ライフサイエンスコーパス: humor

1 drug delivery vehicles through the vitreous humor.

2 iably high ESBA105 concentrations in aqueous humor.

3 ance of nutritional support from the aqueous humor.

4 tration and protein concentration in aqueous humor.

5 olite concentrations in aqueous and vitreous humor.

6 n D(3) were detected in aqueous and vitreous humor.

7 are difficult to determine in human vitreous humor.

8 lony-forming units per milliliter of aqueous humor.

9 c polymerase chain reaction (PCR) in aqueous humor.

10 ansforming growth factor-beta in the aqueous humor.

11 echanical properties of the natural vitreous humor.

12 e critical for the production of the aqueous humor.

13 ated and wild-type myocilin into the aqueous humor.

14 and sufficient for up-regulation by vitreous humor.

15 LM are the peripheral retina and/or vitreous humor.

16 duced pressure-dependent drainage of aqueous humor.

17 ls that separate the cornea from the aqueous humor.

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

19 d leukocytes within the aqueous and vitreous humors.

20 (64 days), amniotic fluid (38 days), aqueous humor (101 days), cerebrospinal fluid (9 months), breast

21 eyes was not different for both the vitreous humor (13,600 vs. 15,000 ng/day/mL; P = 0.73) and retina

22 re ebolavirus (EBOV) was detected in aqueous humor 14 weeks after the onset of EVD and 9 weeks after

23 Hmgb1 is accumulated in the vitreous humor 24 hours after IR.

24 isms were found to predict time to recovery: humor, acting out, emotional hypochondriasis, and projec

25 studies conducted with adults indicate that humor activates specific brain regions, including the te

26 ccumbens in younger participants, indicating humor activation intensity changes during development.

27 ion of regulatory T cells (Tregs) by aqueous humor (AH) and identified TGF-beta as a critical factor.

28 TGFbeta(2)) is often elevated in the aqueous humor (AH) and trabecular meshwork (TM) of patients with

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

30 sure (IOP) resulting from diminished aqueous humor (AH) drainage through the trabecular pathway.

31 concentration of ANGPTL7 protein in aqueous humor (AH) from patients with glaucoma and control patie

32 enzyme-linked immunosorbent assay in aqueous humor (AH) obtained from human donor eyes (POAG and norm

33 To investigate whether the aqueous humor (AH) of Rb eyes has sufficient tumor-derived DNA t

34 of MRP4 in human TM (HTM) cells and aqueous humor (AH) outflow pathway was determined by RT-PCR, imm

35 arising from increased resistance to aqueous humor (AH) outflow through the trabecular meshwork is a

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

37 s from the resistance to drainage of aqueous humor (AH) produced by the ciliary body in a process req

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

39 Aqueous humor (all cohorts), vitreous humor (cohort IV only), an

40 uveitis patients, positive for RV in aqueous humor analysis (polymerase chain reaction [PCR] and/or G

41 ls detectable after 24 hours in the vitreous humor and 4 hours in the RC.

42 leukin (IL)-6 and IL-8 levels in the aqueous humor and a concomitant approximately twofold (P < 0.001

43 secretion of mutant myocilin in the aqueous humor and by decreasing intracellular accumulation of my

44 pears to antagonize the formation of aqueous humor and cause an inhibition of both F(c) and F(u), des

45 NF-alpha, CCL-2/MCP-1, and ICAM-1 in aqueous humor and CCL-2/MCP-1 and ICAM-1 levels in retina were s

46 n unclassified uveitis, aqueous and vitreous humor and cerebrospinal fluid were also analyzed.

47 y and choroid plexus, the sources of aqueous humor and cerebrospinal fluid, respectively.

48 te via soluble agents present in the aqueous humor and implicate Best2 as a critical mediator of that

49 d on elevated levels in glaucomatous aqueous humor and its ability to induce extracellular matrix (EC

50 ular adhesion molecule-1 (ICAM-1) in aqueous humor and retina and nuclear translocation of nuclear fa

51 ncentrations were determined in the vitreous humor and retina for 31 days (on days 2, 8, 15, 22, and

52 and drug content quantified in the vitreous humor and retina-choroid tissue by high-performance liqu

53 between levels of IL-6 and MMP-2 in aqueous humor and the axial lengths of the eye globes (IL-6, bet

54 ug levels were observed in both the vitreous humor and the retina-choroid even on day 21 after diclof

55 form (hDE-117) was maintained in the aqueous humor and the target tissue (iris-ciliary body) up to 24

56 ulate pressure-dependent drainage of aqueous humor and thus intraocular pressure (IOP) are unknown.

