ライフサイエンスコーパス: plexiform layer

1 run in a single, narrow stratum of the inner plexiform layer.

2 ter degree in the OFF sublamina of the inner plexiform layer.

3 retina and dendrites growing into the inner plexiform layer.

4 dendrites in the OFF sublamina of the inner plexiform layer.

5 s in the inner plexiform layer and the outer plexiform layer.

6 e functional ON/OFF subdivision of the inner plexiform layer.

7 centralmost (on and off) bands of the inner plexiform layer.

8 ing to new, more distal regions of the inner plexiform layer.

9 milar to those found in the vertebrate inner plexiform layer.

10 mifying in the different layers of the inner plexiform layer.

11 d to both ON and OFF strata within the inner plexiform layer.

12 on their dendrites and throughout the inner plexiform layer.

13 the dendrites in the sublaminae of the inner plexiform layer.

14 s, sparing the outer retina except the outer plexiform layer.

15 , redirecting their dendrites into the inner plexiform layer.

16 r layer and in synaptic boutons in the inner plexiform layer.

17 e consistent with synaptic loss in the inner plexiform layer.

18 glion cells and their processes in the inner plexiform layer.

19 neuronal connexin, is expressed in the outer plexiform layer.

20 atification in the ON sublamina of the inner plexiform layer.

21 containing histamine terminate in the inner plexiform layer.

22 al M1 positive) in diffusely condensed outer plexiform layer.

23 od vessels abnormally localized in the outer plexiform layer.

24 interactions, respectively, within the inner plexiform layer.

25 wo to three specific sublaminae in the inner plexiform layer.

26 macrine cells located laterally in the inner plexiform layer.

27 y complex, and horizontal cells in the outer plexiform layer.

28 ynapse of the retina as well as in the inner plexiform layer.

29 as to their processes and tips in the outer plexiform layer.

30 athway within the Off sublamina of the inner plexiform layer.

31 ptic and postsynaptic processes in the inner plexiform layer.

32 ons pass through the OFF layers of the inner plexiform layer.

33 c to AII and A17 amacrine cells in the inner plexiform layer.

34 tion of dendrites and axons within the inner plexiform layer.

35 iber layer, inner plexiform layer, and outer plexiform layer.

36 r the outer or the inner border of the inner plexiform layer.

37 mify within the outermost layer of the inner plexiform layer.

38 colocalizations of GluR1 and TH in the inner plexiform layer.

39 es as well as glutamate release in the outer plexiform layer.

40 re generated in both the outer and the inner plexiform layers.

41 e inner and outer nuclear layers and in both plexiform layers.

42 protein predominantly in the inner and outer plexiform layers.

43 cavities in the outer and inner nuclear and plexiform layers.

44 port the robust expression of SNAP25 in both plexiform layers.

45 0.25 mum/y) and the ganglion cell (GC)/inner plexiform layer (0.29 mum/y) on optical coherence tomogr

46 ing exclusively in sublamina S5 of the inner plexiform layer, (2) bistratified cells with dendrites i

47 cose axons arborizing in the inner and outer plexiform layers after glutamatergic synapses depolarize

48 Thus, for each level of the inner plexiform layer all three cell types participate in a si

49 uronal cell types are constrained within the plexiform layers, allowing for establishment of retinal

50 ayers, whereas PKG II was found in the outer plexiform layer, amacrine cells, and somata in the gangl

51 ntibodies labeled RBC dendrites in the outer plexiform layer and axon terminals in the IPL, as well a

52 l of their axon terminal system in the inner plexiform layer and in immunoreactivity for recoverin an

53 ificantly fewer ribbon synapses in the outer plexiform layer and increased ectopic synapses in the ou

54 while the abnormal hyperreflectance of outer plexiform layer and inner nuclear layer on spectral-doma

55 estored; however, the thickness of the inner plexiform layer and one measure of axon branching were s

56 parameters, such as the ganglion cell inner plexiform layer and optic nerve head parameters, also ar

