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

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

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

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

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

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

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

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

13 The melanoblasts delaminated and gathered in the carapacial staging area

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

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

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

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

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

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

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

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

22 Delaminating cardiomyocytes accumulate Cdh2-EGFP on the

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

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

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

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

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

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

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

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

31 Flrt2 is exclusively expressed in the fully delaminated epicardium.

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

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

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

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

36 Cells delaminate from epithelial placodes to form sensory gang

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

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

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

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

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

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

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

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

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

46 Neuroblasts that delaminate from the embryonic epithelium require lgl to

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 To delaminate incoherent from coherent boundary scattering,

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

81 Positively charged delaminated layered double hydroxide lactate nanosheets

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

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

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

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

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

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

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

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

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

91 Delaminated neuroblasts in Drosophila function as stem c

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

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

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

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

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

97 Interestingly, pioneer cells delaminate shortly after ingression.

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

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

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

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

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

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

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

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

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

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

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

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