ライフサイエンスコーパス: laminae

1 in laminae I-II and half of those in deeper laminae).

2 lular expression is the same in all cortical laminae.

3 tin in the new cuticle and organizes it into laminae.

4 to contralateral ventral, medial, and dorsal laminae.

5 of dendritic spine density of neurons in all laminae.

6 n narrow radial columns perpendicular to the laminae.

7 synaptic input to neurons of the superficial laminae.

8 tinct subdivisions of the canonical cortical laminae.

9 nd have dendrites that enter the superficial laminae.

10 onal plasticity of supragranular neocortical laminae.

11 eptors that showed variation across cortical laminae.

12 ted, precluding identification of the normal laminae.

13 disc-shaped neurons, forming fibrodendritic laminae.

14 ecome dorsal horn neurons in the superficial laminae.

15 the brain vasculature, and specialized basal laminae.

16 anular, granular, and infragranular cortical laminae.

17 ignals that guide neuronal migration to form laminae.

18 teries and associated with thickened elastic laminae.

19 ults in the permanent disorganization of its laminae.

20 rimary pathway for the formation of cortical laminae.

21 atS(-/-)LDLR(-/-) mice had preserved elastic laminae.

22 butyric acid-ergic interneurons within the A laminae.

23 almost parallel to other major telencephalic laminae.

24 rons to their proper destinations in retinal laminae.

25 urons were closely aligned with the cellular laminae.

26 entral terminals innervating all dorsal horn laminae.

27 ed boutons were located in other ipsilateral laminae.

28 terminals were found in other contralateral laminae.

29 ofiles representing fetal and adult cortical laminae.

30 ecording arrays sampling across all cortical laminae.

31 sion with a clear indication of isofrequency laminae.

32 re widespread and were now present in deeper laminae.

33 ), with abundant expression in LI and deeper laminae.

34 sual perception is organized within specific laminae.

35 ry transmission in deeper non-nociceptive DH laminae.

36 Of the 17 patients (20 laminae), 1 underwent MOOKP procedure following multiple

37 Resorption was noted in 20 out of 87 laminae (22.98%).

38 Vitritis was the presenting feature (7 of 20 laminae, 35%) indicative of early resorption, and the oc

39 dally before sending collaterals to specific laminae according to neuronal subclass.

40 Retinal laminae across horizontal and vertical meridians were me

41 and project into superficial "pain-specific" laminae after axotomy.

42 bout the orientation of their fibrodendritic laminae and about the morphology of their most distincti

43 ormal, with continuous and organized elastin laminae and abundant alphaActin-expressing SMCs.

44 rous cholinergic cell bodies within the same laminae and compared their density and morphological pro

45 ciated with thickening of the vascular basal laminae and endothelial cell alterations that were visib

46 The names of some of the laminae and fiber tracts were also changed to reflect cu

47 eneration of 3D digital models consisting of laminae and matrix (binary field) with characteristic de

48 odel is presented that incorporates cellular laminae and oriented dendritic growth to form frequency-

49 Robust relationships between laminae and sheath areas also were found, highlighting t

50 (i.e. between leaves within a stem, between laminae and sheaths, and between the mainstem and axilla

51 modern conical aggregates creates contorted laminae and submillimeter-to-millimeter-scale enmeshed b

52 n an accurate assessment of ruptured elastic laminae and the compensatory expression of elastic fiber

53 ers that determine the shape space of finite laminae and thus allows for a comparative study of elong

54 cCP30 is localized with chitin in horizontal laminae and vertically oriented columnar structures in r

55 tes shape sensory processing across cortical laminae and what type of response properties emerge in t

56 reased at later time points from day 4 (deep laminae) and on day 7 (entire dorsal horn).

57 ompartment comprised of elastin and collagen laminae, and grow into the retina.

58 otion encoding is consistent across cortical laminae, and this consistency is maintained during memor

59 lesions, severe degeneration of the elastic laminae, and tunica media of choroidal vessels.

60 ) was closely aligned with that of the Nissl laminae (approximately 25 degrees).

61 Elastic laminae are extracellular matrix constituents that not o

62 The mechanisms for viral escape across basal laminae are unknown.

63 We found a unique relationship between laminae area and leaf rank for the mainstem and its till

64 authors collected juvenile alligator dental laminae at different developmental stages and performed

65 dure following multiple graft failures, 6 (7 laminae) belonged to the chemical injury group, and 10 (

66 The physiological role of basal laminae (BL) and connective tissue (meninges and their p

67 gans during development, occurs nearby basal laminae (BL) overlying connective tissue.

