ライフサイエンスコーパス: retinal pigment epithelium

1 1% intraretinal, 38% subretinal, and 36% sub-retinal pigment epithelium).

2 glia cells, and the basolateral side of the retinal pigment epithelium.

3 hed chromophores and recycling in the nearby retinal pigment epithelium.

4 ar surface ectoderm, lens, neuro-retina, and retinal pigment epithelium.

5 generalized dysfunction at the level of the retinal pigment epithelium.

6 nted when sFlt-1 expression is attenuated in retinal pigment epithelium.

7 and infiltrating myeloid cells but not from retinal pigment epithelium.

8 particularly toxic to photoreceptors and/or retinal pigment epithelium.

9 s </=325 mum or >/=425 mum, and elevation of retinal pigment epithelium.

10 terized by macular atrophy and flecks in the retinal pigment epithelium.

11 etabolite carrier between the retina and the retinal pigment epithelium.

12 al pigmentation consistent with transplanted retinal pigment epithelium.

13 of 11-cis-retinyl esters (11-REs) within the retinal pigment epithelium.

14 hway called the visual cycle in cells of the retinal pigment epithelium.

15 2 in the re-attachment of the retina to the retinal pigment epithelium.

16 ally secreted in exosomes by polarized human retinal pigment epithelium.

17 e physical separation of the retina from the retinal pigment epithelium.

18 n within hyperreflective lesions adherent to retinal pigment epithelium.

19 n early age and peripapillary sparing of the retinal pigment epithelium.

20 posited at the apical and basal sides of the retinal pigment epithelium.

21 e can suppress consumption of glucose by the retinal pigment epithelium.

22 istent with PVR, and reactive changes in the retinal pigment epithelium.

23 on, optic nerve head pallor, and mottling of retinal pigment epithelium.

24 tween the interdigitation zone and an intact retinal pigment epithelium.

25 ning of the cone outer segment closer to the retinal pigment epithelium.

26 in pigment cells, including melanocytes and retinal pigment epithelium.

27 ated retina preparation after removal of the retinal pigmented epithelium.

28 ge, indicative of pathological events in the retinal pigmented epithelium.

29 se was composed of 6 layered components: (1) retinal pigment epithelium, (2) basal laminar deposits,

30 undus photographs were graded for drusen and retinal pigment epithelium abnormalities and were evalua

31 o 17.6% (n = 37) in those 80 years or older, retinal pigment epithelium abnormalities from 4.1% (n =

32 The copresence of medium drusen plus retinal pigment epithelium abnormalities signals a great

33 Retinal pigment epithelium abnormalities, AVLs, neovascu

34 ound the injection site demonstrated diffuse retinal pigment epithelium alterations with dense hard e

35 ion, and position of the CNV relative to the retinal pigment epithelium and Bruch membrane were descr

36 ed to visualize CNV location relative to the retinal pigment epithelium and Bruch's layer and classif

37 location of vitamin A derivatives across the retinal pigment epithelium and Bruch's membrane, 2 tissu

38 thesis that toll-like receptor activation of retinal pigment epithelium and cellular metabolic switch

39 The retinal pigment epithelium and choroid are involved in s

40 ipofuscin accumulate in the lysosomes of the retinal pigment epithelium and display cytotoxic effects

41 Quantifying preserved retinal pigment epithelium and EZ areas on FAF and OCT i

42 tors then export the lactate as fuel for the retinal pigment epithelium and for neighboring Muller gl

43 lly if multimodal imaging supports an intact retinal pigment epithelium and inner retina but an abnor

44 insufficient to alter Fpn levels within the retinal pigment epithelium and Muller cells, but may lim

45 ns in the choriocapillaris in the absence of retinal pigment epithelium and outer retinal abnormaliti

46 cellular adhesion between the retina and the retinal pigment epithelium and prevention of its cellula

47 dal gammadelta T cells in protection against retinal pigment epithelium and retinal injury.

48 Nel is strongly expressed in the presumptive retinal pigment epithelium and RGCs.

49 uter retina and severe damage or loss of the retinal pigment epithelium and the choroid.

