ライフサイエンスコーパス: inner segment

1 inhibits premature cyclase activation in the inner segment.

2 of early redistribution of cone opsin to the inner segment.

3 hodopsin mislocalization in membranes of the inner segment.

4 Ca2+ conductance (gCa) in the photoreceptor inner segment.

5 ith membranes and instead accumulated in the inner segment.

6 orporation of molecules transported from the inner segment.

7 of post-Golgi rhodopsins retains them in the inner segment.

8 tors consist of an outer segment (OS) and an inner segment.

9 ceptors and the periciliary extension of the inner segment.

10 ty is present almost exclusively in the cone inner segment.

11 mtDNA damage, primarily in the photoreceptor inner segments.

12 nd inner plexiform layers, and photoreceptor inner segments.

13 The IR is predominately expressed in rod inner segments.

14 increase was localized to the photoreceptor inner segments.

15 tic terminals and became undetectable in the inner segments.

16 sorganization of the photoreceptor outer and inner segments.

17 not dock properly at the apical edge of the inner segments.

18 in, but only in moving from the outer to the inner segments.

19 plexiform layer as well as to photoreceptor inner segments.

20 ssed constitutively on RPE and photoreceptor inner segments.

21 y on RPE and in high levels on photoreceptor inner segments.

22 ression in the photoreceptor cell bodies and inner segments.

23 e it appeared to be most concentrated in the inner segments.

24 Cone cells in the periphery had remnants of inner segments.

25 ferentiation and was immediately targeted to inner segments.

26 xtracellular vesicles surrounding the distal inner segments.

27 toreceptors, localizing predominantly in the inner segments.

28 e ERG are truncated with shortened outer and inner segments.

29 are retinal cells, especially photoreceptor inner segments.

30 t closely resembles rdgC is localized to rod inner segments.

31 iched in biochemical extracts of retinal rod inner segments.

32 tae openings align with those of neighboring inner segments.

33 tive stress was noted in their photoreceptor inner segments.

34 9-1 and Gbeta5L are primarily located in rod inner segments.

35 GS9-1 from R9AP and redistributing it to rod inner segments.

36 ary dendrites and HR2 mRNA was found in cone inner segments.

37 uperior central retina, within photoreceptor inner segments, 24 hours after light treatment, but decl

38 Of all adult cone inner segments, 88-90% contained L/M opsin mRNA, whereas

39 ctivity and, thus, is likely to regulate the inner segment actin cytoskeleton.

40 s a role in the assembly or stabilization of inner segment and calycal process actin filament bundles

41 actin filament bundles of the photoreceptor inner segment and calycal processes.

42 toresponse, mislocalization of ATP8A2 to the inner segment and cell body, and increased apoptosis in

43 ppears to affect the shape of the OS, as the inner segment and connecting cilium remain intact.

44 with GTP-locked mutants concentrated in the inner segment and GDP-locked mutants concentrated in the

45 remaining P23H-hRho-GFP mislocalizes to the inner segment and outer nuclear layer, with only approxi

46 In control mice REEP6 was localized to the inner segment and outer plexiform layer of rod photorece

47 horoid, retina pigment epithelium (RPE), and inner segment and outer segment (IS/OS) junction.

48 attachment of the ERM (P = .003), and foveal inner segment and outer segment junction disruption (P =

49 ed only in rod photoreceptors, mainly in the inner segment and perinuclear region.

50 ion of vacuole-like structures at the apical inner segment and reduction in selected rod phototransdu

51 It is localized to the inner segment and synapse in photoreceptor cells, and wh

52 ically, IMPDH1 is found predominately in the inner segment and synaptic terminals of retinal photorec

53 in and the ribbons in hair cells, and in the inner segment and the axon of the photoreceptor, consist

54 sed by protein transport defects between the inner segment and the outer segment of the photoreceptor

55 calization and aggregation of S-opsin in the inner segment and the synaptic region of rods, ER stress

56 identified that rhodopsin accumulates in the inner segments and around the nucleus of photoreceptors.

57 soform of Hmgb1 was present in photoreceptor inner segments and bound to a membrane fraction with cha

58 In rods, arrestin-1 moves from the inner segments and cell bodies in the dark to the outer

59 or cell death, rhodopsin was mislocalized in inner segments and cell bodies of Rp1(-/-) rods.