57 lls arborized at various levels of the inner plexiform layer and over fields of different diameters,

58 g: rods retracted their axons from the outer plexiform layer and partially degenerated, whereas cones

59 Cone pedicles remained in the outer plexiform layer and preserved synaptic contacts with OFF

60 eir dendrites to the ON stratum of the inner plexiform layer and provided sufficient membrane area (a

61 l nerve fibre layer, ganglion cell and inner plexiform layer and stopped at the level of the inner nu

62 photoreceptors and in the postsynaptic outer plexiform layer and that interacts with cytoskeletal pro

63 ition of an RGC's dendrites within the inner plexiform layer and that of its axon within the retinore

64 stance between the outer border of the outer plexiform layer and the inner border of the ellipsoid zo

65 er and immunoreactive processes in the inner plexiform layer and the outer plexiform layer.

66 es depolarize TH cell dendrites in the inner plexiform layer and these depolarizations propagate to t

67 ce, hWtEPOR mice had thinner inner and outer plexiform layers and a greater number of amacrine cells.

68 r, ganglion cell, inner plexiform, and outer plexiform layers and increased thickness in the inner nu

69 The SNAP25 immunoreactivity in the plexiform layers and outer nuclear layer fell into at le

70 ons of the inner nuclear layer, in the inner plexiform layer, and along the vitreal surface, but it w

71 ndritic stratification in the retina's inner plexiform layer, and details of dendritic branching.

72 propriately in synaptic laminae in the inner plexiform layer, and functional synapses formed in the r

73 present within the nerve fiber layer, inner plexiform layer, and inner and outer nuclear layers and

74 cant decline with age of only the GCL, inner plexiform layer, and inner nuclear layer thickness with

75 ated in the retinal nerve fiber layer, inner plexiform layer, and outer plexiform layer.

76 e acquired from the nerve fiber layer, outer plexiform layer, and retinal pigmented epithelium using

77 ed from the ganglion cell layer to the inner plexiform layer, and some plaques were observed in the o

78 GCs co-stratify their dendrites in the inner plexiform layer, and that Tenm3(+) ACs require Tenm3 to

79 ner nuclear layer (INL), ~0.087 in the outer plexiform layer, and ~0.026 in the outer nuclear layer (

80 ndria of the ganglion cells, outer and inner plexiform layers, and photoreceptor inner segments.

81 Although the inner plexiform layer appears earlier than the outer plexiform

82 ns without photoreceptors, leaving the outer plexiform layer apposed to the RPE.

83 ition, the synaptic connections in the outer plexiform layer are defective in Oc1-null mice, and phot

84 er, the synaptic mechanisms within the inner plexiform layer are not well characterized within specif

85 ression and synaptic structures in the outer plexiform layer are preserved, and visual responses are

86 r and 4mum for macular ganglion cell + inner plexiform layer are robust thresholds for identifying un

87 tes are segregated within the inner or outer plexiform layers are not known.

88 iated with progression of deformation of the plexiform layers, as central retinal thickness (CRT) did

89 strongly associated with ganglion cell/inner plexiform layer atrophy (P = 0.004) and C1QA and CR1 wer

90 ed genetic predictors of ganglion cell/inner plexiform layer atrophy in a discovery cohort of 374 pat

91 cells occupy strata 2, 3, and 4 of the inner plexiform layer, between the two bands formed by choline

92 uroligin 1 protein was detected in the inner plexiform layer, but its highest levels were detected in

93 ver high-acuity spatial signals to the inner plexiform layer, but outside the fovea, this spatial res

94 major targets of histamine are in the outer plexiform layer, but the retinopetal axons containing hi

95 duction-related machinery is present in both plexiform layers by fetal week 13.

96 nerve fiber (RNFL), ganglion cell, and inner plexiform layers, can be correlated with vision loss cau

97 e attributed to the disorganization of inner plexiform layer cells that occurs in the Dscam mutant re

98 to the inner and outer margins of the inner plexiform layer, co-stratifying with the processes of ot

99 Macular ganglion cell-inner plexiform layer complex (GCIPL) and peripapillary retina

100 drant, and a thinner ganglion cell and inner plexiform layer complex (GCL-IPL).

