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1 oss of transepithelial resistance across the cell sheet.
2  always correlate with stratification of the cell sheet.
3  layer 3 appears as a relatively homogeneous cell sheet.
4  with a thickening and stratification of the cell sheet.
5  extend filopodia at the leading edge of the cell sheet.
6 erall increase in the speed of the migrating cell sheet.
7 M protein and the matrix deposited under the cell sheet.
8 tained level of MAPK activity throughout the cell sheet.
9 rounded cell mass covered with an epithelial cell sheet.
10 ated polarization of cells in the plane of a cell sheet.
11 heet and the other over the perimeter of the cell sheet.
12  polarization of cells within the plane of a cell sheet.
13  polarization of cells within the plane of a cell sheet.
14 d on a silicon wafer and lifted as monolayer cell sheets.
15 ntaining cell-to-cell adhesion in epithelial cell sheets.
16 maintaining cell-cell adhesion in epithelial cell sheets.
17 e kind that promotes migration of epithelial cell sheets.
18 n the elongation and migration of epithelial cell sheets.
19  to provide mechanical support to epithelial cell sheets.
20 tivity in the hiPSC-derived cardiac circular cell sheets.
21  elongated in 2D monolayers to rounded in 3D cell sheets.
22  experiments of confluent corneal epithelial cell sheets.
23 mulating MSC chondrogenic differentiation as cell sheets.
24 nd overall distance covered by the migrating cell sheets.
25  detachment and dissemination from migrating cell sheets.
26 lar buds (cellular aggregates) to epithelial cell sheets.
27 orphologic appearance of cultured epithelial cell sheets.
28 hich RasV12 cells are detected in epithelial cell sheets.
29 ntial of cultivated human corneal epithelial cell sheets.
30 rocesses involve the migration of epithelial cell sheets.
31 n an increase in mechanical integrity of the cell sheets.
32  by digesting agarose blocks imbedded in the cell sheets.
33 ften emerge from mechanical instabilities of cell sheets.
34 expression necessarily persist in stratified cell sheets.
35 e changes and rearrangements within cohesive cell sheets.
36 Furthermore, chondrogenically differentiated cell sheets adhere directly to cartilage surfaces via re
37  and intercellular stresses in an epithelial cell sheet advancing towards an island on which cells ca
38 (m), one that is summed over the area of the cell sheet and the other over the perimeter of the cell
39 tween discrete and continuum descriptions of cell sheets and can be used to probe a wide range of mor
40 rived cardiomyocytes were seeded as circular cell sheets and subjected to different PFA protocols.
41 ssion disrupted the morphology of epithelial cell sheets and three-dimensional cysts ABSTRACT: Collec
42                                              Cell-sheet and rhizoid remains occurred separately or to
43  behaviors over multispatial (single cell to cell sheets) and temporal (minutes to weeks) scales.
44 ape and dynamics of a cell doublet, a planar cell sheet, and a growing cell aggregate.
45 tilage formation in microsphere-incorporated cell sheets, and describe a tailorable system for the ch
46                                   Epithelial cell sheets are often subjected to large-scale deformati
47 a stratified epithelium heal by "sliding" of cell sheets as a coherent unit or do individual cells "l
48 ately after injury, propagates deep into the cell sheet, away from the edge, and then rebounds back t
49 apoptotic cells and contributes force(s) for cell sheet bending.
50 on, resulting in formation of a multilayered cell sheet by mid-gastrulation.
51 dence that movements of embryonic epithelial cell sheets can be controlled by ITRs and suggest that s
52                          Wounding epithelial cell sheets causes activation of the EGFR, which trigger
53                           Cultured epidermal cell sheets (CES) containing undifferentiated cells are
54  of adhesion molecules while maintaining the cell sheets' characteristics.
55 and folding of a distinct epithelial surface cell sheet characterized by strong cell-matrix adhesions
56 ngineered cultivated oral mucosal epithelial cell sheets (COMECS) is a promising newly developed trea
57 ut its effects when activated in PDLSCs as a cell sheet construct and how it would impact bone format
58 mpelling evidence that this SMC-EPC bi-level cell sheet construct can be a promising therapy to repai
59 ared, exploiting spontaneous post-detachment cell sheet contraction, and chondrogenically induced.