60 In the photoreceptor inner segments and cells expressing enhanced green fluor

61 ation of apical cell features: photoreceptor inner segments and cilia in renal and auditory systems.

62 affects retinoid metabolism in photoreceptor inner segments and delays the kinetics of dark adaptatio

63 ic terminals and, to a lesser degree, in rod inner segments and inner retinal neurons.

64 genes at the cell membranes of photoreceptor inner segments and Muller cell apical processes in the z

65 s retained cone nuclei, albeit with abnormal inner segments and OS.

66 erly, and some OS markers mislocalize to the inner segments and outer nuclear layer in the Nphp4(nmf1

67 enolase1 co-localized with arrestin1 in the inner segments and outer nuclear layer, but remained in

68 crystallin localization in the photoreceptor inner segments and outer plexiform layer in the WT contr

69 retina, where it was localized mostly in the inner segments and outer plexiform layer of photorecepto

70 Muller and RPE cells that extend between the inner segments and outer segments of photoreceptors, res

71 Arrestin localizes predominantly to the inner segments and perinuclear region of dark-adapted ro

72 r, mutant receptors were mislocalized to the inner segments and perinuclear region.

73 birth; in the adult, PMCA2 was expressed in inner segments and synaptic terminals of rod photorecept

74 imilarly in the outer retina, especially the inner segments and synaptic terminals of rod photorecept

75 ired to maintain baseline [Ca(2+)](i) in rod inner segments and synaptic terminals.

76 mas at birth but only later were targeted to inner segments and synaptic terminals.

77 a(2+)](i) to below prestimulus levels in rod inner segments and synaptic terminals.

78 gal staining was restricted to photoreceptor inner segments and synaptic termini.

79 sst(2A) immunostaining was seen in the inner segments and terminals of rod and cone photorecept

80 ow that RDH12 localizes to the photoreceptor inner segments and that deletion of this gene in mice sl

81 n, cGK I mRNA was localized to photoreceptor inner segments and the ganglion cell and inner nuclear l

82 MrdgB protein is localized to photoreceptor inner segments and the outer and inner plexiform layers.

83 s showed DRAM2 localization to photoreceptor inner segments and to the apical surface of retinal pigm

84 , it was localized to the connecting cilium, inner segment, and synapse.

85 that opsin accumulates initially within the inner segment, and then in the plasma membrane.

86 retinas, ZBED4 was localized to cone nuclei, inner segments, and pedicles, as well as to Muller cell

87 inner/outer plexiform layers, photoreceptor inner segments, and RPE.

88 d mitochondrial Ca2+ stores in photoreceptor inner segments, and suggest a role for CICR in the regul

89 amounts in ganglion cells and photoreceptor inner segments as well.

90 lecular disulfide bonding may be part of RDS inner-segment assembly in cones but not in rods.

91 ha-GTP complex capable of diffusing from the inner segment back to the outer segment after light-indu

92 or weakly positive before ED13, appeared in inner segments between ED13 and ED15, became subsequentl

93 In primates GCAP2-IR was intense in the rod inner segment but faint in the rod outer segment.

94 mb prevents targeting of Cng channels to the inner segment, by promoting their trafficking through th

95 In contrast, RDH12 in inner segments can protect vital cell organelles against

96 ural subdivisions include the outer segment, inner segment, cell body, and synaptic terminal.

97 psin immunolabeling was also observed in the inner segment, cell body, axon, and axon terminal of pho

98 tissue revealed that MAK is expressed in the inner segments, cell bodies, and axons of rod and cone p

99 85R protein accumulated in the photoreceptor inner segments, cellular bodies, or both.

100 y), outer nuclear layer (ONL) (nasally), and inner segment (centrally and temporally) were found in p

101 human retina showed intense labeling of cone inner segments compared to rods.

102 Prior homogenization of the rod outer-inner segment completely prevented the long-lasting inhi

103 us, sensitization of the photovoltage by rod inner segment conductances appears to extend the operati

104 ment could not be explained by modulation of inner segment conductances or the voltage sensitivity of

105 sin-II is a molecular motor localized to the inner segment, connecting cilium and axoneme of mammalia

106 tor cells, actin and TULP1 colocalize at the inner segment, connecting cilium, and outer limiting mem

107 Photoreceptor inner segments contain LGN, which can bind to the alpha

108 gments were short and disorganized and their inner segments contained stacks of rhodopsin-positive me

109 f free [3H]DHA from ROS to the photoreceptor inner segment contributed to an additional overall incre

110 Preserved inner segments could be identified, but outer segments w

111 discs by palmitoylation, whereas ARL3 is an inner segment cytoplasmic protein.