68 Schwann cells form basal laminae (BLs) containing laminin-2 (Ln-2; heterotrimer a

69 y in the central and caudal parts of the ICC laminae but that contralateral LSO terminals were concen

70 each other within precisely defined synaptic laminae, but the spatial distribution of contacts betwee

71 l and CBV decreased from superficial to deep laminae, but these responses were not well correlated wi

72 present after formation of definitive tectal laminae, but was diffuse and not aligned along RG, which

73 rules that control the formation of synaptic laminae by RGC axons.

74 eper (depth: 0.3-1.2 mm) than in superficial laminae (depth: <0.3 mm) of the dorsal horn (24/67 vs. 9

75 enotypes include severe reduction of leaflet laminae due to a decrease in cell size and number, chang

76 Although axons target specific laminae during development, dendritic lamination has bee

77 ceived excitatory input from the superficial laminae, especially lamina IIi, as well as the II/III bo

78 horn which was concentrated over superficial laminae, especially the substantia gelatinosa (lamina II

79 In most laminae, except in CA3 stratum lucidum, about 15% of PR-

80 uits, and excitatory neurons in different V1 laminae exhibit distinct patterns of layer-specific orga

81 Whereas most cortical laminae exhibited idiosyncratic increases in zinc histoc

82 rons play an important regulatory role in EB laminae formation.

83 These results confirm that neurons in these laminae have extensive collateral projections and sugges

84 fic genes were expressed across at least two laminae, however.

85 thy mice, CACTs were located primarily in DH laminae I (LI) and V (LV) and projected down middle and

86 6 and 7 (GluR5,6,7) in relation to SP within laminae I and II in the rat trigeminal dorsal horn.

87 ive fibers as indicated by c-Fos labeling in laminae I and II of the dorsal horn of the spinal cord.

88 f NMDA NR1-N1, C1, and C2-plus expression in laminae I and II of the spinal cord (T10-L1; L4-S1) in h

89 root ganglion neurons and intensely labeled laminae I and II of the spinal cord dorsal horn.

90 of the spinal superficial dorsal horn (SDH) (laminae I and II) and its relationship to pain and other

91 rficial dorsal horn of the spinal cord (SDH; laminae I and II) receives strong input from thin primar

92 ficial dorsal horn (SDH) of the spinal cord (laminae I and II); however, the effects produced by hypo

93 of the spinal superficial dorsal horn (SDH), laminae I and II, and their electrophysiological propert

94 5-RARE) transgene is seen in interneurons in laminae I and II, as well as in ependymal cells around t

95 vity (HCN1-IR) was predominantly absent from laminae I and II, while a dense band of punctate labelin

96 tified sympathetically correlated neurons in laminae I and II.

97 ell death not only in lamina III but also in laminae I and II.

98 VRL-1 by myelinated nociceptors that target laminae I and IIi and in nonnociceptive Abeta fibers tha

99 sparsity of presynaptic NR1 in terminals in laminae I and IIo and in terminals of peptidergic unmyel

100 PVN cells project also to laminae I and outer II of the Sp5C.

101 ns, whereas VPI receives STT input from both laminae I and V cells, with two different topographic or

102 reporter mouse revealed that many neurons in laminae I and V of the spinal cord dorsal horn and cauda

103 TRPV1+ nociceptors, neurons in the region of laminae I and V of the spinal cord lost responsiveness t

104 restricted to VPI labeled many STT cells in laminae I and V with an anteroposterior topography.

105 d number of NK(1)R-expressing neurons in the laminae I of the dorsal horn in stressed rats.

106 nd prodynorphin labeled puncta and fibers in laminae I, II, and V, as well as some fibers in the rest

107 pAkt and pmTOR were prominent in neurons in laminae I, III, and IV, whereas pmTOR and its downstream

108 Many local circuit neurons in laminae I-II also stained for sGC, but less intensely.

109 pressed by 18% of inhibitory interneurons in laminae I-II and 9% of those in lamina III.

110 the cells receive (over a third of those in laminae I-II and half of those in deeper laminae).

