ライフサイエンスコーパス: photoreceptor outer segment

1 icrovilli, which are interdigitated with the photoreceptor outer segment.

2 gue, Rom-1, to maintain the integrity of the photoreceptor outer segment.

3 in the light-sensitive disc membranes of the photoreceptor outer segment.

4 rans-retinal to all-trans-retinol within the photoreceptor outer segment.

5 ation and maintenance of the light-sensitive photoreceptor outer segment.

6 A prime example is the turnover of the rod photoreceptor outer segment.

7 idate genes involved in the formation of the photoreceptor outer segment.

8 re the RetGC1:GCAP1 complex is formed in the photoreceptor outer segment.

9 pecifically detected at the proximal part of photoreceptor outer segment.

10 unknown function surrounding the base of the photoreceptor outer segment.

11 epithelium and inner retina but an abnormal photoreceptor outer segment.

12 pace K(+) homeostasis in the vicinity of the photoreceptor outer segment.

13 ible for impeding their transport to the rod photoreceptor outer segment.

14 the choroid, retinal pigment epithelium, and photoreceptor outer segments.

15 omplex was observed on endothelial cells and photoreceptor outer segments.

16 showed abnormal disc stacking and shortened photoreceptor outer segments.

17 embly and morphogenesis of the rim region of photoreceptor outer segments.

18 2cr4 verified its expression in the discs of photoreceptor outer segments.

19 nsory cilia formation and the development of photoreceptor outer segments.

20 nd by imaging the fluorescence of retinol in photoreceptor outer segments.

21 l that exceeds the reductive capacity of the photoreceptor outer segments.

22 ase 9 (HDAC9) proteins were detected in cone photoreceptor outer segments.

23 idinium bisretinoid (A2PE) that forms within photoreceptor outer segments.

24 ze the mobility of all-trans retinol in frog photoreceptor outer segments.

25 as revealed progressive vacuolization of the photoreceptor outer segments.

26 CAR was expressed in retina except in photoreceptor outer segments.

27 d the structural and functional integrity of photoreceptor outer segments.

28 but not maintained, producing the absence of photoreceptor outer segments.

29 and GCAP1 immunostaining was absent from the photoreceptor outer segments.

30 pherin/rds protein to the disc rim region of photoreceptor outer segments.

31 ly normal CRX activity, led to shortening of photoreceptor outer segments.

32 ch localized correctly to the axoneme of the photoreceptor outer segments.

33 small extracellular compartment surrounding photoreceptor outer segments.

34 disruption of the normal organization of the photoreceptor outer segments.

35 on in the delivery of 11-cis-retinoid to the photoreceptor outer segments.

36 nt of reactive Muller glia into the layer of photoreceptor outer segments.

37 or other genes that affect the integrity of photoreceptor outer segments.

38 ed to be derived primarily from phagocytosed photoreceptor outer segments.

39 neration slow (rds) mutation completely lack photoreceptor outer segments.

40 um, thus facilitating rhodopsin transport to photoreceptor outer segments.

41 ansplants did not develop parallel layers of photoreceptor outer segments.

42 minently to the microvilli that surround the photoreceptor outer segments.

43 are expressed in the retina and enriched in photoreceptor outer segments.

44 se (PDE) mediates signal transduction in the photoreceptor outer segments.

45 Anti-Yb1 also reacted with photoreceptor outer segments.

46 C-1) is a membrane guanylyl cyclase found in photoreceptor outer segments.

47 on fragments to remodel synapses and recycle photoreceptor outer segments.

48 marked functional defects in phagocytosis of photoreceptor outer segments.

49 ons in the gene for the ABCA4 transporter in photoreceptor outer segments.

50 photoreceptor function and abnormally shaped photoreceptor outer segments.

51 matrix at the interface between the RPE and photoreceptor outer segments.

52 cells primarily through phagocytosis of the photoreceptor outer segments.

53 e ABCA4 gene encodes a protein localizing to photoreceptor outer segments.

54 g of PDE6 and GRK1 to their destination, the photoreceptor outer segments.

55 eflectances appeared dim, suggesting loss of photoreceptor outer segments.

56 es and endfeet, photoreceptor terminals, and photoreceptor outer segments.

