ライフサイエンスコーパス: trabecular meshwork

1 unctional K(ATP) channels are present in the trabecular meshwork.

2 production in both the ciliary body and the trabecular meshwork.

3 a rat model by laser photocoagulation of the trabecular meshwork.

4 that involved laser photocoagulation of the trabecular meshwork.

5 expression of cochlin in human glaucomatous trabecular meshwork.

6 ular matrix protein produced by cells of the trabecular meshwork.

7 ferential flow pathways are present in human trabecular meshwork.

8 of caveolae in the Schlemm's canal (SC) and trabecular meshwork.

9 tion of extracellular matrix material in the trabecular meshwork.

10 nt determinants of fluid outflow through the trabecular meshwork.

11 e cytoskeleton and cell adhesions within the trabecular meshwork.

12 ocilin in the juxtacanalicular region of the trabecular meshwork.

13 f each of eight male monkeys by lasering the trabecular meshwork.

14 t enables it to bind specifically within the trabecular meshwork.

15 ance to outflow of aqueous humor through the trabecular meshwork.

16 in disease and with experiments on perfused trabecular meshwork.

17 ilar to that of the human iris than to human trabecular meshwork.

18 the injected eye by laser application to the trabecular meshwork.

19 than 4% of the genes expressed by the human trabecular meshwork.

20 low structures, Schlemm's canal (SC) and the trabecular meshwork.

21 n of SLT was performed to 360 degrees of the trabecular meshwork.

22 the posterior cornea initiating beneath the trabecular meshwork.

23 lt rhesus macaques by laser treatment to the trabecular meshwork.

24 echiae, and pigmentary dispersion within the trabecular meshwork.

25 chlemm's canal with no visible damage to the trabecular meshwork.

26 9 rhesus macaques by laser treatment to the trabecular meshwork.

27 ered in the ciliary muscle (46 +/- 5.6%) and trabecular meshwork (37 +/- 8.3%) of treated eyes relati

28 Increased levels of beads in pigmented trabecular meshwork adjacent to collector channels sugge

29 The morphology of the bovine trabecular meshwork after perfusion culture was similar

30 se fibronectin syntheses and accumulation in trabecular meshwork and accelerate the depletion of trab

31 ensity fluorescence also was observed in the trabecular meshwork and adjacent cornea.

32 pressed in remodeling tissues, including the trabecular meshwork and ciliary body.

33 COH was induced by laser cauterization of trabecular meshwork and episcleral veins in rat eyes.

34 expressing rats was associated with fibrotic trabecular meshwork and increased levels of F-actin, pho

35 not secreted in two ocular cell types, human trabecular meshwork and retinal pigment epithelial cells

36 120 minutes, label was observed only within trabecular meshwork and Schlemm's canal.

37 pressed within human retina, optic nerve and trabecular meshwork and that ABCA1 and AFAP1 are also ex

38 use of the lack of coagulation damage to the trabecular meshwork and the demonstrated efficacy in pat

39 red cells of both the ciliary epithelium and trabecular meshwork and to lower mouse intraocular press

40 n antioxidant enzyme in protecting the lens, trabecular meshwork, and cornea against oxidative damage

41 ced damage to the anterior chamber angle and trabecular meshwork, and reduced postoperative use of st

42 rat iridocorneal angle (iris, ciliary body, trabecular meshwork, and Schlemm's canal) and used to co

43 inner limiting lamina, the lens capsule, the trabecular meshwork, and the iris.

44 comatous subjects were analyzed to determine trabecular meshwork anteroposterior length and 3 anterio

45 d a significant positive association between trabecular meshwork anteroposterior length and all anter

46 d a significant positive association between trabecular meshwork anteroposterior length and all anter

47 ere used to evaluate the association between trabecular meshwork anteroposterior length and anterior

48 Mean trabecular meshwork anteroposterior length was 824.86 +/

49 ior chamber angle is associated with greater trabecular meshwork anteroposterior length.

50 The preservation of the trabecular meshwork architecture and the demonstrated ef

51 of severely hypomorphic Schlemm's canal and trabecular meshwork, as well as elevated IOP, demonstrat

52 sured as the perpendicular distance from the trabecular meshwork at 500 mum and 750 mum anterior to t

53 -3) cell line and primary cultures of bovine trabecular meshwork (BTM) cells were used in these studi

54 nd/or vehicle, or mechanical blockade of the trabecular meshwork by protein aggregates or contaminant

55 of outflow facility is mediated through the trabecular meshwork CB1 receptor, with an involvement of

56 nces from 1118 clones from this nonamplified trabecular meshwork cDNA library were categorized.

