ライフサイエンスコーパス: inner plexiform layer

1 lls ramifying in the different layers of the inner plexiform layer.

2 ributed to both ON and OFF strata within the inner plexiform layer.

3 ressed on their dendrites and throughout the inner plexiform layer.

4 ns of the dendrites in the sublaminae of the inner plexiform layer.

5 birth, redirecting their dendrites into the inner plexiform layer.

6 nuclear layer and in synaptic boutons in the inner plexiform layer.

7 nt mice consistent with synaptic loss in the inner plexiform layer.

8 nd ganglion cells and their processes in the inner plexiform layer.

9 ic stratification in the ON sublamina of the inner plexiform layer.

10 axons containing histamine terminate in the inner plexiform layer.

11 tical interactions, respectively, within the inner plexiform layer.

12 s to two to three specific sublaminae in the inner plexiform layer.

13 ther amacrine cells located laterally in the inner plexiform layer.

14 irst synapse of the retina as well as in the inner plexiform layer.

15 e On pathway within the Off sublamina of the inner plexiform layer.

16 resynaptic and postsynaptic processes in the inner plexiform layer.

17 eir axons pass through the OFF layers of the inner plexiform layer.

18 stratified mainly in sublamina a or b of the inner plexiform layer.

19 target cells at different sublaminae of the inner plexiform layer.

20 rites and the processes of DA neurons in the inner plexiform layer.

21 C), with brief glutamate applications in the inner plexiform layer.

22 ding a dendritic arbor positioned within the inner plexiform layer.

23 portion of ganglion cells are diffuse in the inner plexiform layer.

24 ynaptic to AII and A17 amacrine cells in the inner plexiform layer.

25 form layer, the inner nuclear layer, and the inner plexiform layer.

26 es, which were seen to ramify throughout the inner plexiform layer.

27 s localized in the ON and OFF regions of the inner plexiform layer.

28 to functionally distinct laminas within the inner plexiform layer.

29 ydroxylase-positive cells in lamina 1 of the inner plexiform layer.

30 n retinal slices by puffing kainate onto the inner plexiform layer.

31 lls that stratify in lamina 3 and 4/5 of the inner plexiform layer.

32 ignificant reduction in the thickness of the inner plexiform layer.

33 tification of dendrites and axons within the inner plexiform layer.

34 ignificant reduction in the thickness of the inner plexiform layer.

35 and their dendrites ramifying throughout the inner plexiform layer.

36 an abnormal distribution of processes in the inner plexiform layer.

37 t generates hyperpolarizing responses in the inner plexiform layer.

38 at the border of the inner nuclear layer and inner plexiform layer.

39 in, intermittently varicose processes in the inner plexiform layer.

40 roject to two distinct sublaminae within the inner plexiform layer.

41 that define the ON and OFF sublamina of the inner plexiform layer.

42 % of the input to bipolar cells (BCs) in the inner plexiform layer.

43 re narrowly stratified in sublamina b of the inner plexiform layer.

44 connections of DB3 bipolar cell axons in the inner plexiform layer.

45 late, coinciding with synaptogenesis in the inner plexiform layer.

46 throughout sublamina a (OFF sublayer) of the inner plexiform layer.

47 ined with processes ramifying throughout the inner plexiform layer.

48 cesses have overlapping distributions in the inner plexiform layer.

49 h dendrites in both ON and OFF strata of the inner plexiform layer.

50 either the outer or the inner border of the inner plexiform layer.

51 hat ramify within the outermost layer of the inner plexiform layer.

52 some colocalizations of GluR1 and TH in the inner plexiform layer.

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

54 a greater degree in the OFF sublamina of the inner plexiform layer.

55 e host retina and dendrites growing into the inner plexiform layer.

56 boreal dendrites in the OFF sublamina of the inner plexiform layer.

57 ess the functional ON/OFF subdivision of the inner plexiform layer.

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

59 rojecting to new, more distal regions of the inner plexiform layer.

60 les similar to those found in the vertebrate inner plexiform layer.

61 SGCs are generated in both the outer and the inner plexiform layers.

62 ith the majority of plaques in the outer and inner plexiform layers.

63 disruption of the nerve fiber layer and the inner plexiform layers.

64 ons showed highest labeling in the outer and inner plexiform layers.

