ライフサイエンスコーパス: delaminate

1 dial and intermediate neuroblasts will later delaminate.

2 pedance change, while the Pt microelectrodes delaminated after 1 million pulses.

3 ebrate development, trunk neural crest cells delaminate along the entire length of the dorsal neural

4 ally express Foxd3 upregulate HNK1 and Cad7, delaminate and emigrate from the neural tube at multiple

5 floor plate precursors and require foxd3 to delaminate and exit the spinal cord.

6 otentials where conventional IR-active films delaminate and fail is reported.

7 ver, for the subset of ectodermal cells that delaminate and form neuroblasts, their polarity requires

8 The cells of the epicardium then delaminate and incorporate into the heart giving rise to

9 erive from caudal neural plate border cells, delaminate and migrate along the paraxial mesoderm on ei

10 ontrast, differentiating neuronal precursors delaminate and migrate laterally, establishing the lamin

11 e floor of the otic vesicle and subsequently delaminate and migrate toward the hindbrain before compl

12 pithelial-to-mesenchymal transition (EMT) to delaminate and migrate, often to distant locations in th

13 there is a reduction of neural precursors to delaminate and populate the developing cochleo-vestibula

14 While the crystals of 1a delaminate and release gaseous N(2) indiscriminately und

15 nd drives those with higher contractility to delaminate and seed the trabecular layer.

16 renew and generate basal progenitors(1) that delaminate and settle in the subventricular zone in enla

17 was subcontinental lithospheric mantle that delaminated and became integrated into the convecting Ar

18 The melanoblasts delaminated and gathered in the carapacial staging area

19 rm, from which the peripheral nervous system delaminates and in the CNS.

20 stiff as the constituent linear polymer, and delaminates and tears along well-defined lines in the ma

21 ence that cross-feeding interactions between delaminating and nondelaminating cells increase each oth

22 ium and cause it to lose cell-cell contacts, delaminate, and invade the extracellular space abutting

23 epithelial-to-mesenchymal transition (EMT), delaminate, and migrate to diverse locations in the embr

24 eventing the most apical daughter cells from delaminating apically following division events.

25 subpopulations of SNSPs (dSNSPs and tSNSPs) delaminate as individual cells from the SNS placode.

26 blasts in the Drosophila melanogaster embryo delaminate as single cells from the embryonic epidermis

27 d around the pouch lumen, and they appear to delaminate as they exit the cell cycle and differentiate

28 gical analyses showed that cells transiently delaminate at the point of closure, and produce cytoplas

29 In mouse embryo gastrulation, epiblast cells delaminate at the primitive streak to form mesoderm and

30 estabilized lower lithosphere that initially delaminated at 180-170 Ma and has relaminated to their o

31 cardiomyocytes lose apicobasal polarity and delaminate basally from the ventricular wall.

32 ns where upwellings are impeded by subducted/delaminated blocks not currently connected to a subducti

33 wrinkles, folds, period-doubles, ridges and delaminated-buckles according to their distinctive topog

34 Delaminating cardiomyocytes accumulate Cdh2-EGFP on the

35 alysis of the tumors allows us to identify a delaminating cell population as the critical one in driv

36 The remaining delaminated cells follow the movement of apically attach

37 ptional program is activated specifically in delaminating cells and drives nonautonomous tissue overg

38 ed signaling molecules and growth factors to delaminating cells, which nonautonomously promote prolif

39 y neural precursor cells including all early delaminating CNS neuroblasts, the encoded Nerfin-1 prote

40 rapid ABHD4 downregulation is necessary for delaminated daughter neuroblasts to escape from anoikis.

41 ur through cell intercalation, and cells can delaminate during epithelial-mesenchymal transitions and

42 rsors from the anterior-lateral otic placode delaminate earlier than those from its medial-posterior

43 fects in apical-basal spindle orientation in delaminated embryonic neuroblasts.

44 effects derived from the differentiating and delaminating endocrine cells nonautonomously regulate th

45 Flrt2 is exclusively expressed in the fully delaminated epicardium.

46 licle cell epithelia and is downregulated in delaminating epithelia as expression of Slbo (C/EBP) is

47 ctronic transport measurements show that the delaminated FL-BP crystals exhibit a high hole mobility

48 Some of the hydrophobic delaminated flakes were discovered to roll into a tubula

49 expression of Keap1 increased the volume of delaminated follicle cells that showed enhanced invasive

50 lowed by sonication in water, the f-Ti3C2 is delaminated forming a stable colloidal solution that is

51 that endocardial cells lacking Alk2 fail to delaminate from AV canal explants.