57 rate that IFT proteins extracted from bovine photoreceptor outer segments, a modified sensory cilium,

58 resulted in atypical accumulation of Rpgr in photoreceptor outer segments, abnormal photoreceptor mor

59 Despite previous reports of diffuse photoreceptor outer segment abnormalities in BVMD, our d

60 creased at night by at least two mechanisms: photoreceptor outer segment activity decreases and synap

61 he optical path length have been observed in photoreceptor outer segments after a flash stimulus via

62 r studies suggest that Grb14 translocates to photoreceptor outer segments after photobleaching of rho

63 f adhesion between RPE apical microvilli and photoreceptor outer segments also declined during peak a

64 nal membrane guanylyl cyclase (RetGC) in the photoreceptor outer segment and suppresses RetGC activat

65 n the cause of acute vision loss to the cone photoreceptor outer segment and will refocus the search

66 luded lamination defects, failure to develop photoreceptor outer segments and a small eye phenotype,

67 Rp1 is required for normal morphogenesis of photoreceptor outer segments and also may play a role in

68 lls are responsible for daily degradation of photoreceptor outer segments and are thus particularly s

69 ce of vacuolar structures that distorted rod photoreceptor outer segments and became more prominent w

70 e and monitor the free Mg2+ concentration in photoreceptor outer segments and examine whether the fre

71 nd their discrete localization in developing photoreceptor outer segments and ganglion cells suggests

72 of mice is associated with nondevelopment of photoreceptor outer segments and gradual death of photor

73 cle in homozygous rds/rds retinas which lack photoreceptor outer segments and heterozygous rds/+ reti

74 alled the retinoid cycle, takes place in the photoreceptor outer segments and in the retinal pigmente

75 us studies have shown that RDH8 localizes to photoreceptor outer segments and is a strong candidate f

76 have highly disorganized, short, fragmented photoreceptor outer segments and lack both rod and cone

77 Crx-/- mice do not elaborate photoreceptor outer segments and lacked rod and cone act

78 osition of debris composed of unphagocytosed photoreceptor outer segments and lipofuscin granules in

79 in RPE further prompted the loss of adjacent photoreceptor outer segments and photoreceptor death, wh

80 receptors-result in blindness from shortened photoreceptor outer segments and progressive photorecept

81 Shortening of photoreceptor outer segments and reduction of the outer

82 thogenic PRPH2 variants, primarily affecting photoreceptor outer segments and retinal pigment epithel

83 parameters of the retinal nerve fiber layer, photoreceptor outer segments and retinal pigment epithel

84 or the retinal nerve fiber layer's features, photoreceptor outer segments and retinal pigment epithel

85 It participates in cellular uptake of photoreceptor outer segments and scavenging of apoptotic

86 ter scale due to the unique structure of the photoreceptor outer segments and sequential stimulation.

87 t-negative form of CRX failed to form proper photoreceptor outer segments and terminals.

88 Only minimal staining was detected in the photoreceptor outer segments and the optic nerve pia and

89 alled the retinoid cycle, takes place in the photoreceptor outer segments and the retinal pigment epi

90 es were observed in the outer nuclear layer, photoreceptor outer segment, and optic nerve.

91 nges; RPE were vacuolated and separated from photoreceptor outer segments, and choriocapillaris fenes

92 cerebrospinal fluid transport, generation of photoreceptor outer segments, and hedgehog signaling.

93 ibroblasts, in all retinal layers except the photoreceptor outer segments, and in the fascicles and a

94 nt disc flattening only minimally alters the photoreceptor outer segment architecture beyond the site

95 Photoreceptor outer segments are continually renewed fro

96 Degenerating rod photoreceptor outer segments are stabilized and develop

97 The proximal portions of mammalian photoreceptor outer segments are synthesized daily by ce

98 ed changes in the optical path length of the photoreceptor outer segment as a response to an optical

99 ning the function and/or organization of the photoreceptor outer segment as reflected by the species-

100 ding cassette (ABC) family that functions in photoreceptor outer segments as a flipase of all-trans r

101 function leads to shortening and loss of the photoreceptor outer segments as observed for various inh

102 as able to reinstate phagocytosis of labeled photoreceptor outer segments at a reduced, but significa

103 hibited normal lamination, but lacked intact photoreceptor outer segments at all ages examined.

104 Excitation signals spread along photoreceptor outer segments away from the site of photo

105 aminins at photoreceptor synapses and around photoreceptor outer segments; both molecules are express

106 Sensitivity was specified at the photoreceptor outer segments by individually correcting

107 ldehyde all-trans retinal is released in rod photoreceptor outer segments by photoactivated rhodopsin

108 a, circadian phagocytosis and degradation of photoreceptor outer segments by the postmitotic retinal

109 iv) the TLR4 participates in phagocytosis of photoreceptor outer segments by the RPE.