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

66 rminating exclusively in sublamina S5 of the inner plexiform layer, (2) bistratified cells with dendr

67 nerve fiber layer, ganglion cell layer, and inner plexiform layer, 86.2 vs. 103.4 microm; inner nucl

68 peripheral reduction in the thickness of the inner plexiform layer, a 15.6% peripheral reduction in t

69 il ED 8, when they showed a reduction of the inner plexiform layer, accompanied by a marked decrease

70 KIF3A is also present in the inner plexiform layer, again at presynaptic ribbons.

71 Thus, for each level of the inner plexiform layer all three cell types participate i

72 elements for receptive field shaping in the inner plexiform layer, although few receptive field mode

73 a has a broad axonal arbor in layer 5 of the inner plexiform layer and a wide dendritic arbor that do

74 ells still target Syntaxin-3 proteins to the inner plexiform layer and have abundant vsx1 mRNA.

75 n level of their axon terminal system in the inner plexiform layer and in immunoreactivity for recove

76 also restored; however, the thickness of the inner plexiform layer and one measure of axon branching

77 acular parameters, such as the ganglion cell inner plexiform layer and optic nerve head parameters, a

78 ive cells arborized at various levels of the inner plexiform layer and over fields of different diame

79 ted their dendrites to the ON stratum of the inner plexiform layer and provided sufficient membrane a

80 retinal nerve fibre layer, ganglion cell and inner plexiform layer and stopped at the level of the in

81 ar position of an RGC's dendrites within the inner plexiform layer and that of its axon within the re

82 ar layer and immunoreactive processes in the inner plexiform layer and the outer plexiform layer.

83 synapses depolarize TH cell dendrites in the inner plexiform layer and these depolarizations propagat

84 e neurons of the inner nuclear layer, in the inner plexiform layer, and along the vitreal surface, bu

85 of dendritic stratification in the retina's inner plexiform layer, and details of dendritic branchin

86 ses appropriately in synaptic laminae in the inner plexiform layer, and functional synapses formed in

87 ng was present within the nerve fiber layer, inner plexiform layer, and inner and outer nuclear layer

88 ignificant decline with age of only the GCL, inner plexiform layer, and inner nuclear layer thickness

89 amacrines and ganglion cells throughout the inner plexiform layer, and much of the labeling was not

90 nd located in the retinal nerve fiber layer, inner plexiform layer, and outer plexiform layer.

91 detected from the ganglion cell layer to the inner plexiform layer, and some plaques were observed in

92 tive RGCs co-stratify their dendrites in the inner plexiform layer, and that Tenm3(+) ACs require Ten

93 itochondria of the ganglion cells, outer and inner plexiform layers, and photoreceptor inner segments

94 Although the inner plexiform layer appears earlier than the outer ple

95 however, the synaptic mechanisms within the inner plexiform layer are not well characterized within

96 r layer and 4mum for macular ganglion cell + inner plexiform layer are robust thresholds for identify

97 most strongly associated with ganglion cell/inner plexiform layer atrophy (P = 0.004) and C1QA and C

98 assessed genetic predictors of ganglion cell/inner plexiform layer atrophy in a discovery cohort of 3

99 crine cells occupy strata 2, 3, and 4 of the inner plexiform layer, between the two bands formed by c

100 In the inner plexiform layer, bipolar cells deliver spatially a

101 It was also seen in ganglion cells and inner plexiform layer but in smaller amounts.

102 e segregated into separate sublaminas of the inner plexiform layer, but early in development these pr

103 ses neuroligin 1 protein was detected in the inner plexiform layer, but its highest levels were detec

104 s deliver high-acuity spatial signals to the inner plexiform layer, but outside the fovea, this spati

105 ns can break the stratification rules of the inner plexiform layer by providing significant synaptic

106 tinal nerve fiber (RNFL), ganglion cell, and inner plexiform layers, can be correlated with vision lo

107 not be attributed to the disorganization of inner plexiform layer cells that occurs in the Dscam mut

108 ricted to the inner and outer margins of the inner plexiform layer, co-stratifying with the processes

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

110 al quadrant, and a thinner ganglion cell and inner plexiform layer complex (GCL-IPL).