112 tochondria cluster at the apical side of the inner segment, directly below the outer segment.

113 inal during synaptic transmission and at the inner segment during protein translocation to the outer

114 dopsin (RHO), which severely mislocalized to inner segments during the initial stage of degeneration.

115 nce from the fovea to the location where the inner segment ellipsoid (ISe) band became undetectable w

116 PURPOSE; The integrity of the inner segment ellipsoid (ISe) band, previously called th

117 d into 5 distinct categories: (1) continuous inner segment ellipsoid (ISe), (2) ISe disruption, (3) I

118 Inner segment ellipsoid and relative ellipsoid reflectiv

119 la demonstrated complete preservation of the inner segment ellipsoid band in 1 patient, with variable

120 onded closely with the lateral extent of the inner segment ellipsoid band in the OCT image.

121 One patient had mild disruption of the inner segment ellipsoid band on OCT and additional mild

122 ipsoid reflectivity (defined as the ratio of inner segment ellipsoid band reflectivity on overall ret

123 Inner segment ellipsoid band reflectivity, global retina

124 inner segment-outer segment junction or the inner segment ellipsoid band was disrupted within 1 degr

125 t in 6 subjects subtle irregularities at the inner segment ellipsoid band were seen.

126 ct outer retina; stage 2 (2 patients [12%]), inner segment ellipsoid line disruption; stage 3 (5 pati

127 Inner segment ellipsoid line loss generally correlated w

128 y, global retinal reflectivity, and relative inner segment ellipsoid reflectivity (defined as the rat

129 he annual rate of change in the width of the inner segment ellipsoid zone (EZ; ie, inner/outer segmen

130 igment epithelium (RPE) band, grading of the inner-segment ellipsoid (ISe) band integrity, and presen

131 TP1 showed specific labeling of rod and cone inner segments, especially in the mitochondria-rich elli

132 velopment leads to opsin accumulation in the inner segment even when the connecting cilium and outer

133 ers of mitochondria (hepatocytes and the rod inner segment) exhibited a punctate fluorescence.

134 e spine density reduction was significant in inner segments following 7 days of treatment.

135 Movement of the inner segments further from the choroid, which occurs in

136 Conversely, unphosphorylated Pd binds to inner segment G protein(s) in the light.

137 Photoreceptor inner segments have a high O(2) demand (QO(2)), and they

138 Photoreceptor inner segments have the highest concentration of Na,K-AT

139 g outer segment light-dependent channels and inner segment hyperpolarization-activated cyclic nucleot

140 s were immunopositive for TRPC1 whereas cone inner segments immunostained with TRPC6 channel antibodi

141 um regulation in the photoreceptor outer and inner segments implies that transduction and synaptic si

142 ated on large punctate structures within the inner segment in ARL3-Q71L retina.

143 analysis, Pd is found almost entirely in the inner segment in both light and dark, most abundantly ne

144 Mutant PRCD C2Y was found in the inner segment in contrast to normal localization of WT P

145 e arrangement of the mitochondria within the inner segment in detail using three-dimensional (3D) ele

146 rding technique and recorded from single rod inner segments in isolated intact neural mouse retinae,

147 Ultrasturctural analysis revealed intact inner segments in light-treated retinas, whereas in untr

148 tet-ARR1), stored in the outer nuclear layer/inner segments in the dark, modulates photoreceptor syna

149 Electron microscopic observations of rat rod inner segments indicated generally excellent survival of

150 dies revealed a mosaic of cone photoreceptor inner segments indistinguishable from that of neonatal r

151 14 months, including improved rod outer and inner segment integrity, less photoreceptor cell loss, a

152 However, RDH12 function in the photoreceptor inner segments is also key, because loss of function mut

153 Transport of these proteins from the inner segments is regulated by the small GTPases Rab6 an

154 major retinal layers being visible, and both inner segment (IS) and outer segment (OS) length were wi

155 e outer segment (OS) in the light and to the inner segment (IS) in the dark.