57 Human trabecular meshwork cell cultures were established from

58 Human primary trabecular meshwork cell cultures were grown in DMEM sup

59 r full-length myocilin purified from a human trabecular meshwork cell expression system alters outflo

60 sistance was used to transduce a transformed trabecular meshwork cell line (TM5).

61 Human trabecular meshwork cells (GTM3 and TM5) and HeLa cells

62 MP1 expression was measured in primary human trabecular meshwork cells (HTM) treated with dexamethaso

63 ferential expression of scAAV-infected human trabecular meshwork cells (HTM) was determined by microa

64 embranes of primary cultures of living human trabecular meshwork cells (hTMC) without the application

65 function in vitro by infecting primary human trabecular meshwork cells and in vivo by injecting livin

66 cular meshwork, which is a scenario toxic to trabecular meshwork cells and leads to early onset of oc

67 ression of CB1 receptors on cultured porcine trabecular meshwork cells and the coupling of these rece

68 B2 cannabinoid receptors on cultured porcine trabecular meshwork cells and the coupling of these rece

69 Key cytoskeleton regulatory pathways in trabecular meshwork cells and their extracellular matrix

70 between high glucose-induced alterations in trabecular meshwork cells and those of vascular endothel

71 e of the actin cytoskeleton and adhesions of trabecular meshwork cells are important determinants of

72 t MYOC appears in the extracellular space of trabecular meshwork cells by an unconventional mechanism

73 Human trabecular meshwork cells can be subjected to increased

74 Mutated myocilin appears to affect trabecular meshwork cells differently from wild-type myo

75 Human trabecular meshwork cells from five donors were cultured

76 ronectin and several other ECM components in trabecular meshwork cells from the anterior segment of t

77 Myocilin purified from human trabecular meshwork cells increased outflow resistance i

78 By visual inspection, human trabecular meshwork cells infected with scAAV2.dnRhoA sh

79 meshwork tissue from glaucoma donors and in trabecular meshwork cells insulted by dexamethasone (DEX

80 Human trabecular meshwork cells isolated from the eye were pla

81 When conditioned media from human trabecular meshwork cells were examined, both native and

82 Primary trabecular meshwork cells were obtained from residual co

83 Primary cultures of human trabecular meshwork cells were used as an in vitro model

84 In MAP kinase assays, treatment of porcine trabecular meshwork cells with 100 nM of JWH015 activate

85 Treatment of trabecular meshwork cells with 30 nM of noladin ether ac

86 ve signals were detected on cultured porcine trabecular meshwork cells with an anti-CB1 antibody in i

87 ve signals were detected on cultured porcine trabecular meshwork cells with an anti-CB2 antibody.

88 lar meshwork and accelerate the depletion of trabecular meshwork cells, a characteristic feature of t

89 , noladin ether treatment caused rounding of trabecular meshwork cells, and there was a decrease of a

90 l CB2 cannabinoid receptors are expressed in trabecular meshwork cells, and these receptors are invol

91 ead to its misfolding and aggregation within trabecular meshwork cells, and ultimately, ER stress-ind

92 h factor-beta induces actin stress fibres in trabecular meshwork cells, indicating that the cells bec

93 bolites may increase oxidative damage to the trabecular meshwork cells, resulting in elevation of int

94 anterior chamber angle, potentially damaging trabecular meshwork cells.

95 he transduction of Chinese hamster ovary and trabecular meshwork cells.

96 n normal human diploid fibroblasts and human trabecular meshwork cells.

97 but not in human diploid fibroblast or human trabecular meshwork cells.

98 cence in human diploid fibroblasts and human trabecular meshwork cells.

99 tor of calcification matrix Gla (MGP) in the trabecular meshwork cells.

100 hanism of extracellular transport of MYOC in trabecular meshwork cells.

101 ed mutant myocilin toxicity in primary human trabecular meshwork cells.

102 YAP and TAZ are both expressed in human trabecular meshwork cells.

103 These tissues include the trabecular meshwork, ciliary body, ciliary epithelium, M

104 between extracellular matrix expression and trabecular meshwork contractility appears to coordinatel

105 OPN was present in the trabecular meshwork, corneal epithelium and endothelium,

106 art in cell-matrix communication and mediate trabecular meshwork cytoskeletal changes.