110 The concentration of all-trans retinol in photoreceptor outer segments can be monitored from its f

111 highly enriched in retina, and localizes to photoreceptor outer segments, ciliary complex, and horiz

112 lysosomal pH with these treatments enhanced photoreceptor outer segment clearance, demonstrating fun

113 nsducin, into and out of the light-sensitive photoreceptor outer segment compartment.

114 Photoreceptor outer segment degeneration was evident, wi

115 Consequently, STGD1 RPE cells have reduced photoreceptor outer segment degradation and abnormal acc

116 Loss in the photoreceptor outer segment detected by SD-OCT co-locali

117 Moreover, although mutant mikre oko photoreceptor outer segments develop only infrequently a

118 F220C mice exhibited minor disruptions of photoreceptor outer segment dimensions without any mislo

119 is a membrane glycoprotein essential for the photoreceptor outer segment disc morphogenesis and maint

120 Imaging of rod photoreceptor outer-segment disc membranes by atomic for

121 lexiform layer simultaneously with the first photoreceptor outer segment discs at 60 hpf; functional

122 uter segments, and phagocytosis of discarded photoreceptor outer segment discs by RPE.

123 rin/rds), which is inserted into the rims of photoreceptor outer segment discs in a complex with rom-

124 lycoprotein is required for the formation of photoreceptor outer segment discs.

125 ase A(2) plays a role in the phagocytosis of photoreceptor outer-segment discs by the retinal pigment

126 rom-1 form a protein complex in the rims of photoreceptor outer segment disk membranes.

127 se results indicate that a rhythm of retinal photoreceptor outer segment disk shedding exists in the

128 Here, we report that the phagocytosis of photoreceptor outer segment disks by the retinal pigment

129 g photoactivated rhodopsin, which moves into photoreceptor outer segments during illumination.

130 ficient mice revealed abnormal morphology of photoreceptor outer segments during the time at which th

131 nner retina and RPE during the time at which photoreceptor outer segments elongate.

132 lar pseudodrusen were deposits juxtaposed to photoreceptor outer segments extending through the outer

133 etinal space developed parallel layers, with photoreceptor outer segments facing the host pigment epi

134 ciliary ectosomes in building the elaborate photoreceptor outer segment filled with hundreds of tigh

135 A2-PE, the A2E precursor, are formed within photoreceptor outer segments following light-induced rel

136 ithelium (RPE), a cell layer adjacent to the photoreceptor outer segments, form the well-established

137 raflagellar transport (IFT) is essential for photoreceptor outer segment formation and maintenance, a

138 lacking ift80 function exhibited defects in photoreceptor outer segment formation and photoreceptor

139 tablish that nephrocystin-5 is essential for photoreceptor outer segment formation but is dispensable

140 ed IQCB1/NPHP5 protein is required for mouse photoreceptor outer segment formation.

141 5 integrin and CD36 receptors to phagocytose photoreceptor outer segment fragments (OS).

142 iurnal bursts of RPE phagocytosis that clear photoreceptor outer segment fragments (POS) shed in a ci

143 ta5 integrin-dependent phagocytosis of spent photoreceptor outer segment fragments by the retinal pig

144 he retinal pigment epithelium (RPE) of spent photoreceptor outer segment fragments is critical for vi

145 oreceptors via diurnal phagocytosis of spent photoreceptor outer segment fragments.

146 apical projections to shield light-sensitive photoreceptor outer segments from photobleaching when fi

147 oplasia of the optic nerve and inhibition of photoreceptor outer segment growth.

148 When photoreceptor outer segment homogenates are preincubated

149 reviously reported and that preincubation of photoreceptor outer segment homogenates with ATP or its

150 is tightly associated with the membranes of photoreceptor outer segments; however, the nature of thi

151 on belt around the basolateral region of the photoreceptor outer segment in humans, and that defects

152 fetal retina can develop parallel layers and photoreceptor outer segments in contact with host pigmen

153 scopic examination confirmed the presence of photoreceptor outer segments in the areas affected by tr

154 al results showed Tgamma c localized to cone photoreceptor outer segments in the normal retina, where

155 required for the elaboration of rod and cone photoreceptor outer segments in the vertebrate retina; i

156 kewise, the autofluorescence of phagocytosed photoreceptor outer segments increased by lysosomal alka

157 Daily phagocytosis of spent photoreceptor outer segments is a critical maintenance f

158 Phagocytosis of daily shed photoreceptor outer segments is an important function of

159 Every day, 10% of rod photoreceptor outer segments is phagocytosed by the neig

160 The reduction of all-trans-retinal in photoreceptor outer segments is the first step in the re

161 pe 1 (ROS-GC1), originally identified in the photoreceptor outer segments, is a member of the subfami

162 binding protein which is highly expressed in photoreceptor outer segments, is also located in 6p21.1.

