ライフサイエンスコーパス: aqueous humor

1 d in reliably high ESBA105 concentrations in aqueous humor.

2 of impedance of nutritional support from the aqueous humor.

3 ll infiltration and protein concentration in aqueous humor.

4 s log colony-forming units per milliliter of aqueous humor.

5 on of transforming growth factor-beta in the aqueous humor.

6 body are critical for the production of the aqueous humor.

7 both mutated and wild-type myocilin into the aqueous humor.

8 -specific polymerase chain reaction (PCR) in aqueous humor.

9 aration at the concentration levels found in aqueous humor.

10 ow that mutant MYOC is not secreted into the aqueous humor.

11 nalyze myocilin complex formation in porcine aqueous humor.

12 which clearly distinguished POAG from normal aqueous humor.

13 a2 levels are elevated in glaucomatous human aqueous humor.

14 (DMEM) or DMEM supplemented with 50% porcine aqueous humor.

15 ents, but only after incubation with porcine aqueous humor.

16 ed by reduced pressure-dependent drainage of aqueous humor.

17 flat cells that separate the cornea from the aqueous humor.

18 when novobiocin (0.1 mM) was present in the aqueous humor.

19 , urine (64 days), amniotic fluid (38 days), aqueous humor (101 days), cerebrospinal fluid (9 months)

20 able Zaire ebolavirus (EBOV) was detected in aqueous humor 14 weeks after the onset of EVD and 9 week

21 ly if myocilin was preincubated with porcine aqueous humor (78% +/- 77% when preincubated in DMEM con

22 generation of regulatory T cells (Tregs) by aqueous humor (AH) and identified TGF-beta as a critical

23 beta 2 (TGFbeta(2)) is often elevated in the aqueous humor (AH) and trabecular meshwork (TM) of patie

24 There were a total of 284 aqueous humor (AH) and/or vitreous fluid (VF) samples.

25 trophozoites can enter the AC; however, the aqueous humor (AH) contains factors that either induce e

26 lar pressure (IOP) resulting from diminished aqueous humor (AH) drainage through the trabecular pathw

27 The concentration of ANGPTL7 protein in aqueous humor (AH) from patients with glaucoma and contr

28 rmed by enzyme-linked immunosorbent assay in aqueous humor (AH) obtained from human donor eyes (POAG

29 To investigate whether the aqueous humor (AH) of Rb eyes has sufficient tumor-deriv

30 ribution of MRP4 in human TM (HTM) cells and aqueous humor (AH) outflow pathway was determined by RT-

31 intraocular pressure (IOP) due to increased aqueous humor (AH) outflow resistance, which is associat

32 tension arising from increased resistance to aqueous humor (AH) outflow through the trabecular meshwo

33 The effects of neuromedin U (NMU) on aqueous humor (AH) outflow were determined in enucleated

34 P results from the resistance to drainage of aqueous humor (AH) produced by the ciliary body in a pro

35 Bicarbonate transport plays a role in aqueous humor (AH) secretion.

36 Aqueous humor (all cohorts), vitreous humor (cohort IV o

37 of all uveitis patients, positive for RV in aqueous humor analysis (polymerase chain reaction [PCR]

38 ed interleukin (IL)-6 and IL-8 levels in the aqueous humor and a concomitant approximately twofold (P

39 ting the secretion of mutant myocilin in the aqueous humor and by decreasing intracellular accumulati

40 Best2 appears to antagonize the formation of aqueous humor and cause an inhibition of both F(c) and F

41 els of TNF-alpha, CCL-2/MCP-1, and ICAM-1 in aqueous humor and CCL-2/MCP-1 and ICAM-1 levels in retin

42 iary body and choroid plexus, the sources of aqueous humor and cerebrospinal fluid, respectively.

43 ommunicate via soluble agents present in the aqueous humor and implicate Best2 as a critical mediator

44 In addition, Gremlin was present in human aqueous humor and in the perfusate medium of perfusion-c

45 AG) based on elevated levels in glaucomatous aqueous humor and its ability to induce extracellular ma

46 ntercellular adhesion molecule-1 (ICAM-1) in aqueous humor and retina and nuclear translocation of nu

47 Freshly secreted aqueous humor and the aqueous humor in the anterior cham

48 ociation between levels of IL-6 and MMP-2 in aqueous humor and the axial lengths of the eye globes (I

49 active form (hDE-117) was maintained in the aqueous humor and the target tissue (iris-ciliary body)

50 that regulate pressure-dependent drainage of aqueous humor and thus intraocular pressure (IOP) are un

51 Analysis of the myocilin in the aqueous humor and TM revealed that PBA significantly imp

52 egment, and comparing myocilin levels in the aqueous humor and trabecular meshwork of Tg-MYOC(Y437H)

53 Tissue, aqueous humor and vitreous concentrations of bimatoprost

54 -conjugate release with detectable levels in aqueous humor and vitreous for at least 105 days.

