ライフサイエンスコーパス: inner plexiform layer

1 axons containing histamine terminate in the inner plexiform layer.

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

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

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

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

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

7 resynaptic and postsynaptic processes in the inner plexiform layer.

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

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

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

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

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

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

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

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

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

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

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

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

20 to functionally distinct laminas within the inner plexiform layer.

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

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

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

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

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

26 and their dendrites ramifying throughout the inner plexiform layer.

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

28 t generates hyperpolarizing responses in the inner plexiform layer.

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

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

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

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

33 % of the input to bipolar cells (BCs) in the inner plexiform layer.

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

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

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

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

38 ined with processes ramifying throughout the inner plexiform layer.

39 cesses have overlapping distributions in the inner plexiform layer.

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

41 extend across the inner nuclear layer to the inner plexiform layer.

42 most strongly staining ones found within the inner plexiform layer.

43 o two sublayers in sublaminae a and b of the inner plexiform layer.

44 he retinal synaptic layers, particularly the inner plexiform layer.

45 e axons of some peripheral cones reached the inner plexiform layer.

46 and stratification of axon terminals in the inner plexiform layer.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 cond postnatal week in the inner nuclear and inner plexiform layers.

69 otoreceptor inner segments and the outer and inner plexiform layers.

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

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

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

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

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

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

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

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

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

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

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

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

82 ately coterminous with synaptogenesis of the inner plexiform layer and may play a role in synaptogene

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

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

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

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

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

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

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

90 associated with presynaptic membranes in the inner plexiform layer and was found only rarely with mem

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

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

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

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

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

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

97 s narrowly in stratum 2 (sublamina a) of the inner plexiform layer, and the A22, which ramifies mostl

98 membrane to the outer limiting membrane, the inner plexiform layer, and the inner nuclear layer (P <

99 It is also absent from axons entering the inner plexiform layer, and their terminals.

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

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

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

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

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

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

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

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

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

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

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 However, labeling was densest in the inner plexiform layer for Kv1.1, more concentrated in th

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 rrowly stratified deep in sublamina 4 of the inner plexiform layer immediately above the rod bipolar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 e axon and axon terminals in lamina 5 of the inner plexiform layer (IPL) and was weakest in the cell

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

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

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

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

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

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

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

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

169 esent in the outer plexiform layer (OPL) and inner plexiform layer (IPL) in three bands corresponding

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

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

172 ratification levels of axon terminals in the inner plexiform layer (IPL) of single L-glutamic acid de

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

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

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

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

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

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

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

180 The nerve fiber layer (NFL) and inner plexiform layer (IPL) show homogeneous backscatter

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

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

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

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

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

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

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

188 rocesses were densely distributed across the inner plexiform layer (IPL) with a maximum density over

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 ted by focal application of glutamate at the inner plexiform layer (IPL).

229 in the distal inner nuclear layer (INL) and inner plexiform layer (IPL).

230 tion that occupies strata 1 through 3 of the inner plexiform layer (IPL).

231 atterns of synaptic relationships within the inner plexiform layer (IPL).

232 mary processes that arborize in the proximal inner plexiform layer (IPL).

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

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

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

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

237 albindin cone bipolar cell suggests that the inner plexiform layer is stratified according to depth,

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

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

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

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

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

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

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

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

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

247 aminae a and b (OFF and ON sublayers) of the inner plexiform layer, occupying the narrow gap separati

248 the retina of the adult goldfish, within the inner plexiform layer of the differentiated retina and t

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

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

251 e a major inhibitory neurotransmitter in the inner plexiform layer of the retinas of all vertebrate s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 The inner plexiform layer surround inhibition comprised GABA

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

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

272 these occur as mirror-image pairs across the inner plexiform layer, the soma of one of each pair bein

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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