50 s were associated with absence of underlying retinal pigment epithelium and were longer (r = -0.62; 9

51 raphy confirmed that these areas had loss of retinal pigmented epithelium and ellipsoids zones, with

52 cal coherence tomography thinning but intact retinal pigment epithelium), and severe (visible bull's-

53 xcavation involving the neurosensory retina, retinal pigment epithelium, and choroid in 4 eyes (44%).

54 e posterior ocular segment (neuronal retina, retinal pigment epithelium, and choroid) of wild-type (W

55 sequential involvement of the outer retina, retinal pigment epithelium, and choroid, as well as freq

56 able degrees of atrophy of the outer retina, retinal pigment epithelium, and choroid, with outer reti

57 extent of structural alterations of the CC, retinal pigment epithelium, and photoreceptors with mult

58 quantitative characteristics of the choroid, retinal pigment epithelium, and retina were compared bet

59 ion, likely by promoting inflammation of the retinal pigment epithelium, and validate TLR2 as a novel

60 totoxicity and genotoxicity studies in human retinal pigment epithelium (ARPE-19) cells.

61 als can stimulate the growth of normal human retinal pigment epithelium (ARPE-19) cells.

62 The atrophic area of the retinal pigment epithelium assessed on the basis of FAF

63 beneath the small irregular elevation of the retinal pigment epithelium at the site of the quiescent

64 bited several nummular perifoveal islands of retinal pigment epithelium atrophy and adjacent pale dep

65 , because of the extent of photoreceptor and retinal pigment epithelium atrophy in the macula.

66 ed with an irregularly thickened and rippled retinal pigment epithelium band in 2 eyes.

67 appeared as hyperreflective debris above the retinal pigment epithelium band in all 3 eyes, and were

68 data highlight an unrecognised link between retinal pigment epithelium bioenergetic status and tissu

69 Retinal pigment epithelium-BM thickness, as measured by

70 hows that fibulin 2 is mainly present in the retinal pigment epithelium, Bruch membrane, choriocapill

71 nce tomography (OCT) revealed a split in the retinal pigment epithelium-Bruch membrane band.

72 the distance between the outer border of the retinal pigment epithelium-Bruch's membrane complex, and

73 retinosomes and condensation products in the retinal pigment epithelium by their characteristic local

74 Suppression of glucose consumption in the retinal pigment epithelium can increase the amount of gl

75 d by the analysis of LC/MS data from a human retinal pigment epithelium cell line (ARPE-19) grown on

76 y AMD, including Bruchs membrane thickening, retinal pigment epithelium cell loss, retinal functional

77 ascularization and a decrease in mesenchymal retinal pigment epithelium cells in alphaB-crystallin kn

78 nly in microglia, whereas both microglia and retinal pigment epithelium cells produced Ccl2.

79 No photoreceptors or retinal pigment epithelium cells were identified at the

80 Retinal pigment epithelium cells were in the centre, pho

81 Finally, in primary human fetal retinal pigment epithelium cells, ligand binding to TLR2

82 ine, bipolar, horizontal, photoreceptor, and retinal pigment epithelium cells, thus exposing the anat

83 served in the mammalian cochlea and in human retinal pigment epithelium cells.

84 n epithelial-mesenchymal transition (EMT) of retinal pigment epithelium cells.

85 IS organelles in the OS region and abnormal retinal pigmented epithelium cells.

86 fundus appearance but later develop mottled retinal pigment epithelium change along the arcades, fol

87 BCA4 mutations lead to clinically detectable retinal pigment epithelium changes remain unclear.

88 be tolerated, such as macular degeneration, retinal pigment epithelium changes, and glaucoma.

89 alized to CNV-associated macrophages and the retinal pigment epithelium/choroid complex.

90 nt component 3 and factor B in plasma and in retinal pigment epithelium/choroid/sclera, establishing

91 ST2 was highly expressed in retinal pigment epithelium, choroidal mast cells, and ch

92 angles, loss of pigment and thinning of the retinal pigment epithelium, choroidal thinning, undiffer

93 orders, resembling congenital hypertrophy of retinal pigment epithelium (CHRPE) lesions.