57 Analysis of the myocilin in the aqueous humor and TM revealed that PBA significantly improved th

58 and comparing myocilin levels in the aqueous humor and trabecular meshwork of Tg-MYOC(Y437H) mice.

59 te release with detectable levels in aqueous humor and vitreous for at least 105 days.

60 , a single dose of DPT-GFX sustained aqueous humor and vitreous humor drug levels during the 24-hour

61 ygen species (ROS) production in the aqueous humor, and caused greater CE cell loss, including loss o

62 re capable of protecting the cornea, aqueous humor, and crystalline lens of rabbits from UV-induced p

63 helium, iris, ciliary body, retina, vitreous humor, and optic nerve.

64 Blood, vitreous humor, and retina samples were collected at predetermine

65 roughout the eye, including cornea, vitreous humor, and retina, suggesting a coordinated protective r

66 liver, spleen, kidney, brain, lung, vitreous humor, and vena cava in comparison to untreated controls

67 r anterior segment of human eyes and aqueous humor antioxidant levels of ascorbate (AsA) and total re

68 munosuppressive molecules within the aqueous humor (AqH) are thought to preserve ocular immune privil

69 Aqueous humor (AqH) from m-EAU and r-EAU was collected and studi

70 aracterized the metabolic profile of aqueous humor (AqH) of patients with HLA-B27-associated AAU (B27

71 ed when the disease was at its peak; aqueous humor (AqH) was collected from one eye, and the other ey

72 LPS injection, eyes were enucleated, aqueous humor (AqH) was collected, and the number of infiltratin

73 after EIU, eyes were enucleated and aqueous humor (AqH) was collected.

74 re killed, eyes were enucleated, and aqueous humor (AqH) was collected.

75 eation of eyes and collection of the aqueous humor (AqH).

76 in which secretion and absorption of aqueous humor are circumferential around and through the iridoco

77 e of psychosocial factors such as the use of humor as a coping style and the level of health care pro

78 multiparametric characterization of vitreous humor as a function of the time since death.

79 soactive peptide that is elevated in aqueous humor as well as circulation of primary open angle glauc

80 A significant decrease in aqueous humor ascorbate was observed in the exposed lotrafilcon

81 VEGF concentrations in aqueous humor at baseline were higher in patients with type 3 NV

82 giogenic factors upregulated in PDR vitreous humor besides VEGF, thus inhibiting their biological act

83 ry had steep oxygen gradients in the aqueous humor between the cornea and lens.

84 scularized structure located in the vitreous humor between the posterior surface of the lens and neur

85 t myocilin was not secreted into the aqueous humor but accumulated in the ER of the trabecular meshwo

86 We do of course also laugh at humor - but can laughter influence how funny we actually

87 min and fibrin into the aqueous and vitreous humor by 8 hours after infection.

88 d therapeutic drug concentrations in aqueous humor can be achieved for long-term (i.e., 28 days) prot

89 Aqueous and vitreous humor cell counts and protein levels and histopathology

90 ter efficacy with significantly less aqueous humor cells and lower vitreous opacity scores (p<0.05).

91 Aqueous humor (all cohorts), vitreous humor (cohort IV only), and blood samples (all cohorts)

92 Pooled data of aqueous humor cytokine concentrations collected at baseline and

93 Aqueous humor cytokine concentrations serve as an early biomarke

94 factor (VEGF) concentrations in the aqueous humor decreased (P = 0.0003), whereas the concentrations

95 It is widely accepted that vitreous humor-derived FGFs are required for the differentiation

96 er treatment with IFN-gamma, porcine aqueous humor, dexamethasone, or a calcium ionophore in cells pr

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

98 cal diseases including muscle, membrane, and humor disorders; optic nerve damage; and eyelid affectio

99 e inflow) and NO release to increase aqueous humor drainage (increase outflow).

