ライフサイエンスコーパス: cell layer

1 d increase in amacrine cells in the ganglion cell layer.

2 terial passage through the plant's epidermal cell layer.

3 rved just below and medial to the inner hair cell layer.

4 cell on the neural aspect of the inner hair cell layer.

5 the hippocampal dentate gyrus (DG) granular cell layer.

6 device to promote adhesion of an immobilized cell layer.

7 eneration of a complete polarized epithelial-cell layer.

8 used to determine the area of the confluent cell layer.

9 pecially prevalent in the innermost ganglion cell layer.

10 cell divisions within the luminal epithelial cell layer.

11 l migration in sepsis beyond the endothelial cell layer.

12 r plexiform layers, rather than the ganglion cell layer.

13 ns and the reduction of the endosperm to one cell layer.

14 particle translocation across an endothelial cell layer.

15 te gyrus and of somatic depth in the granule cell layer.

16 y regulating the excitability of the granule cell layer.

17 in that was predominantly in the endothelial cell layer.

18 with the highest expression noted in the CA3 cell layer.

19 torial and temporal diversity in the granule cell layer.

20 counting the neurons of the retinal ganglion cell layer.

21 d in the molecular layer, hilus, and granule cell layer.

22 elium, without altering the integrity of the cell layer.

23 ll-purification steps or support by a feeder cell layer.

24 istent with lack of HOXA5 expression in this cell layer.

25 rocesses and with visibility on the measured cell layer.

26 bistratified ganglion cells in the ganglion cell layer.

27 terial passage through the plant's epidermal cell layer.

28 tex, and in cerebellum, notably the Purkinje cell layer.

29 a distinct human-specific outer radial glia cell layer.

30 illumination of samples composed of multiple cell layers.

31 erences were measured between live and fixed cell layers.

32 ng circular cell-free areas within confluent cell layers.

33 part of the cell wall of the outer epidermal cell layers.

34 d collagen II and aggrecan deposition in the cell layers.

35 to restrict the rhizobium release to precise cell layers.

36 nts induced damage in cocultured endothelial-cell layers.

37 glucosinolate importers in these peripheral cell layers.

38 ow reduced suberin staining and disorganized cell layers.

39 action of hormones that can target distinct cell layers.

40 cortex and endodermis, as well as additional cell layers.

41 r volumes of aqueous solutions on epithelial cell layers.

42 rather than ion transport across epithelial cell layers.

43 diterpene products into the peripheral root cell layers.

44 is is due to expansion of the differentiated cell layers.

45 d a 2-layer hydrogel with 344SQ and vascular cell layers.

46 dary depletion of the granular and molecular cell layers.

47 rmis and proceeded to include outer cortical cell layers.

48 neuropil layers and weakly stained pyramidal cell layers.

49 was in the hippocampal pyramidal and granule cell layers.

50 ity of large-caliber neurons only (pyramidal cells, layers 3 and 5).

51 might aid PRR-mediated immune activation in cell layers adjacent to infection sites.

52 transfer cell layer (BETL), and the aleurone cell layer (AL).

53 p63 is highly expressed in the epithelial cell layer and acts as a molecular switch that initiates

54 oblasts show retention of procollagen in the cell layer and associated dilated endoplasmic reticulum.

55 ed a strong DNM1L expression in the ganglion cell layer and axons, and comparison between 3-month-old

56 rriers presented by the vascular endothelial cell layer and by the aberrant nature of tumor blood ves

57 gions of reduced cellularity in the ganglion cell layer and damage to optic nerves.

58 rom the subgranular zone through the granule cell layer and ensheathe local synapses and vasculature

59 of GFP-tagged alpha-syn in retinal ganglion cell layer and in the edges of arterial blood vessels in

60 have their soma exclusively in the ganglion cell layer and include a small proportion of bistratifie

61 d immunoreactive cell bodies in the ganglion cell layer and inner nuclear layer and immunoreactive pr

62 hickness (-7.8 mum) and that of the ganglion cell layer and inner plexiform layer (GCIP, -11.3 mum),

63 Atrophy of the macular ganglion cell layer and inner plexiform layer (GCIPL) was -16.42

64 cally, the thickness of the retinal ganglion cell layer and inner plexiform layer (GCL + IPL).