55 Further, a single dose of DPT-GFX sustained aqueous humor and vitreous humor drug levels during the

56 ctive oxygen species (ROS) production in the aqueous humor, and caused greater CE cell loss, includin

57 lenses are capable of protecting the cornea, aqueous humor, and crystalline lens of rabbits from UV-i

58 he ocular anterior segment of human eyes and aqueous humor antioxidant levels of ascorbate (AsA) and

59 Immunosuppressive molecules within the aqueous humor (AqH) are thought to preserve ocular immun

60 Aqueous humor (AqH) from m-EAU and r-EAU was collected a

61 U, we characterized the metabolic profile of aqueous humor (AqH) of patients with HLA-B27-associated

62 tic lymphocytes were found to be absent from aqueous humor (AqH) of virtually all patients with recen

63 ere killed when the disease was at its peak; aqueous humor (AqH) was collected from one eye, and the

64 s after LPS injection, eyes were enucleated, aqueous humor (AqH) was collected, and the number of inf

65 24 hours after EIU, eyes were enucleated and aqueous humor (AqH) was collected.

66 rats were killed, eyes were enucleated, and aqueous humor (AqH) was collected.

67 n, the eyes were enucleated immediately, and aqueous humor (AqH) was collected.

68 by enucleation of eyes and collection of the aqueous humor (AqH).

69 mammals in which secretion and absorption of aqueous humor are circumferential around and through the

70 iliary body and the activity of MMP-2 in the aqueous humor are increased whereas tissue inhibitor of

71 is a vasoactive peptide that is elevated in aqueous humor as well as circulation of primary open ang

72 A significant decrease in aqueous humor ascorbate was observed in the exposed lotr

73 after injection of killed bacteria into the aqueous humor at any time point; however, injection of S

74 VEGF concentrations in aqueous humor at baseline were higher in patients with t

75 my surgery had steep oxygen gradients in the aqueous humor between the cornea and lens.

76 Mutant myocilin was not secreted into the aqueous humor but accumulated in the ER of the trabecula

77 PDGF-D is present in aqueous humor but is not detectable in mature lens or in

78 monstrated a significant reduction in CFU in aqueous humor by 1 hour PI (P </= 0.0044).

79 sustained therapeutic drug concentrations in aqueous humor can be achieved for long-term (i.e., 28 da

80 much better efficacy with significantly less aqueous humor cells and lower vitreous opacity scores (p

81 regions, oxygen levels were decreased in the aqueous humor closest to the pars plicata of the ciliary

82 Tissue and aqueous humor concentrations of bimatoprost, latanoprost

83 Pooled data of aqueous humor cytokine concentrations collected at basel

84 Aqueous humor cytokine concentrations serve as an early

85 l growth factor (VEGF) concentrations in the aqueous humor decreased (P = 0.0003), whereas the concen

86 omes after treatment with IFN-gamma, porcine aqueous humor, dexamethasone, or a calcium ionophore in

87 umor-to-blood direction than in the blood-to-aqueous humor direction, and active.

88 re grown in DMEM supplemented with 50% human aqueous humor (DMEM-AH), heat-denatured DMEM-AH, 10% fet

89 n (reduce inflow) and NO release to increase aqueous humor drainage (increase outflow).

90 odeling of ECM is crucial to maintain normal aqueous humor drainage and intraocular pressure (IOP).

91 cipates in IOP maintenance via modulation of aqueous humor drainage from the eye.

92 sure as the result of abnormal resistance to aqueous humor drainage is a major contributing, and the

93 d intraocular pressure (IOP) due to impaired aqueous humor drainage is a major risk factor for the de

94 of the anterior chamber angle containing the aqueous humor drainage tissue in situ were imaged by TPE

95 is characterized by increased resistance to aqueous humor drainage, elevated IOP, optic nerve degene

96 osing the angle of the eye, thereby limiting aqueous humor drainage.