107 s vector could facilitate the development of trabecular meshwork drugs for gene therapy for glaucoma.

108 n-secreted myocilin leads to HTM cell death, trabecular meshwork dysfunction and, ultimately, a domin

109 ation, ciliary body and iris hypoplasia, and trabecular meshwork dysgenesis.

110 Since precise regulation of the trabecular meshwork ECM composition and organization is

111 Myocilin is a protein found in the trabecular meshwork extracellular matrix tissue of the e

112 d effective long-term gene expression in the trabecular meshwork following intracameral delivery of a

113 py was defined as nonvisibility of posterior trabecular meshwork for at least 2 quadrants.

114 Human trabecular meshworks from glaucoma donors exhibited sign

115 aling pathway inhibitor, in the glaucomatous trabecular meshwork (GTM), and found that key canonical

116 In this clinic-based population, trabecular meshwork height is shorter in PACG patients c

117 Trabecular meshwork height was measured from the scleral

118 queous humor in the human eye is through the trabecular meshwork (HTM) and Schlemm's canal (SC).

119 ed by alizarin red staining in primary human trabecular meshwork (HTM) cells and alkaline phosphatase

120 purpose To determine how primary human trabecular meshwork (HTM) cells are influenced by their

121 media derived from primary cultures of human trabecular meshwork (HTM) cells has confirmed secretion

122 re to determine if oxidative stress on human trabecular meshwork (HTM) cells influences the stability

123 s by Q-PCR and ELISA, respectively, in human trabecular meshwork (HTM) cells transfected with miR-29b

124 Human trabecular meshwork (HTM) cells were cultured on hydroge

125 changes in gene expression profile in human trabecular meshwork (HTM) cells.

126 nium-induced changes in homeostasis of human trabecular meshwork (HTM) cells.

127 idney cells and differentiated primary human trabecular meshwork (HTM) cells.

128 to aqueous humor outflow and a stiffer human trabecular meshwork (HTM).

129 The human trabecular meshwork (HTM-3) cell line and primary cultur

130 n nonpigmented ciliary epithelial (NPCE) and trabecular meshwork (HTM-3) cells were treated with spir

131 creases in human cortical neuronal (HCN-1A), trabecular meshwork (HTMC), and pulmonary artery smooth

132 atment in the media and in the region of the trabecular meshwork in both species.

133 In contrast, the cellularity of the trabecular meshwork in experimental (cyclically pulsed)

134 are consistent with changes observed in the trabecular meshwork in glaucoma and suggest that at leas

135 creased resistance to AH outflow through the trabecular meshwork in ocular hypertension patients.

136 by translimbal laser photocoagulation of the trabecular meshwork in Sprague-Dawley rats.

137 ression is enriched in the smooth muscle and trabecular meshwork in the eye.

138 cible expression of transgenes in the murine trabecular meshwork in vivo.

139 inducible transgene activation in the murine trabecular meshwork in vivo.

140 e most abundant genes expressed by the human trabecular meshwork included ferritin H, eukaryotic tran

141 f the calcification inducer BMP2 gene to the trabecular meshwork induces elevated IOP in living rats

142 Inherited mutations in the trabecular meshwork-inducible glucocorticoid response pr

143 t well understood but has been attributed to trabecular meshwork injury from repeated injections, a p

144 sure by focally ablating and cauterizing the trabecular meshwork/inner wall of Schlemm's canal.

145 ce to aqueous humor (AH) outflow through the trabecular meshwork is a primary risk factor for open-an

146 ance in the aqueous drainage tract distal to trabecular meshwork is potentially an important determin

147 A profile of genes expressed by human trabecular meshwork is presented.

148 h more advanced glaucoma suggesting that the trabecular meshwork is the primary impediment to outflow

149 and a resulting fibrotic activity within the trabecular meshwork may result in ocular hypertension, w

150 e calcification marker, ALP, in glaucomatous trabecular meshworks might be indicative of an undergoin

151 mouse eye, it is difficult to dissect mouse trabecular meshwork (MTM) tissues and establish MTM cell

152 In the trabecular meshwork, MYOC associates with intracellular

153 Optineurin is expressed in trabecular meshwork, nonpigmented ciliary epithelium, re

154 Narrow angles were defined as posterior trabecular meshwork not visible for >/=2 quadrants on no

155 eye tissue sections and primary normal human trabecular meshwork (NTM) cells were studied by Western

156 ) tissue or primary cultures of normal human trabecular meshwork (NTM) cells.