65 The ganglion cell layer and inner plexiform layer thicknesses could p

66 ty (IR) was most noticeable in the pyramidal cell layer and interspersed interneurons, especially tho

67 al synaptic organization between the granule cell layer and its main targets, the Purkinje cells, Gol

68 ed with significant thinning of the ganglion cell layer and nerve fiber layer, as well as a thickenin

69 nal divisions in this lateral root primordia cell layer and perturbed the formation of QC precursor c

70 oliferation of cells in the basal epithelial cell layer and pilosebaceous units of healing tissue.

71 s uncoupled from the folding of the Purkinje cell layer and the basement membrane, leading to disorga

72 y acid analysis of the dentate gyrus granule cell layer and the CA1 pyramidal layer with a 20-mum pix

73 l layer, but only postnatally in the granule cell layer and the dentate nucleus.

74 e dentate gyrus corresponding to the granule cell layer and the subgranular zone and, contrary to pre

75 aquaporin-1 (AQP1), presumably in the ductal cell layer and/or in surviving acinar cells, to drive tr

76 er transport across NCI-H441 lung epithelial cell layers and apical surface liquid (ASL) volumes are

77 intercalation of filopodia into mesothelial cell layers and cell invasion.

78 Instead, the SHR proteins moved multiple cell layers and determined the number of cortex, not end

79 The interwoven organization of the cell layers and extensive extracellular matrix (ECM) for

80 ein allocation, greater numbers of mesophyll cell layers and higher cell mass densities.

81 channeled through the cortex and endodermal cell layers and this movement is dependent on the vacuol

82 the device and first absorbed by the Caco-2 cell layer, and then metabolized by the primary hepatocy

83 spermatogonia, which form part of the basal cell layer, and those with the lowest sensitivity being

84 nuclei in inner nuclear and retinal ganglion cell layers, and HDAC2 activity accounted for approximat

85 half of the calretinin cells in the ganglion cell layer are bistratified ganglion cells resembling th

86 he calretinin positive cells in the ganglion cell layer are ganglion cells, and 20% are displaced ama

87 ype(s) expressing calretinin in the ganglion cell layer are yet to be determined.

88 different endothelial-cell and smooth-muscle-cell layers are coupled.

89 f the reeler mutant, the cadherin-expressing cell layers are dispersed in the radial dimension, where

90 After the four somatic cell layers are generated properly through successive pe

91 influential theoretical work on the granule cell layer as a combinatorial expander, where each granu

92 yers III, IV, and V) and cerebellum (granule cell layer), as well as the caudate nucleus in humans an

93 sa typically originates in the proliferative cell layer at the basement membrane and extends to the u

94 d cells showing palisading in the peripheral cell layer at the dermoepidermal junction and/or in the

95 ification into two layers at E15.5 and three cell layers at E18.5, intermediate cells differentiated

96 cell periphery in a narrow zone of about two cell layers at the nodule apex.

97 of LH to receptors that are located up to 10 cell layers away from the oocyte lowers oocyte cGMP and

98 endosperm (SE), the basal endosperm transfer cell layer (BETL), and the aleurone cell layer (AL).

99 mor section"-like culture by incorporating a cell layer between two diffusion barriers, where an oxyg

100 retinal ganglion cells, because the ganglion cell layer binds D1 and D2 receptor ligands, and display

101 l for electrical uniformity within the given cell layer, but homogenization may be limited by biophys

102 c interneurons in or adjacent to the granule cell layer, but not with the loss of parvalbumin-positiv

103 sed prenatally in the molecular and Purkinje cell layer, but only postnatally in the granule cell lay

104 nfirmed migration of cap cells into the body cell layer, but showed their subsequent preferential eli

105 leukocyte migration through the endothelial cell layer by 93%.

106 umbers of FJ-positive neurons in hippocampal cell layers CA1, CA2 and CA3 (p<0.05 vs Sham) in young a

107 with spatially restricted 344SQ and vascular cell layers confirmed that observed cluster morphologica

108 ferentiated into photoreceptors and formed a cell layer connected with host retinal neurons.

109 ession of DIO2 in the hypothalamic ependymal cell layer containing tanycytes.

110 approach may reconstitute a light-sensitive cell layer de novo and hence repair a structurally damag

111 munoreactivity in the molecular and Purkinje cell layers, demethylation of genome-wide repetitive LIN

112 independent of adrenals in the CA1 pyramidal cell layer, dentate gyrus polymorphic layer, bed nucleus

113 by hyperoxia, but to local retinal ganglion cell layer-derived VEGF.