97 TNF-alpha is elevated in the cornea and aqueous humor during allograft rejection and anterior uv

98 The novel pharmacology and aqueous humor dynamic effects of this molecule suggest i

99 Positional changes in other aqueous humor dynamic parameters may contribute to the c

100 Aqueous humor dynamics (aqueous flow, outflow facility,

101 arding the effects of glaucoma medication on aqueous humor dynamics and the impact of this on intraoc

102 igates the correlation between parameters of aqueous humor dynamics and the influence of CCT in healt

103 underlie bimatoprost's distinctive impact on aqueous humor dynamics are unclear.

104 We investigated the aqueous humor dynamics effects of a cyclodestructive pro

105 on and cellular basis of normal and abnormal aqueous humor dynamics in humans.

106 macologic agents or genetic manipulations on aqueous humor dynamics in mice and other animal models.

107 evaluate the effects of topical 0.005% KL on aqueous humor dynamics in normal monkey eyes.

108 ure of the tissues and cells specialized for aqueous humor dynamics in zebrafish show conservation wi

109 The individual parameters of aqueous humor dynamics may influence each other to maint

110 Linear correlations between individual aqueous humor dynamics parameters and pachymetry were ev

111 Aqueous humor dynamics studies were repeated 3 months af

112 This is the first aqueous humor dynamics study in patients with uveitic gl

113 from their glaucoma medication before their aqueous humor dynamics study measurements at baseline an

114 comprehensive ophthalmic examination before aqueous humor dynamics study measurements, including flu

115 The interplay between parameters of aqueous humor dynamics suggests possible autoregulatory

116 ially influence the individual parameters of aqueous humor dynamics that maintain IOP.

117 on the molecular and cellular mechanisms of aqueous humor dynamics using this species, the authors h

118 Aqueous humor dynamics were compared in Best2(+/+) and B

119 Aqueous humor dynamics were evaluated fluorophotometrica

120 with NO's having a mechanoregulatory role in aqueous humor dynamics, with eNOS induction at elevated

121 itric oxide (NO) increases the rate at which aqueous humor exits the eye; however, the involvement of

122 cantly during the nocturnal period, although aqueous humor flow decreases by 50% or more at night.

123 ecular and cellular mechanisms that regulate aqueous humor flow have remained elusive.

124 The results provide evidence that aqueous humor flow is similar between eyes, that flow va

125 The aqueous humor flow rate was not detectibly different, no

126 However, aqueous humor flow rate was not statistically different

127 measures were tonographic outflow facility, aqueous humor flow rate, and uveoscleral outflow.

128 Aqueous humor flow rate, IOP, and outflow facility were

129 urnal period to compensate for the decreased aqueous humor flow rate.

130 c outflow facility (C) and fluorophotometric aqueous humor flow rates (F) were measured in nine norma

131 is study evaluated the effect of timolol, an aqueous humor flow suppressant, on outflow facility in h

132 d in the regulation of outflow resistance of aqueous humor flow through the trabecular meshwork (TM).

133 This phenomenon may be related to reduced aqueous humor flow, but the precise mechanism remains to

134 These observations support the posit that aqueous humor flow, which is a factor that contributes t

135 trabecular meshwork (TM) cells might detect aqueous humor fluid shear stress via interaction of the

136 of the eye, particularly in the drainage of aqueous humor fluid, which are believed to bring about c

137 r chamber to decreased antioxidant levels in aqueous humor following vitrectomy.

138 as significantly reduced when incubated with aqueous humor for 30 minutes (P </= 0.0001).

139 concentration and neutralization of VEGF in aqueous humor for 8-12 weeks.

140 in understanding the mechanisms controlling aqueous humor formation and thereby intraocular pressure

141 logical functions, such as sperm activation, aqueous humor formation, and metabolic regulation.

142 Aqueous humor formation, or flow (AHF, measured by fluor

143 liary epithelium and is oriented to subserve aqueous humor formation.