60 culture-adherent tension induced spontaneous cell sheet contraction, reducing the diameter 2.4-fold,
61 ed liver tissue in vivo from two-dimensional cell sheets created from small hepatocytes (SHC) and non
62  the world's first use of corneal epithelial cell sheets derived from human induced pluripotent stem
63      To this end, we used corneal epithelial cell sheets detached from the corneas of 2- and 14-month
64 ss magnitude must be reached to overcome the cell sheet displacement barrier.
65 omyosin-based system that facilitates global cell sheet displacements upon serum-stimulated exit from
66 arly, these 2 scFvs, but not others, induced cell sheet dissociation of cultured human keratinocytes,
67                               Wounds in MDCK cell sheets do not close by purse-string contraction but
68 tractile forces near the apical surface of a cell sheet drive out-of-the-plane bending of the sheet a
69 the final maturation of the adjacent luminal cell sheet during pregnancy.
70 e led to increasingly detailed mechanisms of cell sheet dynamics.
71 ions from arrays of many tissues, and we use cell sheet engineering techniques to transfer these comp
72 trast, the flow-like properties of one-sided cell-sheet expansion in confining geometries are not wel
73                        Engineered epithelial cell sheets for clinical replacement of non-functional u
74  to a tissue (the amnioserosa) that promotes cell-sheet fusion (dorsal closure) in the Drosophila emb
75                         To determine whether cell sheets generated with long-term passaged (P10) agin
76 owerful experimental system for studying how cell sheets give rise to complex three-dimensional struc
77                We expect that this method of cell sheet growth and detachment may be useful for low-c
78 on using cultivated human corneal epithelial cell sheets has been used successfully to treat limbal s
79       Tissue engineering using whole, intact cell sheets has shown promise in many cell-based therapi
80                              Self-assembling cell sheets have shown great potential for use in cartil
81 onfluent 2-dimensional hiPSC-derived cardiac cell sheets (hiPSC-CCSs) and optical mapping.
82 e (1 mm i.d.) from aligned human mesenchymal cell sheets (hMSC) as the wall and human endothelial pro
83 geneic human iPSC-derived corneal epithelial cell sheets (iCEPSs) were transplanted onto affected eye
84 as may be a widespread property of polygonal cell sheets in plants and animals.
85             p63 was present in all expanding cell sheets in the first 9 days of culture, but it's pre
86 he emergent collective behavior of migrating cell sheets in vitro has been shown to be disrupted in t
87 , we derive a continuum plate description of cell sheets, in which the effective tissue properties, s
88                                     These 3D cell sheets' initial thickness and cellular densities ma
89  phosphoglycopeptides (sPGPs) transform a 2D cell sheet into 3D cell spheroids.
90 orphogenetic behavior that transforms a flat cell sheet into a pit or groove.
91 rdinated cell shape change drives epithelial cell sheet involution between the oocyte and nurse cell
92 upled to the collective elastic modes of the cell sheet is sufficient to produce swirl-like correlati
93                          This opening in the cell sheet is then repopulated, because the cells on the
94  at low density or when an intact epithelial cell sheet is wounded.
95   Replicate cultures were prepared using RPE cell sheets isolated with Dispase from Royal College of
96  wound interface and also continues into the cell sheet, maintaining a sustained level of MAPK activi
97 e long recognized that dramatic bending of a cell sheet may be driven by even modest shrinking of the
98 isting single cell micro-manipulation and 2D cell sheet mechanical stimulation techniques.
99 and appear to pull the superficial epidermal cell sheet medially.
100 ribution to pores characterizing nematophyte cell-sheet microfossils known as Cosmochlaina.
101 explore these issues: comparison of tube and cell-sheet microfossils with experimentally degraded mod
102                                              Cell sheet microstructure was analyzed through light, sc
103 quired for muscle attachment and for certain cell sheet migrations during embryogenesis.