163 ApoH has been localized to the photoreceptor outer segment layer by immunocytochemistry

164 D OCT revealed an inflammatory lesion in the photoreceptor outer segment layer displacing ELM.

165 a dome-shaped hyper-reflective lesion at the photoreceptor outer segment layer disrupting the ellipso

166 inal eQTL signal, pinpointing the parafoveal photoreceptor outer segment layer.

167 pigment epithelium (RPE) to phagocytize shed photoreceptor outer segments leads to a progressive loss

168 ONL thickness as well as photoreceptor outer segment length are relevant function

169 mong the 32 eyes with subretinal detachment, photoreceptor outer segment length was significantly cor

170 mean EZ-RPE thickness (i.e., a surrogate for photoreceptor outer segment length) and central RFI were

171 opment with lack of a foveal pit and no cone photoreceptor outer segment lengthening.

172 in absence of subretinal drusenoid deposits, photoreceptor outer segment loss, RPE drusen complex vol

173 the RPE resulted in an aberrant assembly of photoreceptor outer segments, loss of fine subcellular u

174 In the mutant RPE, photoreceptor outer segment material was not effectively

175 vestigators and is recognized as an index of photoreceptor outer segment maturity, yet its antigen re

176 )-2 is a Ca2+-binding protein that regulates photoreceptor outer segment membrane guanylate cyclase (

177 ultifunctional molecule that participates in photoreceptor outer segment membrane recognition, oxidan

178 demonstrated that the formation of A2-PE in photoreceptor outer segment membrane was augmented by ex

179 -retinal and phosphatidylethanolamine in the photoreceptor outer segment membrane; (ii) further react

180 found that compartmentalization of GCAP-2 in photoreceptor outer segment membranes is Ca2+- and ionic

181 pigment epithelium (RPE) to phagocytize shed photoreceptor outer segment membranes.

182 (Pgamma kinase) in a GTP-dependent manner in photoreceptor outer segment membranes.

183 s with other phototransduction components to photoreceptor outer segment membranes.

184 n the retina, Rbpr2 loss resulted in shorter photoreceptor outer segments, mislocalization and decrea

185 naling pathways that guide the modulation of photoreceptor outer segment morphogenesis by RPE during

186 nd to light and displayed severely disrupted photoreceptor outer segment morphology and ciliary defec

187 Photoreceptor outer segment morphology was abnormal in t

188 We also observed disorganized photoreceptor outer-segment morphology and defective tra

189 Disease manifests as a loss of rod photoreceptor outer segments, not singly but in microsco

190 In vertebrate photoreceptor outer segments, numerous reactions utilize

191 er than controls in the outer retina (ONL to photoreceptor outer segments). OCT-based retinal sublaye

192 Capn1 expression increased fivefold in photoreceptor outer segments of diabetic mice.

193 detected in vivo in ganglion cells, RPE, and photoreceptor outer segments of rat retina.

194 Strong PDEbeta expression was observed in photoreceptor outer segments only in treated eyes.

195 rds is required for biogenesis of vertebrate photoreceptor outer segment organelles.

196 rotein family required for normal vertebrate photoreceptor outer segment (OS) architecture.

197 ation (PRCD) is a small protein localized to photoreceptor outer segment (OS) disc membranes.

198 rogressive rod-cone degeneration (PRCD) is a photoreceptor outer segment (OS) disc-specific protein w

199 The photoreceptor outer segment (OS) is a sensory compartmen

200 The photoreceptor outer segment (OS) is a unique modificatio

201 The photoreceptor outer segment (OS) is comprised of two com

202 Approximately 10% of the photoreceptor outer segment (OS) is turned over each day

203 marginal zone (CMZ) cell death and decreased photoreceptor outer segment (OS) length, as well as gros

204 irst, the disease-related deformation of the photoreceptor outer segment (OS) may reduce its ability

205 cific tetraspanin glycoprotein essential for photoreceptor outer segment (OS) morphogenesis.

