ライフサイエンスコーパス: delamination

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

2 hiation consequently restrains the film from delamination.

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

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

5 neuroblastoma cell invasion and neural crest delamination.

6 anges in epithelial cell adhesion leading to delamination.

7 l adhesions and protrusive forces during NCC delamination.

8 ol over wrinkle topography without cracks or delamination.

9 ressive apical constriction and, frequently, delamination.

10 ly down-regulated coincident with neuroblast delamination.

11 ofoundly blocks EMT and concomitant mesoderm delamination.

12 autoregulates), neuronal differentiation and delamination.

13 nchymal transition seen in neural crest cell delamination.

14 amination is distinct from neural crest cell delamination.

15 r cell differentiation and during neuroblast delamination.

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

17 ells may also enter the entodermal region by delamination.

18 ctodermal cells and acts prior to neuroblast delamination.

19 ithin the neuroectoderm, prior to neuroblast delamination.

20 amina determined only by the geometry of the delamination.

21 nd eliminating the possibility of multilayer delamination.

22 revealed that this organelle is required for delamination.

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

24 reas overexpression of Gsc greatly increases delamination.

25 Eighteen eyes (4.2%) demonstrated secondary delamination.

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

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

28 including shear banding, crack formation and delamination.

29 showed impaired neural tube closure and CNCC delamination.

30 ell constraints which may contribute to cell delamination.

31 ion to investigate the catalytic benefits of delamination.

32 strate synthesis of Bronsted acid sites upon delamination.

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

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

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

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

37 Examining neurogenesis and delamination after initial placodal patterning and speci

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

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

40 Minimizing delamination and bending energy leads to minimal angles

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

42 Delamination and convective downwelling are two widely r

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

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

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

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

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

48 mal transition is responsible for epithelial delamination and dissolution.

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

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

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

52 G1 delamination and G2 intercalation involve cytoskeletal r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Pillaring and delamination are the primary methods for structural modi

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

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

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

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

93 The delamination buckling approach provides a facile means t

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

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

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

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

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

99 1 or G2 cells, is sufficient to rescue sos-1 delamination defects, revealing that Ras acts non-cell-a

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

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

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

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

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

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

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

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

108 Delamination from FN-muprinted PDMS precluded robust det

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

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

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

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

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

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

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

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

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

118 chanisms generate additional diversity after delamination from the neuroectoderm.

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

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

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

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

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

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

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

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

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

128 The delamination involves a partial or complete epithelium-t

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

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

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

132 Placodal cell delamination is distinct from neural crest cell delamina

133 The delamination is likely due to a perturbed interaction be

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

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

136 This path of delamination is recapitulated by a simple computational

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 1P pathway may also be important for driving delamination of stem cells during differentiation or inv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 or mechanical enhancements against crack and delamination phenomena.

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

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

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

196 tion leaves its original territory through a delamination process.

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

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

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

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

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

202 Pars plana vitrectomy with or without delamination/segmentation.

203 Introducing specific delamination sites by surface modification of embedded c

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

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

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

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

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

209 463 patients) that underwent vitrectomy with delamination, the intraoperative complication rate was 3

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

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

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

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

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

215 1 as well as cadherin-6B can trigger ectopic delamination when co-expressed with the competence facto

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

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

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

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

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

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

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