94 tics of combined hamartoma of the retina and retinal pigment epithelium (CHRRPE) involving the macula

95 f increased autofluorescence as a measure of retinal pigment epithelium damage and lipofuscin accumul

96 Cases recognized before retinal pigment epithelium damage retained foveal archit

97 ansdifferentiation of the dorsal and ventral retinal pigment epithelium, defective optic cup peripher

98 ccelerated accumulation of lipofuscin in the retinal pigment epithelium, degeneration of the neuroret

99 hydroxychloroquine retinopathy involving the retinal pigment epithelium demonstrated progressive dama

100 d a thicker outer nuclear layer and less sub-retinal pigment epithelium deposit accumulation.

101 on; and stage 5 (3 patients [18%]), complete retinal pigment epithelium disruption and/or loss of the

102 s [29%]), optically empty space with partial retinal pigment epithelium disruption; and stage 5 (3 pa

103 l mice had thickening of Bruchs membrane and retinal pigment epithelium dysfunction.

104 gy revealed malformations in the choroid and retinal pigmented epithelium, early cone photoreceptor c

105 ed by quantitative RT-PCR in the retina, the retinal pigment epithelium, fibroblasts, and whole-blood

106 e fellow eye, hemorrhage, and absence of sub-retinal pigment epithelium fluid at baseline were associ

107 ntraretinal fluid, subretinal fluid, and sub-retinal pigment epithelium fluid.

108 s of fibulin 2 dramatically increased in the retinal pigment epithelium following retinal detachment,

109 ons of visual cycle proteins or with reduced retinal pigment epithelium function due to aging.

110 unique to AMD but rather may be a marker for retinal pigment epithelium function.

111 Eyes with elevation of the retinal pigment epithelium had lower risk (aHR, 0.6; CI,

112 oRNA (miRNA)-processing enzyme DICER1 in the retinal pigmented epithelium has been implicated in geog

113 A uptake across the blood-retinal barrier or retinal pigment epithelium have not been identified.

114 , we use human induced pluripotent stem cell-retinal pigment epithelium (hiPSC-RPE) derived from pati

115 hemorrhages in 2 (17%) and 3 (18%); loss of retinal pigment epithelium in 1 (8%) and 4 (24%); and dr

116 id zone and hyperreflectivity underlying the retinal pigment epithelium in 9 eyes (100%), retinal thi

117 monstrate that Mfsd2a is highly expressed in retinal pigment epithelium in embryonic eye, before the

118 LRP3 inflammasome to cause cell death of the retinal pigment epithelium in geographic atrophy, a type

119 TLR2 was robustly expressed by the retinal pigment epithelium in mouse and human eyes, both

120 f subretinal transplantation of hESC-derived retinal pigment epithelium in nine patients with Stargar

121 ine the incidence of atrophic lesions of the retinal pigment epithelium in patients with Stargardt di

122 caused by abnormalities of photoreceptors or retinal pigment epithelium in the retina leading to prog

123 lindrical melanosomes forming the remains of retinal pigment epithelium indicates that it is a verteb

124 classic features of new intraretinal or sub-retinal pigment epithelium infiltration of lymphoma in t

125 le of Bruch's membrane, the Bruch's membrane-retinal pigment epithelium interface, or both in the pat

126 The variable extent of retinal pigment epithelium involvement was reflected in

127 nct morphologies arranged in layers, forming retinal pigment epithelium, is a synapomorphy of vertebr

128 dependent on the level of expression of the retinal pigment epithelium isomerase, Rpe65.

129 Progressive geographic atrophy (GA) of the retinal pigment epithelium leads to loss of central visi

130 associated with a significant enlargement of retinal pigment epithelium lesion area (0.282 mm(2)/year

131 Optical coherence tomography revealed a mean retinal pigment epithelium lesion area of 2.6 mm(2), pre

132 tomography parameters (IS/OS alteration and retinal pigment epithelium lesion area) were obtained in

133 gh closely coupled, the results suggest that retinal pigment epithelium loss is more extensive than p

134 inal lamination, neural retinal attenuation, retinal pigment epithelium loss, or hypertrophy was seen

135 the retinal vasculature, optic atrophy, and retinal pigment epithelium loss.