52 Cranial neural crest cells (CNCCs) delaminate from embryonic neural folds and migrate to ph

53 Cells delaminate from epithelial placodes to form sensory gang

54 Presumptive cochleovestibular neurons delaminate from the anterior ventral part of the otocyst

55 es on their basal side, nTSG-deficient cells delaminate from the apical side of the epithelium and be

56 increase by proliferation, and neural cells delaminate from the cluster, which migrate away to occup

57 he epithelia within the folded wing begin to delaminate from the cuticle and that delamination is com

58 ia, which earlier produced the wing cuticle, delaminate from the cuticle, and the epithelial cells un

59 rns during the period when muscle precursors delaminate from the dermomyotome and migrate into the li

60 pm8 and vpi1 delaminate from the dorsal cyst epithelium and migrate v

61 Trunk neural crest cells delaminate from the dorsal neural tube as an uninterrupt

62 system (PNS) of fas mutants, neurons fail to delaminate from the ectodermal epithelium; in the centra

63 Neuroblasts that delaminate from the embryonic epithelium require lgl to

64 irst present evidence that the putative PGCs delaminate from the endomesoderm upon feeding, migrate i

65 ll dispersal." Premitotic ureteric tip cells delaminate from the epithelium and divide within the lum

66 First, neuroblasts are specified, delaminate from the epithelium of the otocyst, and migra

67 f the mitotic activity showed that NZs cells delaminate from the epithelium, become neuronal precurso

68 acodes occurs, and neuroblasts concomitantly delaminate from the epithelium.

69 During oogenesis, border cells delaminate from the follicular epithelium and migrate.

70 Border cells delaminate from the follicular epithelium and squeeze in

71 Neural precursors delaminate from the groups and occupy positions basal an

72 cent in adult flies but can exit quiescence, delaminate from the hub and convert into CySCs after abl

73 ing limb development Pax3 positive myoblasts delaminate from the hypaxial dermomyotome of limb level

74 basal polarity, mislocalize DE-cadherin, and delaminate from the main epithelium.

75 gregated within the neuroepithelium and then delaminate from the neural tube and migrate into the per

76 ells that arise from the embryonic ectoderm, delaminate from the neural tube in early vertebrate deve

77 me biased toward neuronal lineages when they delaminate from the neural tube, whereas cranial neural

78 g Drosophila neural development, neuroblasts delaminate from the neuroectoderm of each hemisegment in

79 epithelial-mesenchymal transition (EMT), and delaminate from the neuroepithelium.

80 n of early otic progenitors express NEUROG1, delaminate from the otocyst, and coalesce to form the ne

81 epithelial: between E2 and E3.5, neuroblasts delaminate from the otocyst.

82 During cardiac trabeculation, cardiomyocytes delaminate from the outermost (compact) layer to form co

83 astatic outgrowth requires that cancer cells delaminate from the primary tumor, intravasate, survive

84 Epicardially derived cells (EPDCs) delaminate from the primitive epicardium through an epit

85 Unlike other procephalic neuroblasts which delaminate from the surface ectoderm as individual cells

86 rgo epithelial-to-mesenchymal transition and delaminate from the surface of the developing heart subs

87 expressing Wt1, GATA-4, RALDH2 and RXRalpha delaminate from the surface of the liver, intermingle wi

88 Lbx1 mutant mice and limb muscle precursors delaminate from the ventral dermomyotome but fail to mig

89 ting as coalescences of cells that appear to delaminate from the wall of the gut.

90 ersus proliferative expansion and failure to delaminate from their niche.

91 After mitosis, fate-committed daughter cells delaminate from this germinative zone.

92 Archaean oceanic mantle lithosphere that has delaminated from its overlying oceanic crust.

93 Under 2 mM CaCl(2) , insoluble matrix was delaminated from saline washed retinas.

94 A type I PM is delaminated from the entire midgut epithelium and, in so

95 ytes changed their cell-adhesion properties, delaminated from the myocardium and upregulated epicardi

96 free-standing SWNT/polyelectrolyte membranes delaminated from the substrate were found to be exceptio

97 PLP-EGFP was highly expressed as cells delaminated from the VZ.

98 These MMMs can be delaminated from their substrates to create free-standin

99 MP2 delaminates from a cluster of achaete-scute-expressing e

100 les mate repeatedly, a subset of these cells delaminates from and migrates along the apical surface o

101 and rod pattern, has hypoplastic enamel that delaminates from the dentin, and has a deteriorating ena

102 a rare population of endothelial precursors delaminates from the dermomyotome to incorporate exclusi

103 nd G1 pore cells; however, the G1 cell later delaminates from the excretory system to become a neurob

104 ter, a group of anterior follicle cells that delaminates from the follicle epithelium, is disrupted.