157 sociated with glaucoma may be altered in the trabecular meshwork of glaucoma patients.

158 Increased fibronectin accumulation in the trabecular meshwork of glaucomatous eyes may contribute

159 ong-term, safe delivery of transgenes to the trabecular meshwork of living animals.

160 ser photocoagulation was then applied to the trabecular meshwork of one eye to induce chronic elevati

161 ser photocoagulation was then applied to the trabecular meshwork of one eye to induce chronic elevati

162 ser photocoagulation then was applied to the trabecular meshwork of one eye to induce chronic unilate

163 vides prolonged and safe transduction in the trabecular meshwork of rats and monkeys.

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

165 th of cytoskeleton-mediated processes in the trabecular meshwork of the human eye.

166 orylation of ERK1/2 was also observed in the trabecular meshwork of transgenic mice expressing 6-fold

167 ened at least 180 degrees (visible posterior trabecular meshwork on gonioscopy) after laser iridotomy

168 Both ABCA1 and PMM2 are expressed in the trabecular meshwork, optic nerve and other ocular tissue

169 plished by nucleofector electroporation with trabecular meshwork-optimized conditions.

170 f stress fibers in primary cultures of human trabecular meshwork or NIH 3T3 cells.

171 o there is a crescent interest in increasing trabecular meshwork outflow by extracellular matrix remo

172 Modulation of new agents that act mainly on trabecular meshwork outflow may be the future hypotensiv

173 nce and abnormality, pupil edge pigment, and trabecular meshwork pigment.

174 f the amount of missing ruff (P = 0.001) and trabecular meshwork pigmentation (P = 0.006).

175 uced the upregulation of ALP activity in two trabecular meshwork primary cell lines.

176 Primary cell cultures of porcine trabecular meshwork (PTM) and ciliary body (PCB) were tr

177 monophosphate (AMP) and adenosine in porcine trabecular meshwork (PTM) cells treated with adenosine t

178 Porcine trabecular meshwork (pTM) cells were subjected to CMS.

179 m for this complication may be injury to the trabecular meshwork resulting from rapid elevations in I

180 iris, sclera, ciliary muscles, ciliary body, trabecular meshwork, retina and optic nerve were establi

181 the iris and sclera and less actively in the trabecular meshwork, retina, and optic nerve.

182 rols and seven with unilateral laser-induced trabecular meshwork scarification and ocular hypertensio

183 Trabecular meshwork size may play a role in ethnic diffe

184 Human trabecular meshwork stem cells (TMSCs) were isolated as

185 ing of the actin cytoskeleton may render the trabecular meshwork stiffer and more resistant to aqueou

186 logical and pathogenic mechanisms within the trabecular meshwork that are relevant to intraocular pre

187 Immunostaining of trabecular meshwork tissue after exposure to 4MU showed

188 the presence of calcification markers in the trabecular meshwork tissue from glaucoma donors and in t

189 Trabecular meshwork tissue showed moderate ALP activity

190 Trabecular meshwork tissue was obtained from perfused po

191 logical evaluation revealed a well-organized trabecular meshwork tissue, exhibiting denser matrix in

192 protein found in the extracellular matrix of trabecular meshwork tissue, the anatomical region of the

193 adly expressed in most tissues including the trabecular meshwork (TM) and heterozygous Sod2 knockout

194 The trabecular meshwork (TM) and Schlemm's canal (SC) cells

195 (PG) receptors in primary cultures of human trabecular meshwork (TM) and Schlemm's canal (SC) cells

196 conventional outflow pathway comprising the trabecular meshwork (TM) and Schlemm's canal (SC).

197 esistance, its segmental distribution in the trabecular meshwork (TM) and the effect on outflow facil

198 The IOP is maintained by the trabecular meshwork (TM) and the elevation of IOP in ope

199 Various changes in the trabecular meshwork (TM) are responsible for elevated IO

200 oxidation, accumulate in human glaucomatous trabecular meshwork (TM) but not in controls.

201 Normal and glaucomatous trabecular meshwork (TM) cell culture lines were initiat

202 cilin was isolated and purified from porcine trabecular meshwork (TM) cell culture media.

203 Trabecular meshwork (TM) cell lines derived from normal

204 ' effects on hydraulic conductivity of human trabecular meshwork (TM) cell monolayers were evaluated.