136 visualization of structures posterior to the retinal pigment epithelium, may be a useful tool to moni

137 rmal amount of pigment granules deposited in retinal pigment epithelium microvilli area and an abnorm

138 at the interface between photoreceptors and retinal pigment epithelium microvilli, a region critical

139 EDF), an antiangiogenic protein, to regulate retinal pigment epithelium migration.

140 ration, and scarring; blood vessel loss; and retinal pigment epithelium migration.

141 gic functions of photoreceptor cells and the retinal pigmented epithelium necessitate precise gene re

142 n no eye of either groups was atrophy of the retinal pigment epithelium observed in the area of treat

143 arget of TLR2 signaling, was detected in the retinal pigment epithelium of human eyes, particularly i

144 point to subnormal lipofuscin levels in the retinal pigment epithelium or, alternatively, limitation

145 ies, including congenital hypertrophy of the retinal pigment epithelium, ora serrata pearl, TCD, cyst

146 inal hyperreflective foci represent cells of retinal pigment epithelium origin that are similar to th

147 ted with acquired vitelliform lesions are of retinal pigment epithelium origin, and the natural cours

148 pment of ischemic infarction of the choroid, retinal pigment epithelium, outer part of the retina and

149 g vortex vein, congenital hypertrophy of the retinal pigment epithelium, pars plana, ora serrata pear

150 usen phenotypes, including the occurrence of retinal pigment epithelium (RPE) abnormalities, choroida

151 opathy that begins around the age of 30 with retinal pigment epithelium (RPE) and Bruch's membrane ch

152 pear as hyperreflective deposits between the retinal pigment epithelium (RPE) and Bruch's membrane on

153 nced by increased deposition of C5b-9 in the retinal pigment epithelium (RPE) and choroid.

154 in SD-OCT images in eyes with atrophy of the retinal pigment epithelium (RPE) and compared with histo

155 se cause remains elusive, dysfunction of the retinal pigment epithelium (RPE) and dysregulation of co

156 ter segments is an important function of the retinal pigment epithelium (RPE) and it is essential for

157 Histology data show aberrant retinal pigment epithelium (RPE) and late-onset photorec

158 Bestrophin1 (BEST1) is expressed in human retinal pigment epithelium (RPE) and mutations in the BE

159 bi-potential progenitor cells from which the retinal pigment epithelium (RPE) and neural retina fates

160 damage in the diseased retina, damage in the retinal pigment epithelium (RPE) and neural retina from

161 including OV specification and formation of retinal pigment epithelium (RPE) and neural retina proge

162 NH surfaces (BMOM, BMOH) and the terminal of retinal pigment epithelium (RPE) and ONH surfaces (RPEM,

163 xudative AMD that manifests with progressive retinal pigment epithelium (RPE) and photoreceptor degen

164 roduced by neighboring epithelial cells, the retinal pigment epithelium (RPE) and podocytes, respecti

165 We semiautomatically delineated the retinal pigment epithelium (RPE) and RPE drusen complex

166 he interaction between autophagy impaired in retinal pigment epithelium (RPE) and the responses of ma

167 ations in the morphology and function of the retinal pigment epithelium (RPE) are common features sha

168 nner and outer boundaries of the choroid and retinal pigment epithelium (RPE) as well as the inner re

169 outer retinal disruption and atrophy of the retinal pigment epithelium (RPE) associated with ORT on

170 The vitelliform material was above the retinal pigment epithelium (RPE) at any stage of the mac

171 that photoreceptor atrophy can occur without retinal pigment epithelium (RPE) atrophy and that atroph

172 refied choriocapillaris in correspondence of retinal pigment epithelium (RPE) atrophy in 80% (n = 16)

173 est-corrected visual acuity (BCVA), age, and retinal pigment epithelium (RPE) atrophy were recorded a

174 (OS) length, thickness and elevation of the retinal pigment epithelium (RPE) band, grading of the in

175 k of these disorders is the formation of sub-retinal pigment epithelium (RPE) basal deposits.

