ライフサイエンスコーパス: lamina

1 ual processing area of the insect brain (the lamina).

2 d of synaptic inhibition between adjacent EB lamina.

3 r elements (LINEs) to the neutrophil nuclear lamina.

4 constrained to the relative proximity of the lamina.

5 RNA, is pathogenic by disrupting the nuclear lamina.

6 rganization of the lamin meshwork within the lamina.

7 omains are in close contact with the nuclear lamina.

8 dynamic cytoskeletal networks to the nuclear lamina.

9 main of SUN2 that interacts with the nuclear lamina.

10 estrogen establish contacts with the nuclear lamina.

11 main of SUN2 that interacts with the nuclear lamina.

12 aining lineage-relevant genes to the nuclear lamina.

13 ear membrane in association with the nuclear lamina.

14 mined accurately due to lack of clear annual lamina.

15 etally while remaining attached to the basal lamina.

16 osuction and cultured onto both sides of the lamina.

17 meric repeats but not LINE-1 elements to the lamina.

18 ch one daughter loses contact with the basal lamina.

19 s into their role in scaffolding the nuclear lamina.

20 llular activity of antidromically-identified lamina 5b pyramidal-tract type neurons (n = 153) and int

21 are essential building blocks of the nuclear lamina, a filamentous meshwork lining the nucleoplasmic

22 tioned ribosomal DNA and mininucleoli to the lamina-a process that was closely associated with sharpl

23 Five patients received the decellularized lamina alone and 4 patients the recellularized lamina in

24 ve prelamin A processing, leading to nuclear lamina alterations, severe cardiovascular pathology, and

25 by multielectrodes covering several cortical lamina and averaged on spontaneous spikes of thalamocort

26 tude and phase differences between reticular lamina and basilar membrane vibrations are absent in pos

27 by recruiting the inactive X to the nuclear lamina and by doing so enables Xist to spread to activel

28 lamina reflects cell types elsewhere in the lamina and cell types described for other species of Eum

29 The nuclear lamina and chromatin interactions are regulated by estro

30 ole nucleated by deformations of the nuclear lamina and estimate the herniation of chromatin through

31 narrow fluid-filled space between reticular lamina and tectorial membrane.

32 t arises from shearing between the reticular lamina and the tectorial membrane.

33 ycan, which anchor the membrane to the basal lamina and underlying cytoskeletal proteins.

34 chromosomes localized away from the nuclear lamina and were not observed in checkpoint-deficient 293

35 t includes specialized taste buds, the basal lamina, and a lamina propria core with matrix molecules,

36 to basement membranes, the internal elastica lamina, and necrotic cores.

37 whereas, Igkappa remained sequestered at the lamina, and only at the pre-B cell stage located to cent

38 ceptor, an integral component of the nuclear lamina, and that this interaction is required for Xist-m

39 ual mitochondria, undulations in the nuclear lamina, and the HER2 receptor on membrane protrusions in

40 ded CGG repeats into FMRpolyG alters nuclear lamina architecture and drives pathogenesis in FXTAS.

41 rotein LAP2beta and disorganizes the nuclear lamina architecture in neurons differentiated from FXTAS

42 Such lamina-associated domains (LADs) are thought to help org

43 HNRNPU in mouse hepatocytes, the coverage of lamina-associated domains (LADs) in the genome increases

44 Studies have focused either on lamina-associated domains (LADs) or on topologically ass

45 By contrast, A and B compartments, lamina-associated domains and active enhancers and promo

46 te except for a few that are associated with lamina-associated domains and open chromatin.

47 ible euchromatin is protected from UV, while lamina-associated heterochromatin at the nuclear periphe

48 Lamina-associated polypeptide 1 (LAP1) is an integral pr

49 ctivator, the inner nuclear membrane protein lamina-associated polypeptide 1 (LAP1), are required for

50 sh binding of two TorsinA ATPase activators: lamina-associated protein 1 (LAP1) and its paralog, lumi

51 ory of identified BetaM interactors includes lamina-associated protein LAP-1, myocyte nuclear envelop

52 Thus, lamina associations influence internal nuclear organizat

53 meter vibrations directly from the reticular lamina at the apical ends of outer hair cells and from t

54 ng wave vibrates in phase with the reticular lamina at the best frequency, and results in maximal vib

55 pertransmission of light below the RPE-basal lamina band correlated with dissociated RPE.