206 Rod and cone photoreceptor outer segment (OS) structural integrity is

207 spanin protein that plays a pivotal role for photoreceptor outer segment (OS) structure and is involv

208 highly-regulated, biological process wherein photoreceptor outer segment (OS) tips are cyclically pha

209 Mertk is required for the daily ingestion of photoreceptor outer segment (OS) tips.

210 Photoreceptor outer segments (OS) fail to develop proper

211 ARL13b is located exclusively in photoreceptor outer segments (OS) presumably anchored to

212 ions in the gene for ABCA4, a transporter in photoreceptor outer segments (OS) that clears retinaldeh

213 ipitate-like alterations at the level of the photoreceptor outer segments (OS) to choroidal neovascul

214 Here, we show that, in preparations of photoreceptor outer segments (OS), RGS9-1 is readily pho

215 sters are generated by and accumulate in the photoreceptor outer segments (OS), which is the retinal

216 anous whorls that disrupted the integrity of photoreceptor outer segments (OS).

217 essential for the formation of rod and cone photoreceptor outer segments (OS).

218 ipid and protein in the form of phagocytized photoreceptor outer segments (OS).

219 - animals showed progressive degeneration of photoreceptor outer segments (OSs) and increased apoptos

220 Photoreceptor outer segments (OSs) are essential for our

221 the retinal pigment epithelium (RPE) of shed photoreceptor outer segments (OSs), a tissue with one of

222 for the formation of the disc/lamella rim in photoreceptor outer segments (OSs), but plays a differen

223 2 (PRPH2) is essential for the formation of photoreceptor outer segments (OSs), where it functions i

224 loys alphavbeta5 integrin to recognize spent photoreceptor outer segment particles (OS).

225 Diurnal phagocytosis of shed photoreceptor outer-segment particles by retinal pigment

226 In photoreceptor outer segments, particulate guanylyl cycla

227 Mutant RPE exhibited normal photoreceptor outer segment phagocytosis but displayed e

228 absence of Rab28 results in diminished dawn, photoreceptor, outer segment phagocytosis (OSP).

229 rhodopsin to a change in current at the rod photoreceptor outer segment plasma membrane.

230 r early disease features, such as a delay in photoreceptor outer segment (POS) clearance and accumula

231 of phagosomes, derived from the ingestion of photoreceptor outer segment (POS) disk membranes, is a m

232 es; and horizontal extent of the ONL and the photoreceptor outer segment (POS) interdigitation zone (

233 We show here that photoreceptor outer segment (POS) phagocytosis markedly

234 pendently inhibited RPE cell phagocytosis of photoreceptor outer segments (POS) and activated AMP-act

235 of apoptotic cells by macrophages and spent photoreceptor outer segments (POS) by retinal pigment ep

236 Phagocytosis and degradation of photoreceptor outer segments (POS) by retinal pigment ep

237 retina, life-long renewal of light-sensitive photoreceptor outer segments (POS) involves circadian sh

238 fficiency of phagocytosis and degradation of photoreceptor outer segments (POS) necessary for photore

239 at underpin the daily phagocytic turnover of photoreceptor outer segments (POS) required for maintena

240 ed epithelium (RPE) is the clearance of shed photoreceptor outer segments (POS) through a multistep p

241 A main function of RPE is to phagocytose photoreceptor outer segments (POS) which are rich in the

242 ly phagocytosis and lysosomal degradation of photoreceptor outer segments (POS) within the retinal pi

243 its effects measured on the uptake of bovine photoreceptor outer segments (POS), proteolysis of POS r

244 in this medium could also phagocytose human photoreceptor outer segments (POS).

245 s with GC1 and promotes its targeting to the photoreceptor outer segments (POS).

246 red function is that the iPS-RPE phagocytose photoreceptor outer segments (POS).

247 ere they participated in the phagocytosis of photoreceptor outer segments (POSs) and contributed to a

248 ) cells are disorganized and contact between photoreceptor outer segments (POSs) and the RPE apical s

249 Phagocytosis of shed photoreceptor outer segments (POSs) by retinal pigment e

250 and autofluorescent waste products from shed photoreceptor outer segments (POSs).

