ライフサイエンスコーパス: aqueous humor

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

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

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

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

5 aration at the concentration levels found in aqueous humor.

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

7 nalyze myocilin complex formation in porcine aqueous humor.

8 which clearly distinguished POAG from normal aqueous humor.

9 a2 levels are elevated in glaucomatous human aqueous humor.

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

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

12 etermined by direct measurement of aspirated aqueous humor.

13 s and functions to produce components of the aqueous humor.

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

15 ributes to the immunosuppressive activity of aqueous humor.

16 that ranged the level of SOM found in normal 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 d in reliably high ESBA105 concentrations in aqueous humor.

20 of impedance of nutritional support from the aqueous humor.

21 ll infiltration and protein concentration in aqueous humor.

22 ng hormone, at concentrations present in the aqueous humor (10-9 M), as well as melanocyte-stimulatin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43 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

44 SOM is present in aqueous humor and contributes to the immunosuppressive a

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

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

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

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

49 fate proteoglycan (HSPG) was found in bovine aqueous humor and that it directly inhibits binding of b

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

51 antioxidant- and UV-trapping molecule in the aqueous humor and the lens, was used to investigate the

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

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

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

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

56 Tissue, aqueous humor and vitreous concentrations of bimatoprost

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

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

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

60 ions may reach the cornea via the tear film, aqueous humor, and limbal vasculature.

61 modeling, that the concentration of HSPG in aqueous humor (approximately 4 microg/ml), when combined

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

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

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

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

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

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

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

69 24 hours after EIU, eyes were enucleated and aqueous humor (AqH) was collected.

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

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

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

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

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

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

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

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

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

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

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

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

82 and the mechanisms causing elevated IOP from aqueous humor circulation, we pursued proteomic analyses

83 position, and significant obstruction of the aqueous humor circulation.

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

85 Tissue and aqueous humor concentrations of bimatoprost, latanoprost

86 Normal rabbit aqueous humor contained 196 +/- 45 pg/mL (10(-10) M) of

87 a wide range of immunosuppressive factors in aqueous humor contribute to the immune privilege.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 Aqueous humor dynamics (aqueous flow, outflow facility,

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

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

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

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

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

109 Aqueous humor dynamics in NIH Swiss White mice were asse

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

111 fluorescence provides a noninvasive index of aqueous humor dynamics in the mouse eye that facilitates

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

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

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

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 Concentrations of aqueous humor endothelin (ET)-1 are increased in patient

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

123 Aqueous humor flow (Fa) was determined by a dilution met

124 toprost that in humans increases the rate of aqueous humor flow as measured by fluorophotometry.

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

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

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

128 of topical ibopamine on pupillary diameter, aqueous humor flow measured by fluorophotometry, and int

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

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

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

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

133 The transient apparent doubling of aqueous humor flow, measured by fluorescein clearance af

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

135 aocular pressure, despite its stimulation of aqueous humor flow.

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

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

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 cannulation under pentobarbital anesthesia, aqueous humor formation (AHF), anterior chamber volume,

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

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

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

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

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

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

147 rog/ml), when combined with the clearance of aqueous humor from the eye due to circulation, is suffic

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

149 le, with a resultant increase in drainage of aqueous humor from the eye, we compared the effects of t

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

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

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

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

154 n the levels of immunoglobulin G in serum or aqueous humor in microMT mice, and there was no increase

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

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

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

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

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

160 tive conclusions about the relative roles of aqueous humor inflow and outflow in conditions with alte

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

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

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

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

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

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

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

168 Outflow of aqueous humor may be increased by the prostaglandin anal

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

170 y demonstrated presence of leukocytes in the aqueous humor, migration of PMNs into infected tissue, c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 cine eyes produced a significant decrease in aqueous humor outflow facility from baseline of 37% (n =

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

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

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

195 Aqueous humor outflow facility measured with electronic

196 Changes in aqueous humor outflow facility were determined in enucle

197 The effects of LPA and S1P on aqueous humor outflow facility were evaluated by perfusi

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

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

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

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

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

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

204 extracellular matrix turnover and increases aqueous humor outflow facility.

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

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

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

208 lective cannabinoid agonist JWH015 increases aqueous humor outflow facility.

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

210 ilocarpine and latanoprost, known to enhance aqueous humor outflow in humans, accelerated the decay o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 tion and thereby modulates the resistance to 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 Aqueous humor production (F(a)) was measured by the dilu

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

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

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

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

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

246 In this study ibopamine's effect on aqueous humor production was measured while making allow

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

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

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

250 Aqueous humor protein concentrations were measured to es

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

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

253 An aqueous humor sample was obtained during cataract surger

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

255 Aqueous humor samples of patients were subjected to CD44

256 Fresh aqueous humor samples significantly decreased the invasi

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

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

259 Aqueous humor samples were obtained in 10 patients with

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

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

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

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

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

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

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

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

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

269 (0.1 mM) or novobiocin (0.1 mM) added to the aqueous humor side of the tissue, or MK571 (5-(3-(2-(7-c

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

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

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

273 Aqueous humor specimens were taken before each intravitr

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

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

276 Aqueous humor supplementation may maintain cultured trab

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

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

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

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

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

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

283 mouse eye has similar aqueous production and aqueous humor turnover rate as the human eye.

284 Aqueous humor turnover was enhanced more than twofold in

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

286 product that spontaneously formed in rabbit aqueous humor upon incubation with F-ASA.

287 Mean aqueous humor VEGF concentrations before treatment initi

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

289 Fresh rabbit aqueous humor was assayed for SOM by competitive ELISA.

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

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

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

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

294 Aqueous humor was tested whole or fractionated by size e

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

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

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

298 spectively), as well as the turnover rate of aqueous humor, were also calculated.

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

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