176 l and histopathologic evidence suggests that retinal pigment epithelium (RPE) can harbor M tuberculos

177 hannel is localized to the apical aspects of retinal pigment epithelium (RPE) cells and contributes t

178 polar cells, mitochondria, Muller cells, and retinal pigment epithelium (RPE) cells and were visualiz

179 Retinal Pigment Epithelium (RPE) cells generated from a

180 o evaluate the intraretinal migration of the retinal pigment epithelium (RPE) cells in age-related ma

181 Cholesterol accumulation beneath the retinal pigment epithelium (RPE) cells is supposed to co

182 h encodes cadherin-3, a protein expressed in retinal pigment epithelium (RPE) cells that may have a k

183 require trophic and functional support from retinal pigment epithelium (RPE) cells.

184 8A is crucial for volume regulation in human retinal pigment epithelium (RPE) cells.

185 VZV but not HSV-1 infection of human primary retinal pigment epithelium (RPE) cells.

186 s revealed either no abnormalities or foveal retinal pigment epithelium (RPE) changes in 10 and 9 pat

187 eloping murine eye, melanin synthesis in the retinal pigment epithelium (RPE) coincides with neurogen

188 ound TRPV4 expression in the endothelium and retinal pigment epithelium (RPE) components of the BRB,

189 ed macular degeneration and atypical central retinal pigment epithelium (RPE) defects not attributabl

190 ozygous Adamtsl4(tvrm267) mice exhibit focal retinal pigment epithelium (RPE) defects primarily in th

191 Retinal pigment epithelium (RPE) degeneration underpins

192 al dystrophy, characterised by extensive sub-retinal pigment epithelium (RPE) deposits, RPE atrophy,

193 fluid (IRF), subretinal fluid (SRF), and sub-retinal pigment epithelium (RPE) fluid and performed man

194 nal fluid (IRF), subretinal fluid (SRF), sub-retinal pigment epithelium (RPE) fluid, and subretinal t

195 d induced pluripotent stem cells to generate retinal pigment epithelium (RPE) from an individual suff

196 eceptors in three-dimensional optic cups and retinal pigment epithelium (RPE) from iPSCs with this co

197 of pathways necessary for photoreceptor and retinal pigment epithelium (RPE) function is critical to

198 To report on the presence of retinal pigment epithelium (RPE) humps in high myopia, a

199 lipid profiles specifically localized to the retinal pigment epithelium (RPE) in Abca4 (-/-) Stargard

200 Daily, the retinal pigment epithelium (RPE) ingests a bolus of lipi

201 While AMD histopathology involves retinal pigment epithelium (RPE) injury associated with

202 The retinal pigment epithelium (RPE) is a key site of injury

203 The retinal pigment epithelium (RPE) is a monolayer of pigme

204 nd lipid-containing deposits external to the retinal pigment epithelium (RPE) is common in the aging

205 interface between the neural retina and the retinal pigment epithelium (RPE) is critical for several

206 tion of lipofuscin bisretinoids (LBs) in the retinal pigment epithelium (RPE) is the alleged cause of

207 < 0.001-0.03) were: hyperreflective foci and retinal pigment epithelium (RPE) layer atrophy or absenc

208 ber layers (P = 0.024) and diffusely thinned retinal pigment epithelium (RPE) layers (P = 0.009) vers

209 s calculated from the SD-OCT and the area of retinal pigment epithelium (RPE) loss from the FAF.

210 The FAF imaging showed well-defined areas of retinal pigment epithelium (RPE) loss that corresponded

211 e damage to mitochondrial DNA (mtDNA) in the retinal pigment epithelium (RPE) may play a key role in

212 ated kinase 1/2 (ERK1/2) is increased in the retinal pigment epithelium (RPE) of age-related macular

213 lel clinical phenotypes were observed in the retinal pigment epithelium (RPE) of individuals with but

214 sponded to outer retinal atrophy with viable retinal pigment epithelium (RPE) on spectral-domain OCT

215 e NLRP3 inflammasome have been implicated in retinal pigment epithelium (RPE) pathology in age-relate

216 The retinal pigment epithelium (RPE) performs specialized fu

217 s in DPED, estimate of coverage by different retinal pigment epithelium (RPE) phenotypes in the DPED

218 rectly elicit a Wnt/beta-catenin response in retinal pigment epithelium (RPE) progenitors near the op

219 esence of autoantibodies against retinal and retinal pigment epithelium (RPE) proteins.

