ライフサイエンスコーパス: delamination

1 continental mass lost by weathering (40% by delamination).

2 reas overexpression of Gsc greatly increases delamination.

3 Eighteen eyes (4.2%) demonstrated secondary delamination.

4 ta-catenin signalling, which then affects NC delamination.

5 g is transiently inhibited at the time of NC delamination.

6 including shear banding, crack formation and delamination.

7 showed impaired neural tube closure and CNCC delamination.

8 ion to investigate the catalytic benefits of delamination.

9 strate synthesis of Bronsted acid sites upon delamination.

10 luding cell motility, adhesion, mitosis, and delamination.

11 Ras acts non-cell-autonomously to permit G1 delamination.

12 window being around 135 degrees C for ERB-1P delamination.

13 neuroblastoma cell invasion and neural crest delamination.

14 anges in epithelial cell adhesion leading to delamination.

15 l adhesions and protrusive forces during NCC delamination.

16 te more widely to promote orderly progenitor delamination.

17 elamination, whereas decreasing it abrogates delamination.

18 ing to engage in aerobic glycolysis prior to delamination.

19 ressive apical constriction and, frequently, delamination.

20 ly down-regulated coincident with neuroblast delamination.

21 ofoundly blocks EMT and concomitant mesoderm delamination.

22 autoregulates), neuronal differentiation and delamination.

23 nchymal transition seen in neural crest cell delamination.

24 amination is distinct from neural crest cell delamination.

25 r cell differentiation and during neuroblast delamination.

26 x9, cells apoptose prior to or shortly after delamination.

27 ells may also enter the entodermal region by delamination.

28 ctodermal cells and acts prior to neuroblast delamination.

29 ithin the neuroectoderm, prior to neuroblast delamination.

30 ponent increased the film robustness against delamination.

31 d relocalizing apical aPKC partially rescues delamination.

32 f 5 degrees C/km due to density overturn and delamination.

33 ile also influencing differentiation through delamination.

34 plastic tube-wall deformation, and tube-wall delamination.

35 EDOT:PSS coated flat microelectrodes appears delamination.

36 eas the pendant counterpart favors live cell delamination.

37 We demonstrate that MMP14 is required for NC delamination.

38 op can catastrophically propagate intramural delamination.

39 s general importance for the control of cell delamination.

40 termined epigenetically prior to neural tube delamination.

41 morpholinos promotes premature neural crest delamination.

42 non-genetic ciliopathy and premature neuron delamination.

43 k that influences the timing of neural crest delamination.

44 nd inflammatory pathways in IECs, leading to delamination.

45 ctor that promotes loss of cell polarity and delamination.

46 ell constraints which may contribute to cell delamination.

47 hiation consequently restrains the film from delamination.

48 ol over wrinkle topography without cracks or delamination.

49 amina determined only by the geometry of the delamination.

50 rebleeding and what mechanisms prevent clot delamination.

51 nd eliminating the possibility of multilayer delamination.

52 revealed that this organelle is required for delamination.

53 y, required for neural tube closure and CNCC delamination.

54 nd worniu mutants show defects in neuroblast delamination (a form of EMT).

55 roduce a minimal model for curvature-induced delamination accounting for the two buckling motifs that

56 During neuronal delamination, acto-myosin constriction generates a tunne

57 ce ectopic endocrine cell formation and cell delamination after in ovo chicken endoderm electroporati

58 Examining neurogenesis and delamination after initial placodal patterning and speci

59 llular lamellar bilayers, leading to bilayer delamination and "roll-up" in a water milieu after 1 h,

60 of the mitotic spindle correlates with cell delamination and apoptotic death, and that blocking the

61 Minimizing delamination and bending energy leads to minimal angles

62 us differentiation followed by lower crustal delamination and chemical weathering followed by subduct

63 direction, the toughness is much lower since delamination and controlled flexure are expected and des

64 Delamination and convective downwelling are two widely r

65 quatorial fashion, permitted nearly complete delamination and destruction of supported bilayers upon

66 s at the neural plate stage, it delays their delamination and differentiation after neurulation when

67 ate NPC specification with Epb41l5-dependent delamination and differentiation as neurons.

68 n evolutionarily conserved regulator of cell delamination and directed migration.

69 -specifying genes, cell-autonomously driving delamination and directly regulating numerous downstream

70 mal transition is responsible for epithelial delamination and dissolution.

71 (III) in the structure of boehmite inhibited delamination and dissolution.

72 isexpression of Pax2a is sufficient to block delamination and fully suppress the effects of Gsc The o

73 dification resulted in simultaneous chemical delamination and functionalization to targeted CONs.

