ライフサイエンスコーパス: cell layer

1 calized underneath the specialized suberized cell layer.

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

3 torial and temporal diversity in the granule cell layer.

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

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

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

7 rocesses and with visibility on the measured cell layer.

8 bistratified ganglion cells in the ganglion cell layer.

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

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

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

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

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

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

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

16 device to promote adhesion of an immobilized cell layer.

17 eneration of a complete polarized epithelial-cell layer.

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

19 pecially prevalent in the innermost ganglion cell layer.

20 cell divisions within the luminal epithelial cell layer.

21 rmation about the cell growth in a confluent cell layer.

22 taining homeostasis across the photoreceptor cell layer.

23 cells within an otherwise normal epithelial cell layer.

24 representing the average capacitance of the cell layer.

25 age of this processing occurs in the granule cell layer.

26 he retinal nerve fiber layer and/or ganglion cell layer.

27 and in scattered cells within the epithelial cell layer.

28 on cells in the Nubian ibex retinal ganglion cell layer.

29 ent neuron reduction in the retinal ganglion cell layer.

30 igrate inwardly to form the internal granule cell layer.

31 s, and a reduced thickness of the epithelial cell layer.

32 opulations rather than dispersing within the cell layer.

33 fect is associated with increased epithelial cell layers.

34 ity for albumin within confluent endothelial cell layers.

35 echanical forces, albeit active in different cell layers.

36 correlated with a reduced number of cambial cell layers.

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

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

39 dary depletion of the granular and molecular cell layers.

40 rmis and proceeded to include outer cortical cell layers.

41 neuropil layers and weakly stained pyramidal cell layers.

42 was in the hippocampal pyramidal and granule cell layers.

43 illumination of samples composed of multiple cell layers.

44 erences were measured between live and fixed cell layers.

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

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

47 to restrict the rhizobium release to precise cell layers.

48 nts induced damage in cocultured endothelial-cell layers.

49 glucosinolate importers in these peripheral cell layers.

50 ns dominate and hinder formation of discrete cell layers.

51 nodule organogenesis initiated in inner root cell layers.

52 intaining distinct epithelial and fibroblast cell layers.

53 , with alpha equaling ~0.050 in the ganglion cell layer, ~0.122 in the inner plexiform layer (IPL), ~

54 ted, with schitic spaces within the ganglion cell layer (13/17 eyes; 76.5%) observed to be perifoveal

55 s (calcium indicator GCaMP6s, 10 Hz, 100-250 cells, layer 2/3 of primary visual cortex, i.e., V1) in

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

57 s in the retinal pigment epithelium (RPE), a cell layer adjacent to the photoreceptor outer segments,

58 11 d, is confined to one to three endosperm cell layers adjacent to the embryonic scutellum.

59 tant corneal epithelium contained 1-2 or 2-3 cell layers after Dox induction from embryonic day 0 (E0

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

61 lum and brainstem revealed a reduced granule cell layer and a reduction in size of pontine nuclei.

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

63 eptor, neuron number in the retinal ganglion cell layer and axon number in the optic nerve were marke

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 CPE) associated to the interface between the cell layer and the electrolyte.

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

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

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

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

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

84 gradient from the epidermis to the interior cell layers, and this gradient is essential for the stem

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 Skin and other epithelial cell layers are frequently subjected to extensive deform

91 outer plexiform, inner nuclear and ganglion cell layers are the strongest biomarkers for discriminat

92 hibitory interneuron observed in the granule cell layer, are well suited to perform normalization or

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

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

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

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

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

98 littermate controls, which consisted of 5-6 cell layers at postnatal day 21 (P21), the mutant cornea

99 rked atrophy of the nerve fiber and ganglion cell layers at the central macula.

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

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

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

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

104 cifically labels all neurons in the ganglion cell layer but is largely excluded from otherwise molecu

105 ier function typically requires a contiguous cell layer but since teeth penetrate the oral epithelium

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

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

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

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

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

111 t only saponin alters the capacitance of the cell layer by two orders of magnitude.

112 e extracellular matrix underlying epithelial cell layers can strongly affect the speed and morphology

113 Hence, cell layer capacitance and TEER represent two independen

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

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

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

117 In our model, utilizing heterogeneous cell-layer contractility and elastic moduli values based

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

119 ion and their migration into the subgranular cell layer demonstrating that MCs-generated Shh is a key

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

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

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

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

124 Furthermore, the ependymal cell layer does not form in the conditional knockout, re

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

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

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

128 rther, that this shift occurs throughout the cell layer, even in regions where associated changes in

129 nction (TJ) formation between the enveloping cell layer (EVL) and the yolk syncytial layer (YSL) in t

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

131 the sole source of inhibition to the granule cell layer, express both nicotinic and muscarinic cholin

132 r, transports immunoglobuline G (IgG) across cell layers, extending IgG half-life in circulation and

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

134 Ganglion cell layer, ganglion cell complex, and inner nuclear lay

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

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

137 pne5, 6, and 9 are expressed in the ganglion cell layer (GCL) and inner nuclear layer (INL) in both a

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

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

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

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

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

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

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

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

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

147 er (RNFL) thickness measurement and ganglion cell layer (GCL) volume determination.

148 , in both eyes, a thickening of the ganglion cell layer (GCL) with a hyperreflective opacity as a cap

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

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

151 tinal nerve fiber layer (RNFL), the ganglion cell layer (GCL), and the choroidal thickness (CT).