111 L5 segment GFAP expression was increased in laminae I-II and Iba1 in deep laminae on day 1, in the e

112 somatosensory (S1) cortices and terminate in laminae I-II and III-V of the Sp5C, respectively.

113 received excitatory synaptic input from both laminae I-II and the outer part of III-IV, especially th

114 synaptic release of glutamate in superficial laminae I-II of the DH, while GABA release was spared.

115 so significantly inhibited Fos expression in laminae I-II of the spinal cord in the sham-operated rat

116 ase in L1 expression in Lissauer's tract and laminae I-II on the deafferented side.

117 pERK-positive neurons clearly overlapped in laminae I-II with normal unmyelinated and thin myelinate

118 r terminals in superficial dorsal horn (SDH; laminae I-II) constitute two separate subpopulations: th

119 in 13-15% of VGAT-immunoreactive boutons in laminae I-II, and 5% of those in lamina III.

120 - 4.0 (7-75) minutes in 9 neurons located in laminae I-II, and 9 neurons located in laminae III-V.

121 for intense labeling in Lissauer's tract, in laminae I-II, and on dorsolateral funicular axons.

122 5) minutes after CSD in 7 neurons located in laminae I-II, or after a latency of 25.1 +/- 4.0 (7-75)

123 ls (<2/section) were observed in superficial laminae I-II.

124 al recordings were restricted to lamina I or laminae I-II.

125 in neurokinin 1 receptor-positive neurons in laminae I-III after peripheral inflammation.

126 orsolateral funiculus and numerous puncta in laminae I-III and V of the dorsal horn.

127 Between 25-40% of neurons in laminae I-III are GABAergic, and some of these express n

128 IGRs are expressed in GABAergic terminals in laminae I-III of the dorsal horn.

129 -gamma, and calretinin-expressing neurons in laminae I-III were markedly reduced, but the ventral cor

130 We found that 4-6% of neurons in laminae I-III were NPY-immunoreactive and based on the p

131 rd to characterize and label interneurons in laminae I-III with Neurobiotin.

132 proportion of the inhibitory interneurons in laminae I-III, and that their axons preferentially targe

133 terminals of Adelta and C afferent fibers in laminae I-III, presynaptic IGRs may play a role in inhib

134 al and mature dorsal horn, especially within laminae I-III.

135 vation in neurons in the superficial layers (laminae I-IIo) of the dorsal horn.

136 d neurons were found in the dorsal Vi/Vc and laminae I-IV of Vc.

137 as only present in 4-7% of VGLUT2 boutons in laminae I-IV, it was found in 58% of the VGLUT2 boutons

138 pre- or postsynaptically, or both, in spinal laminae I-IV.

139 rs that projected throughout the dorsal horn laminae I-V.

140 ha1-3 and alpha5 subunit immunoreactivity in laminae I-V.

141 C-Fos expression was localized to spinal laminae I-VI, with a modest decrease observed in the sup

142 terally, labeled boutons were located within laminae I-X, with the densest distribution found in lami

143 (LTMR) afferents "sprout" into pain-specific laminae (I-II) of the dorsal horn and are responsible fo

144 tions throughout the superficial dorsal horn laminae (I-II).

145 ls with varied morphology in the superficial laminae (I-III) of the dorsal horn of the spinal cord.

146 ely suppressed Fos expression in superficial laminae (I/II) and activated it in deeper laminae (III/I

147 e TrkB+ and TrkC+ afferents terminate (i.e., laminae II, III, IV, and VI) exhibit the highest levels

148 resence of a plexus of cholinergic fibers in laminae II-III of the dorsal horn of the macaque monkey.

149 o axon varicosities of neurons recorded from laminae II-V, although the occurrence of immunolabeling

150 itatory pyramidal neurons somata situated in laminae III and V, the excitatory neurons in rat S1 were

151 correlated neurons were found in dorsal horn laminae III, IV, and V.

152 We tested the hypothesis that dorsal horn laminae III-IV cell receptive fields (RFs) are initially

153 transition between the dorsal input zones of laminae III-IV neurons and the ventral input zones of la

154 give local synaptic inputs) for dorsal horn laminae III-IV neurons, in parasagittal and transverse s

155 neurons in lamina I, together with those in laminae III-IV that express the neurokinin 1 receptor (N

156 eurons in lamina I, together with neurons in laminae III-IV that express the neurokinin 1 receptor (N

157 Inhibitory input from laminae III-IV was found in a subpopulation of neurons o

158 s), mediolateral, and dorsoventral (reaching laminae III-IV) distribution.