251 In the absence of phagocytic challenge with photoreceptor outer segments, postconfluent RPE cultures

252 s (53.3%), irregular hyporeflectivity in the photoreceptor outer segments (PROS) was observed in 17 e

253 he previously characterized ROS-GC1 from the photoreceptor outer segments (PROS), and its new modulat

254 synaptic proteins are correctly trafficked, photoreceptor outer segment proteins fail to be transpor

255 dherin, a known interactor of PROM1, and rod photoreceptor outer segment proteins, including rhodopsi

256 motors has been implicated in trafficking of photoreceptor outer segment proteins.

257 he light-activated currents generated at the photoreceptor outer segment provide an easily observed r

258 feration and migration, RPE atrophy, loss of photoreceptor outer segments, reactive gliosis, retinal

259 ific human retinal pigment epithelial (HRPE) photoreceptor outer segment recognition and oxidant prod

260 equired for morphogenesis and maintenance of photoreceptor outer segments, regions that collect light

261 Mammalian photoreceptor outer segment renewal is a highly coordina

262 Daily renewal of 10% of photoreceptor outer segments requires stringent control

263 fish consisting of disorganized rod and cone photoreceptor outer segments resulting in abnormal visua

264 Light detection by vertebrate rod photoreceptor outer segments results in the destruction

265 nterestingly, although it is associated with photoreceptor outer segments, retbindin's expression is

266 er nuclear layer (ONL) and the length of rod photoreceptor outer segment (ROS) were made.

267 High resolution maps of the interface photoreceptor outer segments (ROS) and the RPE apical si

268 RPE) and plays a role in the phagocytosis of photoreceptor outer segments (ROS), a function critical

269 ated in in vitro models of lipid rafts, from photoreceptor outer segments (ROS), and the localization

270 acid (DHA, 22:6n-3) in their plasma and rod photoreceptor outer segments (ROS).

271 adhesion), and 3) Adhesion of the RPE to the photoreceptor outer segments (RPE-POS adhesion).

272 ess to the confined space within the retinal photoreceptor outer segment signaling compartment and di

273 xhibited small eyes, kidney cysts, and short photoreceptor outer segments, some of which were disorga

274 this degeneration on the localization of two photoreceptor outer segment-specific integral membrane p

275 Development of photoreceptor outer segments stopped, and rod cells were

276 5 photoreceptor-specific knock-out mice, the photoreceptor outer segment structure was severely impai

277 mt-deficient mice trafficked normally to the photoreceptor outer segment, suggesting that the failure

278 tinal pigment epithelium (RPE) with adjacent photoreceptor outer segments that are essential for visi

279 hich are crucial for forming and maintaining photoreceptor outer segments that are PUFA-enriched cili

280 fluorescent spots appeared to originate from photoreceptor outer segments that were arranged within r

281 f key signaling proteins into and out of the photoreceptor outer segment, the cellular compartment wh

282 matographies of a cytosolic fraction of frog photoreceptor outer segments, the Pgamma kinase activity

283 stinct scattering bands corresponding to the photoreceptor outer segment tips, RPE, and Bruch's membr

284 Photoreceptor outer-segment tips are imaged on a charge-

285 the second procedure showed that exposure of photoreceptor outer segments to light resulted in the in

286 d that constitutes .15% of all lipids in the photoreceptor outer segment, to produce beta-HB.

287 The structure of photoreceptor outer segment was compared using electron

288 olved in binding and internalization of shed photoreceptor outer segments was subjected to changes in

289 rans-retinal to all-trans-retinol within the photoreceptor outer segment, was the first visual cycle

290 Notably, photoreceptor outer segments were drastically smaller, o

291 e positive for S-antigen, but well-developed photoreceptor outer segments were not present.

292 Although photoreceptor outer segments were shortened by 36%, ligh

293 histochemistry localizes the PHR1 protein to photoreceptor outer segments where chemical extraction s

294 dX) is a polytopic membrane protein found in photoreceptor outer segments where it is the principal e

295 otoreceptors, rather than at the base of the photoreceptor outer segments, where PROM1 is normally lo

296 and reduction to all-trans-retinol occur in photoreceptor outer segments whereas enzymatic esterific

297 affect the structure of the light-sensitive photoreceptor outer segment, which is composed of a stac

298 lial (RPE) cells phagocytize and digest shed photoreceptor outer segment, which provides a rich sourc

299 Vision begins in photoreceptor outer segments with light captured by opsi

300 ght exposure promotes "oxidative tagging" of photoreceptor outer segments with structurally defined c