220 ean (SD) height of 45.3 (36.1) mum above the retinal pigment epithelium (RPE) reference plane that wa

221 absolute measurements of vitreous (VIT) and retinal pigment epithelium (RPE) signal intensities, whi

222 A central macular patch of retinal pigment epithelium (RPE) sparing was evident in

223 thelial growth factor (VEGF) inhibitors, (2) retinal pigment epithelium (RPE) tear, (3) subretinal he

224 To investigate when retinal pigment epithelium (RPE) tears occur and their a

225 ted to OCT measurement parameters, including retinal pigment epithelium (RPE) thickness, central macu

226 abolite transport is a major function of the retinal pigment epithelium (RPE) to support the neural r

227 tiated, biologically and genetically defined retinal pigment epithelium (RPE) to the diseased human e

228 Retinectomies expose the retinal pigment epithelium (RPE) to the vitreous cavity;

229 To conditionally inactivate genes in the retinal pigment epithelium (RPE) transgenic mouse strain

230 In contrast, the canonical retinal pigment epithelium (RPE) visual cycle produces e

231 The retinal pigment epithelium (RPE) was absent (n = 2), thi

232 rmalities in regions with normally appearing retinal pigment epithelium (RPE) were the loss of the PO

233 lated macular degeneration (AMD) affects the retinal pigment epithelium (RPE), a cell monolayer essen

234 te mechanisms that modulate autophagy in the retinal pigment epithelium (RPE), a key site of insult i

235 t), (3) retinal projection through SHRM onto retinal pigment epithelium (RPE), and (4) masking of cho

236 intensities were lower at the photoreceptor, retinal pigment epithelium (RPE), and choroid layers (st

237 tina, resulting from loss of photoreceptors, retinal pigment epithelium (RPE), and underlying chorioc

238 this reisomerization occurs in the adjacent retinal pigment epithelium (RPE), but because ipRGCs are

239 on was found in the photoreceptor-supporting retinal pigment epithelium (RPE), especially in a zone c

240 h the coordinated terminal maturation of the retinal pigment epithelium (RPE), fenestrated choroid en

241 ty, which was then compared with that of the retinal pigment epithelium (RPE), generating an optical

242 ioretinopathy, congenital hypertrophy of the retinal pigment epithelium (RPE), hemorrhagic RPE detach

243 tinoid-containing lipofuscin pigments in the retinal pigment epithelium (RPE), increased oxidative st

244 n abundant membrane-associate protein in the retinal pigment epithelium (RPE), is a key retinoid isom

245 d by many cell types, including those of the retinal pigment epithelium (RPE), is a regulatory protei

246 of TGF-beta signaling in the entire eye, the retinal pigment epithelium (RPE), or the vascular endoth

247 assic 'fingerprint' lysosomal storage in the retinal pigment epithelium (RPE), replicating the human

248 educe cytotoxic bisretinoid formation in the retinal pigment epithelium (RPE), which is associated wi

249 ciations of ocular and systemic factors with retinal pigment epithelium (RPE)-Bruch's membrane (BM) c

250 all interfering RNA (siRNA) to transfect the retinal pigment epithelium (RPE)-derived cell line ARPE-

251 The volumes of retinal pigment epithelium (RPE)-drusen complex, RPE-dru

252 ia 9.7, P = .001; SE -2.27 D [SD 4.65]), and retinal pigment epithelium (RPE)-related dystrophies (OR

253 epends on the retinoid cycle in the adjacent retinal pigment epithelium (RPE).

254 espread pigment clumping at the level of the retinal pigment epithelium (RPE).

255 mice lacking caveolin-1 specifically in the retinal pigment epithelium (RPE).

256 ls in a model of chronic degeneration of the retinal pigment epithelium (RPE).

257 (POS) disk membranes, is a major role of the retinal pigment epithelium (RPE).