56 was preceded by thickening of the RPE-basal lamina band.

57 specific reference segment external elastic lamina-based stent optimisation strategy was safe and re

58 acterized the rice (Oryza sativa) LESION AND LAMINA BENDING (LLB) gene that encodes a chloroplast-tar

59 l peri-implant epithelial sealing with basal lamina (BL) attachment at the interface of the implant a

60 astrocytes, and pericytes embedded in basal lamina (BL).

61 a-catenin/Wnt pathway activity in the dental lamina bulge.

62 low sharply tuned responses of the reticular lamina, but only a slow tuned response of the basilar me

63 and found average volumes of 6.5 mum(3) for lamina cells and 3.8 mum(3) for medulla cells.

64 hat communication between photoreceptors and lamina cells requires a signaling relay through glia.

65 keleton to the LINC complex and then through lamina-chromatin interactions to directly stretch chroma

66 rypanosomatid coiled-coil NUP-1 protein is a lamina component functionally analogous to lamins, the m

67 todomain shedding to become a synaptic basal lamina component.

68 ing NUP-2 as a second trypanosomatid nuclear lamina component.

69 To find additional trypanosomatid lamina components we identified NUP-1 interacting protei

70 t the inner nuclear membrane and the nuclear lamina contributes to the aging process.

71 we identify cells in different parts of the lamina corresponding to the three different regions of t

72 sitions into GIS 15.2 and 14, constrained by lamina counting, lasted 74 and 27 yr, respectively, both

73 en the excellent relative uncertainty of its lamina-counting chronology.

74 essel shift inside the ONH occurs within the lamina cribrosa (LC) or the prelaminar tissue.

75 an increased pressure difference across the lamina cribrosa (LC) related to a low intracranial press

76 y segmented (prelamina, choroid, sclera, and lamina cribrosa [LC]).

77 intracranial pressure (ICP) at the level of lamina cribrosa could have important implications for un

78 In glaucoma patients, lamina cribrosa depth changes are detected with similar

79 To determine whether: (1) change in lamina cribrosa depth occurs more frequently than change

80 Lamina cribrosa depth should be measured from an anterio

81 The trans-lamina cribrosa pressure difference (TLCPD) was calculat

82 Trans-lamina cribrosa pressure difference (TLCPD) was calculat

83 To estimate the pressures at the lamina cribrosa, geometrical distances were estimated fr

84 tinal layers, optic nerve head, choroid, and lamina cribrosa.

85 ch allows systematic integration of Hi-C and lamina-DamID data for complete three-dimensional genome

86 be directly observed in the original Hi-C or lamina-DamID data.

87 e chromosome conformation capture (Hi-C) and lamina-DamID experiments.

88 s or the LINC complex did not rescue nuclear lamina defects, a previously identified determinant of n

89 lear membrane ruptures at sites with nuclear lamina defects.

90 -/-) mice, which presented decreased elastic lamina degradation and aortic expansion.

91 heritable skin disease manifesting with sub-lamina densa blistering, erosions, and chronic ulcers.

92 ha3 IV), the GBM is irregularly swollen, the lamina densa is absent, and permeation is increased.

93 cate that size-dependent permeation into the lamina densa of the GBM and the podocyte glycocalyx, tog

94 nanoparticles show that permeation into the lamina densa of the GBM is size-sensitive.

95 Particles traversing the lamina densa tend to accumulate upstream of the podocyte

96 ized particles permeate extensively into the lamina densa.

97 ceptor degeneration, multilayered RPE, basal lamina deposits, and accumulations of monocytes/macropha

98 requency is an eigenvalue of the delaminated lamina determined only by the geometry of the delaminati

99 r defects including aberrant shapes, nuclear lamina disruption and reductions to peripheral heterochr

100 stem cells associated with the shark dental lamina (DL) emerge from a field of epithelial progenitor

101 c3) organizes heterochromatin at the nuclear lamina during cardiac progenitor lineage restriction.

102 that phosphorylation at this site increases lamina dynamics, providing a mechanistic explanation for

103 heterochromatin and nucleoli to the nuclear lamina facilitates the folding of the neutrophil genome

104 limited, there is evidence that the nuclear lamina filament protein Lamin A/C protects RB from prote

105 d of a stalagmite with well-developed annual lamina from Xinglong Cave, northern China, covering DO 1

106 different stiffness and the four-sublaminate lamina has a consistent global vibration mode.