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

153 erpixels thickness measurements for ganglion cell layer (GCL), ganglion cell/inner plexiform layer (G

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

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

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

157 s a density using the volume of the granular cell layer (GCLv) for standardization; and (d) these tot

158 Each cell layer has a specialized function in mediating diges

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

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

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

162 The endodermis is a key cell layer in plant roots that contributes to the contro

163 A specialized cell layer in roots called the endodermis, which has cel

164 pathways are distinguished, however, by the cell layer in which they operate - mesophyll at a two-ce

165 sented and linked to the constituents of the cell layer in which various electrical elements have bee

166 ts that the EAS is a dynamic zone from which cell layers in contact with the embryo are regularly eli

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

168 yed by distinct vascular beds and epithelial cell layers in response to infection by SARS-CoV-2 is st

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

170 a range within the epidermis and across the cell layers in which these peptides influence patterns.

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

172 nal nerve fiber layer thickness and ganglion cell layer - inner plexiform layer thickness).

173 cell layer volume (GCL, p = 0.003), ganglion cell layer - inner plexiform layer volume (GCL-IPL, p =

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

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

176 limit, vertical stacking of multiple memory cell layers, innovative device concepts, and novel mater

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

178 unctions, substrate adhesion, and epithelial cell layer integrity.

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

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

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

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

183 nd jammed, the leading edge of the advancing cell layer is shown to become progressively more migrato

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

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

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

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

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

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

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

191 curs at the electrode and declines with each cell layer, is present in thin biofilms (<5 um) and full

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

193 through the intestinal mucus and epithelial cell layer, leading to low absorption and bioavailabilit

194 nal Pigment Epithelium (RPE) in-vitro at the cell layer level using impedance spectroscopy measuremen

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

196 well as in the tumor, but within the wounded cell layer little is known about the link between mechan

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

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

199 retinal nerve fiber layer, macular ganglion cell layer (mGCL), and macular inner plexiform layer (mI

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

201 lation increased activity in cones, ganglion cell layer neurons, and cortical neurons, and enabled mi

202 ids undergo reduced proliferation, decreased cell layer number, urothelial program activation, and ac

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

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

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

206 el was also elevated in the retinal ganglion cell layer of aged M(1) receptor-deficient mice.

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

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

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

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

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

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

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

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

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

216 ed to transcriptomically profile the granule cell layer of the dentate gyrus (DG-GCL) in human hippoc

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

218 preproglucagon (PPG) neurons in the granule cell layer of the olfactory bulb.

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

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

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

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

223 ting and quantifying small RNAs in different cell layers of early developmental stage maize anthers t

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

225 H and qPCR revealed Ddr1 expression in basal cell layers of the oral epithelia and in immune cells.

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

227 oxorubicin-containing liposomes to the outer cell layers of the spheroids, followed by doxorubicin re

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

229 ate, as expected, a clear degradation of the cell layer opposed to a relative stability of the not lo

230 rrent inputs than GCs closer to the Purkinje cell layer (outer-zone GCs).

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

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

233 d: nerve fiber layer plexus (NFLP), ganglion cell layer plexus (GCLP), superficial vascular complex (

234 cting an integrate-and-fire model of granule cell layer population activity, we find that the directi

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

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

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

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

239 , A6 and A12 being capable of colonising the cell layer regardless of host species or disease status

240 ated with time from surgery for the ganglion cell layer region of interest (R = -0.74, P < 0.0001) an

241 esected brain tissue volume and the ganglion cell layer region of interest (R = -0.78, P < 0.0001) an

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

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

244 derlying cellular mechanism of lesion at the cell layer scale is analyzed by impedance spectroscopy.

245 se tissues are commonly composed of discrete cell layers-sheets of cells that are one-cell thick.

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

247 role not continuously, but when the granule cell layer starts receiving a high amount of excitatory

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

249 We then computed cell-layer stress distributions using finite element con

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

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

252 Recent evidence suggests that granule cell layer synaptic integration can be contextually modi

253 tigate the role of ACh in regulating granule cell layer synaptic integration in male rats and mice of

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

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

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

259 the model and the physiological state of the cell layer, the same procedure is applied to blue light

260 generation of a tensional 'skin', only a few cell layers thick, at the spheroid surface, which correl

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

262 Multivariate regression indicated ganglion cell layer thickness was a significant independent predi

263 Increased ganglion cell layer thickness was associated with worse BCVA.

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

265 integration and coordination across several cell layers through ligand-activated plasma membrane rec

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

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

268 ots and animal guts have evolved specialized cell layers to control mineral nutrient homeostasis.

269 e-dimensional mechanical model with multiple cell layers to interrogate the flattening of organs duri

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 totic activity decreases, from the center of cell layers to the edge.

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

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

279 ur cell sorting-based study of the epidermal cell layer transcriptome confirms that core UV-B stress

280 s total retinal volume (p = 0.037), ganglion cell layer volume (GCL, p = 0.003), ganglion cell layer

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

282 nd neurofilament H indicate that the granule cell layer was composed of two sublamina.

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

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

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

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

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

292 e sublamination of the molecular and granule cell layers, which is not observed in the domestic ferre

293 after germination in epidermal and mesophyll cell layers, which undergo endoreplication to increment

294 l nerve fiber layer and the retinal ganglion cell layer with spectral-domain optical coherence tomogr

295 uniform but that PIP2;5 may be saturated in cell layers with apoplastic barriers, i.e. the endodermi

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

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

300 rimordia (LRP) must traverse three overlying cell layers within the parent root.