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1  layer 3 appears as a relatively homogeneous cell sheet.
2  extend filopodia at the leading edge of the cell sheet.
3 erall increase in the speed of the migrating cell sheet.
4 M protein and the matrix deposited under the cell sheet.
5 tained level of MAPK activity throughout the cell sheet.
6 rounded cell mass covered with an epithelial cell sheet.
7 ated polarization of cells in the plane of a cell sheet.
8 heet and the other over the perimeter of the cell sheet.
9  polarization of cells within the plane of a cell sheet.
10  polarization of cells within the plane of a cell sheet.
11 oss of transepithelial resistance across the cell sheet.
12 rocesses involve the migration of epithelial cell sheets.
13 lar buds (cellular aggregates) to epithelial cell sheets.
14 n an increase in mechanical integrity of the cell sheets.
15  by digesting agarose blocks imbedded in the cell sheets.
16 ften emerge from mechanical instabilities of cell sheets.
17 e changes and rearrangements within cohesive cell sheets.
18 orphologic appearance of cultured epithelial cell sheets.
19 d on a silicon wafer and lifted as monolayer cell sheets.
20 ntaining cell-to-cell adhesion in epithelial cell sheets.
21 maintaining cell-cell adhesion in epithelial cell sheets.
22 e kind that promotes migration of epithelial cell sheets.
23 hich RasV12 cells are detected in epithelial cell sheets.
24 n the elongation and migration of epithelial cell sheets.
25  to provide mechanical support to epithelial cell sheets.
26  and intercellular stresses in an epithelial cell sheet advancing towards an island on which cells ca
27 (m), one that is summed over the area of the cell sheet and the other over the perimeter of the cell
28 tween discrete and continuum descriptions of cell sheets and can be used to probe a wide range of mor
29                                              Cell-sheet and rhizoid remains occurred separately or to
30  behaviors over multispatial (single cell to cell sheets) and temporal (minutes to weeks) scales.
31 tilage formation in microsphere-incorporated cell sheets, and describe a tailorable system for the ch
32 a stratified epithelium heal by "sliding" of cell sheets as a coherent unit or do individual cells "l
33 ately after injury, propagates deep into the cell sheet, away from the edge, and then rebounds back t
34 apoptotic cells and contributes force(s) for cell sheet bending.
35 on, resulting in formation of a multilayered cell sheet by mid-gastrulation.
36 dence that movements of embryonic epithelial cell sheets can be controlled by ITRs and suggest that s
37                          Wounding epithelial cell sheets causes activation of the EGFR, which trigger
38                           Cultured epidermal cell sheets (CES) containing undifferentiated cells are
39 ngineered cultivated oral mucosal epithelial cell sheets (COMECS) is a promising newly developed trea
40 ed liver tissue in vivo from two-dimensional cell sheets created from small hepatocytes (SHC) and non
41 arly, these 2 scFvs, but not others, induced cell sheet dissociation of cultured human keratinocytes,
42                               Wounds in MDCK cell sheets do not close by purse-string contraction but
43 the final maturation of the adjacent luminal cell sheet during pregnancy.
44 e led to increasingly detailed mechanisms of cell sheet dynamics.
45 trast, the flow-like properties of one-sided cell-sheet expansion in confining geometries are not wel
46  to a tissue (the amnioserosa) that promotes cell-sheet fusion (dorsal closure) in the Drosophila emb
47                         To determine whether cell sheets generated with long-term passaged (P10) agin
48 owerful experimental system for studying how cell sheets give rise to complex three-dimensional struc
49                We expect that this method of cell sheet growth and detachment may be useful for low-c
50       Tissue engineering using whole, intact cell sheets has shown promise in many cell-based therapi
51                              Self-assembling cell sheets have shown great potential for use in cartil
52 e (1 mm i.d.) from aligned human mesenchymal cell sheets (hMSC) as the wall and human endothelial pro
53 as may be a widespread property of polygonal cell sheets in plants and animals.
54 , we derive a continuum plate description of cell sheets, in which the effective tissue properties, s
55  phosphoglycopeptides (sPGPs) transform a 2D cell sheet into 3D cell spheroids.
56 orphogenetic behavior that transforms a flat cell sheet into a pit or groove.
57 rdinated cell shape change drives epithelial cell sheet involution between the oocyte and nurse cell
58                          This opening in the cell sheet is then repopulated, because the cells on the
59  at low density or when an intact epithelial cell sheet is wounded.
60   Replicate cultures were prepared using RPE cell sheets isolated with Dispase from Royal College of
61  wound interface and also continues into the cell sheet, maintaining a sustained level of MAPK activi
62 e long recognized that dramatic bending of a cell sheet may be driven by even modest shrinking of the
63 isting single cell micro-manipulation and 2D cell sheet mechanical stimulation techniques.
64 and appear to pull the superficial epidermal cell sheet medially.
65 ribution to pores characterizing nematophyte cell-sheet microfossils known as Cosmochlaina.
66 explore these issues: comparison of tube and cell-sheet microfossils with experimentally degraded mod
67 quired for muscle attachment and for certain cell sheet migrations during embryogenesis.
68 hila development, provide a model system for cell sheet morphogenesis and wound healing.
69 in dorsal closure, controlling cell fate and cell sheet morphogenesis during embryogenesis.
70 al closure in Drosophila, a model system for cell sheet morphogenesis.
71 We find that Drosophila MYPT is required for cell sheet movement during dorsal closure, morphogenesis
72 on pathways coordinately regulate epithelial cell sheet movement during the process of dorsal closure
73 chain (MHC encoded by zipper is required for cell sheet movements in Drosophila embryos.
74   Dorsal closure is characterized by complex cell sheet movements, driven by multiple tissue specific
75 optotic force is used by the embryo to drive cell-sheet movements during development, a role not clas
76  conserved contractile protein likely drives cell-sheet movements throughout phylogeny.
77 erated from morphologically simple monolayer cell sheets of SHC and NPC.
78              Furthermore, substrate-released cell sheets of wild-type podocytes were readily dissocia
79 ough transplantation of autologous epidermal cell sheets or seeded decellularized biological scaffold
80 the moving edge is shared with an epithelial cell sheet; peripheral microfilament bundles at the lead
81           The dynamic behavior of epithelial cell sheets plays a central role during numerous develop
82 gregates in suspension or substrate-released cell sheets readily dissociated when subjected to mechan
83          Here, we describe a new approach to cell sheet release surfaces based on silicone oil-infuse
84 yospheroid mutants ultimately fails when the cell sheets rip themselves apart, our analysis indicates
85 s form cell streams, which support suspended cell sheets (SCS) of various sizes and curvatures.
86 e study motion within a confluent epithelial cell sheet, simultaneously measuring collective migratio
87 ides with neighboring cells in an epithelial cell sheet that was undergoing migration as a wound-heal
88                                   Within the cell sheet there arise unanticipated fluctuations of mec
89  recapitulate closure dynamics of epithelial cell sheets, they fail to capture how a wounded fibrous
90 rofabrication techniques to allow epithelial cell sheets to migrate into strips whose width was varie
91                       A migrating epithelial cell sheet usually produces finger-like projections of c
92 calculate stress maps in two dimensions, the cell sheet was assumed to behave like an elastic materia
93 etal eyes were dissected on arrival, and RPE cell sheets were mechanically separated from the choroid
94 uces single cell segmentation from confluent cell sheets with high accuracy.
95 a and the rate of seam formation between the cell sheets (zipping), key processes that contribute to

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