease.
9 be used with caution in patients with prior corneal disease.
10 ulation, followed by cataract, glaucoma, and corneal disease.
11 d exciting possibilities in the treatment of corneal disease.
12 nal ganglia were inversely proportional with corneal disease.
13 nd underappreciated role in the treatment of corneal disease.
14 creasing number and variety of patients with corneal disease.
15 rneal development and to study the causes of corneal disease.
16 increased amounts of MIP133 and more severe corneal disease.
17 stimulates MIP133 secretion, and exacerbates corneal disease.
18 and its absence in MMP-9(-/-) mice decreased corneal disease.
19 in a significantly reduced capacity to cause corneal disease.
20 m or more should be evaluated for potential corneal disease.
21 ctions in triggering immune complex-mediated corneal disease.
22 IL-1beta polyclonal Ab significantly reduced corneal disease.
23 eal PMN number and significantly exacerbated corneal disease.
24 Both groups developed invasive corneal disease.
25 utic vaccine against recurrent HSV-1-induced corneal disease.
26 AS4 significantly decreased postreactivation corneal disease.
27 hod may also be applicable to other heredity corneal diseases.
28 and explains how two SNPs may contribute to corneal diseases.
29 rategy for the pathogenesis and treatment of corneal diseases.
30 itical defect tightly linked to common human corneal diseases.
31 mental models and therapeutic strategies for corneal diseases.
32 dry eye after refractive surgery, and other corneal diseases.
33 s a significant problem associated with many corneal diseases.
34 s, healthy subjects, and patients with other corneal diseases.
35 us, normal subjects, and patients with other corneal diseases.
39 cal protection against primary HSV-1-induced corneal disease, a local ocular vaccine may prove more e
41 MIP-133 production is necessary to initiate corneal disease and plays an important role in the subse
42 LPS before challenge reduced the severity of corneal disease and protected challenged mice against pe
43 peutic topical application of CD ameliorated corneal disease and reduced the bacterial count in the e
44 vation are separable, (ii) the phenotypes of corneal disease and spontaneous reactivation are separab
45 33 production might be necessary to initiate corneal disease and that it may play an important role i
49 cal processes central to the pathogenesis of corneal disease, as well as other conditions including t
50 we found that two SNPs linked previously to corneal diseases, astigmatism, and Stevens-Johnson syndr
51 ce keratitis mimicking the onchocercal human corneal disease, BALB/c mice preimmunized with the bindi
53 motility contributed to the role of pili in corneal disease but was not involved in the role of pili
54 ease, compared with the production of severe corneal disease by 2 x 10(5) PFU of marker-rescued virus
58 (8) PFU per eye, d34.5 produced virtually no corneal disease, compared with the production of severe
61 d histopathologically, the human onchocercal corneal disease, demonstrating the antigenic specificity
66 m solani and Fusarium oxysporum cause severe corneal disease in the United States and worldwide and w
68 eal physiology and in the pathophysiology of corneal disease, including modulation of keratocyte apop
69 g-h3) and furthermore that some of the human corneal disease-inducing substitutions identified in bet
71 ever, delaying oral immunization until after corneal disease is established fails to mitigate keratit
75 chs corneal dystrophy (FCD) is a progressive corneal disease marked by the development of guttae, foc
78 h the changes observed in previously studied corneal diseases nor did they correlate with genes encod
79 ival, or it can promote diseases such as HSV corneal disease (or herpes stromal keratitis [HSK] in hu
80 important implications for the treatment of corneal disease, particularly corneal blindness due to L
84 ic neutralization of IL-2 after the onset of corneal disease resulted in a rapid regression of inflam
87 d that extended to the cornea, such that HSV corneal disease severity was reduced in susceptible BALB
88 ct on the cornea also depends on preexisting corneal disease, severity and chronicity of intraocular
90 efficacious against HSV-1-induced recurrent corneal disease than against recurrent HSV-1 ocular shed
91 ng elderly individuals; keratoconus (27%), a corneal disease that slowly deforms the cornea in young
92 ralization exacerbated P. aeruginosa-induced corneal disease, TIMP pAb- and normal rabbit serum (NRS)
93 val scarring (using Tauber staging), central corneal disease (vascularization, scarring, ulceration,
96 entral nervous system (CNS) inflammation and corneal disease was evaluated, and responses in genetica
97 PAK strains in the cornea and development of corneal disease was impaired in DeltaexoS, DeltaexoT, an
101 the homotypic gD1 vaccine against recurrent corneal disease, whereas the homotypic vaccine was much
102 role for endosymbiotic Wolbachia bacteria in corneal disease, which is characterized by neutrophil in
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