114 loss of glutamatergic neurons in hippocampal cell layers, diminished loss of inhibitory interneurons

115 al. (2014) show that the basal myoepithelial cell layer directs the final maturation of the adjacent

116 us deletion of LIS1 exhibited robust granule cell layer dispersion, and adult-born granule cells labe

117 It subsequently interacted with the MCF-7 cell layer, distributed in the lung, heart and fat tissu

118 king activity that sweep across the ganglion cell layer during a limited period of development before

119 to recruit an entirely exogenous mesothelial cell layer during development.

120 ous species, the endosperm is reduced to one cell layer during seed maturation and reserves such as o

121 a collagenous stroma and an innermost single-cell layered endothelium and providing 2/3 of the refrac

122 The epicardium, a mesothelial cell layer enveloping the myocardium, is activated to pr

123 The epicardium is a mesothelial cell layer essential for vertebrate heart development an

124 ess involving coordinated epithelial surface cell layer expansion and mesenchymal deep cell intercala

125 etwork and localized adjacent to endothelial cell layer expressing CD31, indicating potential roles o

126 he fovea, neuronal densities in the ganglion cell layer form a broadly ovoid and asymmetric plateau i

127 rmined the number of cortex, not endodermal, cell layers formed in the root.

128 Ramifying terminals branched in the squamous cell layer, forming horizontal fibers that ran parallel

129 ll surfaces of the human body to protect the cell layer from a myriad of insults.

130 gnificantly thinner RNFL (nasally), ganglion cell layer (GCL) (nasally and temporally), inner plexifo

131 , the dentate gyrus (DG) including a granule cell layer (GCL) and a molecular layer (ML) that continu

132 (dpf), and was mainly found in the ganglion cell layer (GCL) and inner part of the inner nuclear lay

133 on laser-microdissected hippocampal granule cell layer (GCL) and on plasma, at different time points

134 acrine cells, one positioned in the ganglion cell layer (GCL) and the other in the inner nuclear laye

135 resolve into a single-cell retinal ganglion cell layer (GCL) are not well understood.

136 ining and supported for the retinal ganglion cell layer (GCL) by laser capture microdissection (LCM)

137 natorial expansion by the cerebellar granule cell layer (GCL) is fundamental to theories of cerebella

138 u(2J) mutation on PC layer (PCL) and granule cell layer (GCL) neuronal spiking activity and, also, in

139 sion of Npas2 and Adcy1 mRNA in the ganglion cell layer (GCL) of the retina.

140 cysts were seen parafoveally in the ganglion cell layer (GCL) or nerve fiber layer (NFL) in 4 eyes.

141 synapses on granule cells within the granule cell layer (GCL) that can be activated by orthodromic st

142 thinned (<30% of normal thickness) ganglion cell layer (GCL) that colocalized in 7 of 8 eyes with a

143 e fiber layer (RNFL) thickness, the ganglion cell layer (GCL) thickness, macular thickness and visual

144 GN and glial number, and DG and granule cell layer (GCL) volumes were stereologically estimated.

145 r normal stopping site at the inner granular cell layer (GCL), and became misplaced in the outer GCL

146 tinal nerve fiber layer (RNFL), the ganglion cell layer (GCL), and choroid thickness (CT) in patients

147 race- and NeuN-stained cells in the ganglion cell layer (GCL), and RBPMS is not expressed in syntaxin

148 ing of total macula, central fovea, ganglion cell layer (GCL), ganglion cell complex (GCC), and some

149 eled fibers were found mostly in the granule cell layer (GCL), not the GL.

150 ostratified cells with somas in the ganglion cell layer (GCL).

151 ) and a few cell bodies were in the ganglion cell layer (GCL).

152 Experiments are conducted in parallel using cell layers grown and stimulated under the same conditio

153 Each cell layer has a specialized function in mediating diges

154 llel activity profiling for oxygen consuming cell layers has been recently developed for extracellula

155 ained neurons per hippocampus in the granule cell layer, hilus, and pyramidal cell layer of CA3, CA2,

156 The thicknesses of the ganglion cell layer (I3 and N6 sectors), inner plexiform layer (S

157 role for Fat4 and Dchs1 in signaling between cell layers, implicate Dchs1 as a Fat4 receptor for stro

158 ration of neutrophils through an endothelial cell layer in vitro.