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

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

102 the result of abnormal resistance to aqueous humor drainage is a major contributing, and the only pre

103 cular pressure (IOP) due to impaired aqueous humor drainage is a major risk factor for the developmen

104 nterior chamber angle containing the aqueous humor drainage tissue in situ were imaged by TPEF to loc

105 acterized by increased resistance to aqueous humor drainage, elevated IOP, optic nerve degeneration a

106 e angle of the eye, thereby limiting aqueous humor drainage.

107 DPT-GFX sustained aqueous humor and vitreous humor drug levels during the 24-hour study, with a t(1/2

108 -alpha is elevated in the cornea and aqueous humor during allograft rejection and anterior uveitis.

109 Nanotubes persisted in the vitreous humor during the 15 days study and pazopanib levels in t

110 The novel pharmacology and aqueous humor dynamic effects of this molecule suggest it may be

111 Positional changes in other aqueous humor dynamic parameters may contribute to the change in

112 Aqueous humor dynamics (aqueous flow, outflow facility, and uveo

113 he correlation between parameters of aqueous humor dynamics and the influence of CCT in healthy volun

114 We investigated the aqueous humor dynamics effects of a cyclodestructive procedure a

115 ellular basis of normal and abnormal aqueous humor dynamics in humans.

116 c agents or genetic manipulations on aqueous humor dynamics in mice and other animal models.

117 he tissues and cells specialized for aqueous humor dynamics in zebrafish show conservation with that

118 The individual parameters of aqueous humor dynamics may influence each other to maintain intr

119 near correlations between individual aqueous humor dynamics parameters and pachymetry were evaluated

120 Aqueous humor dynamics studies were repeated 3 months after the

121 This is the first aqueous humor dynamics study in patients with uveitic glaucoma/O

122 eir glaucoma medication before their aqueous humor dynamics study measurements at baseline and the 3-

123 ensive ophthalmic examination before aqueous humor dynamics study measurements, including fluorophoto

124 The interplay between parameters of aqueous humor dynamics suggests possible autoregulatory mechanis

125 fluence the individual parameters of aqueous humor dynamics that maintain IOP.

126 molecular and cellular mechanisms of aqueous humor dynamics using this species, the authors have char

127 Aqueous humor dynamics were compared in Best2(+/+) and Best2(-/-

128 Aqueous humor dynamics were evaluated fluorophotometrically and

129 s having a mechanoregulatory role in aqueous humor dynamics, with eNOS induction at elevated IOPs lea

130 clude fibrillar degeneration of the vitreous humor, early-onset cataract, minute crystalline deposits

131 o humor, suggesting these regions may form a humor-essential neural network already present in childh

132 ide (NO) increases the rate at which aqueous humor exits the eye; however, the involvement of soluble

133 uring the nocturnal period, although aqueous humor flow decreases by 50% or more at night.

134 nd cellular mechanisms that regulate aqueous humor flow have remained elusive.

135 The aqueous humor flow rate was not detectibly different, nor did th

136 However, aqueous humor flow rate was not statistically different (2.47 +/

137 s were tonographic outflow facility, aqueous humor flow rate, and uveoscleral outflow.

138 Aqueous humor flow rate, IOP, and outflow facility were measured

139 riod to compensate for the decreased aqueous humor flow rate.

140 evaluated the effect of timolol, an aqueous humor flow suppressant, on outflow facility in healthy e

141 regulation of outflow resistance of aqueous humor flow through the trabecular meshwork (TM).

142 phenomenon may be related to reduced aqueous humor flow, but the precise mechanism remains to be dete

143 lar meshwork (TM) cells might detect aqueous humor fluid shear stress via interaction of the extracel

144 eye, particularly in the drainage of aqueous humor fluid, which are believed to bring about changes i

145 r to decreased antioxidant levels in aqueous humor following vitrectomy.

146 DEX was detected in the retina and vitreous humor for 6 months, with peak concentrations during the

147 ration and neutralization of VEGF in aqueous humor for 8-12 weeks.

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

149 Analysis of aqueous humor from patients with primary open-angle glaucoma (PO

150 ork (TM) tissue controls drainage of aqueous humor from the anterior chamber of the eye primarily by

151 intain fluid homeostasis by draining aqueous humor from the eye into the systemic circulation.