205 Primary cultures of human trabecular meshwork (TM) cell monolayers were treated wi

206 ueous of patients with POAG, affects RGC and trabecular meshwork (TM) cell survival in vitro.

207 tween nitric oxide (NO)-induced decreases in trabecular meshwork (TM) cell volume and NO-induced incr

208 aqueous humor outflow; agents that decrease trabecular meshwork (TM) cell volume increase the rate o

209 Ecto-ATPases from transformed human trabecular meshwork (TM) cells (TM5) and explant-derived

210 Primary human trabecular meshwork (TM) cells and corneoscleral explant

211 e expression and distribution of MRP4 in the trabecular meshwork (TM) cells and its role in homeostas

212 t-soluble CD44 (sCD44)-which is cytotoxic to trabecular meshwork (TM) cells and retinal ganglion cell

213 tagonist gremlin is elevated in glaucomatous trabecular meshwork (TM) cells and tissues and elevates

214 production in low-passage porcine and human trabecular meshwork (TM) cells and transformed human TM

215 Trabecular meshwork (TM) cells appear to sense changes i

216 ular matrix (ECM) proteins were evaluated in trabecular meshwork (TM) cells by cDNA microarray, q-PCR

217 tudy was to determine whether cultured human trabecular meshwork (TM) cells express BMP1, BMP1 expres

218 A percentage of trabecular meshwork (TM) cells in tissue and organ cultu

219 Elevated cAMP in the trabecular meshwork (TM) cells increases the aqueous hum

220 the release of exosomes containing MYOC from trabecular meshwork (TM) cells is constitutive or regula

221 We have previously shown that trabecular meshwork (TM) cells might detect aqueous humo

222 matrix metalloproteinase (MMP)-2 and -14 on trabecular meshwork (TM) cells that resemble podosomes o

223 Interactions were also examined in bovine trabecular meshwork (TM) cells through a mammalian two-h

224 he present study was to examine responses of trabecular meshwork (TM) cells to cyclic biomechanical s

225 To challenge human trabecular meshwork (TM) cells using lactate to mimic ce

226 took advantage of the phagocytic property of trabecular meshwork (TM) cells, and developed a novel ma

227 GRbeta and Hsp90 in normal and glaucomatous trabecular meshwork (TM) cells, as well as in TM cells o

228 PE cells, human lens epithelial cells, human trabecular meshwork (TM) cells, human choroidal endothel

229 re (IOP), sensed as mechanical stretching by trabecular meshwork (TM) cells, triggers extracellular m

230 rane localization of GTP-binding proteins in trabecular meshwork (TM) cells, using immunofluorescence

231 ng on ET-1 expression and secretion by human trabecular meshwork (TM) cells.

232 iber formation and contractility in cultured trabecular meshwork (TM) cells.

233 G-protein expression and activation in human trabecular meshwork (TM) cells.

234 role in the regulation of RhoA signaling in trabecular meshwork (TM) cells.

235 ation of matrix metalloproteinases (MMPs) in trabecular meshwork (TM) cells.

236 ositol) profiles of control and glaucomatous trabecular meshwork (TM) derived from human donors.

237 ix metalloproteinases (MMPs) are involved in trabecular meshwork (TM) extracellular matrix metabolism

238 irculation, we pursued proteomic analyses of trabecular meshwork (TM) from glaucoma and age-matched c

239 GC-induced myocilin expression in the trabecular meshwork (TM) has been suggested to play an i

240 To determine if trabecular meshwork (TM) height differs between primary

241 c lens in enucleated porcine eyes and of the trabecular meshwork (TM) in human corneoscleral rim tiss

242 sure by increasing outflow resistance in the trabecular meshwork (TM) in some individuals.

243 However, their potential role in the trabecular meshwork (TM) in the eye, which regulates int

244 -1 (matrix metalloproteinase [MMP]-3) by the trabecular meshwork (TM) initiates extracellular matrix

245 f extracellular matrix (ECM) proteins in the trabecular meshwork (TM) is associated with TM dysfuncti

246 The function of hevin in trabecular meshwork (TM) is unknown.

247 relationship between SPARC and TGF-beta2 in trabecular meshwork (TM) is unknown.

248 Trabecular meshwork (TM) matrix metalloproteinase (MMP),

249 o increase aqueous outflow resistance in the trabecular meshwork (TM) of glaucomatous eyes.