74 G1 delamination and G2 intercalation involve cytoskeletal r

75 d onto treated PDMS with no visible signs of delamination and geometrically scaling resistance under

76 utant embryonic brains, abnormal radial glia delamination and heterotopia volume were significantly r

77 he encompassing epithelial sheet, leading to delamination and ingression into the mesenchyme where th

78 epithelial-mesenchymal transformation after delamination and initial migration, but before definitiv

79 best characterized as a combination of mass-delamination and invagination.

80 ithelialization of the neural crest prior to delamination and is required for the overall epithelial

81 tomyosin contractility rescues cardiomyocyte delamination and is sufficient to drive cardiomyocyte fa

82 icate that two independent processes, apical delamination and JAK/STAT activation, are concurrently r

83 bly Sox9/10, are essential for NC induction, delamination and lineage specification.

84 tory relationships that orchestrate neuronal delamination and may inform mechanisms underlying pathol

85 afic lower crust and consequent deep crustal delamination and melting--leading to abundant tonalite-t

86 sion of Pt-Ets4 is sufficient to induce cell delamination and migration by inducing a mesoderm-like c

87 rise to all muscles of the limbs through the delamination and migration of cells into the limb buds.

88 during the progressive events leading to the delamination and migration of neural crest cells.

89 th the absence of SOX17 leading to premature delamination and migration of parietal endoderm.

90 l crest (NC), and has been implicated in the delamination and migration of the NC cells.

91 CC) polarity is prerequisite for directional delamination and migration, which in turn is essential f

92 ctions that control NCC motility during both delamination and migration.

93 lated in epithelial cell clusters to control delamination and migration.

94 and suggest that its removal may cause pole delamination and mitotic failure when spindle forces are

95 genin pathway in ferret progenitors promoted delamination and outward migration.

96 esting to the pivotal role of DE-cadherin in delamination and polarized division of neuroblasts.

97 ausible unifying mechanism for the premature delamination and precocious differentiation of progenito

98 that ion exchange is coupled to the dynamic delamination and restacking of clay layers, which create

99 ring mitosis in epithelial cells just before delamination and selection of a proneural cell fate in t

100 view that stratification occurs through the delamination and subsequent movement of epidermal cells,

101 oxidation of any of these layers to help aid delamination and subsequently, recovery.

102 However, issues such as delamination and substructure resistance are generated b

103 echanically induced phase transition without delamination and their overall crystal integrity is reta

104 ributed to tectonic shortening, lithospheric delamination and unloading due to deglaciation and erosi

105 n in mutants, including focal subendothelial delamination and widespread podocyte foot process broade

106 or thermal expansion can result in membrane delamination and, thereby, device failure.

107 ural crest cells that are required for their delamination and/or migration.

108 here Twist1 is required both for proper cNCC delamination, and for emigration from the dorsal neural

109 y cellular behaviors including invagination, delamination, and ingression.

110 hitecture, including overproliferation, cell delamination, and migration.

111 developmental processes such as neural crest delamination, and new tissue organizations such as the b

112 Protrusions, efflorescence, delamination, and opacity decreasing are severe degradat

113 hesis, structure, properties, intercalation, delamination, and potential applications.

114 tic region of high proliferation, neuroblast delamination, and programmed cell death at stage 20/21 (

115 e neuronal progenitor domain upon neuroblast delamination, and reveals that the order and place of ne

116 for the vestibuloacoustic neurons and their delamination appeared to be unaffected in the absence of

117 lecular mechanisms that mediate neural crest delamination are also likely to be involved in the sprea

118 Pillaring and delamination are the primary methods for structural modi

119 Cell-biological mechanisms mediating delamination are, however, poorly understood.

120 microfissures, the starting points of paint delamination, are the result of an overall expansion of

121 on to examine potential mechanisms of aortic delamination arising from smooth muscle cell (SMC) dysfu

122 We demonstrate that conjugate delamination arrays are the result of elastic strain ene

123 These results implicate IEC delamination as a protective UPR-mediated response to ch

124 But delamination as the primary cause of uplift is questione

125 ores do not cause microtubule detachment and delamination at SPBs.

126 ation, nor has the mechanism controlling SAG delamination been elucidated.

127 nal crack modes--such as enamel chipping and delamination--began to manifest themselves, leading to m

128 Our results show possible large-scale delamination beneath the Songpan-Ganzi and Qiangtang ter

129 Delamination between the S(1) and S(2) layers of trachei

130 The delamination buckling approach provides a facile means t

131 ysis was initiated at the time of neuroblast delamination by labeling progenitors with replication-de

132 helia and removes the less fit; extrusion or delamination can remove apoptotic or defective cells fro

133 Because live-cell delamination constitutes a mechanistic link between epit

134 dentified a subpopulation of NCCs that, upon delamination, crossed the dorsal midline to colonize spa

135 te that pulse current can effectively reduce delamination damage and residual deformation.