159 to examine neuronal atrophy in the ganglion cell layer in wild-type and Bax-deficient mice.

160 form of extracellular matrix that underlies cell layers in nearly all animal tissues.

161 ked thinning of the nerve fiber and ganglion cell layers in the inferior retinas.

162 NCR169 was induced in the cell layers in which bacteroid elongation was most prono

163 neuron density in the dentate gyrus granule cell layer, increased proliferation of granule cell prec

164 i67(+) cells in the basal and the suprabasal cell layers, increased loricrin expression, and also inc

165 ve fiber layer as well as composite ganglion cell layer+inner plexiform layer thicknesses in the eyes

166 , mGCL, and mIPL parameters and the ganglion cell layer-inner plexiform layer (mGCL-IPL) was determin

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

168 tifying extracellular changes in endothelial cell layer integrity following the activation of the pro

169 hese findings prioritize the loss of granule cell layer interneurons for further testing as a potenti

170 s under the retinal pigment epithelial (RPE) cell layer is a pathognomonic feature of AMD.

171 ntibodies, and antibody transport across the cell layer is dramatically increased upon addition of to

172 elopment suggests that PSP1 activity in this cell layer is essential in pollen development.

173 the inner nuclear layer and in the ganglion cell layer is glutamic acid decarboxylase-positive and s

174 r show that although MP activity in a single-cell layer is sufficient to promote polarity convergence

175 Collective migration of mechanically coupled cell layers is a notable feature of wound healing, embry

176 The spreading of mesenchymal-like cell layers is critical for embryo morphogenesis and tis

177 ns are generated, but their integration into cell layers is disrupted.

178 Mechanical coherence of cell layers is essential for epithelia to function as ti

179 affecting Vmem of the ectoderm and no other cell layers is sufficient to cause CFAs, but only during

180 The shedding of epithelial cell layers is usually effective for controlling biofilm

181 ng its reserve HFSCs and SC-inhibitory inner cell layer, is lost.

182 f inhibition and gain throughout the granule cell layer, it is not known whether this spontaneous act

183 of marked atypia on melanocytes in the basal cell layer; it presented with lower ABCD Total Dermoscop

184 t root tips, accumulation of Na in the outer cell layers likely contributed to reduction of Na in inn

185 ntrast to other ECs, which form a continuous cell layer, liver sinusoidal ECs (LSECs) constitute disc

186 Backscatter at the basal epithelial cell layer measured by IVCM predicts the need for EK aft

187 nerve fiber layer (mRNFL), macular ganglion cell layer (mGCL), macular inner plexiform layer (mIPL),

188 f the outer retina beginning at the ganglion cell layer (n = 1), outer plexiform layer (n = 4), outer

189 Quantitation of retinal ganglion cell layer neurons in young mice confirmed age-related r

190 mice, which had 20.8% more retinal ganglion cell layer neurons than non-transplanted AD controls.

191 filament-tau, and decreased retinal ganglion cell layer neurons.

192 creased oxidative damage in retinal ganglion cell layer neurons.

193 blocks free diffusion across the epithelial cell layer, occurred.

194 eld potentials from the dorsal CA1 pyramidal cell layer of 7- to 8-month-old wild-type and rTg4510 mi

195 eld potentials from the dorsal CA1 pyramidal cell layer of 7-8 month old wild-type and rTg4510 mice a

196 the granule cell layer, hilus, and pyramidal cell layer of CA3, CA2, and CA1 subfields.

197 erior-localized clonal cells in the follicle cell layer of developing ovarioles with down-regulated e

198 uronal thinning was observed in the ganglion cell layer of eyes affected by acute optic neuritis 3 an

199 profilaggrin in the differentiating granular cell layer of human skin.

200 phic distribution of neurons in the ganglion cell layer of insectivorous, nectarivorous, and frugivor

201 ressed in the inner nuclear and the ganglion cell layer of marmoset retina, however, the specific cel

202 ofluorescence detected TP in the endothelial cell layer of MCA.