105 We propose that Wt1 expression in cells delaminating from the coelomic epithelium is essential f

106 arity proteins, including Crumbs2 (CRB2) and delaminate in a stepwise manner; live imaging shows that

107 In addition, dorsal ectodermal cells delaminate in blf morphants during late somitogenesis.

108 To delaminate incoherent from coherent boundary scattering,

109 e resulting MXenes, Ti(3)C(2)Cl(2), was then delaminated into few-layer flakes by intercalating lithi

110 vibration frequency is an eigenvalue of the delaminated lamina determined only by the geometry of th

111 Positively charged delaminated layered double hydroxide lactate nanosheets

112 CONs have graphene-like layered morphology (delaminated layers), unlike the COFs from which they wer

113 ocks not currently connected to a subducting/delaminating lithosphere ('remnant blocks' for simplicit

114 ) on the regional and global scales in arcs, delaminated lower crust, and river waters.

115 A partially dealuminated delaminated material displays a 2.3-fold enhancement in

116 precursor to single and curved layers in the delaminated material.

117 me and increase in external surface area for delaminated materials relative to their calcined 3D zeol

118 During development, endocrine progenitors delaminate, migrate radially and cluster to form islets.

119 e lateral borders of the neural plate before delaminating, migrating and differentiating into various

120 lly increase capacity, as observed mainly in delaminated MXenes and confirmed by DFT calculations and

121 The particular topology of the delaminated nanosheets, with quite distant cobalt center

122 with measurements of pressure and tension of delaminating NCC and neighboring neuroepithelial cells,

123 atory morphology classically associated with delaminating NCC.

124 e topography of central projections, and (2) delaminated neuroblasts differentiate in close contact w

125 Delaminated neuroblasts in Drosophila function as stem c

126 rix, we were able to readily distinguish the delaminating neuroblasts and to describe progressive sta

127 ctodermal thickenings, called placodes, that delaminate or invaginate to form cranial ganglia and sen

128 membranes, preventing them from slipping and delaminating over the cell-laden bioink of the biotrache

129 s governed by their propensity to buckle and delaminate partially, under minute levels of compression

130 n the contact of neural crest cells with the delaminated placode-derived cells.

131 as they proliferate and by the LECs as they delaminate (push/pull coordination).

132 uter nuclear layer (ONL) surrounded by thick delaminated retina with intraretinal hyperreflective les

133 he archenteron, but particularly strongly in delaminating secondary mesenchyme cells.

134 Interestingly, pioneer cells delaminate shortly after ingression.

135 CT(x) MXenes from their chemically unstable delaminated single-layer flakes.

136 genes result in the absence or reduction of delaminating SNSPs; loss of function of neurogenic genes

137 rce-driven rolling-up process can be used to delaminate synthetic SnS(2)/WSe(2) vdW heterostructures

138 ds coalesce into a single gap and eventually delaminate the interface in Li, whereas the voids split

139 fective, thermally insulating structures and delaminates the device from the skin, thereby eliminatin

140 Mechanical peeling then delaminates the PI film from glass along the middle of t

141 In contrast, we show that delaminating the samples at the metal/organic interface

142 As these cardiomyocytes delaminate, the remodeling of adhesion junctions must be

143 manner; live imaging shows that as one cell delaminates, the next cell ratchets up, the dmNes+RG end

144 ng rather than on stresses at the tip of the delaminated tissue.

145 favored, whereas Dia1-negative cells tend to delaminate to a suprabasal compartment.

146 main of the ear epithelium, from which cells delaminate to form the cochleovestibular ganglion, is ex

147 c epithelium and among those neurons that do delaminate to form the CVG.

148 t of cells within the otic vesicle that will delaminate to form the octaval (statoacoustic) ganglion.

149 UiO-67 and two-dimensional hxl UiO-67 can be delaminated to form metal-organic nanosheets.

150 Shortly after generation, BPs delaminate towards the subventricular zone, where they f

151 VIGS, showed no water resistance, completely delaminating upon soaking in water.

152 nthesized COFs (all eight) were successfully delaminated using a simple, safe, and environmentally fr

153 epicardium, migrating epithelial epicardium, delaminated vasculogenic mesenchyme and vascular smooth

154 avian and aquatic species revealed that NCC delaminate via an epithelial-mesenchymal transition (EMT

155 cate zeolite precursor ERB-1P (Si/B = 11) is delaminated via isomorphous substitution of Al for B usi

156 These materials, if delaminated, would prove an interesting new family of 2D

157 nd broad implementation for the synthesis of delaminated zeolite catalysts.