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1 d its impact on nanoparticle behavior in the tear fluid.
2 al of 174 proteins that were detected in the tear fluid.
3 hydrodynamic diameter after interacting with tear fluid.
4 conduct the first O-glycoproteomic study of tear fluid.
5 nds regulate the production and secretion of tear fluid.
6 9 activity assay in 1 microL of unstimulated tear fluid.
7 n composition and amount of O-glycans in the tear fluid.
8 icrobial peptides have been described in the tear fluid.
9 bead assay were used to quantify IL-1beta in tear fluid.
10 lm is also dictated by the amount of aqueous tear fluid.
11 ction between the lipid film and the aqueous tear fluid.
12 biologically inactive precursor IL-1 beta in tear fluid.
13 ace of the human eye and is present in human tear fluid.
14 human corneal epithelium and are present in tear fluid.
15 ase B (92 kDa) activity (P < 0.001) in their tear fluid.
16 ymphocytes, and increased bioavailability in tear fluids.
17 ntrations in rosacea-affected than in normal tear fluids.
19 sed by fluorometric measurement of collected tear fluid 15 minutes after instillation of 1% sodium fl
21 t of tear fluid was less cytoprotective than tear fluid (80% protection with tear fluid, 48% with sul
22 When nanoparticles are introduced into the tear fluid, a layer of protein corona is formed on their
25 on in both tear fluid and sulfacetamide, but tear fluid also blocked bacterial swimming motility.
27 th as the source of the aqueous component of tear fluid and as the site of autoimmune pathology in th
28 s cytokines in cultured CECs, its absence in tear fluid and CIC samples suggests that IL-1beta does n
29 y revealed bacterial chain formation in both tear fluid and sulfacetamide, but tear fluid also blocke
30 factant protein D (SP-D) is present in human tear fluid and that it can protect corneal epithelial ce
33 rstanding of the interplay between bacteria, tear fluid, and the corneal epithelium that determines h
34 peptides that are likely to be components of tear fluid are expressed by acinar cells and show pronou
35 xpression pattern of inflammatory markers in tear fluids at baseline might serve as a prognostic fact
36 These cytokines were also measured in normal tear fluid before and after nasal stimulation to induce
39 e assumed to contribute to the production of tear fluid, but little is known about their function.
41 We tested the hypothesis that whole human tear fluid can protect corneal epithelia against P. aeru
44 RER1, ACTB, GAPDH, PGK1, UBC, and AP3D1) in tear fluid collected from individuals with dry eye disea
45 ic, five invasive)/ml with or without reflex tear fluid collected from the conjunctival sacs of human
46 e was evaluated by measuring fluorescence in tear fluid collected from the inferior meniscus 15 minut
51 s correlated with delayed tear clearance and tear fluid concentration of interleukin-1alpha, a proinf
53 chia coli-induced travelers' diarrhea and in tear fluid derived from virally associated corneal disea
55 tions between gold nanoaprticles (AuNPs) and tear fluid, focusing on the physicochemical changes of t
57 work for future biochemical investigation of tear fluid glycoproteins and their application as diagno
58 e most comprehensive characterization of the tear fluid glycoproteome to date, elucidating the glycos
60 sity of corneal fluorescein staining and the tear fluid IL-1 alpha concentration (r(2) = 0.17, P < 0.
63 omoter polymorphisms and TNF-alpha levels in tear fluid in scarring trachoma, a large matched-pair ca
65 a, precursor IL-1 beta, and IL-1Ra in reflex tear fluid, indicating that the lacrimal glands may secr
67 WB assay, assessment of lactoferrin in human tear fluid is demonstrated with a goal of advancing towa
75 ivity was evaluated by gelatin zymography in tear fluid obtained from 13 patients with ocular rosacea
76 IL-1 beta, was significantly elevated in the tear fluid of both dry-eye groups compared with normal s
78 mined whether nucleases are deficient in the tear fluid of dry eye disease (DED) patients, and whethe
83 cin MUC5AC were significantly reduced in the tear fluid of patients with Sjogren syndrome, corroborat
87 inoculation was performed ex vivo to exclude tear fluid or corneas were pretreated with EGTA to disru
89 r surface epithelia but is also found in the tear fluid, presumably in a soluble form, as found on th
90 ctrometry (MS) was performed to quantify the tear fluid proteins from chronic SJS/TEN patients (n = 2
95 alomucin complex was immunoprecipitated from tear fluid samples and both corneal and conjunctival epi
96 ntagonist (IL-1Ra) were measured by ELISA in tear fluid samples obtained from normal individuals and
98 nM, which when delivered topically increased tear fluid secretion in mice and showed efficacy in an e
99 In vivo pharmacokinetic studies in rabbit tear fluid showed significant increase in mean residence
103 tion of RNA and gene expression changes from tear fluid that could be used to monitor or study eye di
105 of rigorous validation in studies involving tear fluid to ensure accurate gene expression results, t
106 c channel in contact lens sensors allows for tear fluid to flow through the sensing region, enabling
113 on of IL-1 alpha and mature IL-1 beta in the tear fluid was increased, and the concentration of precu
114 ith bacteriostatic activity matching that of tear fluid was less cytoprotective than tear fluid (80%
115 Without perturbing the eyeball, 3 microL of tear fluid was sampled from the marginal conjunctiva und
116 concentrations of IL-1beta and TNF-alpha in tear fluid washings and in corneal and conjunctival epit
117 the concentrations of IL-1beta and MMP-9 in tear fluid washings and the concentrations of IL-1beta a
118 se (MMP)-9 concentration and activity in the tear fluid were evaluated with gelatin zymography and wi
120 ro-MMP-9 and IL-1alpha concentrations in the tear fluid were measured by enzyme-linked immunosorbent
123 hich showed marked upregulation in patients' tear fluid when normalized with the top-rated reference
125 f corneal sizes and then quickly dissolve in tear fluid within a minute, enabling an initial burst re