203 aging of neuronal activity, in the pyramidal cell layer of mouse hippocampal in vitro preparations, d

204 ication, was reduced in the retinal ganglion cell layer of MS patients and in a transgenic mouse mode

205 K expression was detected in the endothelial cell layer of nonatherosclerotic vessels but was absent

206 The outermost cell layer of plants, the epidermis, and its outer (late

207 spaces, including the vascular smooth muscle cell layer of rat and pig coronary arteries, promotes va

208 We report that in the ganglion cell layer of rat retinas, all spiking amacrine interneu

209 sory information transmission in the granule cell layer of the cerebellum.

210 ion in hippocampus, cortex, and the Purkinje cell layer of the cerebellum.

211 iciency of adult neurogenesis in the granule cell layer of the dentate gyrus and rescues hippocampal

212 The ameloblast cell layer of the enamel organ is in contact with the fo

213 the retinal specializations in the ganglion cell layer of the giraffe.

214 tenascin-R (TNR) is produced in the granule cell layer of the OB and that its expression increases d

215 ted in impaired neurogenesis at the granular cell layer of the olfactory bulb and the DG in the adult

216 ution of somatic mesoderm to the mesothelial cell layer of the PE.

217 n, ABCA1 is highly expressed in the ganglion cell layer of the retina, a finding consistent with it h

218 was predominantly localized to the ganglion cell layer of the retina, the cell type most affected by

219 tein accumulates in the epidermis, the outer cell layer of the root, and also in the pericycle cells

220 to reduce arsenate to arsenite in the outer cell layer of the root, facilitating efflux of arsenic a

221 ochlear epithelium, forming the intermediate cell layer of the stria vascularis.

222 dosperm (nkd) mutants produce multiple outer cell layers of partially differentiated cells that show

223 lopment of the exine occurs in the innermost cell layers of the anther, direct observations of this p

224 ocalized to the epidermal and outer cortical cell layers of the DTZ in the Al-resistant NIL, and the

225 ree diffusion of molecules between the inner cell layers of the root and the outer environment.

226 t is transmitted from the outer to the inner cell layers of the root.

227 es was limited to the epidermal and palisade cell layers of the seed coat.

228 in dense surface-attached communities where cells layer on top of one another such that only those a

229 morphology and the arrangement of epidermal cell layers, on whose activity cuticle formation depends

230 , and RPE (P = 0.0001), and thicker ganglion cell layer (P = 0.003) and outer plexiform layer (OPL) (

231 ity set point angle, differences in cortical cell layer patterning, stem cell niche structure, and ra

232 sts another germinal site along the Purkinje cell layer (PCL), in which Bergmann glia are generated u

233 the retinal nerve fibre layer, the ganglion cell layer plus inner plexiform layer, the INL plus oute

234 Theta burst stimulation of the granule cell layer potentiated CA3 responses not only to granule

235 rast, theta burst stimulation of the granule cell layer potentiated responses throughout the molecula

236 antially enrich our understanding of granule cell layer processing, which seems to promote spatial gr

237 ption factor determines the number of cortex cell layers produced in the roots of B. distachyon and O

238 igration, translocation to the photoreceptor cell layer, proliferation, and phagocytosis of dying cel

239 Their genes are expressed in peripheral cell layers prone to pathogen entry and are lineage spec

240 Ganglion cell layer reduction was associated with increased axona

241 The mean thickness of each ganglion cell layer region was correlated to the mean thickness o

242 orithm, the thickness of 66 macular ganglion cell layer regions and the thickness of 12 peripapillary

243 tions in both the inner nuclear and ganglion cell layers, respectively, and to distinguish them from

244 t various light intensities in the BHJ solar cell layer reveals that Ba prevents trap assisted Shockl

245 inal nerve fiber (RNFL) and retinal ganglion cell layer (RGCL) in the macula were segmented using an

246 isin supporting interactions between retinal cell layers, so disassembly would prevent structural cou

247 otentiated CA3 responses not only to granule cell layer stimulation but also to perforant path stimul

248 liferation leading to numerous, disorganized cell layers, suggesting a synergistic interaction betwee

249 owever, high levels of EC-SOD in the granule cell layer supported normal maturation of newborn neuron

250 Hyaluronan was present in the smooth muscle cell layer surrounding the pulmonary vasculature and in

251 Bundle sheath (BS) cells form a single cell layer surrounding the vascular tissue in leaves.

252 tein is specifically expressed in the anther cell layers surrounding the meiocytes and microspores, s

253 which establish dynamic and highly organized cell layers surrounding the oocyte.