159 y and inhibitory synaptic inputs from within laminae III-IV, while a subset of neurons also received

160 pulation also received excitatory input from laminae III-IV.

161 central terminals of myelinated afferents in laminae III-V and lamina IX of the rat spinal cord.

162 fibers and intrinsic discharge properties of laminae III-V neurons that may significantly influence i

163 dapting type II (SAII) afferent terminals in laminae III-V of the rat spinal cord.

164 ry postsynaptic currents (EPSCs) recorded in laminae III-V showed enhanced sensitivity to Ca(2+)-perm

165 ntralateral) afferents, while for boutons in laminae III-V, VGLUT1 levels were reduced by 50-70%.

166 ed in laminae I-II, and 9 neurons located in laminae III-V.

167 regions of the dorsal horn corresponding to laminae III-V.

168 ng localized the increase in GluA4 levels in laminae III-V.

169 ossessed axons that projected ventrally into laminae III-V; six of these were hyperpolarized by DAMGO

170 d in nonnociceptive Abeta fibers that target laminae III/IV.

171 was found in lamina I, inner lamina II, and laminae III/IV.

172 al laminae (I/II) and activated it in deeper laminae (III/IV) of the spinal dorsal horn.

173 e results show that iron is distributed over laminae in a pattern that is suggestive of each region's

174 modest decrease observed in the superficial laminae in IT CHA-treated rats.

175 TE6 disrupt the formation of elliptical leaf laminae in mature leaves, whereas overexpression of GTE6

176 (LGN), and in the formation of eye-specific laminae in other species.

177 ncided with the fragmentation of the elastic laminae in the arterial wall, which is hypothesized to i

178 lamina/extrusion was noted in 3 out of the 7 laminae in the chemical injury group and 8 out of the 12

179 ubiquity of disrupted, curled, and contorted laminae in the crests of many Mesoproterozoic, Paleoprot

180 To study the biology of basal laminae in the developing nervous system the protein com

181 on functional differences of these distinct laminae in the dorsal spinal cord.

182 rmal innervation zones terminate in adjacent laminae in the dorsal spinal cord.

183 tact their synaptic partners within specific laminae in the inner and outer retina, provide a good sy

184 ed their processes appropriately in synaptic laminae in the inner plexiform layer, and functional syn

185 constraints on scan times and does not show laminae in the medial temporal lobe.

186 he chemical injury group and 8 out of the 12 laminae in the SJS group.

187 the anatomic spatial resolution of frequency laminae in the thalamus, supporting a growing consensus

188 ent populations are restricted to particular laminae in their target area.

189 gs demonstrate the importance of the elastic laminae in vascular injury, and reveal an unexpected rol

190 interneurons confined to the retinorecipient laminae, in which retinal axons arborize and form synaps

191 The exposure of monocytes to elastic laminae induced activation of SIRP alpha, which in turn

192 ells often migrate laterally along forebrain laminae into still-developing brain areas.

193 wly born neurons to their prospective target laminae is a prerequisite for neural circuit assembly in

194 f axons and dendrites to particular synaptic laminae is an important mechanism by which precise patte

195 the SG-to-CN projections into frequency band laminae is clearly evident despite severe auditory depri

196 ic restriction of fibers into frequency band laminae is significantly less precise in perinatal kitte

197 at an important function of arterial elastic laminae is to prevent monocyte adhesion, which is mediat

198 Thus, the formation of synaptic laminae is ultimately dispensable for the correct wiring

199 ic patterns of active neurons change between laminae is unknown.

200 neurones were observed in the spinal cord in laminae IV and V, in the region of the central canal and

201 forming type II glomeruli), while boutons in laminae IV-V had only simple, nonglomerular interactions

202 urons were most commonly observed in Rexed's laminae IV-VI and the dorsal portions of laminae VII-VII

203 section) were also observed in contralateral laminae IV-VI and the lateral spinal nucleus, with fewer

204 trast, afferents from the deeper dorsal horn laminae (IV-V) were found to course in the dorsolateral

205 found in lamina VII and, to a lesser extent, laminae IX and VI.