101 ter degree in the OFF sublamina of the inner plexiform layer, corroborating the hypothesis that RGCs

102 the visibility of the SCS: disarrangement of plexiform layers, CRT, and multiple adhesion points betw

103 lls that terminate in stratum 3 of the inner plexiform layer (DB4) express more Ret-PCP2 than those t

104 including both glomerular layer and external plexiform layer (EPL) computations and incorporating bot

105 We found that, whereas external plexiform layer (EPL) interneurons show broadly distribu

106 , including granule cells (GCs) and external plexiform layer (EPL) interneurons.

107 odendritic synaptic circuits in the external plexiform layer (EPL).

108 ateral dendrites in the superficial external plexiform layer (EPL); (2) axodendritic synapses onto GC

109 photoreceptor axons, which changed the outer plexiform layer from a thin sheet of synaptic pedicles i

110 f the perifoveal retinal ganglion cell-inner plexiform layer (GC-IPL) and the peripapillary retinal n

111 e fiber layer (RNFL) and ganglion cell-inner plexiform layer (GC-IPL) of patients with DOA were evalu

112 as to study the macular ganglion cell- inner plexiform layer (GC-IPL) thickness in healthy 6.5 year-

113 thickness, rim area, and ganglion cell-inner plexiform layer (GC-IPL) thickness measurements were eva

114 thickness (CST), macular ganglion cell-inner plexiform layer (GC-IPL) thickness, and peripapillary re

115 Rates of ganglion cell + inner plexiform layer (GCIP) and whole-brain (r = 0.45; p < 0.

116 AAs (p = 0.047), whereas ganglion cell/inner plexiform layer (GCIP) thickness did not differ by race.

117 nd that of the ganglion cell layer and inner plexiform layer (GCIP, -11.3 mum), whereas the thickness

118 The common ganglion cell and inner plexiform layer (GCIPL) and inner nuclear layer (INL) vo

119 NFL) and macular retinal ganglion cell-inner plexiform layer (GCIPL) change over time in healthy and

120 RNFL) thickness, macular ganglion cell-inner plexiform layer (GCIPL) thickness and optic nerve head (

121 er (pRNFL) and macular ganglion cell + inner plexiform layer (GCIPL) thinning in multiple sclerosis (

122 of the macular ganglion cell layer and inner plexiform layer (GCIPL) was -16.42 mum (-19.23 to -13.60

123 nglion cell layer (GCL), ganglion cell/inner plexiform layer (GCIPL), ganglion cell complex (GCC), an

124 nerve fiber layer, ganglion cell plus inner plexiform layer (GCIPL), whole-brain, gray matter and th

125 n cell complex (GCC) and ganglion cell inner plexiform layer (GCIPL), with the accuracy of RNFL param

126 e fiber layer (RNFL) and ganglion cell-inner plexiform layer (GCIPL).

127 cular (including the ganglion cell and inner plexiform layer [GCIPL], inner retina [IR], outer retina

128 of the retinal ganglion cell layer and inner plexiform layer (GCL + IPL).

129 Thicknesses of the ganglion cell layer/inner plexiform layer (GCL+IPL), RNFL, outer plexiform/inner n

130 omplex formed by the ganglion cell and inner plexiform layers (GCL + IPL) provided the highest probab

131 t 50%) of the GlyRalpha4 puncta in the inner plexiform layer, however, was found to lack GlyRbeta and

132 cted to specific sublaminae within the inner plexiform layer in adulthood, but acquire their restrict

133 of significantly thicker GCL, IPL, and outer plexiform layer in the central retinal area (i.e., fovea

134 zed to the outer nuclear layer and the outer plexiform layer in the CNGB3(-/-) retina.