250 ctional changes in the unlasered portions of trabecular meshwork (TM) of laser-treated primate eyes a

251 often elevated in the aqueous humor (AH) and trabecular meshwork (TM) of patients with primary open-a

252 Because the trabecular meshwork (TM) plays an important role in aque

253 by the MGP gene promoter specifically to the trabecular meshwork (TM) provides a new tool for specifi

254 Given that the trabecular meshwork (TM) provides most of aqueous humor

255 ion (SHG), were used to obtain images of the trabecular meshwork (TM) region within an intact mouse e

256 excitation fluorescence (TPEF) of the human trabecular meshwork (TM) reveals beams of heterogeneous

257 The study was designed to determine trabecular meshwork (TM) stiffness and its relationship

258 was to determine the localization of TNC in trabecular meshwork (TM) tissue and to analyze the effec

259 The trabecular meshwork (TM) tissue controls drainage of aqu

260 Trabecular meshwork (TM) tissue in the eye is under cons

261 emistry, and inside-out patch clamp in human trabecular meshwork (TM) tissue or primary cultures of n

262 he MMP-3 increase that occurs in response to trabecular meshwork (TM) treatment by laser trabeculopla

263 ly in the regulation of ECM synthesis in the trabecular meshwork (TM) under basal and TGF-beta2 stimu

264 The trabecular meshwork (TM), a specialized eye tissue, is b

265 s morphologic and biochemical changes in the trabecular meshwork (TM), an ocular tissue involved in r

266 10 most highly expressed genes in the human trabecular meshwork (TM), and its expression is affected

267 tes from outflow pathway tissues such as the trabecular meshwork (TM), but the associated molecular e

268 In the trabecular meshwork (TM), interleukin (IL)-1alpha is a p

269 The trabecular meshwork (TM), iris, ciliary body, and sclera

270 ptor activation in primary cultures of human trabecular meshwork (TM), Schlemm's canal (SC), and cili

271 to endoplasmic reticulum (ER) stress in the trabecular meshwork (TM), the tissue that regulates IOP.

272 ueous humor but accumulated in the ER of the trabecular meshwork (TM), thereby inducing ER stress in

273 a resistance to aqueous humor outflow in the trabecular meshwork (TM).

274 signaling pathway genes are expressed in the trabecular meshwork (TM).

275 on of extracellular matrix metabolism in the trabecular meshwork (TM).

276 extracellular matrix (ECM) remodeling in the trabecular meshwork (TM).

277 ir mRNA levels and protein expression in the trabecular meshwork (TM).

278 istance of aqueous humor outflow through the trabecular meshwork (TM).

279 resistance of aqueous humor flow through the trabecular meshwork (TM).

280 h morphologic and biochemical changes in the trabecular meshwork (TM).

281 etalloproteinase-3 (MMP-3) expression in the trabecular meshwork (TM).

282 was associated with chronic ER stress of the trabecular meshwork (TM).

283 liary body (CB) and its drainage through the trabecular meshwork (TM).

284 atrix (ECM) synthesis and/or turnover in the trabecular meshwork (TM).

285 ) in many tissues and is highly expressed in trabecular meshwork (TM).

286 Both TSP1 and TSP2 are found in the trabecular meshwork (TM).

287 50]) and angle opening (all 4 quadrants with trabecular meshwork [TM] visible on gonioscopy after LPI

288 interacts with a prostamide receptor in the trabecular meshwork to increase outflow facility.

289 re associated with increased exposure of the trabecular meshwork to oxygen.

290 he juxtacanalicular connective tissue of the trabecular meshwork together with inner wall endothelium

291 In contrast, scAAV2 transduced the trabecular meshwork very efficiently, with a fast onset

292 A direct effect on the trabecular meshwork was not indicated by these in vivo s

293 eyes were classified as narrow if posterior trabecular meshwork was not visible and open if the angl

294 l of glaucoma with laser photocoagulation of trabecular meshwork was used.

295 Wedges of trabecular meshwork were dissected and some wedges immed

296 sly thought to be primarily expressed in the trabecular meshwork, which are highly expressed by RGCs

297 acellularly instead of being secreted to the trabecular meshwork, which is a scenario toxic to trabec

298 aint staining of collagen type I in areas of trabecular meshwork with high MMP1 transgene expression.

299 CF increased in the trabecular meshwork with increasing perfusion time.

300 trates efficient transgene activation in the trabecular meshwork, with additional sites of transgene