111 a greater degree in the OFF sublamina of the inner plexiform layer, corroborating the hypothesis that

112 lar cells that terminate in stratum 3 of the inner plexiform layer (DB4) express more Ret-PCP2 than t

113 nglion cells, laminar dissection through the inner plexiform layer, disorganization of the outer plex

114 ck, neural retina neurocan is present in the inner plexiform layer from day 7 on, and the GalNAcPTase

115 tion of the perifoveal retinal ganglion cell-inner plexiform layer (GC-IPL) and the peripapillary ret

116 l nerve fiber layer (RNFL) and ganglion cell-inner plexiform layer (GC-IPL) of patients with DOA were

117 pose was to study the macular ganglion cell- inner plexiform layer (GC-IPL) thickness in healthy 6.5

118 RNFL) thickness, rim area, and ganglion cell-inner plexiform layer (GC-IPL) thickness measurements we

119 field thickness (CST), macular ganglion cell-inner plexiform layer (GC-IPL) thickness, and peripapill

120 Rates of ganglion cell + inner plexiform layer (GCIP) and whole-brain (r = 0.45;

121 er in AAs (p = 0.047), whereas ganglion cell/inner plexiform layer (GCIP) thickness did not differ by

122 mum) and that of the ganglion cell layer and inner plexiform layer (GCIP, -11.3 mum), whereas the thi

123 The common ganglion cell and inner plexiform layer (GCIPL) and inner nuclear layer (I

124 yer (RNFL) and macular retinal ganglion cell-inner plexiform layer (GCIPL) change over time in health

125 FL (cpRNFL) thickness, macular ganglion cell-inner plexiform layer (GCIPL) thickness and optic nerve

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

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

128 for ganglion cell layer (GCL), ganglion cell/inner plexiform layer (GCIPL), ganglion cell complex (GC

129 etinal nerve fiber layer, ganglion cell plus inner plexiform layer (GCIPL), whole-brain, gray matter

130 anglion cell complex (GCC) and ganglion cell inner plexiform layer (GCIPL), with the accuracy of RNFL

131 l nerve fiber layer (RNFL) and ganglion cell-inner plexiform layer (GCIPL).

132 of macular (including the ganglion cell and inner plexiform layer [GCIPL], inner retina [IR], outer

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

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

135 the complex formed by the ganglion cell and inner plexiform layers (GCL + IPL) provided the highest

136 (about 50%) of the GlyRalpha4 puncta in the inner plexiform layer, however, was found to lack GlyRbe

137 are generally located in adjacent puncta in inner plexiform layer, implying paracrine interactions.

138 restricted to specific sublaminae within the inner plexiform layer in adulthood, but acquire their re

139 extended thickness of the ON sublayer of the inner plexiform layer in the microbat retina, more ON th

140 he outer limiting membrane and the outer and inner plexiform layers in the retina.

141 OS) was localized primarily in puncta in the inner plexiform layer, in amacrine cells, and in somata

142 Functionally, the inner plexiform layer, in which bipolar cells synapse on

143 mmediate proximity to one another within the inner plexiform layer, indicating that they do not engag

144 rom moderate glaucoma was mGCL combined with inner plexiform layer (IPL) (AUC = 0.915) and cpRNFL (AU

145 n cell layer (GCL) (nasally and temporally), inner plexiform layer (IPL) (nasally), outer nuclear lay

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

147 However, amacrine cell signalling in the inner plexiform layer (IPL) also contributes to the stea

148 ll types stratify at different levels in the inner plexiform layer (IPL) and can interact with costra

149 inals ramified in 70-85% of the depth of the inner plexiform layer (IPL) and DBC(R)-like DeltaI(C) se

150 tes ramifying at different strata within the inner plexiform layer (IPL) and each carrying a unique r

151 el(s) of axon terminal stratification in the inner plexiform layer (IPL) and exhibiting light respons

152 ed obliquely through the scleral half of the inner plexiform layer (IPL) and formed a loose, tangenti

153 on synapses in the innermost ON layer of the inner plexiform layer (IPL) and from dopaminergic amacri

154 s), nerve fiber layer (NFL), and also in the inner plexiform layer (IPL) and inner nuclear layer (INL

155 ty reveals two dendritic plexuses within the inner plexiform layer (IPL) and morphologically heteroge

156 es into a discrete synaptic layer called the inner plexiform layer (IPL) and only rarely extend proce

157 Functional Ca(2+) imaging at the inner plexiform layer (IPL) and outer plexiform layer (O

158 The location of the inner plexiform layer (IPL) and outer plexiform layer (O

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

160 axons to the retina where they branch in the inner plexiform layer (IPL) and synapse onto several inn

161 ple neurite targeting defects in the retinal inner plexiform layer (IPL) and tectal neuropil.