135 ed thickness of the ON sublayer of the inner plexiform layer in the microbat retina, more ON than OFF

136 n the photoreceptor inner segments and outer plexiform layer in the WT controls with EAU; but such st

137 and their terminals in the outer nuclear and plexiform layers in a developmentally regulated manner.

138 While the developmental sequence of plexiform layers in human retina has been characterized,

139 ll structures in the inner nuclear and outer plexiform layers in paraneoplastic vitelliform retinopat

140 s localized primarily in puncta in the inner plexiform layer, in amacrine cells, and in somata in the

141 Functionally, the inner plexiform layer, in which bipolar cells synapse onto ama

142 te proximity to one another within the inner plexiform layer, indicating that they do not engage in m

143 splicing in the retinal ganglia cells, outer plexiform layer, inner nuclear layer, and outer nuclear

144 cystoid spaces (72% vs 40%, P < .038), outer plexiform layer involvement (5% vs 96%, P < .001), ellip

145 derate glaucoma was mGCL combined with inner plexiform layer (IPL) (AUC = 0.915) and cpRNFL (AUC = 0

146 layer (GCL) (nasally and temporally), inner plexiform layer (IPL) (nasally), outer nuclear layer (ON

147 with ONHD had a significantly thinner inner plexiform layer (IPL) (P = 0.02), nerve fiber layer (P =

148 es stratify at different levels in the inner plexiform layer (IPL) and can interact with costratifyin

149 iquely through the scleral half of the inner plexiform layer (IPL) and formed a loose, tangential ple

150 apses in the innermost ON layer of the inner plexiform layer (IPL) and from dopaminergic amacrine cel

151 rve fiber layer (NFL), and also in the inner plexiform layer (IPL) and inner nuclear layer (INL).

152 eals two dendritic plexuses within the inner plexiform layer (IPL) and morphologically heterogeneous

153 o a discrete synaptic layer called the inner plexiform layer (IPL) and only rarely extend processes i

154 The location of the inner plexiform layer (IPL) and outer plexiform layer (OPL) wa

155 from bipolar and amacrine cells in the inner plexiform layer (IPL) and send information to the brain

156 urite targeting defects in the retinal inner plexiform layer (IPL) and tectal neuropil.

157 nal amacrine cells migrate towards the inner plexiform layer (IPL) and then retract their trailing pr

158 subunits are widely distributed in the inner plexiform layer (IPL) and therefore are likely contribut

159 branching in the outermost part of the inner plexiform layer (IPL) and weakly melanopsin-positive M2

160 t dACs send processes into the forming inner plexiform layer (IPL) before migrating through it and in

161 he division between the ON and the OFF inner plexiform layer (IPL) is not structurally absolute.

162 In the inner plexiform layer (IPL) of the mouse retina, ~70 neuronal

163 te arbors and form synapses within the inner plexiform layer (IPL) of the vertebrate retina.

164 xon collaterals or terminals in the internal plexiform layer (IPL) on both sides of each bulb.

165 ls ramifying between 0% and 30% of the inner plexiform layer (IPL) receive mixed inputs from rods and

166 upregulated in regrowing RGC axons and inner plexiform layer (IPL) synapses, respectively.

167 cific arbor specializations within the inner plexiform layer (IPL) that occur consistently at defined

168 dor columns through synapses in the internal plexiform layer (IPL) to produce an intrabulbar map.

169 scleral half or "Off" sublamina of the inner plexiform layer (IPL) undergo the greatest changes, wher

170 e combined nerve fiber layer (NFL) and inner plexiform layer (IPL) were manually segmented and thickn

171 form functional neural circuits in the inner plexiform layer (IPL), a laminar region that is conventi

172 In the distal 80% of the inner plexiform layer (IPL), dense GC dendrites coexisted with

173 SAC, found at the outer border of the inner plexiform layer (IPL), forms a synaptic subband "a" with

174 cally branched into sublamina a of the inner plexiform layer (IPL), i.e., the OFF inner plexiform sub

175 on the dendritic stratification in the inner plexiform layer (IPL), those monostratified in the Off s

176 l axon terminals in sublamina-b of the inner plexiform layer (IPL), we investigated the possibility t

177 regation of ON and OFF pathways in the inner plexiform layer (IPL), where glutamate is released from

178 nals in the innermost sublamina of the inner plexiform layer (IPL), which is typical for mammals.

