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1 ated EVs, though subsequent pipetting caused reaggregation.
2                                        After reaggregation, 600 islet equivalents of the purified bet
3 sive function of C-cadherin in standard cell reaggregation and additional assays, C-cadherin levels w
4  of the starting material, is stable against reaggregation and can achieve solutions containing exclu
5                                  Both forced reaggregation and endogenous cell mixing reveals how rob
6 n-5 (alpha3beta1 integrin ligand), A431 cell reaggregation and motility functions were markedly impai
7 lly, in vitro cultures and cell dissociation-reaggregation assays suggest that Myo10 may be critical
8                      We have used short-term reaggregation assays to compare the adhesive properties
9 adhesion, promotes cell-sorting behaviors in reaggregation assays, and inhibits medial-lateral cell i
10 l adhesion activity in cell dissociation and reaggregation assays.
11                After transgene silencing and reaggregation culture, the specified cells generate hema
12                                       Thymic reaggregation cultures demonstrated that CD4(+) T cells
13 C, suggest that positive selection in thymus reaggregation cultures is an exclusive property of corti
14                                           In reaggregation cultures with CD81-transfected fibroblasts
15 selection of T cells were examined in thymus reaggregation cultures, a system in which dispersed popu
16 f nanomaterials typically focus on retarding reaggregation, for example via surface modification, as
17 y affects neutrophil aggregation and permits reaggregation in the presence of a heterologous stimulus
18 th-forming capability after dissociation and reaggregation in vitro to investigate the mechanism that
19         We found that after dissociation and reaggregation, incisor, but not molar, mesenchyme exhibi
20  and CD47-overexpressing phenotype and their reaggregation into human HIP pseudoislets (p-islets).
21 onic exfoliation method from graphite, where reaggregation is prevented by the addition of common cat
22 ation of organoid size and shape using quick reaggregation methods, retinal organoids were highly rep
23 tion remained available to pyrene even after reaggregation occurred, suggesting an irreversible effec
24 ed as twin and larger sets by separation and reaggregation of blastomeres of cleavage-stage embryos.
25 spreading on laminin-5, and had no effect on reaggregation of cells plated on collagen I (alpha2beta1
26 s fiber formation, and temperature-dependent reaggregation of FmetHb S suggests that IHP stabilizes p
27 e direct observation of a rapid and specific reaggregation of retinal cell types into two discrete ty
28 nction as a strong stabilizing agent against reaggregation of single-layer nanosheets for greatly imp
29 ation-dispersion, and aggregation-dispersion-reaggregation of the NPs, are observed during the penetr
30 tes homophilic adhesion, as evidenced by the reaggregation of the transfected cells and the specific
31                           Disaggregation and reaggregation of Xnr-2-producing tissues also extends th
32 of hiPSC in 2D cultures followed by a forced reaggregation step that leads to highly enriched (>90% c
33 lar mechanisms thought to promote islet cell reaggregation, summarize methods that optimize pseudoisl
34 diated physiological T-cell development upon reaggregation with T-cell progenitors.