162 itive cells appeared after I/R injury in the inner plexiform layer (IPL) and the inner nuclear layer

163 , retinal amacrine cells migrate towards the inner plexiform layer (IPL) and then retract their trail

164 Cx45) subunits are widely distributed in the inner plexiform layer (IPL) and therefore are likely con

165 ous varicose processes in all laminae of the inner plexiform layer (IPL) and to the outer plexiform l

166 cells branching in the outermost part of the inner plexiform layer (IPL) and weakly melanopsin-positi

167 With the formation of the inner plexiform layer (IPL) at S18, ChAT-immunoreactive

168 at most dACs send processes into the forming inner plexiform layer (IPL) before migrating through it

169 polar terminals were first identified in the inner plexiform layer (IPL) by labeling for the photorec

170 nded their processes in the sublamina of the inner plexiform layer (IPL) closest to the INL/IPL borde

171 the number of V-1L-positive synapses in the inner plexiform layer (IPL) compared with the percentage

172 y 180-350 microm stratifying near 70% of the inner plexiform layer (IPL) depth.

173 Puncta were present throughout the inner plexiform layer (IPL) for beta(1) and 62-3G1, but

174 that the division between the ON and the OFF inner plexiform layer (IPL) is not structurally absolute

175 ified and ramified in specific strata of the inner plexiform layer (IPL) of retina to synapse with di

176 In the inner plexiform layer (IPL) of the mouse retina, ~70 neu

177 sc and had varicose terminal branches in the inner plexiform layer (IPL) of the peripheral retina.

178 synaptic connectivity of Y1 processes in the inner plexiform layer (IPL) of the rat retina.

179 tions of the visual world is embodied in the inner plexiform layer (IPL) of the retina, in which ligh

180 The inner plexiform layer (IPL) of the vertebrate retina com

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

182 erminals ramifying between 0% and 30% of the inner plexiform layer (IPL) receive mixed inputs from ro

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

184 Labelling was weaker in the inner plexiform layer (IPL) than in nuclear layers, thou

185 ctate CB1R-IR in the distal one-third of the inner plexiform layer (IPL) that could not be assigned t

186 er-specific arbor specializations within the inner plexiform layer (IPL) that occur consistently at d

187 o the scleral half or "Off" sublamina of the inner plexiform layer (IPL) undergo the greatest changes

188 The combined nerve fiber layer (NFL) and inner plexiform layer (IPL) were manually segmented and

189 lls terminate in different sublaminas of the inner plexiform layer (IPL) where they form synapses wit

190 ns to form functional neural circuits in the inner plexiform layer (IPL), a laminar region that is co

191 n cell layer, (2) dendritic processes in the inner plexiform layer (IPL), and (3) axons in the optic

192 as P3, prior to synapse formation within the inner plexiform layer (IPL), and again in the INL at P22

193 re found in the outer plexiform layer (OPL), inner plexiform layer (IPL), and optic fiber layer (OFL)

194 axon boutons only in the ON sublamina of the inner plexiform layer (IPL), and seven B(off) types with

195 itecture, level of stratification within the inner plexiform layer (IPL), and tracer coupling pattern

196 In the distal 80% of the inner plexiform layer (IPL), dense GC dendrites coexiste

197 type-I SAC, found at the outer border of the inner plexiform layer (IPL), forms a synaptic subband "a

198 s typically branched into sublamina a of the inner plexiform layer (IPL), i.e., the OFF inner plexifo

199 ences in the dye accumulation pattern in the inner plexiform layer (IPL), suggesting a dynamic, light

200 based on the dendritic stratification in the inner plexiform layer (IPL), those monostratified in the

201 punctate immunolabeling, exclusively in the inner plexiform layer (IPL), was observed for each of th

202 ar cell axon terminals in sublamina-b of the inner plexiform layer (IPL), we investigated the possibi

203 at retinal synaptic layers, particularly the inner plexiform layer (IPL), where communication between

204 he segregation of ON and OFF pathways in the inner plexiform layer (IPL), where glutamate is released

205 terminals in the innermost sublamina of the inner plexiform layer (IPL), which is typical for mammal

206 tivity; (4) restricted lamination within the inner plexiform layer (IPL), which renders J-RGCs respon

207 50 in the ganglion cell layer, ~0.122 in the inner plexiform layer (IPL), ~0.025 in the inner nuclear

208 is embodied as separate strata that span the inner plexiform layer (IPL).