206 between the earplug (sum of contaminants in laminae layers) and blubber samples from the same organi

207 naturally in insect wings, leaves, and other laminae-like organelles.

208 y was an unusually smooth surface of elastic laminae, manifesting the loss of cell attachments that a

209 Similarly sized fossil bubbles and contorted laminae may be present only in the crestal zones of some

210 nd GAL-containing neurons in the deep lumbar laminae may contribute to the establishment of known sex

211 stages T2* changes involved deeper cortical laminae, multiple cortical areas and gyri.

212 ventrally extending dendrites of superficial laminae neurons.

213 Kenyon cell axons into the adult pattern of laminae occurs gradually over the course of nymphal deve

214 IP upregulation in the neuron of superficial laminae of dorsal spinal horn.

215 upying a specialised niche beneath the basal laminae of myofibres.

216 these different inputs, in terms of both the laminae of origin and those in which the recorded cells

217 on (LTD) vary depending on cortical area and laminae of presynaptic and postsynaptic neurons.

218 that binds to receptors in the retinotectal laminae of the amphibian optic tectum.

219 le projections were present in ventral motor laminae of the cord, including putative synapses directl

220 ar dominance of neurons in thalamo-recipient laminae of the cortex, and the amplitude of the thalamoc

221 er, Na(v)1.3-LI fibers terminate in the deep laminae of the dorsal horn and in the ventral horn.

222 CB1 receptor immunoreactivity in superficial laminae of the dorsal horn of the spinal cord was consis

223 ioceptive sensory axons into the superficial laminae of the dorsal horn where cutaneous sensory axons

224 sal horn) and day 7 after nerve injury (deep laminae of the dorsal horn) at spinal L5 segment.

225 -related peptide project only to superficial laminae of the dorsal horn, where uninjured nociceptive

226 n potentials did not sprout into superficial laminae of the dorsal horn.

227 to both superficial (I-II) and deep (III-V) laminae of the dorsal horn.

228 lateral to dorsomedial along the axis of the laminae of the ICC and perpendicular to the tonotopic ax

229 alized to numerous varicose processes in all laminae of the inner plexiform layer (IPL) and to the ou

230 d that bNOS is expressed in neurons in the A laminae of the LGN as early as postnatal day 7 (P7), a t

231 el, single-unit recordings were taken across laminae of the midbrain SC of the awake, passively liste

232 at sensory and motor neurons comingle within laminae of the SC to support rapid sensorimotor integrat

233 a activation was elevated in the superficial laminae of the spinal cord dorsal horn in TOW mice, spec

234 their projecting fibers into the superficial laminae of the spinal dorsal horn.

235 nd interpeduncular nuclei, as well as select laminae of the superior colliculus.

236 that neuronal cell bodies in the superficial laminae of the Vc positively stained for sGC.

237 Case records of 18 eyes (20 laminae) of 17 patients who showed evidence of lamina re

238 of lamina resorption out of the 85 eyes (87 laminae) of 82 patients that underwent MOOKP procedure b

239 s increased in laminae I-II and Iba1 in deep laminae on day 1, in the entire dorsal horn on day 4 and

240 y confirmed the inhibitory effect of elastic laminae on monocyte adhesion.

241 lly mediate the inhibitory effect of elastic laminae on monocyte adhesion.

242 receptors in GABAergic terminals in the same laminae, on the other hand, presynaptic IGRs may have an

243 al annual rainfall and frustule densities in laminae over a longer 83-year record were weakly and neg

244 measured and the thickness of photoreceptor laminae overlying drusen and in retinal regions neighbor

245 Reductions in the photoreceptor laminae overlying drusen were detectable and this is con

246 chrony between superficial and deep cortical laminae (phase-dependent power correlations, and phase c

247 nerve 1 month later at L5 and found ventral laminae projections similar to those in intact animals,

248 Although the intestinal laminae propriae of Rag-gammac(-/-) mice have a higher f

249 nctional dissociation of attention within SC laminae provides a subcortical basis for the oculomotor

250 al kidneys revealed anionic sites along both laminae rarae of the GBM that became most prominent alon

251 ppearance and spontaneously formed primitive laminae, reminiscent of the developing retina.