254 listic structural context of (1) the granule cell layer that contains all somata and (2) the molecula

255 as cells located >100 mum from the Purkinje cell layer that did not exhibit complex spikes.

256 d events: expansion of the cumulus granulosa cell layer that encloses the oocyte and meiotic maturati

257 The intestinal epithelium is a single cell layer that facilitates the absorption of nutrients

258 The endodermis is the innermost cortical cell layer that features rings of hydrophobic cell wall

259 tages Xenopus displays a superficial granule cell layer that is not proliferative and expresses both

260 onductance and gradients at key "gatekeeper" cell layers that impact on whole plant water flow and pl

261 ng a highly restricted zone, essentially one cell layer thick, immediately below the lamina I/II bord

262 Assessment of ganglion cell layer thickness by OCT after ON onset can be used a

263 The ganglion cell layer thickness was inversely correlated with disea

264 The retinal nerve fiber layer and ganglion cell layer thicknesses were inversely correlated with th

265 at the extra-embryonic epithelial enveloping cell layer, thought mainly to provide protection to the

266 confluent normal rat kidney (NRK) epithelial cell layer to osmotic stress are studied by both convent

267 in layers spanning from the retinal ganglion cell layer to outer plexiform layer (standardized beta =

268 bles random neuronal networks in the granule cell layer to provide the necessary signal separation an

269 h chemical and mechanical cross talk between cell layers to allow for development of new lateral orga

270 esophageal mucosa of controls (median, 25.5 cell layers to surface; interquartile range [IQR], 21.4-

271 patients with NERD-both distal (median, 9.5 cell layers to surface; IQR, 1.5-13.3; P < .0001 vs ERD,

272 21.4-28.8) vs patients with ERD (median, 23 cell layers to surface; IQR, 16-27.5), or patients with

273 16-27.5), or patients with BE (median, 21.5 cell layers to surface; IQR, 16.1-27.5).

274 BE, and controls) and proximal (median, 5.0 cell layers to surface; IQR, 2.5-9.3 vs median 10.4 cell

275 yers to surface; IQR, 2.5-9.3 vs median 10.4 cell layers to surface; IQR, 8.0-16.9; P = .0098 vs cont

276 cer metastasis, clearance of the mesothelial cell layer, to examine the clearance ability of a large

277 endothelium have illuminated how this single cell layer toggles between quiescence and activation to

278 ted immature neurons repopulated the granule cell layer upon termination of the toxin treatment.

279 , we quantify the contributions of different cell layers, using the measured parameters.

280 oliferation, resulting in decreased neuronal cell-layer volume resembling microcephaly.

281 Neuropil and cell layer volumes were reduced in cornu ammonis (CA)1 a

282 f the adult-born neurons through the granule cell layer was only altered in wild-type mice.

283 coefficient of value (CV) of the endothelial cell layer were calculated by the instruments' built-in

284 somas in the inner nuclear and the ganglion cell layer were filled with the lipophilic dye DiI.

285 ular, formation of the suprabasal epithelial cell layer were impaired.

286 axosomatic symmetric synapses in the granule cell layer were reconstructed from serial electron micro

287 l thickness and cell numbers in the ganglion cell layer were reduced in the IGFBP-3 KO mice.

288 Recombined cells in the hippocampal granule cell layer were visualized and quantified by yellow fluo

289 The distal cell layer where the receptors accumulate at the cell pe

290 tissue-specific strategy to identify the key cell layers where ABA signaling acts to regulate growth.

291 the superficial portion of the CA1 pyramidal cell layer, whereas it is absent from deep-layer cells.

292 olk cell and defects in the outer enveloping cell layer, which are both known mediators of epiboly mo

293 es as they transition to a mature protective cell layer, which includes a marked increase in NO dilat

294 expression of Sox4 and Sox11 in the ganglion cell layer while deletion of Brn3b has no effect on the

295 er wall, which comprises the outer epidermal cell layer, whose turgor pressure is related to its hydr

296 ke cells typically had somas in the ganglion cell layer, with 23% displaced to the inner nuclear laye

297 ce modulates H3ac and H3K4me3 in the granule cell layer, with concomitant rescue of both the neurogen

298 ternalised and transported across the Calu-3 cell layers, with B12 conjugation not only enhancing cel

299 tivated interneurons were distributed across cell layers, with somatostatin-expressing cells predomin

300 that form the inner luminal and outer basal cell layers, with stem and progenitor cells contributing