179 ; (4) restricted lamination within the inner plexiform layer (IPL), which renders J-RGCs responsive t

180 the ganglion cell layer, ~0.122 in the inner plexiform layer (IPL), ~0.025 in the inner nuclear layer

181 the inner or the outer portion of the inner plexiform layer (IPL).

182 ayering, or lamination, of the retinal inner plexiform layer (IPL).

183 and a dense layer in the middle of the inner plexiform layer (IPL).

184 odied as separate strata that span the inner plexiform layer (IPL).

185 ple retinal neuron subtypes within the inner plexiform layer (IPL).

186 ar cells in distinct sublaminae of the inner plexiform layer (IPL).

187 amina a (OFF sublamina) of the retinal inner plexiform layer (IPL).

188 dense layer of neuropil, the so-called inner plexiform layer (IPL).

189 mified in strata 1, 3, 4, and 5 of the inner plexiform layer (IPL).

190 to the outer plexiform layer (OPL) and inner plexiform layer (IPL); the beta(3) subunit was localized

191 irregularity (18%), outer nuclear and outer plexiform layer irregularity (8%), and inner nuclear lay

192 onal synapses and gap junctions in the inner plexiform layer is also observed.

193 that Gbeta5S expression in the retinal outer plexiform layer is eliminated, as is the ERG b-wave.

194 suggests that the organization of the outer plexiform layer is more complex than classically thought

195 We found that: (a) the outer plexiform layer is the most discriminative layer for cla

196 ing from the inner nuclear layer (INL)/outer plexiform layer junction to involve the full-thickness I

197 ation of photoreceptor synapses in the outer plexiform layer, leading to a progressive functional det

198 in the glomerular layer but not the external plexiform layer, leading to an imbalance in OB circuitry

199 Average and quadrant ganglion cell-inner plexiform layer measures demonstrated CVs </=4.5% with e

200 her predominantly macula ganglion cell-inner plexiform layer (mGCIPL), predominantly peripapillary re

201 parameters and the ganglion cell layer-inner plexiform layer (mGCL-IPL) was determined by combining t

202 anglion cell layer (mGCL), and macular inner plexiform layer (mIPL) were significantly thinner in the

203 ar ganglion cell layer (mGCL), macular inner plexiform layer (mIPL), macular inner nuclear layer (mIN

204 ar inner nuclear layer (mINL), macular outer plexiform layer (mOPL), macular outer nuclear layer (mON

205 ng at the ganglion cell layer (n = 1), outer plexiform layer (n = 4), outer nuclear layer (n = 12), o

206 plexiform layer neurites, and varicose outer plexiform layer neurites all bear spines, that some of t

207 TH cell somata, tapering and varicose inner plexiform layer neurites, and varicose outer plexiform l

208 lion cell layer (NFL/GCL), NFL/GCL and inner plexiform layer (NFL/GCL + IPL), and total retina thickn

209 was localized to the inner segment and outer plexiform layer of rod photoreceptors.

210 f synapses and synaptic ribbons in the outer plexiform layer of Sfxn3 (-/-) mice.

211 select neurons concentrated in the internal plexiform layer of the main olfactory bulb.

212 tina and were found to interact in the outer plexiform layer of the retina containing the photorecept

213 he organization of cells making up the outer plexiform layer of the retina in the absence of Dscam.