104 hila development, provide a model system for cell sheet morphogenesis and wound healing.
105 in dorsal closure, controlling cell fate and cell sheet morphogenesis during embryogenesis.
106 al closure in Drosophila, a model system for cell sheet morphogenesis.
107 We find that Drosophila MYPT is required for cell sheet movement during dorsal closure, morphogenesis
108 on pathways coordinately regulate epithelial cell sheet movement during the process of dorsal closure
109 chain (MHC encoded by zipper is required for cell sheet movements in Drosophila embryos.
110   Dorsal closure is characterized by complex cell sheet movements, driven by multiple tissue specific
111 optotic force is used by the embryo to drive cell-sheet movements during development, a role not clas
112  conserved contractile protein likely drives cell-sheet movements throughout phylogeny.
113 erated from morphologically simple monolayer cell sheets of SHC and NPC.
114              Furthermore, substrate-released cell sheets of wild-type podocytes were readily dissocia
115                    The transplanted bi-level cell sheet on the ischemic heart provides a biomimetic m
116 ough transplantation of autologous epidermal cell sheets or seeded decellularized biological scaffold
117 the moving edge is shared with an epithelial cell sheet; peripheral microfilament bundles at the lead
118 cle cells (SMC) as a scaffold-free, bi-level cell sheet platform to improve ventricular remodeling an
119           The dynamic behavior of epithelial cell sheets plays a central role during numerous develop
120 gregates in suspension or substrate-released cell sheets readily dissociated when subjected to mechan
121          Here, we describe a new approach to cell sheet release surfaces based on silicone oil-infuse
122 ns within the hiPSC-derived cardiac circular cell sheets, resulting in areas of conduction block.
123 yospheroid mutants ultimately fails when the cell sheets rip themselves apart, our analysis indicates
124 s form cell streams, which support suspended cell sheets (SCS) of various sizes and curvatures.
125 e study motion within a confluent epithelial cell sheet, simultaneously measuring collective migratio
126 lated the collective migration of epithelial cell sheets Stimulation with epidermal growth factor, a
127 lamide) (PNIPAm) is widely used to fabricate cell sheet surfaces for cell culturing, however copolyme
128                This review aims to introduce cell sheet technology as a breakthrough cell therapy wit
129  this end, this study explored scaffold-free cell sheet technology as a new 3D platform.
130  Together, these data support the utility of cell sheet technology for fabricating scaffold-free, hya
131                                              Cell sheet technology maintains cell functionality as sc
132 tunities and anticipated clinical impacts of cell sheet technology using MSCs are discussed.
133 ides with neighboring cells in an epithelial cell sheet that was undergoing migration as a wound-heal
134                                   Within the cell sheet there arise unanticipated fluctuations of mec
135  recapitulate closure dynamics of epithelial cell sheets, they fail to capture how a wounded fibrous
136 SC therapeutic potency can be enhanced by 3D cell sheet tissue structure.
137                        On transferring these cell sheets to a confluent layer of fibroblasts, the epi
138 rofabrication techniques to allow epithelial cell sheets to migrate into strips whose width was varie
139 der zone myocardium, were observed following cell sheet transplantation.
140 , this study developed a new allogeneic stem cell sheet using human umbilical cord mesenchymal stem c
141 ality of cultivated human corneal epithelial cell sheets using time-lapse imaging of the cell culture
142                       A migrating epithelial cell sheet usually produces finger-like projections of c
143 calculate stress maps in two dimensions, the cell sheet was assumed to behave like an elastic materia
144             On confocal scanning, epithelial cell sheets were detected in the interface leading to th
145 etal eyes were dissected on arrival, and RPE cell sheets were mechanically separated from the choroid
146    Epithelial monolayers are two-dimensional cell sheets which compartmentalize the body and organs o
147 uces single cell segmentation from confluent cell sheets with high accuracy.
148 a and the rate of seam formation between the cell sheets (zipping), key processes that contribute to

 
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