136 defects, including leaflet discontinuities, delamination defects, and deposition of acellular extrac

137 tethering excess aPKC is sufficient to cause delamination defects, and relocalizing apical aPKC parti

138 1 or G2 cells, is sufficient to rescue sos-1 delamination defects, revealing that Ras acts non-cell-a

139 ons exist between these different phenomena: delamination depends on the dynamics of crack hopping, w

140 inates containing an embedded, through-width delamination dividing the laminate into four sub-laminat

141 We also show that delamination does not occur uniformly across the film.

142 ar films that cause problems in cracking and delamination during flexing or heating.

143 key degradation modes including gas-induced delamination, electrode layer collapse and propagation o

144 view will summarize our current knowledge on delamination, EMT and migration of NC cells using key ex

145 onic brain from the consequences of sporadic delamination errors and teratogenic insults.

146 bers form mainly by direct branching, unlike delamination events that create ventricular trabeculae.

147 We find that just preceding cell cluster delamination, expression of transmembrane immunoglobulin

148 theoretical modeling to understand thin film delamination from an indium tin oxide (ITO) current coll

149 Delamination from FN-muprinted PDMS precluded robust det

150 l muscle has been challenging due to myotube delamination from synthetic culture substrates approxima

151 itoses of NSCs; coordinating abscission with delamination from the apical membrane; timing of neuroge

152 ugh a combination of bulk flow of lipids and delamination from the cell cortex via the formation and

153 as characterized by a late phase of cellular delamination from the dorsal and lateral neural tube, a

154 ecome committed to the myogenic lineage upon delamination from the dorsomedial and dorsolateral lips

155 rects cluster asymmetry essential for timing delamination from the epithelium.

156 t neuroepithelial cells to suppress cellular delamination from the neural tube and thereby preserve n

157 sses during embryonic development, including delamination from the neural tube by epithelial-to-mesen

158 proper timing of neural crest emigration and delamination from the neural tube of the avian embryo.

159 transition (EMT) that promotes neural crest delamination from the neural tube; however, little is kn

160 chanisms generate additional diversity after delamination from the neuroectoderm.

161 y and acquire motile properties before their delamination from the neuroepithelium.

162 als that the order and place of neuroblasts' delamination from the otic epithelium prefigure their po

163 opic basal progenitors, suggesting premature delamination from the ventricular zone.

164 (SBH), likely to be initiated by progenitor delamination from the VZ early during corticogenesis.

165 The motion of a small region of the delamination front, where the shear component of interfa

166 Other NSAIDs did not induce IEC delamination; however, Glafenine also displays off-targe

167 a subset of MDR inhibitors also induced IEC delamination, implicating MDR efflux pumps as cellular t

168 s during sensory neurogenesis and neuroblast delamination in the differing placodes.

169 monolayer interfaces accessed through sample delamination in ultrahigh vacuum (UHV).

170 pre-migratory NC cells, are required for NC delamination in Xenopus and chick embryos, whereas they

171 t elastically by expansion or plastically by delamination into slabs that glide along slip planes.

172 Cellular events driving these movements are delamination, invagination, and intercalation as well as

173 The delamination involves a partial or complete epithelium-t

174 This process, also known as delamination, involves adherens-junction disassembly and

175 We hypothesized that veneer chipping/delamination is a result of the propagation of near-cont

176 egin to delaminate from the cuticle and that delamination is complete when the wing has fully expande

177 Placodal cell delamination is distinct from neural crest cell delamina

178 ccurring hair-cortex degradation and cuticle delamination is increased in fibers with increased PAH c

179 The delamination is likely due to a perturbed interaction be

180 We show that this process of delamination is mechanistically distinct from apoptosis-

181 heir role in neural crest cell formation and delamination is not.

182 This path of delamination is recapitulated by a simple computational

183 When the direction of delamination is reversed through suppression of RhoGEF2,

184 Following NCC delamination, low level of TWIST1-CRM activity is instru

185 imple, surfactant- and sonication-free, mild delamination method is expected to find broad implementa

186 synthetic studies demonstrate that this new delamination method requires (i) a borosilicate layered

187 in endocrine progenitor cells, allowing for delamination, migration and/or appropriate cell fate dec

188 ry network (GRN) controls the specification, delamination, migration, and differentiation of this fas

189 However, not all Ngn1-positive cells undergo delamination, nor has the mechanism controlling SAG dela

190 ction, accounting for the crack patterns and delamination observed after repeated cycling.