214 Synapses in the inner plexiform layer of the retina undergo short-term plastic

215 , Gbeta5 and R9AP, were reduced in the outer plexiform layer of the RGS11(-/-) and RGS7(Delta/Delta)/

216 ts highest levels were detected in the outer plexiform layer on the tips of horizontal cell dendrites

217 ment (OS) and outer nuclear layer plus outer plexiform layer (ONL+) thicknesses fell below the 95% co

218 nesses of the outer nuclear layer plus outer plexiform layer (ONL+), outer segment (OS), and retinal

219 S) layer, the outer nuclear layer plus outer plexiform layer (ONL+), the retinal pigment epithelium p

220 er ganglion cell layer (P = 0.003) and outer plexiform layer (OPL) (P < 0.001) compared with controls

221 pointing toward the inner limit of the outer plexiform layer (OPL) adjacent to the margin between the

222 hese areas included: subsidence of the outer plexiform layer (OPL) and inner nuclear layer (INL), and

223 ; the beta(2) subunit localized to the outer plexiform layer (OPL) and inner plexiform layer (IPL); t

224 es of HC axons fail to stratify in the outer plexiform layer (OPL) and invade the outer nuclear layer

225 l and optical property features of the outer plexiform layer (OPL) and the complex formed by the gang

226 n above (type 1) or below (type 2) the outer plexiform layer (OPL) at 6 tertiary referral centers.

227 correlating confirmed expansion of the outer plexiform layer (OPL) by optical coherence tomography (O

228 or terminals are ensheathed within the outer plexiform layer (OPL) by the processes of one type of gl

229 s by puffing kainic acid (KA) into the outer plexiform layer (OPL) caused a positive voltage shift an

230 d as inner nuclear layer thinning with outer plexiform layer (OPL) disruption.

231 tinal layers limited externally by the outer plexiform layer (OPL) in 15 eyes (93.7%).

232 receptors mediating this action in the outer plexiform layer (OPL) is not clear.

233 is localized primarily throughout the outer plexiform layer (OPL) of the distal retina, a synaptic l

234 l confined to the inner portion of the outer plexiform layer (OPL) on PD-OCT.

235 drites (ORDs) either ramify within the outer plexiform layer (OPL) or the inner nuclear layer, and wh

236 he internal limiting membrane (ILM) to outer plexiform layer (OPL) was correlated with better postope

237 of the inner plexiform layer (IPL) and outer plexiform layer (OPL) was identified at each age, and it

238 ribbon synapses established within the outer plexiform layer (OPL), initiating retinal visual process

239 not in the inner nuclear layer (INL), outer plexiform layer (OPL), or outer segment (OS) layer.

240 body, near the distal boundary of the outer plexiform layer (OPL), suggesting that apical synapses a

241 tina expresses several laminins in the outer plexiform layer (OPL), where they may provide an extrace

242 n the organization and assembly of the outer plexiform layer (OPL).

243 (ELM), outer nuclear layer (ONL), and outer plexiform layer (OPL).

244 orm a third independent network in the outer plexiform layer (OPL).

245 thinning over an anteriorly displaced outer plexiform layer (OPL).

246 the inner nuclear layer (INL), and the outer plexiform layer (OPL).

247 thickening of the inner nuclear layer, outer plexiform layer, or full retina.

248 dependent cellular interactions in the outer plexiform layer overcome this variability to ensure the

249 .006) or thinner average ganglion cell-inner plexiform layer (P = .028) along with higher baseline VF

250 Reduction of the ganglion cell and inner plexiform layers predicted greater axonal damage in pati

251 of idiopathic ERM, deformation of the outer plexiform layer progresses and is associated with decrea

252 ent types of amacrine cells across the inner plexiform layer prompts that they should be also involve

253 IMS2 localization in the human retinal outer plexiform layer, Purkinje cells, and pancreatic islets.

254 at the margin of the inner nuclear and inner plexiform layers, rather than the ganglion cell layer.

255 .74, P < 0.0001) and the ganglion cell inner plexiform layer region of interest (R = -0.51, P < 0.000

256 = -0.78, P < 0.0001) and ganglion cell inner plexiform layer region of interest (R = -0.65, P = 0.000

257 ral macular retinal ganglion cell plus inner plexiform layer (RGC+IPL) loss identified by spectral-do

258 the combined retinal ganglion cell and inner plexiform layers (RGCL+), and the inner nuclear layer (I

259 nglion cell layer (I3 and N6 sectors), inner plexiform layer (S6 and N6 sectors), inner nuclear layer

260 nuclear layer (T6 and N6 sectors), and outer plexiform layer (S6 sector), as well as the overall reti

261 ed by OB neurons in the superficial external plexiform layer (sEPL) and glomerular layer (GL).

