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 e organized into distinct lineage-associated laminae.

3 ed boutons were located in other ipsilateral laminae.

4 terminals were found in other contralateral laminae.

5 ofiles representing fetal and adult cortical laminae.

6 ecording arrays sampling across all cortical laminae.

7 central nucleus of the IC cross isofrequency laminae.

8 sion with a clear indication of isofrequency laminae.

9 re widespread and were now present in deeper laminae.

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

11 sual perception is organized within specific laminae.

12 layers, late born ones innervate superficial laminae.

13 ry transmission in deeper non-nociceptive DH laminae.

14 lular expression is the same in all cortical laminae.

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

16 to contralateral ventral, medial, and dorsal laminae.

17 of dendritic spine density of neurons in all laminae.

18 n narrow radial columns perpendicular to the laminae.

19 illae and maxillae lacking external (facial) laminae.

20 ed into subgroups across dorsoventral spinal laminae.

21 synaptic input to neurons of the superficial laminae.

22 tinct subdivisions of the canonical cortical laminae.

23 nd have dendrites that enter the superficial laminae.

24 ere suggested to send terminals to accessory laminae.

25 onal plasticity of supragranular neocortical laminae.

26 eptors that showed variation across cortical laminae.

27 ted, precluding identification of the normal laminae.

28 disc-shaped neurons, forming fibrodendritic laminae.

29 ecome dorsal horn neurons in the superficial laminae.

30 the brain vasculature, and specialized basal laminae.

31 tively, by the internal and external elastic laminae.

32 anular, granular, and infragranular cortical laminae.

33 ignals that guide neuronal migration to form laminae.

34 g that distinctly varied between regions and laminae.

35 teries and associated with thickened elastic laminae.

36 o simultaneously measure activity across all laminae.

37 s vFHs (26 g) also activated the superficial laminae.

38 ally attract neural processes to specific FB laminae.

39 ity in cellular phenotype within and between laminae.

40 y in vascular cells that produce the elastic laminae.

41 ults in the permanent disorganization of its laminae.

42 entral terminals innervating all dorsal horn laminae.

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

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

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

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

47 Retinal laminae across horizontal and vertical meridians were me

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

49 , including prominent spinopostyzgopophyseal laminae (also present in non-tetanurans and metriacantho

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

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

52 are nanostructurally distinct between spinal laminae and across age groups.

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

54 orn V3 INs became fate-restricted to ventral laminae and displayed mostly descending and local commis

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

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

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

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

59 Group 3 spiders had laminae and some evidence of reduced medullae and mushro

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

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

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

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

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

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

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

67 llae and premaxillae with facial and palatal laminae, and that these bones underwent divergent evolut

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

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

70 Elastic laminae are extracellular matrix constituents that not o

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

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

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

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

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

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

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

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

79 for blue wing color, we found that thickened laminae caused a color shift from brown to blue.

80 n to the arterial wall and how local elastic laminae defects may contribute to cardiovascular disease

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

82 ypes as well as neurons located in different laminae display distinct stimulus response profiles.

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

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

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

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

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

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

89 However, sensitivity in V1 is higher in the laminae (extragranular) and recording modalities (local

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

91 cle cells (SMCs) produce the layered elastic laminae found in elastic arteries but synthesize little

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

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

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

95 6 and 7 (GluR5,6,7) in relation to SP within laminae I and II in the rat trigeminal dorsal horn.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 - 4.0 (7-75) minutes in 9 neurons located in laminae I-II, and 9 neurons located in laminae III-V.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Laminae I/II INs drive chemical itch-induced scratching,

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

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

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

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

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

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

148 Activity mapping suggested dorsal horn laminae II-IV was activated in females but showed net in

149 l parasympathetic nucleus (SPN), dorsal horn laminae II-IV, and dorsal commissural nucleus (SDCom).

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

151 INs drive chemical itch-induced scratching, laminae II/III INs generate paw withdrawal movements, an

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

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

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

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

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

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

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

159 urons located deeper within the dorsal horn (laminae III-IV) are important for both types of injuries

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

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

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

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

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

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

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

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

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

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

170 I INs generate paw withdrawal movements, and laminae III/IV INs modulate dynamic corrective reflexes.

171 d in nonnociceptive Abeta fibers that target 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 o measure neural activations across cortical laminae in M1 while participants either tapped their thu

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

176 ng Sm22aCre resulted in depletion of elastic laminae in the arterial wall with the exception of the I

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

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

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

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

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

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

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

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

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

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

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

191 elements converge on specific cell types and laminae involved in cerebral cortical expansion.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 ers had the most complex systems, with large laminae, medullae formed from optical glomeruli, and rob

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

208 ventrally extending dendrites of superficial laminae neurons.

209 Group 2 spiders had large laminae, no medullae and large mushroom bodies.

210 Group 1 spiders had small, underdeveloped laminae, no medullae, and no mushroom bodies.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 aneously record neuronal activity across all laminae of the spinal dorsal horn.

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

230 her connect ipsilaterally to retinorecipient laminae of the tectum and pretectum or bilaterally to bo

231 4-binding C fiber populations in superficial laminae of the thoracic dorsal horn.

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

233 rostat, a structure consisting of aggregated laminae of unidirectional muscle fibers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

249 gray matter, in particular its intermediate laminae, represents a growth-promoting environment for s

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

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

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

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

254 these data provide a spatiotemporal map for laminae-specific molecules and suggest that diverse neur

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

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

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

258 nical organ (SFO) and the organum vasculosum laminae terminalis (OVLT) are two sensory circumventricu

259 d gliovascular markers of organon vasculosum laminae terminalis (OVLT) in three planes.

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

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

262 this is mediated via the organum vasculosum laminae terminalis (OVLT).

263 greater activity in the superficial and deep laminae than the innocuous control (30 degrees C).

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

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

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

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

268 e-dimensional soft bodies by simply adhering laminae to their surfaces.

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

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

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

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

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

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

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

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

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

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

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

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

281 Segmentally, the CSP to contralateral laminae VII and IX preferentially innervated C5-C7, whic

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

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

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

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

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

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

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

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

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

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

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

293 In addition, up to seven laminae were evident in the dentate gyrus.

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

295 redominantly activated intermediate and deep laminae whereas noxious vFHs (26 g) also activated the s

296 on and genetic regulation of butterfly scale laminae, which are simple photonic nanostructures.

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

298 in auditory cortices were stronger in deeper laminae, while attentional influences were greatest at t

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

300 anical stimuli were also detected across the laminae with the technique, as were the effects of the a