191 Ngn1 in partially overlapping domains, with delamination occurring primarily in the zone of overlap.

192 roperties than the flat one, and no crack or delamination occurs after electroplating PEDOT:PSS and p

193 be stretched to over twice its length before delamination occurs.

194 The process involves delamination of a group of 6 to 10 follicle cells from t

195 autonomous role for RTK-Ras signaling in the delamination of a neuroblast from an epithelial organ.

196 on molecule polarity regulates asymmetry and delamination of an epithelial cell cluster.

197 Functionalization may result in spontaneous delamination of bulk COF materials into solution-stable

198 ls is an elaborate process that requires the delamination of cells from an epithelium and cell moveme

199 xamine in chick the mechanism underlying the delamination of cells from the epibranchial placodal ect

200 extends beyond the initial specification and delamination of cells from the epithelium.

201 t the endodermal secretory products promoted delamination of cells from the precardiac mesoderm and e

202 By progressive delamination of cells, the placode generated a series of

203 modified graphene films, featuring wrinkles, delamination of close-packed laminates, their ordered an

204 nded by mesenchymal cells derived from local delamination of coelomic epithelium.

205 on of graphene oxide and the electrochemical delamination of CVD grown graphene, are currently on par

206 y a combination both of delayed or defective delamination of CVG neuroblast precursors from the otic

207 tachment of progenitor cells from the normal delamination of daughter neuroblasts in the developing m

208 endocrine cell types owing to defects in the delamination of early endocrine progenitors from the tru

209 When overexpressed in chick, Wise causes delamination of ectodermal cells and attracts migrating

210 velopment they do not efficiently induce the delamination of ectopic neural crest cells from the neur

211 E-cadherin gene expression, thereby allowing delamination of endocrine cells from the trunk epitheliu

212 initial step of endocardial formation, i.e., delamination of endothelial precursor cells from precard

213 Delamination of hcp UiO-67 occurs through the cleavage o

214 e for dermomyotome and myotome formation and delamination of limb myogenic progenitors.

215 todermal cadherin genes to contribute to the delamination of mesendodermal precursors at gastrulation

216 al molecules that control the generation and delamination of muscle precursor cells have been identif

217 ation of single SiNS arises from spontaneous delamination of nanosheets from their substrate due to d

218 gulate adhesions and motility during initial delamination of NCCs from the neuroepithelium.

219 Delamination of neural crest (NC) cells is a bona fide p

220 of rho activity by C3 exotoxin prevents the delamination of neural crest cells from neural tube expl

221 results suggest that rhoB has a role in the delamination of neural crest cells from the dorsal neura

222 inhibition of SOX2 signaling results in the delamination of neural progenitor cells from the ventric

223 dynamics in the Spemann organizer, regulates delamination of neuroblasts in the otic vesicle.

224 data resolve a genetic mechanism controlling delamination of otic neuroblasts.

225 The limb musculature arises by delamination of premyogenic cells from the lateral dermo

226 isexpression of Ngn1 and Gsc induces ectopic delamination of some cells from the medial wall of the o

227 1P pathway may also be important for driving delamination of stem cells during differentiation or inv

228 epithelial invasions can result in complete delamination of stromal tissue and subsequent inclusion

229 usions, large loose bodies, and bubbling and delamination of the cartilage with exposure of subchondr

230 mage as corrosion of steel reinforcement and delamination of the concrete itself.

231 South America and the Gibraltar arc, and to delamination of the entire lithospheric mantle, as aroun

232 As cracks hop they locally initiate the delamination of the film which warps with a timescale mu

233 schisis (XLRS), a dystrophy characterized by delamination of the inner retinal layers, leading to vis

234 nterneuron loss; and (iv) optic atrophy with delamination of the lateral geniculate nuclei.

235 No discernible delamination of the layers or leakage between channels w

236 re exchanged by water molecules, producing a delamination of the material, where the individual doubl

237 to the underlying electron conductor and in delamination of the membrane from the electrode body, bo

238 g (Snai2) are not required for formation and delamination of the neural crest in mice.

239 he neural cell fate determinant Prospero and delamination of the neural precursors from the epitheliu

240 orations often fracture from chipping and/or delamination of the porcelain veneers.

