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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.

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