107 e association of Rif1 with insoluble nuclear lamina has thus far hampered exhaustive characterization

108 e induces long-term synaptic facilitation in lamina I and II neurons within the rodent spinal dorsal

109 ced ADS in the monosynaptic C fiber input to lamina I neurokinin 1 receptor-expressing neurons (1-10

110 nd on miniature (m)EPSCs recorded from large lamina I neurons in horizontal spinal cord slices.

111 iated NMDA currents in spinal lamina IIo not lamina I neurons.

112 from low-threshold Abeta mechanoreceptors to lamina I output neurons.

113 nd cutaneous afferent synapses onto immature lamina I projection neurons, which convey nociceptive in

114 tiation (LTP) at sensory synapses onto adult lamina I projection neurons, which serve as a major outp

115 mouse primary afferent synapses onto mature lamina I projection neurons, which serve as a major outp

116 utaneous afferent synapses onto immature rat lamina I spino-parabrachial neurons, which serve as a ma

117 es within the Vc/C2 superficial dorsal horn (lamina I) 3 weeks post-CCI-ION.

118 the dorsal horn, besides KChIP3 in the inner lamina II and lamina III, we detected DPP10 in most proj

119 a-2 is associated with AMPARs at synapses in lamina II but excluded from those at C-fiber inputs, a v

120 ed from the somata of nociceptors and spinal lamina II excitatory interneurons, which sense and modul

121 with Kv4.3 in the cell bodies of a subset of lamina II excitatory interneurons, while KChIP1, KChIP2,

122 ociceptors and Kv4.2/Kv4.3 in certain spinal lamina II excitatory interneurons.

123 as boosted to the adapting-firing excitatory lamina II interneurons while GABAergic and glycinergic i

124 In the tonic-firing inhibitory lamina II interneurons, glutamatergic drive was reduced

125 Type I TARPs, evoked whole-cell currents in lamina II neurons, but such currents were severely atten

126 ype I TARP gamma-2 (stargazin) is present in lamina II of the superficial dorsal horn, an area involv

127 primed mice activates a subset of neurons in lamina III and IV of the dorsal horn that coexpress PAX2

128 n, besides KChIP3 in the inner lamina II and lamina III, we detected DPP10 in most projection neurons

129 t of GluN2B-mediated NMDA currents in spinal lamina IIo not lamina I neurons.

130 lamins are major constituents of the nuclear lamina in all metazoan cells, yet have specific roles in

131 vibration characters of the four-sublaminate lamina in macroscopic and microscopic mechanism.

132 py reveals a significantly disrupted nuclear lamina in postmortem tissue from human Alzheimer's disea

133 the ecto-AMPase activity in the nociceptive lamina in the brainstem.

134 perimentally demonstrate that the lower thin lamina in the white cover scales causes the blue iridesc

135 some chains and the filaments of the nuclear lamina, in situ.

136 Additionally, llb shows an increased lamina inclination and enhanced early seedling growth du

137 packing of epithelial cells along the basal lamina increases, but density is later restored by activ

138 ed in part through dynamic chromatin-nuclear lamina interactions and that competence of a progenitor

139 These include the loss of DNA-nuclear lamina interactions, the distension of centromeres, and

140 portion of CTCF associated with the nuclear lamina interacts with enhancer regions, limiting the for

141 mina alone and 4 patients the recellularized lamina into a femtosecond-assisted 9.5-mm diameter lamel

142 The nuclear lamina is a filamentous structure subtending the nuclear

143 The nuclear lamina is a fundamental constituent of metazoan nuclei.

144 ing structural stability to the nucleus, the lamina is involved in many nuclear activities, including

145 , the structural organization of the nuclear lamina is poorly understood.

146 Lamina IX boutons were also elevated in two frontopariet

147 Posterior movement of the lamina (LD-BM increase or LD-AS increase) occurred with

148 rting basement membrane and internal elastic lamina macromolecules with minimal deformation of the se

149 , hexoses, quercitol and starch) in the leaf lamina, main veins and twigs over 24 h.

150 ording to reference segment external elastic lamina measurements.

151 s suggest that disintegration of the nuclear lamina mediated by gamma134.5 promotes HSV replication.

152 s for carrying out spatial summation are the lamina monopolar cells (LMCs) of the first visual proces

153 ating heminodes in the distal osseous spiral lamina, NaV1.1 partly overlapped NaV1.6 and ankyrin-G.