152 e in the eye that functions to drain aqueous humor from the intraocular chamber into systemic circula

153 tify the effect of dynamic motion of aqueous humor from the posterior to the anterior chamber, and (3

154 Human aqueous humor (hAH) provides nutrition and immunity within the a

155 Hyposecretion of aqueous humor has been postulated to adversely affect the health

156 nvolved in the detection and appreciation of humor in childhood.

157 in the primary drainage pathway for aqueous humor in the eye is responsible for ocular hypertension,

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

159 udy to date has used neuroimaging to examine humor in typically developing children.

160 to migrate from the plasma into the aqueous humor, increasing intraocular pressure.

161 A single injection of FIV(HuMOR) into the temporomandibular joints of Col1-IL-1bet

162 Humor is a vital component of human well-being.

163 heir apical surface, in contact with aqueous humor is hexagonal, whereas their basal surface is irreg

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

165 owth factor-beta2 (TGF-beta2) in the aqueous humor is the main cause of fibrosis of TM in POAG patien

166 ncentrations in intraocular tissues (aqueous humor, lens, and iris) versus eyes not receiving Y-27632

167 ts with AMD had significantly higher aqueous humor levels of cadmium (median: 0.70 micromol/L, IQR: 0

168 ificant differences were observed in aqueous humor levels of manganese and selenium between patients

169 MMC to the endothelium and into the aqueous humor may lead surgeons to reassess appropriate dosing a

170 When cultured in media containing aqueous humor, MYOC-associated exosomes increased 514% over cont

171 underwent aqueous humor (n = 5) or vitreous humor (n = 2) analysis and cerebrospinal fluid analysis

172 ssified uveitis, 7 of whom underwent aqueous humor (n = 5) or vitreous humor (n = 2) analysis and cer

173 respiratory samples, biopsies, and vitreous humor) obtained longitudinally or from different anatomi

174 nic acid (KA) was injected into the vitreous humor of B6.Cg-Tg(Thy1-YFP)HJrs/J mice.

175 Here, we provide evidence in both vitreous humor of diabetic patients and in retina of a murine mod

176 of the innate immune system, in the aqueous humor of patients undergoing repeat DMEK for graft failu

177 g 16 clinical samples collected from aqueous humor of patients undergoing therapeutic anterior chambe

178 e the cytokine concentrations in the aqueous humor of patients with acute nonarteritic anterior ische

179 erations of trace elements levels in aqueous humor of patients with non-exsudative (dry) AMD.

180 ch is found in higher amounts in the aqueous humor of patients with POAG.

181 free metalloproteinases (MMP) in the aqueous humor of patients with primary open angle glaucoma (POAG

182 ase family that are increased in the aqueous humor of POAG arising from a variety of conditions, it i

183 ological media such as blood or the vitreous humor of the eye in situ.

184 ed with the collagen network of the vitreous humor of the eye.

185 that the authors discovered in the vitreous humor of the eye.

186 boxyfluorescein elimination from the aqueous humor of the perfused eye was reduced 80% when novobioci

187 we assessed the cytokine pattern in aqueous humors of 10 affected patients.

188 that direct the movement of fluid (vitreous humor or cerebrospinal fluid) into and under the retina.

189 been proposed to underlie increased aqueous humor outflow (AHO) resistance, which leads to elevated

190 acterized by increased resistance to aqueous humor outflow and a stiffer human trabecular meshwork (H

191 sruptor that decreases resistance to aqueous humor outflow and decreases intraocular pressure.

192 e eye, plays a key role in promoting aqueous humor outflow and maintenance of normal intraocular pres

193 that offer the potential to improve aqueous humor outflow and protect RGCs simultaneously, and prese

194 th a reduction in available area for aqueous humor outflow and the confinement of outflow to the vici

195 Presumably as a consequence of aqueous humor outflow blockage, they rapidly developed multiple

196 cked both PEA-induced enhancement of aqueous humor outflow facility and PEA-induced phosphorylation o

197 the administration of AEA increases aqueous humor outflow facility and that this effect of AEA invol

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

199 Aqueous humor outflow facility measured with electronic Schiotz

200 was to investigate the variation of aqueous humor outflow facility with body position changes.

201 gnificantly reduced IOP and improved aqueous humor outflow facility, which was sustained for at least

202 ar meshwork (TM) cells increases the aqueous humor outflow facility.