209 multiple retinal neuron subtypes within the inner plexiform layer (IPL).

210 bipolar cells in distinct sublaminae of the inner plexiform layer (IPL).

211 n sublamina a (OFF sublamina) of the retinal inner plexiform layer (IPL).

212 bution from the center to sublamina a of the inner plexiform layer (IPL).

213 respectively, and in their processes in the inner plexiform layer (IPL).

214 in a dense layer of neuropil, the so-called inner plexiform layer (IPL).

215 s) form synapses on dendrites of RGCs in the inner plexiform layer (IPL).

216 s ramified across the vertical extent of the inner plexiform layer (IPL).

217 polar that ramifies in stratum 3 (s3) of the inner plexiform layer (IPL).

218 ayer (INL), and in two distinct bands of the inner plexiform layer (IPL).

219 inergic bands were clearly identified in the inner plexiform layer (IPL).

220 e synaptic neuropil in the inner retina, the inner plexiform layer (IPL).

221 esponse attributes to different parts of the inner plexiform layer (IPL).

222 (OPL) and in many synaptic terminals in the inner plexiform layer (IPL).

223 ata 6-9 and a minor band in stratum 3 of the inner plexiform layer (IPL).

224 strating the presence of transporters in the inner plexiform layer (IPL).

225 ither the outer plexiform layer (OPL) or the inner plexiform layer (IPL).

226 of a vertical stack of neural strata at the inner plexiform layer (IPL).

227 ndrites confined to On and Off strata of the inner plexiform layer (IPL).

228 diffuse ramification (n = 14) throughout the inner plexiform layer (IPL).

229 orizontal cells and future OPL, reaching the inner plexiform layer (IPL).

230 ses ramified in strata 1, 3, 4, and 5 of the inner plexiform layer (IPL).

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

232 the layering, or lamination, of the retinal inner plexiform layer (IPL).

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

234 ion patterns identified three regions in the inner plexiform layer (IPL): a thick sublamina a, with t

235 lized to the outer plexiform layer (OPL) and inner plexiform layer (IPL); the beta(3) subunit was loc

236 nventional synapses and gap junctions in the inner plexiform layer is also observed.

237 ginating synapses appear normal, whereas the inner plexiform layer is undisturbed; finally, the rate

238 evel, immunocytochemistry showed that in the inner plexiform layer KCC2's density increased gradually

239 Bipolar cell terminals in the inner plexiform layer made normal ribbon synapses; thus,

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

241 as either predominantly macula ganglion cell-inner plexiform layer (mGCIPL), predominantly peripapill

242 mIPL parameters and the ganglion cell layer-inner plexiform layer (mGCL-IPL) was determined by combi

243 ular ganglion cell layer (mGCL), and macular inner plexiform layer (mIPL) were significantly thinner

244 macular ganglion cell layer (mGCL), macular inner plexiform layer (mIPL), macular inner nuclear laye

245 e that TH cell somata, tapering and varicose inner plexiform layer neurites, and varicose outer plexi

246 l ganglion cell layer (NFL/GCL), NFL/GCL and inner plexiform layer (NFL/GCL + IPL), and total retina

247 y branched extensively and terminated in the inner plexiform layer, occasionally alongside retinal bl

248 Synapses in the inner plexiform layer of the retina undergo short-term p

249 ATP release from Muller cells into the inner plexiform layer of the retina was shown using the

250 glaucoma may represent abnormalities in the inner plexiform layer of the temporal retina, where clas

251 nges were demonstrated in both the outer and inner plexiform layers of the retina by immunofluorescen

252 the CNS, in neurons of the inner nuclear and inner plexiform layers of the retina, and in the kidney

253 mmunoreactivity was intense in the outer and inner plexiform layers (OPL and IPL, respectively).