154 on, as well as the spatiotemporal pattern of lamina neuron differentiation.

155 produce insulin-like peptides, which induce lamina neuronal differentiation.

156 nd Dscam2, which together repel dendrites of lamina neurons, L1 and L2, in the visual system.

157 ng their target field in the optic lobe, the lamina neurons, with a secreted differentiation cue, epi

158 The overall size of the lamina neuropil did not correlate with the size of its L

159 This ensures tiling of the lamina neuropil through heterotypic interactions.

160 malian genome is associated with the nuclear lamina (NL), it is interesting to study how native genes

161 The opening lacks nuclear lamina, nuclear pore complexes, and nuclear membrane, bu

162 5/28 [89%]) in whom anterior movement of the lamina occurred with the Bruch's membrane, but not the a

163 tion and mitophagy in the axons of the glial lamina of aged E50K(-tg) mice in vivo.

164 ing transition by stretching and imaging the lamina of isolated cell nuclei.

165 ex ridge-lamellar architectures in the upper lamina of the cover scales.

166 and ecto-AMPase activity in the nociceptive lamina of the trigeminal subnucleus caudalis (TSNC) in t

167 oriented along nanotube domains, or layered lamina or multiple cantilevered sheets).

168 tions suggests a mechanism by which abnormal lamina organization prevents the egress of these RNAs vi

169 re weak membrane areas, caused by defects in lamina organization, rupture because of an increase in i

170 as floral organ abscission and lateral organ lamina outgrowth.

171 instead, they actively vibrate the reticular lamina over a broad frequency range.

172 rate sufficient force to drive the reticular lamina over all audible frequencies in living cochleae.

173 e of the mnemonic "CLOSE": Cribriform plate, Lamina papyracea, Onodi cell, Sphenoid sinus pneumatizat

174 Lamin B1, a key component of the nuclear lamina, plays an important role in brain development and

175 Lamin B1, a key component of the nuclear lamina, plays an important role in brain development.

176 remodelling after 12 weeks, both within the lamina propria (decreased thickness, p = 0.005) and with

177 sion in cells residing in the lung, airways, lamina propria (LP) of the small intestine, brain, visce

178 cular basement membrane (Rbm) and underlying lamina propria (LP).

179 nduction among lymphocytes in the intestinal lamina propria (LPL) and cervical lymph nodes (CLN).

180 AR was elevated in inflammatory cells in the lamina propria (P = 0.0019), bronchial epithelial (P = 0

181 sidual cells persist in the small intestinal lamina propria (siLP) of adult and neonatal Il7ra(-/-) m

182 d numbers of CD4(+) alphabeta T cells in the lamina propria and activation of T cell receptor gammade

183 fibrocytes of the tunica adventitia and the lamina propria and an inner epithelial lining composed o

184 s identified within lymphatic vessels of the lamina propria and in spaces of >5 mum between a small n

185 opy studies revealed a lack of lipids in the lamina propria and intercellular space in Gpat3(-/-) mic

186 onal dendritic cells (cDC) in the intestinal lamina propria and mesenteric lymph nodes were GFP(+) Ho

187 sically activated macrophages in the colonic lamina propria and worsened the severity of inflammation

188 Infiltration of the lamina propria by peripherally expanded CD8(+) T cells w

189 indings demonstrate that intraepithelial and lamina propria CD8(+) T cells exhibit different dynamics

190 h muscle precursors further diversified into lamina propria cells directly adjacent to the ureteric e

191 olone or 2,4,6-trinitrobenzenesulfonic acid; lamina propria cells from these mice expressed lower lev

192 Lamina propria cells in colon tissues of patients with I

193 Macrophages were isolated from lamina propria cells of mice, IL1beta production was mea

194 CX3CR1(+) macrophages in the intestinal lamina propria contribute to gut homeostasis through the

195 cialized taste buds, the basal lamina, and a lamina propria core with matrix molecules, fibroblasts,

196 Although both TLR5 and CD172alpha(+) lamina propria dendritic cells (LPDC) have been shown to

197 nd dilated intercellular spaces; P < .0001), lamina propria eosinophilia (P < .0001), and fibrosis (P

198 red eighty-six biopsy specimens had adequate lamina propria for evaluation of subepithelial remodelin

199 n pre-diabetic male PAT mice, the intestinal lamina propria had lower Th17 and Treg proportions and i

200 5 to sustain ILC2 homeostasis in the resting lamina propria in mice.