203 (4) receptor stimulation facilitated aqueous humor outflow facility.

204 EA caused a transient enhancement of aqueous humor outflow facility.

205 icacious in both, increasing ex vivo aqueous humor outflow in porcine eyes and inhibiting myosin ligh

206 sure (IOP) caused by a resistance to aqueous humor outflow in the trabecular meshwork (TM).

207 nt regulator of TEK signaling in the aqueous humor outflow pathway and identify a new therapeutic tar

208 or alterations in morphology of the aqueous humor outflow pathway were observed after treatment with

209 able targets within the conventional aqueous humor outflow pathway, which is thought to be regulated/

210 nization is required to maintain the aqueous humor outflow resistance and intraocular pressure homeos

211 cular meshwork (TM) provides most of aqueous humor outflow resistance in the eye, an in vitro bioengi

212 ersican's potential contributions to aqueous humor outflow resistance, its segmental distribution in

213 mediated IOP elevation and increased aqueous humor outflow resistance.

214 PCG, defects in the anterior chamber aqueous humor outflow structures of the eye result in elevated i

215 e performed 3D SD-OCT imaging of the aqueous humor outflow structures with 2 devices: The Cirrus HD-O

216 caused by developmental defects in 2 aqueous humor outflow structures, Schlemm's canal (SC) and the t

217 surgeries reduce IOP by facilitating aqueous humor outflow through a vent fashioned from the wall of

218 sults demonstrate that PEA increases aqueous humor outflow through the TM pathway and these effects a

219 ssure due to increased resistance of aqueous humor outflow through the trabecular meshwork (TM).

220 r pressure (IOP) due to insufficient aqueous humor outflow through the trabecular meshwork and Schlem

221 able inner core designed to modulate aqueous humor outflow to provide immediate IOP reduction, preven

222 The effects of GGTI-DU40 on aqueous humor outflow were determined using organ-cultured, perf

223 The effects of AEA on aqueous humor outflow were measured using a porcine anterior seg

224 he aqueous outflow pathway increases aqueous humor outflow, possibly through altered cell adhesive in

225 thereby modulates the resistance to aqueous humor outflow.

226 Ps caused by increased resistance to aqueous humor outflow.

227 nd pressure-dependent (conventional) aqueous humor outflow.

228 TM) cell volume increase the rate of aqueous humor outflow.

229 l intraocular pressure by regulating aqueous humor outflow.

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

231 e changes and changes in the rate of aqueous humor outflow; agents that decrease trabecular meshwork

232 cells may also provide resistance to aqueous humor outflow; therefore, this study tests the involveme

233 Ranibizumab concentration in aqueous humor peaked the first day after injection (range, 36.9-

234 To study the value and safety of aqueous humor polymerase chain reaction (PCR) analysis for Herpe

235 nics drive angle opening rather than aqueous humor pressurization.

236 ial link in studying the neurodevelopment of humor processing across the lifespan, our findings contr

237 bilateral TOPJ activation may be specific to humor processing and not part of a general constellation

238 onventional outflow facility (C(t)), aqueous humor production (F(a)), and anterior chamber volume (V(

239 mouse eye results in a reduction in aqueous humor production and complete loss of the vitreous chamb

240 stent with a major role of alpha2 in aqueous humor production and suggests that, potentially, alpha2-

241 However, aqueous humor production in the same mice appears to be normal b

242 he effect of medications that reduce aqueous humor production on outflow facility in living human eye

243 ibit the Na,K-ATPase, hence reducing aqueous humor production.

244 onic anhydrase (CA) enzyme to reduce aqueous humor production.

245 the enclosed spaces are filled with aqueous humor rather than circulating blood.

246 luorescence or ELISA in homogenized vitreous humor, reflecting the greater spatial resolution of in s

247 s study and pazopanib levels in the vitreous humor, retina, and choroid-RPE at the end of the study w

248 es were developed and tested in the vitreous humor, RPE cell homogenates and intact RPE cells.