252 diminished the inhibitory effect of elastic laminae, resulting in a significant increase in monocyte

253 al preservation, these stromatolites contain laminae rich in organic carbon, interpreted as the fossi

254 Sixteen out of 20 laminae showed evidence of resorption superiorly.

255 owever, CBF changes were quite stable across laminae, similar to LFP.

256 integrated functional organization within SC laminae supports rapid and local integration of sensory

257 of cells was found in the organum vasculosum laminae terminalis (OV) and the median preoptic nucleus

258 neurones in the forebrain organum vasculosum laminae terminalis (OVLT) and hypothalamic paraventricul

259 neurons of the forebrain organum vasculosum laminae terminalis (OVLT) play a pivotal role in trigger

260 moreceptor neurons in the organum vasculosum laminae terminalis (OVLT), which then activates downstre

261 horn of the spinal cord consists of distinct laminae that serve as a pivotal region for relaying a va

262 g of axons and dendrites to defined zones or laminae, the recognition of individual target cells, the

263 at the visual DVR is organized in three main laminae, the thalamorecipient nucleus entopallium; a dor

264 ruct a precise chronology, and variations in laminae thickness provide an annual growth-rate record t

265 ged to the chemical injury group, and 10 (12 laminae) to the Stevens-Johnson syndrome (SJS) group.

266 ge numbers of labeled cells predominantly in laminae V and VII (more than half as many as from massiv

267 that VL receives STT input originating from laminae V and VII neurons that may be coextensive with i

268 These findings support the role of laminae V and VII STT cells in sensorimotor integration

269 n VL labeled STT cells almost exclusively in laminae V and VII, in segments consistent with the coars

270 nt medial part of the grey matter of Rexed's laminae V to VII, but sparing the dorsolateral CST and m

271 entified, namely to the intermediate region (laminae V, VI and VII) and to ventral horn region (lamin

272 ts input from three cell populations: medial laminae V-VI, lateral lamina V, and medial laminae VII-V

273 All interneurons were located in laminae V-VII of the L3-L7 segments.

274 from projection neurons of deep spinal cord laminae V-VIII and targets the 5HT neurons of the NRM, b

275 edominantly (63-69%) in lamina I but also in laminae V-VIII and the thoracic lateral horn (intermedio

276 ed, most CST axons terminated in spinal cord laminae V-VIII, as well as the laterodorsal motoneuronal

277 Ipsilaterally, boutons were found in laminae V-X.

278 medial dorsal horn, dorsal gray commissure, laminae VI and X and dorsal lateral gray were activated

279 al increases in contralateral M2 labeling in laminae VII and IX, the added effect of adjacent parieta

280 atter which include the intermediate region, laminae VII and VIII.

281 A population of rat lumbar laminae VII and X putative spinothalamic (STT) neurons t

282 l gray matter labeled cells in contralateral laminae VII-VIII (approximately 6-9/section) with fewer

283 d's laminae IV-VI and the dorsal portions of laminae VII-VIII.

284 l laminae V-VI, lateral lamina V, and medial laminae VII-VIII.

285 cord, numerous neurons located primarily in laminae VII-X, were retrogradely labeled with Fluoro-Rub

286 Because laminae VIII and IX collectively harbor axial, proximal,

287 gement in medial lamina VII and ventromedial laminae VIII and IX contralaterally.

288 ticularly dense BDA labeling was observed in laminae VIII and IX ipsilaterally at the C6 and C8 level

289 e V, VI and VII) and to ventral horn region (laminae VIII and IX).

290 it medial geniculate body (MGV) has cellular laminae visible in routine Nissl stains, allowing a dire

291 arteries, except that degradation of elastic laminae was evident in uPA-transduced arteries.

292 Resorption of the laminae was noted to occur along the aspect with thinner

293 terial reconstruction model in vivo, elastic laminae were resistant to leukocyte adhesion and transmi

294 map putative stem cells in alligator dental laminae, which contain quiescent odontogenic progenitors

295 inate, the immunostaining in all dorsal horn laminae, which indicates that VRL-1 expression derives f

296 It was more concentrated in some superficial laminae, which might support directional movement.

297 or quantitative neuroimaging across cortical laminae with calibrated fMRI methods.

298 reactivity was widespread in all spinal cord laminae, with higher intensities in LII and lateral LV,

299 ar axons targeted multiple or all geniculate laminae, with little laminar selectivity in the distribu

300 The formation of laminae within the retina requires the coordinate regula