201 ls was not observed in ileum, and the entire lamina propria in sections of duodenum, jejunum, and ile

202 lium, often accompanied by loosely organized lamina propria infiltrates.

203 was increased in airway epithelial cells and lamina propria inflammatory cells in severe asthma compa

204 amples were collected from patients with CD; lamina propria leukocytes were isolated and expression o

205 Incubation of intestinal lamina propria leukocytes with granulocyte-macrophage co

206 d within the intestinal epithelium and among lamina propria lymphocytes.

207 Whether IL10R regulates lamina propria macrophage function during infant develop

208 Lamina propria macrophages (LpMs) preferentially express

209 Mainly the transcriptome of lamina propria mononuclear cells (LPMC) was affected by

210 Lamina propria mononuclear cells and T cells were isolat

211 agonists is recapitulated in vitro in mouse lamina propria mononuclear cells, human colonic epitheli

212 y, NLRP3(R258W) functions exclusively in the lamina propria mononuclear phagocytes to directly enhanc

213 e number of perforin-expressing cells in the lamina propria of acutely HIV-infected patients was posi

214 decreased CD4 and CD8 T-cell numbers in the lamina propria of both small and large intestines under

215 c CD8(+) T cell activity, was evident in the lamina propria of seronegative acutely HIV-infected pati

216 ents and most nerve fibers were found in the lamina propria of the cervical region of the vagina, whe

217 tissue MPhis, such as those residing in the lamina propria of the colon and the dermis, as well as i

218 optively transferred cells isolated from the lamina propria of the large intestine from wild type or

219 ondary lymphoid organs (SLOs) and within the lamina propria of the small intestine, respectively (C.

220 we demonstrate reprogramming of oral mucosal lamina propria progenitor cells from patients undergoing

221 In conclusion, oral mucosal lamina propria progenitor cells represent a source of ce

222 We observed increased expression of GATA3 by lamina propria T cells from mice with colitis compared w

223 In addition, we found that the abundance of lamina propria Th17, but not Th1, cells is highly correl

224 nd was characterized by increased numbers of lamina propria TH2 cells, mast cells, and eosinophils, s

225 CEACAM6 in the lamina propria was localized to neutrophils predominantl

226 itro but it increases the width of the nasal lamina propria when delivered intranasally.

227 an increased ST2 content, restricted to the lamina propria's cellular infiltrate.

228 expansion and proteolytic remodeling of the lamina propria, but few studies have examined these chan

229 perforin expression was downregulated in the lamina propria, but not in the epithelium.

230 T lymphocytes residing in the human colonic lamina propria, encountered by Shigella upon its crossin

231 +) alphabeta T cells in the small intestinal lamina propria, this increase was absent in antibiotic-t

232 stine, pT(regs) are located primarily in the lamina propria, whereas intraepithelial CD4(+) T cells (

233 in SI; Mf3 formed a dense network in mucosal lamina propria, whereas Mf4 was enriched in submucosa.

234 ing the basal epithelium from the underlying lamina propria.

235 tory population highly enriched in the colon lamina propria.

236 )CD64(+)CX3CR1(+) macrophages in the gastric lamina propria.

237 etwork of phagocytes in the small intestinal lamina propria.

238 ers of DCs in the mesenteric lymph nodes and lamina propria.

239 01b(+) antigen-presenting cells (APC) in the lamina propria.

240 ose tissue, skeletal muscle, and the colonic lamina propria.

241 roducing macrophages in the inflamed colonic lamina propria.

242 EoE, in addition to select cells within the lamina propria.

243 increased in the epithelium, but not in the lamina propria.

244 Lamina protein incorporation was assessed using precurso

245 SASP), and reduced expression of the nuclear lamina protein LaminB1 (LMNB1) [1].

246 FMRpolyG interacts with the nuclear lamina protein LAP2beta and disorganizes the nuclear lam

247 functionally analogous to lamins, the major lamina proteins of metazoa.

248 ell proliferation and transcription of basal lamina receptor genes, both necessary for radial sorting

249 Our results demonstrate that lamina recruitment changes the 3D structure of DNA, enab

250 alves, the general morphology of the midband lamina reflects cell types elsewhere in the lamina and c

251 liferation, the development of a normal leaf lamina requires photomorphogenesis-like hormonal respons

252 Thickening of the lamina reticularis, a feature of remodeling in the asthm

253 that produce matrix proteins and thicken the lamina reticularis.