249 An aqueous humor sample was obtained during cataract surgery betwee

250 After RLB, aqueous humor samples harvested from nontreated eyes but not fro

251 t protein 1 (MCP-1) was reported in vitreous humor samples of patients with RD and diabetic retinopat

252 ines, and correlate levels with IOP, aqueous humor samples were analyzed from 23 eyes with open angle

253 For this pilot study, aqueous humor samples were collected from patients undergoing ca

254 Aqueous humor samples were obtained in 10 patients with acute NA

255 Aqueous humor samples were taken at the time of IVB pretreatment

256 echanisms: CA inhibition to decrease aqueous humor secretion (reduce inflow) and NO release to increa

257 lar anterior segment responsible for aqueous humor secretion and absorption have been well characteri

258 d to identify and study the sites of aqueous humor secretion and absorption in adult zebrafish eyes.

259 is controlled by the balance between aqueous humor secretion from the ciliary body (CB) and its drain

260 Zebrafish eyes show aqueous humor secretion primarily from the dorsal ciliary region

261 l culture from blood, saliva, urine, aqueous humor, semen, and breast milk from infected or convalesc

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

263 ion detected parasite DNA in 8/60 OT aqueous humor specimens but failed to identify Type II strain al

264 A total of 132 aqueous humor specimens were collected before intravitreal aflib

265 Aqueous humor specimens were obtained for antioxidant analysis o

266 A total of 859 aqueous humor specimens were taken before each intravitreal rani

267 Aqueous humor specimens were taken before each intravitreal rani

268 , IL-1beta released by PMNs into the aqueous humor stimulates FGF-2 synthesis in corneal endothelium

269 and are now being investigated as a vitreous humor substitute.

270 alcium ionophore, and a component of aqueous humor, suggesting that TM cells respond to environmental

271 olimbic activation in children's response to humor, suggesting these regions may form a humor-essenti

272 was diminished in cells treated with aqueous humor that was first passed through a 3-kDa or a 30-kDa,

273 ntraocular environment (aqueous and vitreous humors), the capsular tissue, and the intraocular lens (

274 ian eye is responsible for secreting aqueous humor to maintain intraocular pressure, which is elevate

275 e Ussing chambers was greater in the aqueous humor-to-blood direction than in the blood-to-aqueous hu

276 ively, surgical procedures can shunt aqueous humor too well, leading to hypotony.

277 Aqueous humor turnover was enhanced more than twofold in Best2(-

278 oscleral outflow (F(u)), and rate of aqueous humor turnover, were calculated from measured data.

279 o significant difference in baseline aqueous humor VEGF concentration was noted, while at the 2-month

280 Mean aqueous humor VEGF concentrations before treatment initiation we

281 a recognition and quantification of vitreous humor (VH) cystine as well as provide the portability fo

282 90DeltatarO were cultured in bovine vitreous humor (VH) in vitro or inoculated into the vitreous cham

283 g velocity of the suspension in the vitreous humor was 3 cm/h.

284 mized versus vitrectomized eyes for vitreous humor was 791 ng/mL (day 22) versus 731 ng/mL (day 22),

285 pressure and the level of Hmgb1 in vitreous humor was analyzed 24 hours after reperfusion.

286 g, and IL-1beta concentration in the aqueous humor was elevated in a time-dependent manner after free

287 nd caspase-3 ELISA; ascorbate in the aqueous humor was evaluated by nuclear magnetic resonance spectr

288 eaction (PCR) testing of aqueous or vitreous humor was positive for herpes simplex virus (HSV) or var

289 Conversely, VEGF in aqueous humor was significantly lower in the highly myopic eyes

290 n the iridocorneal angle tissues and aqueous humor was studied by immunohistochemistry and Western bl

291 Aqueous humor was tested whole or fractionated by size exclusion

292 0) and 47,200 ng . d/g, and for the vitreous humor were 213 ng/mL (day 60) and 11,300 ng . d/mL, resp

293 acility and total TGFbeta2 levels in aqueous humor were measured.

294 th Cytomegalovirus DNA in plasma and aqueous humor were positive.

295 average, VEGF concentrations in the aqueous humor were suppressed below the lower limit of quantific

296 ibited 3.5-fold lower solubility in vitreous humor, when compared with its sodium salt.

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

298 easured in the central plane of the vitreous humor with an SLO.

299 jection of fluorescein targeted the vitreous humor with no significant selectivity for posterior vers

300 m between production and drainage of aqueous humor, with compromised drainage generally viewed as the