156 le fiber outer nuclear layer (HFONL) and the inner segment (IS) layer, but not in the inner nuclear l

157 proteins from their site of synthesis in the inner segment (IS) to the outer segment (OS) is critical

158 ro-tetramers with Rom-1 in the photoreceptor inner segment (IS), while higher-order, disulfide-linked

159 her photoreceptor compartments including the inner segments (IS) and synaptic terminals (ST) is recog

160 al antibody showed staining localized to the inner segments (IS) of photoreceptor cells, as well as t

161 The inner segments (IS) of the photoreceptors in vertebrates

162 ion in length and broadening of rod and cone inner segments (IS) was next observed, followed by the f

163 outer plexiform (OPL) layers, photoreceptor inner segments (IS), and retinal pigment epithelium (RPE

164 GB1-P/rds interaction, were initiated within inner segments (ISs) before trafficking to OSs.

165 he plasma membrane (PM) of rod photoreceptor inner segments (ISs), and causes autosomal dominant RP.

166 or disruption of the photoreceptor outer and inner segment junction was noted.

167 cetacoplan exhibited a thicker photoreceptor inner segment layer along the 5.16 degrees -contour-line

168 sin was sequestered to the photoreceptor rod inner segment layer with a concomitant increase in photo

169 e ONL and that of the rod outer-segment plus inner-segment layer were measured at several points alon

170 In its absence, rod photoreceptor outer and inner segment length was reduced, and cone cell numbers

171 hondria are elongated and extend most of the inner-segment length, where they supply energy for prote

172 ause retention of ABCA4 in the photoreceptor inner segment, likely by impairing correct folding, resu

173 of stable rhodopsin/arrestin complex in the inner segment may be an important mechanism for triggeri

174 ecting cilium and consequent accumulation of inner segment membrane proteins in the outer segment, al

175 ization signal distributed to both outer and inner segment membranes.

176 Morphology of the inner segment mitochondria was examined by electron micr

177 Due to the often close proximity to the inner-segment mitochondria, they may, too, play a role i

178 ged and had reduced alignment to neighboring inner-segment mitochondria.

179 ochondria, they may, too, play a role in the inner-segment mitochondrial arrangement as well as metab

180 Photoreceptor inner segment morphology was markedly affected in RS(-)(

181 EM revealed abnormal inner segment morphology, particularly in rods, and diso

182 Grb14 is localized predominantly to the inner segment, nuclear layer, and synapse in dark-adapte

183 f Phd isoforms with CRX predominantly in the inner segment of cone cells, with additional costaining

184 rences in the localization of RNA within the inner segment of cone photoreceptors, suggesting that mo

185 PDE6 present in the inner segment of Rce1-deficient photoreceptor cells was

186 ffective when applied either to the outer or inner segment of red-sensitive cones.

187 bonate exerted an effect when applied to the inner segment of rods but had little efficacy when appli

188 pted retina but was more concentrated in the inner segments of dark-adapted retina.

189 Within photoreceptors, only the inner segments of frog double cones are strongly labeled

190 l layer, inner and outer nuclear layers, and inner segments of photoreceptor cells in all 17 eyes.

191 the day and night was in the vicinity of the inner segments of photoreceptor cells, supporting the id

192 the outer plexiform layer (OPL), and in the inner segments of photoreceptor cells.

193 cein-conjugated PEDF stained exclusively the inner segments of photoreceptors and cells of the gangli

194 trans-retinaldehyde, which diffuses into the inner segments of photoreceptors from illuminated rhodop

195 and human retinas, NOS-1 is expressed in the inner segments of photoreceptors, cells in the inner nuc

196 ccumulation of intracellular vesicles in the inner segments of photoreceptors, whereas immunohistoche

197 s, C.O. and NOS levels were both high in the inner segments of retinal photoreceptor cells where ener

198 Intensity of the GCAP1-IR was strong in inner segments of rods in all species but weaker in oute

199 eadily discernible changes in [Ca2+]i in the inner segments of rods, but not cones.

200 that GFP was predominantly localized to the inner segments of the major rods; a smaller amount was i

201 immunoreactivity was observed in the OPL and inner segments of the photoreceptor cells.

202 ayers of the retina but in neither outer nor inner segments of the photoreceptor layers in mice beari

203 d expression pattern but is expressed in the inner segments of the photoreceptors whilst Cds2 shows a

204 els to the more hypoxic environment near the inner segments of the photoreceptors.