262 ses extending into the ON-layer of the inner plexiform layer, similar to A8 amacrine cells described

263 rom the retinal ganglion cell layer to outer plexiform layer (standardized beta = 0.657 to 0.777, all

264 specific types of RGCs and of specific inner plexiform layer sublaminae, opening new avenues for iden

265 naptic layers beginning in stereotyped inner plexiform layer sublaminae.

266 The inner plexiform layer surround inhibition comprised GABAergic

267 exiform layer appears earlier than the outer plexiform layer, synaptic proteins, and ribbons are firs

268 us inner plexiform layer, the INL plus outer plexiform layer (the combined thickness of these layers

269 re layer, the ganglion cell layer plus inner plexiform layer, the INL plus outer plexiform layer (the

270 nglion cell layer (GCL) as well as the inner plexiform layer, the inner nuclear layer (INL), and the

271 mple, changes in the ganglion cell and inner plexiform layers, the sites of the retinal ganglion cell

272 Minimum rim width (MRW), ganglion cell-inner plexiform layer thickness (GC-IPLT), and circumpapillary

273 (ETDRS </=35) had normal ganglion cell-inner plexiform layer thickness and normal mfERG findings.

274 between CS at 6 cpd and ganglion cell/inner plexiform layer thickness at inferotemporal and inferona

275 mRNFL) and macular ganglion cell layer-inner plexiform layer thickness were 3.5, 4.5, 3.0, 3.0, 2.5,

276 al retinal thickness and ganglion cell-inner plexiform layer thickness were measured using custom-des

277 er thickness and ganglion cell layer - inner plexiform layer thickness).

278 reproducible measures of ganglion cell-inner plexiform layer thickness.

279 cell complex, inner nuclear layer, and outer plexiform layer thickness.

280 polar cell markers and preservation of outer plexiform layer thickness.

281 The ganglion cell layer and inner plexiform layer thicknesses could predict axonal damage

282 well as composite ganglion cell layer+inner plexiform layer thicknesses in the eyes of patients with

283 is and increased nerve fibre layer and inner plexiform layer thicknesses.

284 be obtained by measuring the areas of outer plexiform layer thinning (adjusted R(2) = 0.93), externa

285 milar set of analyses of ganglion cell/inner plexiform layer thinning in a replication cohort (n = 37

286 threshold of 5mum and ganglion cell + inner plexiform layer threshold of 4mum for identifying unilat

287 GCL, p = 0.003), ganglion cell layer - inner plexiform layer volume (GCL-IPL, p = 0.005) and inner re

288 Inner plexiform layer volume of both eyes (IPL, right eye: p =

289 lls and the ON-OFF organization in the inner plexiform layer was largely preserved.

290 Imaging throughout the inner plexiform layer, we found transient, rectified release a

291 and stratification of terminals in the outer plexiform layer were comparable among coneless, conefull

292 l complement, and the extension of the outer plexiform layer were diminished.

293 The synapses in the outer plexiform layer were extensively degenerated and replace

294 copically, the inner nuclear layer and outer plexiform layer were the most affected retinal structure

295 f the combined outer nuclear layer and outer plexiform layer when we compared MSNON or MSON eyes with

296 his functional diversity arises in the inner plexiform layer, where inhibitory amacrine cells modulat

297 GL-dSACs are located in the internal plexiform layer, where they integrate centrifugal cholin

298 d in bipolar cells, ganglion cells, and both plexiform layers, whereas PKG II was found in the outer

299 especially high concentrations in the outer plexiform layer, while lutein is much more diffuse at re

300 dritic reduction to sublamina b of the inner plexiform layer without retinal ganglion cell loss, show