144 Analysis of aqueous humor from patients with primary open-angle glau

145 ar meshwork (TM) tissue controls drainage of aqueous humor from the anterior chamber of the eye prima

146 ns to maintain fluid homeostasis by draining aqueous humor from the eye into the systemic circulation

147 structure in the eye that functions to drain aqueous humor from the intraocular chamber into systemic

148 to quantify the effect of dynamic motion of aqueous humor from the posterior to the anterior chamber

149 Human aqueous humor (hAH) provides nutrition and immunity with

150 This study demonstrates that aqueous humor has a potent host defense capability and t

151 Hyposecretion of aqueous humor has been postulated to adversely affect th

152 Freshly secreted aqueous humor and the aqueous humor in the anterior chamber angle are relative

153 athology in the primary drainage pathway for aqueous humor in the eye is responsible for ocular hyper

154 The principal outflow pathway for aqueous humor in the human eye is through the trabecular

155 Recombinant myocilin in porcine aqueous humor increased outflow resistance in cultured h

156 es water to migrate from the plasma into the aqueous humor, increasing intraocular pressure.

157 Their apical surface, in contact with aqueous humor is hexagonal, whereas their basal surface

158 Vectorial flow of zebrafish aqueous humor is in contrast to that in mammals in which

159 The protein component of aqueous humor is responsible for these changes.

160 rming growth factor-beta2 (TGF-beta2) in the aqueous humor is the main cause of fibrosis of TM in POA

161 drug concentrations in intraocular tissues (aqueous humor, lens, and iris) versus eyes not receiving

162 Patients with AMD had significantly higher aqueous humor levels of cadmium (median: 0.70 micromol/L

163 No significant differences were observed in aqueous humor levels of manganese and selenium between p

164 ation of MMC to the endothelium and into the aqueous humor may lead surgeons to reassess appropriate

165 When cultured in media containing aqueous humor, MYOC-associated exosomes increased 514% o

166 an unclassified uveitis, 7 of whom underwent aqueous humor (n = 5) or vitreous humor (n = 2) analysis

167 liary body and level of IL-18 protein in the aqueous humor of DBA/2J mice are dramatically increased

168 ytokines of the innate immune system, in the aqueous humor of patients undergoing repeat DMEK for gra

169 r testing 16 clinical samples collected from aqueous humor of patients undergoing therapeutic anterio

170 d compare the cytokine concentrations in the aqueous humor of patients with acute nonarteritic anteri

171 sure alterations of trace elements levels in aqueous humor of patients with non-exsudative (dry) AMD.

172 ta2, which is found in higher amounts in the aqueous humor of patients with POAG.

173 os with free metalloproteinases (MMP) in the aqueous humor of patients with primary open angle glauco

174 lloprotease family that are increased in the aqueous humor of POAG arising from a variety of conditio

175 of 6-carboxyfluorescein elimination from the aqueous humor of the perfused eye was reduced 80% when n

176 asmosis, we assessed the cytokine pattern in aqueous humors of 10 affected patients.

177 f SC has been proposed to underlie increased aqueous humor outflow (AHO) resistance, which leads to e

178 is characterized by increased resistance to aqueous humor outflow and a stiffer human trabecular mes

179 leton disruptor that decreases resistance to aqueous humor outflow and decreases intraocular pressure

180 on of the eye, plays a key role in promoting aqueous humor outflow and maintenance of normal intraocu

181 ligands that offer the potential to improve aqueous humor outflow and protect RGCs simultaneously, a

182 cides with a reduction in available area for aqueous humor outflow and the confinement of outflow to

183 Presumably as a consequence of aqueous humor outflow blockage, they rapidly developed m

184 or 96 hours caused a significant increase in aqueous humor outflow facility (110%) compared with cont

185 way, blocked both PEA-induced enhancement of aqueous humor outflow facility and PEA-induced phosphory

186 ate that the administration of AEA increases aqueous humor outflow facility and that this effect of A

187 as used to measure the effects of statins on aqueous humor outflow facility in the anterior segments

188 001) and mouse (110%, P < 0.001) and reduced aqueous humor outflow facility in the mouse.

189 dding 3, 30, or 300 nM of noladin ether, the aqueous humor outflow facility increased concentration d

190 Aqueous humor outflow facility measured with electronic

191 Changes in aqueous humor outflow facility were determined in enucle

192 The effects of noladin ether on aqueous humor outflow facility were measured in a porcin

193 is study was to investigate the variation of aqueous humor outflow facility with body position change

194 ed to significantly reduced IOP and improved aqueous humor outflow facility, which was sustained for

195 trabecular meshwork (TM) cells increases the aqueous humor outflow facility.

196 that EP(4) receptor stimulation facilitated aqueous humor outflow facility.

197 ion of AEA caused a transient enhancement of aqueous humor outflow facility.

198 extracellular matrix turnover and increases aqueous humor outflow facility.