205 as restricted to the outer nuclear layer and inner segments of the retina.

206 etina, though it is clearly expressed in the inner segments of the rod photoreceptors.

207 of free Ca2+ concentration ([Ca2+]i) in the inner segments of vertebrate photoreceptors.

208 ants, despite the visibility of remnant cone inner segments on the AO images.

209 mbrane (INL-ELM); external limiting membrane-inner segment outer segment (ELM-ISOS); and inner segmen

210 -inner segment outer segment (ELM-ISOS); and inner segment outer segment-retinal pigment epithelium (

211 demonstrate that disruption of photoreceptor inner segment-outer segment (ellipsoid) layer on SD-OCT

212 fluid, size and location of cystoid changes, inner segment-outer segment (IS-OS) continuity, quantity

213 Retinal sensitivity over lesions with intact inner segment-outer segment (IS-OS) junction was 13.35 +

214 yer (ONL), external limiting membrane (ELM), inner segment-outer segment (IS-OS) junction, outer phot

215 rence of several abnormalities, for example, inner segment-outer segment alterations were found in 60

216 E nodularity (8%), photoreceptor loss (43%), inner segment-outer segment junction (IS-OS) irregularit

217 The inner segment-outer segment junction or the inner segmen

218 The intensity of inner segment/outer segment (ellipsoid zone line) reflec

219 rence tomography (SD-OCT), disruption of the inner segment/outer segment (IS/OS) band, and thinning o

220 ellipsoid (ISe) band, previously called the inner segment/outer segment (IS/OS) border, seen on opti

221 (P < .001), regardless of the photoreceptor inner segment/outer segment (IS/OS) condition.

222 red autofluorescence patterns, the status of inner segment/outer segment (IS/OS) interface, and retin

223 ers evaluated the integrity of photoreceptor inner segment/outer segment (IS/OS) junction and externa

224 The SDOCT scans showed disruption of inner segment/outer segment (IS/OS) junction in 54.6% of

225 OCT data showed a loss of the photoreceptor inner segment/outer segment (IS/OS) junction in the cent

226 d on 8 eyes and the horizontal extent of the inner segment/outer segment (IS/OS) junction was measure

227 Disrupted inner segment/outer segment (IS/OS) junction was noted i

228 ild-type mice demonstrated visibility of the inner segment/outer segment (IS/OS) junction, external l

229 macular defects, including disruption of the inner segment/outer segment and outer segment/retinal pi

230 er (n = 4), outer nuclear layer (n = 12), or inner segment/outer segment junction (n = 1).

231 erence tomography showed preservation of the inner segment/outer segment junction at the fovea.

232 Generalized loss of the photoreceptor inner segment/outer segment junction was seen more frequ

233 Focal loss of the inner segment/outer segment junction was seen most commo

234 Evaluation of the photoreceptor inner segment/outer segment junction, using this approac

235 SD OCT results with preserved photoreceptor inner segment/outer segment junction, whereas this junct

236 e associated with concomitant defects of the inner segment/outer segment layer.

237 In all patients, a disrupted inner segment/outer segment line and the external limiti

238 In the midperipheral retina, the rod inner segment/outer segment line was disrupted and blurr

239 s most apparent for the foveal photoreceptor inner segment (p=0.001).

240 We recorded with patch electrodes the inner segment photovoltages and with suction electrodes

241 ted (Cng) channels, which accumulates on the inner segment plasma membrane in addition to its normal

242 PNPLA6 localizes mostly at the inner segment plasma membrane in photoreceptors and muta

243 sruption of the myosin-tail homology domain, inner segment plasma membrane proteins, including syntax

244 ated primarily with the outer leaflet of the inner segment plasma membrane through anionic phospholip

245 he sodium-potassium ATPase (NKAalpha) on the inner segment plasma membrane.

246 ntaining the protocadherin, PCDH21, with the inner segment plasma membrane.

247 iles in the interphotoreceptor space and the inner segment plasma membranes are immunoreactive for rh

248 ic activity (EC 3.6.1.37) in a rat rod outer-inner segment preparation.

249 Photoreceptor inner segments produce the highest of these reflections

250 The rod inner segments projected through the cone mosaic in a pr

251 estricted membrane microdomain at the apical inner segment recess that wraps around the connecting ci

252 xpression occurred almost exclusively in the inner segment region of photoreceptors.