241 ted mechanical stress does not result in the delamination of the sensing and reference membranes, lea

242 s unusual phenomenon to a reversible partial delamination of the topmost atomic layers, which then mi

243 of premigratory neural crest cell fate, the delamination of these cells from the neural epithelium a

244 ce membranes are held in place mechanically, delamination of these membranes from the underlying soli

245 Intercalation and delamination of two-dimensional solids in many cases is

246 They exhibit no physical delamination or degradation even after 1 million biphasi

247 preciable complication rate, particularly if delamination or segmentation are required.

248 e paint layers (leading to, e.g., cracks and delamination) or can lead to a visual change of the imag

249 or mechanical enhancements against crack and delamination phenomena.

250 pattern with key regulators of neural crest delamination, Phf12 and Snail2, and interacts with their

251 cal response including surface striation and delamination, photosalient effect (ballistic disintegrat

252 material shows a "memory effect" during the delamination-pillarization process.

253 After NCC delamination, planar cell polarity signaling acts via Rh

254 in their structural integrity throughout the delamination process and also remain stable in aqueous,

255 ures of AKNA are important for mediating the delamination process in the formation of the subventricu

256 flakes are produced using an amine-assisted delamination process.

257 tion leaves its original territory through a delamination process.

258 dings to native closure by showing that cell delamination represents a locally patterned and collecti

259 e interlaminar fracture toughness, hardness, delamination resistance, in-plane mechanical properties,

260 in the formation of shear bands, and enhance delamination resistance.

261 Defects in delamination result in thickened, hyperplastic valves, a

262 to prevent thermomechanical problems such as delamination; robust performance in the presence of surf

263 the lipid structure is disrupted by lamellar delamination ("roll-up").

264 Pars plana vitrectomy with or without delamination/segmentation.

265 he two buckling motifs that underlie partial delamination: shallow "rucks" and localized "folds".

266 Introducing specific delamination sites by surface modification of embedded c

267 K s(-1), nucleate exclusively at interfacial delamination sites in composite solids.

268 Herein, a hydrogen-free electrochemical delamination strategy through weak Lewis acid intercalat

269 seismic structures as a continuing regional, delamination-style foundering of lower crust and contine

270 ycycline and topical corticosteroid, alcohol delamination, substance P-derived peptide and ILGF-I dro

271 dering the high number of cell divisions and delaminations taking place during embryonic development,

272 Finally, we demonstrate that these delaminations tend to populate layers that are enriched

273 Based on the cyclic delamination test, the adhesive bond durability of bio-a

274 scopy, water contact angle measurements, and delamination tests confirm the covalent attachment of th

275 Based on reduced diametric error, and delamination, tests with a feed rate (FR) of 0.08 mm/rev

276 ify a novel process of crowding-induced cell delamination that balances growth to ensure the developm

277 patients) that underwent vitrectomy without delamination, the intraoperative complication rate was 1

278 463 patients) that underwent vitrectomy with delamination, the intraoperative complication rate was 3

279 nery in cardiomyocytes to restrict excessive delamination, thereby preserving the architecture of the

280 iated de-epithelialization, and a subsequent delamination through the basement membrane.

281 ed postsynthetic modifications, and chemical delamination to CONs for potential advantageous targeted

282 Delamination toughening associated with intensive but co

283 2 gigapascals can be achieved by activating delamination toughening coupled with transformation-indu

284 crine commitment, cell cycle exit, and rapid delamination toward proto-islet clusters.

285 nical instabilities, including wrinkling and delamination, underlie the morphogenesis program of grow

286 chieve in situ thermal remending of internal delamination via dynamic bond re-association.

287 rspective, sub-laminates above and below the delamination vibrate in exactly the same mode in spite o

288 ymer films such as mass variation, swelling, delamination, viscoelasticity, and pore formation.

289 1 as well as cadherin-6B can trigger ectopic delamination when co-expressed with the competence facto

290 cycled electrode showed mud-cracks and film delamination whereas SiCN-MoS2 electrodes were intact an

291 in the compact layer cardiomyocytes augments delamination, whereas decreasing it abrogates delaminati

292 Loss of Gsc severely inhibits delamination, whereas overexpression of Gsc greatly incr

293 , including directed cell migration and cell delamination, which are also involved in other physiolog

294 s AJ defect is consistent with impaired CNCC delamination, which requires AJ dissolution.

295 mbedded channels is achieved via interfacial delamination, which requires less energy to create a new

296 against crack propagation due to interfacial delamination, which substantially increases their risk o

297 Non-MDF sample's surface shows spalling and delamination, while the dominated wear mechanism of fina

298 micro buckles occur on the interfaces of the delamination with amplitude about 10(-3) times of that o

299 that we have devised--silicene encapsulated delamination with native electrodes.

300 Using this UHV delamination XPS, we examine titanium vapor deposited on