199 st selective for the CB1 receptor, increases aqueous humor outflow facility.

200 was used to measure the effects of JWH015 on aqueous humor outflow facility.

201 ical role for myosin II in the regulation of aqueous humor outflow facility.

202 lective cannabinoid agonist JWH015 increases aqueous humor outflow facility.

203 bute to overall physiological homeostasis of aqueous humor outflow facility.

204 was efficacious in both, increasing ex vivo aqueous humor outflow in porcine eyes and inhibiting myo

205 lar pressure (IOP) caused by a resistance to aqueous humor outflow in the trabecular meshwork (TM).

206 important regulator of TEK signaling in the aqueous humor outflow pathway and identify a new therape

207 hat selective inhibition of myosin II in the aqueous humor outflow pathway leads to increased aqueous

208 tructure or alterations in morphology of the aqueous humor outflow pathway were observed after treatm

209 fy druggable targets within the conventional aqueous humor outflow pathway, which is thought to be re

210 line, which caused sclerosis and blockade of aqueous humor outflow pathways.

211 and organization is required to maintain the aqueous humor outflow resistance and intraocular pressur

212 ontribute to the homeostatic modification of aqueous humor outflow resistance are also upregulated or

213 he trabecular meshwork (TM) provides most of aqueous humor outflow resistance in the eye, an in vitro

214 assess versican's potential contributions to aqueous humor outflow resistance, its segmental distribu

215 se, they make homeostatic corrections in the aqueous humor outflow resistance, partially by increasin

216 TGFbeta-mediated IOP elevation and increased aqueous humor outflow resistance.

217 ity of the TM tissue and consequently impede aqueous humor outflow resulting in elevated intraocular

218 In PCG, defects in the anterior chamber aqueous humor outflow structures of the eye result in el

219 We performed 3D SD-OCT imaging of the aqueous humor outflow structures with 2 devices: The Cir

220 and is caused by developmental defects in 2 aqueous humor outflow structures, Schlemm's canal (SC) a

221 laucoma surgeries reduce IOP by facilitating aqueous humor outflow through a vent fashioned from the

222 Our results demonstrate that PEA increases aqueous humor outflow through the TM pathway and these e

223 ular pressure due to increased resistance of aqueous humor outflow through the trabecular meshwork (T

224 traocular pressure (IOP) due to insufficient aqueous humor outflow through the trabecular meshwork an

225 a degradable inner core designed to modulate aqueous humor outflow to provide immediate IOP reduction

226 The effects of GGTI-DU40 on aqueous humor outflow were determined using organ-cultur

227 The effects of AEA on aqueous humor outflow were measured using a porcine ante

228 ins in the aqueous outflow pathway increases aqueous humor outflow, possibly through altered cell adh

229 leral) and pressure-dependent (conventional) aqueous humor outflow.

230 ained IOPs caused by increased resistance to aqueous humor outflow.

231 shwork (TM) cell volume increase the rate of aqueous humor outflow.

232 in normal intraocular pressure by regulating aqueous humor outflow.

233 tion and thereby modulates the resistance to aqueous humor outflow.

234 eshwork (TM) damage, which leads to impaired aqueous humor outflow.

235 ll volume changes and changes in the rate of aqueous humor outflow; agents that decrease trabecular m

236 al (SC) cells may also provide resistance to aqueous humor outflow; therefore, this study tests the i

237 Ranibizumab concentration in aqueous humor peaked the first day after injection (rang

238 To study the value and safety of aqueous humor polymerase chain reaction (PCR) analysis f

239 al mechanics drive angle opening rather than aqueous humor pressurization.

240 (EVP), conventional outflow facility (C(t)), aqueous humor production (F(a)), and anterior chamber vo

241 m of the mouse eye results in a reduction in aqueous humor production and complete loss of the vitreo

242 is consistent with a major role of alpha2 in aqueous humor production and suggests that, potentially,

243 However, aqueous humor production in the same mice appears to be

244 wever, the effect of medications that reduce aqueous humor production on outflow facility in living h

245 normal monkeys appeared to have no effect on aqueous humor production or tonographic outflow facility

246 and inhibit the Na,K-ATPase, hence reducing aqueous humor production.

247 the carbonic anhydrase (CA) enzyme to reduce aqueous humor production.

248 n, as there was no significant difference in aqueous humor protein concentration between treated and

249 Aqueous humor protein concentrations were measured to es

250 sis that the enclosed spaces are filled with aqueous humor rather than circulating blood.