254 (P = .006) or thinner average ganglion cell-inner plexiform layer (P = .028) along with higher basel

255 Reduction of the ganglion cell and inner plexiform layers predicted greater axonal damage i

256 different types of amacrine cells across the inner plexiform layer prompts that they should be also i

257 terminals ramify in the proximal half of the inner plexiform layer, raising the possibility that thes

258 found at the margin of the inner nuclear and inner plexiform layers, rather than the ganglion cell la

259 R = -0.74, P < 0.0001) and the ganglion cell inner plexiform layer region of interest (R = -0.51, P <

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

261 transcript expressed in the vicinity of the inner plexiform layer, revealed its role in cell type co

262 tructural macular retinal ganglion cell plus inner plexiform layer (RGC+IPL) loss identified by spect

263 NFL), the combined retinal ganglion cell and inner plexiform layers (RGCL+), and the inner nuclear la

264 the ganglion cell layer (I3 and N6 sectors), inner plexiform layer (S6 and N6 sectors), inner nuclear

265 processes extending into the ON-layer of the inner plexiform layer, similar to A8 amacrine cells desc

266 irst conventional synapses appear within the inner plexiform layer simultaneously with the first phot

267 Plaques were embedded in the inner plexiform layer strata displaying syntaxin 1 and C

268 th of specific types of RGCs and of specific inner plexiform layer sublaminae, opening new avenues fo

269 the synaptic layers beginning in stereotyped inner plexiform layer sublaminae.

270 The inner plexiform layer surround inhibition comprised GABA

271 ve fibre layer, the ganglion cell layer plus inner plexiform layer, the INL plus outer plexiform laye

272 the ganglion cell layer (GCL) as well as the inner plexiform layer, the inner nuclear layer (INL), an

273 or example, changes in the ganglion cell and inner plexiform layers, the sites of the retinal ganglio

274 Muller cells may secrete ACBP in the inner plexiform layer, thereby decreasing the sensitivit

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

276 ation (ETDRS </=35) had normal ganglion cell-inner plexiform layer thickness and normal mfERG finding

277 found between CS at 6 cpd and ganglion cell/inner plexiform layer thickness at inferotemporal and in

278 ness (mRNFL) and macular ganglion cell layer-inner plexiform layer thickness were 3.5, 4.5, 3.0, 3.0,

279 Total retinal thickness and ganglion cell-inner plexiform layer thickness were measured using cust

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

281 ighly reproducible measures of ganglion cell-inner plexiform layer thickness.

282 The ganglion cell layer and inner plexiform layer thicknesses could predict axonal d

283 yer as well as composite ganglion cell layer+inner plexiform layer thicknesses in the eyes of patient

284 poptosis and increased nerve fibre layer and inner plexiform layer thicknesses.

285 d a similar set of analyses of ganglion cell/inner plexiform layer thinning in a replication cohort (

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

287 to diffuse long distances from axons in the inner plexiform layer to receptors in other retinal laye

288 lume (GCL, p = 0.003), ganglion cell layer - inner plexiform layer volume (GCL-IPL, p = 0.005) and in

289 Inner plexiform layer volume of both eyes (IPL, right ey

290 ine cells and the ON-OFF organization in the inner plexiform layer was largely preserved.

291 Reaction product within the inner plexiform layer was observed in processes of gangl

292 Imaging throughout the inner plexiform layer, we found transient, rectified rel

293 er part of sublamina a (OFF sublayer) of the inner plexiform layer where it costratifies with the den

294 h of this functional diversity arises in the inner plexiform layer, where inhibitory amacrine cells m

295 a synaptic terminal in the outer half of the inner plexiform layer, where it contacts an OFF midget g

296 hese cells are present at every level of the inner plexiform layer, which suggests that they affect m

297 Labeled puncta were observed in the inner plexiform layer with each of these antisera to glu

298 es in that VRL1-IR was most prominent in the inner plexiform layer, with scattered compact projection

299 tina, cGK I protein was most abundant in the inner plexiform layer, with significant amounts in gangl

300 ed dendritic reduction to sublamina b of the inner plexiform layer without retinal ganglion cell loss