253 sis during development, to be present in the inner segment region of these postmitotic cells in sever

254 trafficking regulators in the mammalian rod inner segment remain undefined.

255 They developed inner segments rich in mitochondria.

256 er (mean 47, range 20-76 ppm), photoreceptor inner segments (RIS) ellipsoid zone, outer limiting memb

257 mistry, ZCRDH was abundantly present in cone inner segments, similar to the reported distribution of

258 t GCIP identified high levels of GCIP in the inner segments, somata and synaptic terminals of frog co

259 dult retinas, anti-TULP1 labels cone and rod inner segments, somata, and synapses; outer segments are

260 g with anti-GCAP2 antibodies was in the cone inner segments, somata, and synaptic terminals and, to a

261 ucin translocates from rod outer segments to inner segments/spherules in bright light, but the functi

262 e adhesion, in maintaining the photoreceptor inner segment stability and architecture.

263 nstitutive GITRL expression on photoreceptor inner segments suggests that photoreceptors participate

264 fter methanol intoxication, with evidence of inner segment swelling and mitochondrial disruption.

265 ium regulation in the outer segment (OS) and inner segment/synaptic terminal (IS/ST) regions of rods

266 kre oko photoreceptor cells, including their inner segments, the nuclear regions, and the synaptic te

267 r photoreceptors are present in the cavefish inner segments, the outer segments of the photoreceptors

268 is localized primarily in the photoreceptor inner segments, the site of mitochondrial oxidative stre

269 lace at or near the plasma membrane from the inner segment through the connecting cilium into the out

270 ransported from the site of synthesis in the inner segment through the connecting cilium, followed by

271 within the rod photoreceptor cells from the inner segments, through the rod nuclei to the rod photor

272 ed GFP immunoreactivity in rod photoreceptor inner segments throughout the retina, indicating the rod

273 tion mechanism of 11-cis-retinal in the cone inner segment to regenerate visual pigment.

274 ts of lipid and protein to be moved from the inner segment to the OS.

275 to regulate the export of proteins from the inner segment to the outer segment sensory axoneme.

276 extending from the outer segment through the inner segment to the synaptic terminals.

277 ng PDE6) from their site of synthesis in the inner segment to their final destination in the outer se

278 achment, severely reduces the ability of the inner segments to obtain O(2), even for detachment heigh

279 ique, nonredundant role in the photoreceptor inner segments to regulate the flow of retinoids in the

280 nts aberrant transport of rhodopsin from the inner segments to the nascent disc membranes of the oute

281 to light, a leak of retinoids from outer to inner segments was detected in rods from both wild-type

282 etina due to shortening of the rod outer and inner segments was observed when compared to control lit

283 hereas in untreated retinas only remnants of inner segments were observed.

284 However, the inner segments were significantly disrupted after incuba

285 Caffeine-evoked Ca2+ responses in cone inner segments were unmasked in the presence of inhibito

286 and outer nuclear layer, but remained in the inner segments when arrestin1 translocated in response t

287 nol is transported from Muller cells to cone inner segments, where it is oxidized to 11-cis-retinal.

288 rder neurons and, to a lesser extent, to the inner segments, where polarized protein translocation oc

289 ghly expressed in rod and cone photoreceptor inner segments, where they shape the light response, mut

290 s mostly restricted to the rod photoreceptor inner segments, whereas GCAP1 immunofluorescence was con

291 e localized exclusively in the photoreceptor inner segments, which are known to be densely populated

292 ntral cones had 2-microm-wide outer (OS) and inner segments, which came straight off the cell body.

293 conditions require a large O(2) flux to the inner segments, which in turn requires high choroidal ox

294 of the plasma membrane of the photoreceptor inner segments, which synthesize and secrete it.

295 stin, and membranes within the photoreceptor inner segment, while the localization of alpha-transduci

296 scopy showed increased autophagosomes in rod inner segments with HDAC inhibitor (HDACi) treatment, po

297 EM showed abnormal cone inner segments with swollen mitochondria.

298 dentified as cones by dual labeling of their inner segments with the lectin peanut agglutinin or by c

299 s the majority of recoverin was found in rod inner segments, with approximately 12% present in the ou

300 e most intense immunolabeling was in the rod inner segments, with weaker labeling of cone myoids, som