251 Addition of human aqueous humor rather than FBS to trabecular monolayer ce

252 An aqueous humor sample was obtained during cataract surger

253 After RLB, aqueous humor samples harvested from nontreated eyes but

254 Aqueous humor samples of patients were subjected to CD44

255 ry cytokines, and correlate levels with IOP, aqueous humor samples were analyzed from 23 eyes with op

256 For this pilot study, aqueous humor samples were collected from patients under

257 Aqueous humor samples were obtained in 10 patients with

258 Aqueous humor samples were taken at the time of IVB pret

259 urther by determining the phosphorylation of aqueous humor sCD44 in normal and primary open-angle gla

260 The normal aqueous humor sCD44 was positive for serine-threonine ph

261 gh two mechanisms: CA inhibition to decrease aqueous humor secretion (reduce inflow) and NO release t

262 the ocular anterior segment responsible for aqueous humor secretion and absorption have been well ch

263 were used to identify and study the sites of aqueous humor secretion and absorption in adult zebrafis

264 IOP is controlled by the balance between aqueous humor secretion from the ciliary body (CB) and i

265 Zebrafish eyes show aqueous humor secretion primarily from the dorsal ciliar

266 d by cell culture from blood, saliva, urine, aqueous humor, semen, and breast milk from infected or c

267 (0.1 mM) or novobiocin (0.1 mM) added to the aqueous humor side of the tissue, or MK571 (5-(3-(2-(7-c

268 in reaction detected parasite DNA in 8/60 OT aqueous humor specimens but failed to identify Type II s

269 A total of 132 aqueous humor specimens were collected before intravitre

270 Aqueous humor specimens were obtained for antioxidant an

271 A total of 859 aqueous humor specimens were taken before each intravitr

272 Aqueous humor specimens were taken before each intravitr

273 freezing, IL-1beta released by PMNs into the aqueous humor stimulates FGF-2 synthesis in corneal endo

274 oid, a calcium ionophore, and a component of aqueous humor, suggesting that TM cells respond to envir

275 Aqueous humor supplementation may maintain cultured trab

276 yocilin appears to form a complex in porcine aqueous humor that enables it to bind specifically withi

277 ncrease was diminished in cells treated with aqueous humor that was first passed through a 3-kDa or a

278 e from an increased resistance to outflow of aqueous humor through the trabecular meshwork.

279 chnique was developed to measure the flow of aqueous humor through the uveoscleral pathway in porcine

280 e mammalian eye is responsible for secreting aqueous humor to maintain intraocular pressure, which is

281 dy in the Ussing chambers was greater in the aqueous humor-to-blood direction than in the blood-to-aq

282 Alternatively, surgical procedures can shunt aqueous humor too well, leading to hypotony.

283 Aqueous humor turnover was enhanced more than twofold in

284 and uveoscleral outflow (F(u)), and rate of aqueous humor turnover, were calculated from measured da

285 No significant difference in baseline aqueous humor VEGF concentration was noted, while at the

286 Mean aqueous humor VEGF concentrations before treatment initi

287 when preincubated in DMEM containing porcine aqueous humor versus 13% +/- 15% when preincubated with

288 freezing, and IL-1beta concentration in the aqueous humor was elevated in a time-dependent manner af

289 TUNEL and caspase-3 ELISA; ascorbate in the aqueous humor was evaluated by nuclear magnetic resonanc

290 The bactericidal activity of rabbit aqueous humor was investigated in vitro.

291 Conversely, VEGF in aqueous humor was significantly lower in the highly myop

292 ocilin in the iridocorneal angle tissues and aqueous humor was studied by immunohistochemistry and We

293 Aqueous humor was tested whole or fractionated by size e

294 (2)) and myeloperoxidase (MPO) activities of aqueous humor were determined up to 25 hours postinfecti

295 utflow facility and total TGFbeta2 levels in aqueous humor were measured.

296 Both Cytomegalovirus DNA in plasma and aqueous humor were positive.

297 On average, VEGF concentrations in the aqueous humor were suppressed below the lower limit of q

298 endothelial (CE) cells and is present in the aqueous humor, which bathes CE cells in vivo.

299 yocilin appears to form a complex in porcine aqueous humor with a heat-labile protein(s).

300 uilibrium between production and drainage of aqueous humor, with compromised drainage generally viewe