254 potentially contribute to thickening of the lamina reticularis.

255 a show some specializations not found in the lamina serving the upper and lower eye halves, the gener

256 racellular matrix (ECM) incorporates a basal lamina significantly denser than the loosely organized C

257 junction (T/TJ), and (ii) deep successional lamina (SL) where tooth regeneration initiates.

258 cific plastic processes that correlated with lamina-specific changes in responses to further, repeate

259 elded a large number of genes expressed in a lamina-specific manner in the tectum, which may have oth

260 te gamma oscillations induced two different, lamina-specific plastic processes that correlated with l

261 Elucidation of the lamina structure provides insight into its contribution

262 e mutant mice, the organization of the basal lamina surrounding developing follicles is severely defe

263 estry, suggesting the presence of a distinct lamina system in trypanosomes.

264 projections to the organum vasculosum of the lamina terminalis (OVLT) and median preoptic nucleus (Mn

265 nucleus (MnPO) and organum vasculosum of the lamina terminalis (OVLT) are known to regulate fluid/ele

266 Neurons in the organum vasculosum of the lamina terminalis (OVLT) sense changes in extracellular

267 nucleus (MnPO) and organum vasculosum of the lamina terminalis (OVLT), a region that has also been im

268 on neurons in the organum vasculosum of the lamina terminalis (OVLT), these observations suggest OVL

269 hed in cell cycle regulator genes to nuclear lamina that mediates the CTCF function.

270 s on the structure and neuronal types of the lamina, the first optic neuropil in the stomatopod visua

271 around the nucleus that disrupts the nuclear lamina, the main structure limiting nuclear deformabilit

272 determine their association with the nuclear lamina, their dynamic links with other nuclear compartme

273 ca nigra that localized FR enrichment at the lamina tip induces upward leaf movement (hyponasty) from

274 The phase relation of reticular lamina to basilar membrane vibration changes with freque

275 Igh relocated from the nuclear lamina to central domains only at the pro-B cell stage,

276 ticipated interplay between CTCF and nuclear lamina to control the transcription of ER target genes,

277 nn cells interact with neurons and the basal lamina to myelinate axons using known receptors, signals

278 g to reposition the Bcl11b enhancer from the lamina to the nuclear interior and to juxtapose the Bcl1

279 s, the Bcl11b enhancer repositioned from the lamina to the nuclear interior.

280 bundle, the tectorial membrane and reticular lamina, to the transverse motion of the basilar membrane

281 cacy of decellularized human corneal stromal lamina transplantation with or without autologous adipos

282 Decellularized human corneal stromal laminas transplantation seems safe and moderately effect

283 zed to mitochondria-ER junctions and nuclear lamina, two compartments that are recalcitrant to classi

284 connectivity pattern of a sub-population of lamina V inhibitory sensory relay neurons marked during

285 The outer hair cell-driven reticular lamina vibration collaboratively interacts with the basi

286 se cochleae that the sound-induced reticular lamina vibration is substantially larger than the basila

287 s occurred in lamina VIII, at the expense of lamina VII bouton labeling.

288 ina VIII and the adjacent ventral sectors of lamina VII, which are involved in axial/proximal limb se

289 located between L2 and L5 segments in medial lamina VII, with a maximal density within L4.

290 Increases occurred in lamina VIII and the adjacent ventral sectors of lamina V

291 ontrols, elevated bouton numbers occurred in lamina VIII, at the expense of lamina VII bouton labelin

292 Anterior movement of the lamina was detected more frequently with the Bruch's mem

293 V effect was highest for delta(18) O of leaf lamina water, but 40% lower on delta(18) O of main vein

294 ions of the tectorial membrane and reticular lamina were tuned.

295 assisted 120-mum thickness and 9-mm diameter laminas were obtained from the anterior stroma of human

296 ocilia, the tectorial membrane and reticular lamina, were sharply tuned in the radial direction.

297 of basally migrating GC and a weakened basal lamina, whereas GC migration was minimal in DBP-FW anima

298 sis and extrusion of cells through the basal lamina, which are then engulfed by blood-borne phagocyte

299 ipid bilayer attached to a viscoelastic gel (lamina) whose elasticity and viscosity primarily depend

300 factory bulbs, the prefrontal cortex and the lamina X of the cervical spinal cord.