258 and cone pigment regeneration driven by the retinal pigment epithelium (RPE).

259 play late-onset morphological changes in the retinal pigment epithelium (RPE).

260 e photoreceptors, as well as the choroid and retinal pigment epithelium (RPE).

261 ans, and is characterized by the loss of the retinal pigment epithelium (RPE).

262 examine the effects of smoke exposure on the retinal pigment epithelium (RPE).

263 of the internal limiting membrane, RNFL, and retinal pigment epithelium (RPE).

264 the retina, the ciliary margin (CM), and the retinal pigment epithelium (RPE).

265 d epithelial mesenchymal transition (EMT) of retinal pigment epithelium (RPE).

266 may regulate the phagocytosis of OSs by the retinal pigment epithelium (RPE).

267 teristics, especially the involvement of the retinal pigment epithelium (RPE).

268 e (ELM) and mild transient thickening of the retinal pigment epithelium (RPE)/Bruch's complex (Bc).

269 lammatory IL-1beta was markedly increased in retinal pigment epithelium (RPE)/choroid and positively

270 ntally regulated manner in chicken embryonic retinal pigment epithelium (RPE)/choroid in the absence

271 CT B-scans showed 2 distinct profiles of the retinal pigment epithelium (RPE): a slight RPE detachmen

272 mophore through a series of reactions in the retinal pigmented epithelium (RPE visual cycle).

273 elated macular degeneration characterized by retinal pigmented epithelium (RPE) death; the RPE also e

274 The retinal pigmented epithelium (RPE) forms the outer blood

275 Accumulation of bis-retinoids in the retinal pigmented epithelium (RPE) is a hallmark of agin

276 One of the major biological functions of the retinal pigmented epithelium (RPE) is the clearance of s

277 ession, we delivered a wild-type Mfrp to the retinal pigmented epithelium (RPE) of Mfrp (rd6) /Mfrp (

278 y both the intraretinal visual cycle and the retinal pigmented epithelium (RPE) visual cycle.

279 neration (AMD) characterized by death of the retinal pigmented epithelium (RPE), causes untreatable b

280 types, photoreceptor cells and the adjacent retinal pigmented epithelium (RPE), reportedly display t

281 alysis revealed predominant up-regulation of retinal pigmented epithelium (RPE)-specific genes associ

282 ns that occur in photoreceptor cells and the retinal pigmented epithelium (RPE).

283 iRNA)-processing enzyme DICER1 in the mature retinal pigmented epithelium (RPE).

284 pecialized phagocytes: Sertoli cells and the retinal pigmented epithelium (RPE).

285 iber layer, photoreceptor outer segments and retinal pigment epithelium show promise for the diagnost

286 n area >/=196350 mum2) and depigmentation of retinal pigment epithelium (slope of -19.17 for the NEI-

287 decreased levels of CFH led to increased sub-retinal pigmented epithelium (sub-RPE) deposit formation

288 PGS2 when cultured with interleukin-33-rich retinal pigment epithelium supernatant.

289 Retinal pigment epithelium tears act differently dependi

290 We excluded 5 eyes from analysis (4 had retinal pigment epithelium tears, and 1 had a laser scar

291 hat included the ectopic island of surviving retinal pigment epithelium that had been exposed to vect

292 se enzymatic effect on photoreceptors or the retinal pigment epithelium that is not limited to areas

293 Loss of retinal pigment epithelium, the presence of a thin choro

294 rystal mutant lacks pigmentation also in the retinal pigment epithelium, therefore enabling optical a

295 from the choroidal blood passes through the retinal pigment epithelium to the retina where photorece

296 r displacement of the temporal peripapillary retinal pigment epithelium (tRPE) from its position in c

297 91/266), and 16.9% (45/266) were type 1 (sub-retinal pigment epithelium), type 2 (subretinal), type 3

298 bilateral soft drusen and depigmentation of retinal pigment epithelium was associated with substanti

299 Labeling of retinal pigment epithelium was observed in some cases of

300 s features, photoreceptor outer segments and retinal pigment epithelium when 23 diabetic eyes with mi

301 calcium-activated chloride channel from the retinal pigment epithelium, where mutations are associat